Cargando…

Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats

Bats have been identified as natural reservoir hosts of several zoonotic viruses, prompting suggestions that they have unique immunological adaptations. Among bats, Old World fruit bats (Pteropodidae) have been linked to multiple spillovers. To test for lineage-specific molecular adaptations in thes...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Shilin, Zeng, Jiaming, Jiao, Hengwu, Zhang, Dejing, Zhang, Libiao, Lei, Cao-qi, Rossiter, Stephen J., Zhao, Huabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162675/
https://www.ncbi.nlm.nih.gov/pubmed/37146151
http://dx.doi.org/10.1126/sciadv.add0141
_version_ 1785037744281485312
author Tian, Shilin
Zeng, Jiaming
Jiao, Hengwu
Zhang, Dejing
Zhang, Libiao
Lei, Cao-qi
Rossiter, Stephen J.
Zhao, Huabin
author_facet Tian, Shilin
Zeng, Jiaming
Jiao, Hengwu
Zhang, Dejing
Zhang, Libiao
Lei, Cao-qi
Rossiter, Stephen J.
Zhao, Huabin
author_sort Tian, Shilin
collection PubMed
description Bats have been identified as natural reservoir hosts of several zoonotic viruses, prompting suggestions that they have unique immunological adaptations. Among bats, Old World fruit bats (Pteropodidae) have been linked to multiple spillovers. To test for lineage-specific molecular adaptations in these bats, we developed a new assembly pipeline to generate a reference-quality genome of the fruit bat Cynopterus sphinx and used this in comparative analyses of 12 bat species, including six pteropodids. Our results reveal that immunity-related genes have higher evolutionary rates in pteropodids than in other bats. Several lineage-specific genetic changes were shared across pteropodids, including the loss of NLRP1, duplications of PGLYRP1 and C5AR2, and amino acid replacements in MyD88. We introduced MyD88 transgenes containing Pteropodidae-specific residues into bat and human cell lines and found evidence of dampened inflammatory responses. By uncovering distinct immune adaptations, our results could help explain why pteropodids are frequently identified as viral hosts.
format Online
Article
Text
id pubmed-10162675
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-101626752023-05-06 Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats Tian, Shilin Zeng, Jiaming Jiao, Hengwu Zhang, Dejing Zhang, Libiao Lei, Cao-qi Rossiter, Stephen J. Zhao, Huabin Sci Adv Biomedicine and Life Sciences Bats have been identified as natural reservoir hosts of several zoonotic viruses, prompting suggestions that they have unique immunological adaptations. Among bats, Old World fruit bats (Pteropodidae) have been linked to multiple spillovers. To test for lineage-specific molecular adaptations in these bats, we developed a new assembly pipeline to generate a reference-quality genome of the fruit bat Cynopterus sphinx and used this in comparative analyses of 12 bat species, including six pteropodids. Our results reveal that immunity-related genes have higher evolutionary rates in pteropodids than in other bats. Several lineage-specific genetic changes were shared across pteropodids, including the loss of NLRP1, duplications of PGLYRP1 and C5AR2, and amino acid replacements in MyD88. We introduced MyD88 transgenes containing Pteropodidae-specific residues into bat and human cell lines and found evidence of dampened inflammatory responses. By uncovering distinct immune adaptations, our results could help explain why pteropodids are frequently identified as viral hosts. American Association for the Advancement of Science 2023-05-05 /pmc/articles/PMC10162675/ /pubmed/37146151 http://dx.doi.org/10.1126/sciadv.add0141 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Tian, Shilin
Zeng, Jiaming
Jiao, Hengwu
Zhang, Dejing
Zhang, Libiao
Lei, Cao-qi
Rossiter, Stephen J.
Zhao, Huabin
Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title_full Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title_fullStr Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title_full_unstemmed Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title_short Comparative analyses of bat genomes identify distinct evolution of immunity in Old World fruit bats
title_sort comparative analyses of bat genomes identify distinct evolution of immunity in old world fruit bats
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10162675/
https://www.ncbi.nlm.nih.gov/pubmed/37146151
http://dx.doi.org/10.1126/sciadv.add0141
work_keys_str_mv AT tianshilin comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT zengjiaming comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT jiaohengwu comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT zhangdejing comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT zhanglibiao comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT leicaoqi comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT rossiterstephenj comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats
AT zhaohuabin comparativeanalysesofbatgenomesidentifydistinctevolutionofimmunityinoldworldfruitbats