Exhaled aerosol transmission of pandemic and seasonal H1N1 influenza viruses in the ferret
Person-to-person transmission of influenza viruses occurs by contact (direct and fomites) and non-contact (droplet and small particle aerosol) routes, but the quantitative dynamics and relative contributions of these routes are incompletely understood. The transmissibility of influenza strains estim...
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creator | Koster, Frederick Gouveia, Kristine Zhou, Yue Lowery, Kristin Russell, Robert MacInnes, Heather Pollock, Zemmie Layton, R Colby Cromwell, Jennifer Toleno, Denise Pyle, John Zubelewicz, Michael Harrod, Kevin Sampath, Rangarajan Hofstadler, Steven Gao, Peng Liu, Yushi Cheng, Yung-Sung |
description | Person-to-person transmission of influenza viruses occurs by contact (direct and fomites) and non-contact (droplet and small particle aerosol) routes, but the quantitative dynamics and relative contributions of these routes are incompletely understood. The transmissibility of influenza strains estimated from secondary attack rates in closed human populations is confounded by large variations in population susceptibilities. An experimental method to phenotype strains for transmissibility in an animal model could provide relative efficiencies of transmission. We developed an experimental method to detect exhaled viral aerosol transmission between unanesthetized infected and susceptible ferrets, measured aerosol particle size and number, and quantified the viral genomic RNA in the exhaled aerosol. During brief 3-hour exposures to exhaled viral aerosols in airflow-controlled chambers, three strains of pandemic 2009 H1N1 strains were frequently transmitted to susceptible ferrets. In contrast one seasonal H1N1 strain was not transmitted in spite of higher levels of viral RNA in the exhaled aerosol. Among three pandemic strains, the two strains causing weight loss and illness in the intranasally infected 'donor' ferrets were transmitted less efficiently from the donor than the strain causing no detectable illness, suggesting that the mucosal inflammatory response may attenuate viable exhaled virus. Although exhaled viral RNA remained constant, transmission efficiency diminished from day 1 to day 5 after donor infection. Thus, aerosol transmission between ferrets may be dependent on at least four characteristics of virus-host relationships including the level of exhaled virus, infectious particle size, mucosal inflammation, and viral replication efficiency in susceptible mucosa. |
doi_str_mv | 10.1371/journal.pone.0033118 |
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The transmissibility of influenza strains estimated from secondary attack rates in closed human populations is confounded by large variations in population susceptibilities. An experimental method to phenotype strains for transmissibility in an animal model could provide relative efficiencies of transmission. We developed an experimental method to detect exhaled viral aerosol transmission between unanesthetized infected and susceptible ferrets, measured aerosol particle size and number, and quantified the viral genomic RNA in the exhaled aerosol. During brief 3-hour exposures to exhaled viral aerosols in airflow-controlled chambers, three strains of pandemic 2009 H1N1 strains were frequently transmitted to susceptible ferrets. In contrast one seasonal H1N1 strain was not transmitted in spite of higher levels of viral RNA in the exhaled aerosol. Among three pandemic strains, the two strains causing weight loss and illness in the intranasally infected 'donor' ferrets were transmitted less efficiently from the donor than the strain causing no detectable illness, suggesting that the mucosal inflammatory response may attenuate viable exhaled virus. Although exhaled viral RNA remained constant, transmission efficiency diminished from day 1 to day 5 after donor infection. Thus, aerosol transmission between ferrets may be dependent on at least four characteristics of virus-host relationships including the level of exhaled virus, infectious particle size, mucosal inflammation, and viral replication efficiency in susceptible mucosa.