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Host specificity and geographic dispersion shape virome diversity in Rhinolophus bats

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Abstract Background Many zoonotic viruses originated from bats. Notably, Rhinolophus bats have been identified as natural reservoirs for some viruses with global health implications, including severe acute respiratory syndrome–related coronaviruses (SARSr-CoVs) and swine acute diarrhea syndrome-related coronavirus (SADSr-CoVs). Understanding the diversity and evolution of the viral communities in Rhinolophus bats becomes an essential step if our aims are to enhance preparedness for emerging zoonotic viruses. However, the current knowledge of viral diversity within and among Rhinolophus species remains neglected, leaving underestimated spillover risks. Results We characterized 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 related bat species. The massive metatranscriptomic data revealed substantial viral genome resources of 133 vertebrate-infecting vANI80s, which contain occasional cross-species transmission across mammalian orders and specially across bat families. Notably, those viruses included many 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. Conclusions 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.
Title: Host specificity and geographic dispersion shape virome diversity in Rhinolophus bats
Description:
Abstract Background Many zoonotic viruses originated from bats.
Notably, Rhinolophus bats have been identified as natural reservoirs for some viruses with global health implications, including severe acute respiratory syndrome–related coronaviruses (SARSr-CoVs) and swine acute diarrhea syndrome-related coronavirus (SADSr-CoVs).
Understanding the diversity and evolution of the viral communities in Rhinolophus bats becomes an essential step if our aims are to enhance preparedness for emerging zoonotic viruses.
However, the current knowledge of viral diversity within and among Rhinolophus species remains neglected, leaving underestimated spillover risks.
Results We characterized 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 related bat species.
The massive metatranscriptomic data revealed substantial viral genome resources of 133 vertebrate-infecting vANI80s, which contain occasional cross-species transmission across mammalian orders and specially across bat families.
Notably, those viruses included many 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.
Conclusions 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.

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