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Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019)
Mozambique introduced the monovalent rotavirus vaccine (Rotarix(®), GSK Biologicals, Rixensart, Belgium) in September 2015. Previous analysis, showed that Nampula province continues reporting a high frequency of Rotavirus A (RVA) infection and the emergence of G9P[6], G9P[4] and G3P[4] genotypes. Th...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8345880/ https://www.ncbi.nlm.nih.gov/pubmed/34358275 http://dx.doi.org/10.1371/journal.pone.0255720 |
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author | Chissaque, Assucênio Bauhofer, Adilson Fernando Loforte Cossa-Moiane, Idalécia Sitoe, Ezequias Munlela, Benilde João, Eva Dora Langa, Jerónimo S. Chilaúle, Jorfélia José Boene, Simone Salvador Cassocera, Marta Guimarães, Esperança Lourenço Kellogg, Timothy A. Gonçalves, Luzia de Deus, Nilsa |
author_facet | Chissaque, Assucênio Bauhofer, Adilson Fernando Loforte Cossa-Moiane, Idalécia Sitoe, Ezequias Munlela, Benilde João, Eva Dora Langa, Jerónimo S. Chilaúle, Jorfélia José Boene, Simone Salvador Cassocera, Marta Guimarães, Esperança Lourenço Kellogg, Timothy A. Gonçalves, Luzia de Deus, Nilsa |
author_sort | Chissaque, Assucênio |
collection | PubMed |
description | Mozambique introduced the monovalent rotavirus vaccine (Rotarix(®), GSK Biologicals, Rixensart, Belgium) in September 2015. Previous analysis, showed that Nampula province continues reporting a high frequency of Rotavirus A (RVA) infection and the emergence of G9P[6], G9P[4] and G3P[4] genotypes. This analysis aimed to determine the RVA frequency; risk factors; genotype distribution by vaccination status and age between pre- and post-vaccine periods in children under-five years old with diarrhea in Nampula. A cross-sectional, hospital-based surveillance study was conducted in the Hospital Central de Nampula in Mozambique. Socio-demographic and clinical data were collected to assess factors related to RVA infection in both periods. Stool specimens were screened to detect RVA by ELISA, and positive samples were genotyped. Between 2015 (pre-vaccine period) and 2016–2019 (post-vaccine period), 614 stool specimens were collected and tested for RVA in which 34.9% (67/192) were positive in pre-vaccine period and 21.8% (92/422) in post-vaccine (p = 0.001). In the post-vaccine period, age, year, and contact with different animal species (chicken, duck, or multiple animals) were associated with RVA infection. RVA infection was higher in children partially vaccinated (40.7%, 11/27) followed by the fully vaccinated (29.3%, 56/191) and the unvaccinated (15.3%, 21/137) (p = 0.002). G1P[8] and G9P[4] were common in vaccinated children less than 12 months. The present analysis showed that RVA infection reduced slightly in the post-vaccine period, with a high proportion of infection and genotype diversity in children, under 12 months of age, vaccinated. Further research on factors associated with RVA infection on vaccinated compared to unvaccinated children and vaccination optimization should be done. |
format | Online Article Text |
id | pubmed-8345880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83458802021-08-07 Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) Chissaque, Assucênio Bauhofer, Adilson Fernando Loforte Cossa-Moiane, Idalécia Sitoe, Ezequias Munlela, Benilde João, Eva Dora Langa, Jerónimo S. Chilaúle, Jorfélia José Boene, Simone Salvador Cassocera, Marta Guimarães, Esperança Lourenço Kellogg, Timothy A. Gonçalves, Luzia de Deus, Nilsa PLoS One Research Article Mozambique introduced the monovalent rotavirus vaccine (Rotarix(®), GSK Biologicals, Rixensart, Belgium) in September 2015. Previous analysis, showed that Nampula province continues reporting a high frequency of Rotavirus A (RVA) infection and the emergence of G9P[6], G9P[4] and G3P[4] genotypes. This analysis aimed to determine the RVA frequency; risk factors; genotype distribution by vaccination status and age between pre- and post-vaccine periods in children under-five years old with diarrhea in Nampula. A cross-sectional, hospital-based surveillance study was conducted in the Hospital Central de Nampula in Mozambique. Socio-demographic and clinical data were collected to assess factors related to RVA infection in both periods. Stool specimens were screened to detect RVA by ELISA, and positive samples were genotyped. Between 2015 (pre-vaccine period) and 2016–2019 (post-vaccine period), 614 stool specimens were collected and tested for RVA in which 34.9% (67/192) were positive in pre-vaccine period and 21.8% (92/422) in post-vaccine (p = 0.001). In the post-vaccine period, age, year, and contact with different animal species (chicken, duck, or multiple animals) were associated with RVA infection. RVA infection was higher in children partially vaccinated (40.7%, 11/27) followed by the fully vaccinated (29.3%, 56/191) and the unvaccinated (15.3%, 21/137) (p = 0.002). G1P[8] and G9P[4] were common in vaccinated children less than 12 months. The present analysis showed that RVA infection reduced slightly in the post-vaccine period, with a high proportion of infection and genotype diversity in children, under 12 months of age, vaccinated. Further research on factors associated with RVA infection on vaccinated compared to unvaccinated children and vaccination optimization should be done. Public Library of Science 2021-08-06 /pmc/articles/PMC8345880/ /pubmed/34358275 http://dx.doi.org/10.1371/journal.pone.0255720 Text en © 2021 Chissaque et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chissaque, Assucênio Bauhofer, Adilson Fernando Loforte Cossa-Moiane, Idalécia Sitoe, Ezequias Munlela, Benilde João, Eva Dora Langa, Jerónimo S. Chilaúle, Jorfélia José Boene, Simone Salvador Cassocera, Marta Guimarães, Esperança Lourenço Kellogg, Timothy A. Gonçalves, Luzia de Deus, Nilsa Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title | Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title_full | Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title_fullStr | Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title_full_unstemmed | Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title_short | Rotavirus A infection in pre- and post-vaccine period: Risk factors, genotypes distribution by vaccination status and age of children in Nampula Province, Northern Mozambique (2015-2019) |
title_sort | rotavirus a infection in pre- and post-vaccine period: risk factors, genotypes distribution by vaccination status and age of children in nampula province, northern mozambique (2015-2019) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8345880/ https://www.ncbi.nlm.nih.gov/pubmed/34358275 http://dx.doi.org/10.1371/journal.pone.0255720 |
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