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

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