Patent Application
20210010072
The present disclosure relates to a device, a preparator's skill evaluating method, program, and device, and a testing device performance evaluating method, program, and device.
Polymerase chain reactions (PCR) and quantitative polymerase chain reactions (qPCR) are used for, for example, qualitative evaluation and quantitative evaluation of nucleic acids. Lately, PCR is also used for, for example, negative tests for genetically modified crops or foods (GMO) and negative tests for virus contamination. Therefore, it is demanded that reliability of the results be ensured.
For ensuring the results, ensurance of device performance and management of measuring systems have been carried out based on device temperature control management and users' maintenance management.
A series of nucleic acid samples used for qualitative evaluation and quantitative evaluation of nucleic acids are produced by serial dilution of a nucleic acid sample having a known concentration. For example, there has been proposed a method for diluting DNA fragments having a specific base sequence by a limiting dilution method and selecting a diluted solution including the intended copy number based on the result of real-time PCR of the obtained diluted solutions (for example, see PTL 1).
There has also been proposed a standard nucleic acid kit obtained by sealing standard nucleic acid solutions serially diluted to different concentrations in a plurality of sample filling portions (for example, see PTL 2).
Further, for management of the measuring systems, it has been proposed to ensure the results of measurement based on temperature management during PCR reactions (for example, see NPL 1).
In recent years, real-time polymerase chain reactions (real-time PCR) have become increasingly important in qualitation and quantification in genetic testing. Performance evaluation for real-time polymerase chain reactions, particularly, inter-device or inter-facility performance evaluation is important. Currently, calibration curves based on external standards utilizing absorbance are used. However, these calibration curves do not accurately prescribe the absolute numbers of nucleic acids. Particularly, the failure to accurately prescribe the absolute numbers is considerably influential for low copy numbers.
A series of nucleic acid samples for such calibration curves are produced by serial dilution of a nucleic acid sample having a known concentration. For example, there has been proposed a method for diluting DNA fragments having a specific base sequence by a limiting dilution method and selecting a diluted solution including the intended copy number based on the result of real-time PCR of the obtained diluted solutions (for example, see PTL 1).
Recently, there has also been proposed a method of introducing a specific number (copy number) of DNA fragment molecules into cells by a gene recombination technique, culturing the cells, and isolating the cultured cells by manipulation, to prepare a sample containing one copy of DNA having an intended base sequence (for example, see PTL 3).
The present disclosure has an object to provide a device used for appropriately evaluating the skill of a preparator who prepares a reagent composition, or a device capable of appropriately evaluating in-plane uniformity of a testing device, inter-testing device performance, and inter-testing facility performance.
According to one aspect of the present disclosure, a device includes a plurality of wells, and two or more groups into which the wells are divided to be varied in composition in the wells.
The present disclosure can provide a device used for appropriately evaluating the skill of a preparator who prepares a reagent composition, or a device capable of appropriately evaluating in-plane uniformity of a testing device, inter-testing device performance, and inter-testing facility performance.
(Device)
A device of the present disclosure includes a plurality of wells, and two or more groups into which the wells are divided to be varied in composition in the wells. The device further includes other members as needed.
It is preferable that the device of the present disclosure include a plurality of wells in each of which a reagent composition containing an amplifiable reagent in a specific copy number is located, and two or more groups into which the wells are divided to have the amplifiable reagent located in the same specific copy number but to be varied in composition of the reagent composition except for the specific copy number.
The device of the present disclosure is based on the following finding. Existing diluting methods may probabilistically result in failure to fill some portions with copies or may result in failure to locate a copy as designed when the absolute number to be located is only one copy. Therefore, the performance of a measuring system cannot be evaluated with a high accuracy.
The device of the present disclosure is also based on the following finding. With existing standard nucleic acid kits, it has been impossible to overcome a problem that probabilistic variation of sample nucleic acids in a low copy number region is not taken into consideration.
The device of the present disclosure is also based on the following finding. Existing methods for evaluating measuring systems have evaluated the measuring systems only based on temperature, which is an indirect factor, and have not been able to appropriately evaluate influences on the measuring systems due to manual operations.
The device of the present disclosure including two or more groups of wells between which the specific copy number of the amplifiable reagent contained in the reagent composition is the same but the composition of the reagent composition is varied except for the specific copy number can be used for appropriately evaluating the skill of a preparator who prepares a reagent composition. Note that the copy number of the amplifiable reagent may be associated with the number of molecules.
It is preferable that the device of the present disclosure include a plurality of wells in each of which an amplifiable reagent is located in a specific copy number, and two or more groups into which the wells are divided to be varied in the specific copy number of the amplifiable reagent.
The device of the present disclosure is based on the following finding. Existing diluting methods may probabilistically result in failure to fill some portions with copies or may result in failure to locate a copy as designed when the absolute number to be located is only one copy. Therefore, existing diluting methods cannot be used for evaluation of an in-plane property of a testing device and quantitative evaluation.
The device of the present disclosure is also based on the following finding. Existing methods employing manipulation are techniques relating to the method for preparing a sample solution. Performance evaluation for testing devices is neither described nor suggested. Besides, these techniques are problematic in throughput.
The device of the present disclosure including two or more groups into which a plurality of wells in each of which an amplifiable reagent is located in a specific copy number are divided such that the specific copy number of the amplifiable reagent is varied between the groups makes it possible to appropriately evaluate in-plane uniformity of a testing device, inter-testing device performance, and inter-testing facility performance.
When the same base sequence is not to be introduced in a plural number into one molecule, “a number of molecules” may be used in the same meaning as “a copy number”.
<Well>
For example, the shape, the number, the volume, the material, and the color of the well are not particularly limited and may be appropriately selected depending on the intended purpose.
The shape of the well is not particularly limited and may be appropriately selected depending on the intended purpose so long as a reagent composition containing an amplifiable reagent in a specific copy number can be located in the well. Examples of the shape of the well include: concaves such as a flat bottom, a round bottom, a U bottom, and a V bottom; and sections on a substrate.
The number of wells is preferably a plural number of 2 or greater, more preferably 5 or greater, and yet more preferably 50 or greater.
A multi-well plate with the number of wells of 2 or greater is suitably used.
Examples of the multi-well plate include a 24-well, 48-well, 96-well, 384-well, or 1,536-well plate.
The volume of the well is not particularly limited, may be appropriately selected depending on the intended purpose, and is preferably 10 microliters or greater but 1,000 microliters or less in consideration of the amount of a sample used in a common nucleic acid testing device.
The material of the well is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the material of the well include polystyrene, polypropylene, polyethylene, fluororesins, acrylic resins, polycarbonate, polyurethane, polyvinyl chloride, and polyethylene terephthalate.
Examples of the color of the well include transparent colors, semi-transparent colors, chromatic colors, and complete light-shielding colors.
Wettability of the well is not particularly limited and may be appropriately selected depending on the intended purpose. The wettability of the well is preferably water repellency. When the wettability of the well is water repellency, adsorption of the amplifiable reagent to the internal wall of the well can be reduced. Further, when the wettability of the well is water repellency, the amplifiable reagent, a primer, and an amplifying reagent in the well can be moved in a state of a solution.
The method for imparting water repellency to the internal wall of the well is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include a method of forming a fluororesin coating film, a fluorine plasma treatment, and an embossing treatment. Particularly, by applying a water repellency imparting treatment that imparts a contact angle of 100 degrees or greater, it is possible to suppress reduction of the amplifiable reagent due to spill of the liquid and suppress increase of uncertainty (or coefficient of variation).
<Base Material>
The device is preferably a plate-shaped device obtained by providing a well in a base material, but may be linking-type well tubes such as 8-series tubes.
For example, the material, the shape, the size, and the structure of the base material are not particularly limited and may be appropriately selected depending on the intended purpose.
The material of the base material is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the material of the base material include semiconductors, ceramics, metals, glass, quartz glass, and plastics. Among these materials, plastics are preferable.
Examples of the plastics include polystyrene, polypropylene, polyethylene, fluororesins, acrylic resins, polycarbonate, polyurethane, polyvinyl chloride, and polyethylene terephthalate.
The shape of the base material is not particularly limited and may be appropriately selected depending on the intended purpose. For example, board shapes and plate shapes are preferable.
The structure of the base material is not particularly limited, may be appropriately selected depending on the intended purpose, and may be, for example, a single-layer structure or a multilayered structure.
<Identifier Unit>
It is preferable that the device include an identifier unit that enables identifying information on the specific copy number of the amplifiable reagent.
The identifier unit is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the identifier unit include a memory, an IC chip, a barcode, a QR code (registered trademark), a Radio Frequency Identifier (hereinafter may also be referred to as “RFID”), color coding, and printing.
The position at which the identifier unit is provided and the number of identifier units are not particularly limited and may be appropriately selected depending on the intended purpose.
Examples of the information to be stored in the identifier unit include not only the information on the specific copy number of the amplifiable reagent, but also results of analyses (for example, activity value and emission intensity), the number of amplifiable reagents (for example, the number of cells), whether cells are alive or dead, a copy number of a specific base sequence, which of a plurality of wells is filled with the amplifiable reagent, the kind of the amplifiable reagent, the measurement date and time, and the name of the person in charge of measurement.
The information stored in the identifier unit can be read with various kinds of reading units. For example, when the identifier unit is a barcode, a barcode reader is used as the reading unit.
The method for writing information in the identifier unit is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include manual input, a method of directly writing data through a liquid droplet forming device configured to count the number of amplifiable reagents during dispensing of the amplifiable reagents into the wells, transfer of data stored in a server, and transfer of data stored in a cloud system.
<Other Members>
The other members are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the other members include a sealing member.
—Sealing Member—
It is preferable that the device include a sealing member in order to prevent mixing of foreign matters into the wells and outflow of the filled materials.
It is preferable that the sealing member be configured to be capable of sealing at least one well and separable at a perforation in order to be capable of sealing or opening each one of the wells individually.
The shape of the sealing member is preferably a cap shape matching the inner diameter of a well, or a film shape for covering the well opening.
Examples of the material of the sealing member include polyolefin resins, polyester resins, polystyrene resins, and polyamide resins.
It is preferable that the sealing member have a film shape that can seal all wells at a time. It is also preferable that the sealing member be configured to have different adhesive strengths for wells that need to be reopened and wells that need not, in order that the user can reduce improper use.
The device of the present disclosure includes a plurality of wells, and reagent compositions located in the plurality of wells and each containing an amplifiable reagent in a specific copy number.
A copy number means the number of target or specific base sequences in an amplifiable reagent contained in the well.
The target base sequence refers to a base sequence including defined base sequences in at least primer and probe regions. Specifically, a base sequence having a defined total length is also referred to as specific base sequence.
A specific copy number refers to the aforementioned copy number that specifies the number of target base sequences at accuracy of a certain level or higher.
This means that the specific copy number is known as the number of target base sequences actually contained in a well. That is, the specific copy number in the present disclosure is more accurate or reliable as a number than a predetermined copy number (calculated estimated value) obtained according to existing serial dilution methods, and is a controlled value that has no dependency on a Poisson distribution even if the value is within a low copy number region of 1,000 or lower in particular. When it is said that the specific copy number is a controlled value, it is preferable that a coefficient of variation CV expressing uncertainty roughly satisfy either CV<1/√x with respect to an average copy number x or CV≤20%. Hence, use of a device including wells in which a target base sequence is contained in the specific copy number makes it possible to perform qualitative or quantitative testing of samples containing the target base sequence more accurately than ever.
When the number of target base sequences and the number of nucleic acid molecules including the sequence coincide with each other, “copy number” and “number of molecules” may be associated with each other.
Specifically, for example, in the case of norovirus, when the number of viruses is 1, the number of nucleic acid molecules is 1 and the specific copy number is 1. In the case of yeast at a GI phase, when the number of yeast cells is 1, the number of nucleic acid molecules (the number of same chromosomes) is 1 and the specific copy number is 1. In the case of human cell at a G0/GI phase, when the number of human cells is 1, the number of nucleic acid molecules (the number of same chromosomes) is 2 and the copy number is 2.
Further, in the case of yeast at a GI phase having the target base sequence introduced at two positions, when the number of yeast cells is 1, the number of nucleic acid molecules (the number of same chromosomes) is 1 and the copy number is 2.
In the present disclosure, a specific copy number of the amplifiable reagent may also be referred to as absolute number of the amplifiable reagent.
When there are a plurality of wells containing the amplifiable reagent, it is at least needed that the amplifiable reagent be contained in the wells in the same specific copy number.
When it is said that the amplifiable reagent is contained in the wells in the same specific copy number, it is meant that the variation in the number of amplifiable reagents is within a tolerable range, where the variation occurs when the amplifiable reagents are filled in the device. Whether the variation in the number of amplifiable reagents is within the tolerable range can be determined based on information on uncertainty described below.
Information on the specific copy number of the amplifiable reagent is not particularly limited and may be appropriately selected depending on the intended purpose so long as the information is information regarding the amplifiable reagent in the device. Examples of the information include information on uncertainty, information on a carrier described below, and information on the amplifiable reagent.
“Uncertainty” is defined in ISO/IEC Guide 99:2007 [International Vocabulary of Metrology-Basics and general concepts and related terms (VIM)] as “a parameter that characterizes measurement result-incidental variation or dispersion of values rationally linkable to the measured quantity”.
Here, “values rationally linkable to the measured quantity” means candidates for the true value of the measured quantity. That is, uncertainty means information on the variation of the results of measurement due to operations and devices involved in production of a measurement target. With a greater uncertainty, a greater variation is predicted in the results of measurement.
For example, the uncertainty may be standard deviation obtained from the results of measurement, or a half value of a reliability level, which is expressed as a numerical range in which the true value is contained at a predetermined probability or higher. The uncertainty may be calculated according to the methods based on, for example, Guide to the Expression of Uncertainty in Measurement (GUM:ISO/IEC Guide 98-3), and Japan Accreditation Board Note 10, Guideline on Uncertainty in Measurement in Test. As the method for calculating the uncertainty, for example, there are two types of applicable methods: a type-A evaluation method using, for example, statistics of the measured values, and a type-B evaluation method using information on uncertainty obtained from, for example, calibration certificate, manufacturer's specification, and information open to the public.
All uncertainties due to factors such as operations and measurement can be expressed by the same reliability level, by conversion of the uncertainties to standard uncertainty. Standard uncertainty indicates variation in the average value of measured values.
In an example method for calculating the uncertainty, for example, factors that may cause uncertainties are extracted, and uncertainties (standard deviations) due to the respective factors are calculated. Then, the calculated uncertainties due to the respective factors are synthesized according to the sum-of-squares method, to calculate a synthesized standard uncertainty. In the calculation of the synthesized standard uncertainty, the sum-of-squares method is used. Therefore, a factor that causes a sufficiently small uncertainty can be ignored, among the factors that cause uncertainties.
In the device of the present disclosure, a coefficient of variation of the amplifiable reagent filled in the wells may be used as the information on the uncertainty. The coefficient of variation means a relative value of the variation in the number of cells (or the number of amplifiable reagents) filled in each concave, where the variation occurs when cells are filled in the concave. That is, the coefficient of variation means the filling accuracy in terms of the number of cells (or amplifiable reagents) filled in the concave. The coefficient of variation is a value obtained by dividing standard deviation G by an average value x. Here, the coefficient of variation CV is assumed to be a value obtained by dividing standard deviation G by an average copy number (average number of copies filled) x. In this case, a relational expression represented by Formula 1 below is established.
Generally, cells (or amplifiable reagents) have a random distribution state of a
Poisson distribution in a dispersion liquid. Therefore, in a random distribution state by a serial dilution method, i.e., of a Poisson distribution, standard deviation σ can be regarded as satisfying a relational expression represented by Formula 2 below with an average copy number x. Hence, in the case where a dispersion liquid of cells (or amplifiable reagents) is diluted by a serial dilution method, when coefficients of variation CV (CV values) for average copy numbers x are calculated according to Formula 3 below derived from Formula 1 above and Formula 2 based on the standard deviation σ and the average copy numbers x, the results are as presented in Table 1 and
From the results of Table 1 and
As regards the copy number of the amplifiable reagent, it is preferable that the coefficient of variation CV and an average specific copy number x of the amplifiable reagent satisfy a relationship: CV<1/√x, and more preferably satisfy CV<1/2√x.
