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Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion

ABSTRACTS: BACKGROUND: Highly pathogenic avian influenza A virus has been shown to infect organs other than the lung, and this is likely to be mediated by systemic spread resulting from viremia which has been detected in blood in severe cases of infection with avian H5N1 viruses. The infectivity of...

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Autores principales: Wang, Xue, Tan, Jiying, Zhao, Jiangqin, Ye, Zhiping, Hewlett, Indira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101865/
https://www.ncbi.nlm.nih.gov/pubmed/24712669
http://dx.doi.org/10.1186/1471-2334-14-192
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author Wang, Xue
Tan, Jiying
Zhao, Jiangqin
Ye, Zhiping
Hewlett, Indira
author_facet Wang, Xue
Tan, Jiying
Zhao, Jiangqin
Ye, Zhiping
Hewlett, Indira
author_sort Wang, Xue
collection PubMed
description ABSTRACTS: BACKGROUND: Highly pathogenic avian influenza A virus has been shown to infect organs other than the lung, and this is likely to be mediated by systemic spread resulting from viremia which has been detected in blood in severe cases of infection with avian H5N1 viruses. The infectivity of virus in blood and the potential for virus transmission by transfusion has not been investigated. METHODS: Using a susceptible ferret animal model, we evaluated viremia and transmission by blood transfusion. Blood was collected on day 2, 4, 6, and 10 post-infection (or before death) from donor ferrets infected with either low dose (1.0 × 10(2.6) EID(50)/ml) or high dose (1.0 × 10(3.6) EID(50)/ml) of H5N1 virus, A/VN/1203/04 and transfused to recipient animals. RESULTS: Viremia was observed in 2/12 (16.67%) recipients that received blood from donor ferrets infected with low dose and 7/12 (58.33%) recipients who received blood from high dose infected donors. 1/12 (8.3%) low dose recipients and 6/12 (50%) high dose recipients died within 11 days after transfusion. Increased changes in body weight and temperatures were observed in high dose recipients, and high levels of viral RNA were detected in recipient ferrets after transfusion of blood from the early viremic phase, which also correlated with adverse impact on their survival. CONCLUSION: These data suggest that highly pathogenic avian influenza A virus, H5N1, is transmissible by blood transfusion in ferrets. Low levels of viremia were detected around the time of onset of symptoms and later in ferrets infected with highly pathogenic H5N1 virus. These findings may have implication for pathogenesis and transmissibility of H5N1.
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spelling pubmed-41018652014-07-18 Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion Wang, Xue Tan, Jiying Zhao, Jiangqin Ye, Zhiping Hewlett, Indira BMC Infect Dis Research Article ABSTRACTS: BACKGROUND: Highly pathogenic avian influenza A virus has been shown to infect organs other than the lung, and this is likely to be mediated by systemic spread resulting from viremia which has been detected in blood in severe cases of infection with avian H5N1 viruses. The infectivity of virus in blood and the potential for virus transmission by transfusion has not been investigated. METHODS: Using a susceptible ferret animal model, we evaluated viremia and transmission by blood transfusion. Blood was collected on day 2, 4, 6, and 10 post-infection (or before death) from donor ferrets infected with either low dose (1.0 × 10(2.6) EID(50)/ml) or high dose (1.0 × 10(3.6) EID(50)/ml) of H5N1 virus, A/VN/1203/04 and transfused to recipient animals. RESULTS: Viremia was observed in 2/12 (16.67%) recipients that received blood from donor ferrets infected with low dose and 7/12 (58.33%) recipients who received blood from high dose infected donors. 1/12 (8.3%) low dose recipients and 6/12 (50%) high dose recipients died within 11 days after transfusion. Increased changes in body weight and temperatures were observed in high dose recipients, and high levels of viral RNA were detected in recipient ferrets after transfusion of blood from the early viremic phase, which also correlated with adverse impact on their survival. CONCLUSION: These data suggest that highly pathogenic avian influenza A virus, H5N1, is transmissible by blood transfusion in ferrets. Low levels of viremia were detected around the time of onset of symptoms and later in ferrets infected with highly pathogenic H5N1 virus. These findings may have implication for pathogenesis and transmissibility of H5N1. BioMed Central 2014-04-08 /pmc/articles/PMC4101865/ /pubmed/24712669 http://dx.doi.org/10.1186/1471-2334-14-192 Text en Copyright © 2014 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Xue
Tan, Jiying
Zhao, Jiangqin
Ye, Zhiping
Hewlett, Indira
Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title_full Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title_fullStr Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title_full_unstemmed Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title_short Highly pathogenic avian influenza A virus (H5N1) can be transmitted in ferrets by transfusion
title_sort highly pathogenic avian influenza a virus (h5n1) can be transmitted in ferrets by transfusion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101865/
https://www.ncbi.nlm.nih.gov/pubmed/24712669
http://dx.doi.org/10.1186/1471-2334-14-192
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