Department of Pharmaceutical Sciences, The University of Tennessee Health Science Centergrid.267301.1, Memphis, Tennessee, USA.
Department of Microbiology, Immunology and Biochemistry, The University of Tennessee Health Science Centergrid.267301.1, Memphis, Tennessee, USA.
Microbiol Spectr. 2022 Jun 29;10(3):e0277521. doi: 10.1128/spectrum.02775-21. Epub 2022 Apr 21.
Analysis of dissemination and colonization of sex organs in rodents is of significant value as it queries the possibility of mammal-to-mammal venereal transmission. The aim of our study was to evaluate the presence and viability of Leptospira interrogans in testes of mice using models of infection that we previously developed. Using sublethal and lethal doses of bioluminescent strains of L. interrogans serovars Manilae and Copenhageni, we visualized the presence of leptospires in testes of C57BL/6 mice as early as 30 min and up to days 3-4 postinfection. This was confirmed by qPCR for the Copenhageni serovar after lethal infection of C3H/HeJ mice. In this model, no histopathological changes were noticed in testis. We further studied persistence of serovar Copenhageni in C3H/HeJ testes after lethal and sublethal infection, with different doses of leptospires. No viable leptospires were recovered from testes of lethally infected mice. However, we found live culturable in testes of 19/19 (100%) sublethally infected mice at the acute phase but not at 15 days postinfection, which corresponds to the chronic phase of renal colonization. The data suggest that colonization of testes with live and potentially infectious leptospires is transient and limited to the spirochetemic phase of infection. Further studies are necessary to evaluate if presence of in testes of mice leads to excretion in semen and to venereal transmission to female mice. Analysis of venereal transmission of is important to determine if direct animal to animal transmission occurs, which could impact measures to prevent and treat leptospirosis. The goal of this study was to determine if live colonize mouse testes. We found that colonization of mouse testes with live was transient and limited to the acute spirochetemic phase of infection and that transient colonization of the testes was insufficient to cause histopathological changes.
分析啮齿动物性器官的传播和定植具有重要意义,因为它可以探究哺乳动物之间性传播的可能性。我们的研究目的是使用我们之前开发的感染模型来评估睾丸中问号钩端螺旋体(Leptospira interrogans)的存在和活力。使用亚致死和致死剂量的发光菌株血清型 Manilae 和 Copenhageni,我们早在感染后 30 分钟至 3-4 天即可在 C57BL/6 小鼠的睾丸中观察到钩端螺旋体的存在。在致死性感染 C3H/HeJ 小鼠后,通过 qPCR 对 Copenhageni 血清型进行了确认。在该模型中,睾丸未观察到组织病理学变化。我们进一步研究了致死和亚致死感染不同剂量钩端螺旋体后,C3H/HeJ 睾丸中血清型 Copenhageni 的持续存在。从致死性感染的小鼠睾丸中未回收活的钩端螺旋体。然而,我们发现 19/19(100%)亚致死感染的急性期小鼠睾丸中有可培养的活钩端螺旋体,但在感染后 15 天未发现,这对应于肾脏定植的慢性期。数据表明,睾丸中活的和潜在感染性钩端螺旋体的定植是短暂的,仅限于感染的螺旋体血症期。需要进一步研究以评估小鼠睾丸中存在的是否会导致在精液中排出,并传播给雌性小鼠。分析的性传播对确定是否发生直接的动物到动物传播很重要,这可能会影响预防和治疗钩端螺旋体病的措施。本研究的目的是确定活是否定植于小鼠睾丸。我们发现,活在小鼠睾丸中的定植是短暂的,仅限于感染的急性螺旋体血症期,睾丸的短暂定植不足以引起组织病理学变化。