Regulatory Mutations Impacting Antibiotic Susceptibility in an Established Staphylococcus aureus Biofilm

Author:

Atwood Danielle N.1ORCID,Beenken Karen E.1,Lantz Tamara L.1,Meeker Daniel G.1,Lynn William B.1,Mills Weston B.1,Spencer Horace J.2,Smeltzer Mark S.134

Affiliation:

1. Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA

2. Department of Biostatistics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA

3. Department of Orthopaedic Surgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA

4. Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA

Abstract

ABSTRACT We previously determined the extent to which mutations of different Staphylococcus aureus regulatory loci impact biofilm formation as assessed under in vitro conditions. Here we extend these studies to determine the extent to which those regulatory loci that had the greatest effect on biofilm formation also impact antibiotic susceptibility. The experiments were done under in vitro and in vivo conditions using two clinical isolates of S. aureus (LAC and UAMS-1) and two functionally diverse antibiotics (daptomycin and ceftaroline). Mutation of the staphylococcal accessory regulator ( sarA ) or sigB was found to significantly increase susceptibilities to both antibiotics and in both strains in a manner that could not be explained by changes in the MICs. The impact of a mutation in sarA was comparable to that of a mutation in sigB and greater than the impact observed with any other mutant. These results suggest that therapeutic strategies targeting sarA and/or sigB have the greatest potential to facilitate the ability to overcome the intrinsic antibiotic resistance that defines S. aureus biofilm-associated infections.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

DOD | Congressionally Directed Medical Research Programs

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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