As regards the information on the uncertainty, it is preferable that the device include a plurality of wells in each of which the amplifiable reagent is contained, and that the information on the uncertainty include information on uncertainty of the device as a whole based on the specific copy number of the amplifiable reagent contained in each well.
There are some conceivable factors that cause uncertainties. For example, in a production process of introducing the intended amplifiable reagent into cells and dispensing the cells while counting the number of cells, examples of the conceivable factors include the number of amplifiable reagents in a cell (for example, the cell cycl of the cell), the unit configured to locate the cells in the device (including any outcomes of operations of an inkjet device or each section of the device, such as operation timings of the device, and the number of cells included in a liquid droplet when the cell suspension is formed into the form of a liquid droplet), the frequency at which cells are located at appropriate positions of the device (for example, the number of cells located in a well), and contamination due to destruction of cells in a cell suspension and consequent mixing of the amplifiable reagent into the cell suspension (hereinafter may also be described as mixing of contaminants).
Examples of information on the number of the amplifiable reagent as the information on the amplifiable reagent include information on uncertainty of the number of amplifiable reagents contained in the device.
In addition to the amplifiable reagent in the specific copy number, the reagent composition contains components needed for amplifying the amplifiable reagent (for example, a nucleic acid), and, for example, contains a primer and an amplifying reagent.
A primer is a synthetic oligonucleotide having a complementary base sequence that includes 18 or more but 30 or less bases and is specific to a template DNA of a polymerase chain reaction (PCR). A pair of primers, namely a forward primer and a reverse primer, are set at two positions in a manner to sandwich the region to be amplified.
Examples of the amplifying reagent for, for example, a polymerase chain reaction (PCR) include enzymes such as DNA polymerase, matrices such as the four kinds of bases (dGTP, dCTP, dATP, and dTTP), Mg2+ (2 mM magnesium chloride), and a buffer for maintaining the optimum pH (pH of from 7.5 through 9.5).
The state of the amplifiable reagent, a primer, and an amplifying reagent in the well is not particularly limited and may be appropriately selected depending on the intended purpose. For example, the state of the amplifiable reagent, a primer, and an amplifying reagent may be a state of either a solution or a solid. In terms of convenience of use, the state of the amplifiable reagent, a primer, and an amplifying reagent is particularly preferably a state of a solution. In a state of a solution, a user can use the amplifiable reagent, a primer, and an amplifying reagent for a test immediately. In terms of transportation, the state of the amplifiable reagent, a primer, and an amplifying reagent is particularly preferably a state of a solid and more preferably a dry state. In a solid dry state, a reaction speed at which the amplifiable reagent is decomposed by, for example, a breakdown enzyme, can be reduced, and storage stability of the amplifiable reagent, a primer, and an amplifying reagent can be improved.
It is preferable that the amplifiable reagent, a primer, and an amplifying reagent be filled in appropriate amounts in the device in the solid dry state, in order to make it possible to use the amplifiable reagent, a primer, and an amplifying reagent in the form of a reaction solution immediately by dissolving the amplifiable reagent, a primer, and an amplifying reagent in a buffer or water immediately before use of the device.
The drying method is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the drying method include freeze drying, heating drying, hot-air drying, vacuum drying, steam drying, suction drying, infrared drying, barrel drying, and spin drying.
The device includes two or more groups of wells between which the specific copy number of the amplifiable reagent is the same but the composition of the reagent composition is varied except for the specific copy number. For example, when the base material of the device is a plate including a plurality of wells, a “region” of each group is formed on the plate by each group. Two or more regions between which the specific copy number of the amplifiable reagent in the reagent composition is varied may adjoin each other or may be apart from each other.
For example, being varied in composition except for the specific copy number of the amplifiable reagent means that it is possible to provide combinations that may or may not contain any other primer or amplifying reagent than the nucleic acid serving as the amplifiable reagent. For example, a first group of the device includes (1) a composition containing a nucleic acid, a primer, and an amplifying reagent, a second group of the device includes (2) a composition containing a nucleic acid and a primer, and a third group of the device includes (3) a composition containing only a nucleic acid. A preparator adds at least any one of a primer and an amplifying reagent to the compositions of (2) and (3) by a manual operation in preparation of the reagent composition, and use the reagent composition for a PCR reaction. Hence, the device enables, for example, evaluation of the skill of a preparator who prepares the reagent composition.
When a nucleic acid is used as the amplifiable reagent, examples of the skill of the preparator include a pipetting operation, an amount of the amplifying reagent to be prepared, and addition of a reagent to a well plate.
In preparation, the preparator may have a previous knowledge of the kinds, amounts, and concentrations of nucleic acids, primers (or primer sets including a plurality of kinds of primers), and amplifying reagents to be contained in the respective groups of the device used. This makes it also possible for the preparator to prepare the reagent composition in a manner to suit to the kinds, amounts, and concentrations in the respective groups, and use the reagent composition for a PCR reaction. This enables more appropriate evaluation of the skill of the preparator.
Further, it is possible to employ a mode in which the device includes a plurality of wells, and reagent compositions located in the plurality of wells and each containing at least a composition selected from the group consisting of an amplifiable reagent, a primer, and an amplifying reagent, wherein the reagent compositions include two or more groups varied in the composition.
This configuration makes it possible to evaluate the skill of a preparator who prepares arbitrary compositions.
Furthermore, it is preferable that the device include groups varied from each other in the specific copy number of the amplifiable reagent. That is, it is preferable that there be two or more specific copy numbers of the amplifiable reagent varied between one well and any other well(s). Examples of the combination of the two or more specific copy numbers include a combination of 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10, a combination of 1, 3, 5, 7, and 9, and a combination of 2, 4, 6, 8, and 10.
In the device of the present disclosure, it is preferable that the specific copy number of the amplifiable reagent in one well be 10N1, and that the specific copy number of the amplifiable reagent in another well be 10N2 (where N1 and N2 are mutually continuous integers). Examples of the combination of such specific copy numbers include a combination of 1, 10, 100, and 1,000, and a combination of 100, 1,000, 10,000, 100,000, and 1,000,000. Hence, a calibration curve for a wide range ranging from a low copy number to a high copy number can be easily generated with the device of the present disclosure.
The device of the present disclosure includes two or more groups of wells varied in the specific copy number of the amplifiable reagent. For example, when the base material of the device is a plate including a plurality of wells, a “region” of each group is formed on the plate by each group. In the “regions” formed by two or more groups between which the specific copy number of the amplifiable reagent is varied, wells may adjoin each other or may be apart from each other.
Hence, when a testing device subjected to real-time PCR, which is one kind of performance evaluation, using the device of the present disclosure turns out to include a well (an unqualified well) unsuitable for use as compared with another well present at a different position and sharing the same specific copy number, it is possible to judge whether to calibrate the testing device by real-time PCR again or to exclude the unqualified well from actual sample application. Furthermore, by measuring a testing device on a regular basis using the device of the present disclosure, it is possible to obtain information on temporal changes of Ct value at an in-plane position of the testing device and evaluate an in-plane property of the testing device based on the information. Moreover, use of devices on which the same specific copy number is located enables comparison between a testing device subjected to measurement and another testing device.
It is preferable that at least one group of the groups of wells be a group in which the specific copy number of the amplifiable reagent is close to the limit of detection.
The limit of detection (LOD) represents the least copy number of amplifiable reagent detectable by a method that can detect an amplifiable reagent (for example, a nucleic acid). The limit of detection is not particularly limited, may be appropriately selected depending on a measuring method, and may be, for example, average value+3σ.
In the present specification, when there are sample sets varied in the specific copy number and each including 21 samples with the same specific copy number, and any of the sample sets result(s) in non-detection from one sample among the 21 samples (corresponding to 2σ judged by a probability of 95%), the least copy number among the specific copy numbers of such sample sets may be used as the limit of detection.
Being close to the limit of detection means a copy number in a range of ±1 from the limit of detection copy number.
It is assumed that the device of the present disclosure includes at least a group in which the specific copy number of the amplifiable reagent is close to the limit of detection. For example, it is assumed that the device of the present disclosure includes groups with the specific copy number of the amplifiable reagent of “1”, “2”, “3”, “4”, and “5”, respectively. In this case, when a testing device subjected to performance evaluation using the device of the present disclosure turns out to be able to amplify the amplifiable reagent in the groups with the specific copy number of “3” or greater but unable to amplify the amplifiable reagent in the groups with the specific copy number of “2” or less, it can be revealed that the lower limit value representing the limit of detection of the specific copy number of the amplifiable reagent in the testing device is “3”. Furthermore, when another similar testing device subjected to performance evaluation using the device of the present disclosure turns out to be able to amplify the amplifiable reagent in the groups with the specific copy number of “4” or greater but unable to amplify the amplifiable reagent in the groups with the specific copy number of “3” or less, it can be revealed that the lower limit value representing the limit of detection of the specific copy number of the amplifiable reagent in the testing device is “4”. Hence, it is possible to determine the least specific copy number of the amplifiable reagent detectable by a testing device.
It is preferable that at least one group among the groups in which the amplifiable reagent is located in specific copy numbers be a group in which the specific copy number of the amplifiable reagent is a copy number greater than a limit of quantification.
The limit of quantification (LOQ) indicates the least copy number of amplifiable reagent quantifiable by a method that can quantify an amplifiable reagent (for example, a nucleic acid), where “quantifiable” means that the result of quantification can be sufficiently reliable. The limit of quantification is not particularly limited and may be appropriately selected depending on a measuring method.
In the present specification, a value representing a copy number deviating from linearity of a calibration curve generated using samples formed of a plurality of molecular species (for example, a plurality of nucleic acid samples with different specific numbers of molecules (with different copy numbers)) may be used as the limit of quantification. Alternatively, uncertainty of a calibration curve may be expressed by CV value. In a graph plotting CV value by representing copy number on a horizontal axis and Ct value on a vertical axis, for example, a value (a copy number) with a CV value of lower than 5% or 10% may be used as the limit of quantification.
In a quantitative evaluation, not a Ct value per se, but a number of molecules (a copy number or a concentration) corresponding to a Ct value can be obtained from a calibration curve and PCR efficiency. Therefore, the limit of quantification may be set based on CV value converted to a number of molecules (a copy number or a concentration).
When the device of the present disclosure includes at least a group in which the specific copy number of the amplifiable reagent (for example, a nucleic acid) is a copy number greater than the limit of quantification, for example, it is possible to determine the least specific copy number of the amplifiable reagent that can be ensured quantitative detection by a testing device, like it is possible to find a testing device to be capable of ensuring quantitative detection when the specific copy number of the amplifiable reagent is 10 or greater, and find another testing device to be capable of ensuring quantitative detection when the specific coy number of nucleic acid is 20 or greater.
In the device of the present disclosure, it is preferable that at least one group of the groups of wells be a negative control group in which the specific copy number of the amplifiable reagent is 0.
With at least one group of the groups of wells provided as a negative control group in which the specific copy number of the amplifiable reagent is 0 in the device of the present disclosure, any detection of an amplifiable reagent from the negative control group suggests abnormality of the detection system (the reagent or the device). With the negative control group provided in the device, the user can immediately recognize a problem when the problem occurs, and can stop the measurement and inspect the root of the problem.
In the device of the present disclosure, it is preferable that at least one group of the groups of wells be a positive control group in which the specific copy number of the amplifiable reagent is 100 or greater.
With at least one group of the groups of wells provided as a positive control group in which the specific copy number of the amplifiable reagent is 100 or greater in the device of the present disclosure, any non-detection of an amplifiable reagent from the positive control group suggests abnormality of the detection system (the reagent or the device). With the positive control group provided in the device, the user can immediately recognize a problem when the problem occurs, and can stop the measurement and inspect the root of the problem.
In the device of the present disclosure, it is further preferable that at least one group of the groups of wells be a group (a group with the least copy number) having the least copy number except for the negative control group, and that the group with the least copy number be positioned at least at wells that are approximately at the periphery of the device.
Wells that are approximately at the periphery means wells on the outermost periphery and wells on some lines that are inward from the outermost periphery among the wells arranged two-dimensionally on the device. Examples of the wells on the outermost periphery and the wells on some lines that are inward from the outermost periphery include wells on the first line or a line with a greater ordinal number but on the 47th line or a line with a less ordinal number.
Unlike the wells positioned near the center of the device, the wells positioned on the outermost periphery of the device have no other wells on the outer side and define the boundary between the device and the outside of the device. Therefore, (1) the wells on the outermost periphery physically have uneven thermal conduction on the device, and (2) the wells on the outermost periphery are susceptible to temperature fluctuating factors of a PCR device because the wells are set on the periphery of a temperature controlling member, which is a component constituting the PCR device. Therefore, by at least one group of the groups of wells being provided in the device of the present disclosure as a group (a group with the least copy number) having the least copy number except for the negative control group and by the group with the least copy number being positioned at least at the wells that are approximately at the periphery of the device, it is possible to detect failures of the PCR device with a higher sensitivity.
It is preferable that the amplifiable reagent be a nucleic acid. It is preferable that the nucleic acid be incorporated into the nucleus of a cell.
—Nucleic Acid—
A nucleic acid means a polymeric organic compound in which a nitrogen-containing base derived from purine or pyrimidine, sugar, and phosphoric acid are bonded with one another regularly. Examples of the nucleic acid also include a fragment of a nucleic acid or an analog of a nucleic acid or of a fragment of a nucleic acid.
The nucleic acid is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the nucleic acid include DNA, RNA, and cDNA.
The nucleic acid or nucleic acid fragment may be a natural product obtained from a living thing, or a processed product of the natural product, or a product produced by utilizing a genetic recombination technique, or a chemically synthesized artificially synthesized nucleic acid molecule. One of these nucleic acids may be used alone or two or more of these nucleic acids may be used in combination. With an artificially synthesized nucleic acid molecule, it is possible to suppress impurities and set the molecular weight to a low level. This makes it possible to improve the initial reaction efficiency.
An artificially synthesized nucleic acid means an artificially synthesized nucleic acid produced to have the same constituent components (base, deoxyribose, and phosphoric acid) as naturally existent DNA or RNA. Examples of the artificially synthesized nucleic acid include not only a nucleic acid having a base sequence coding a protein, but also a nucleic acid having an arbitrary base sequence.
Examples of the analog of a nucleic acid or a nucleic acid fragment include a nucleic acid or a nucleic acid fragment bonded with a non-nucleic acid component, a nucleic acid or a nucleic acid fragment labeled with a labeling agent such as a fluorescent dye or an isotope (e.g., a primer or a probe labeled with a fluorescent dye or a radioisotope), and an artificial nucleic acid, which is a nucleic acid or a nucleic acid fragment in which the chemical structure of some of the constituent nucleotides is changed (e.g., PNA, BNA, and LNA).
The form of the nucleic acid is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the form of the nucleic acid include double-strand nucleic acid, single-strand nucleic acid, and partially double-strand or single-strand nucleic acid. Cyclic or straight-chain plasmids can also be used. The nucleic acid may be modified or mutated.
It is preferable that the nucleic acid have a specific base sequence. The term “specific” means “particularly specified”.
The specific base sequence is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the specific base sequence include base sequences used for infectious disease testing, naturally non-existent non-natural base sequences, animal cell-derived base sequences, plant cell-derived base sequences, fungal cell-derived base sequences, bacterium-derived base sequences, and virus-derived base sequences. One of these base sequences may be used alone or two or more of these base sequences may be used in combination.
When using a non-natural base sequence, the specific base sequence preferably has a GC content of 30% or higher but 70% or lower, and preferably has a constant GC content (for example, see SEQ ID NO. 1).
