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Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal

PROBLEM: Rhinoviruses (RVs), the most common causes of acute respiratory infections in young children and infants, are highly diverse genetically. OBJECTIVE: To characterize the RV types detected with respiratory illness episodes in infants in Nepal. STUDY METHODS: Infants born to women enrolled in...

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Autores principales: Kuypers, Jane, Perchetti, Garrett A., Chu, Helen Y., Newman, Kira L., Katz, Joanne, Khatry, Subarna K., LeClerq, Steven C., Jerome, Keith R., Tielsch, James M., Englund, Janet A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800797/
https://www.ncbi.nlm.nih.gov/pubmed/31389049
http://dx.doi.org/10.1002/jmv.25563
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author Kuypers, Jane
Perchetti, Garrett A.
Chu, Helen Y.
Newman, Kira L.
Katz, Joanne
Khatry, Subarna K.
LeClerq, Steven C.
Jerome, Keith R.
Tielsch, James M.
Englund, Janet A.
author_facet Kuypers, Jane
Perchetti, Garrett A.
Chu, Helen Y.
Newman, Kira L.
Katz, Joanne
Khatry, Subarna K.
LeClerq, Steven C.
Jerome, Keith R.
Tielsch, James M.
Englund, Janet A.
author_sort Kuypers, Jane
collection PubMed
description PROBLEM: Rhinoviruses (RVs), the most common causes of acute respiratory infections in young children and infants, are highly diverse genetically. OBJECTIVE: To characterize the RV types detected with respiratory illness episodes in infants in Nepal. STUDY METHODS: Infants born to women enrolled in a randomized trial of maternal influenza immunization in rural, southern Nepal were followed with household‐based weekly surveillance until 180 days of age. Infants with respiratory symptoms had nasal swabs tested for twelve respiratory viruses. A subset with RV alone was selected for sequencing of the VP4/2 gene to identify RV types. RESULTS: Among 547 RV‐only positive illnesses detected from December 2012 to April 2014, 285 samples (52%) were sequenced. RV‐A, B, and C species were detected in 193 (68%), 18 (6%), and 74 (26%) specimens, respectively. A total of 94 unique types were identified from the sequenced samples, including 52 RV‐A, 11 RV‐B, and 31 RV‐C. Multiple species and types circulated simultaneously throughout the study period. No seasonality was observed. The median ages at illness onset were 88, 104, and 88 days for RV‐A, B, and C, respectively. The median polymerase chain reaction cycle threshold values did not differ between RV species. No differences between RV species were observed for reported respiratory symptoms, including pneumonia, or for medical care‐seeking. CONCLUSIONS: Among very young, symptomatic infants in rural Nepal, all three species and many types of RV were identified; RV‐A was detected most frequently. There was no association between RV species and disease severity.
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spelling pubmed-68007972020-04-21 Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal Kuypers, Jane Perchetti, Garrett A. Chu, Helen Y. Newman, Kira L. Katz, Joanne Khatry, Subarna K. LeClerq, Steven C. Jerome, Keith R. Tielsch, James M. Englund, Janet A. J Med Virol Research Articles PROBLEM: Rhinoviruses (RVs), the most common causes of acute respiratory infections in young children and infants, are highly diverse genetically. OBJECTIVE: To characterize the RV types detected with respiratory illness episodes in infants in Nepal. STUDY METHODS: Infants born to women enrolled in a randomized trial of maternal influenza immunization in rural, southern Nepal were followed with household‐based weekly surveillance until 180 days of age. Infants with respiratory symptoms had nasal swabs tested for twelve respiratory viruses. A subset with RV alone was selected for sequencing of the VP4/2 gene to identify RV types. RESULTS: Among 547 RV‐only positive illnesses detected from December 2012 to April 2014, 285 samples (52%) were sequenced. RV‐A, B, and C species were detected in 193 (68%), 18 (6%), and 74 (26%) specimens, respectively. A total of 94 unique types were identified from the sequenced samples, including 52 RV‐A, 11 RV‐B, and 31 RV‐C. Multiple species and types circulated simultaneously throughout the study period. No seasonality was observed. The median ages at illness onset were 88, 104, and 88 days for RV‐A, B, and C, respectively. The median polymerase chain reaction cycle threshold values did not differ between RV species. No differences between RV species were observed for reported respiratory symptoms, including pneumonia, or for medical care‐seeking. CONCLUSIONS: Among very young, symptomatic infants in rural Nepal, all three species and many types of RV were identified; RV‐A was detected most frequently. There was no association between RV species and disease severity. John Wiley and Sons Inc. 2019-08-21 2019-12 /pmc/articles/PMC6800797/ /pubmed/31389049 http://dx.doi.org/10.1002/jmv.25563 Text en © 2019 Wiley Periodicals, Inc. This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.
spellingShingle Research Articles
Kuypers, Jane
Perchetti, Garrett A.
Chu, Helen Y.
Newman, Kira L.
Katz, Joanne
Khatry, Subarna K.
LeClerq, Steven C.
Jerome, Keith R.
Tielsch, James M.
Englund, Janet A.
Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title_full Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title_fullStr Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title_full_unstemmed Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title_short Phylogenetic characterization of rhinoviruses from infants in Sarlahi, Nepal
title_sort phylogenetic characterization of rhinoviruses from infants in sarlahi, nepal
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800797/
https://www.ncbi.nlm.nih.gov/pubmed/31389049
http://dx.doi.org/10.1002/jmv.25563
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