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

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Emily R Bryan, Julia McRae, Vishnu Kumar, Logan K Trim, Toby I Maidment, Jacob A D Tickner, Emma L Sweeney, Elizabeth D Williams, David M Whiley, Kenneth W Beagley
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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.

利用蕈样奈瑟氏菌模拟男性生殖器奈瑟氏菌感染的新型小鼠模型。
淋病奈瑟菌每年约有 7 800 万病例,由于抗菌药耐药性的不断出现,淋病奈瑟菌已成为全球公共卫生的一个紧迫威胁。在男性生殖道中,未经治疗的感染可能会造成永久性损伤、精子质量低下,进而导致不育。目前,淋球菌感染的动物模型很少,而淋球菌对人类有严格的致病性。缺乏适当的模型阻碍了重要的新诊断和治疗方法的开发。然而,小鼠口腔奈瑟氏菌的发现带来了巨大的希望。这种细菌已被用于建立口腔奈瑟氏菌感染模型,但建立泌尿生殖道淋球菌模型的可行性还没有被探索。我们通过阴茎内途径给小鼠接种了蕈样淋球菌。我们评估了整个雄性生殖道的细菌负荷、感染后两周的全身和组织特异性免疫反应以及感染对精子健康的影响。在阴茎(2/5)和输精管(3/5)组织中发现了蕈样奈瑟菌。感染改变了免疫细胞数量:与未感染的小鼠相比,CD19+(脾脏、淋巴结、阴茎)、F4/80+(脾脏、淋巴结、附睾)和 Gr1+(阴茎)。这导致感染小鼠的精子存活率、活力和形态都很差。我们假设,在没有睾丸感染的情况下,其他生殖系统的感染和炎症足以损害精子质量。本文中的许多结果与淋病感染的结果一致,这表明该模型有可能成为一种工具,用于加深对奈瑟氏菌感染人类男性生殖道的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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