The base length of the specific base sequence is not particularly limited, may be appropriately selected depending on the intended purpose, and may be, for example, a base length of 20 base pairs (or mer) or greater but 10,000 base pairs (or mer).
When using a base sequence used for infectious disease testing, the base sequence is not particularly limited and may be appropriately selected depending on the intended purpose so long as the base sequence includes a base sequence specific to the intended infectious disease. It is preferable that the base sequence include a base sequence designated in official analytical methods or officially announced methods (for example, see SEQ ID NOS. 2 and 3).
The nucleic acid may be a nucleic acid derived from the cells to be used, or a nucleic acid introduced by transgenesis. When a nucleic acid introduced by transgenesis and a plasmid are used as the nucleic acid, it is preferable to confirm that one copy of the nucleic acid is introduced per cell. The method for confirming that one copy of the nucleic acid is introduced is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include a sequencer, a PCR method, and a Southern blotting method.
One kind or two or more kinds of nucleic acids having specific base sequences may be introduced by transgenesis. Also in the case of introducing only one kind of a nucleic acid by transgenesis, base sequences of the same kind may be introduced in tandem depending on the intended purpose.
The method for transgenesis is not particularly limited and may be appropriately selected depending on the intended purpose so long as the method can introduce an intended copy number of specific nucleic acid sequences at an intended position. Examples of the method include homologous recombination, CRISPR/Cas9, CRISPR/Cpf1, TALEN, Zinc finger nuclease, Flip-in, and Jump-in. In the case of yeast fungi, homologous recombination is preferable among these methods in terms of a high efficiency and ease of controlling.
—Carrier—
It is preferable to handle the amplifiable reagent in a state of being carried on a carrier. When the amplifiable reagent is a nucleic acid, a preferable form is the nucleic acid being carried (or more preferably encapsulated) by the carrier having a particle shape (carrier particles).
The carrier is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the carrier include a cell, a resin, liposome, and microcapsule.
—Cells—
A cell means a structural, functional unit that includes an amplifiable reagent (for example, a nucleic acid) and forms an organism.
The cells are not particularly limited and may be appropriately selected depending on the intended purpose. All kinds of cells can be used regardless of whether the cells are eukaryotic cells, prokaryotic cells, multicellular organism cells, and unicellular organism cells. One of these kinds of cells may be used alone or two or more of these kinds of cells may be used in combination.
The eukaryotic cells are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the eukaryotic cells include animal cells, insect cells, plant cells, fungi, algae, and protozoans. One of these kinds of eukaryotic cells may be used alone or two or more of these kinds of eukaryotic cells may be used in combination. Among these eukaryotic cells, animal cells and fungi are preferable.
Adherent cells may be primary cells directly taken from tissues or organs, or may be cells obtained by passaging primary cells directly taken from tissues or organs a few times. Adherent cells may be appropriately selected depending on the intended purpose. Examples of adherent cells include differentiated cells and undifferentiated cells.
Differentiated cells are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of differentiated cells include: hepatocytes, which are parenchymal cells of a liver; stellate cells; Kupffer cells; endothelial cells such as vascular endothelial cells, sinusoidal endothelial cells, and corneal endothelial cells; fibroblasts; osteoblasts; osteoclasts; periodontal ligament-derived cells; epidermal cells such as epidermal keratinocytes; epithelial cells such as tracheal epithelial cells, intestinal epithelial cells, cervical epithelial cells, and corneal epithelial cells; mammary glandular cells; pericytes; muscle cells such as smooth muscle cells and myocardial cells; renal cells; pancreatic islet cells; nerve cells such as peripheral nerve cells and optic nerve cells; chondrocytes; and bone cells.
Undifferentiated cells are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of undifferentiated cells include: pluripotent stem cells such as embryotic stem cells, which are undifferentiated cells, and mesenchymal stem cells having pluripotency; unipotent stem cells such as vascular endothelial progenitor cells having unipotency; and iPS cells.
Fungi are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of fungi include molds and yeast fungi. One of these kinds of fungi may be used alone or two or more of these kinds of fungi may be used in combination. Among these kinds of fungi, yeast fungi are preferable because the cell cycles are adjustable and monoploids can be used.
The cell cycle means a cell proliferation process in which cells undergo cell division and cells (daughter cells) generated by the cell division become cells (mother cells) that undergo another cell division to generate new daughter cells.
Yeast fungi are not particularly limited and may be appropriately selected depending on the intended purpose. For example, yeast fungi that are synchronously cultured to synchronize at a G0/G1 phase, and fixed at a G1 phase are preferable.
Further, for example, as yeast fungi, Bar1-deficient yeasts with enhanced sensitivity to a pheromone (sex hormone) that controls the cell cycle at a G1 phase are preferable. When yeast fungi are Bar1-deficient yeasts, the abundance ratio of yeast fungi with uncontrolled cell cycles can be reduced. This makes it possible to, for example, prevent a specific nucleic acid from increasing in number in the cells contained in a well.
The prokaryotic cells are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the prokaryotic cells include eubacteria and archaea. One of these kinds of prokaryotic cells may be used alone or two or more of these kinds of prokaryotic cells may be used in combination.
As the cells, dead cells are preferable. With dead cells, it is possible to prevent occurrence of cell division after fractionation.
As the cells, cells that can emit light upon reception of light are preferable. With cells that can emit light upon reception of light, it is possible to land the cells into wells while having a highly accurate control on the number of cells.
Reception of light means receiving of light.
An optical sensor means a passive sensor configured to collect, with a lens, any light in the range from visible light rays visible by human eyes to near infrared rays, short-wavelength infrared rays, and thermal infrared rays that have longer wavelengths than the visible light rays, to obtain, for example, shapes of target cells in the form of image data.
—Cells that can Emit Light Upon Reception of Light—
The cells that can emit light upon reception of light are not particularly limited and may be appropriately selected depending on the intended purpose so long as the cells can emit light upon reception of light. Examples of the cells include cells stained with a fluorescent dye, cells expressing a fluorescent protein, and cells labeled with a fluorescent-labeled antibody.
A cellular site stained with a fluorescent dye, expressing a fluorescent protein, or labeled with a fluorescent-labeled antibody is not particularly limited. Examples of the cellular site include a whole cell, a cell nucleus, and a cellular membrane.
—Fluorescent Dye—
Examples of the fluorescent dye include fluoresceins, azo dyes, rhodamines, coumarins, pyrenes, cyanines. One of these fluorescent dyes may be used alone or two or more of these fluorescent dyes may be used in combination. Among these fluorescent dyes, fluoresceins, azo dyes, and rhodamines are preferable, and eosin, Evans blue, trypan blue, rhodamine 6G, rhodamine B, and rhodamine 123 are more preferable.
As the fluorescent dye, a commercially available product may be used. Examples of the commercially available product include product name: EOSIN Y (available from Wako Pure Chemical Industries, Ltd.), product name: EVANS BLUE (available from Wako Pure Chemical Industries, Ltd.), product name: TRYPAN BLUE (available from Wako Pure Chemical Industries, Ltd.), product name: RHODAMINE 6G (available from Wako Pure Chemical Industries, Ltd.), product name: RHODAMINE B (available from Wako Pure Chemical Industries, Ltd.), and product name: RHODAMINE 123 (available from Wako Pure Chemical Industries, Ltd.).
—Fluorescent Protein—
Examples of the fluorescent protein include Sirius, EBFP, ECFP, mTurquoise, TagCFP, AmCyan, mTFP1, MidoriishiCyan, CFP, TurboGFP, AcGFP, TagGFP, Azami-Green, ZsGreen, EmGFP, EGFP, GFP2, HyPer, TagYFP, EYFP, Venus, YFP, PhiYFP, PhiYFP-m, TurboYFP, ZsYellow, mBanana, KusabiraOrange, mOrange, TurboRFP, DsRed-Express, DsRed2, TagRFP, DsRed-Monomer, AsRed2, mStrawberry, TurboFP602, mRFP1, JRed, KillerRed, mCherry, mPlum, PS-CFP, Dendra2, Kaede, EosFP, and KikumeGR. One of these fluorescent proteins may be used alone or two or more of these fluorescent proteins may be used in combination.
—Fluorescent-Labeled Antibody—
The fluorescent-labeled antibody is not particularly limited and may be appropriately selected depending on the intended purpose so long as the fluorescent-labeled antibody is fluorescent-labeled. Examples of the fluorescent-labeled antibody include CD4-FITC and CD8-PE. One of these fluorescent-labeled antibodies may be used alone or two or more of these fluorescent-labeled antibodies may be used in combination.
The volume average particle diameter of the cells is preferably 30 micrometers or less, more preferably 10 micrometers or less, and particularly preferably 7 micrometers or less in a free state. When the volume average particle diameter of the cells is 30 micrometers or less, the cells can be suitably used in an inkjet method or a liquid droplet discharging unit such as a cell sorter.
The volume average particle diameter of the cells can be measured by, for example, a measuring method described below.
Ten microliters is extracted from a produced stained yeast dispersion liquid and poured onto a plastic slide formed of PMMA. Then, with an automated cell counter (product name: COUNTESS AUTOMATED CELL COUNTER, available from Invitrogen), the volume average particle diameter of the cells can be measured. The cell number can be obtained by a similar measuring method.
The concentration of the cells in a cell suspension is not particularly limited, may be appropriately selected depending on the intended purpose, and is preferably 5×104 cells/mL or higher but 5×108 cells/mL or lower and more preferably 5×104 cells/mL or higher but 5×107 cells/mL or lower. When the cell number is 5×104 cells/mL or higher but 5×108 cells/mL or lower, it can be ensured that cells be contained in a discharged liquid droplet without fail. The cell number can be measured with an automated cell counter (product name: COUNTESS AUTOMATED CELL COUNTER, available from Invitrogen) in the same manner as measuring the volume average particle diameter.
The cell number of cells including a nucleic acid is not particularly limited and may be appropriately selected depending on the intended purpose so long as the cell number is a plural number.
—Resin—
The material, the shape, the size, and the structure of the resin are not particularly limited and may be appropriately selected depending on the intended purpose so long as the resin can carry the amplifiable reagent (for example, a nucleic acid).
—Liposome—
A liposome is a lipid vesicle formed of a lipid bilayer containing lipid molecules. Specifically, the liposome means a lipid-containing closed vesicle including a space separated from the external environment by a lipid bilayer produced based on the polarities of a hydrophobic group and a hydrophilic group of lipid molecules.
The liposome is a closed vesicle formed of a lipid bilayer using a lipid, and contains an aqueous phase (internal aqueous phase) in the space in the closed vesicle. The internal aqueous phase contains, for example, water. The liposome may be single-lamellar (single-layer lamellar or unilamellar with a single bilayer) or multilayer lamellar (multilamellar, with an onion-like structure including multiple bilayers, with the individual layers separated by watery layers).
As the liposome, a liposome that can encapsulate an amplifiable reagent (for example, a nucleic acid) is preferable. The form of encapsulation is not particularly limited. “Encapsulation” means a form of a nucleic acid being contained in the internal aqueous phase and the layer of the liposome. Examples of the form include a form of encapsulating a nucleic acid in the closed space formed of the layer, a form of encapsulating a nucleic acid in the layer per se, and a combination of these forms.
The size (average particle diameter) of the liposome is not particularly limited so long as the liposome can encapsulate an amplifiable reagent (for example, a nucleic acid). It is preferable that the liposome have a spherical form or a form close to the spherical form.
The component (layer component) constituting the lipid bilayer of the liposome is selected from lipids. As the lipid, an arbitrary lipid that can dissolve in a mixture solvent of a water-soluble organic solvent and an ester-based organic solvent can be used. Specific examples of the lipid include phospholipids, lipids other than phospholipids, cholesterols, and derivatives of these lipids. These components may be formed of a single kind of a component or a plurality of kinds of components.
—Microcapsule—
A microcapsule means a minute particle having a wall material and a hollow structure, and can encapsulate an amplifiable reagent (for example, a nucleic acid) in the hollow structure.
The microcapsule is not particularly limited, and, for example, the wall material and the size of the microcapsule may be appropriately selected depending on the intended purpose.
Examples of the wall material of the microcapsule include polyurethane resins, polyurea, polyurea-polyurethane resins, urea-formaldehyde resins, melamine-formaldehyde resins, polyamide, polyester, polysulfone amide, polycarbonate, polysulfinate, epoxyr, acrylic acid ester, methacrylic acid ester, vinyl acetate, and gelatin. One of these wall materials may be used alone or two or more of these wall materials may be used in combination.
The size of the microcapsule is not particularly limited and may be appropriately selected depending on the intended purpose so long as the microcapsule can encapsulate an amplifiable reagent (for example, a nucleic acid).
The method for producing the microcapsule is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include an in-situ method, an interfacial polymerization method, and a coacervation method.
Real-time PCR is performed using the device of
For example, in the real-time PCR, first, a master mix (available from Thermo Fisher Scientific Inc., TAQMAN UNIVERSAL PCR MASTER MIX) (1 microliter), a forward primer and a reverse primer for amplifying a specific base sequence (0.5 nmol each), and a probe (0.4 nmol) are added to each sample in the device. Subsequently, amplification and detection can be performed with a real-time PCR device (available from Thermo Fisher Scientific Inc., QUANTSTUDIO 7 FLEX).
Ct value indicates the cycle number at a timing when a fluorescence signal of a reaction crosses Threshold Line. Because Ct value is linearly decreased to the logarithm of the initial amount of the target, the initial copy number of DNA can be calculated based on Ct value.
Threshold Line indicates the signal level at which a statistically significant increase from a calculated baseline signal is observed, and means the threshold of a real-time PCR reaction.
Hence, an in-plane property of the device can be evaluated based on, for example, the average Ct value, the standard deviation of the Ct values, the CV value [(standard deviation/average Ct value)×100], and [(Ct value (Max)−Ct value (min))/2·average Ct value]×100.
In the device of
Real-time PCR is performed using the device of
For example, by performing measurement for a certain period of time using the devices described with reference to
In a 96-well plate illustrated in
Real-time PCR is performed using the device of
In the device of
In the device of
In the device of
In the device of
In the device of
By performing measurement for a certain period of time using the devices described with reference to
<Device Producing Method>
A device producing method using cells including a specific nucleic acid will be described below.
The device producing method of the present disclosure includes a cell suspension producing step of producing a cell suspension containing a plurality of cells including a specific nucleic acid and a solvent, a liquid droplet landing step of discharging the cell suspension in the form of liquid droplets to sequentially land the liquid droplets in wells of a plate, a cell number counting step of counting the number of cells contained in the liquid droplets with a sensor after the liquid droplets are discharged and before the liquid droplets land in the wells, and a nucleic acid extracting step of extracting nucleic acids from cells in the wells, preferably includes a step of calculating the degrees of certainty of estimated numbers of nucleic acids in the cell suspension producing step, the liquid droplet landing step, and the cell number counting step, an outputting step, and a recording step, and further includes other steps as needed.
<<Cell Suspension Producing Method>>
The cell suspension producing step is a step of producing a cell suspension containing a plurality of cells including a specific nucleic acid and a solvent.
The solvent means a liquid used for dispersing cells.
Suspension in the cell suspension means a state of cells being present dispersedly in the solvent.
Producing means a producing operation.
—Cell Suspension—
The cell suspension contains a plurality of cells including a specific nucleic acid and a solvent, preferably contains an additive, and further contains other components as needed.
The plurality of cells including a specific nucleic acid are as described above.
—Solvent—
The solvent is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the solvent include water, a culture fluid, a separation liquid, a diluent, a buffer, an organic matter dissolving liquid, an organic solvent, a polymeric gel solution, a colloid dispersion liquid, an electrolytic aqueous solution, an inorganic salt aqueous solution, a metal aqueous solution, and mixture liquids of these liquids. One of these solvents may be used alone or two or more of these solvents may be used in combination. Among these solvents, water and a buffer are preferable, and water, a phosphate buffered saline (PBS), and a Tris-EDTA buffer (TE) are more preferable.
