Inhibitors of bacterial H 2 S biogenesis targeting antibiotic resistance and tolerance

Author:

Shatalin Konstantin1ORCID,Nuthanakanti Ashok1ORCID,Kaushik Abhishek1ORCID,Shishov Dmitry2ORCID,Peselis Alla1,Shamovsky Ilya1ORCID,Pani Bibhusita1,Lechpammer Mirna1ORCID,Vasilyev Nikita1ORCID,Shatalina Elena1,Rebatchouk Dmitri3,Mironov Alexander4ORCID,Fedichev Peter2,Serganov Alexander1ORCID,Nudler Evgeny15ORCID

Affiliation:

1. Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA.

2. Gero LLC, Moscow, Russia.

3. Ellyris LLC, Union, NJ 07083, USA.

4. Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Moscow 119991, Russia.

5. Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.

Abstract

Turning down tolerance Persister cells, which are found in abundance in biofilms, adopt a quiescent state and survive antimicrobial treatments, seeding disease recurrence and incubating new resistance mutations. Building on work implicating the reactive small-molecule hydrogen sulfide in bacterial defense against antibiotics, Shatalin et al. conducted a structure-based screen for inhibitors of a bacterial hydrogen sulfide–producing enzyme and found a group of inhibitors that act through an allosteric mechanism (see the Perspective by Mah). These inhibitors potentiated bactericidal antibiotics in vitro and in mouse infection models. They also suppressed persister bacteria and disrupted biofilm formation. This strategy of taking out persister cells may be promising for treating recalcitrant infections and holding the line against drug-resistant bacteria. Science , abd8377, this issue p. 1169 ; see also abj3062, p. 1153

Funder

U.S. Department of Defense

Howard Hughes Medical Institute

New York University

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference99 articles.

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