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0033118</identifier><identifier>PMID: 22509254</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aerosols ; Air flow ; Airflow ; Analysis ; Animals ; Apoptosis ; Biology ; Cell culture ; Chemistry ; Cross infection ; Disease transmission ; Eggs ; Exhalation ; Experimental methods ; Ferrets - virology ; Fomites ; Health aspects ; Human populations ; Humans ; Humidity ; Infections ; Infectious diseases ; Inflammation ; Inflammatory response ; Influenza ; Influenza A Virus, H1N1 Subtype - metabolism ; Influenza A Virus, H1N1 Subtype - pathogenicity ; Influenza A Virus, H1N1 Subtype - physiology ; Laboratories ; Lung - virology ; Male ; Medicine ; Mucosa ; Nebulizers and Vaporizers ; Orthomyxoviridae ; Orthomyxoviridae Infections - transmission ; Pandemics ; Pandemics - prevention & control ; Particle size ; Phenotypes ; Ribonucleic acid ; RNA ; RNA viruses ; RNA, Viral - metabolism ; Science ; Seasons ; Species Specificity ; Strains (organisms) ; Swine flu ; Swine influenza ; Time Factors ; Transmission efficiency ; Veterinary Science ; Viral Load ; Viruses</subject><ispartof>PloS one, 2012-04, Vol.7 (4), p.e33118-e33118</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Koster et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Koster et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-58fa05899fdfdc19030a44fd61b6ef8183740436d2e889b380e0afc6d8e945c43</citedby><cites>FETCH-LOGICAL-c758t-58fa05899fdfdc19030a44fd61b6ef8183740436d2e889b380e0afc6d8e945c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317934/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317934/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23871,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22509254$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Guan, Yi</contributor><creatorcontrib>Koster, Frederick</creatorcontrib><creatorcontrib>Gouveia, Kristine</creatorcontrib><creatorcontrib>Zhou, Yue</creatorcontrib><creatorcontrib>Lowery, Kristin</creatorcontrib><creatorcontrib>Russell, Robert</creatorcontrib><creatorcontrib>MacInnes, Heather</creatorcontrib><creatorcontrib>Pollock, Zemmie</creatorcontrib><creatorcontrib>Layton, R Colby</creatorcontrib><creatorcontrib>Cromwell, Jennifer</creatorcontrib><creatorcontrib>Toleno, Denise</creatorcontrib><creatorcontrib>Pyle, John</creatorcontrib><creatorcontrib>Zubelewicz, Michael</creatorcontrib><creatorcontrib>Harrod, Kevin</creatorcontrib><creatorcontrib>Sampath, Rangarajan</creatorcontrib><creatorcontrib>Hofstadler, Steven</creatorcontrib><creatorcontrib>Gao, Peng</creatorcontrib><creatorcontrib>Liu, Yushi</creatorcontrib><creatorcontrib>Cheng, Yung-Sung</creatorcontrib><title>Exhaled aerosol transmission of pandemic and seasonal H1N1 influenza viruses in the ferret</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Person-to-person transmission of influenza viruses occurs by contact (direct and fomites) and non-contact (droplet and small particle aerosol) routes, but the quantitative dynamics and relative contributions of these routes are incompletely understood. The transmissibility of influenza strains estimated from secondary attack rates in closed human populations is confounded by large variations in population susceptibilities. An experimental method to phenotype strains for transmissibility in an animal model could provide relative efficiencies of transmission. We developed an experimental method to detect exhaled viral aerosol transmission between unanesthetized infected and susceptible ferrets, measured aerosol particle size and number, and quantified the viral genomic RNA in the exhaled aerosol. During brief 3-hour exposures to exhaled viral aerosols in airflow-controlled chambers, three strains of pandemic 2009 H1N1 strains were frequently transmitted to susceptible ferrets. In contrast one seasonal H1N1 strain was not transmitted in spite of higher levels of viral RNA in the exhaled aerosol. Among three pandemic strains, the two strains causing weight loss and illness in the intranasally infected 'donor' ferrets were transmitted less efficiently from the donor than the strain causing no detectable illness, suggesting that the mucosal inflammatory response may attenuate viable exhaled virus. Although exhaled viral RNA remained constant, transmission efficiency diminished from day 1 to day 5 after donor infection. Thus, aerosol transmission between ferrets may be dependent on at least four characteristics of virus-host relationships including the level of exhaled virus, infectious particle size, mucosal inflammation, and viral replication efficiency in susceptible mucosa.</description><subject>Aerosols</subject><subject>Air flow</subject><subject>Airflow</subject><subject>Analysis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biology</subject><subject>Cell culture</subject><subject>Chemistry</subject><subject>Cross infection</subject><subject>Disease transmission</subject><subject>Eggs</subject><subject>Exhalation</subject><subject>Experimental methods</subject><subject>Ferrets - virology</subject><subject>Fomites</subject><subject>Health aspects</subject><subject>Human populations</subject><subject>Humans</subject><subject>Humidity</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Influenza</subject><subject>Influenza A Virus, H1N1 Subtype - metabolism</subject><subject>Influenza A Virus, H1N1 Subtype - pathogenicity</subject><subject>Influenza A Virus, H1N1 