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Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana
BACKGROUND: Acute lower respiratory tract infection (ALRTI) in children under 5 years is known to be predominantly caused by respiratory syncytial virus (RSV). In recent times, however, human metapneumovirus (HMPV) has also been implicated. This study sought to investigate and genotype respiratory s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229459/ https://www.ncbi.nlm.nih.gov/pubmed/35751110 http://dx.doi.org/10.1186/s12887-022-03419-7 |
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author | Kafintu-Kwashie, Anna Aba Nii-Trebi, Nicholas Israel Obodai, Evangeline Neizer, Margaret Adiku, Theophilus Korku Odoom, John Kofi |
author_facet | Kafintu-Kwashie, Anna Aba Nii-Trebi, Nicholas Israel Obodai, Evangeline Neizer, Margaret Adiku, Theophilus Korku Odoom, John Kofi |
author_sort | Kafintu-Kwashie, Anna Aba |
collection | PubMed |
description | BACKGROUND: Acute lower respiratory tract infection (ALRTI) in children under 5 years is known to be predominantly caused by respiratory syncytial virus (RSV). In recent times, however, human metapneumovirus (HMPV) has also been implicated. This study sought to investigate and genotype respiratory syncytial virus and human metapneumovirus in children presenting with ALRTIs infection at the Princess Marie Louis Children’s Hospital in Accra, Ghana. METHODS: Children below 5 years who were clinically diagnosed of ALRTI and on admission at the study site were recruited between September 2015 and November 2016 for this study. Demographic data information was obtained by means of a standardized questionnaire; and relevant clinical information was obtained from medical records. Nasopharyngeal swabs were collected from 176 children recruited for the study. Ribonucleic acid was extracted from swabs and cDNA syntheses were performed by RT-PCR. RSV-positive amplicons were sequenced and analyzed for genotype assignment. RESULTS: RSV and HMPV prevalence among the sampled subjects were 11.4 and 1.7% respectively. Of the RSV positives, 8/20 (40%) were RSV-A and 12/20 (60%) were RSV-B. The highest prevalence was observed in children less than 12 months old. Phylogenetic analysis of the second hypervariable region of the RSV G-gene revealed that all RSV group A viruses belonged to the “novel” ON1 genotype containing the 72-nucleotide duplication; and RSV group B viruses belong to the BA IX genotype. CONCLUSION: RSV is frequently detected in children aged under 5 years admitted with ALRTI in Ghana. Continued surveillance of viral aetiological agents is warranted to elucidate the prevalence and transmission patterns of viral pathogens that cause respiratory tract infections among children. This will help inform appropriate intervention approaches. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03419-7. |
format | Online Article Text |
id | pubmed-9229459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92294592022-06-25 Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana Kafintu-Kwashie, Anna Aba Nii-Trebi, Nicholas Israel Obodai, Evangeline Neizer, Margaret Adiku, Theophilus Korku Odoom, John Kofi BMC Pediatr Research BACKGROUND: Acute lower respiratory tract infection (ALRTI) in children under 5 years is known to be predominantly caused by respiratory syncytial virus (RSV). In recent times, however, human metapneumovirus (HMPV) has also been implicated. This study sought to investigate and genotype respiratory syncytial virus and human metapneumovirus in children presenting with ALRTIs infection at the Princess Marie Louis Children’s Hospital in Accra, Ghana. METHODS: Children below 5 years who were clinically diagnosed of ALRTI and on admission at the study site were recruited between September 2015 and November 2016 for this study. Demographic data information was obtained by means of a standardized questionnaire; and relevant clinical information was obtained from medical records. Nasopharyngeal swabs were collected from 176 children recruited for the study. Ribonucleic acid was extracted from swabs and cDNA syntheses were performed by RT-PCR. RSV-positive amplicons were sequenced and analyzed for genotype assignment. RESULTS: RSV and HMPV prevalence among the sampled subjects were 11.4 and 1.7% respectively. Of the RSV positives, 8/20 (40%) were RSV-A and 12/20 (60%) were RSV-B. The highest prevalence was observed in children less than 12 months old. Phylogenetic analysis of the second hypervariable region of the RSV G-gene revealed that all RSV group A viruses belonged to the “novel” ON1 genotype containing the 72-nucleotide duplication; and RSV group B viruses belong to the BA IX genotype. CONCLUSION: RSV is frequently detected in children aged under 5 years admitted with ALRTI in Ghana. Continued surveillance of viral aetiological agents is warranted to elucidate the prevalence and transmission patterns of viral pathogens that cause respiratory tract infections among children. This will help inform appropriate intervention approaches. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12887-022-03419-7. BioMed Central 2022-06-24 /pmc/articles/PMC9229459/ /pubmed/35751110 http://dx.doi.org/10.1186/s12887-022-03419-7 Text en © The Author(s) 2022 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 Kafintu-Kwashie, Anna Aba Nii-Trebi, Nicholas Israel Obodai, Evangeline Neizer, Margaret Adiku, Theophilus Korku Odoom, John Kofi Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title | Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title_full | Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title_fullStr | Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title_full_unstemmed | Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title_short | Molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in Accra, Ghana |
title_sort | molecular epidemiological surveillance of viral agents of acute lower respiratory tract infections in children in accra, ghana |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9229459/ https://www.ncbi.nlm.nih.gov/pubmed/35751110 http://dx.doi.org/10.1186/s12887-022-03419-7 |
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