IP Library › Granted Patent US 12,545,964
Granted Patent B2
US 12,545,964 · App. 17/805,721 · Granted Feb 10, 2026

Detection of infectious agents from environmental air dust

Inventor: Kenneth S. Henderson (Wilmington, MA)
Assignee: Charles River Laboratories International, Inc.
C12Q1/6888A01K1/031C12Q1/6806C12Q1/689C12Q1/6893G01N1/2205G01N1/2247G01N1/2273
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Quick Facts
Patent No.
US 12,545,964
App. No.
17/805,721
Granted
Feb 10, 2026
Kind
B2
Abstract

Embodiments of the present disclosure are directed to systems and methods for collection and analysis of environmental air dust (EAD) within an individually ventilated cage rack (IVR) environment for detecting pathogens. The method includes collection of an EAD sample by a collection media, isolation of a plurality of nucleic acids (e.g., RNA and/or DNA) representative of one or more infectious agents from the EAD sample, optional reverse transcription of RNA to cDNA if the isolated nucleic acids contain RNA, amplification of the cDNA and/or DNA (e.g., by polymerase chain reaction (PCR)), and assay interpretation. Optionally, the EAD sample may be analyzed with one or more other sample types (e.g., fecal pellets, oral swabs, body swabs, tissue, etc.) to improve detection of low-copy organisms.

Claims (62)

1 . A method for identifying one or more infectious agents carried by environmental air dust within a single cage for housing an animal, the environmental air dust released by agitation of soiled bedding disposed within the single cage, wherein the single cage is not within an individually ventilated cage rack system, the method comprising:

disposing collection media within the single cage containing the soiled bedding and not containing the animal;

agitating the single cage to release the environmental air dust comprising a test sample from the soiled bedding, while the single cage is containing the soiled bedding and not containing the animal;

collecting the test sample within the environmental air dust on the collection media during agitation of the single cage;

isolating a plurality of nucleic acids from the test sample, the nucleic acids being representative of the one or more infectious agents;

amplifying at least one of the isolated plurality of nucleic acids; and

analyzing the amplified at least one nucleic acid to identify a presence or absence of the one or more infectious agents.

2 . The method of claim 1 , wherein the single cage is configured to receive the animal therein.

3 . The method of claim 1 , wherein

isolating the plurality of nucleic acids comprises extracting an RNA sample from the test sample and reverse transcribing the extracted RNA sample into a cDNA sample,

amplifying the at least one of the isolated plurality of nucleic acids comprises amplifying the cDNA sample by real-time polymerase chain reaction (PCR), and

analyzing the amplified at least one nucleic acid comprises measuring a threshold cycle (Ct) value of the amplified cDNA sample.

4 . The method of claim 1 , wherein

isolating the plurality of nucleic acids comprises extracting a DNA sample from the test sample,

amplifying the at least one of the isolated plurality of nucleic acids comprises amplifying the DNA sample by real-time PCR, and

analyzing the amplified at least one nucleic acid comprises measuring a Ct value of the amplified DNA sample.

5 . The method of claim 1 , wherein isolating the plurality of nucleic acids comprises at least one of magnetic isolation, column-based nucleic acid isolation, organic extraction, and/or alkaline lysis.

6 . The method of claim 1 , further comprising reverse transcribing an RNA sample of the isolated plurality of nucleic acids into a cDNA sample.

7 . The method of claim 1 , wherein amplifying the at least one of the isolated plurality of nucleic acids comprises at least one of loop mediated isothermic amplification (LAMP) and/or PCR.

8 . The method of claim 1 , wherein amplifying the at least one of the isolated plurality of nucleic acids comprises PCR.

9 . The method of claim 1 , wherein

amplifying the at least one of the isolated plurality of nucleic acids comprises PCR, and

analyzing the amplified at least one nucleic acid comprises time-of-flight analysis of PCR products.

10 . The method of claim 1 , wherein analyzing the amplified at least one nucleic acid comprises measuring sample Ct values and evaluating the sample Ct values.

11 . The method of claim 1 , wherein the one or more infectious agents are selected from the group consisting of: Staphylococcus spp., Pasteurella spp., Proteus spp., Klebsiella spp., Giardia spp., Cryptosporidium spp., Entamoeba spp., Spironucleus spp., Murine norovirus, Pseudomonas spp., and beta-hemolytic Streptococcus spp.

12 . The method of claim 1 , wherein the collection media comprises a mechanical filter.

13 . The method of claim 1 , wherein disposing the collection media in the single cage comprises suspending the collection media within the single cage containing the soiled bedding.

14 . The method of claim 1 , wherein disposing the collection media in the single cage comprises positioning the collection media within the single cage so as to impinge at least a portion of the environmental air dust released by agitation of the single cage.