—Additive—
An additive is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the additive include a surfactant, a nucleic acid, and a resin. One of these additives may be used alone or two or more of these additives may be used in combination.
The surfactant can prevent mutual aggregation of cells and improve continuous discharging stability.
The surfactant is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the surfactant include ionic surfactants and nonionic surfactants. One of these surfactants may be used alone or two or more of these surfactants may be used in combination. Among these surfactants, nonionic surfactants are preferable because proteins are neither modified nor deactivated by nonionic surfactants, although depending on the addition amount of the nonionic surfactants.
Examples of the ionic surfactants include fatty acid sodium, fatty acid potassium, alpha-sulfo fatty acid ester sodium, sodium straight-chain alkyl benzene sulfonate, alkyl sulfuric acid ester sodium, alkyl ether sulfuric acid ester sodium, and sodium alpha-olefin sulfonate. One of these ionic surfactants may be used alone or two or more of these ionic surfactants may be used in combination. Among these ionic surfactants, fatty acid sodium is preferable and sodium dodecyl sulfonate (SDS) is more preferable.
Examples of the nonionic surfactants include alkyl glycoside, alkyl polyoxyethylene ether (e.g., BRIJ series), octyl phenol ethoxylate (e.g., TRITON X series, IGEPAL CA series, NONIDET P series, and NIKKOL OP series), polysorbates (e.g., TWEEN series such as TWEEN 20), sorbitan fatty acid esters, polyoxyethylene fatty acid esters, alkyl maltoside, sucrose fatty acid esters, glycoside fatty acid esters, glycerin fatty acid esters, propylene glycol fatty acid esters, and fatty acid monoglyceride. One of these nonionic surfactants may be used alone or two or more of these nonionic surfactants may be used in combination. Among these nonionic surfactants, polysorbates are preferable.
The content of the surfactant is not particularly limited, may be appropriately selected depending on the intended purpose, and is preferably 0.001% by mass or greater but 30% by mass or less relative to the total amount of the cell suspension. When the content of the surfactant is 0.001% by mass or greater, an effect of adding the surfactant can be obtained. When the content of the surfactant is 30% by mass or less, aggregation of cells can be suppressed, making it possible to strictly control the copy number of nucleic acid in the cell suspension.
The nucleic acid is not particularly limited and may be appropriately selected depending on the intended purpose so long as the nucleic acid does not affect detection of the detection target nucleic acid. Examples of the nucleic acid include ColE1 DNA. With such a nucleic acid, it is possible to prevent the nucleic acid having a specific base sequence from adhering to the wall surface of a well.
The resin is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the resin include polyethyleneimide.
—Other Materials—
Other materials are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the other materials include a crosslinking agent, a pH adjustor, an antiseptic, an antioxidant, an osmotic pressure regulator, a humectant, and a dispersant.
<Method for Dispersing Cells>
The method for dispersing the cells is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include a medium method such as a bead mill, an ultrasonic method such as an ultrasonic homogenizer, and a method using a pressure difference such as a French press. One of these methods may be used alone or two or more of these methods may be used in combination. Among these methods, the ultrasonic method is more preferable because the ultrasonic method has low damage on the cells. With the medium method, a high crushing force may destroy cellular membranes or cell walls, and the medium may mix as contamination.
<Method for Screening Cells>
The method for screening the cells is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the method include screening by wet classification, a cell sorter, and a filter. One of these methods may be used alone or two or more of these methods may be used in combination. Among these methods, screening by a cell sorter and a filter is preferable because the method has low damage on the cells.
It is preferable to estimate the number of nucleic acids having a target base sequence from the cell number contained in the cell suspension, by measuring the cell cycles of the cells.
Measuring the cell cycles means quantifying the cell number due to cell division.
Estimating the number of nucleic acids means obtaining the copy number of nucleic acids based on the cell number.
What is to be counted needs not be the cell number, but may be the number of target base sequences. Typically, it is safe to consider that the number of target base sequences is equal to the cell number, because the cells to be selected as the cells to be counted are cells each including one target base sequence (=one target base sequence per cell), or because one target base sequence is introduced per cell by gene recombination. However, nucleic acid replication occurs in cells in order for the cells to undergo cell division at specific cycles. Cell cycles are different depending on the kinds of cells. By extracting a predetermined amount of the solution from the cell suspension and measuring the cycles of a plurality of cells, it is possible to calculate an expected value of the number of target base sequences included in one cell and the degree of certainty of the estimated value. This can be realized by, for example, observing nuclear stained cells with a flow cytometer.
Degree of certainty means a probability of occurrence of one specific event, predicted beforehand, when there are possibilities of occurrence of some events. Calculation means deriving a needed value by a calculating operation.
It is preferable to perform an operation of controlling the cell cycles before producing the cell suspension. By preparing the cells uniformly to a state before replication occurs or a state after replication has occurred, it is possible to calculate the number of target base sequences based on the cell number more accurately.
It is preferable to calculate the degree of certainty (probability) for the estimated specific copy number. By calculating the degree of certainty (probability), it is possible to express and output the degree of certainty as a variance or a standard deviation based on these values. When adding up influences of a plurality of factors, it is possible use a square root of the sum of the squares of the standard deviation commonly used. For example, a correct answer percentage for the number of cells discharged, the number of DNA in a cell, and a landing ratio at which discharged cells land in wells can be used as the factors. A highly influential factor may be selected for calculation.
<<Liquid Droplet Landing Step>>
The liquid droplet landing step is a step of discharging the cell suspension in the form of liquid droplets to sequentially land the liquid droplets in wells of a plate.
A liquid droplet means a gathering of a liquid formed by a surface tension.
Discharging means making the cell suspension fly in the form of liquid droplets. “Sequentially” means “in order”.
Landing means making liquid droplets reach the wells.
As a discharging unit, a unit configured to discharge the cell suspension in the form of liquid droplets (hereinafter may also be referred to as “discharging head”) can be suitably used.
Examples of the method for discharging the cell suspension in the form of liquid droplets include an on-demand method and a continuous method that are based on the inkjet method. Of these methods, in the case of the continuous method, there is a tendency that the dead volume of the cell suspension used is high, because of, for example, empty discharging until the discharging state becomes stable, adjustment of the amount of liquid droplets, and continued formation of liquid droplets even during transfer between the wells. In the present disclosure, in terms of cell number adjustment, it is preferable to suppress influence due to the dead volume. Hence, of the two methods, the on-demand method is more preferable.
Examples of the on-demand method include a plurality of known methods such as a pressure applying method of applying a pressure to a liquid to discharge the liquid, a thermal method of discharging a liquid by film boiling due to heating, and an electrostatic method of drawing liquid droplets by electrostatic attraction to form liquid droplets. Among these methods, the pressure applying method is preferable for the reason described below.
In the electrostatic method, there is a need for disposing an electrode in a manner to face a discharging unit that is configured to retain the cell suspension and form liquid droplets. In the device producing method, a plate for receiving liquid droplets is disposed at the facing position. Hence, it is preferable not to provide an electrode, in order to increase the degree of latitude in the plate configuration.
In the thermal method, there are a risk of local heating concentration that may affect the cells, which are a biomaterial, and a risk of kogation to the heater portion. Influences by heat depend on the components contained or the purpose for which the plate is used. Therefore, there is no need for flatly rejecting the thermal method. However, the pressure applying method is preferable because the pressure applying method has a lower risk of kogation to the heater portion than the thermal method.
Examples of the pressure applying method include a method of applying a pressure to a liquid using a piezo element, and a method of applying a pressure using a valve such as an electromagnetic valve. The configuration example of a liquid droplet generating device usable for discharging liquid droplets of the cell suspension is illustrated in
As the electromagnetic valve-type discharging head, for example, a dispenser available from Tech Elan LLC can be suitably used.
As the piezo-type discharging head, for example, a single cell printer available from Cytena GmbH can be suitably used.
Any of these discharging heads may be used. However, the pressure applying method by the electromagnetic valve is not capable of forming liquid droplets at a high speed repeatedly. Therefore, it is preferable to use the piezo method in order to increase the throughput of producing a plate. A piezo-type discharging head using a common piezoelectric element 13b may cause unevenness in the cell concentration due to settlement, or may have nozzle clogging.
Therefore, a more preferable configuration is the configuration illustrated in
In the discharging head of
Examples of any other method than the on-demand method include a continuous method for continuously forming liquid droplets. When pushing out liquid droplets from a nozzle by pressurization, the continuous method applies regular fluctuations using a piezoelectric element or a heater, to make it possible to continuously form minute liquid droplets. Further, the continuous method can select whether to land a flying liquid droplet into a well or to recover the liquid droplet in a recovery unit, by controlling the discharging direction of the liquid droplet with voltage application. Such a method is employed in a cell sorter or a flow cytometer. For example, a device named: CELL SORTER SH800Z available from Sony Corporation can be used.
During a period in which liquid droplets are not discharged, inputting a plurality of pulses that are not high enough to discharge liquid droplets enables the cell suspension in the liquid chamber to be stirred, making it possible to suppress occurrence of a concentration distribution due to settlement of the cells.
The liquid droplet forming operation of the discharging head that can be used in the present disclosure will be described below.
The discharging head can discharge liquid droplets with application of a pulsed voltage to the upper and lower electrodes formed on the piezoelectric element.
In
Next, as illustrated in
Finally, as illustrated in
In the device producing method, a plate in which wells are formed is secured on a movable stage, and by combination of driving of the stage with formation of liquid droplets from the discharging head, liquid droplets are sequentially landed in the concaves. A method of moving the plate along with moving the stage is described here. However, naturally, it is also possible to move the discharging head.
The plate is not particularly limited, and a plate that is commonly used in bio fields and in which wells are formed can be used.
The number of wells in the plate is not particularly limited and may be appropriately selected depending on the intended purpose. The number of wells may be a single number or a plural number.
As illustrated in
In the dispensing device 400, the plate 700 is disposed over a movable stage 800. The plate 700 has a plurality of wells 710 (concaves) in which liquid droplets 310 discharged from a discharging head of the liquid droplet forming device 401 land. The control device 900 is configured to move the stage 800 and control the relative positional relationship between the discharging head of the liquid droplet forming device 401 and each well 710. This enables liquid droplets 310 containing fluorescent-stained cells 350 to be discharged sequentially into the wells 710 from the discharging head of the liquid droplet forming device 401.
The control device 900 may be configured to include, for example, a CPU, a ROM, a RAM, and a main memory. In this case, various functions of the control device 900 can be realized by a program recorded in, for example, the ROM being read out into the main memory and executed by the CPU. However, a part or the whole of the control device 900 may be realized only by hardware. Alternatively, the control device 900 may be configured with, for example, physically a plurality of devices.
When landing the cell suspension into the wells, it is preferable to land the liquid droplets to be discharged into the wells, in a manner that a plurality of levels are obtained.
A plurality of levels mean a plurality of references serving as standards.
As the plurality of levels, it is preferable that a plurality of cells including a specific nucleic acid have a predetermined concentration gradient in the wells. With a concentration gradient, the nucleic acid can be favorably used as a reagent for calibration curve. The plurality of levels can be controlled using values counted by a sensor.
As the plate, it is preferable to use, for example, a 1-well microtube, 8-series tubes, a 96-well plate, and a 384-well plate. When the number of wells are a plural number, it is possible to dispense the same number of cells into the wells of these plates, or it is also possible to dispense numbers of cells of different levels into the wells. There may be a well in which no cells are contained. Particularly, for producing a plate used for evaluating a real-time PCR device or digital PCR device configured to quantitatively evaluate an amount of nucleic acids, it is preferable to dispense numbers of nucleic acids of a plurality of levels. For example, it is conceivable to produce a plate into which cells (or nucleic acids) are dispensed at 7 levels, namely about 1 cell, 2 cells, 4 cells, 8 cells, 16 cells, 32 cells, and 64 cells. Using such a plate, it is possible to inspect, for example, quantitativity, linearity, and lower limit of evaluation of a real-time PCR device or digital PCR device.
<<Cell Number Counting Step>>
The cell number counting step is a step of counting the number of cells contained in the liquid droplets with a sensor after the liquid droplets are discharged and before the liquid droplets land in the wells.
A sensor means a device configured to, by utilizing some scientific principles, change mechanical, electromagnetic, thermal, acoustic, or chemical properties of natural phenomena or artificial products or spatial information/temporal information indicated by these properties into signals, which are a different medium easily handleable by humans or machines.
Counting means counting of numbers.
The cell number counting step is not particularly limited and may be appropriately selected depending on the intended purpose, so long as the cell number counting step counts the number of cells contained in the liquid droplets with a sensor after the liquid droplets are discharged and before the liquid droplets land in the wells. The cell number counting step may include an operation for observing cells before discharging and an operation for counting cells after landing.
For counting the number of cells contained in the liquid droplets after the liquid droplets are discharged and before the liquid droplets land in the wells, it is preferable to observe cells in a liquid droplet at a timing at which the liquid droplet is at a position that is immediately above a well opening and at which the liquid droplet is predicted to enter the well in the plate without fail.
Examples of the method for observing cells in a liquid droplet include an optical detection method and an electric or magnetic detection method.
—Optical Detection Method—
With reference to
In
Irradiation of light means application of light.
The discharging head 10 includes a liquid chamber 11, a membrane 12, and a driving element 13 and can discharge a cell suspension 300 suspending fluorescent-stained cells 350 in the form of liquid droplets.
The liquid chamber 11 is a liquid retaining portion configured to retain the cell suspension 300 suspending the fluorescent-stained cells 350. A nozzle 111, which is a through hole, is formed in the lower surface of the liquid chamber 11. The liquid chamber 11 may be formed of, for example, a metal, silicon, or a ceramic. Examples of the fluorescent-stained cells 350 include inorganic particles and organic polymer particles stained with a fluorescent pigment.
The membrane 12 is a film-shaped member secured on the upper end portion of the liquid chamber 11. The planar shape of the membrane 12 may be, for example, a circular shape, but may also be, for example, an elliptic shape or a quadrangular shape.
The driving element 13 is provided on the upper surface of the membrane 12. The shape of the driving element 13 may be designed to match the shape of the membrane 12. For example, when the planar shape of the membrane 12 is a circular shape, it is preferable to provide a circular driving element 13.
The membrane 12 can be vibrated by supplying a driving signal to the driving element 13 from a driving unit 20. The vibration of the membrane 12 can cause a liquid droplet 310 containing the fluorescent-stained cells 350 to be discharged through the nozzle 111.
When a piezoelectric element is used as the driving element 13, for example, the driving element 13 may have a structure obtained by providing the upper surface and the lower surface of the piezoelectric material with electrodes across which a voltage is to be applied. In this case, when the driving unit 20 applies a voltage across the upper and lower electrodes of the piezoelectric element, a compressive stress is applied in the horizontal direction of the drawing sheet, making it possible for the membrane 12 to vibrate in the upward-downward direction of the drawing sheet. As the piezoelectric material, for example, lead zirconate titanate (PZT) may be used. In addition, various piezoelectric materials can be used, such as bismuth iron oxide, metal niobate, barium titanate, or materials obtained by adding metals or different oxides to these materials.
The light source 30 is configured to irradiate a flying liquid droplet 310 with light L. A flying state means a state from when the liquid droplet 310 is discharged from a liquid droplet discharging unit 10 until when the liquid droplet 310 lands on the landing target. A flying liquid droplet 310 has an approximately spherical shape at the position at which the liquid droplet 310 is irradiated with the light L. The beam shape of the light L is an approximately circular shape.
It is preferable that the beam diameter of the light L be from about 10 times through 100 times as great as the diameter of the liquid droplet 310. This is for ensuring that the liquid droplet 310 is irradiated with the light L from the light source 30 without fail even when the position of the liquid droplet 310 fluctuates.
However, it is not preferable if the beam diameter of the light L is much greater than 100 times as great as the diameter of the liquid droplet 310. This is because the energy density of the light with which the liquid droplet 310 is irradiated is reduced, to lower the light volume of fluorescence Lf to be emitted upon the light L serving as excitation light, making it difficult for the light receiving element 60 to detect the fluorescence Lf.
