Patent Application
20070042453
1. Field of the Invention
The invention relates to the improvement of antimicrobial screening techniques for chemical formulations and more specifically, to a method of increasing the speed and throughput at which the antimicrobial effects of chemical formulations can be evaluated.
2. Description of the Related Art
The discovery of new sanitizing agents for industrial and household applications involves antimicrobial screening. Antimicrobial screening provides a way to evaluate the ability of various chemical compounds to inhibit bacterial growth. Normally there is a very slow turnaround for evaluating effects of sanitizers such as ethanol, ozone, chlorine, various salts, acids, bases, and reducing agents on microorganism survival. Traditionally, the antimicrobial effects of chemical compounds are tested individually on pure cultures of select microorganisms of interest by exposure followed by growth and evaluation hours to days later using a selective growth medium.
One method of measuring the antimicrobial effectiveness of a chemical agent is to determine its zone of inhibition. In the agar diffusion method, one species of microorganism is uniformly swabbed onto a nutrient agar plate. A chemical agent is placed on paper disks. These discs are added to the surface of the agar. During incubation, the chemical agent diffuses from the disk into the surrounding agar. An effective agent will inhibit bacterial growth, and measurements can be made to quantify the size of the zones of inhibition around the disks. The relative effectiveness of a compound is determined by comparing the diameter of the zone of inhibition with values in a standard table. Zones of inhibition with larger diameters indicate stronger and more effective antimicrobial agents.
While the agar diffusion method measures relative antimicrobial effectiveness, the dilution method is used to determine whether a chemical is bactericidal (kills bacteria) or bacteriostatic (inhibits bacteria). In the dilution method, the chemical compound of interest is placed in a tube containing the microorganism which is being tested. The microorganism is then deposited onto a nutrient agar plate. If the microorganism grows on the nutrient agar the chemical is bacteriostatic; if not, the microorganism was killed by the chemical, in which case the chemical is then termed bactericidal. Unfortunately, treatments followed by plating on selective media for growth usually take more than a few days to obtain results for just one antimicrobial compound.
Therefore, there remains a need for a high throughput screening method to evaluate the antimicrobial effects of chemical formulations on different microorganisms.
Embodiments of the invention generally provide methods and systems for increasing the speed and throughput at which the antimicrobial effects of chemical formulations can be evaluated. In one embodiment, the invention provides a method for screening antimicrobial chemical formulations, comprising depositing microorganisms on a slide, depositing chemical formulations onto the deposited microorganisms, removing the chemical formulations from the deposited microorganisms after a given treatment time, depositing fluorescent dyes onto the deposited microorganisms after removing the chemical formulations, and scanning the slide for fluorescence to evaluate viability of the microorganisms after depositing the fluorescent dyes.
In another aspect, the invention provides a method for screening antimicrobial chemical formulations, comprising placing a slide in an atmosphere controlled chamber, depositing microorganisms on a slide, depositing chemical formulations onto the deposited microorganisms, removing the chemical formulations from the deposited microorganisms after a given treatment time, depositing fluorescent dyes onto the deposited microorganisms after removing the chemical formulations, and scanning the slide for fluorescence to evaluate viability of the microorganisms after depositing the fluorescent dyes.
In another aspect, the invention provides a system for evaluating the antimicrobial effects of numerous chemical formulations, comprising a microarray printer to deposit a plurality of spots containing combinations of chemical formulations, microorganisms, and fluorescent dyes onto a slide, a microarray scanner to detect live and dead microorganisms in each spot through fluorescence markers, and an execution unit which, upon executing code, is configured to analyze the fluorescence marker data of each spot collected from the microarray scanner.
For a further understanding of the nature and objects of the present invention, reference should be made to the following detailed description, taken in conjunction with the accompanying drawings, in which like elements are given the same or analogous reference numbers and wherein:
The words and phrases used herein should be given their ordinary and customary meaning in the art by one skilled in the art unless otherwise further defined.
Normally, there is a very slow turnaround for evaluating effects of antimicrobial agents such as ethanol, ozone, chlorine, salts, acids, bases, and reducing agents on microorganism survival. Exposing microorganisms to antimicrobial compounds and plating the treated microorganisms on selective media for growth is a lengthy screening process, and efficacy results for just one antimicrobial compound usually takes more than a few days. Embodiments of the present invention enable rapid, automated microbial evaluation of thousands of chemical formulations at once. A particular embodiment of the invention involves the use of a microarray printer to deposit thousands of sanitizer/microorganism combinations on a slide. A microarray scanner is then used to detect live and dead specimens on the slide as indicated by a viability dye. By scanning thousands of spots in a short period of time, the microarray scanner analysis can expedite the time needed for evaluations of microbial susceptibility to chemical formulations.
