| Literature DB >> 33309526 |
Richa Mishra1, Vikas Yadav1, Madhura Guha1, Amit Singh2.
Abstract
Successful treatment of tuberculosis (TB) depends on the eradication of its causative agent Mycobacterium tuberculosis (Mtb) in the host. However, the emergence of phenotypically drug-resistant Mtb in the host environment tempers the ability of antibiotics to cure disease. Host immunity produces diverse microenvironmental niches that are exploited by Mtb to mobilize adaptation programs. Such differential interactions amplify pre-existing heterogeneity in the host-pathogen milieu to influence disease pathology and therapy outcome. Therefore, comprehending the intricacies of phenotypic heterogeneity can be an empirical step forward in potentiating drug action. With this goal, we review the interconnectedness of the lesional, cellular, and bacterial heterogeneity underlying phenotypic drug resistance. Based on this information, we anticipate the development of new therapeutic strategies targeting host-pathogen heterogeneity to cure TB.Entities:
Keywords: drug tolerance; phagosomal acidification; phenotypic heterogeneity; redox metabolism
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Year: 2020 PMID: 33309526 PMCID: PMC7611257 DOI: 10.1016/j.tim.2020.10.013
Source DB: PubMed Journal: Trends Microbiol ISSN: 0966-842X Impact factor: 17.079