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Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens

In contrast to human influenza viruses that replicate in the respiratory tract and are airborne transmitted, avian viruses also replicate in gut epithelial cells and are transmitted via the fecal-oral route. On this route, the virus is exposed to destructive fluids of the digestive tract, which are...

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Autores principales: Han, Xuejiao, Bertzbach, Luca D., Veit, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126190/
https://www.ncbi.nlm.nih.gov/pubmed/31767100
http://dx.doi.org/10.1016/j.vetmic.2019.108462
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author Han, Xuejiao
Bertzbach, Luca D.
Veit, Michael
author_facet Han, Xuejiao
Bertzbach, Luca D.
Veit, Michael
author_sort Han, Xuejiao
collection PubMed
description In contrast to human influenza viruses that replicate in the respiratory tract and are airborne transmitted, avian viruses also replicate in gut epithelial cells and are transmitted via the fecal-oral route. On this route, the virus is exposed to destructive fluids of the digestive tract, which are acidic and contain the proteases pepsin (gizzard) or chymotrypsin and trypsin (intestine). Only the latter enzyme activates virus by cleaving hemagglutinin (HA) into HA(1) and HA(2) subunits. We mimicked the passage of viruses through the gastrointestinal tract by treating them with digestive fluids from chicken and determined titers and integrity of HA by western-blot. Gizzard fluid completely inactivated virions and degrades HA even at a high dilution, but only if the pH was kept acidic. If the fluid is diluted with neutral buffer (mimicking virus uptake with seawater) particles were more resistant. Virions containing an uncleaved HA were even activated suggesting that gastric juice contains a trypsin-like protease. Undiluted intestinal fluid inactivated particles and destroyed HA, but diluted fluid activated virions. A virus isolated from the duck´s intestine is more tolerant against intestinal fluid compared to fowl plague virus suggesting that the former is better adapted to grow in the intestine. We also demonstrate that influenza viruses replicate to high titers in a novel chicken epithelial gut cell line. While viruses with a monobasic HA cleavage site require addition of trypsin, these cells effectively process HA with a polybasic cleavage site, which could be blocked with an inhibitor of the cellular furin protease.
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spelling pubmed-71261902020-04-08 Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens Han, Xuejiao Bertzbach, Luca D. Veit, Michael Vet Microbiol Article In contrast to human influenza viruses that replicate in the respiratory tract and are airborne transmitted, avian viruses also replicate in gut epithelial cells and are transmitted via the fecal-oral route. On this route, the virus is exposed to destructive fluids of the digestive tract, which are acidic and contain the proteases pepsin (gizzard) or chymotrypsin and trypsin (intestine). Only the latter enzyme activates virus by cleaving hemagglutinin (HA) into HA(1) and HA(2) subunits. We mimicked the passage of viruses through the gastrointestinal tract by treating them with digestive fluids from chicken and determined titers and integrity of HA by western-blot. Gizzard fluid completely inactivated virions and degrades HA even at a high dilution, but only if the pH was kept acidic. If the fluid is diluted with neutral buffer (mimicking virus uptake with seawater) particles were more resistant. Virions containing an uncleaved HA were even activated suggesting that gastric juice contains a trypsin-like protease. Undiluted intestinal fluid inactivated particles and destroyed HA, but diluted fluid activated virions. A virus isolated from the duck´s intestine is more tolerant against intestinal fluid compared to fowl plague virus suggesting that the former is better adapted to grow in the intestine. We also demonstrate that influenza viruses replicate to high titers in a novel chicken epithelial gut cell line. While viruses with a monobasic HA cleavage site require addition of trypsin, these cells effectively process HA with a polybasic cleavage site, which could be blocked with an inhibitor of the cellular furin protease. Elsevier B.V. 2019-12 2019-10-18 /pmc/articles/PMC7126190/ /pubmed/31767100 http://dx.doi.org/10.1016/j.vetmic.2019.108462 Text en © 2019 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Han, Xuejiao
Bertzbach, Luca D.
Veit, Michael
Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title_full Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title_fullStr Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title_full_unstemmed Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title_short Mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
title_sort mimicking the passage of avian influenza viruses through the gastrointestinal tract of chickens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126190/
https://www.ncbi.nlm.nih.gov/pubmed/31767100
http://dx.doi.org/10.1016/j.vetmic.2019.108462
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