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Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses

The Chandipura virus (CHPV) belonging to the Vesiculovirus genus and Rhabdoviridae family, has recently been associated with a number of encephalitis epidemics, with high mortality in children, in different parts of India. No full length genome sequences of CHPV isolates were available in GenBank an...

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Autores principales: Cherian, Sarah S., Gunjikar, Rashmi S., Banerjee, Arpita, Kumar, Satyendra, Arankalle, Vidya A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260278/
https://www.ncbi.nlm.nih.gov/pubmed/22272333
http://dx.doi.org/10.1371/journal.pone.0030315
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author Cherian, Sarah S.
Gunjikar, Rashmi S.
Banerjee, Arpita
Kumar, Satyendra
Arankalle, Vidya A.
author_facet Cherian, Sarah S.
Gunjikar, Rashmi S.
Banerjee, Arpita
Kumar, Satyendra
Arankalle, Vidya A.
author_sort Cherian, Sarah S.
collection PubMed
description The Chandipura virus (CHPV) belonging to the Vesiculovirus genus and Rhabdoviridae family, has recently been associated with a number of encephalitis epidemics, with high mortality in children, in different parts of India. No full length genome sequences of CHPV isolates were available in GenBank and little is known about the molecular markers for pathogenesis. In the present study, we provide the complete genomic sequences of four isolates from epidemics during 2003–2007. These sequences along with the deduced sequence of the prototype isolate of 1965 were analysed using phylogeny, motif search, homology modeling and epitope prediction methods. Comparison with other rhaboviruses was also done for functional extrapolations. All CHPV isolates clustered with the Isfahan virus and maintained several functional motifs of other rhabdoviruses. A notable difference with the prototype vesiculovirus, Vesicular Stomatitis Virus was in the L-domain flanking sequences of the M protein that are known to be crucial for interaction with host proteins. With respect to the prototype isolate, significant additional mutations were acquired in the 2003–2007 isolates. Several mutations in G mapped onto probable antigenic sites. A mutation in N mapped onto regions crucial for N-N interaction and a putative T-cell epitope. A mutation in the Casein kinase II phosphorylation site in P may attribute to increased rates of phosphorylation. Gene junction comparison revealed changes in the M-G junction of all the epidemic isolates that may have implications on read-through and gene transcription levels. The study can form the basis for further experimental verification and provide additional insights into the virulence determinants of the CHPV.
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spelling pubmed-32602782012-01-23 Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses Cherian, Sarah S. Gunjikar, Rashmi S. Banerjee, Arpita Kumar, Satyendra Arankalle, Vidya A. PLoS One Research Article The Chandipura virus (CHPV) belonging to the Vesiculovirus genus and Rhabdoviridae family, has recently been associated with a number of encephalitis epidemics, with high mortality in children, in different parts of India. No full length genome sequences of CHPV isolates were available in GenBank and little is known about the molecular markers for pathogenesis. In the present study, we provide the complete genomic sequences of four isolates from epidemics during 2003–2007. These sequences along with the deduced sequence of the prototype isolate of 1965 were analysed using phylogeny, motif search, homology modeling and epitope prediction methods. Comparison with other rhaboviruses was also done for functional extrapolations. All CHPV isolates clustered with the Isfahan virus and maintained several functional motifs of other rhabdoviruses. A notable difference with the prototype vesiculovirus, Vesicular Stomatitis Virus was in the L-domain flanking sequences of the M protein that are known to be crucial for interaction with host proteins. With respect to the prototype isolate, significant additional mutations were acquired in the 2003–2007 isolates. Several mutations in G mapped onto probable antigenic sites. A mutation in N mapped onto regions crucial for N-N interaction and a putative T-cell epitope. A mutation in the Casein kinase II phosphorylation site in P may attribute to increased rates of phosphorylation. Gene junction comparison revealed changes in the M-G junction of all the epidemic isolates that may have implications on read-through and gene transcription levels. The study can form the basis for further experimental verification and provide additional insights into the virulence determinants of the CHPV. Public Library of Science 2012-01-17 /pmc/articles/PMC3260278/ /pubmed/22272333 http://dx.doi.org/10.1371/journal.pone.0030315 Text en Cherian 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cherian, Sarah S.
Gunjikar, Rashmi S.
Banerjee, Arpita
Kumar, Satyendra
Arankalle, Vidya A.
Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title_full Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title_fullStr Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title_full_unstemmed Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title_short Whole Genomes of Chandipura Virus Isolates and Comparative Analysis with Other Rhabdoviruses
title_sort whole genomes of chandipura virus isolates and comparative analysis with other rhabdoviruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260278/
https://www.ncbi.nlm.nih.gov/pubmed/22272333
http://dx.doi.org/10.1371/journal.pone.0030315
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