Patent Application
20060014298
This invention relates to a method and a kitset for collecting and storing a plurality of biological samples for later identification of individual samples. It is particularly suited for the collection and storage of sources of DNA, for example of blood. In a particularly preferred embodiment it may be used in a system for tracing meat specimens back to the carcass from which the meat originated.
U.S. Pat. No. 5,092,466 describes a very sophisticated storage system for storing very large numbers of samples of protein gene products or hybridoma cells. The samples are collected on a porous medium such as filter paper. The samples are then lyophilised and placed in an air tight packet. This packet is then welded on to motion picture film stock with appropriate identification such as a bar code. The sample can be punched out of the film. The film can be spliced in the same manner as normal movie stock. This is a very convenient system for storing millions of samples in a retrievable compact storage system.
U.S. Pat. No. 5,460,057 describes a method and apparatus particularly adapted for handling blood samples. This also involves the use of filter paper to collect the samples.
The filter paper is attached to an identification label. When the samples are to be analysed a punch is used to punch out a small portion of the sample on the filter paper and it is then analysed.
A suitable filter paper medium for absorbing and storing of DNA samples is described in U.S. Pat. No. 5,496,562. This is a solid matrix impregnated with a compound or composition which protects against degradation of DNA which is incorporated into or absorbed on the matrix. The matrix claimed is a cellulose based matrix. The impregnated DNA stabilising composition consists of a weak base, a chelating agent, an ionic surfactant or detergent and optionally uric acid or a urate salt.
Other DNA storage matrices are described in U.S. Pat. Nos. 5,756,126; 5,807,527; 5,972,360; 5,976,572 and 5,985,327. Similar DNA storage matrices are described in WO 90/03959 and AU 691,114.
EP 0741 296A relates to a pre-transfusion card designed to determine the compatibility of donor and recipient blood.
U.S. Pat. No. 2,734,503 describes a bandage comprising a polymeric elastic backing on which is superimposed an adherent pad dressing, one side of the backing being covered with an adhesive.
FR 2621690A relates to a device intended to act as a support for samples, in particular biological samples.
While systems are known from the prior art described above for the identification storage and retrieval of DNA samples under laboratory conditions. When samples are to be taken from large numbers of animals in a race or pen or moving carcasses on the killing chain of an animal slaughterhouse quick and accurate sample taking is required.
It is an object of this invention to go some way towards achieving this desideratum or at least to offer the public a useful choice.
Although the present invention was conceived in the environment of a killing chain, its use is not limited thereto and can be used in any system where biological samples need to be taken from a plurality of individual sources, stored and then are able to be individually traced back to their original sources.
Accordingly, the invention may be said broadly to consist in a method for collecting and storing a biological sample for later identification of the source of said sample which comprises the steps of:
Preferably said biological sample is a source of DNA.
Preferably said source of DNA is blood, lymph or saliva.
Preferably said biological sample is taken from an animal carcass.
In one embodiment said identification substrate is a carcass ticket.
Alternatively said DNA sample is taken from a live animal.
In another embodiment said substrate is a document of description.
Preferably said method is used within a system to trace the origin of meat or other food stuffs.
Preferably said marked combined substrate/strip is stored in dry storage.
Preferably said marking is done on said identification substrate before said sampling strip is affixed thereto.
In another embodiment the invention may be said broadly to consist in a biological specimen sample storage and identification kitset comprising:
Preferably said biological sample is a source of DNA.
More preferably said sample is blood, lymph or saliva.
Preferably said adhesive is selected for high stickability and to maintain adhesion at cold storage temperatures.
Preferably said adhesive is a food grade adhesive.
Preferably said adsorbing sheet is DNA sampling paper.
Preferably said filter paper is treated to maintain DNA in a stable state.
Preferably said sampling strip is supplied with said adhesive and sampling sheet face down on a sheet of roll stock whose surface has low adhesivity to allow quick removal of said sampling strip.
Preferably there are perforations through said backing sheet along outer periphery of said sampling sheet.
In one embodiment said substrate is a carcass ticket.
In another embodiment said substrate is a document of description.
In an alternative embodiment a first portion of said sampling strip is adhered to or is integral with said substrate and a second portion faces away from said substrate, a release sheet being releasably adhered to said second portion of said sampling strip, said substrate being adapted to receive said second portion and to be adhered thereto when said release sheet has been removed and said second portion is applied thereto.
The invention may also be said to consist in a method as defined above which comprises using said alternative kitset embodiment, removing said release sheet, applying said sample absorbing sheet to said source of DNA and sticking said second portion of said sampling strip to said substrate.
