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

Author:

Bryan Emily R1234,McRae Julia12,Kumar Vishnu5,Trim Logan K12,Maidment Toby I1234,Tickner Jacob A D34,Sweeney Emma L34,Williams Elizabeth D67,Whiley David M34,Beagley Kenneth W12

Affiliation:

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

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

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

4. The University of Queensland , Faculty of Medicine, , Brisbane, Queensland 4029, Australia

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

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

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

Abstract

Abstract 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.

Funder

Australian Research Council Research Hub for Antimicrobial Resistance

National Health and Medical Research Council

Division of Arctic Sciences

Researcher Exchange and Development with Industry

PA Research Foundation

Publisher

Oxford University Press (OUP)

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