It is preferable that the light L emitted by the light source 30 be pulse light. It is preferable to use, for example, a solid-state laser, a semiconductor laser, and a dye laser. When the light L is pulse light, the pulse width is preferably 10 microseconds or less and more preferably 1 microsecond or less. The energy per unit pulse is preferably roughly 0.1 microjoules or higher and more preferably 1 microjoule or higher, although significantly depending on the optical system such as presence or absence of light condensation.
The light receiving element 60 is configured to receive fluorescence Lf emitted by the fluorescent-stained cell 350 upon absorption of the light L as excitation light, when the fluorescent-stained cell 350 is contained in a flying liquid droplet 310. Because the fluorescence Lf is emitted to all directions from the fluorescent-stained cell 350, the light receiving element 60 can be disposed at an arbitrary position at which the fluorescence Lf is receivable. Here, in order to improve contrast, it is preferable to dispose the light receiving element 60 at a position at which direct incidence of the light L emitted by the light source 30 to the light receiving element 60 does not occur.
The light receiving element 60 is not particularly limited and may be appropriately selected depending on the intended purpose so long as the light receiving element 60 is an element capable of receiving the fluorescence Lf emitted by the fluorescent-stained cell 350. An optical sensor configured to receive fluorescence from a cell in a liquid droplet when the liquid droplet is irradiated with light having a specific wavelength is preferable. Examples of the light receiving element 60 include one-dimensional elements such as a photodiode and a photosensor. When high-sensitivity measurement is needed, it is preferable to use a photomultiplier tube and an Avalanche photodiode. As the light receiving element 60, two-dimensional elements such as a CCD (Charge Coupled Device), a CMOS (Complementary Metal Oxide Semiconductor), and a gate CCD may be used.
The fluorescence Lf emitted by the fluorescent-stained cell 350 is weaker than the light L emitted by the light source 30. Therefore, a filter configured to attenuate the wavelength range of the light L may be installed at a preceding stage (light receiving surface side) of the light receiving element 60. This enables the light receiving element 60 to obtain an extremely highly contrastive image of the fluorescent-stained cell 350. As the filter, for example, a notch filter configured to attenuate a specific wavelength range including the wavelength of the light L may be used.
As described above, it is preferable that the light L emitted by the light source 30 be pulse light. The light L emitted by the light source 30 may be continuously oscillating light. In this case, it is preferable to control the light receiving element 60 to be capable of receiving light at a timing at which a flying liquid droplet 310 is irradiated with the continuously oscillating light, to make the light receiving element 60 receive the fluorescence Lf.
The control unit 70 has a function of controlling the driving unit 20 and the light source 30. The control unit 70 also has a function of obtaining information that is based on the light volume received by the light receiving element 60 and counting the number of fluorescent-stained cells 350 contained in the liquid droplet 310 (the case where the number is zero is also included). With reference to
As illustrated in
The CPU 71 is configured to control various functions of the control unit 70. The ROM 72 serving as a memory unit is configured to store programs to be executed by the CPU 71 for controlling the various functions of the control unit 70 and various information. The RAM 73 serving as a memory unit is configured to be used as, for example, the work area of the CPU 71. The RAM 73 is also configured to be capable of storing predetermined information for a temporary period of time. The I/F 74 is an interface configured to couple the liquid droplet forming device 401 to, for example, another device. The liquid droplet forming device 401 may be coupled to, for example, an external network via the I/F 74.
As illustrated in
With reference to
In the step S11, the discharging control unit 701 of the control unit 70 outputs an instruction for discharging to the driving unit 20. Upon reception of the instruction for discharging from the discharging control unit 701, the driving unit 20 supplies a driving signal to the driving element 13 to vibrate the membrane 12. The vibration of the membrane 12 causes a liquid droplet 310 containing a fluorescent-stained cell 350 to be discharged through the nozzle 111.
Next, in the step S12, the light source control unit 702 of the control unit 70 outputs an instruction for lighting to the light source 30 in synchronization with the discharging of the liquid droplet 310 (in synchronization with a driving signal supplied by the driving unit 20 to the liquid droplet discharging unit 10). In accordance with this instruction, the light source 30 is turned on to irradiate the flying liquid droplet 310 with the light L.
Here, the light is emitted by the light source 30, not in synchronization with discharging of the liquid droplet 310 by the liquid droplet discharging unit 10 (supplying of the driving signal to the liquid droplet discharging unit 10 by the driving unit 20), but in synchronization with the timing at which the liquid droplet 310 has come flying to a predetermined position in order for the liquid droplet 310 to be irradiated with the light L. That is, the light source control unit 702 controls the light source 30 to emit light at a predetermined period of time of delay from the discharging of the liquid droplet 310 by the liquid droplet discharging unit 10 (from the driving signal supplied by the driving unit 20 to the liquid droplet discharging unit 10).
For example, the speed v of the liquid droplet 310 to be discharged when the driving signal is supplied to the liquid droplet discharging unit 10 may be measured beforehand. Based on the measured speed v, the time t taken from when the liquid droplet 310 is discharged until when the liquid droplet 310 reaches the predetermined position may be calculated, in order that the timing of light irradiation by the light source 30 may be delayed from the timing at which the driving signal is supplied to the liquid droplet discharging unit 10 by the period of time of t. This enables a good control on light emission, and can ensure that the liquid droplet 310 is irradiated with the light from the light source 30 without fail.
Next, in the step S13, the cell number counting unit 703 of the control unit 70 counts the number of fluorescent-stained cells 350 contained in the liquid droplet 310 (the case where the number is zero is also included) based on information from the light receiving element 60. The information from the light receiving element 60 indicates the luminance (light volume) and the area value of the fluorescent-stained cell 350.
The cell number counting unit 703 can count the number of fluorescent-stained cells 350 by, for example, comparing the light volume received by the light receiving element 60 with a predetermined threshold. In this case, a one-dimensional element may be used or a two-dimensional element may be used as the light receiving element 60.
When a two-dimensional element is used as the light receiving element 60, the cell number counting unit 703 may use a method of performing image processing for calculating the luminance or the area of the fluorescent-stained cell 350 based on a two-dimensional image obtained from the light receiving element 60. In this case, the cell number counting unit 703 can count the number of fluorescent-stained cells 350 by calculating the luminance or the area value of the fluorescent-stained cell 350 by image processing and comparing the calculated luminance or area value with a predetermined threshold.
The fluorescent-stained cell 350 may be a cell or a stained cell. A stained cell means a cell stained with a fluorescent pigment or a cell that can express a fluorescent protein.
The fluorescent pigment for the stained cell is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the fluorescent pigment include fluoresceins, rhodamines, coumarins, pyrenes, cyanines, and azo pigments. One of these fluorescent pigments may be used alone or two or more of these fluorescent pigments may be used in combination. Among these fluorescent pigments, eosin, Evans blue, trypan blue, rhodamine 6G, rhodamine B, and Rhodamine 123 are more preferable.
Examples of the fluorescent protein include Sirius, EBFP, ECFP, mTurquoise, TagCFP, AmCyan, mTFP1, MidoriishiCyan, CFP, TurboGFP, AcGFP, TagGFP, Azami-Green, ZsGreen, EmGFP, EGFP, GFP2, HyPer, TagYFP, EYFP, Venus, YFP, PhiYFP, PhiYFP-m, TurboYFP, ZsYellow, mBanana, KusabiraOrange, mOrange, TurboRFP, DsRed-Express, DsRed2, TagRFP, DsRed-Monomer, AsRed2, mStrawberry, TurboFP602, mRFP1, JRed, KillerRed, mCherry, mPlum, PS-CFP, Dendra2, Kaede, EosFP, and KikumeGR. One of these fluorescent proteins may be used alone or two or more of these fluorescent proteins may be used in combination.
In this way, in the liquid droplet forming device 401, the driving unit 20 supplies a driving signal to the liquid droplet discharging unit 10 retaining the cell suspension 300 suspending fluorescent-stained cells 350 to cause the liquid droplet discharging unit 10 to discharge a liquid droplet 310 containing the fluorescent-stained cell 350, and the flying liquid droplet 310 is irradiated with the light L from the light source 30. Then, the fluorescent-stained cell 350 contained in the flying liquid droplet 310 emits the fluorescence Lf upon the light L serving as excitation light, and the light receiving element 60 receives the fluorescence Lf. Then, the cell number counting unit 703 counts the number of fluorescent-stained cells 350 contained in the flying liquid droplet 310, based on information from the light receiving element 60.
That is, the liquid droplet forming device 401 is configured for on-the-spot actual observation of the number of fluorescent-stained cells 350 contained in the flying liquid droplet 310. This can realize a better accuracy than hitherto obtained, in counting the number of fluorescent-stained cells 350. Moreover, because the fluorescent-stained cell 350 contained in the flying liquid droplet 310 is irradiated with the light L and emits the fluorescence Lf that is to be received by the light receiving element 60, an image of the fluorescent-stained cell 350 can be obtained with a high contrast, and the frequency of occurrence of erroneous counting of the number of fluorescent-stained cells 350 can be reduced.
In the liquid droplet forming device 401A, arranging the mirror 40 at the perceiving stage of the light receiving element 60 can improve the degree of latitude in the layout of the light receiving element 60.
For example, in the layout of
That is, by changing the layout of the light receiving element 60 as illustrated in
The fluorescences Lf1 and Lf2 represent parts of fluorescence emitted to all directions from the fluorescent-stained cell 350. The light receiving elements 60 and 61 can be disposed at arbitrary positions at which the fluorescence emitted to different directions by the fluorescent-stained cell 350 is receivable. Three or more light receiving elements may be disposed at positions at which the fluorescence emitted to different directions by the fluorescent-stained cell 350 is receivable. The light receiving elements may have the same specifications or different specifications.
With one light receiving element, when a plurality of fluorescent-stained cells 350 are contained in a flying liquid droplet 310, there is a risk that the cell number counting unit 703 may erroneously count the number of fluorescent-stained cells 350 contained in the liquid droplet 310 (a risk that a counting error may occur) because the fluorescent-stained cells 350 may overlap each other.
As described above, the cell number counting unit 703 can count the number of fluorescent particles, by calculating the luminance or the area value of fluorescent particles by image processing and comparing the calculated luminance or area value with a predetermined threshold.
When two or more light receiving elements are installed, it is possible to suppress occurrence of a counting error, by adopting the data indicating the maximum value among the luminance values or area values obtained from these light receiving elements. This will be described in more detail with reference to
However, actually, when n is 2 or greater, because particles may overlap each other, the luminance to be actually measured is Lu≤Le≤nLu (the half-tone dot meshed portion in
When a plurality of light receiving elements are installed, the number of cells may be determined according to an algorithm for estimating the number of cells based on a plurality of shape data to be obtained.
As can be understood, with the plurality of light receiving elements configured to receive fluorescence emitted to different directions by the fluorescent-stained cell 350, the liquid droplet forming device 401B can further reduce the frequency of occurrence of erroneous counting of the number of fluorescent-stained cells 350.
The liquid droplet discharging unit 10C includes a liquid chamber 11C, a membrane 12C, and a driving element 13C. At the top, the liquid chamber 11C has an atmospherically exposed portion 115 configured to expose the interior of the liquid chamber 11C to the atmosphere, and bubbles mixed in the cell suspension 300 can be evacuated through the atmospherically exposed portion 115.
The membrane 12C is a film-shaped member secured at the lower end of the liquid chamber 11C. A nozzle 121, which is a through hole, is formed in approximately the center of the membrane 12C, and the vibration of the membrane 12C causes the cell suspension 300 retained in the liquid chamber 11C to be discharged through the nozzle 121 in the form of a liquid droplet 310. Because the liquid droplet 310 is formed by the inertia of the vibration of the membrane 12C, it is possible to discharge the cell suspension 300 even when the cell suspension 300 has a high surface tension (a high viscosity). The planer shape of the membrane 12C may be, for example, a circular shape, but may also be, for example, an elliptic shape or a quadrangular shape.
The material of the membrane 12C is not particularly limited. However, if the material of the membrane 12C is extremely flexible, the membrane 12C easily undergo vibration and is not easily able to stop vibration immediately when there is no need for discharging. Therefore, a material having a certain degree of hardness is preferable. As the material of the membrane 12C, for example, a metal material, a ceramic material, and a polymeric material having a certain degree of hardness can be used.
Particularly, when a cell is used as the fluorescent-stained cell 350, the material of the membrane is preferably a material having a low adhesiveness with the cell or proteins. Generally, adhesiveness of cells is said to be dependent on the contact angle of the material with respect to water. When the material has a high hydrophilicity or a high hydrophobicity, the material has a low adhesiveness with cells. As the material having a high hydrophilicity, various metal materials and ceramics (metal oxides) can be used. As the material having a high hydrophobicity, for example, fluororesins can be used.
Other examples of such materials include stainless steel, nickel, and aluminum, and silicon dioxide, alumina, and zirconia. In addition, it is conceivable to reduce cell adhesiveness by coating the surface of the material. For example, it is possible to coat the surface of the material with the metal or metal oxide materials described above, or coat the surface of the material with a synthetic phospholipid polymer mimicking a cellular membrane (e.g., LIPIDURE available from NOF Corporation).
It is preferable that the nozzle 121 be formed as a through hole having a substantially perfect circle shape in approximately the center of the membrane 12C. In this case, the diameter of the nozzle 121 is not particularly limited but is preferably twice or more greater than the size of the fluorescent-stained cell 350 in order to prevent the nozzle 121 from being clogged with the fluorescent-stained cell 350. When the fluorescent-stained cell 350 is, for example, an animal cell, particularly, a human cell, the diameter of the nozzle 121 is preferably 10 micrometers or greater and more preferably 100 micrometers or greater in conformity with the cell used, because a human cell typically has a size of about from 5 micrometers through 50 micrometers.
On the other hand, when a liquid droplet is extremely large, it is difficult to achieve an object of forming a minute liquid droplet. Therefore, the diameter of the nozzle 121 is preferably 200 micrometers or less. That is, in the liquid droplet discharging unit 10C, the diameter of the nozzle 121 is typically in the range of from 10 micrometers through 200 micrometers.
The driving element 13C is formed on the lower surface of the membrane 12C. The shape of the driving element 13C can be designed to match the shape of the membrane 12C. For example, when the planar shape of the membrane 12C is a circular shape, it is preferable to form a driving element 13C having an annular (ring-like) planar shape around the nozzle 121. The driving method for driving the driving element 13C may be the same as the driving method for driving the driving element 13.
The driving unit 20 can selectively (for example, alternately) apply to the driving element 13C, a discharging waveform for vibrating the membrane 12C to form a liquid droplet 310 and a stirring waveform for vibrating the membrane 12C to an extent until which a liquid droplet 310 is not formed.
For example, the discharging waveform and the stirring waveform may both be rectangular waves, and the driving voltage for the stirring waveform may be set lower than the driving voltage for the discharging waveform. This makes it possible for a liquid droplet 310 not to be formed by application of the stirring waveform. That is, it is possible to control the vibration state (degree of vibration) of the membrane 12C depending on whether the driving voltage is high or low.
In the liquid droplet discharging unit 10C, the driving element 13C is formed on the lower surface of the membrane 12C. Therefore, when the membrane 12 is vibrated by means of the driving element 13C, a flow can be generated in a direction from the lower portion to the upper portion in the liquid chamber 11C.
Here, the fluorescent-stained cells 350 move upward from lower positions, to generate a convection current in the liquid chamber 11C to stir the cell suspension 300 containing the fluorescent-stained cells 350. The flow from the lower portion to the upper portion in the liquid chamber 11C disperses the settled, aggregated fluorescent-stained cells 350 uniformly in the liquid chamber 11C.
