Cargando…
Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats
Previous studies have shown that bats are reservoirs of a large number of viruses, many of which cause illness and mortality in humans and other animals. However, these bat-associated pathogens cause little, if any, clinicopathology in bats. This long-term adaptation should be reflected somewhat in...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079974/ https://www.ncbi.nlm.nih.gov/pubmed/28013457 http://dx.doi.org/10.1007/s00251-016-0966-2 |
_version_ | 1783507931798437888 |
---|---|
author | Jiang, Haiying Li, Juan Li, Linmiao Zhang, Xiujuan Yuan, Lihong Chen, Jinping |
author_facet | Jiang, Haiying Li, Juan Li, Linmiao Zhang, Xiujuan Yuan, Lihong Chen, Jinping |
author_sort | Jiang, Haiying |
collection | PubMed |
description | Previous studies have shown that bats are reservoirs of a large number of viruses, many of which cause illness and mortality in humans and other animals. However, these bat-associated pathogens cause little, if any, clinicopathology in bats. This long-term adaptation should be reflected somewhat in the immune system. Toll-like receptors (TLRs) are the first line of immune defense against pathogens in vertebrates. Therefore, this study focuses on the selection of TLRs involved in virus recognition. The coding sequences of TLR3, TLR7, TLR8, and TLR9 were sequenced in ten bats. The selection pressure acting on each gene was also detected using branch- and site-specific methods. The results showed that the ancestor of bats and certain other bat sublineages evolved under positive selection for TLR7, TLR8, and TLR9. The highest proportion of positive selection occurred in TLR9, followed by TLR8 and TLR7. All of the positively selected sites were located in the leucine-rich repeat (LRR) domain, which implied their important roles in pathogen recognition. However, TLR3 evolved under negative selection. Our results are not in line with previous studies which identified more positively selected sites in TLR8 in mammalian species. In this study, the most positively selected sites were found in TLR9. This study encompassed more species that were considered natural reservoirs of viruses. The positive selection for TLR7, TLR8, and TLR9 might contribute to the adaptation of pathogen-host interaction in bats, especially in bat TLR9. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00251-016-0966-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7079974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70799742020-03-23 Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats Jiang, Haiying Li, Juan Li, Linmiao Zhang, Xiujuan Yuan, Lihong Chen, Jinping Immunogenetics Original Article Previous studies have shown that bats are reservoirs of a large number of viruses, many of which cause illness and mortality in humans and other animals. However, these bat-associated pathogens cause little, if any, clinicopathology in bats. This long-term adaptation should be reflected somewhat in the immune system. Toll-like receptors (TLRs) are the first line of immune defense against pathogens in vertebrates. Therefore, this study focuses on the selection of TLRs involved in virus recognition. The coding sequences of TLR3, TLR7, TLR8, and TLR9 were sequenced in ten bats. The selection pressure acting on each gene was also detected using branch- and site-specific methods. The results showed that the ancestor of bats and certain other bat sublineages evolved under positive selection for TLR7, TLR8, and TLR9. The highest proportion of positive selection occurred in TLR9, followed by TLR8 and TLR7. All of the positively selected sites were located in the leucine-rich repeat (LRR) domain, which implied their important roles in pathogen recognition. However, TLR3 evolved under negative selection. Our results are not in line with previous studies which identified more positively selected sites in TLR8 in mammalian species. In this study, the most positively selected sites were found in TLR9. This study encompassed more species that were considered natural reservoirs of viruses. The positive selection for TLR7, TLR8, and TLR9 might contribute to the adaptation of pathogen-host interaction in bats, especially in bat TLR9. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00251-016-0966-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-12-24 2017 /pmc/articles/PMC7079974/ /pubmed/28013457 http://dx.doi.org/10.1007/s00251-016-0966-2 Text en © Springer-Verlag Berlin Heidelberg 2016 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Jiang, Haiying Li, Juan Li, Linmiao Zhang, Xiujuan Yuan, Lihong Chen, Jinping Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title | Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title_full | Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title_fullStr | Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title_full_unstemmed | Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title_short | Selective evolution of Toll-like receptors 3, 7, 8, and 9 in bats |
title_sort | selective evolution of toll-like receptors 3, 7, 8, and 9 in bats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7079974/ https://www.ncbi.nlm.nih.gov/pubmed/28013457 http://dx.doi.org/10.1007/s00251-016-0966-2 |
work_keys_str_mv | AT jianghaiying selectiveevolutionoftolllikereceptors378and9inbats AT lijuan selectiveevolutionoftolllikereceptors378and9inbats AT lilinmiao selectiveevolutionoftolllikereceptors378and9inbats AT zhangxiujuan selectiveevolutionoftolllikereceptors378and9inbats AT yuanlihong selectiveevolutionoftolllikereceptors378and9inbats AT chenjinping selectiveevolutionoftolllikereceptors378and9inbats |