Sampling and Storage
Illustrated in
On the neck 14 of the carcass 10 is the blood or lymph sample 16 to be collected. An operator standing next to the chain will remove a sampling strip 20 from the roll stock 28 being dispensed from a dispenser 27 (described below with reference to
At a point in the killing chain earlier than where the DNA sampling is done the carcass ticket 30 will have been labelled with identification indicia, such as bar coding, to identify the particular carcass 10.
A unique code could optionally be printed on the DNA-sampling strip 20 at the time of initial manufacture, or during delivery of the strip 20 via the dispenser 27.
DNA Tracing
The purpose of storing DNA samples 16 with records of the individual sources of those samples on carcass tickets 30 is to allow tracing from meat cuts. Referring to
Sampling Strip
The structure of the sampling strip is illustrated in
This product is compliant with the regulations of the US Food and Drug Administration (FPA) and thus may come into contact with meat carcasses intended for human consumption.
The adhesive 24 attached to backing strip 22 is “550” adhesive sold by Green Bay Packaging Inc of Green Bay, Wis., USA. It is intended for use in a cold environment. It may be applied at temperatures above minus 15 C. The minimum temperature for retaining adhesiveness is minus 49 C.
The absorbent sheet 26 on sample collecting strip 20 is preferably selected from two types of absorbent paper:
Both types of paper are suitable for direct contact with fatty and aqueous food. The latter product is a class 11 medical device listed by the FDA. The weight range is 185 to 210 gsm.
As illustrated in
The roll stock is a 70 gsm densified kraft sheet commonly used in the self adhesive industry. It has a soventless silicon release coating on the face to which the sampling strip 20 is attached so as to release the strip as required.
There are a series of perforations 25 through backing sheet 22. These are at either edge of absorbent sheet 26.
In a preferred embodiment absorbent sheet 26 has an orientation. One end is for handling and the other is where the sample 16 is collected as shown. The orientation can be indicated by making the backing sheet 22 transparent at the sample end and translucent or opaque at the handling end.
Another alternative manner of using a sampling strip 20 will be described with reference to
In a further alternative the portion of the sampling strip 20 to the right of line X-Y is integral with a substrate. In such an embodiment the absorbent sheet 26 and the adhesive layer 24 would not be present on the portion of the backing sheet 22 which is integral with substrate 28.
When a genetic analysis is to be made of a sample 16 from a sampling strip 20 as described with reference to
Carcass Ticket
A carcass ticket 30 is illustrated in
In a preferred embodiment the carcass ticket 30 is a white polypropylene base sheet coated on one side with a thermal imaging coating with which to produce the identification information. The thermal coating is protected with an additional environmental protection coating to provide oil, water, heat, light and plasticiser resistance to the thermal coating. The imaging is black.
Documents of Description
Another use of the method of the invention is to provide positive identification on a document describing one or more animals. Such documents are referred to in this specification as “documents of description”. A document of description may be a single page, a folder or a book. It will contain a written number or letter identifier and a sample strip with a sample attached to a page of the document, the page being a substrate. Common examples of where a document of description is used include: animal registration or licensing systems, in animal health control programmes, bills of sale, entry form for a contest; during movement or import and export of animals or products from animals (animal passport). If there is any doubt as to the documentation then a DNA sample is taken from the animal and compared to the DNA sample in the document of description produced in relation to that animal.
Illustrated in
At the time that the passport is being issued a blood sample may be taken on the sampling strip 20 which is then attached to the passport sample page 44 for the permanent record. The page may be laminated with a clear plastics material for additional security and for a longer storage life.
Collection, Storage and Tracing of DNA Sample from Carcass Samples were collected by wiping a volume of blood from the neck of a carcass onto a DNA-sampling strip 20. The DNA-sampling strip was then attached by permanent adhesive 24 to the carcass identification ticket 30 hanging from the carcass 10. This procedure was used to sample all carcasses processed for a 10 metric tonne consignment of meat requiring traceability. The carcass identification tickets 30 with DNA sampling strips 20 attached were stored in cardboard boxes containing approximately 1000 tickets in numbered bunches of approximately 60 tickets. The tickets in each bunch were tied securely in the order of cutting. The boxes of DNA samples were entered onto an inventory system and stored at −20 C. DNA analysis of these stored tickets samples was used to trace meat from the market.
A trace was requested on 3 portions of meat from the market. Samples of the meat were taken by slicing open the meat and placing an FTA@ Card (Flinders Technologies PTY Ltd) into the cut, then closing the cut tightly until the FTA Card was saturated. The FTA Card was then air dried and mailed to a laboratory for analysis. Once received, a 1.2 mm diameter punch of each bloodstain was removed using a HARRIS MICRO-PUNCH (Shunderson Communications) and placed into a separate bar-coded or otherwise uniquely identified tube or receptacle. The identification of the receptacle and of the meat sample were entered into a spreadsheet or database. These data were used at a later date to relate the DNA profile to the sample identification. Both the FTA Card and Harris MICRO-PUNCH were obtained from the distributor Life Technologies, Inc., Gathersburg, Md., USA.
