Comparative Genome Sequence Analysis of Multidrug-Resistant Acinetobacter baumannii

Author:

Adams Mark D.1,Goglin Karrie1,Molyneaux Neil1,Hujer Kristine M.2,Lavender Heather1,Jamison Jennifer J.3,MacDonald Ian J.3,Martin Kristienna M.3,Russo Thomas3456,Campagnari Anthony A.36,Hujer Andrea M.2,Bonomo Robert A.72,Gill Steven R.38

Affiliation:

1. Department of Genetics

2. Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio

3. New York State Center of Excellence in Bioinformatics and Life Sciences

4. Veterans Administration Western New York Healthcare System

5. Department of Medicine

6. Department of Microbiology & Immunology

7. Departments of Pharmacology and Molecular Biology and Microbiology, Case Western Reserve University School of Medicine, Cleveland, Ohio

8. Department of Oral Biology, The State University of New York at Buffalo, Buffalo, New York

Abstract

ABSTRACT The recent emergence of multidrug resistance (MDR) in Acinetobacter baumannii has raised concern in health care settings worldwide. In order to understand the repertoire of resistance determinants and their organization and origins, we compared the genome sequences of three MDR and three drug-susceptible A. baumannii isolates. The entire MDR phenotype can be explained by the acquisition of discrete resistance determinants distributed throughout the genome. A comparison of closely related MDR and drug-susceptible isolates suggests that drug efflux may be a less significant contributor to resistance to certain classes of antibiotics than inactivation enzymes are. A resistance island with a variable composition of resistance determinants interspersed with transposons, integrons, and other mobile genetic elements is a significant but not universal contributor to the MDR phenotype. Four hundred seventy-five genes are shared among all six clinical isolates but absent from the related environmental species Acinetobacter baylyi ADP1. These genes are enriched for transcription factors and transporters and suggest physiological features of A. baumannii that are related to adaptation for growth in association with humans.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3