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2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016

BACKGROUND: Respiratory syncytial virus (RSV) is a major cause of severe acute respiratory illnesses (ARI) in young children. Circulation of RSV subgroups A and B can vary by season and geographic location, and may have implications for disease susceptibility, outcomes, and prevention measures. We i...

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Autores principales: Rha, Brian, Peret, Teresa C T, Wang, Lijuan, Lively, Joana Y, Curns, Aaron, Campbell, Angela P, Boom, Julie A, Azimi, Parvin H, Weinberg, Geoffrey A, Staat, Mary A, Selvarangan, Rangaraj, Halasa, Natasha B, Englund, Janet A, Klein, Eileen J, Harrison, Christopher J, Stewart, Laura S, Szilagyi, Peter G, Nayakwadi. Singer, Monica, Avadhanula, Vasanthi, McNeal, Monica, Figueroa-Downing, Daniella, Prill, Mila M, Whitaker, Brett L, Payne, Daniel C, Lindstrom, Stephen, Thornburg, Natalie J, Gerber, Susan I, Langley, Gayle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810179/
http://dx.doi.org/10.1093/ofid/ofz360.2006
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author Rha, Brian
Peret, Teresa C T
Wang, Lijuan
Lively, Joana Y
Curns, Aaron
Campbell, Angela P
Boom, Julie A
Azimi, Parvin H
Weinberg, Geoffrey A
Staat, Mary A
Selvarangan, Rangaraj
Halasa, Natasha B
Englund, Janet A
Klein, Eileen J
Harrison, Christopher J
Stewart, Laura S
Szilagyi, Peter G
Nayakwadi. Singer, Monica
Avadhanula, Vasanthi
McNeal, Monica
Figueroa-Downing, Daniella
Prill, Mila M
Whitaker, Brett L
Payne, Daniel C
Lindstrom, Stephen
Thornburg, Natalie J
Gerber, Susan I
Langley, Gayle
Langley, Gayle
author_facet Rha, Brian
Peret, Teresa C T
Wang, Lijuan
Lively, Joana Y
Curns, Aaron
Campbell, Angela P
Boom, Julie A
Azimi, Parvin H
Weinberg, Geoffrey A
Staat, Mary A
Selvarangan, Rangaraj
Halasa, Natasha B
Englund, Janet A
Klein, Eileen J
Harrison, Christopher J
Stewart, Laura S
Szilagyi, Peter G
Nayakwadi. Singer, Monica
Avadhanula, Vasanthi
McNeal, Monica
Figueroa-Downing, Daniella
Prill, Mila M
Whitaker, Brett L
Payne, Daniel C
Lindstrom, Stephen
Thornburg, Natalie J
Gerber, Susan I
Langley, Gayle
Langley, Gayle
author_sort Rha, Brian
collection PubMed
description BACKGROUND: Respiratory syncytial virus (RSV) is a major cause of severe acute respiratory illnesses (ARI) in young children. Circulation of RSV subgroups A and B can vary by season and geographic location, and may have implications for disease susceptibility, outcomes, and prevention measures. We investigated RSV subgroup distribution among samples collected in the New Vaccine Surveillance Network. METHODS: Prospective active surveillance for hospitalized ARI was conducted from November 1, 2015 to June 30, 2016 among children < 12 months of age at seven pediatric hospital sites. Mid-turbinate nasal and throat flocked swabs (combined when both available) and/or tracheal aspirates were collected and tested for RSV at each site using real-time reverse transcription polymerase chain reaction (rRT–PCR) assays; RSV A/B subgroup results were available from four sites that did their own subgroup testing (Cincinnati, Kansas City, Houston, and Oakland). At three sites (Rochester, Nashville, Seattle), approximately 50 RSV-positive specimens were sampled based on the monthly distribution for each site and 1:1 distribution by gender, and then assayed for subgroup at CDC. Patient information was obtained from medical records; chi-square tests were used to compare the distribution of A and B subgroups by site. RESULTS: Of 704 RSV-positive hospitalized infants, subgroup data from 586 were analyzed; 340 (58%) were RSV A and 246 (42%) were RSV B. The median age for both RSV A and RSV B patients was 2 months. Subgroup distribution varied by geographic location, with the overall proportion of RSV A ranging from 18–83% across sites (P < 0.01). Peak RSV A and B detections by month varied by site, occurring from November–February (figure). CONCLUSION: During the 2015–2016 season, RSV A and B subgroups co-circulated among hospitalized infants enrolled at seven US sites. The predominance of RSV subgroup varied by geographic location. Continued surveillance and additional subgroup testing over multiple seasons should improve understanding of the epidemiologic significance of RSV infections by subgroup. