Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models

BACKGROUND: Influenza A virus causes respiratory disease in many animal species as well as in humans. Due to the high human-animal interface, the monitoring of canine influenza in dogs and the study of the transmission and pathogenicity of canine influenza in animals are important. METHODS: Eight-we...

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Published in:Virology Journal
Main Authors: Tangwangvivat, Ratanaporn, Chaiyawong, Supassama, Nonthabenjawan, Nutthawan, Charoenkul, Kamonpan, Janethanakit, Taveesak, Udom, Kitikhun, Kesdangsakonwut, Sawang, Tantilertcharoen, Rachod, Thontiravong, Aunyaratana, Amonsin, Alongkorn
Format: Text
Language:English
Published: BioMed Central 2022
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559841/
https://doi.org/10.1186/s12985-022-01888-x
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spelling ftpubmed:oai:pubmedcentral.nih.gov:9559841 2023-05-15T15:50:50+02:00 Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models Tangwangvivat, Ratanaporn Chaiyawong, Supassama Nonthabenjawan, Nutthawan Charoenkul, Kamonpan Janethanakit, Taveesak Udom, Kitikhun Kesdangsakonwut, Sawang Tantilertcharoen, Rachod Thontiravong, Aunyaratana Amonsin, Alongkorn 2022-10-12 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559841/ https://doi.org/10.1186/s12985-022-01888-x en eng BioMed Central http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559841/ http://dx.doi.org/10.1186/s12985-022-01888-x © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. CC0 PDM CC-BY Virol J Research Text 2022 ftpubmed https://doi.org/10.1186/s12985-022-01888-x 2022-10-16T01:05:11Z BACKGROUND: Influenza A virus causes respiratory disease in many animal species as well as in humans. Due to the high human-animal interface, the monitoring of canine influenza in dogs and the study of the transmission and pathogenicity of canine influenza in animals are important. METHODS: Eight-week-old beagle dogs (Canis lupus familaris) (n = 13) were used for the intraspecies transmission model. The dogs were inoculated intranasally with 1 ml of 10(6) EID(50) per ml of canine H3N2 influenza virus (A/canine/Thailand/CU-DC5299/2012) (CIV-H3N2). In addition, 4-week-old guinea pigs (Cavia porcellus) (n = 20) were used for the interspecies transmission model. The guinea pigs were inoculated intranasally with 300 µl of 10(6) EID(50) per ml of CIV-H3N2. RESULTS: For the Thai CIV-H3N2 challenged in the dog model, the incoculated and direct contact dogs developed respiratory signs at 2 dpi. The dogs shed the virus in the respiratory tract at 1 dpi and developed an H3-specific antibody against the virus at 10 dpi. Lung congestion and histopathological changes in the lung were observed. For the Thai CIV-H3N2 challenge in the guinea pig model, the incoculated, direct contact and aerosol-exposed guinea pigs developed fever at 1–2 dpi. The guinea pigs shed virus in the respiratory tract at 2 dpi and developed an H3-specific antibody against the virus at 7 dpi. Mild histopathological changes in the lung were observed. CONCLUSION: The result of this study demonstrated evidence of intraspecies and interspecies transmission of CIV-H3N2 in a mammalian model. Text Canis lupus PubMed Central (PMC) Virology Journal 19 1
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research
spellingShingle Research
Tangwangvivat, Ratanaporn
Chaiyawong, Supassama
Nonthabenjawan, Nutthawan
Charoenkul, Kamonpan
Janethanakit, Taveesak
Udom, Kitikhun
Kesdangsakonwut, Sawang
Tantilertcharoen, Rachod
Thontiravong, Aunyaratana
Amonsin, Alongkorn
Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
topic_facet Research
description BACKGROUND: Influenza A virus causes respiratory disease in many animal species as well as in humans. Due to the high human-animal interface, the monitoring of canine influenza in dogs and the study of the transmission and pathogenicity of canine influenza in animals are important. METHODS: Eight-week-old beagle dogs (Canis lupus familaris) (n = 13) were used for the intraspecies transmission model. The dogs were inoculated intranasally with 1 ml of 10(6) EID(50) per ml of canine H3N2 influenza virus (A/canine/Thailand/CU-DC5299/2012) (CIV-H3N2). In addition, 4-week-old guinea pigs (Cavia porcellus) (n = 20) were used for the interspecies transmission model. The guinea pigs were inoculated intranasally with 300 µl of 10(6) EID(50) per ml of CIV-H3N2. RESULTS: For the Thai CIV-H3N2 challenged in the dog model, the incoculated and direct contact dogs developed respiratory signs at 2 dpi. The dogs shed the virus in the respiratory tract at 1 dpi and developed an H3-specific antibody against the virus at 10 dpi. Lung congestion and histopathological changes in the lung were observed. For the Thai CIV-H3N2 challenge in the guinea pig model, the incoculated, direct contact and aerosol-exposed guinea pigs developed fever at 1–2 dpi. The guinea pigs shed virus in the respiratory tract at 2 dpi and developed an H3-specific antibody against the virus at 7 dpi. Mild histopathological changes in the lung were observed. CONCLUSION: The result of this study demonstrated evidence of intraspecies and interspecies transmission of CIV-H3N2 in a mammalian model.
format Text
author Tangwangvivat, Ratanaporn
Chaiyawong, Supassama
Nonthabenjawan, Nutthawan
Charoenkul, Kamonpan
Janethanakit, Taveesak
Udom, Kitikhun
Kesdangsakonwut, Sawang
Tantilertcharoen, Rachod
Thontiravong, Aunyaratana
Amonsin, Alongkorn
author_facet Tangwangvivat, Ratanaporn
Chaiyawong, Supassama
Nonthabenjawan, Nutthawan
Charoenkul, Kamonpan
Janethanakit, Taveesak
Udom, Kitikhun
Kesdangsakonwut, Sawang
Tantilertcharoen, Rachod
Thontiravong, Aunyaratana
Amonsin, Alongkorn
author_sort Tangwangvivat, Ratanaporn
title Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
title_short Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
title_full Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
title_fullStr Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
title_full_unstemmed Transmission and pathogenicity of canine H3N2 influenza virus in dog and guinea pig models
title_sort transmission and pathogenicity of canine h3n2 influenza virus in dog and guinea pig models
publisher BioMed Central
publishDate 2022
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559841/
https://doi.org/10.1186/s12985-022-01888-x
genre Canis lupus
genre_facet Canis lupus
op_source Virol J
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9559841/
http://dx.doi.org/10.1186/s12985-022-01888-x
op_rights © The Author(s) 2022
https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
op_rightsnorm CC0
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CC-BY
op_doi https://doi.org/10.1186/s12985-022-01888-x
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