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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...

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Autores principales: Jiang, Haiying, Li, Juan, Li, Linmiao, Zhang, Xiujuan, Yuan, Lihong, Chen, Jinping
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
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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.
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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
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