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Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus

Peste des Petits Ruminants (PPR) is an acute, highly contagious, and febrile viral disease that affects both domestic and wild small ruminants. The disease has become a major obstacle to the development of sustainable Agriculture. Hemagglutinin (H), the envelope glycoprotein of Peste des Petits Rumi...

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Autores principales: Liang, Zhongxiang, Yuan, Ruyi, Chen, Lei, Zhu, Xueliang, Dou, Yongxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818033/
https://www.ncbi.nlm.nih.gov/pubmed/27035347
http://dx.doi.org/10.1371/journal.pone.0152587
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author Liang, Zhongxiang
Yuan, Ruyi
Chen, Lei
Zhu, Xueliang
Dou, Yongxi
author_facet Liang, Zhongxiang
Yuan, Ruyi
Chen, Lei
Zhu, Xueliang
Dou, Yongxi
author_sort Liang, Zhongxiang
collection PubMed
description Peste des Petits Ruminants (PPR) is an acute, highly contagious, and febrile viral disease that affects both domestic and wild small ruminants. The disease has become a major obstacle to the development of sustainable Agriculture. Hemagglutinin (H), the envelope glycoprotein of Peste des Petits Ruminants Virus (PPRV), plays a crucial role in regulating viral adsorption and entry, thus determining pathogenicity, and release of newly produced viral particles. In order to accurately understand the epidemic of the disease and the interactions between the virus and host, we launch the work. Here, we examined H gene from all four lineages of the PPRV to investigate evolutionary and epidemiologic dynamics of PPRV by the Bayesian method. In addition, we predicted positive selection sites due to selective pressures. Finally, we studied the interaction between H protein and SLAM receptor based on homology model of the complex. Phylogenetic analysis suggested that H gene can also be used to investigate evolutionary and epidemiologic dynamics of PPRV. Positive selection analysis identified four positive selection sites in H gene, in which only one common site (aa246) was detected by two methods, suggesting strong operation structural and/or functional constraint of changes on the H protein. This target site may be of interest for future mutagenesis studies. The results of homology modeling showed PPRVHv-shSLAM binding interface and MVH-maSLAM binding interface were consistent, wherein the groove in the B4 blade and B5 of the head domain of PPRVHv bound to the AGFCC′ β-sheets of the membrane-distal ectodomain of shSLAM. The binding regions could provide insight on the nature of the protein for epitope vaccine design, novel drug discovery, and rational drug design against PPRV.
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spelling pubmed-48180332016-04-19 Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus Liang, Zhongxiang Yuan, Ruyi Chen, Lei Zhu, Xueliang Dou, Yongxi PLoS One Research Article Peste des Petits Ruminants (PPR) is an acute, highly contagious, and febrile viral disease that affects both domestic and wild small ruminants. The disease has become a major obstacle to the development of sustainable Agriculture. Hemagglutinin (H), the envelope glycoprotein of Peste des Petits Ruminants Virus (PPRV), plays a crucial role in regulating viral adsorption and entry, thus determining pathogenicity, and release of newly produced viral particles. In order to accurately understand the epidemic of the disease and the interactions between the virus and host, we launch the work. Here, we examined H gene from all four lineages of the PPRV to investigate evolutionary and epidemiologic dynamics of PPRV by the Bayesian method. In addition, we predicted positive selection sites due to selective pressures. Finally, we studied the interaction between H protein and SLAM receptor based on homology model of the complex. Phylogenetic analysis suggested that H gene can also be used to investigate evolutionary and epidemiologic dynamics of PPRV. Positive selection analysis identified four positive selection sites in H gene, in which only one common site (aa246) was detected by two methods, suggesting strong operation structural and/or functional constraint of changes on the H protein. This target site may be of interest for future mutagenesis studies. The results of homology modeling showed PPRVHv-shSLAM binding interface and MVH-maSLAM binding interface were consistent, wherein the groove in the B4 blade and B5 of the head domain of PPRVHv bound to the AGFCC′ β-sheets of the membrane-distal ectodomain of shSLAM. The binding regions could provide insight on the nature of the protein for epitope vaccine design, novel drug discovery, and rational drug design against PPRV. Public Library of Science 2016-04-01 /pmc/articles/PMC4818033/ /pubmed/27035347 http://dx.doi.org/10.1371/journal.pone.0152587 Text en © 2016 Liang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liang, Zhongxiang
Yuan, Ruyi
Chen, Lei
Zhu, Xueliang
Dou, Yongxi
Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title_full Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title_fullStr Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title_full_unstemmed Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title_short Molecular Evolution and Characterization of Hemagglutinin (H) in Peste des Petits Ruminants Virus
title_sort molecular evolution and characterization of hemagglutinin (h) in peste des petits ruminants virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4818033/
https://www.ncbi.nlm.nih.gov/pubmed/27035347
http://dx.doi.org/10.1371/journal.pone.0152587
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