Cargando…

Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11

BACKGROUND: Human metapneumovirus (HMPV) is an important global cause of severe acute respiratory infections in young children and the elderly. The epidemiology of HMPV in sub-Saharan Africa is poorly described and factors that allow its recurrent epidemics in communities not understood. METHODS: We...

Descripción completa

Detalles Bibliográficos
Autores principales: Owor, Betty E., Masankwa, Geoffrey N., Mwango, Lilian C., Njeru, Regina W., Agoti, Charles N., Nokes, D. James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912817/
https://www.ncbi.nlm.nih.gov/pubmed/27316548
http://dx.doi.org/10.1186/s12879-016-1605-0
_version_ 1782438333318692864
author Owor, Betty E.
Masankwa, Geoffrey N.
Mwango, Lilian C.
Njeru, Regina W.
Agoti, Charles N.
Nokes, D. James
author_facet Owor, Betty E.
Masankwa, Geoffrey N.
Mwango, Lilian C.
Njeru, Regina W.
Agoti, Charles N.
Nokes, D. James
author_sort Owor, Betty E.
collection PubMed
description BACKGROUND: Human metapneumovirus (HMPV) is an important global cause of severe acute respiratory infections in young children and the elderly. The epidemiology of HMPV in sub-Saharan Africa is poorly described and factors that allow its recurrent epidemics in communities not understood. METHODS: We undertook paediatric inpatient surveillance for HMPV in Kilifi County Hospital (KCH) of Coastal Kenya between 2007 and 2011. Nasopharyngeal samples collected from children aged 1 day–59 months admitted with severe or very severe pneumonia, were tested for HMPV using real-time polymerase chain reaction (RT-PCR). Partial nucleotide sequences of the attachment (G) and fusion (F) surface proteins of positive samples were determined and phylogenetically analyzed. RESULTS: HMPV was detected in 4.8 % (160/3320) of children [73.8 % (118/160) of these less than one year of age], ranging between 2.9 and 8.8 % each year over the 5 years of study. HMPV infections were seasonal in occurrence, with cases predominant in the months of November through April. These months frequently coincided with low rainfall, high temperature and low relative humidity in the location. Phylogenetic analysis of partial F and G sequences revealed three subgroups of HMPV, A2 (74 %, 91/123), B1 (3.2 %, 4/123) and B2 (22.8 %, 28/123) in circulation, with subgroup A2 predominant in majority of the epidemic seasons. Comparison of G sequences (local and global) provided a greater phylogenetic resolution over comparison of F sequences and indicated presence of probable multiple G antigenic variants within the subgroups due to differences in amino acid sequence, encoded protein length and glycosylation patterns. CONCLUSION: The present study reveals HMPV is an important seasonal contributor to respiratory disease hospitalization in coastal Kenya, with an evolutionary pattern closely relating to that of respiratory syncytial virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-016-1605-0) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4912817
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-49128172016-06-20 Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11 Owor, Betty E. Masankwa, Geoffrey N. Mwango, Lilian C. Njeru, Regina W. Agoti, Charles N. Nokes, D. James BMC Infect Dis Research Article BACKGROUND: Human metapneumovirus (HMPV) is an important global cause of severe acute respiratory infections in young children and the elderly. The epidemiology of HMPV in sub-Saharan Africa is poorly described and factors that allow its recurrent epidemics in communities not understood. METHODS: We undertook paediatric inpatient surveillance for HMPV in Kilifi County Hospital (KCH) of Coastal Kenya between 2007 and 2011. Nasopharyngeal samples collected from children aged 1 day–59 months admitted with severe or very severe pneumonia, were tested for HMPV using real-time polymerase chain reaction (RT-PCR). Partial nucleotide sequences of the attachment (G) and fusion (F) surface proteins of positive samples were determined and phylogenetically analyzed. RESULTS: HMPV was detected in 4.8 % (160/3320) of children [73.8 % (118/160) of these less than one year of age], ranging between 2.9 and 8.8 % each year over the 5 years of study. HMPV infections were seasonal in occurrence, with cases predominant in the months of November through April. These months frequently coincided with low rainfall, high temperature and low relative humidity in the location. Phylogenetic analysis of partial F and G sequences revealed three subgroups of HMPV, A2 (74 %, 91/123), B1 (3.2 %, 4/123) and B2 (22.8 %, 28/123) in circulation, with subgroup A2 predominant in majority of the epidemic seasons. Comparison of G sequences (local and global) provided a greater phylogenetic resolution over comparison of F sequences and indicated presence of probable multiple G antigenic variants within the subgroups due to differences in amino acid sequence, encoded protein length and glycosylation patterns. CONCLUSION: The present study reveals HMPV is an important seasonal contributor to respiratory disease hospitalization in coastal Kenya, with an evolutionary pattern closely relating to that of respiratory syncytial virus. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-016-1605-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-17 /pmc/articles/PMC4912817/ /pubmed/27316548 http://dx.doi.org/10.1186/s12879-016-1605-0 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Owor, Betty E.
Masankwa, Geoffrey N.
Mwango, Lilian C.
Njeru, Regina W.
Agoti, Charles N.
Nokes, D. James
Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title_full Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title_fullStr Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title_full_unstemmed Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title_short Human metapneumovirus epidemiological and evolutionary patterns in Coastal Kenya, 2007-11
title_sort human metapneumovirus epidemiological and evolutionary patterns in coastal kenya, 2007-11
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4912817/
https://www.ncbi.nlm.nih.gov/pubmed/27316548
http://dx.doi.org/10.1186/s12879-016-1605-0
work_keys_str_mv AT oworbettye humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711
AT masankwageoffreyn humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711
AT mwangolilianc humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711
AT njerureginaw humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711
AT agoticharlesn humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711
AT nokesdjames humanmetapneumovirusepidemiologicalandevolutionarypatternsincoastalkenya200711