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Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes
Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) causes SARS. The pathogenic mechanisms of SARS-CoV remain poorly understood. Six cynomolgus monkeys were inoculated with the HKU39849 isolate of SARS-CoV via four routes. After intranasal inoculation, the virus was isolated from res...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2517337/ https://www.ncbi.nlm.nih.gov/pubmed/18039277 http://dx.doi.org/10.1111/j.1365-2613.2007.00567.x |
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author | Nagata, Noriyo Iwata, Naoko Hasegawa, Hideki Sato, Yuko Morikawa, Shigeru Saijo, Masayuki Itamura, Shigeyuki Saito, Takehiko Ami, Yasushi Odagiri, Takato Tashiro, Masato Sata, Tetsutaro |
author_facet | Nagata, Noriyo Iwata, Naoko Hasegawa, Hideki Sato, Yuko Morikawa, Shigeru Saijo, Masayuki Itamura, Shigeyuki Saito, Takehiko Ami, Yasushi Odagiri, Takato Tashiro, Masato Sata, Tetsutaro |
author_sort | Nagata, Noriyo |
collection | PubMed |
description | Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) causes SARS. The pathogenic mechanisms of SARS-CoV remain poorly understood. Six cynomolgus monkeys were inoculated with the HKU39849 isolate of SARS-CoV via four routes. After intranasal inoculation, the virus was isolated from respiratory swabs on days 2–7 postinoculation (p.i.) and virus genome was detected in intestinal tissues on day 7 p.i. Virus was not detected after intragastric inoculation. After intravenous inoculation, infectious virus was isolated from rectal swabs, and virus antigen was detected in intestinal cells on day 14 p.i. After intratracheal (i.t.) inoculation, virus antigen-positive alveolar cells and macrophages were found in lung and infectious virus was detected in lymphoid and intestinal tissues. The peribronchial lymph nodes showed evidence of an immune response. Lung tissue and/or fluid and/or the peribronchial lymph node of the intratracheally inoculated animals had high TNF-α, IL-8 and IL-12 levels. SARS lung lesions are only generated in monkeys by i.t. inoculation. The virus appears to spread into and perhaps via the intestinal and lymphatic systems. It has been suggested previously that viraemia may cause intestinal infections in SARS patients. |
format | Text |
id | pubmed-2517337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-25173372011-11-29 Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes Nagata, Noriyo Iwata, Naoko Hasegawa, Hideki Sato, Yuko Morikawa, Shigeru Saijo, Masayuki Itamura, Shigeyuki Saito, Takehiko Ami, Yasushi Odagiri, Takato Tashiro, Masato Sata, Tetsutaro Int J Exp Pathol Original Articles Severe acute respiratory syndrome-associated coronavirus (SARS-CoV) causes SARS. The pathogenic mechanisms of SARS-CoV remain poorly understood. Six cynomolgus monkeys were inoculated with the HKU39849 isolate of SARS-CoV via four routes. After intranasal inoculation, the virus was isolated from respiratory swabs on days 2–7 postinoculation (p.i.) and virus genome was detected in intestinal tissues on day 7 p.i. Virus was not detected after intragastric inoculation. After intravenous inoculation, infectious virus was isolated from rectal swabs, and virus antigen was detected in intestinal cells on day 14 p.i. After intratracheal (i.t.) inoculation, virus antigen-positive alveolar cells and macrophages were found in lung and infectious virus was detected in lymphoid and intestinal tissues. The peribronchial lymph nodes showed evidence of an immune response. Lung tissue and/or fluid and/or the peribronchial lymph node of the intratracheally inoculated animals had high TNF-α, IL-8 and IL-12 levels. SARS lung lesions are only generated in monkeys by i.t. inoculation. The virus appears to spread into and perhaps via the intestinal and lymphatic systems. It has been suggested previously that viraemia may cause intestinal infections in SARS patients. Blackwell Publishing Ltd 2007-12 /pmc/articles/PMC2517337/ /pubmed/18039277 http://dx.doi.org/10.1111/j.1365-2613.2007.00567.x Text en © 2007 The Authors Journal compilation © 2007 Blackwell Publishing Ltd |
spellingShingle | Original Articles Nagata, Noriyo Iwata, Naoko Hasegawa, Hideki Sato, Yuko Morikawa, Shigeru Saijo, Masayuki Itamura, Shigeyuki Saito, Takehiko Ami, Yasushi Odagiri, Takato Tashiro, Masato Sata, Tetsutaro Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title | Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title_full | Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title_fullStr | Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title_full_unstemmed | Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title_short | Pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
title_sort | pathology and virus dispersion in cynomolgus monkeys experimentally infected with severe acute respiratory syndrome coronavirus via different inoculation routes |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2517337/ https://www.ncbi.nlm.nih.gov/pubmed/18039277 http://dx.doi.org/10.1111/j.1365-2613.2007.00567.x |
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