Synergy Screening Identifies a Compound That Selectively Enhances the Antibacterial Activity of Nitric Oxide.

TitleSynergy Screening Identifies a Compound That Selectively Enhances the Antibacterial Activity of Nitric Oxide.
Publication TypeJournal Article
Year of Publication2020
AuthorsChou, WKang, Vaikunthan, M, Schröder, HV, A Link, J, Kim, H, Brynildsen, MP
JournalFront Bioeng Biotechnol
Volume8
Pagination1001
Date Published2020
ISSN2296-4185
Abstract

<p>Antibiotic resistance poses a serious threat to global health. To reinforce the anti-infective arsenal, many novel therapeutic strategies to fight bacterial infections are being explored. Among them, anti-virulence therapies, which target pathways important for virulence, have attracted much attention. Nitric oxide (NO) defense systems have been identified as critical for the pathogenesis of various bacteria, making them an appealing therapeutic target. In this study, we performed chemical screens to identify inhibitors of NO detoxification in . We found that 2-mercaptobenzothiazole (2-MBT) can potently inhibit cellular detoxification of NO, achieving a level of inhibition that resembled the effect of genetically removing Hmp, the dominant detoxification enzyme under oxygenated conditions. Further analysis revealed that in the presence of NO, 2-MBT impaired the catalysis of Hmp and synthesis of Hmp and other proteins, whereas in its absence there were minimal perturbations to growth and protein synthesis. In addition, by studying the structure-activity relationship of 2-MBT, we found that both sulfur atoms in 2-MBT were vital for its inhibition of NO detoxification. Interestingly, when 2-mercaptothiazole (2-MT), which lacked the benzene ring, was used, differing biological activities were observed, although they too were NO dependent. Specifically, 2-MT could still prohibit NO detoxification, though it did not interfere with Hmp catalysis; rather, it was a stronger inhibitor of protein synthesis and it reduced the transcript levels of , which was not observed with 2-MBT. Overall, these results provide a strong foundation for further exploration of 2-MBT and 2-MT for therapeutic applications.</p>

DOI10.3389/fbioe.2020.01001
Alternate JournalFront Bioeng Biotechnol
PubMed ID32984281
PubMed Central IDPMC7477088