Colistin Resistance in Acinetobacter baumannii Is Mediated by Complete Loss of Lipopolysaccharide Production

Author:

Moffatt Jennifer H.1,Harper Marina12,Harrison Paul3,Hale John D. F.4,Vinogradov Evgeny5,Seemann Torsten3,Henry Rebekah1,Crane Bethany1,St. Michael Frank5,Cox Andrew D.5,Adler Ben123,Nation Roger L.4,Li Jian4,Boyce John D.12

Affiliation:

1. Department of Microbiology, Monash University, Clayton, Victoria, Australia

2. Australian Research Council Centre of Excellence in Structural and Functional Microbial Genomics, Monash University, Clayton, Victoria, Australia

3. Victorian Bioinformatics Consortium, Monash University, Clayton, Victoria, Australia

4. Facility for Anti-Infective Drug Development and Innovation, Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University, Clayton, Victoria, Australia

5. Institute for Biological Sciences, National Research Council, Ottawa, Ontario, Canada

Abstract

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.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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