Cargando…
Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013
Background: Kenya introduced the monovalent Rotarix® rotavirus group A (RVA) vaccine nationally in mid-2014. Long-term surveillance data is important prior to wide-scale vaccine use to assess the impact on disease and to investigate the occurrence of heterotypic strains arising through immune selec...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6464063/ https://www.ncbi.nlm.nih.gov/pubmed/31020048 http://dx.doi.org/10.12688/wellcomeopenres.14908.2 |
_version_ | 1783410827597971456 |
---|---|
author | Owor, Betty E. Mwanga, Mike J. Njeru, Regina Mugo, Robert Ngama, Mwanajuma Otieno, Grieven P. Nokes, D.J. Agoti, C.N. |
author_facet | Owor, Betty E. Mwanga, Mike J. Njeru, Regina Mugo, Robert Ngama, Mwanajuma Otieno, Grieven P. Nokes, D.J. Agoti, C.N. |
author_sort | Owor, Betty E. |
collection | PubMed |
description | Background: Kenya introduced the monovalent Rotarix® rotavirus group A (RVA) vaccine nationally in mid-2014. Long-term surveillance data is important prior to wide-scale vaccine use to assess the impact on disease and to investigate the occurrence of heterotypic strains arising through immune selection. This report presents baseline data on RVA genotype circulation patterns and intra-genotype genetic diversity over a 7-year period in the pre-vaccine era in Kilifi, Kenya, from 2002 to 2004 and from 2010 to 2013. Methods: A total of 745 RVA strains identified in children admitted with acute gastroenteritis to a referral hospital in Coastal Kenya, were sequenced using the di-deoxy sequencing method in the VP4 and VP7 genomic segments (encoding P and G proteins, respectively). Sequencing successfully generated 569 (76%) and 572 (77%) consensus sequences for the VP4 and VP7 genes respectively. G and P genotypes were determined by use of BLAST and the online RotaC v2 RVA classification tool. Results: The most common GP combination was G1P[8] (51%), similar to the Rotarix® strain, followed by G9P[8] (15%) , G8P[4] (14%) and G2P[4] (5%). Unusual GP combinations—G1P[4], G2P[8], G3P[4,6], G8P[8,14], and G12P[4,6,8]—were observed at frequencies of <5%. Phylogenetic analysis showed that the infections were caused by both locally persistent strains as evidenced by divergence of local strains occurring over multiple seasons from the global ones, and newly introduced strains, which were closely related to global strains. The circulating RVA diversity showed temporal fluctuations both season by season and over the longer-term. None of the unusual strains increased in frequency over the observation period. Conclusions: The circulating RVA diversity showed temporal fluctuations with several unusual strains recorded, which rarely caused major outbreaks. These data will be useful in interpreting genotype patterns observed in the region during the vaccine era. |
format | Online Article Text |
id | pubmed-6464063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-64640632019-04-23 Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 Owor, Betty E. Mwanga, Mike J. Njeru, Regina Mugo, Robert Ngama, Mwanajuma Otieno, Grieven P. Nokes, D.J. Agoti, C.N. Wellcome Open Res Research Article Background: Kenya introduced the monovalent Rotarix® rotavirus group A (RVA) vaccine nationally in mid-2014. Long-term surveillance data is important prior to wide-scale vaccine use to assess the impact on disease and to investigate the occurrence of heterotypic strains arising through immune selection. This report presents baseline data on RVA genotype circulation patterns and intra-genotype genetic diversity over a 7-year period in the pre-vaccine era in Kilifi, Kenya, from 2002 to 2004 and from 2010 to 2013. Methods: A total of 745 RVA strains identified in children admitted with acute gastroenteritis to a referral hospital in Coastal Kenya, were sequenced using the di-deoxy sequencing method in the VP4 and VP7 genomic segments (encoding P and G proteins, respectively). Sequencing successfully generated 569 (76%) and 572 (77%) consensus sequences for the VP4 and VP7 genes respectively. G and P genotypes were determined by use of BLAST and the online RotaC v2 RVA classification tool. Results: The most common GP combination was G1P[8] (51%), similar to the Rotarix® strain, followed by G9P[8] (15%) , G8P[4] (14%) and G2P[4] (5%). Unusual GP combinations—G1P[4], G2P[8], G3P[4,6], G8P[8,14], and G12P[4,6,8]—were observed at frequencies of <5%. Phylogenetic analysis showed that the infections were caused by both locally persistent strains as evidenced by divergence of local strains occurring over multiple seasons from the global ones, and newly introduced strains, which were closely related to global strains. The circulating RVA diversity showed temporal fluctuations both season by season and over the longer-term. None of the unusual strains increased in frequency over the observation period. Conclusions: The circulating RVA diversity showed temporal fluctuations with several unusual strains recorded, which rarely caused major outbreaks. These data will be useful in interpreting genotype patterns observed in the region during the vaccine era. F1000 Research Limited 2019-05-15 /pmc/articles/PMC6464063/ /pubmed/31020048 http://dx.doi.org/10.12688/wellcomeopenres.14908.2 Text en Copyright: © 2019 Owor BE et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Owor, Betty E. Mwanga, Mike J. Njeru, Regina Mugo, Robert Ngama, Mwanajuma Otieno, Grieven P. Nokes, D.J. Agoti, C.N. Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title | Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title_full | Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title_fullStr | Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title_full_unstemmed | Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title_short | Molecular characterization of rotavirus group A strains circulating prior to vaccine introduction in rural coastal Kenya, 2002-2013 |
title_sort | molecular characterization of rotavirus group a strains circulating prior to vaccine introduction in rural coastal kenya, 2002-2013 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6464063/ https://www.ncbi.nlm.nih.gov/pubmed/31020048 http://dx.doi.org/10.12688/wellcomeopenres.14908.2 |
work_keys_str_mv | AT oworbettye molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT mwangamikej molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT njeruregina molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT mugorobert molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT ngamamwanajuma molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT otienogrievenp molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT nokesdj molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 AT agoticn molecularcharacterizationofrotavirusgroupastrainscirculatingpriortovaccineintroductioninruralcoastalkenya20022013 |