Department of Biology, Georgetown University, Washington, DC, USA.
Department of Biology, University of Oklahoma, Norman, OK, USA.
Trends Parasitol. 2021 Feb;37(2):117-129. doi: 10.1016/j.pt.2020.10.012. Epub 2020 Nov 17.
Because most emerging human pathogens originate in mammals, many studies aim to identify host traits that determine the risk of sourcing zoonotic outbreaks. Studies regularly assert that 'fast-lived' mammal species exhibiting greater fecundity and shorter lifespans tend to host more zoonoses; however, the causes of this association remain poorly understood and they cover a range of immune and nonimmune mechanisms. We discuss these drivers in the context of evolutionary ecology and wildlife-human interactions. Ultimately, differentiating these mechanisms will require linking interspecific variation in life history with immunity, pathogen diversity, transmissibility, and zoonotic risk, and critical data gaps currently limit our ability to do so. We highlight sampling and analytical frameworks to address this gap and to better inform zoonotic reservoir prediction.
由于大多数新发人类病原体起源于哺乳动物,因此许多研究旨在确定宿主特征,这些特征决定了引发人畜共患病暴发的风险。研究经常声称,“寿命短”的哺乳动物物种表现出更高的繁殖力和更短的寿命,往往会携带更多的人畜共患病;然而,这种关联的原因仍不清楚,它涵盖了一系列免疫和非免疫机制。我们在进化生态学和野生动物与人类相互作用的背景下讨论这些驱动因素。最终,区分这些机制需要将物种间生活史的差异与免疫、病原体多样性、传染性和人畜共患病风险联系起来,而目前关键的数据差距限制了我们这样做的能力。我们强调了采样和分析框架,以解决这一差距,并更好地预测人畜共患病的储存库。