The date and time of production information on packaging of the meat was supplied to the ticket storage facility. The appropriate box of stored carcass tickets was identified and sent to the laboratory. A 1.2 mm diameter punch from the blood stain attached to each relevant ticket was removed using a HARRIS MICRO PUNCH (Shunderson Communications) and placed into a separate bar-coded (or otherwise uniquely identified) tube or receptacle. The identification of the receptacle and of the carcass ticket were entered into a spreadsheet or database and stored for later use in relating the DNA profile to the carcass information.
Punches from FTA® card and from the sampling strip 20 were each washed as follows. Using a Biomek 2000 Automated Workstation (Beckman Instruments, USA), 160 μl aliquots of FTA™ PURIFICATION REAGENT (Flinders Technologies PTY Ltd, supplied by Life Technologies Gibco-BRL) were dispensed into each well. Reagent was allowed to sit for 5 min at room temperature. After the 5 min incubation the reagent not soaked into the punch was removed. The above steps were repeated an additional two times for a total of three washes with the FTA™ Purification Reagent. After the FTA™ Purification Reagent has been removed for the third time, 160 l of TE (10 mM Tris-HCl, pH 8.0 m 0.1 mM EDTA) was dispersed into each well and mixed. The mixtures were allowed to sit for 5 min at room temperature. After the 5 min incubation most of the TE was aspirated. An additional 160 μl of TE buffer was added. After the final TE buffer had been removed, 160 μl 96% ethanol was added, incubated for 5 min and aspirated.
The FTA paper punch was allowed to air dry completely (approximately 2 hours at room temperature). Alternatively, drying was accelerated by incubating the plate of punches at 60 C for 30 min.
The washed punches were analysed by the polymerase chain reaction. The resulting samples from the meat specimen punch and the carcass sample punch were loaded onto separate lanes of ABI 377 gel (36 cm plate); Run module GS 36C/2400 (Applied Biosystems Inc.).
The output of ABI377 was analysed using Genescan and Genotyper Software (Applied Biosystems Inc.). The results from each carcass ticket sample were compared with the profile from the meat sample. Profiles identical within the tolerance of the analysis system (plus or minus lbp) are selected as “matches”. The likelihood that this match could have occurred by chance was calculated using standard methods and allele frequency data derived from the other animals analysed at the time. A single matching carcass ticket sample was identified for each meat sample. In each case the likelihood that such a DNA match could occur with a carcass ticket from a different animal was less than one chance in one million tests.
The DNA link between the sample of meat from the market place and the stored carcass sample was used relate information previously only associated the carcass to the submitter of the sample of the meat cut. The data included farm of origin, farm and transport quality assurance data, weight and grade of carcass.
Other Applications
Although the method of the invention has been described in relation to DNA sampling, other potential analyses which could be done on the samples taken using the DNA sampling strip include:
The method and kitset of the invention can be used in any application requiring rapid sampling of fluid from plant or animal tissue for diagnostic or reference purposes and clear identification of the sample is paramount.
Possible applications including taking samples from live animals including humans, dead animals/humans or tissue. Samples would include blood, saliva, mucus, plasma, body fluid such as milk and crushed or homogenised tissue such as muscle. The sampling strip with the sample is stuck to pre-existing, or custom printed document of description concerning the animal or human (including a book, passport, photograph, card, tag, ticket-any format for printed material).
For example, when animals are being tagged or handled a sample of blood is collected using a lancet to prick the ear and soaking one or two drops of blood onto the DNA sampling strip 20 label. The sampling strip is then permanently stuck to a substrate 30 in the form of a card, book or passport, or photograph which lists all details concerning the animal tag (eg: colour, number, radio or other electromagnetic frequency emission). This information could be pre-existing or could be printed just prior to or during the sample being taken.
The method and kitset of this invention could also be used in the same way to trace the plant origin of materials. The plant products to be traced could be sap, fruit juice, or crushed or homogenised plant tissue.
Other variations and permutations within the scope of the claims will be apparent to those skilled in the art.
| Number | Date | Country | Kind |
|---|---|---|---|
| 335233 | Apr 1999 | NZ | national |
This is a continuation of application Ser. No. 09/958,898 filed Jan. 18, 2002, which is a Continuation Application of PCT Application No. PCT/NZ00/00050 filed Apr. 7, 2000. The entire disclosure(s) of the prior application(s), application Ser. No. 09/958,898 is hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 09958898 | Jan 2002 | US |
| Child | 11232010 | Sep 2005 | US |
| Parent | PCT/NZ00/00050 | Apr 2000 | US |
| Child | 09958898 | Jan 2002 | US |
