RcsB Contributes to the Distinct Stress Fitness among Escherichia coli O157:H7 Curli Variants of the 1993 Hamburger-Associated Outbreak Strains

Author:

Carter Michelle Q.,Parker Craig T.,Louie Jacqueline W.,Huynh Steven,Fagerquist Clifton K.,Mandrell Robert E.

Abstract

ABSTRACTCurli are adhesive fimbriae ofEnterobactericaeaeand are involved in surface attachment, cell aggregation, and biofilm formation. We reported previously that curli-producing (C+) variants ofE. coliO157:H7 (EcO157) were much more acid sensitive than their corresponding curli-deficient (C) variants; however, this difference was not linked to the curli fimbriaeper se. Here, we investigated the underlying molecular basis of this phenotypic divergence. We identified large deletions in thercsBgene of C+variants isolated from the 1993 U.S. hamburger-associated outbreak strains.rcsBencodes the response regulator of the RcsCDB two-component signal transduction system, which regulates curli biogenesis negatively but acid resistance positively. Further comparison of stress fitness revealed that C+variants were also significantly more sensitive to heat shock but were resistant to osmotic stress and oxidative damage, similar to Cvariants. Transcriptomics analysis uncovered a large number of differentially expressed genes between the curli variants, characterized by enhanced expression in C+variants of genes related to biofilm formation, virulence, catabolic activity, and nutrient uptake but marked decreases in transcription of genes related to various types of stress resistance. Supplying C+variants with a functionalrcsBrestored resistance to heat shock and acid challenge in cells but blocked curli production, confirming that inactivation of RcsB in C+variants was the basis of fitness segregation within the EcO157 population. This study provides an example of how genome instability of EcO157 promotes intrapopulation diversification, generating subpopulations carrying an array of distinct phenotypes that may confer the pathogen with survival advantages in diverse environments.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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