15 . The method of claim 1 , wherein disposing the collection media in the single cage comprises disposing the collection media configured to capture dust particles having a size ranging from about 0.1 nm to about 10.0 mm.

16 . A method for identifying one or more infectious agents carried by environmental air dust within a single enclosure, the environmental air dust released by agitation of soiled bedding disposed within the single enclosure, wherein the single enclosure is not within an individually ventilated cage rack system, the method comprising:

disposing collection media within the single enclosure containing the soiled bedding and not containing an animal;

agitating the single enclosure to release the environmental air dust comprising a test sample from the soiled bedding, while the single enclosure is containing the soiled bedding;

collecting the test sample within the environmental air dust on the collection media during agitation of the single enclosure;

isolating a plurality of nucleic acids from the test sample, the nucleic acids being representative of the one or more infectious agents;

amplifying at least one of the isolated plurality of nucleic acids; and

analyzing the amplified at least one nucleic acid to identify a presence or absence of the one or more infectious agents.

17 . The method of claim 16 , wherein the single enclosure is adapted to receive no more than a single cage therein.

18 . The method of claim 17 , wherein the single enclosure further comprises a single chamber adapted to receive the single cage therein.

19 . The method of claim 17 , wherein the soiled bedding and the collection media are disposed within the single cage within the single enclosure.

20 . The method of claim 16 , wherein the single enclosure is configured to receive the animal therein.

21 . The method of claim 16 , wherein

isolating the plurality of nucleic acids comprises extracting an RNA sample from the test sample and reverse transcribing the extracted RNA sample into a cDNA sample,

amplifying the at least one of the isolated plurality of nucleic acids comprises amplifying the cDNA sample by real-time polymerase chain reaction (PCR), and

analyzing the amplified at least one nucleic acid comprises measuring a threshold cycle (Ct) value of the amplified cDNA sample.

22 . The method of claim 16 , wherein

isolating the plurality of nucleic acids comprises extracting a DNA sample from the test sample,

amplifying the at least one of the isolated plurality of nucleic acids comprises amplifying the DNA sample by real-time PCR, and

analyzing the amplified at least one nucleic acid comprises measuring a Ct value of the amplified DNA sample.

23 . The method of claim 16 , wherein isolating the plurality of nucleic acids comprises at least one of magnetic isolation, column-based nucleic acid isolation, organic extraction, and/or alkaline lysis.

24 . The method of claim 16 , further comprising reverse transcribing an RNA sample of the isolated plurality of nucleic acids into a cDNA sample.

25 . The method of claim 16 , wherein amplifying the at least one of the isolated plurality of nucleic acids comprises at least one of loop mediated isothermic amplification (LAMP) and/or PCR.

26 . The method of claim 16 , wherein amplifying the at least one of the isolated plurality of nucleic acids comprises PCR.

27 . The method of claim 16 , wherein

amplifying the at least one of the isolated plurality of nucleic acids comprises PCR, and

analyzing the amplified at least one nucleic acid comprises time-of-flight analysis of PCR products.

28 . The method of claim 16 , wherein analyzing the amplified at least one nucleic acid comprises measuring sample Ct values and evaluating the sample Ct values.

29 . The method of claim 16 , wherein the one or more infectious agents are selected from the group consisting of: Staphylococcus spp., Pasteurella spp., Proteus spp., Klebsiella spp., Giardia spp., Cryptosporidium spp., Entamoeba spp., Spironucleus spp., Murine norovirus, Pseudomonas spp., and beta-hemolytic Streptococcus spp.

30 . The method of claim 16 , wherein the collection media comprises a mechanical filter.

31 . The method of claim 16 , wherein disposing the collection media in the single enclosure comprises suspending the collection media within the single enclosure containing the soiled bedding.

32 . The method of claim 16 , wherein disposing the collection media in the single enclosure comprises positioning the collection media within the single enclosure so as to impinge at least a portion of the environmental air dust released by agitation of the single enclosure.

33 . The method of claim 16 , wherein disposing the collection media in the single enclosure comprises disposing the collection media configured to capture dust particles having a size ranging from about 0.1 nm to about 10.0 mm.

34 . The method of claim 16 , wherein the single enclosure is not configured to receive the animal therein.

Assignments (2)
SECURITY INTEREST Recorded Dec 13, 2024
From: CHARLES RIVER LABORATORIES INTERNATIONAL, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 069582/0600 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2022
From: HENDERSON, KENNETH S.
To: CHARLES RIVER LABORATORIES INTERNATIONAL, INC.
Reel/Frame 061010/0286 →
Continuity (5)
Continuation 17178608 · Feb 18, 2021
Continuation 15170660 · Jun 1, 2016
Provisional Application 62280057 · Jan 18, 2016
Provisional Application 62169438 · Jun 1, 2015
Related Publication 20220298585A1 · Sep 22, 2022
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