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Generation of a recombinant temperature-sensitive influenza D virus

Influenza D virus (IDV) is a causative agent of the bovine respiratory disease complex (BRDC), which is the most common and costly disease affecting the cattle industry. For developing a candidate vaccine virus against IDV, we sought to produce a temperature-sensitive strain, similar to the live att...

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Autores principales: Ishida, Hiroho, Murakami, Shin, Kamiki, Haruhiko, Matsugo, Hiromichi, Katayama, Misa, Sekine, Wataru, Ohira, Kosuke, Takenaka-Uema, Akiko, Horimoto, Taisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992382/
https://www.ncbi.nlm.nih.gov/pubmed/36882459
http://dx.doi.org/10.1038/s41598-023-30942-z
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author Ishida, Hiroho
Murakami, Shin
Kamiki, Haruhiko
Matsugo, Hiromichi
Katayama, Misa
Sekine, Wataru
Ohira, Kosuke
Takenaka-Uema, Akiko
Horimoto, Taisuke
author_facet Ishida, Hiroho
Murakami, Shin
Kamiki, Haruhiko
Matsugo, Hiromichi
Katayama, Misa
Sekine, Wataru
Ohira, Kosuke
Takenaka-Uema, Akiko
Horimoto, Taisuke
author_sort Ishida, Hiroho
collection PubMed
description Influenza D virus (IDV) is a causative agent of the bovine respiratory disease complex (BRDC), which is the most common and costly disease affecting the cattle industry. For developing a candidate vaccine virus against IDV, we sought to produce a temperature-sensitive strain, similar to the live attenuated, cold-adapted vaccine strain available against the influenza A virus (IAV). To this end, we produced a recombinant IDV (designated rD/OK-AL) strain by introducing mutations responsible for the adaptation of the IAV vaccine strain to cold conditions and conferring sensitivity to high temperatures into PB2 and PB1 proteins using reverse genetics. The rD/OK-AL strain grew efficiently at 33 °C but did not grow at 37 °C in the cell culture, indicating its high-temperature sensitivity. In mice, rD/OK-AL was attenuated following intranasal inoculation. It mediated the production of high levels of antibodies against IDV in the serum. When the rD/OK-AL-inoculated mice were challenged with the wild-type virus, the virus was not detected in respiratory organs after the challenge, indicating complete protection against IDV. These results imply that the rD/OK-AL might be a potential candidate for the development of live attenuated vaccines for IDV that can be used to control BRDC.
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spelling pubmed-99923822023-03-09 Generation of a recombinant temperature-sensitive influenza D virus Ishida, Hiroho Murakami, Shin Kamiki, Haruhiko Matsugo, Hiromichi Katayama, Misa Sekine, Wataru Ohira, Kosuke Takenaka-Uema, Akiko Horimoto, Taisuke Sci Rep Article Influenza D virus (IDV) is a causative agent of the bovine respiratory disease complex (BRDC), which is the most common and costly disease affecting the cattle industry. For developing a candidate vaccine virus against IDV, we sought to produce a temperature-sensitive strain, similar to the live attenuated, cold-adapted vaccine strain available against the influenza A virus (IAV). To this end, we produced a recombinant IDV (designated rD/OK-AL) strain by introducing mutations responsible for the adaptation of the IAV vaccine strain to cold conditions and conferring sensitivity to high temperatures into PB2 and PB1 proteins using reverse genetics. The rD/OK-AL strain grew efficiently at 33 °C but did not grow at 37 °C in the cell culture, indicating its high-temperature sensitivity. In mice, rD/OK-AL was attenuated following intranasal inoculation. It mediated the production of high levels of antibodies against IDV in the serum. When the rD/OK-AL-inoculated mice were challenged with the wild-type virus, the virus was not detected in respiratory organs after the challenge, indicating complete protection against IDV. These results imply that the rD/OK-AL might be a potential candidate for the development of live attenuated vaccines for IDV that can be used to control BRDC. Nature Publishing Group UK 2023-03-07 /pmc/articles/PMC9992382/ /pubmed/36882459 http://dx.doi.org/10.1038/s41598-023-30942-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Ishida, Hiroho
Murakami, Shin
Kamiki, Haruhiko
Matsugo, Hiromichi
Katayama, Misa
Sekine, Wataru
Ohira, Kosuke
Takenaka-Uema, Akiko
Horimoto, Taisuke
Generation of a recombinant temperature-sensitive influenza D virus
title Generation of a recombinant temperature-sensitive influenza D virus
title_full Generation of a recombinant temperature-sensitive influenza D virus
title_fullStr Generation of a recombinant temperature-sensitive influenza D virus
title_full_unstemmed Generation of a recombinant temperature-sensitive influenza D virus
title_short Generation of a recombinant temperature-sensitive influenza D virus
title_sort generation of a recombinant temperature-sensitive influenza d virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992382/
https://www.ncbi.nlm.nih.gov/pubmed/36882459
http://dx.doi.org/10.1038/s41598-023-30942-z
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