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Human Metapneumovirus Genetic Variability, South Africa

The molecular epidemiology and genetic diversity of the human metapneumovirus (hMPV) were characterized for a 3-year period (2000–2002) from viruses that were identified in South Africa. Two major genetic groups (A and B) and 2 subgroups (1 and 2) of hMPV were identified, as well as 2–6 possible gen...

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Autores principales: Ludewick, Herbert P., Abed, Yacine, van Niekerk, Nadia, Boivin, Guy, Klugman, Keith P., Madhi, Shabir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371776/
https://www.ncbi.nlm.nih.gov/pubmed/16022783
http://dx.doi.org/10.3201/eid1107.050500
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author Ludewick, Herbert P.
Abed, Yacine
van Niekerk, Nadia
Boivin, Guy
Klugman, Keith P.
Madhi, Shabir A.
author_facet Ludewick, Herbert P.
Abed, Yacine
van Niekerk, Nadia
Boivin, Guy
Klugman, Keith P.
Madhi, Shabir A.
author_sort Ludewick, Herbert P.
collection PubMed
description The molecular epidemiology and genetic diversity of the human metapneumovirus (hMPV) were characterized for a 3-year period (2000–2002) from viruses that were identified in South Africa. Two major genetic groups (A and B) and 2 subgroups (1 and 2) of hMPV were identified, as well as 2–6 possible genotypes within the subgroups. A shift in the predominant group was documented in successive seasons. Whereas the F gene was relatively conserved between subgroups, a high degree of variation was observed in the extracellular domain of the G gene of the virus. The G protein identities between groups A and B were 45.1%–53.1% at the nucleotide level and 22.4%–27.6% at the amino acid level. These results provide evidence for the diversity of both surface glycoproteins of hMPV in Africa, which may be a prerequisite to understanding protective immunity against hMPV.
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spelling pubmed-33717762012-06-19 Human Metapneumovirus Genetic Variability, South Africa Ludewick, Herbert P. Abed, Yacine van Niekerk, Nadia Boivin, Guy Klugman, Keith P. Madhi, Shabir A. Emerg Infect Dis Research The molecular epidemiology and genetic diversity of the human metapneumovirus (hMPV) were characterized for a 3-year period (2000–2002) from viruses that were identified in South Africa. Two major genetic groups (A and B) and 2 subgroups (1 and 2) of hMPV were identified, as well as 2–6 possible genotypes within the subgroups. A shift in the predominant group was documented in successive seasons. Whereas the F gene was relatively conserved between subgroups, a high degree of variation was observed in the extracellular domain of the G gene of the virus. The G protein identities between groups A and B were 45.1%–53.1% at the nucleotide level and 22.4%–27.6% at the amino acid level. These results provide evidence for the diversity of both surface glycoproteins of hMPV in Africa, which may be a prerequisite to understanding protective immunity against hMPV. Centers for Disease Control and Prevention 2005-07 /pmc/articles/PMC3371776/ /pubmed/16022783 http://dx.doi.org/10.3201/eid1107.050500 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
Ludewick, Herbert P.
Abed, Yacine
van Niekerk, Nadia
Boivin, Guy
Klugman, Keith P.
Madhi, Shabir A.
Human Metapneumovirus Genetic Variability, South Africa
title Human Metapneumovirus Genetic Variability, South Africa
title_full Human Metapneumovirus Genetic Variability, South Africa
title_fullStr Human Metapneumovirus Genetic Variability, South Africa
title_full_unstemmed Human Metapneumovirus Genetic Variability, South Africa
title_short Human Metapneumovirus Genetic Variability, South Africa
title_sort human metapneumovirus genetic variability, south africa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371776/
https://www.ncbi.nlm.nih.gov/pubmed/16022783
http://dx.doi.org/10.3201/eid1107.050500
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