Department of Biology, Indiana University, Bloomington, IN, USA.
Center for the Ecology of Infectious Disease, University of Georgia, Athens, GA, USA.
Mol Ecol. 2020 Apr;29(8):1534-1549. doi: 10.1111/mec.15422. Epub 2020 Apr 21.
Most emerging pathogens can infect multiple species, underlining the importance of understanding the ecological and evolutionary factors that allow some hosts to harbour greater infection prevalence and share pathogens with other species. However, our understanding of pathogen jumps is based primarily around viruses, despite bacteria accounting for the greatest proportion of zoonoses. Because bacterial pathogens in bats (order Chiroptera) can have conservation and human health consequences, studies that examine the ecological and evolutionary drivers of bacterial prevalence and barriers to pathogen sharing are crucially needed. Here were studied haemotropic Mycoplasma spp. (i.e., haemoplasmas) across a species-rich bat community in Belize over two years. Across 469 bats spanning 33 species, half of individuals and two-thirds of species were haemoplasma positive. Infection prevalence was higher for males and for species with larger body mass and colony sizes. Haemoplasmas displayed high genetic diversity (21 novel genotypes) and strong host specificity. Evolutionary patterns supported codivergence of bats and bacterial genotypes alongside phylogenetically constrained host shifts. Bat species centrality to the network of shared haemoplasma genotypes was phylogenetically clustered and unrelated to prevalence, further suggesting rare-but detectable-bacterial sharing between species. Our study highlights the importance of using fine phylogenetic scales when assessing host specificity and suggests phylogenetic similarity may play a key role in host shifts not only for viruses but also for bacteria. Such work more broadly contributes to increasing efforts to understand cross-species transmission and the epidemiological consequences of bacterial pathogens.
大多数新出现的病原体可以感染多种物种,这突显出理解允许某些宿主具有更高感染流行率并与其他物种共享病原体的生态和进化因素的重要性。然而,我们对病原体跳跃的理解主要围绕病毒展开,尽管细菌占人畜共患病的比例最大。由于蝙蝠(翼手目)中的细菌病原体可能对保护和人类健康产生影响,因此迫切需要研究检查细菌流行率和病原体共享障碍的生态和进化驱动因素。在这里,我们在伯利兹的一个物种丰富的蝙蝠群落中研究了两年的血液传染性支原体属(即支原体)。在跨越 33 个物种的 469 只蝙蝠中,有一半的个体和三分之二的物种呈支原体阳性。雄性和体重较大、群体规模较大的物种的感染率更高。支原体表现出高度的遗传多样性(21 种新基因型)和强烈的宿主特异性。进化模式支持蝙蝠和细菌基因型的共同进化以及受系统发育限制的宿主转移。共享支原体基因型网络中蝙蝠物种的中心性在系统发育上是聚类的,与流行率无关,这进一步表明物种之间存在罕见但可检测到的细菌共享。我们的研究强调了在评估宿主特异性时使用精细的系统发育尺度的重要性,并表明系统发育相似性可能不仅对病毒,而且对细菌的宿主转移都起着关键作用。此类工作更广泛地有助于增加对跨物种传播和细菌病原体的流行病学后果的理解。