Immunology-Vaccinology (B43b), Department of Infectious and Parasitic Diseases, Faculty of Veterinary Medicine, University of Liège, Liège, Belgium.
PLoS Pathog. 2013;9(4):e1003292. doi: 10.1371/journal.ppat.1003292. Epub 2013 Apr 4.
Transmission is a matter of life or death for pathogen lineages and can therefore be considered as the main motor of their evolution. Gammaherpesviruses are archetypal pathogenic persistent viruses which have evolved to be transmitted in presence of specific immune response. Identifying their mode of transmission and their mechanisms of immune evasion is therefore essential to develop prophylactic and therapeutic strategies against these infections. As the known human gammaherpesviruses, Epstein-Barr virus and Kaposi's Sarcoma-associated Herpesvirus are host-specific and lack a convenient in vivo infection model; related animal gammaherpesviruses, such as murine gammaherpesvirus-68 (MHV-68), are commonly used as general models of gammaherpesvirus infections in vivo. To date, it has however never been possible to monitor viral excretion or virus transmission of MHV-68 in laboratory mice population. In this study, we have used MHV-68 associated with global luciferase imaging to investigate potential excretion sites of this virus in laboratory mice. This allowed us to identify a genital excretion site of MHV-68 following intranasal infection and latency establishment in female mice. This excretion occurred at the external border of the vagina and was dependent on the presence of estrogens. However, MHV-68 vaginal excretion was not associated with vertical transmission to the litter or with horizontal transmission to female mice. In contrast, we observed efficient virus transmission to naïve males after sexual contact. In vivo imaging allowed us to show that MHV-68 firstly replicated in penis epithelium and corpus cavernosum before spreading to draining lymph nodes and spleen. All together, those results revealed the first experimental transmission model for MHV-68 in laboratory mice. In the future, this model could help us to better understand the biology of gammaherpesviruses and could also allow the development of strategies that could prevent the spread of these viruses in natural populations.
传播对于病原体谱系来说是生死攸关的,因此可以被视为它们进化的主要动力。γ疱疹病毒是典型的致病持续性病毒,它们已经进化到能够在特定的免疫反应存在的情况下进行传播。因此,确定它们的传播方式和免疫逃避机制对于开发针对这些感染的预防和治疗策略至关重要。由于已知的人类γ疱疹病毒,如 EBV 和卡波西肉瘤相关疱疹病毒,都是宿主特异性的,缺乏方便的体内感染模型;相关的动物γ疱疹病毒,如鼠γ疱疹病毒-68(MHV-68),通常被用作体内γ疱疹病毒感染的通用模型。到目前为止,还从未有可能监测到 MHV-68 在实验室小鼠群体中的病毒排泄或病毒传播。在这项研究中,我们使用与全球荧光素酶成像相关的 MHV-68 来研究该病毒在实验室小鼠中的潜在排泄部位。这使我们能够在雌性小鼠中确定 MHV-68 在鼻腔感染和潜伏期建立后的生殖器排泄部位。这种排泄发生在外阴的外部边界,并且依赖于雌激素的存在。然而,MHV-68 的阴道排泄并不与垂直传播到后代或与雌性小鼠的水平传播相关。相反,我们观察到在性接触后,病毒能够有效地传播到未感染的雄性。体内成像使我们能够显示出 MHV-68 首先在阴茎上皮和海绵体中复制,然后传播到引流淋巴结和脾脏。所有这些结果揭示了 MHV-68 在实验室小鼠中的第一个实验性传播模型。在未来,该模型可以帮助我们更好地了解γ疱疹病毒的生物学,并且还可以开发出能够阻止这些病毒在自然种群中传播的策略。