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Shipworm symbiosis ecology-guided discovery of an antibiotic that kills colistin-resistant Acinetobacter.

Authors :
Miller BW
Lim AL
Lin Z
Bailey J
Aoyagi KL
Fisher MA
Barrows LR
Manoil C
Schmidt EW
Haygood MG
Source :
Cell chemical biology [Cell Chem Biol] 2021 Nov 18; Vol. 28 (11), pp. 1628-1637.e4. Date of Electronic Publication: 2021 Jun 18.
Publication Year :
2021

Abstract

Teredinibacter turnerae is an intracellular bacterial symbiont in the gills of wood-eating shipworms, where it is proposed to use antibiotics to defend itself and its animal host. Several biosynthetic gene clusters are conserved in T. turnerae and their host shipworms around the world, implying that they encode defensive compounds. Here, we describe turnercyclamycins, lipopeptide antibiotics encoded in the genomes of all sequenced T. turnerae strains. Turnercyclamycins are bactericidal against challenging Gram-negative pathogens, including colistin-resistant Acinetobacter baumannii. Phenotypic screening identified the outer membrane as the likely target. Turnercyclamycins and colistin operate by similar cellular, although not necessarily molecular, mechanisms, but turnercyclamycins kill colistin-resistant A. baumannii, potentially filling an urgent clinical need. Thus, by exploring environments that select for the properties we require, we harvested the fruits of evolution to discover compounds with potential to target unmet health needs. Investigating the symbionts of shipworms is a powerful example of this principle.<br />Competing Interests: Declaration of interests The authors have filed a provisional patent application for the turnercyclamycins.<br /> (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
2451-9448
Volume :
28
Issue :
11
Database :
MEDLINE
Journal :
Cell chemical biology
Publication Type :
Academic Journal
Accession number :
34146491
Full Text :
https://doi.org/10.1016/j.chembiol.2021.05.003