Thin film culture device with carbon dioxide generant

Patent metadata

Field	Value
Publication number	US-10723992-B2
Application number	US-201615569451-A
Country	US
Kind code	B2
Filing date	Apr 26, 2016
Priority date	Apr 29, 2015
Publication date	Jul 28, 2020
Grant date	Jul 28, 2020

Abstract

The present disclosure provides a culture device for enumerating colonies of microorganisms. The device can comprise a base, a coversheet, and a nonporous spacer member disposed therebetween. The spacer member comprises an aperture that defines a growth compartment. At least one adhesive layer is adhered to the base or the coversheet in the growth compartment. A cold water-soluble gelling agent and an effective amount of a dry carbon dioxide-generating reagent are adhered to the at least one adhesive layer. The carbon dioxide-generating reagent consists essentially of particles having a diameter of less than 106 microns.

First claim

The invention claimed is:

1. A culture device for enumerating colonies of microorganisms, the device comprising:
a base having opposing inner and outer surfaces;
a coversheet having opposing inner and outer surfaces;
a spacer member disposed between the base and the coversheet, wherein the spacer member is coupled to the base or the coversheet, wherein the spacer member comprises an aperture that defines a shape and a depth of a growth compartment, wherein the spacer member and the growth compartment are disposed between the inner surface of the base and the inner surface of the coversheet;
a first adhesive layer adhered to the base in the growth compartment or a second adhesive layer adhered to the coversheet in the growth compartment;
an effective amount of a dry carbon dioxide-generating reagent adhered to the first adhesive layer or the second adhesive layer in the growth compartment;
a dry, cold-water-soluble gelling agent adhered to the base or the coversheet in the growth compartment;
an amount of a dry oxygen-scavenging reagent adhered to the first adhesive layer or the second adhesive layer in the growth compartment that is effective to consume 0.54 μmoles or more of oxygen in a period of 120 minutes or less at about 22 degrees C. to about 42 degrees C.; and
a first indicator reagent for detecting growth of a target anaerobic microorganism;
wherein the coversheet is coupled to the base or to the spacer member and wherein the culture device either
further comprises an effective amount of a selective agent to inhibit growth of a non-target microorganism, wherein the selective agent is adhered to the base or the coversheet in the growth compartment, or
further comprises an effective amount of a reducing agent, wherein the reducing agent is adhered to the base or the coversheet in the growth compartment, or
further comprises a second indicator reagent disposed in fluid communication with the growth compartment, wherein the second indicator reagent indicates a presence of non-target microorganisms and target microorganisms, or
more than one of the foregoing.

2. The culture device of claim 1 , wherein the carbon dioxide-generating reagent consists essentially of particles having a diameter of less than 106 microns.

3. The culture device of claim 1 , wherein the oxygen-scavenging reagent consists essentially of particles having a diameter of less than 106 microns.

4. The culture device of claim 3 , wherein the carbon dioxide-generating reagent comprises a metal carbonate.

5. The culture device of claim 1 , wherein the spacer member is nonporous.

6. The culture device of claim 1 , further comprising an effective amount of a dry buffer reagent disposed in the growth compartment.

7. The culture device of claim 1 , further comprising a dry nutrient to facilitate growth of a target microorganism, wherein the nutrient is adhered to the base or the coversheet in the growth compartment.

8. The culture device of claim 1 , further comprising an effective amount of a selective agent to inhibit growth of a non-target microorganism, wherein the selective agent is adhered to the base or the coversheet in the growth compartment.

9. The culture device of claim 1 , further comprising an effective amount of a reducing agent, wherein the reducing agent is adhered to the base or the coversheet in the growth compartment.

10. The culture device of claim 1 :
wherein the inner surface of the base has the first adhesive adhered thereto;
wherein one or more first component disposed in the growth compartment is adhered to the first adhesive;
wherein the first component is selected from the group consisting of the gelling agent, the oxygen-scavenging reagent, a buffer reagent, a nutrient, the indicator reagent, a selective agent, a reducing agent, and a combination of any two or more of the foregoing first components.

11. The culture device of claim 1 , wherein the oxygen-scavenging reagent comprises ferrous iron or a salt thereof, ascorbic acid or a salt of ascorbic acid, or an enzyme that catalyzes an oxygen-consuming reaction.

12. The culture device of claim 1 , further comprising a second indicator reagent disposed in fluid communication with the growth compartment, wherein the second indicator reagent indicates a presence of non-target microorganisms and target microorganisms.

13. A method of detecting a microorganism in a sample, the method comprising:
placing the culture device of claim 1 into an open configuration that provides access to the growth compartment therein;
placing a predefined volume of aqueous liquid into the growth compartment;
placing a sample into the growth compartment;
closing the culture device;
wherein placing the aqueous liquid and the sample into the growth compartment and closing the culture device comprises forming a semi-solid microbial culture medium enclosed by the base, the coversheet, and the spacer of the culture device;

incubating the culture device for a period of time sufficient to permit formation of a microbial colony in the culture medium; and
detecting the microbial colony.

14. The method of claim 13 , wherein closing the culture device comprises leaving an open fluid pathway from a gaseous environment outside the culture device to the semisolid microbial culture medium enclosed in the growth compartment.

15. The method of claim 13 , wherein placing the sample into the growth compartment comprises placing an additive into the growth compartment, wherein the additive comprises an effective amount of a selective agent or an indicator for detecting microbial growth.

16. The method of claim 15 , wherein the effective amount of the selective agent substantially permits growth of lactic acid bacteria in the culture device and the effective amount of selective agent substantially inhibits growth of E. coli, S. aureus, C. sporogenes, C. perfringens, Bacteroides fragilis, Prevotella melaninogencia , and/or a Fusobacterium species.

17. The method of claim 15 wherein, after incubating the culture device, detecting the microbial colony further comprises enumerating one or more optically-detectable colonies in the culture device.

18. The method of claim 17 , wherein enumerating one or more microbial colonies further comprises distinguishing carbon dioxide-producing colonies from non-carbon dioxide-producing colonies.

19. The method of claim 13 , wherein incubating the culture device for a period of time comprises incubating the culture device for the period of time in an aerobic atmosphere.

Assignees

• 3M Innovative Properties Co

Inventors

• Bjork Jason W
• Brutinel Evan D
• Stanenas Adam J

Classifications

• C12M41/36 Primary

  of biomass, e.g. colony counters or by turbidity measurements (electrooptical investigation of individual particles G01N15/14, flow cytometers G01N15/1404) · CPC title

• C12M41/34

  of gas · CPC title

• C12M25/06

  Plates; Walls; Drawers; Multilayer plates · CPC title

• C12M23/34

  Internal compartments or partitions · CPC title

• C12M23/20

  Material Coatings (immunocoatings C12M25/00) · CPC title