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Article: Surgical Mask Partition Reduces the Risk of Noncontact Transmission in a Golden Syrian Hamster Model for Coronavirus Disease 2019 (COVID-19)

TitleSurgical Mask Partition Reduces the Risk of Noncontact Transmission in a Golden Syrian Hamster Model for Coronavirus Disease 2019 (COVID-19)
Authors
Keywordscoronavirus
COVID-19
SARS-CoV-2
mask
transmission
Issue Date2020
PublisherOxford University Press. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/cid/
Citation
Clinical Infectious Diseases, 2020, v. 71 n. 16, p. 2139-2149 How to Cite?
AbstractBackground: Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is believed to be mostly transmitted by medium- to large-sized respiratory droplets, although airborne transmission may be possible in healthcare settings involving aerosol-generating procedures. Exposure to respiratory droplets can theoretically be reduced by surgical mask usage. However, there is a lack of experimental evidence supporting surgical mask usage for prevention of COVID-19. Methods: We used a well-established golden Syrian hamster SARS-CoV-2 model. We placed SARS-CoV-2-challenged index hamsters and naive hamsters into closed system units each comprising 2 different cages separated by a polyvinyl chloride air porous partition with unidirectional airflow within the isolator. The effect of a surgical mask partition placed between the cages was investigated. Besides clinical scoring, hamster specimens were tested for viral load, histopathology, and viral nucleocapsid antigen expression. Results: Noncontact transmission was found in 66.7% (10/15) of exposed naive hamsters. Surgical mask partition for challenged index or naive hamsters significantly reduced transmission to 25% (6/24, P = .018). Surgical mask partition for challenged index hamsters significantly reduced transmission to only 16.7% (2/12, P = .019) of exposed naive hamsters. Unlike the severe manifestations of challenged hamsters, infected naive hamsters had lower clinical scores, milder histopathological changes, and lower viral nucleocapsid antigen expression in respiratory tract tissues. Conclusions: SARS-CoV-2 could be transmitted by respiratory droplets or airborne droplet nuclei which could be reduced by surgical mask partition in the hamster model. This is the first in vivo experimental evidence to support the possible benefit of surgical mask in prevention of COVID-19 transmission, especially when masks were worn by infected individuals.
Persistent Identifierhttp://hdl.handle.net/10722/289445
ISSN
2021 Impact Factor: 20.999
2020 SCImago Journal Rankings: 3.440
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, JFW-
dc.contributor.authorYuan, S-
dc.contributor.authorZhang, AJ-
dc.contributor.authorPoon, VKM-
dc.contributor.authorChan, CCS-
dc.contributor.authorLee, ACY-
dc.contributor.authorFan, Z-
dc.contributor.authorLi, C-
dc.contributor.authorLiang, R-
dc.contributor.authorCao, J-
dc.contributor.authorTang, K-
dc.contributor.authorLuo, C-
dc.contributor.authorCheng, VCC-
dc.contributor.authorCai, JP-
dc.contributor.authorChu, H-
dc.contributor.authorChan, KH-
dc.contributor.authorTo, KKW-
dc.contributor.authorSridhar, S-
dc.contributor.authorYuen, KY-
dc.date.accessioned2020-10-22T08:12:46Z-
dc.date.available2020-10-22T08:12:46Z-
dc.date.issued2020-
dc.identifier.citationClinical Infectious Diseases, 2020, v. 71 n. 16, p. 2139-2149-
dc.identifier.issn1058-4838-
dc.identifier.urihttp://hdl.handle.net/10722/289445-