That is, by applying the discharging waveform to the driving element 13C and controlling the vibration state of the membrane 12C, the driving unit 20 can cause the cell suspension 300 retained in the liquid chamber 11C to be discharged through the nozzle 121 in the form of a liquid droplet 310. Further, by applying the stirring waveform to the driving element 13C and controlling the vibration state of the membrane 12C, the driving unit 20 can stir the cell suspension 300 retained in the liquid chamber 11C. During stirring, no liquid droplet 310 is discharged through the nozzle 121.
In this way, stirring the cell suspension 300 while no liquid droplet 310 is being formed can prevent settlement and aggregation of the fluorescent-stained cells 350 over the membrane 12C and can disperse the fluorescent-stained cells 350 in the cell suspension 300 without unevenness. This can suppress clogging of the nozzle 121 and variation in the number of fluorescent-stained cells 350 in the liquid droplets 310 to be discharged. This makes it possible to stably discharge the cell suspension 300 containing the fluorescent-stained cells 350 in the form of liquid droplets 310 continuously for a long time.
In the liquid droplet forming device 401C, bubbles may mix in the cell suspension 300 in the liquid chamber 11C. Also in this case, with the atmospherically exposed portion 115 provided at the top of the liquid chamber 11C, the liquid droplet forming device 401C can be evacuated of the bubbles mixed in the cell suspension 300 to the outside air through the atmospherically exposed portion 115. This enables continuous, stable formation of liquid droplets 310 without a need for disposing of a large amount of the liquid for bubble evacuation.
That is, the discharging state is affected when mixed bubbles are present at a position near the nozzle 121 or when many mixed bubbles are present over the membrane 12C. Therefore, in order to perform stable formation of liquid droplets for a long time, there is a need for eliminating the mixed bubbles. Typically, mixed bubbles present over the membrane 12C move upward autonomously or by vibration of the membrane 12C. Because the liquid chamber 11C is provided with the atmospherically exposed portion 115, the mixed bubbles can be evacuated through the atmospherically exposed portion 115. This makes it possible to prevent occurrence of empty discharging even when bubbles mix in the liquid chamber 11C, enabling continuous, stable formation of liquid droplets 310.
At a timing at which a liquid droplet is not being formed, the membrane 12C may be vibrated to an extent until which a liquid droplet is not formed, in order to positively move the bubbles upward in the liquid chamber 11C.
—Electric or Magnetic Detection Method—
In the case of the electric or magnetic detection method, as illustrated in
<Operation for Observing Cells Before Discharging>
The operation for observing cells before discharging may be performed by, for example, a method for counting cells 350′ that have passed through a micro-flow path 250 illustrated in
As the discharging head 10′ illustrated in
<Operation for Counting Cells after Landing>
The operation for counting cells after landing may be performed by a method for detecting fluorescent-stained cells by observing the wells in the plate with, for example, a fluorescence microscope. This method is described in, for example, Sangjun et al., PLoS One, Volume 6(3), e17455.
Methods for observing cells before discharging a liquid droplet or after landing have the problems described below. Depending on the kind of the plate to be produced, it is the most preferable to observe cells in a liquid droplet that is being discharged. In the method for observing cells before discharging, the number of cells that are considered to have landed is counted based on the number of cells that have passed through a flow path and image observation before discharging (and after discharging). Therefore, it is not confirmed whether the cells have actually been discharged, and an unexpected error may occur. For example, there may be a case where because the nozzle portion is stained, a liquid droplet is not discharged appropriately but adheres to the nozzle plate, thus failing to make the cells in the liquid droplet land. Moreover, there may occur a problem that the cells stay behind in a narrow region of the nozzle portion, or a discharging operation causes the cells to move beyond assumption and go outside the range of observation.
The method for detecting cells on the plate after landing also have problems. First, there is a need for preparing a plate that can be observed with a microscope. As a plate that can be observed, it is common to use a plate having a transparent, flat bottom surface, particularly a plate having a bottom surface formed of glass. However, there is a problem that such a special plate is incompatible with use of ordinary wells. Further, when the number of cells is large, such as some tens of cells, there is a problem that correct counting is impossible because the cells may overlap with each other. Accordingly, it is preferable to perform the operation for observing cells before discharging and the operation for counting cells after landing, in addition to counting the number of cells contained in a liquid droplet with a sensor and a cell number counting unit after the liquid droplet is discharged and before the liquid droplet lands in a well.
As the light receiving element, a light receiving element including one or a small number of light receiving portion(s), such as a photodiode, an Avalanche photodiode, and a photomultiplier tube may be used. In addition, a two-dimensional sensor including light receiving elements in a two-dimensional array formation, such as a CCD (Charge Coupled Device), a CMOS (Complementary Metal Oxide Semiconductor), and a gate CCD may be used.
When using a light receiving element including one or a small number of light receiving portion(s), it is conceivable to determine the number of cells contained, based on the fluorescence intensity, using a calibration curve prepared beforehand. Here, binary detection of whether cells are present or absent in a flying liquid droplet is common. When the cell suspension is discharged in a state that the cell concentration is so sufficiently low that almost only 1 or 0 cell(s) will be contained in a liquid droplet, sufficiently accurate counting is available by the binary detection. On the premise that cells are randomly distributed in the cell suspension, the cell number in a flying liquid droplet is considered to conform to a Poisson distribution, and the probability P (>2) at which two or more cells are contained in a liquid droplet is represented by a formula (1) below.
P(>2)=1−(1+λ)×e−λ formula (1)
<<<Step of Calculating Degrees of Certainty of Estimated Numbers of Nucleic Acids in Cell Suspension Producing Step, Liquid Droplet Landing Step, and Cell Number Counting Step>>>
The step of calculating degrees of certainty of estimated numbers of nucleic acids in the cell suspension producing step, the liquid droplet landing step, and the cell number counting step is a step of calculating the degree of certainty in each of the cell suspension producing step, the liquid droplet landing step, and the cell number counting step.
The degree of certainty of an estimated number of nucleic acids can be calculated in the same manner as calculating the degree of certainty in the cell suspension producing step.
The timing at which the degrees of certainty are calculated may be collectively in the next step to the cell number counting step, or may be at the end of each of the cell suspension producing step, the liquid droplet landing step, and the cell number counting step in order for the degrees of certainty to be summed in the next step to the cell number counting step. In other words, the degrees of certainty in these steps need only to be calculated at arbitrary timings by the time when summing is performed.
<<Outputting Step>>
The outputting step is a step of outputting a counted value of the number of cells contained in the cell suspension that has landed in a well, counted by a particle number counting unit based on a detection result measured by a sensor.
The counted value means a number of cells contained in the well, calculated by the particle number counting unit based on the detection result measured by the sensor.
Outputting means sending a value counted by a device such as a motor, communication equipment, and a calculator upon reception of an input to an external server serving as a count result memory unit in the form of electronic information, or printing the counted value as a printed matter.
In the outputting step, an observed value or an estimated value obtained by observing or estimating the number of cells or the number of nucleic acids in each well of a plate during production of the plate is output to an external memory unit.
Outputting may be performed at the same time as the cell number counting step, or may be performed after the cell number counting step.
<<Recording Step>>
The recording step is a step of recording the observed value or the estimated value output in the outputting step.
The recording step can be suitably performed by a recording unit.
Recording may be performed at the same time as the outputting step, or may be performed after the outputting step.
Recording means not only supplying information to a recording medium but also storing information in a memory unit.
<<Nucleic Acid Extracting Step>>
The nucleic acid extracting step is a step of extracting nucleic acids from cells in the well.
Extracting means destroying, for example, cellular membranes and cell walls to pick out nucleic acids.
As the method for extracting nucleic acids from cells, there is known a method of thermally treating cells at from 90 degrees C. through 100 degrees C. By a thermal treatment at 90 degrees C. or lower, there is a possibility that DNA may not be extracted. By a thermal treatment at 100 degrees C. or higher, there is a possibility that DNA may be decomposed. Here, it is preferable to perform thermal treatment with addition of a surfactant.
The surfactant is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the surfactant include ionic surfactants and nonionic surfactants. One of these surfactants may be used alone or two or more of these surfactants may be used in combination. Among these surfactants, nonionic surfactants are preferable because proteins are neither modified nor deactivated by nonionic surfactants, although depending on the addition amount of the nonionic surfactants.
Examples of the ionic surfactants include fatty acid sodium, fatty acid potassium, alpha-sulfo fatty acid ester sodium, sodium straight-chain alkyl benzene sulfonate, alkyl sulfuric acid ester sodium, alkyl ether sulfuric acid ester sodium, and sodium alpha-olefin sulfonate. One of these ionic surfactants may be used alone or two or more of these ionic surfactants may be used in combination. Among these ionic surfactants, fatty acid sodium is preferable and sodium dodecyl sulfate (SDS) is more preferable.
Examples of the nonionic surfactants include alkyl glycoside, alkyl polyoxyethylene ether (e.g., BRIJ series), octyl phenol ethoxylate (e.g., TRITON X series, IGEPAL CA series, NONIDET P series, and NIKKOL OP series), polysorbates (e.g., TWEEN series such as TWEEN 20), sorbitan fatty acid esters, polyoxyethylene fatty acid esters, alkyl maltoside, sucrose fatty acid esters, glycoside fatty acid esters, glycerin fatty acid esters, propylene glycol fatty acid esters, and fatty acid monoglyceride. One of these nonionic surfactants may be used alone or two or more of these nonionic surfactants may be used in combination. Among these nonionic surfactants, polysorbates are preferable.
The content of the surfactant is preferably 0.01% by mass or greater but 5.00% by mass or less relative to the total amount of the cell suspension in the well. When the content of the surfactant is 0.01% by mass or greater, the surfactant can be effective for DNA extraction. When the content of the surfactant is 5.00% by mass or less, inhibition against amplification can be prevented during PCR. As a numerical range in which both of these effects can be obtained, the range of 0.01% by mass or greater but 5.00% by mass or less is preferable.
The method described above may not be able to sufficiently extract DNA from a cell that has a cell wall. Examples of methods for such a case include an osmotic shock procedure, a freeze-thaw method, an enzymic digestive method, use of a DNA extraction kit, an ultrasonic treatment method, a French press method, and a homogenizer method. Among these methods, an enzymic digestive method is preferable because the method can save loss of extracted DNA.
<<Other Steps>>
The other steps are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the other steps include an enzyme deactivating step and a step of changing the composition except for the specific copy number of the amplifiable reagent.
—Enzyme Deactivating Step—
The enzyme deactivating step is a step of deactivating an enzyme.
Examples of the enzyme include DNase, RNase, and an enzyme used in the nucleic acid extracting step in order to extract a nucleic acid.
The method for deactivating an enzyme is not particularly limited and may be appropriately selected depending on the intended purpose. A known method can be suitably used.
<<Step of Changing Composition Except for Specific Copy Number of Amplifiable Reagent>>
What is meant by the step of changing the composition except for the specific copy number of the amplifiable reagent is that it is possible to provide combinations that may or may not contain any other primer or amplifying reagent than the nucleic acid serving as the amplifiable reagent. Specifically, one well includes (1) a composition containing a nucleic acid, a primer, and an amplifying reagent, another well includes (2) a composition containing a nucleic acid and a primer, and yet another well includes (3) a composition containing only a nucleic acid. A preparator who prepares reagent compositions adds a primer and an amplifying reagent to the compositions of (2) and (3) by a manual operation in preparation of the reagent compositions, and use the reagent compositions for a PCR reaction.
The step of changing the composition except for the specific copy number of the amplifiable reagent may be performed by machine dispensing instead of a manual operation. This makes it possible to accurately dispense the primer and the amplifying reagent.
Hence, the device enables, for example, evaluation of the skill of the preparator who prepares the reagent compositions.
The device of the present disclosure is widely used in, for example, biotechnology-related industries, life science industries, and health care industries, and can be used suitably for, for example, equipment calibration or generation of calibration curves, and management of the accuracy of a testing device.
In the case of working the device for infectious diseases, the device is applicable to methods stipulated as official analytical methods or officially announced methods.
(Preparator's Skill Evaluating Method, Preparator's Skill Evaluating Device, and Preparator's Skill Evaluating Program)
A preparator's skill evaluating method of the present disclosure is a preparator's skill evaluating method for evaluating the skill of a preparator who prepares a reagent composition, includes a Ct value information obtaining step of obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure and a skill evaluating step of evaluating the skill of a preparator based on the obtained information on the Ct value, and further includes other steps as needed.
A preparator's skill evaluating device of the present disclosure is a preparator's skill evaluating device configured to evaluate the skill of a preparator who prepares a reagent composition, includes a Ct value information obtaining unit configured to obtain information on a Ct value in the device of the present disclosure using the device of the present disclosure and a skill evaluating unit configured to evaluate the skill of a preparator based on the obtained information on the Ct value, and further includes other units as needed.
A preparator's skill evaluating program of the present disclosure is a preparator's skill evaluating program for evaluating the skill of a preparator who prepares a reagent composition, and causes a computer to execute a process including obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure, and evaluating the skill of a preparator based on the obtained information on the Ct value.
Control being performed by, for example, a control unit of the preparator's skill evaluating device of the present disclosure has the same meaning as the preparator's skill evaluating method of the present disclosure being carried out. Therefore, details of the preparator's skill evaluating method will also be specified through description of the preparator's skill evaluating device of the present disclosure. Further, the preparator's skill evaluating program of the present disclosure realizes the preparator's skill evaluating device of the present disclosure with the use of, for example, computers as hardware resources. Therefore, details of the preparator's skill evaluating program of the present disclosure will also be specified through description of the preparator's skill evaluating device of the present disclosure.
<Ct Value Information Obtaining Step and Ct Value Information Obtaining Unit>
The Ct value information obtaining step is a step of obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure, and is performed by the Ct value information obtaining unit.
Ct value indicates the cycle number at a timing when a fluorescence signal of a reaction crosses Threshold Line. Because Ct value is linearly decreased to the logarithm of the initial amount of the target, the initial copy number of DNA can be calculated based on Ct value.
Threshold Line indicates the signal level at which a statistically significant increase from a calculated baseline signal is observed, and means the threshold of a real-time PCR reaction.
Baseline means the signal level in PCR initial cycles during which the fluorescence signal does not almost change.
Examples of the information on the Ct value include a Ct value, average Ct, standard deviation, CV value [(standard deviation/average Ct)×100], and [(Ct(Max)−Ct(min))/2·average Ct]×100.
<Skill Evaluating Step and Skill Evaluating Unit>
The skill evaluating step is a step of evaluating the skill of a preparator based on the information on the Ct value, and is performed by the skill evaluating unit.
Examples of the skill of the preparator include a skill of the preparator to prepare a reagent composition by a manual operation as regards the composition other than a nucleic acid in the device.
It is possible to evaluate the skill of the preparator, based on a PCR reaction of a prepared reagent composition performed using the device of the present disclosure, and comparison of information on Ct values to be obtained.
For evaluation of the skill of the preparator, the preparator may prepare samples on the same device on which the standard samples with which the samples are to be compared are provided, or may prepare samples on a different device. As the method for evaluating the skill of the preparator by letting the preparator prepare samples on the same device on which the standard samples with which the samples are to be compared are provided, for example, an automatic dispensing device or a certified skill holder prepares reagents on wells, and the preparator to be evaluated prepares reagents on different wells on the same device. Then, Ct values obtained from PCR reactions in the respective wells are compared with each other. In this way, it is possible to evaluate the skill of the preparator. As the method for evaluating the skill of the preparator by letting the preparator prepare samples on a device different from the device on which the standard samples with which the samples are to be compared are provided, for example, an automatic dispensing device or a certified skill holder prepares reagents on a first device, and the preparator to be evaluated prepares reagents on a second device. Then, Ct values obtained from PCR reactions using the prepared first and second devices are compared with each other. In this way, it is possible to evaluate the skill of the preparator to be evaluated.
<Other Steps and Other Units>
The other steps and other units are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the other steps and other units include a displaying step and a display unit.
The process according to the preparator's skill evaluating program of the present disclosure can be executed using a computer including a control unit constituting the preparator's skill evaluating device.
