Distinct Signature of Oxylipid Mediators of Inflammation during Infection and Asymptomatic Colonization byE. coliin the Urinary Bladder

Author:

Packiriswamy Nandakumar1,Gandy Jeff1,Smith Sara N.2,Mobley Harry L. T.2,Sordillo Lorraine M.1ORCID,Subashchandrabose Sargurunathan3ORCID

Affiliation:

1. Department of Large Animal Clinical Sciences, Michigan State University, East Lansing, MI, USA

2. Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA

3. Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC, USA

Abstract

Urinary tract infection (UTI) is an extremely common infectious disease. UropathogenicEscherichia coli(UPEC) is the predominant etiological agent of UTI. Asymptomatic bacteriuricE. coli(ABEC) strains successfully colonize the urinary tract resulting in asymptomatic bacteriuria (ABU) and do not induce symptoms associated with UTI. Oxylipids are key signaling molecules involved in inflammation. Based on the distinct clinical outcomes ofE. colicolonization, we hypothesized that UPEC triggers the production of predominantly proinflammatory oxylipids and ABEC leads to production of primarily anti-inflammatory or proresolving oxylipids in the urinary tract. We performed quantitative detection of 39 oxylipid mediators with proinflammatory, anti-inflammatory, and proresolving properties, during UTI and ABU caused by genetically distinctE. colistrains in the murine urinary bladder. Our results reveal that infection with UPEC causes an increased accumulation of proinflammatory oxylipids as early as 6 h postinoculation, compared to controls. To the contrary, ABEC colonization leads to decreased accumulation of proinflammatory oxylipids at the early time point compared to UPEC infection but does not affect the level of proresolving oxylipids. This report represents the first comprehensive investigation on the oxylipidome during benign ABEC colonization observed in ABU and acute inflammation triggered by UPEC leading to UTI.

Funder

U.S. Department of Agriculture

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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