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A shift in circulating rotaviral genotypes among hospitalized neonates

In neonates, rotavirus (RV) infection is generally nosocomial. The control of rotaviral infection within hospital settings is challenging due to prolonged shedding of the virus and contamination of the surrounding environment. There are few studies that have reported asymptomatic infection within ne...

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Autores principales: Reju, Sudhabharathi, Srikanth, Padma, Selvarajan, Sribal, Thomas, Reuben Kuruvilla, Barani, Ramya, Amboiram, Prakash, Palani, Gunasekaran, Kang, Gagandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857175/
https://www.ncbi.nlm.nih.gov/pubmed/35181717
http://dx.doi.org/10.1038/s41598-022-06506-y
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author Reju, Sudhabharathi
Srikanth, Padma
Selvarajan, Sribal
Thomas, Reuben Kuruvilla
Barani, Ramya
Amboiram, Prakash
Palani, Gunasekaran
Kang, Gagandeep
author_facet Reju, Sudhabharathi
Srikanth, Padma
Selvarajan, Sribal
Thomas, Reuben Kuruvilla
Barani, Ramya
Amboiram, Prakash
Palani, Gunasekaran
Kang, Gagandeep
author_sort Reju, Sudhabharathi
collection PubMed
description In neonates, rotavirus (RV) infection is generally nosocomial. The control of rotaviral infection within hospital settings is challenging due to prolonged shedding of the virus and contamination of the surrounding environment. There are few studies that have reported asymptomatic infection within neonates. In this study, neonates were screened for RV infection and possible clinical manifestations that may play a role in RV acquisition were analysed. Stool samples were collected from 523 hospitalized neonates admitted for > 48 h in a low-cost and higher-cost tertiary centre. RV antigen was screened using ELISA and the samples which tested positive were confirmed by semi-nested RT-PCR. RV was detected in 34% of participants and genotypes identified included G12P[11] (44.4%), G10 P[11] (42.6%), G10G12P[11] (10.1%) and G3P[8] (2.9%). ICU admissions were associated with higher viral shedding (p < 0.05). Hospitalization in the low-cost facility ICU was associated with higher RV acquisition risk (p < 0.05). RV was detected in higher rates (36.9%) among neonates with gastrointestinal manifestations. G10P[11] was the predominant genotype for several years (1988–2016) among neonates within India. The preponderance of an emerging G12P[11] genotype and heterotypic distribution was documented. RV surveillance is important to identify emerging strains and establish the road ahead in managing RV infection.
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spelling pubmed-88571752022-02-22 A shift in circulating rotaviral genotypes among hospitalized neonates Reju, Sudhabharathi Srikanth, Padma Selvarajan, Sribal Thomas, Reuben Kuruvilla Barani, Ramya Amboiram, Prakash Palani, Gunasekaran Kang, Gagandeep Sci Rep Article In neonates, rotavirus (RV) infection is generally nosocomial. The control of rotaviral infection within hospital settings is challenging due to prolonged shedding of the virus and contamination of the surrounding environment. There are few studies that have reported asymptomatic infection within neonates. In this study, neonates were screened for RV infection and possible clinical manifestations that may play a role in RV acquisition were analysed. Stool samples were collected from 523 hospitalized neonates admitted for > 48 h in a low-cost and higher-cost tertiary centre. RV antigen was screened using ELISA and the samples which tested positive were confirmed by semi-nested RT-PCR. RV was detected in 34% of participants and genotypes identified included G12P[11] (44.4%), G10 P[11] (42.6%), G10G12P[11] (10.1%) and G3P[8] (2.9%). ICU admissions were associated with higher viral shedding (p < 0.05). Hospitalization in the low-cost facility ICU was associated with higher RV acquisition risk (p < 0.05). RV was detected in higher rates (36.9%) among neonates with gastrointestinal manifestations. G10P[11] was the predominant genotype for several years (1988–2016) among neonates within India. The preponderance of an emerging G12P[11] genotype and heterotypic distribution was documented. RV surveillance is important to identify emerging strains and establish the road ahead in managing RV infection. Nature Publishing Group UK 2022-02-18 /pmc/articles/PMC8857175/ /pubmed/35181717 http://dx.doi.org/10.1038/s41598-022-06506-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Reju, Sudhabharathi
Srikanth, Padma
Selvarajan, Sribal
Thomas, Reuben Kuruvilla
Barani, Ramya
Amboiram, Prakash
Palani, Gunasekaran
Kang, Gagandeep
A shift in circulating rotaviral genotypes among hospitalized neonates
title A shift in circulating rotaviral genotypes among hospitalized neonates
title_full A shift in circulating rotaviral genotypes among hospitalized neonates
title_fullStr A shift in circulating rotaviral genotypes among hospitalized neonates
title_full_unstemmed A shift in circulating rotaviral genotypes among hospitalized neonates
title_short A shift in circulating rotaviral genotypes among hospitalized neonates
title_sort shift in circulating rotaviral genotypes among hospitalized neonates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857175/
https://www.ncbi.nlm.nih.gov/pubmed/35181717
http://dx.doi.org/10.1038/s41598-022-06506-y
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