dc.description.abstractBackground: Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is believed to be mostly transmitted by medium- to large-sized respiratory droplets, although airborne transmission may be possible in healthcare settings involving aerosol-generating procedures. Exposure to respiratory droplets can theoretically be reduced by surgical mask usage. However, there is a lack of experimental evidence supporting surgical mask usage for prevention of COVID-19. Methods: We used a well-established golden Syrian hamster SARS-CoV-2 model. We placed SARS-CoV-2-challenged index hamsters and naive hamsters into closed system units each comprising 2 different cages separated by a polyvinyl chloride air porous partition with unidirectional airflow within the isolator. The effect of a surgical mask partition placed between the cages was investigated. Besides clinical scoring, hamster specimens were tested for viral load, histopathology, and viral nucleocapsid antigen expression. Results: Noncontact transmission was found in 66.7% (10/15) of exposed naive hamsters. Surgical mask partition for challenged index or naive hamsters significantly reduced transmission to 25% (6/24, P = .018). Surgical mask partition for challenged index hamsters significantly reduced transmission to only 16.7% (2/12, P = .019) of exposed naive hamsters. Unlike the severe manifestations of challenged hamsters, infected naive hamsters had lower clinical scores, milder histopathological changes, and lower viral nucleocapsid antigen expression in respiratory tract tissues. Conclusions: SARS-CoV-2 could be transmitted by respiratory droplets or airborne droplet nuclei which could be reduced by surgical mask partition in the hamster model. This is the first in vivo experimental evidence to support the possible benefit of surgical mask in prevention of COVID-19 transmission, especially when masks were worn by infected individuals.-
dc.languageeng-
dc.publisherOxford University Press. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/cid/-
dc.relation.ispartofClinical Infectious Diseases-
dc.rightsPre-print: Journal Title] ©: [year] [owner as specified on the article] Published by Oxford University Press [on behalf of xxxxxx]. All rights reserved. Pre-print (Once an article is published, preprint notice should be amended to): This is an electronic version of an article published in [include the complete citation information for the final version of the Article as published in the print edition of the Journal.] Post-print: This is a pre-copy-editing, author-produced PDF of an article accepted for publication in [insert journal title] following peer review. The definitive publisher-authenticated version [insert complete citation information here] is available online at: xxxxxxx [insert URL that the author will receive upon publication here].-
dc.subjectcoronavirus-
dc.subjectCOVID-19-
dc.subjectSARS-CoV-2-
dc.subjectmask-
dc.subjecttransmission-
dc.titleSurgical Mask Partition Reduces the Risk of Noncontact Transmission in a Golden Syrian Hamster Model for Coronavirus Disease 2019 (COVID-19)-
dc.typeArticle-
dc.identifier.emailChan, JFW: jfwchan@hku.hk-
dc.identifier.emailYuan, S: yuansf@hku.hk-
dc.identifier.emailZhang, AJ: zhangajx@hkucc.hku.hk-
dc.identifier.emailPoon, VKM: vinpoon@hku.hk-
dc.identifier.emailChan, CCS: cschan@hku.hk-
dc.identifier.emailLee, ACY: cyalee@hku.hk-
dc.identifier.emailFan, Z: fanzm@HKUCC-COM.hku.hk-
dc.identifier.emailLi, C: canlee@hku.hk-
dc.identifier.emailLiang, R: liangrh@HKUCC-COM.hku.hk-
dc.identifier.emailTang, K: kmtang20@hku.hk-
dc.identifier.emailLuo, C: cuiting@hku.hk-
dc.identifier.emailCheng, VCC: vcccheng@hkucc.hku.hk-
dc.identifier.emailCai, JP: caijuice@hku.hk-
dc.identifier.emailChu, H: hinchu@hku.hk-
dc.identifier.emailChan, KH: chankh2@hkucc.hku.hk-
dc.identifier.emailTo, KKW: kelvinto@hku.hk-
dc.identifier.emailSridhar, S: sid8998@hku.hk-
dc.identifier.emailYuen, KY: kyyuen@hkucc.hku.hk-
dc.identifier.authorityChan, JFW=rp01736-
dc.identifier.authorityYuan, S=rp02640-
dc.identifier.authorityZhang, AJ=rp00413-
dc.identifier.authorityChu, H=rp02125-
dc.identifier.authorityChan, KH=rp01921-
dc.identifier.authorityTo, KKW=rp01384-
dc.identifier.authoritySridhar, S=rp02249-
dc.identifier.authorityYuen, KY=rp00366-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1093/cid/ciaa644-
dc.identifier.pmid32472679-
dc.identifier.pmcidPMC7314229-
dc.identifier.scopuseid_2-s2.0-85096509214-
dc.identifier.hkuros317198-
dc.identifier.volume71-
dc.identifier.issue16-
dc.identifier.spage2139-
dc.identifier.epage2149-
dc.identifier.isiWOS:000595479200017-
dc.publisher.placeUnited States-
dc.identifier.issnl1058-4838-

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