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Cedar Virus: A Novel Henipavirus Isolated from Australian Bats

The genus Henipavirus in the family Paramyxoviridae contains two viruses, Hendra virus (HeV) and Nipah virus (NiV) for which pteropid bats act as the main natural reservoir. Each virus also causes serious and commonly lethal infection of people as well as various species of domestic animals, however...

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Autores principales: Marsh, Glenn A., de Jong, Carol, Barr, Jennifer A., Tachedjian, Mary, Smith, Craig, Middleton, Deborah, Yu, Meng, Todd, Shawn, Foord, Adam J., Haring, Volker, Payne, Jean, Robinson, Rachel, Broz, Ivano, Crameri, Gary, Field, Hume E., Wang, Lin-Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410871/
https://www.ncbi.nlm.nih.gov/pubmed/22879820
http://dx.doi.org/10.1371/journal.ppat.1002836
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author Marsh, Glenn A.
de Jong, Carol
Barr, Jennifer A.
Tachedjian, Mary
Smith, Craig
Middleton, Deborah
Yu, Meng
Todd, Shawn
Foord, Adam J.
Haring, Volker
Payne, Jean
Robinson, Rachel
Broz, Ivano
Crameri, Gary
Field, Hume E.
Wang, Lin-Fa
author_facet Marsh, Glenn A.
de Jong, Carol
Barr, Jennifer A.
Tachedjian, Mary
Smith, Craig
Middleton, Deborah
Yu, Meng
Todd, Shawn
Foord, Adam J.
Haring, Volker
Payne, Jean
Robinson, Rachel
Broz, Ivano
Crameri, Gary
Field, Hume E.
Wang, Lin-Fa
author_sort Marsh, Glenn A.
collection PubMed
description The genus Henipavirus in the family Paramyxoviridae contains two viruses, Hendra virus (HeV) and Nipah virus (NiV) for which pteropid bats act as the main natural reservoir. Each virus also causes serious and commonly lethal infection of people as well as various species of domestic animals, however little is known about the associated mechanisms of pathogenesis. Here, we report the isolation and characterization of a new paramyxovirus from pteropid bats, Cedar virus (CedPV), which shares significant features with the known henipaviruses. The genome size (18,162 nt) and organization of CedPV is very similar to that of HeV and NiV; its nucleocapsid protein displays antigenic cross-reactivity with henipaviruses; and it uses the same receptor molecule (ephrin- B2) for entry during infection. Preliminary challenge studies with CedPV in ferrets and guinea pigs, both susceptible to infection and disease with known henipaviruses, confirmed virus replication and production of neutralizing antibodies although clinical disease was not observed. In this context, it is interesting to note that the major genetic difference between CedPV and HeV or NiV lies within the coding strategy of the P gene, which is known to play an important role in evading the host innate immune system. Unlike HeV, NiV, and almost all known paramyxoviruses, the CedPV P gene lacks both RNA editing and also the coding capacity for the highly conserved V protein. Preliminary study indicated that CedPV infection of human cells induces a more robust IFN-β response than HeV.
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spelling pubmed-34108712012-08-09 Cedar Virus: A Novel Henipavirus Isolated from Australian Bats Marsh, Glenn A. de Jong, Carol Barr, Jennifer A. Tachedjian, Mary Smith, Craig Middleton, Deborah Yu, Meng Todd, Shawn Foord, Adam J. Haring, Volker Payne, Jean Robinson, Rachel Broz, Ivano Crameri, Gary Field, Hume E. Wang, Lin-Fa PLoS Pathog Research Article The genus Henipavirus in the family Paramyxoviridae contains two viruses, Hendra virus (HeV) and Nipah virus (NiV) for which pteropid bats act as the main natural reservoir. Each virus also causes serious and commonly lethal infection of people as well as various species of domestic animals, however little is known about the associated mechanisms of pathogenesis. Here, we report the isolation and characterization of a new paramyxovirus from pteropid bats, Cedar virus (CedPV), which shares significant features with the known henipaviruses. The genome size (18,162 nt) and organization of CedPV is very similar to that of HeV and NiV; its nucleocapsid protein displays antigenic cross-reactivity with henipaviruses; and it uses the same receptor molecule (ephrin- B2) for entry during infection. Preliminary challenge studies with CedPV in ferrets and guinea pigs, both susceptible to infection and disease with known henipaviruses, confirmed virus replication and production of neutralizing antibodies although clinical disease was not observed. In this context, it is interesting to note that the major genetic difference between CedPV and HeV or NiV lies within the coding strategy of the P gene, which is known to play an important role in evading the host innate immune system. Unlike HeV, NiV, and almost all known paramyxoviruses, the CedPV P gene lacks both RNA editing and also the coding capacity for the highly conserved V protein. Preliminary study indicated that CedPV infection of human cells induces a more robust IFN-β response than HeV. Public Library of Science 2012-08-02 /pmc/articles/PMC3410871/ /pubmed/22879820 http://dx.doi.org/10.1371/journal.ppat.1002836 Text en © 2012 Marsh 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
Marsh, Glenn A.
de Jong, Carol
Barr, Jennifer A.
Tachedjian, Mary
Smith, Craig
Middleton, Deborah
Yu, Meng
Todd, Shawn
Foord, Adam J.
Haring, Volker
Payne, Jean
Robinson, Rachel
Broz, Ivano
Crameri, Gary
Field, Hume E.
Wang, Lin-Fa
Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title_full Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title_fullStr Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title_full_unstemmed Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title_short Cedar Virus: A Novel Henipavirus Isolated from Australian Bats
title_sort cedar virus: a novel henipavirus isolated from australian bats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410871/
https://www.ncbi.nlm.nih.gov/pubmed/22879820
http://dx.doi.org/10.1371/journal.ppat.1002836
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