Overcoming Mycobacterium tuberculosis through small molecule inhibitors to break down cell wall synthesis.
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ABSTRACT: Mycobacterium tuberculosis (MTB) utilizes multiple mechanisms to obtain antibiotic resistance during the treatment of infections. In addition, the biofilms, secreted by MTB, can further protect the latter from the contact with drug molecules and immune cells. These self-defending mechanisms lay a formidable challenge to develop effective therapeutic agents against chronic and recurring antibiotic-tolerant MTB infections. Although several inexpensive and effective drugs (isoniazid, rifampicin, pyrazinamide and ethambutol) have been discovered for the treatment regimen, MTB continues to cause considerable morbidity and mortality worldwide. Antibiotic resistance and tolerance remain major global issues, and innovative therapeutic strategies are urgently needed to address the challenges
SUBMITTER: Kuang W
PROVIDER: S-EPMC9366312 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
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