Characterization of outer membrane vesicles released by clinical isolates of Neisseria gonorrhoeae

Author:

Dhital Subhash1,Deo Pankaj1,Stuart Isabella1,Huang Cheng12,Zavan Lauren34,Han Mei‐Ling5,Kaparakis‐Liaskos Maria34ORCID,Ramm Georg16,Schittenhelm Ralf B.12,Howden Benjamin7,Naderer Thomas1ORCID

Affiliation:

1. Department of Biochemistry & Molecular Biology Biomedicine Discovery Institute Monash University Clayton Victoria Australia

2. Monash Proteomics and Metabolomics Platform Biomedicine Discovery Institute Monash University Clayton Victoria Australia

3. Department of Microbiology Anatomy, Physiology, and Pharmacology La Trobe University Melbourne Victoria Australia

4. Research Centre for Extracellular Vesicles School of Molecular Science La Trobe University Melbourne Victoria Australia

5. Department of Microbiology Biomedicine Discovery Institute Monash University Clayton Victoria Australia

6. Monash Ramaciotti Centre for Cryo Electron Microscopy Monash University Melbourne Victoria Australia

7. Microbiological Diagnostic Unit Public Health Laboratory Department of Microbiology & Immunology The University of Melbourne at The Doherty Institute for Infection and Immunity Melbourne Victoria Australia

Abstract

AbstractThe sexually transmitted pathogen Neisseria gonorrhoeae releases membrane vesicles including outer membrane vesicles (OMVs) during infections. OMVs traffic outer membrane molecules, such as the porin PorB and lipo‐oligosaccharide (LOS), into host innate immune cells, eliciting programmed cell death pathways, and inflammation. Little is known, however, about the proteome and LOS content of OMVs released by clinical strains isolated from different infection sites, and whether these vesicles similarly activate immune responses. Here, we characterized OMVs from four N. gonorrhoeae isolates and determined their size, abundance, proteome, LOS content, and activation of inflammatory responses in macrophages. The overall proteome of the OMVs was conserved between the four different isolates, which included major outer membrane and periplasm proteins. Despite this, we observed differences in the rate of OMV biogenesis and the relative abundance of membrane proteins and LOS. Consequently, OMVs from clinical isolates induced varying rates of macrophage cell death and the secretion of interleukin‐1 family members, such as IL‐1α and IL‐1β. Overall, these findings demonstrate that clinical isolates of N. gonorrhoeae utilize membrane vesicles to release proteins and lipids, which affects innate immune responses.

Funder

Australian Research Council

National Health and Medical Research Council

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Extracellular vesicles—An omics view;PROTEOMICS;2024-04-26

2. Extracellular Vesicles and Bacterial Infection;Extracellular Vesicles in Human Health and Diseases;2024

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