Subtype - physiology</subject><subject>Laboratories</subject><subject>Lung - virology</subject><subject>Male</subject><subject>Medicine</subject><subject>Mucosa</subject><subject>Nebulizers and Vaporizers</subject><subject>Orthomyxoviridae</subject><subject>Orthomyxoviridae Infections - transmission</subject><subject>Pandemics</subject><subject>Pandemics - prevention & control</subject><subject>Particle size</subject><subject>Phenotypes</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA viruses</subject><subject>RNA, Viral - metabolism</subject><subject>Science</subject><subject>Seasons</subject><subject>Species Specificity</subject><subject>Strains (organisms)</subject><subject>Swine flu</subject><subject>Swine influenza</subject><subject>Time 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one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koster, Frederick</au><au>Gouveia, Kristine</au><au>Zhou, Yue</au><au>Lowery, Kristin</au><au>Russell, Robert</au><au>MacInnes, Heather</au><au>Pollock, Zemmie</au><au>Layton, R Colby</au><au>Cromwell, Jennifer</au><au>Toleno, Denise</au><au>Pyle, John</au><au>Zubelewicz, Michael</au><au>Harrod, Kevin</au><au>Sampath, Rangarajan</au><au>Hofstadler, Steven</au><au>Gao, Peng</au><au>Liu, Yushi</au><au>Cheng, Yung-Sung</au><au>Guan, Yi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exhaled aerosol transmission of pandemic and seasonal H1N1 influenza viruses in the ferret</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-04-03</date><risdate>2012</risdate><volume>7</volume><issue>4</issue><spage>e33118</spage><epage>e33118</epage><pages>e33118-e33118</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Person-to-person transmission of influenza viruses occurs by contact (direct and fomites) and non-contact (droplet and small particle aerosol) routes, but the quantitative dynamics and relative contributions of these routes are incompletely understood. The transmissibility of influenza strains estimated from secondary attack rates in closed human populations is confounded by large variations in population susceptibilities. An experimental method to phenotype strains for transmissibility in an animal model could provide relative efficiencies of transmission. We developed an experimental method to detect exhaled viral aerosol transmission between unanesthetized infected and susceptible ferrets, measured aerosol particle size and number, and quantified the viral genomic RNA in the exhaled aerosol. During brief 3-hour exposures to exhaled viral aerosols in airflow-controlled chambers, three strains of pandemic 2009 H1N1 strains were frequently transmitted to susceptible ferrets. In contrast one seasonal H1N1 strain was not transmitted in spite of higher levels of viral RNA in the exhaled aerosol. Among three pandemic strains, the two strains causing weight loss and illness in the intranasally infected 'donor' ferrets were transmitted less efficiently from the donor than the strain causing no detectable illness, suggesting that the mucosal inflammatory response may attenuate viable exhaled virus. Although exhaled viral RNA remained constant, transmission efficiency diminished from day 1 to day 5 after donor infection. Thus, aerosol transmission between ferrets may be dependent on at least four characteristics of virus-host relationships including the level of exhaled virus, infectious particle size, mucosal inflammation, and viral replication efficiency in susceptible mucosa.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22509254</pmid><doi>10.1371/journal.pone.0033118</doi><tpages>e33118</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2012-04, Vol.7 (4), p.e33118-e33118 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2009660461 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Aerosols Air flow Airflow Analysis Animals Apoptosis Biology Cell culture Chemistry Cross infection Disease transmission Eggs Exhalation Experimental methods Ferrets - virology Fomites Health aspects Human populations Humans Humidity Infections Infectious diseases Inflammation Inflammatory response Influenza Influenza A Virus, H1N1 Subtype - metabolism Influenza A Virus, H1N1 Subtype - pathogenicity Influenza A Virus, H1N1 Subtype - physiology Laboratories Lung - virology Male Medicine Mucosa Nebulizers and Vaporizers Orthomyxoviridae Orthomyxoviridae Infections - transmission Pandemics Pandemics - prevention & control Particle size Phenotypes Ribonucleic acid RNA RNA viruses RNA, Viral - metabolism Science Seasons Species Specificity Strains (organisms) Swine flu Swine influenza Time Factors Transmission efficiency Veterinary Science Viral Load Viruses |
title | Exhaled aerosol transmission of pandemic and seasonal H1N1 influenza viruses in the ferret |
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