The processing steps 202-210 according to the embodiments of the invention are described below. The embodiments described herein are provided to illustrate the invention and the particular embodiments shown should not be used to limit the scope of the invention.
The first processing step 202 of the invention involves depositing selected microorganisms on a slide. Microorganisms of concern, such as Escherichia coli, Salmonella, Campylobacter, Listeria monocytogenes, Staphylococcus aureus, and various species of Candida, Bacilli, Clostridia and Enterobacter sakazakii can be deposited on slides to form an array of spots, or a microarray. One embodiment of this invention employs the use of an inkjet printer to deposit solutions containing microorganisms on a slide. Various mixtures of microorganisms can be spotted on slides using an inkjet printer that enables 100 μm spots and up to 10,000 different spots per standard microscope slide (1 mm×25 mm×76 mm). Microorganisms can be deposited at each spot in different concentrations or combinations to approximate realistic environmental conditions. The microorganisms should be dried onto the slide surface prior to depositing any antimicrobial compounds. The specimens can be quick-dried in a dryer void of contamination.
An example of a printer consists of an inkjet head with nozzles through which a solution containing the microorganisms can be deposited on the slide. The nozzles are controlled by a computer which directs where on the slide to deposit the microorganisms, and how much solution to deposit. The printer also contains cartridges that act as reservoirs holding a supply of solution containing the desired microorganisms. After a first set of microorganisms is deposited, the reservoirs are emptied and rinsed. The inkjet head is then washed and flushed thoroughly so that there is no cross-contamination with a next round of microorganisms to be deposited.
The deposition of microorganisms on the slide is preferably conducted in an atmosphere/gas-controlled chamber. It is important to control contamination, humidity, and dust during spotting of the slides. Foreign substances can contaminate the deposited antimicrobial compound/microorganism mixtures. Dust can interfere with data collection from the microarray scanner later in the process. Humidity must be maintained below 75% in order to prevent condensation on the slide. Certain gas mixtures containing variations in nitrogen, hydrogen, carbon dioxide, and oxygen from standard air will be more effective in preparing the slides for analyses. Ideally the deposition process can be performed at room temperature.
The next main processing step 204 of the invention involves depositing various antimicrobial chemicals on the microorganisms in exact recorded locations on the slide. Examples of antimicrobial formulations that can be deposited include antibiotics, quaternary ammonium compounds, ethanol, reducing agents or other chemical combinations. The chemical permutations may be added directly on top of specific microorganisms dried on the slide. As an example according to one embodiment of this invention,
The deposited microorganisms in each sample spot of the microarray are then fluorescently tagged to observe the efficacy of the respective antimicrobial formulation. The processing step 208 of the invention involves depositing fluorescent dyes onto the deposited microorganisms using a microarray printer similar to that used in processing step 202. In one preferred embodiment, Live/Dead BacLight assay reagents (available from Invitrogen Corp., Eugene, Oreg.) can be deposited on each sample spot. The reagents are two fluorescent nucleid acid dyes, Syto 9 and propidium iodide, which indicate cell viability through fluorescence tagging. Syto 9 is a smaller green dye only visible in the absence of propidium iodide, a larger red dye. If cell membranes are damaged, indicating cell death, both fluorescent dyes freely enter the cells to bind nucleic acids, and only red fluorescence is observed. If a cell's membrane is intact, only Syto 9 is small enough to freely enter the cell, and the live undamaged cell would appear to be fluorescent green.
The survival of microorganisms with respect to specific chemical treatments or formulations would then be scanned in processing step 210 using a microarray scanner. In a preferred embodiment, the scanner is tuned to detect Syto 9 green-fluorescent nucleic acid stains at 480-500 nm and propidium iodide red-fluorescent nucleic acid stains at 490-635 nm.
Preferred processes and apparatus for practicing the present invention have been described. It will be understood and readily apparent to the skilled artisan that many changes and modifications may be made to the above-described embodiments without departing from the spirit and the scope of the present invention. The foregoing is illustrative only and that other embodiments of the integrated processes and apparatus may be employed without departing from the true scope of the invention defined in the following claims.
This application claims the benefit under 35 U.S.C. § 119(e) to provisional application No. 60/710,340, filed Aug. 22, 2005, the entire contents of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 60710340 | Aug 2005 | US |
