IP Library Granted Patent US 12,442,035
Granted Patent B2
US 12,442,035 · App. 17/271,496 · Granted Oct 14, 2025

Compositions and methods for detecting antibiotic responsive mRNA expression signatures and uses thereof

Inventors: Deborah Hung (Cambridge, MA); Roby Bhattacharyya (Boston, MA); Jonathan Livny (Cambridge, MA); Peijun Ma (Cambridge, MA)
Assignees: THE BROAD INSTITUTE, INC.; THE GENERAL HOSPITAL CORPORATION
C12Q1/6816C12N1/06C12N1/20C12Q1/6876C12Q1/689
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Quick Facts
Patent No.
US 12,442,035
App. No.
17/271,496
Granted
Oct 14, 2025
Kind
B2
Abstract

The present disclosure relates to compositions, methods, and kits for rapid phenotypic detection of antibiotic resistance/susceptibility.

Claims (30)

1. A method, comprising:

obtaining a sample including one or more bacterial cells, wherein the sample is obtained from a patient;

processing the sample to enrich the one or more bacterial cells;

contacting the sample with one or more antibiotic compounds;

lysing the sample to release messenger ribonucleic acid (mRNA) from the one or more bacterial cells;

hybridizing the released mRNA to at least one set of two nucleic acid probes, wherein each nucleic acid probe includes a unique barcode or tag and wherein the at least one set of nucleic acid probes includes one or more probes from SEQ ID NOs: 74-86 and one or more probes from SEQ ID NOs: 91-103;

detecting the hybridized nucleic acid probes;

identifying one or more genetic resistance determinants;

determining antibiotic susceptibility of the one or more bacterial cells using a machine learning algorithm trained on a susceptibility classification dataset, wherein the machine learning algorithm generates a ranked list of two or more susceptibility features, thereby determining antibiotic susceptibility of the one or more bacterial cells; and

selecting an appropriate antibiotic based on the determined antibiotic susceptibility of the one or more bacterial cells; and

administering the appropriate antibiotic to the patient.

2. The method of claim 1 , wherein the hybridizing occurs at a temperature between about 64° C. and about 69° C.

3. The method of claim 1 , wherein the hybridizing occurs at a temperature between about 65° C. and about 67° C.

4. The method of claim 1 , wherein the hybridizing occurs at about 65° C. or about 66° C. or about 67° C.

5. The method of claim 1 , wherein the at least one set of two nucleic acid probes is selected from the group consisting of: SEQ ID NO: 74 and SEQ ID NO: 91; SEQ ID NO: 75 and SEQ ID NO: 92; SEQ ID NO: 76 and SEQ ID NO: 93; SEQ ID NO: 77 and SEQ ID NO: 94; SEQ ID NO: 78 and SEQ ID NO: 95; SEQ ID NO: 79 and SEQ ID NO: 96; SEQ ID NO: 80 and SEQ ID NO: 97; SEQ ID NO: 81 and SEQ ID NO: 98; SEQ ID NO: 82 and SEQ ID NO: 99; SEQ ID NO: 83 and SEQ ID NO: 100; SEQ ID NO: 84 and SEQ ID NO: 101; SEQ ID NO: 85 and SEQ ID NO: 102; and SEQ ID NO: 86 and SEQ ID NO: 103.

6. The method of claim 5 , wherein the at least one set of two nucleic acid probes is selected from the group consisting of: SEQ ID NO: 74 and SEQ ID NO: 91; SEQ ID NO: 75 and SEQ ID NO: 92; SEQ ID NO: 76 and SEQ ID NO: 93; SEQ ID NO: 77 and SEQ ID NO: 94; SEQ ID NO: 78 and SEQ ID NO: 95; SEQ ID NO: 80 and SEQ ID NO: 97; SEQ ID NO: 82 and SEQ ID NO: 99; SEQ ID NO: 83 and SEQ ID NO: 100; and SEQ ID NO: 85 and SEQ ID NO: 102.

7. The method of claim 1 , wherein at least two sets of nucleic acid probes are selected.

8. The method of claim 1 , wherein at least three sets of nucleic acid probes are selected.

9. The method of claim 1 , wherein at least four sets of nucleic acid probes are selected.

10. A method, comprising:

obtaining a sample including one or more bacterial cells, wherein the sample is obtained from a patient;

processing the sample to enrich the one or more bacterial cells;

contacting the sample with one or more antibiotic compounds;

lysing the sample to release messenger ribonucleic acid (mRNA) from the one or more bacterial cells;

hybridizing the released mRNA to at least five nucleic acid probe sets, wherein each nucleic acid probe includes a unique barcode or tag and wherein the at least one set of nucleic acid probes includes one or more probes from SEQ ID NOs: 74-86 and one or more probes from SEQ ID NOs: 91-103;

detecting the hybridized nucleic acid probes;

identifying one or more genetic resistance determinants;

determining antibiotic susceptibility of the one or more bacterial cells using a machine learning algorithm trained on a susceptibility classification dataset, wherein the machine learning algorithm generates a ranked list of two or more susceptibility features, thereby determining antibiotic susceptibility of the one or more bacterial cells; and

selecting an appropriate antibiotic based on the determined antibiotic susceptibility of the one or more bacterial cells and administering the appropriate antibiotic to the patient.

11. The method of claim 10 , wherein the at least five nucleic acid probe sets comprise: SEQ ID NO: 74 and SEQ ID NO: 91; SEQ ID NO: 75 and SEQ ID NO: 92; SEQ ID NO: 76 and SEQ ID NO: 93; SEQ ID NO: 78 and SEQ ID NO: 95; and SEQ ID NO: 84 and SEQ ID NO: 101.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2025
From: LIVNY, JONATHAN
To: THE BROAD INSTITUTE, INC.
Reel/Frame 072129/0684 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2025
From: MA, PEIJUN
To: THE BROAD INSTITUTE, INC.
Reel/Frame 071444/0234 →
Continuity (3)
Provisional Application 62834786 · Apr 16, 2019
Provisional Application 62723417 · Aug 27, 2018
Related Publication 20210230675A1 · Jul 29, 2021
References Cited (11)
US 9885088B2 · Hung et al. · 2018 [cited by applicant]
US 20100136534A1 · Wang et al. · 2010 [cited by applicant]
EP 3231874A1 · 2017 [cited by applicant]
WO 2011094514A1 · 2011 [cited by applicant]
WO 2018144918A1 · 2018 [cited by applicant]
Codjoe et al. (“Carbapenem resistance: a review.” Medical Sciences 6.1 (2017)). [cited by examiner]
Klebsiella pneumoniae capsular polysaccharide biosynthesis gene cluster, type: KL106-1: Genbank Accession LT174576.1; Publication [online]. Jun. 13, 2013 [retrieved Dec. 17, 2019]. Retrieved from the internet: <https://… [cited by applicant]
Klebsiella pneumoniae strain KpMDU1 cpsC capsular synthesis gene cluster, complete sequence: Genbank Accession KR007677.1; Publication [online]. Jun. 8, 2015 [retrieved Dec. 17, 2017]. Retrieved from the internet: <http… [cited by applicant]
International Search Report dated Jan. 9, 2020 for related Application No. PCT/US2019/048114. [cited by applicant]
International Search Report dated Mar. 11, 2021 for related Application No. PCT/US2019/048114. [cited by applicant]
Extended European Search Report in corresponding application No. 19853410.9 dated May 13, 2022. [cited by applicant]