Putri Dira S, Shepherd Frances K, Sanders Autumn E, Roach Shanley N, Jay Sridevi, Pierson Mark J, Wieking Garritt, Anderson Jodi L, Meyerholz David K, Schacker Timothy W, Langlois Ryan A
Department of Microbiology and Immunology, University of Minnesota, Minneapolis, Minnesota, USA.
Microbiology, Immunology and Cancer Biology Graduate Program, University of Minnesota, Minneapolis, Minnesota, USA.
J Virol. 2025 Jun 17;99(6):e0018725. doi: 10.1128/jvi.00187-25. Epub 2025 May 28.
Specific-pathogen-free (SPF) mice are widely used in biomedical research to model human infections. However, these animals do not always accurately recapitulate human immune responses. This is due, in part, to their lack of infection history. A growing number of studies show that the host microbiome influences the development, progression, and responses of many diseases. To date, the majority of research on the microbiome has focused on the bacterial populations and less on the eukaryotic virome of the host. Here, we characterize a transmission model where SPF mice are exposed to natural mouse pathogens at physiologic doses and routes. We found that pet store mice acquired from different sources have distinct viromes and infection histories. We also found significant heterogeneity in the kinetics of the transmission of natural mouse viruses. A common virus found in our model was murine Kobuvirus. Surprisingly, murine Kobuvirus infection was found in the glandular stomach epithelia and not intestinal epithelia like other enteric picornaviruses. Together, these data characterize the heterogeneity of the dirty mouse cohousing system and provide a foundation for studying the biology of natural mouse viruses.
Increasing evidence supports microbial exposure as a critical factor in shaping responses to immune challenges such as infections and vaccinations. However, many experimental models introducing microbial exposure into laboratory animals have confounding factors that may impact phenotypes and are not well characterized. Here, we characterized the pet store reservoir virome diversity, prior infection history, and transmission kinetics. We found significant heterogeneity across these features of the pet store cohousing model. Moreover, we leveraged this model to investigate the tropism of two less characterized viruses-murine Kobuvirus and murine astrovirus 2-in a natural transmission setting. These findings highlight the importance of characterizing the virome of pet store reservoirs to better mimic microbial exposure in humans.
无特定病原体(SPF)小鼠在生物医学研究中被广泛用于模拟人类感染。然而,这些动物并不总是能准确重现人类免疫反应。部分原因在于它们缺乏感染史。越来越多的研究表明,宿主微生物群会影响许多疾病的发生、发展和反应。迄今为止,大多数关于微生物群的研究都集中在细菌群体上,而对宿主的真核病毒组关注较少。在这里,我们描述了一种传播模型,即让SPF小鼠以生理剂量和途径接触天然小鼠病原体。我们发现,从不同来源获得的宠物店小鼠具有不同的病毒组和感染史。我们还发现天然小鼠病毒传播动力学存在显著异质性。我们模型中发现的一种常见病毒是鼠科杯状病毒。令人惊讶的是,在腺胃上皮中发现了鼠科杯状病毒感染,而不像其他肠道小核糖核酸病毒那样在肠道上皮中发现。总之,这些数据描述了脏小鼠同笼饲养系统的异质性,并为研究天然小鼠病毒的生物学特性提供了基础。
越来越多的证据支持微生物暴露是塑造对感染和疫苗接种等免疫挑战反应的关键因素。然而,许多将微生物暴露引入实验动物的实验模型存在可能影响表型且未得到充分表征的混杂因素。在这里,我们描述了宠物店宿主病毒组的多样性、既往感染史和传播动力学。我们发现宠物店同笼饲养模型的这些特征存在显著异质性。此外,我们利用这个模型在自然传播环境中研究了两种特征较少的病毒——鼠科杯状病毒和鼠星状病毒2型的嗜性。这些发现凸显了表征宠物店宿主病毒组以更好模拟人类微生物暴露的重要性。