Genetic factors affecting storage and utilization of lipids during dormancy in Mycobacterium tuberculosis

Author:

Sturm Alexander123ORCID,Sun Penny1,Avila-Pacheco Julian4,Clatworthy Anne E.123ORCID,Bloom-Ackermann Zohar123,Wuo Michael G.5,Gomez James E.123,Jin Soomin1,Clish Clary B.4,Kiessling Laura L.5,Hung Deborah T.123ORCID

Affiliation:

1. Infectious Disease and Microbiome Program, Broad Institute, Cambridge, Massachusetts, USA

2. Department of Molecular Biology and Center for Computational and Integrative Biology, Massachusetts General Hospital, Boston, Massachusetts, USA

3. Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA

4. Metabolomics Platform, Broad Institute, Cambridge, Massachusetts, USA

5. Department of Chemistry, MIT, Cambridge, Massachusetts, USA

Abstract

Tuberculosis is a global threat, with ~10 million yearly active cases. Many more people, however, live with “latent” infection, where Mycobacterium tuberculosis survives in a non-replicative form. When latent bacteria activate and regrow, they elicit immune responses and result in significant host damage. Replicating and non-growing bacilli can co-exist; however, non-growing bacteria are considerably less sensitive to antibiotics, thus complicating treatment by necessitating long treatment durations. Here, we sought to identify genes important for bacterial survival in this non-growing state using a carbon starvation model. We found that a previously uncharacterized gene, omamC , is involved in storing and utilizing fatty acids as bacteria transition between these two states. Importantly, inhibiting lipid metabolism using a lipase inhibitor eradicates non-growing bacteria. Thus, targeting lipid metabolism may be a viable strategy for treating the non-growing population in strategies to shorten treatment durations of tuberculosis.

Funder

Broad Institute TB Gift Donors

Publisher

American Society for Microbiology

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