A novel murine model mimicking male genital Neisseria species infection using Neisseria musculi†.

Mouse model Neisseria gonorrhoeae Neisseria musculi immune response male sperm

Journal

Biology of reproduction
ISSN: 1529-7268
Titre abrégé: Biol Reprod
Pays: United States
ID NLM: 0207224

Informations de publication

Date de publication:
08 Jul 2024
Historique:
received: 09 12 2023
revised: 25 04 2024
medline: 7 7 2024
pubmed: 7 7 2024
entrez: 7 7 2024
Statut: aheadofprint

Résumé

With ~78 million cases yearly, the sexually transmitted bacterium Neisseria gonorrhoeae is an urgent threat to global public health due to continued emergence of antimicrobial resistance. In the male reproductive tract, untreated infections may cause permanent damage, poor sperm quality, and subsequently subfertility. Currently, few animal models exist for N. gonorrhoeae infection, which has strict human tropism, and available models have limited translatability to human disease. The absence of appropriate models inhibits the development of vital new diagnostics and treatments. However, the discovery of Neisseria musculi, a mouse oral cavity bacterium, offers much promise. This bacterium has already been used to develop an oral Neisseria infection model, but the feasibility of establishing urogenital gonococcal models is unexplored. We inoculated mice via the intrapenile route with N. musculi. We assessed bacterial burden throughout the male reproductive tract, the systemic and tissue-specific immune response 2-weeks postinfection, and the effect of infection on sperm health. Neisseria musculi was found in penis (2/5) and vas deferens (3/5) tissues. Infection altered immune cell counts: CD19+ (spleen, lymph node, penis), F4/80+ (spleen, lymph node, epididymus), and Gr1+ (penis) compared with noninfected mice. This culminated in sperm from infected mice having poor viability, motility, and morphology. We hypothesize that in the absence of testis infection, infection and inflammation in other reproductive is sufficient to damage sperm quality. Many results herein are consistent with outcomes of gonorrhoea infection, indicating the potential of this model as a tool for enhancing the understanding of Neisseria infections of the human male reproductive tract.

Identifiants

pubmed: 38972067
pii: 7708810
doi: 10.1093/biolre/ioae100
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Australian Research Council Research Hub for Antimicrobial Resistance
ID : IH190100021
Organisme : National Health and Medical Research Council
ID : APP1145825
Organisme : Division of Arctic Sciences
Organisme : Researcher Exchange and Development with Industry
Organisme : PA Research Foundation

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Society for the Study of Reproduction. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Emily R Bryan (ER)

Faculty of Health, School of Biomedical Science, Centre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland 4006, Australia.
Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.

Julia McRae (J)

Faculty of Health, School of Biomedical Science, Centre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland 4006, Australia.

Vishnu Kumar (V)

Justus-Liebig-University Giessen, Institute for Anatomy and Cell Biology, 35385 Giessen, Germany.

Logan K Trim (LK)

Faculty of Health, School of Biomedical Science, Centre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland 4006, Australia.

Toby I Maidment (TI)

Faculty of Health, School of Biomedical Science, Centre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland 4006, Australia.
Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.

Jacob A D Tickner (JAD)

Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.

Emma L Sweeney (EL)

Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.

Elizabeth D Williams (ED)

Faculty of Health, School of Biomedical Science at Translational Research Institute, Centre for Genomics and Personalised Health, Queensland University of Technology, Brisbane, Queensland 4102, Australia.

David M Whiley (DM)

Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland 4029, Australia.

Kenneth W Beagley (KW)

Faculty of Health, School of Biomedical Science, Centre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland 4006, Australia.

Classifications MeSH