Hand contamination with human rhinovirus in Bangladesh

As one step in developing a measure of hand contamination with respiratory viruses, this study assessed if human rhinovirus (HRV) was detectable on hands in a low income non‐temperate community where respiratory disease is a leading cause of child death. Research assistants observed residents in a l...

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Veröffentlicht in:Journal of medical virology 2014-12, Vol.86 (12), p.2177-2180
Hauptverfasser: Luby, Stephen P., Lu, Xiaoyan, Cromeans, Theresa, Sharker, M.A. Yushuf, Kadir, Mohammad Abdul, Erdman, Dean D.
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container_end_page 2180
container_issue 12
container_start_page 2177
container_title Journal of medical virology
container_volume 86
creator Luby, Stephen P.
Lu, Xiaoyan
Cromeans, Theresa
Sharker, M.A. Yushuf
Kadir, Mohammad Abdul
Erdman, Dean D.
description As one step in developing a measure of hand contamination with respiratory viruses, this study assessed if human rhinovirus (HRV) was detectable on hands in a low income non‐temperate community where respiratory disease is a leading cause of child death. Research assistants observed residents in a low income community in Dhaka, Bangladesh. When they observed a resident sneeze or pick their nose, they collected a hand rinse and anterior nare sample from the resident. Samples were first tested for HRV RNA by real‐time RT‐PCR (rRT‐PCR). A subset of rRT‐PCR positive samples were cultured into MRC‐5 and HeLa Ohio cells. Among 177 hand samples tested for HRV by real‐time RT‐PCR, 52 (29%) were positive. Among 15 RT‐PCR positive hand samples that were cultured, two grew HRV. HRV was detected in each of the sampling months (January, February, June, July, November, and December). This study demonstrates in the natural setting that, at least after sneezing or nasal cleaning, hands were contaminated commonly with potentially infectious HRV. Future research could explore if HRV RNA is present consistently and is associated sufficiently with the incidence of respiratory illness in communities that it may provide a proxy measure of respiratory viral hand contamination. J. Med. Virol. 86:21772180, 2014. © Published 2014. This article is a U.S. Government work and is in the public domain in the USA.
doi_str_mv 10.1002/jmv.23959
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Research assistants observed residents in a low income community in Dhaka, Bangladesh. When they observed a resident sneeze or pick their nose, they collected a hand rinse and anterior nare sample from the resident. Samples were first tested for HRV RNA by real‐time RT‐PCR (rRT‐PCR). A subset of rRT‐PCR positive samples were cultured into MRC‐5 and HeLa Ohio cells. Among 177 hand samples tested for HRV by real‐time RT‐PCR, 52 (29%) were positive. Among 15 RT‐PCR positive hand samples that were cultured, two grew HRV. HRV was detected in each of the sampling months (January, February, June, July, November, and December). This study demonstrates in the natural setting that, at least after sneezing or nasal cleaning, hands were contaminated commonly with potentially infectious HRV. Future research could explore if HRV RNA is present consistently and is associated sufficiently with the incidence of respiratory illness in communities that it may provide a proxy measure of respiratory viral hand contamination. J. Med. Virol. 86:21772180, 2014. © Published 2014. 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Med. Virol</addtitle><description>As one step in developing a measure of hand contamination with respiratory viruses, this study assessed if human rhinovirus (HRV) was detectable on hands in a low income non‐temperate community where respiratory disease is a leading cause of child death. Research assistants observed residents in a low income community in Dhaka, Bangladesh. When they observed a resident sneeze or pick their nose, they collected a hand rinse and anterior nare sample from the resident. Samples were first tested for HRV RNA by real‐time RT‐PCR (rRT‐PCR). A subset of rRT‐PCR positive samples were cultured into MRC‐5 and HeLa Ohio cells. Among 177 hand samples tested for HRV by real‐time RT‐PCR, 52 (29%) were positive. Among 15 RT‐PCR positive hand samples that were cultured, two grew HRV. HRV was detected in each of the sampling months (January, February, June, July, November, and December). This study demonstrates in the natural setting that, at least after sneezing or nasal cleaning, hands were contaminated commonly with potentially infectious HRV. Future research could explore if HRV RNA is present consistently and is associated sufficiently with the incidence of respiratory illness in communities that it may provide a proxy measure of respiratory viral hand contamination. J. Med. Virol. 86:21772180, 2014. © Published 2014. 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subjects Adolescent
Adult
Bangladesh
Cell Line
Child
Child, Preschool
Disease transmission
Female
hand
Hand - virology
handwashing
Human rhinovirus
Humans
Hygiene
Infant
Male
Nose - virology
Real-Time Polymerase Chain Reaction
Respiratory diseases
Reverse Transcriptase Polymerase Chain Reaction
rhinovirus
Rhinovirus - isolation & purification
RNA, Viral - analysis
RNA, Viral - genetics
Viral infections
Virology
Virus Cultivation
Young Adult
title Hand contamination with human rhinovirus in Bangladesh
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