Host-pathogen genetic interactions underlie tuberculosis susceptibility in genetically diverse mice

Author:

Smith Clare M12ORCID,Baker Richard E1,Proulx Megan K1ORCID,Mishra Bibhuti B13ORCID,Long Jarukit E1,Park Sae Woong4ORCID,Lee Ha-Na4ORCID,Kiritsy Michael C1ORCID,Bellerose Michelle M1ORCID,Olive Andrew J1ORCID,Murphy Kenan C1ORCID,Papavinasasundaram Kadamba1ORCID,Boehm Frederick J1ORCID,Reames Charlotte J1ORCID,Meade Rachel K25ORCID,Hampton Brea K67ORCID,Linnertz Colton L6ORCID,Shaw Ginger D68ORCID,Hock Pablo6,Bell Timothy A6ORCID,Ehrt Sabine4ORCID,Schnappinger Dirk4,Pardo-Manuel de Villena Fernando68ORCID,Ferris Martin T6ORCID,Ioerger Thomas R9,Sassetti Christopher M1ORCID

Affiliation:

1. Department of Microbiology and Physiological Systems, University of Massachusetts Medical School

2. Department of Molecular Genetics and Microbiology, Duke University

3. Department of Immunology and Microbial Disease, Albany Medical College

4. Department of Microbiology and Immunology, Weill Cornell Medical College

5. University Program in Genetics and Genomics, Duke University

6. Department of Genetics, University of North Carolina at Chapel Hill

7. Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill

8. Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill

9. Department of Computer Science and Engineering, Texas A&M University

Abstract

The outcome of an encounter withMycobacterium tuberculosis(Mtb) depends on the pathogen’s ability to adapt to the variable immune pressures exerted by the host. Understanding this interplay has proven difficult, largely because experimentally tractable animal models do not recapitulate the heterogeneity of tuberculosis disease. We leveraged the genetically diverse Collaborative Cross (CC) mouse panel in conjunction with a library ofMtbmutants to create a resource for associating bacterial genetic requirements with host genetics and immunity. We report that CC strains vary dramatically in their susceptibility to infection and produce qualitatively distinct immune states. Global analysis ofMtbtransposon mutant fitness (TnSeq) across the CC panel revealed that many virulence pathways are only required in specific host microenvironments, identifying a large fraction of the pathogen’s genome that has been maintained to ensure fitness in a diverse population. Both immunological and bacterial traits can be associated with genetic variants distributed across the mouse genome, making the CC a unique population for identifying specific host-pathogen genetic interactions that influence pathogenesis.

Funder

National Institute of Allergy and Infectious Diseases

Howard Hughes Medical Institute

National Human Genome Research Institute

Bank of America

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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