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68101792019-10-28 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016 Rha, Brian Peret, Teresa C T Wang, Lijuan Lively, Joana Y Curns, Aaron Campbell, Angela P Boom, Julie A Azimi, Parvin H Weinberg, Geoffrey A Staat, Mary A Selvarangan, Rangaraj Halasa, Natasha B Englund, Janet A Klein, Eileen J Harrison, Christopher J Stewart, Laura S Szilagyi, Peter G Nayakwadi. Singer, Monica Avadhanula, Vasanthi McNeal, Monica Figueroa-Downing, Daniella Prill, Mila M Whitaker, Brett L Payne, Daniel C Lindstrom, Stephen Thornburg, Natalie J Gerber, Susan I Langley, Gayle Langley, Gayle Open Forum Infect Dis Abstracts BACKGROUND: Respiratory syncytial virus (RSV) is a major cause of severe acute respiratory illnesses (ARI) in young children. Circulation of RSV subgroups A and B can vary by season and geographic location, and may have implications for disease susceptibility, outcomes, and prevention measures. We investigated RSV subgroup distribution among samples collected in the New Vaccine Surveillance Network. METHODS: Prospective active surveillance for hospitalized ARI was conducted from November 1, 2015 to June 30, 2016 among children < 12 months of age at seven pediatric hospital sites. Mid-turbinate nasal and throat flocked swabs (combined when both available) and/or tracheal aspirates were collected and tested for RSV at each site using real-time reverse transcription polymerase chain reaction (rRT–PCR) assays; RSV A/B subgroup results were available from four sites that did their own subgroup testing (Cincinnati, Kansas City, Houston, and Oakland). At three sites (Rochester, Nashville, Seattle), approximately 50 RSV-positive specimens were sampled based on the monthly distribution for each site and 1:1 distribution by gender, and then assayed for subgroup at CDC. Patient information was obtained from medical records; chi-square tests were used to compare the distribution of A and B subgroups by site. RESULTS: Of 704 RSV-positive hospitalized infants, subgroup data from 586 were analyzed; 340 (58%) were RSV A and 246 (42%) were RSV B. The median age for both RSV A and RSV B patients was 2 months. Subgroup distribution varied by geographic location, with the overall proportion of RSV A ranging from 18–83% across sites (P < 0.01). Peak RSV A and B detections by month varied by site, occurring from November–February (figure). CONCLUSION: During the 2015–2016 season, RSV A and B subgroups co-circulated among hospitalized infants enrolled at seven US sites. The predominance of RSV subgroup varied by geographic location. Continued surveillance and additional subgroup testing over multiple seasons should improve understanding of the epidemiologic significance of RSV infections by subgroup. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6810179/ http://dx.doi.org/10.1093/ofid/ofz360.2006 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Rha, Brian
Peret, Teresa C T
Wang, Lijuan
Lively, Joana Y
Curns, Aaron
Campbell, Angela P
Boom, Julie A
Azimi, Parvin H
Weinberg, Geoffrey A
Staat, Mary A
Selvarangan, Rangaraj
Halasa, Natasha B
Englund, Janet A
Klein, Eileen J
Harrison, Christopher J
Stewart, Laura S
Szilagyi, Peter G
Nayakwadi. Singer, Monica
Avadhanula, Vasanthi
McNeal, Monica
Figueroa-Downing, Daniella
Prill, Mila M
Whitaker, Brett L
Payne, Daniel C
Lindstrom, Stephen
Thornburg, Natalie J
Gerber, Susan I
Langley, Gayle
Langley, Gayle
2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title_full 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title_fullStr 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title_full_unstemmed 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title_short 2328. Human Respiratory Syncytial Virus Subgroups among Hospitalized Infants in the United States, 2015–2016
title_sort 2328. human respiratory syncytial virus subgroups among hospitalized infants in the united states, 2015–2016
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810179/
http://dx.doi.org/10.1093/ofid/ofz360.2006
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