Colistin Resistance in <i>Acinetobacter baumannii</i> Is Mediated by Complete Loss of Lipopolysaccharide Production

Jennifer H. Moffatt(Monash University), Marina Harper(Australian Research Council), Paul F. Harrison(Melbourne Bioinformatics), John Hale(Monash University), Evgeny Vinogradov(Institute for Biological Sciences), Torsten Seemann(Melbourne Bioinformatics), Rebekah Henry(Monash University), Bethany Crane(Monash University), Frank St. Michael(Institute for Biological Sciences), Andrew D. Cox(Institute for Biological Sciences), Ben Adler(Australian Research Council), Roger L. Nation(Monash University), Jian Li(Monash University), John D. Boyce(Australian Research Council)
Antimicrobial Agents and Chemotherapy
September 21, 2010
Cited by 789

Abstract

Infections caused by multidrug-resistant (MDR) Gram-negative bacteria represent a major global health problem. Polymyxin antibiotics such as colistin have resurfaced as effective last-resort antimicrobials for use against MDR Gram-negative pathogens, including Acinetobacter baumannii. Here we show that A. baumannii can rapidly develop resistance to polymyxin antibiotics by complete loss of the initial binding target, the lipid A component of lipopolysaccharide (LPS), which has long been considered to be essential for the viability of Gram-negative bacteria. We characterized 13 independent colistin-resistant derivatives of A. baumannii type strain ATCC 19606 and showed that all contained mutations within one of the first three genes of the lipid A biosynthesis pathway: lpxA, lpxC, and lpxD. All of these mutations resulted in the complete loss of LPS production. Furthermore, we showed that loss of LPS occurs in a colistin-resistant clinical isolate of A. baumannii. This is the first report of a spontaneously occurring, lipopolysaccharide-deficient, Gram-negative bacterium.


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