Host Specificity and Geographic Dispersion Shape Virome Diversity in Rhinolophus Bats

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Daxi Wang, Linmiao Li, Zirui Ren, Yepin Yu, Zhipeng Zhang, Jiabin Zhou, Hailong Zhao, Zhiwen Zhao, Peibo Shi, Xinrui Mi, Xin Jin, Ziqing Deng, Junhua Li, Jinping Chen
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Abstract

Rhinolophus bats have been identified as natural reservoirs for viruses with global health implications, including severe acute respiratory syndrome–related coronaviruses (SARSr-CoV) and swine acute diarrhoea syndrome-related coronavirus (SADSr-CoV). In this study, we characterised the individual viromes of 603 bats to systematically investigate the diversity, abundance and geographic distribution of viral communities within R. affinis, R. sinicus and 11 other bat species. The massive metatranscriptomic data revealed substantial viral genome resources of 133 vertebrate-infecting viral clusters, which contain occasional cross-species transmission across mammalian orders and especially across bat families. Notably, those viruses included nine clusters closely related to human and/or livestock pathogens, such as SARS-CoVs and SADS-CoVs. The investigation also highlighted distinct features of viral diversity between and within bat colonies, which appear to be influenced by the distinct host population genetics of R. affinis and R. sinicus species. The comparison of SARSr-CoVs further showed varied impact of host specificity along genome-wide diversification and modular viral evolution among Rhinolophus species. Overall, the findings point to a complex interaction between host genetic diversity, and the way viruses spread and structure within natural populations, calling for continued surveillance efforts to understand factors driving viral transmission and emergence in human populations. These results present the underestimated spillover risk of bat viruses, highlighting the importance of enhancing preparedness and surveillance for emerging zoonotic viruses.

鼻鼻蝠宿主特异性和地理分散形成病毒组多样性。
鼻蝠已被确定为具有全球健康影响的病毒的天然宿主,包括严重急性呼吸综合征相关冠状病毒(SARSr-CoV)和猪急性腹泻综合征相关冠状病毒(SADSr-CoV)。本研究通过对603只蝙蝠的个体病毒组特征分析,系统地研究了亲和蝙蝠、sinicus蝙蝠和其他11种蝙蝠中病毒群落的多样性、丰度和地理分布。大量的超转录组学数据揭示了133种脊椎动物感染病毒簇的大量病毒基因组资源,这些病毒簇偶尔在哺乳动物目之间,特别是在蝙蝠科之间进行跨物种传播。值得注意的是,这些病毒包括与人类和/或牲畜病原体密切相关的9个聚集性病毒,如sars - cov和sads - cov。调查还强调了蝙蝠种群之间和内部病毒多样性的明显特征,这似乎受到affinis R.和sinicus R.不同宿主种群遗传的影响。sars - cov的比较进一步表明,随着病毒的全基因组多样化和模块化进化,宿主特异性对鼻犀牛物种的影响存在差异。总的来说,这些发现指出了宿主遗传多样性与病毒在自然种群中的传播方式和结构之间的复杂相互作用,呼吁继续进行监测工作,以了解驱动病毒在人类种群中传播和出现的因素。这些结果表明蝙蝠病毒的溢出风险被低估了,突出了加强对新出现的人畜共患病毒的防范和监测的重要性。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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