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Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012

BACKGROUND: Human Coronaviruses (HCoV) are a common cause of respiratory illnesses and are responsible for considerable morbidity and hospitalization across all age groups especially in individuals with compromised immunity. There are six known species of HCoV: HCoV-229E, HCoV-NL63, HCoV-HKU1, HCoV-...

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Autores principales: Sipulwa, Lenata A., Ongus, Juliette R., Coldren, Rodney L., Bulimo, Wallace D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736488/
https://www.ncbi.nlm.nih.gov/pubmed/26833249
http://dx.doi.org/10.1186/s12985-016-0474-x
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author Sipulwa, Lenata A.
Ongus, Juliette R.
Coldren, Rodney L.
Bulimo, Wallace D.
author_facet Sipulwa, Lenata A.
Ongus, Juliette R.
Coldren, Rodney L.
Bulimo, Wallace D.
author_sort Sipulwa, Lenata A.
collection PubMed
description BACKGROUND: Human Coronaviruses (HCoV) are a common cause of respiratory illnesses and are responsible for considerable morbidity and hospitalization across all age groups especially in individuals with compromised immunity. There are six known species of HCoV: HCoV-229E, HCoV-NL63, HCoV-HKU1, HCoV-OC43, MERS-CoV and SARS-HCoV. Although studies have shown evidence of global distribution of HCoVs, there is limited information on their presence and distribution in Kenya. METHODS: HCoV strains that circulated in Kenya were retrospectively diagnosed and molecularly characterized. A total of 417 nasopharyngeal specimens obtained between January 2009 and December 2012 from around Kenya were analyzed by a real time RT-PCR using HCoV-specific primers. HCoV-positive specimens were subsequently inoculated onto monolayers of LL-CMK2 cells. The isolated viruses were characterized by RT-PCR amplification and sequencing of the partial polymerase (pol) gene. RESULTS: The prevalence of HCoV infection was as follows: out of the 417 specimens, 35 (8.4 %) were positive for HCoV, comprising 10 (2.4 %) HCoV-NL63, 12 (2.9 %) HCoV-OC43, 9 (2.1 %) HCoV-HKU1, and 4 (1 %) HCoV-229E. The Kenyan HCoV strains displayed high sequence homology to the prototypes and contemporaneous strains. Evolution analysis showed that the Kenyan HCoV-OC43 and HCoV-NL63 isolates were under purifying selection. Phylogenetic evolutionary analyses confirmed the identities of three HCoV-HKU1, five HCoV-NL63, eight HCoV-OC43 and three HCoV-229E. CONCLUSIONS: There were yearly variations in the prevalence and circulation patterns of individual HCoVs in Kenya. This paper reports on the first molecular characterization of human Coronaviruses in Kenya, which play an important role in causing acute respiratory infections among children.
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spelling pubmed-47364882016-02-03 Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012 Sipulwa, Lenata A. Ongus, Juliette R. Coldren, Rodney L. Bulimo, Wallace D. Virol J Research BACKGROUND: Human Coronaviruses (HCoV) are a common cause of respiratory illnesses and are responsible for considerable morbidity and hospitalization across all age groups especially in individuals with compromised immunity. There are six known species of HCoV: HCoV-229E, HCoV-NL63, HCoV-HKU1, HCoV-OC43, MERS-CoV and SARS-HCoV. Although studies have shown evidence of global distribution of HCoVs, there is limited information on their presence and distribution in Kenya. METHODS: HCoV strains that circulated in Kenya were retrospectively diagnosed and molecularly characterized. A total of 417 nasopharyngeal specimens obtained between January 2009 and December 2012 from around Kenya were analyzed by a real time RT-PCR using HCoV-specific primers. HCoV-positive specimens were subsequently inoculated onto monolayers of LL-CMK2 cells. The isolated viruses were characterized by RT-PCR amplification and sequencing of the partial polymerase (pol) gene. RESULTS: The prevalence of HCoV infection was as follows: out of the 417 specimens, 35 (8.4 %) were positive for HCoV, comprising 10 (2.4 %) HCoV-NL63, 12 (2.9 %) HCoV-OC43, 9 (2.1 %) HCoV-HKU1, and 4 (1 %) HCoV-229E. The Kenyan HCoV strains displayed high sequence homology to the prototypes and contemporaneous strains. Evolution analysis showed that the Kenyan HCoV-OC43 and HCoV-NL63 isolates were under purifying selection. Phylogenetic evolutionary analyses confirmed the identities of three HCoV-HKU1, five HCoV-NL63, eight HCoV-OC43 and three HCoV-229E. CONCLUSIONS: There were yearly variations in the prevalence and circulation patterns of individual HCoVs in Kenya. This paper reports on the first molecular characterization of human Coronaviruses in Kenya, which play an important role in causing acute respiratory infections among children. BioMed Central 2016-02-01 /pmc/articles/PMC4736488/ /pubmed/26833249 http://dx.doi.org/10.1186/s12985-016-0474-x Text en © Sipulwa et al. 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
Sipulwa, Lenata A.
Ongus, Juliette R.
Coldren, Rodney L.
Bulimo, Wallace D.
Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title_full Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title_fullStr Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title_full_unstemmed Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title_short Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012
title_sort molecular characterization of human coronaviruses and their circulation dynamics in kenya, 2009–2012
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736488/
https://www.ncbi.nlm.nih.gov/pubmed/26833249
http://dx.doi.org/10.1186/s12985-016-0474-x
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