The hardware configuration and the functional configuration of the preparator's skill evaluating device will be described below.
<Hardware Configuration of Preparator's Skill Evaluating Device>
As illustrated in
The CPU 101 is a processing device configured to execute various controls and operations. The CPU 101 realizes various functions by executing an OS (Operating System) and programs stored in, for example, the main memory device 102. That is, in the present example, the CPU 101 functions as a control unit 130 of the preparator's skill evaluating device 100 by executing the preparator's skill evaluating program.
The CPU 101 also controls the operation of the preparator's skill evaluating device 100 on the whole. In the present example, the CPU 101 is used as the device configured to control the operation of the preparator's skill evaluating device 100 on the whole. However, this is non-limiting. For example, a FPGA (Field Programmable Gate Array) may be used.
The preparator's skill evaluating program and various databases need not be stored in, for example, the main memory device 102 or the auxiliary memory device 103. The preparator's skill evaluating program and various databases may be stored in, for example, any other information processing device that is coupled to the preparator's skill evaluating device 100 via, for example, the Internet, a LAN (Local Area Network), and a WAN (Wide Area Network). The preparator's skill evaluating device 100 may be configured to receive the preparator's skill evaluating program and various databases from such another information processing device and execute the preparator's skill evaluating program and various databases.
The main memory device 102 is configured to store various programs and store, for example, data needed for execution of the various programs.
The main memory device 102 includes a ROM (Read Only Memory) and a RAM (Random Access Memory) unillustrated.
The ROM stores, for example, various programs such as BIOS (Basic Input/Output System).
The RAM functions as a work area to be developed when the various programs stored in the ROM are executed by the CPU 101. The RAM is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the RAM include a DRAM (Dynamic Random Access Memory) and an SRAM (Static Random Access Memory).
The auxiliary memory device 103 is not particularly limited and may be appropriately selected depending on the intended purpose so long as the auxiliary memory device 103 can store various information. Examples of the auxiliary memory device 103 include a solid-state drive and a hard disk drive. As the auxiliary memory device 103, for example, portable memory devices such as a CD (Compact Disc) drive, a DVD (Digital Versatile Disc) drive, and a BD (Blu-ray (registered trademark) Disc) drive may also be used.
As the output device 104, for example, a display and a speaker can be used. The display is not particularly limited and an appropriate known display may be used. Examples of the display include a liquid crystal display and an organic EL display.
The input device 105 is not particularly limited and an appropriate known input device may be used so long as the input device can receive various requests to the preparator's skill evaluating device 100. Examples of the input device include a keyboard, a mouse, and a touch panel.
The communication interface (communication I/F) 106 is not particularly limited and an appropriate known communication interface may be used. Examples of the communication interface include a wireless or wired communication device.
The hardware configuration described above can realize the process functions of the preparator's skill evaluating device 100.
<Functional Configuration of Preparator's Skill Evaluating Device>
As illustrated in
The control unit 130 includes a Ct value information obtaining unit 131 and a skill evaluating unit 132. The control unit 130 is configured to control the preparator's skill evaluating device 100 on the whole.
The memory unit 140 includes a Ct value information database 141 and a skill evaluation result database 142. Hereinafter, “database” may also be referred to as “DB”.
The Ct value information obtaining unit 131 is configured to obtain information on a Ct value, using data representing the information on a Ct value stored in the Ct value information DB 141 of the memory unit 140. As described above, the Ct value information DB 141 stores, for example, data representing a Ct value previously obtained by an experiment. Note that information on a Ct value associated with the device may be stored in the Ct value information DB 141. Inputting to the DB may be performed via another information processing device coupled to the preparator's skill evaluating device 100 or performed by a human operator.
The skill evaluating unit 132 is configured to evaluate the skill of a preparator based on information on a Ct value. Examples of a specific method for evaluating the skill of a preparator include a method of calculating a standard deviation from the obtained Ct value and evaluating the skill of the preparator based on the calculated standard deviation.
The result of evaluating the skill of the preparator by the skill evaluating unit 132 is stored in the skill evaluation result DB 142 of the memory unit 140.
Next, the process procedures of the preparator's skill evaluating program of the present disclosure will be described.
In the step S110, the Ct value information obtaining unit 131 of the control unit 130 of the preparator's skill evaluating device 100 obtains data representing the information on a Ct value stored in the Ct value information DB 141 of the memory unit 140, and moves the process to the step S111.
In the step S111, the skill evaluating unit 132 of the control unit 130 of the preparator's skill evaluating device 100 evaluates the skill of the preparator based on the obtained information on the Ct value, and moves the process to the step S112.
In the step S112, the control unit 130 of the preparator's skill evaluating device 100 stores the obtained result of evaluation of the skill of the preparator in the skill evaluation result DB 142 of the memory unit 140, and ends the process.
(Testing Device Performance Evaluating Method, Testing Device Performance Evaluating Device, and Testing Device Performance Evaluating Program)
A testing device performance evaluating method of the present disclosure is a testing device performance evaluating method for evaluating the performance of a testing device configured to test a testing target, includes a Ct value information obtaining step of obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure, and a performance evaluating step of evaluating the performance of the testing device based on the information on the Ct value, and further includes other steps as needed.
A testing device performance evaluating device of the present disclosure is a testing device performance evaluating device configured to evaluate the performance of a testing device configured to test a testing target, and includes a Ct value information obtaining unit configured to obtain information on a Ct value in the device of the present disclosure using the device of the present disclosure, and a performance evaluating unit configured to evaluate the performance of the testing device based on the information on the Ct value, and further includes other units as needed.
A testing device performance evaluating program of the present disclosure is a testing device performance evaluating program for evaluating the performance of a testing device configured to test a testing target, and causes a computer to execute a process including obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure and evaluating the performance of the testing device based on the information on the Ct value.
Control being performed by, for example, a control unit of the testing device performance evaluating device of the present disclosure has the same meaning as the testing device performance evaluating method of the present disclosure being carried out. Therefore, details of the testing device performance evaluating method will also be specified through description of the testing device performance evaluating device of the present disclosure. Further, the testing device performance evaluating program of the present disclosure realizes the testing device performance evaluating device of the present disclosure with the use of, for example, computers as hardware resources. Therefore, details of the testing device performance evaluating program of the present disclosure will also be specified through description of the testing device performance evaluating device of the present disclosure.
<Ct Value Information Obtaining Step and Ct Value Information Obtaining Unit>
The Ct value information obtaining step is a step of obtaining information on a Ct value in the device of the present disclosure using the device of the present disclosure, and is performed by the Ct value information obtaining unit.
A Ct value can be obtained by performing real-time PCR using the device of the present disclosure.
Examples of the information on the Ct value include an average Ct value, standard deviation of Ct values, a CV value [(standard deviation/average Ct value)×100], and [(Ct value (Max)−Ct value (min))/2·average Ct value]×100.
Information on the Ct value may be obtained for each of two or more groups provided in the device and varied in the specific copy number of the amplifiable reagent.
<Performance Evaluating Step and Performance Evaluating Unit>
The performance evaluating step is a step of evaluating the performance of the testing device based on the information on the Ct value, and is performed by the performance evaluating unit.
In a qualitative evaluation, real-time PCR is performed using the device of the present disclosure to measure Ct values and calculate the average Ct value. An in-plane property can be evaluated by grading a well as “◯” when the Ct value in the well is within 10% of the average Ct value, and grading a well as “x” when the Ct value in the well is greater than 10% of the average Ct value.
By performing measurement for a certain period of time using the device of the present disclosure, it is possible to obtain temporal changes of the Ct values. Hence, like the in-plane property, when the Ct value of a well is greater than 10% of the average Ct value, it is possible to perform calibration of the testing device or to adopt a measure of not using the measured position. Furthermore, because the specific copy number of the copies located is an absolute value, use of devices with copies located in the same specific copy number enables comparison of the performance between testing devices.
In a quantitative evaluation, by performing measurement for a certain period of time using the device of the present disclosure, it is possible to obtain temporal changes of the Ct values. Hence, like the in-plane property, when a value deviating from a quality control value is obtained, it is possible to perform calibration of the testing device or to adopt a measure of not using the measured position. Furthermore, because the copy number of the copies located is an absolute value, use of devices with copies located in the same copy number enables comparison of the performance between testing devices.
In a quantitative evaluation, not a Ct value per se, but a number of molecules (a copy number or a concentration) corresponding to a Ct value can be obtained from a calibration curve and PCR efficiency. Therefore, the performance evaluation between testing devices may be performed using such values as a number of molecules (a copy number or a concentration), or a CV value converted to a number of molecules (a copy number of a concentration), and (Max−Min)/2·average value×100 calculated for a number of molecules (converted to a copy number or a concentration).
<Other Steps and Other Units>
The other steps and the other units are not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the other steps and the other units include a displaying step and a display unit.
The process according to the testing device performance evaluating program of the present disclosure can be executed using a computer including a control unit constituting the testing device performance evaluating device.
The hardware configuration and the functional configuration of the testing device performance evaluating device will be described below.
<Hardware Configuration of Testing Device Performance Evaluating Device>
As illustrated in
The CPU 101 is a processing device configured to execute various controls and operations. The CPU 101 realizes various functions by executing an OS (Operating System) and programs stored in, for example, the main memory device 102. That is, in the present example, the CPU 101 functions as a control unit 130 of the testing device performance evaluating device 100 by executing the testing device performance evaluating program.
The CPU 101 also controls the operation of the testing device performance evaluating device 100 on the whole. In the present example, the CPU 101 is used as the device configured to control the operation of the testing device performance evaluating device 100 on the whole. However, this is non-limiting. For example, a FPGA (Field Programmable Gate Array) may be used.
The testing device performance evaluating program and various databases need not be stored in, for example, the main memory device 102 or the auxiliary memory device 103. The testing device performance evaluating program and various databases may be stored in, for example, any other information processing device that is coupled to the testing device performance evaluating device 100 via, for example, the Internet, a LAN (Local Area Network), and a WAN (Wide Area Network). The testing device performance evaluating device 100 may be configured to receive the testing device performance evaluating program and various databases from such another information processing device and execute the testing device performance evaluating program and various databases.
The main memory device 102 is configured to store various programs and store, for example, data needed for execution of the various programs.
The main memory device 102 includes a ROM (Read Only Memory) and a RAM (Random Access Memory) unillustrated.
The ROM stores, for example, various programs such as BIOS (Basic Input/Output System).
The RAM functions as a work area to be developed when the various programs stored in the ROM are executed by the CPU 101. The RAM is not particularly limited and may be appropriately selected depending on the intended purpose. Examples of the RAM include a DRAM (Dynamic Random Access Memory) and an SRAM (Static Random Access Memory).
The auxiliary memory device 103 is not particularly limited and may be appropriately selected depending on the intended purpose so long as the auxiliary memory device 103 can store various information. Examples of the auxiliary memory device 103 include a solid-state drive and a hard disk drive. As the auxiliary memory device 103, for example, portable memory devices such as a CD (Compact Disc) drive, a DVD (Digital Versatile Disc) drive, and a BD (Blu-ray (registered trademark) Disc) drive may also be used.
As the output device 104, for example, a display and a speaker can be used. The display is not particularly limited and an appropriate known display may be used. Examples of the display include a liquid crystal display and an organic EL display.
The input device 105 is not particularly limited and an appropriate known input device may be used so long as the input device can receive various requests to the testing device performance evaluating device 100. Examples of the input device include a keyboard, a mouse, and a touch panel.
The communication interface (communication I/F) 106 is not particularly limited and an appropriate known communication interface may be used. Examples of the communication interface include a wireless or wired communication device.
The hardware configuration described above can realize the process functions of the testing device performance evaluating device 100.
<Functional Configuration of Testing Device Performance Evaluating Device>
As illustrated in
The control unit 130 includes a Ct value information obtaining unit 131 and a performance evaluating unit 132. The control unit 130 is configured to control the testing device performance evaluating device 100 on the whole.
The memory unit 140 includes a Ct value information database 141 and a performance evaluation result database 142. Hereinafter, “database” may also be referred to as “DB”.
The Ct value information obtaining unit 131 is configured to obtain information on a Ct value, using data representing the information on a Ct value stored in the Ct value information DB 141 of the memory unit 140. As described above, the Ct value information DB 141 stores, for example, data representing a Ct value previously obtained by an experiment. Note that information on a Ct value associated with the device may be stored in the Ct value information DB 141. Inputting to the DB may be performed via another information processing device coupled to the testing device performance evaluating device 100 or performed by a human operator.
The performance evaluating unit 132 is configured to evaluate the performance of a testing device based on information on a Ct value. The specific method for evaluating the performance of a testing device is as described above.
The result of evaluating the performance of the testing device by the performance evaluating unit 132 is stored in the performance evaluation result DB 142 of the memory unit 140.
Next, the process procedures of the testing device performance evaluating program of the present disclosure will be described.
In the step S110, the Ct value information obtaining unit 131 of the control unit 130 of the testing device performance evaluating device 100 obtains data representing the information on a Ct value stored in the Ct value information DB 141 of the memory unit 140, and moves the process to the step S111.
In the step S111, the performance evaluating unit 132 of the control unit 130 of the testing device performance evaluating device 100 evaluates the performance of the testing device based on the obtained information on the Ct value, and moves the process to the step S112.
In the step S112, the control unit 130 of the testing device performance evaluating device 100 stores the obtained result of evaluation of the performance of the testing device in the performance evaluation result DB 142 of the memory unit 140, and ends the process.
The present disclosure will be described below by way of Examples. The present disclosure should not be construed as being limited to these Examples.
<Production of Device>
A device was produced in the manner described below.
—Gene Recombinant Yeast—
For producing a recombinant, a budding yeast YIL015W BY4741 (available from ATCC, ATCC4001408) was used as a carrier cell for one copy of a specific nucleic acid sequence. The specific nucleic acid sequence was a dense nucleic acid sample DNA600-G (available from National Institute of Advanced Industrial Science and Technology, NMIJ CRM 6205-a, see SEQ ID NO. 1). In the form of a plasmid produced by arranging the specific nucleic acid sequence in tandem with URA3, which was a selectable marker, one copy of the specific nucleic acid sequence was introduced into yeast genome DNA by homologous recombination, targeting a BAR1 region of the carrier cell, to produce a gene recombinant yeast.
—Culturing and Cell-Cycle Control—
In an Erlenmeyer flask, a 90-mL fraction of the gene recombinant yeast cultured in 50 g/L of a YPD medium (available from Takara Bio Inc., CLN-630409) was mixed with 900 microliters of α1-MATING FACTOR ACETATE SALT (available from Sigma-Aldrich Co., LLC, T6901-5MG, hereinafter referred to as “a factor”) prepared to 500 micrograms/mL with a Dulbecco's phosphate buffered saline (available from Thermo Fisher Scientific Inc., 14190-144, hereinafter referred to as “DPBS”).
Next, the resultant was incubated with a bioshaker (available from Taitec Corporation, BR-23FH) at a shaking speed of 250 rpm at a temperature of 28 degrees C. for 2 hours, to synchronize the yeast at a G0/G1 phase, to obtain a yeast suspension. For confirmation of the cell cycle of the synchronized cells, the cells were stained with SYTOX GREEN NUCLEIC ACID STAIN (device name: S7020, available from Thermo Fisher Scientific Inc.) and subjected to flow cytometry using a flow cytometer (device name: SH800, available from Sony Corporation) at an excitation wavelength of 488 nm. As a result, it was confirmed that the cells were synchronized at a G0/G1 phase. The ratio of cells at a G1 phase was 99.5% and the ratio of cells at a G2 phase was 0.5%.
