Genetic factors affecting storage and utilization of lipids during dormancy in <i>Mycobacterium tuberculosis</i>
Alexander Sturm, Penny Sun, Julián Ávila-Pacheco, Anne E. Clatworthy, Zohar Bloom‐Ackermann, Michael Wuo, James Gomez, Soomin Jin, et al. (11 authors)
mBio · 2024-01
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.
MeSH terms
- Dormancy
- Mycobacterium tuberculosis
- Tuberculosis
- Biology
- Biotechnology
- Microbiology