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Development of a murine model to study the pathogenesis of rotavirus infection
A murine model to study enteritis induced by bovine (BRV) and murine rotavirus (MRV) has been developed. The course of infection was determined by clinical symptoms of diarrhea and virus isolation as well as histopathological, immunohistochemical, and electron microscopic methods. Both isolates were...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
1989
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130208/ https://www.ncbi.nlm.nih.gov/pubmed/2553474 http://dx.doi.org/10.1016/0014-4800(89)90019-1 |
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author | Ijaz, M.K. Dent, D. Haines, D. Babiuk, L.A. |
author_facet | Ijaz, M.K. Dent, D. Haines, D. Babiuk, L.A. |
author_sort | Ijaz, M.K. |
collection | PubMed |
description | A murine model to study enteritis induced by bovine (BRV) and murine rotavirus (MRV) has been developed. The course of infection was determined by clinical symptoms of diarrhea and virus isolation as well as histopathological, immunohistochemical, and electron microscopic methods. Both isolates were able to replicate and produce clinical symptoms in neonatal mice. Rotavirus-free neonates were orally inoculated with MRV or BRV and observed over a 192-hr postinoculation (HPI) period. Following infection with 10(4) PFU of virus, diarrhea and maximal intestinal dysfunction, as measured by xylose absorption, did not occur until beyond 20 hr postinfection even though maximal virus production occurred at 10–15 HPI. Immunohistochemically and by electron microscopy we were able to demonstrate viral antigen and virus particles in the enterocytes of villous tips at 5–8 HPI. The appearance of diarrheal symptoms was dependent on the virus dose and the type of virus isolate inoculated. The disease could be induced with doses as low as 1 × 10(2) PFU/mouse of BRV and 1 × 10(1) PFU/mouse of MRV. On the basis of these results, MRV was found to be more virulent than BRV in this model. The model should prove useful for studies designed to assess rotavirus virulence genes and for vaccine protection studies. This work emphasizes the need for early sample collection for critical evaluation of any vaccine or antiviral agent using this model. |
format | Online Article Text |
id | pubmed-7130208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71302082020-04-08 Development of a murine model to study the pathogenesis of rotavirus infection Ijaz, M.K. Dent, D. Haines, D. Babiuk, L.A. Exp Mol Pathol Article A murine model to study enteritis induced by bovine (BRV) and murine rotavirus (MRV) has been developed. The course of infection was determined by clinical symptoms of diarrhea and virus isolation as well as histopathological, immunohistochemical, and electron microscopic methods. Both isolates were able to replicate and produce clinical symptoms in neonatal mice. Rotavirus-free neonates were orally inoculated with MRV or BRV and observed over a 192-hr postinoculation (HPI) period. Following infection with 10(4) PFU of virus, diarrhea and maximal intestinal dysfunction, as measured by xylose absorption, did not occur until beyond 20 hr postinfection even though maximal virus production occurred at 10–15 HPI. Immunohistochemically and by electron microscopy we were able to demonstrate viral antigen and virus particles in the enterocytes of villous tips at 5–8 HPI. The appearance of diarrheal symptoms was dependent on the virus dose and the type of virus isolate inoculated. The disease could be induced with doses as low as 1 × 10(2) PFU/mouse of BRV and 1 × 10(1) PFU/mouse of MRV. On the basis of these results, MRV was found to be more virulent than BRV in this model. The model should prove useful for studies designed to assess rotavirus virulence genes and for vaccine protection studies. This work emphasizes the need for early sample collection for critical evaluation of any vaccine or antiviral agent using this model. Published by Elsevier Inc. 1989-10 2004-04-11 /pmc/articles/PMC7130208/ /pubmed/2553474 http://dx.doi.org/10.1016/0014-4800(89)90019-1 Text en Copyright © 1989 Published by Elsevier Inc. 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 Ijaz, M.K. Dent, D. Haines, D. Babiuk, L.A. Development of a murine model to study the pathogenesis of rotavirus infection |
title | Development of a murine model to study the pathogenesis of rotavirus infection |
title_full | Development of a murine model to study the pathogenesis of rotavirus infection |
title_fullStr | Development of a murine model to study the pathogenesis of rotavirus infection |
title_full_unstemmed | Development of a murine model to study the pathogenesis of rotavirus infection |
title_short | Development of a murine model to study the pathogenesis of rotavirus infection |
title_sort | development of a murine model to study the pathogenesis of rotavirus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130208/ https://www.ncbi.nlm.nih.gov/pubmed/2553474 http://dx.doi.org/10.1016/0014-4800(89)90019-1 |
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