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Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate)
Nipah virus (NiV) is a high-risk pathogen which can cause fatal infections in humans. The Indian isolate from the 2018 outbreak in the Kerala state of India showed ~ 4% nucleotide and amino acid difference in comparison to the Bangladesh strains of NiV and the substitutions observed were mostly not...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281463/ https://www.ncbi.nlm.nih.gov/pubmed/37312405 http://dx.doi.org/10.1080/21505594.2023.2224642 |
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author | Mohandas, Sreelekshmy Shete, Anita Sarkale, Prasad Kumar, Abhinendra Mote, Chandrasekhar Yadav, Pragya |
author_facet | Mohandas, Sreelekshmy Shete, Anita Sarkale, Prasad Kumar, Abhinendra Mote, Chandrasekhar Yadav, Pragya |
author_sort | Mohandas, Sreelekshmy |
collection | PubMed |
description | Nipah virus (NiV) is a high-risk pathogen which can cause fatal infections in humans. The Indian isolate from the 2018 outbreak in the Kerala state of India showed ~ 4% nucleotide and amino acid difference in comparison to the Bangladesh strains of NiV and the substitutions observed were mostly not present in the region of any functional significance except for the phosphoprotein gene. The differential expression of viral genes was observed following infection in Vero (ATCC® CCL−81™) and BHK−21 cells. Intraperitoneal infection in the 10–12-week-old, Syrian hamster model induced dose dependant multisystemic disease characterized by prominent vascular lesions in lungs, brain, kidney and extra vascular lesions in brain and lungs. Congestion, haemorrhages, inflammatory cell infiltration, thrombosis and rarely endothelial syncitial cell formation were seen in the blood vessels. Intranasal infection resulted in respiratory tract infection characterised by pneumonia. The model showed disease characteristics resembling the human NiV infection except that of myocarditis similar to that reported by NiV-Malaysia and NiV-Bangladesh isolates in hamster model. The variation observed in the genome of the Indian isolate at the amino acid levels should be explored further for any functional significance. |
format | Online Article Text |
id | pubmed-10281463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-102814632023-06-21 Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) Mohandas, Sreelekshmy Shete, Anita Sarkale, Prasad Kumar, Abhinendra Mote, Chandrasekhar Yadav, Pragya Virulence Research Paper Nipah virus (NiV) is a high-risk pathogen which can cause fatal infections in humans. The Indian isolate from the 2018 outbreak in the Kerala state of India showed ~ 4% nucleotide and amino acid difference in comparison to the Bangladesh strains of NiV and the substitutions observed were mostly not present in the region of any functional significance except for the phosphoprotein gene. The differential expression of viral genes was observed following infection in Vero (ATCC® CCL−81™) and BHK−21 cells. Intraperitoneal infection in the 10–12-week-old, Syrian hamster model induced dose dependant multisystemic disease characterized by prominent vascular lesions in lungs, brain, kidney and extra vascular lesions in brain and lungs. Congestion, haemorrhages, inflammatory cell infiltration, thrombosis and rarely endothelial syncitial cell formation were seen in the blood vessels. Intranasal infection resulted in respiratory tract infection characterised by pneumonia. The model showed disease characteristics resembling the human NiV infection except that of myocarditis similar to that reported by NiV-Malaysia and NiV-Bangladesh isolates in hamster model. The variation observed in the genome of the Indian isolate at the amino acid levels should be explored further for any functional significance. Taylor & Francis 2023-06-16 /pmc/articles/PMC10281463/ /pubmed/37312405 http://dx.doi.org/10.1080/21505594.2023.2224642 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Paper Mohandas, Sreelekshmy Shete, Anita Sarkale, Prasad Kumar, Abhinendra Mote, Chandrasekhar Yadav, Pragya Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title | Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title_full | Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title_fullStr | Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title_full_unstemmed | Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title_short | Genomic characterization, transcriptome analysis, and pathogenicity of the Nipah virus (Indian isolate) |
title_sort | genomic characterization, transcriptome analysis, and pathogenicity of the nipah virus (indian isolate) |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281463/ https://www.ncbi.nlm.nih.gov/pubmed/37312405 http://dx.doi.org/10.1080/21505594.2023.2224642 |
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