A Gram-negative-selective antibiotic that spares the gut microbiome.
Publication Date: 2024 Jun
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Authors
Kristen A Muñoz; Rebecca J Ulrich; Archit K Vasan; Matt Sinclair; Po-Chao Wen; Jessica R Holmes; Hyang Yeon Lee; Chien-Che Hung; Christopher J Fields; Emad Tajkhorshid; Gee W Lau; Paul J HergenrotherAbstract
OBJECTIVE
Infections caused by Gram-negative pathogens are increasingly prevalent and are typically treated with broad-spectrum antibiotics, resulting in disruption of the gut microbiome and susceptibility to secondary infections. There is a critical need for antibiotics that are selective both for Gram-negative bacteria over Gram-positive bacteria, as well as for pathogenic bacteria over commensal bacteria. Here we report the design and discovery of lolamicin, a Gram-negative-specific antibiotic targeting the lipoprotein transport system. Lolamicin has activity against a panel of more than 130 multidrug-resistant clinical isolates, shows efficacy in multiple mouse models of acute pneumonia and septicaemia infection, and spares the gut microbiome in mice, preventing secondary infection with Clostridioides difficile. The selective killing of pathogenic Gram-negative bacteria by lolamicin is a consequence of low sequence homology for the target in pathogenic bacteria versus commensals; this doubly selective strategy can be a blueprint for the development of other microbiome-sparing antibiotics.
Source
Nature
Pub Types(s)
Journal Article
Language
English
PubMed ID
38811738