—Fixing—
Forty-five milliliters of the synchronization-confirmed yeast suspension was transferred to a centrifuge tube (available from As One Corporation, VIO-50R) and centrifuged with a centrifugal separator (available from Hitachi, Ltd., F16RN,) at a rotation speed of 3,000 rpm for 5 minutes, with subsequent supernatant removal, to obtain yeast pellets. Four milliliters of formalin (available from Wako Pure Chemical Industries, Ltd., 062-01661) was added to the obtained yeast pellets, and the resultant was left to stand still for 5 minutes, then centrifuged with subsequent supernatant removal, and suspended with addition of 10 mL of ethanol, to obtain a fixed yeast suspension.
—Staining—
Five hundred microliters of the fixed yeast suspension was transferred to a 1.5 mL light-shielding tube (available from Watson, 131-915BR), centrifuged with a centrifugal separator at a rotation speed of 3,000 rpm for 5 minutes with subsequent supernatant removal, suspended sufficiently by pipetting with addition of 400 microliters of DPBS (1 mM EDTA) prepared to 1 mM EDTA (available from Tocris Bioscience, 200-449-4), then centrifuged with a centrifugal separator at a rotation speed of 3,000 rpm for 5 minutes with subsequent supernatant removal, to obtain yeast pellets. One milliliter of an Evans blue aqueous solution (available from Wako Pure Chemical Industries, Ltd., 054-04061) prepared to 1 mg/mL was added to the obtained pellets, and the resultant was stirred with a vortex for 5 minutes, then centrifuged with a centrifugal separator at a rotation speed of 3,000 rpm for 5 minutes with subsequent supernatant removal, and stirred with a vortex with addition of DPBS (1 mM EDTA), to obtain a stained yeast suspension.
—Dispersing—
The stained yeast suspension was subjected to dispersion treatment using an ultrasonic homogenizer (available from Yamato Scientific Co., Ltd., device name: LUH150) at a power output of 30% for 10 seconds, centrifuged with a centrifugal separator at a rotation speed of 3,000 rpm for 5 minutes with subsequent supernatant removal, and then washed with addition of 1 mL of DPBS. Centrifugal separation and supernatant removal were performed twice in total, and the resultant was again suspended in 1 mL of DPBS, to obtain a yeast suspension ink.
—Dispensing and Cell Counting—
A plate with a known cell number was produced by counting the number of yeast cells in liquid droplets in the manner described below to discharge 10 cells per well. Specifically, with the use of the liquid droplet forming device illustrated in
An image of yeast cells in a liquid droplet discharged was captured using a high-sensitivity camera (available from Tokyo Instruments Inc., SCMOS PCO.EDGE) as a light receiving unit and using a YAG laser (available from Spectra-Physics, Inc., EXPLORER ONE-532-200-KE) as a light source, and the cell number was counted by image processing with image processing software IMAGE J serving as a particle number counting unit for the captured image. In this way, a plate with a known cell number of 1 was produced.
—Extraction of Nucleic Acids—
With a Tris-EDTA (TE) buffer and ColE1 DNA (available from Wako Pure Chemical Industries, Ltd., 312-00434), ColE1/TE was prepared at 5 ng/microliter. With ColE1/TE, a Zymolyase solution of Zymolyase® 100T (available from Nacalai Tesque Inc., 07665-55) was prepared at 1 mg/mL.
Four microliters of the Zymolyase solution was added into each well of the produced plate with a known cell number, incubated at 37.2 degrees C. for 30 minutes, to dissolve cell walls (extraction of nucleic acids), and then thermally treated at 95 degrees C. for 2 minutes, to produce a plate.
Next, in order to consider the reliability of a result obtained from a plate with a known cell number, a plate with a known cell number was produced by dispensing cells in a specific copy number into wells and the uncertainty for a cell number of 1 was calculated. Note that it is possible to calculate uncertainties for various copy numbers, by using the method described below for each specific copy number.
—Calculation of Uncertainty—
In the present Example, the number of cells in a liquid droplet, the copy number of amplifiable reagents in a cell, the number of cells in a well, and contamination were used as the factors for uncertainty.
As the number of cells in a liquid droplet, the number of cells in a liquid droplet, counted based on an analysis of an image of the liquid droplet discharged by a discharging unit, and the number of cells obtained based on microscopic observation of each liquid droplet landed on a glass slide among liquid droplets discharged by a discharging unit so as to be landed on the glass slide were used.
The copy number of nucleic acids in a cell (cell cycle) was calculated using the ratio of cells that were at a G1 phase of the cell cycle (99.5%) and the ratio of cells that were at a G2 phase (0.5%).
As the number of cells in a well, the number of discharged liquid droplets landed in a well was counted. However, in counting 96 samples in total, all of the samples were landed in the wells as liquid droplets. Therefore, as a factor, the number of cells in a well was excluded from calculation of the uncertainty.
To confirm contamination, a filtrate (4 microliters) of the ink was subjected to real-time PCR to see whether any other nucleic acid than the amplifiable reagents in the cell was mixed in the ink liquid. This was tried three times. The result was the limit of detection in all of the three tries. Therefore, as a factor, contamination was also excluded from calculation of the uncertainty.
For the uncertainty, standard deviation was calculated from the measured values of each factor and multiplied by a sensitivity coefficient, to obtain a standard uncertainty unified in the unit of the measured quantity. Based on such standard uncertainties, a synthesized standard uncertainty was calculated according to the sum-of-squares method. The synthesized standard uncertainty covered only the values in a range of about 68% of a normal distribution. Therefore, by doubling the synthesized standard uncertainty, it was possible to obtain an expanded uncertainty, which was an uncertainty that took into account a range of about 95% of the normal distribution. The results are presented in the budget sheet of Table 2 below.
In Table 2, “Symbol” means an arbitrary symbol associated with a factor of the uncertainty.
In Table 2, “Value (±)” indicates an experimental standard deviation in average value, obtained by dividing a calculated experimental standard deviation by the square root of the number of data.
In Table 2, “Probability distribution” is a probability distribution of a factor of the uncertainty. The field was left blank for type-A uncertainty evaluation, whereas either normal distribution or rectangular distribution was filled in the field for type-B uncertainty evaluation. In the present Example, only type-A uncertainty evaluation was performed. Therefore, the probability distribution field was left blank.
In Table 2, “Divisor” means a number that normalizes the uncertainty of each factor.
In Table 2, “Standard uncertainty” is a value obtained by dividing “Value (±)” by “Divisor”.
In Table 2, “Sensitivity coefficient” means a value used for unification to the unit of the measured quantity.
Next, average specific copy numbers of nucleic acid samples filled in wells and uncertainties were calculated. The results are presented in Table 3. The coefficients of variation CV were calculated by dividing the uncertainty values by the average specific copy numbers.
According to the inkjet method, the accuracy for dispensing a specific copy number of 1 of a nucleic acid sample, i.e., one copy of a nucleic acid sample (one yeast cell) per well was found to be ±0.1281 copies. In the case of filling one or more copies per well, the accuracy at which a specific copy number of nucleic acid samples would be filled would be determined by accumulation of this accuracy.
In the present disclosure, a nucleic acid may be dispensed in a specific copy number into wells not only by the inkjet method described above but also by a method using a cell sorter described below. A case where a cell sorter was used will be described below. Until the fixing of the yeast suspension, the same methods as described above were used. Therefore, description about the procedure up to the fixing will be skipped.
—Nuclear Staining—
Two hundred microliters of the fixed yeast suspension was fractionated, washed with DPBS once, and resuspended in 480 microliters of DPBS.
Next, to the resultant, 20 microliters of 20 mg/mL RNase A (available from Nippon Gene Co., Ltd., 318-06391) was added, followed by incubation with a bioshaker at 37 degrees C. for 2 hours.
Next, to the resultant, 25 microliters of 20 mg/mL proteinase K (available from Takara Bio Inc., TKR-9034) was added, followed by incubation with PETIT COOL (available from Waken B Tech Co., Ltd., PETIT COOL MINI T-C) at 50 degrees C. for 2 hours.
Finally, to the resultant, 6 microliters of 5 mM SYTOX GREEN NUCLEIC ACID STAIN (available from Thermo Fisher Scientific Inc., 57020) was added, followed by staining in a light-shielded environment for 30 minutes.
—Dispersing—
The stained yeast suspension was subjected to dispersion treatment using an ultrasonic homogenizer (available from Yamato Scientific Co., Ltd., LUH150,) at a power output of 30% for 10 seconds, to obtain a yeast suspension ink.
<Filling of Nucleic Acid Samples>
—Dispensing of Yeast Suspension with Number Counting—
After a filling container (96-well flat bottom plate (available from Watson Co., Ltd., 4846-96-FS)) was filled with a dissolving liquid for dissolving cell walls in an amount of 4 microliters per well beforehand, the series of nucleic acid samples were dispensed one cell per well, using a cell sorter (available from Sony Corporation, SH800Z).
Next, with a Tris-EDTA (TE) buffer (available from Thermo Fisher Scientific Inc., AM9861) serving as a cell wall dissolving liquid and ColE1 DNA (available from Nippon Gene Co., Ltd., 312-00434), ColE1/TE was prepared at 5 ng/microliter. With ColE1/TE, a Zymolyase solution of Zymolyase® 100T (available from Nacalai Tesque Inc., 07665-55) was prepared at 1 mg/mL.
Next, during dispensing by a cell sorter, the cell cycle was analyzed at an excitation wavelength of 488 nm, to select only a region in which G0/G1 phase cells were present and dispense a prescribed number of yeast cells by a single cell mode.
—Extraction of Nucleic Acids from Dispensed Yeast Cells—
For extraction of nucleic acids from the yeast cells, the filling container was incubated at 37 degrees C. for 30 minutes, to dissolve the cell walls (extraction of nucleic acids), and then thermally treated at 95 degrees C. for 2 minutes.
<Calculation of Uncertainty of Series of Nucleic Acid Samples>
The series of nucleic acid samples filled had certain uncertainties for the respective specific copy number levels, due to the following factor of uncertainty.
Factor i: Uncertainty regarding a percentage at which the yeast cell number in each discharged liquid droplet matched
The uncertainty regarding the factor i was calculated based on the percentage at which the numbers of yeast cells in landed liquid droplets discharged into another container under the same conditions as in the filling method matched the intended numbers of yeast cells.
In the present experiment system, the accuracy of the cell sorter for dispensing one yeast cell (specific copy number of 1) per well was 99.2%. In the case of dispensing a greater number of yeast cells (a greater copy number), it is safe to consider that the accuracy for dispensing a specific copy number of yeast cells would be determined by accumulation of the accuracy for one cell.
In the way described above, an average specific copy number and the uncertainty were calculated for each nucleic acid sample filled. The results are presented in Table 4. The coefficient of variation CV was calculated by dividing the uncertainty by the average specific copy number.
—Association of Uncertainty with Each Filled Portion—
The calculated uncertainty was associated with each well.
In this way, it was possible to calculate the average copy number of nucleic acids of the series of nucleic acid samples and the uncertainty of the average copy number, and associate the average copy number and the uncertainty with each well.
Next, a device (plate) with a known cell number was produced according to the same manner as described above, except that the number of cells to be dispensed per well was changed to 10 cells.
On the produced plate, amplification and detection by real-time PCR was performed according to the protocol illustrated in
The composition of the amplifying reagent was as follows.
After the preparation of the plate, amplification and detection was performed using a real-time PCR device (available from Thermo Fisher Scientific Inc., QUANTSTUDIO 7FLEX). The results are presented in
Aspects of the present disclosure are as follows, for example.
<1> A device including:
a plurality of wells; and
two or more groups into which the wells are divided to be varied in composition in the wells.
<2> A device including:
a plurality of wells;
a reagent composition located in each of the wells and containing an amplifiable reagent in a specific copy number; and
two or more groups into which the wells are divided to have the amplifiable reagent located in the same specific copy number but to be varied in composition of the reagent composition except for the specific copy number.
<3> The device according to <2>, including groups varied in the specific copy number.
<4> A device including:
a plurality of wells;
an amplifiable reagent located in a specific copy number in each of the wells; and
two or more groups into which the wells are divided to be varied in the specific copy number of the amplifiable reagent.
<5> The device according to any one of <2> to <4>,
wherein at least one group of the groups into which the wells are divided is a group in which the specific copy number of the amplifiable reagent is close to a limit of detection.
<6> The device according to any one of <2> to <4>,
wherein at least one group of the groups into which the wells are divided is a group in which the specific copy number of the amplifiable reagent is a copy number greater than a limit of quantification.
<7> The device according to any one of <2> to <6>,
wherein at least one group of the groups into which the wells are divided is a negative control group in which the specific copy number of the amplifiable reagent is 0.
<8> The device according to any one of <2> to <7>,
wherein at least one group of the groups into which the wells are divided is a positive control group in which the specific copy number of the amplifiable reagent is 100 or greater.
<9> The device according to any one of <2> to <8>,
wherein at least one group of the groups into which the wells are divided is a group having the least copy number except for the negative control group, the at least one group being positioned at least at wells that are approximately at a periphery of the device.
<10> The device according to any one of <2> to <9>,
wherein each of the wells contains at least any one of a primer and an amplifying agent.
<11> The device according to any one of <2> to <10>, including
an identifier unit configured to enable identifying information on the specific copy number of the amplifiable reagent in the wells.
<12> The device according to any one of <2> to <11>,
wherein the amplifiable reagent is a nucleic acid.
<13> The device according to <12>,
wherein the nucleic acid is incorporated in a nucleic acid in a nucleus of a cell.
<14> The device according to <13>,
wherein the cell is a yeast cell.
<15> The device according to any one of <2> to <14>,
wherein the specific copy number is a counted copy number of the amplifiable reagent.
<16> The device according to any one of <13> to <15>,
wherein the cell is discharged by an inkjet method.
<17> A preparator's skill evaluating method for evaluating skill of a preparator who prepares a reagent composition, the preparator's skill evaluating method including: obtaining information on a Ct value in the device according to any one of <1> to <16>; and
evaluating the skill of the preparator based on the obtained information on the Ct value.
<18> A preparator's skill evaluating program for evaluating skill of a preparator who prepares a reagent composition, the preparator's skill evaluating program causing a computer to execute a process including:
obtaining information on a Ct value in the device according to any one of <1> to <16>; and
evaluating the skill of the preparator based on the obtained information on the Ct value.
<19> A preparator's skill evaluating device configured to evaluate skill of a preparator who prepares a reagent composition, the preparator's skill evaluating device including: a Ct value information obtaining unit configured to obtain information on a Ct value in the device according to any one of <1> to <16>; and
a skill evaluating unit configured to evaluate the skill of the preparator based on the obtained information on the Ct value.
<20> A testing device performance evaluating method for evaluating performance of a testing device configured to test a testing target, the testing device performance evaluating method including:
obtaining information on a Ct value in the device according to any one of <1> to <16>; and
evaluating the performance of the testing device based on the information on the Ct value.
<21> A testing device performance evaluating program for evaluating performance of a testing device configured to test a testing target, the testing device performance evaluating program causing a computer to execute a process including:
obtaining information on a Ct value in the device according to any one of <1> to <16>; and
evaluating the performance of the testing device based on the information on the Ct value.
<22> A testing device performance evaluating device configured to evaluate performance of a testing device configured to test a testing target, the testing device performance evaluating device including:
a Ct value information obtaining unit configured to obtain information on a Ct value in the device according to any one of <1> to <16>; and
a performance evaluating unit configured to evaluate the performance of the testing device based on the information on the Ct value.
The device according to any one of <1> to <16>, the preparator's skill evaluating method according to <17>, the preparator's skill evaluating program according to <18>, the preparator's skill evaluating device according to <19>, the testing device performance evaluating method according to <20>, the testing device performance evaluating program according to <21>, and the testing device performance evaluating device according to <22> can solve the various problems in the related art and can achieve the object of the present disclosure.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-226081 | Nov 2017 | JP | national |
| 2017-226082 | Nov 2017 | JP | national |
| 2018-073410 | Apr 2018 | JP | national |
| 2018-187453 | Oct 2018 | JP | national |
| 2018-216110 | Nov 2018 | JP | national |
| 2018-218612 | Nov 2018 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2018/043287 | 11/22/2018 | WO | 00 |
