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Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic

OBJECTIVE: Rotavirus A (RVA) remains the main causative agent of gastroenteritis in young children and the young of many mammalian and avian species. In this study we describe a RVA strain detected from a 6-month-old child from Central African Republic (CAR). RESULTS: We report the 11 open reading f...

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Autores principales: Banga-Mingo, Virginie, Esona, Mathew D., Betrapally, Naga S., Gautam, Rashi, Jaimes, Jose, Katz, Eric, Waku-Kouomou, Diane, Bowen, Michael D., Gouandjika-Vasilache, Ionela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166134/
https://www.ncbi.nlm.nih.gov/pubmed/34059133
http://dx.doi.org/10.1186/s13104-021-05634-4
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author Banga-Mingo, Virginie
Esona, Mathew D.
Betrapally, Naga S.
Gautam, Rashi
Jaimes, Jose
Katz, Eric
Waku-Kouomou, Diane
Bowen, Michael D.
Gouandjika-Vasilache, Ionela
author_facet Banga-Mingo, Virginie
Esona, Mathew D.
Betrapally, Naga S.
Gautam, Rashi
Jaimes, Jose
Katz, Eric
Waku-Kouomou, Diane
Bowen, Michael D.
Gouandjika-Vasilache, Ionela
author_sort Banga-Mingo, Virginie
collection PubMed
description OBJECTIVE: Rotavirus A (RVA) remains the main causative agent of gastroenteritis in young children and the young of many mammalian and avian species. In this study we describe a RVA strain detected from a 6-month-old child from Central African Republic (CAR). RESULTS: We report the 11 open reading frame sequences of a G29-P[6]-I2-R2-C2-M2-A2-N2-T2-E2-H2 rotavirus strain, RVA/Human-wt/CAR/CAR91/2014/G29P[6]. Nine genes (VP1–VP3, VP6, NSP1–NSP5) shared 90–100% sequence similarities with genogroup 2 rotaviruses. Phylogenetically, backbone genes, except for VP3 and NSP4 genes, were linked with cognate gene sequences of human DS-1-like genogroup 2, hence their genetic origin. The VP3 and NSP4 genes, clustered genetically with both human and animal strains, an indication genetic reassortment human and animal RVA strains has taken place. The VP7 gene shared nucleotide (93–94%) and amino acid (95.5–96.7%) identities with Kenyan and Belgian human G29 strains, as well as to buffalo G29 strain from South Africa, while the VP4 gene most closely resembled P[6]-lineage I strains from Africa and Bangladesh (97%).
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spelling pubmed-81661342021-06-02 Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic Banga-Mingo, Virginie Esona, Mathew D. Betrapally, Naga S. Gautam, Rashi Jaimes, Jose Katz, Eric Waku-Kouomou, Diane Bowen, Michael D. Gouandjika-Vasilache, Ionela BMC Res Notes Research Note OBJECTIVE: Rotavirus A (RVA) remains the main causative agent of gastroenteritis in young children and the young of many mammalian and avian species. In this study we describe a RVA strain detected from a 6-month-old child from Central African Republic (CAR). RESULTS: We report the 11 open reading frame sequences of a G29-P[6]-I2-R2-C2-M2-A2-N2-T2-E2-H2 rotavirus strain, RVA/Human-wt/CAR/CAR91/2014/G29P[6]. Nine genes (VP1–VP3, VP6, NSP1–NSP5) shared 90–100% sequence similarities with genogroup 2 rotaviruses. Phylogenetically, backbone genes, except for VP3 and NSP4 genes, were linked with cognate gene sequences of human DS-1-like genogroup 2, hence their genetic origin. The VP3 and NSP4 genes, clustered genetically with both human and animal strains, an indication genetic reassortment human and animal RVA strains has taken place. The VP7 gene shared nucleotide (93–94%) and amino acid (95.5–96.7%) identities with Kenyan and Belgian human G29 strains, as well as to buffalo G29 strain from South Africa, while the VP4 gene most closely resembled P[6]-lineage I strains from Africa and Bangladesh (97%). BioMed Central 2021-05-31 /pmc/articles/PMC8166134/ /pubmed/34059133 http://dx.doi.org/10.1186/s13104-021-05634-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Banga-Mingo, Virginie
Esona, Mathew D.
Betrapally, Naga S.
Gautam, Rashi
Jaimes, Jose
Katz, Eric
Waku-Kouomou, Diane
Bowen, Michael D.
Gouandjika-Vasilache, Ionela
Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title_full Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title_fullStr Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title_full_unstemmed Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title_short Whole gene analysis of a genotype G29P[6] human rotavirus strain identified in Central African Republic
title_sort whole gene analysis of a genotype g29p[6] human rotavirus strain identified in central african republic
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166134/
https://www.ncbi.nlm.nih.gov/pubmed/34059133
http://dx.doi.org/10.1186/s13104-021-05634-4
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