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Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice
BACKGROUND: Respiratory Syncytial Virus (RSV) infection is usually restricted to the respiratory epithelium. Few studies have documented the presence of RSV in the systemic circulation, however there is no consistent information whether virus detection in the blood correlates with disease severity....
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946301/ https://www.ncbi.nlm.nih.gov/pubmed/20843364 http://dx.doi.org/10.1186/1465-9921-11-125 |
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author | Torres, Juan Pablo Gomez, Ana M Khokhar, Shama Bhoj, Vijay G Tagliabue, Claudia Chang, Michael L Kiener, Peter A Revell, Paula A Ramilo, Octavio Mejias, Asuncion |
author_facet | Torres, Juan Pablo Gomez, Ana M Khokhar, Shama Bhoj, Vijay G Tagliabue, Claudia Chang, Michael L Kiener, Peter A Revell, Paula A Ramilo, Octavio Mejias, Asuncion |
author_sort | Torres, Juan Pablo |
collection | PubMed |
description | BACKGROUND: Respiratory Syncytial Virus (RSV) infection is usually restricted to the respiratory epithelium. Few studies have documented the presence of RSV in the systemic circulation, however there is no consistent information whether virus detection in the blood correlates with disease severity. METHODS: Balb/c mice were inoculated with live RSV, heat-inactivated RSV or medium. A subset of RSV-infected mice was treated with anti-RSV antibody 72 h post-inoculation. RSV RNA loads were measured by PCR in peripheral blood from day 1-21 post-inoculation and were correlated with upper and lower respiratory tract viral loads, the systemic cytokine response, lung inflammation and pulmonary function. Immunohistochemical staining was used to define the localization of RSV antigens in the respiratory tract and peripheral blood. RESULTS: RSV RNA loads were detected in peripheral blood from day 1 to 14 post-inoculation, peaked on day 5 and significantly correlated with nasal and lung RSV loads, airway obstruction, and blood CCL2 and CXCL1 expression. Treatment with anti-RSV antibody reduced blood RSV RNA loads and improved airway obstruction. Immunostaining identified RSV antigens in alveolar macrophages and peripheral blood monocytes. CONCLUSIONS: RSV RNA was detected in peripheral blood upon infection with live RSV, followed a time-course parallel to viral loads assessed in the respiratory tract and was significantly correlated with RSV-induced airway disease. |
format | Text |
id | pubmed-2946301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29463012010-09-28 Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice Torres, Juan Pablo Gomez, Ana M Khokhar, Shama Bhoj, Vijay G Tagliabue, Claudia Chang, Michael L Kiener, Peter A Revell, Paula A Ramilo, Octavio Mejias, Asuncion Respir Res Research BACKGROUND: Respiratory Syncytial Virus (RSV) infection is usually restricted to the respiratory epithelium. Few studies have documented the presence of RSV in the systemic circulation, however there is no consistent information whether virus detection in the blood correlates with disease severity. METHODS: Balb/c mice were inoculated with live RSV, heat-inactivated RSV or medium. A subset of RSV-infected mice was treated with anti-RSV antibody 72 h post-inoculation. RSV RNA loads were measured by PCR in peripheral blood from day 1-21 post-inoculation and were correlated with upper and lower respiratory tract viral loads, the systemic cytokine response, lung inflammation and pulmonary function. Immunohistochemical staining was used to define the localization of RSV antigens in the respiratory tract and peripheral blood. RESULTS: RSV RNA loads were detected in peripheral blood from day 1 to 14 post-inoculation, peaked on day 5 and significantly correlated with nasal and lung RSV loads, airway obstruction, and blood CCL2 and CXCL1 expression. Treatment with anti-RSV antibody reduced blood RSV RNA loads and improved airway obstruction. Immunostaining identified RSV antigens in alveolar macrophages and peripheral blood monocytes. CONCLUSIONS: RSV RNA was detected in peripheral blood upon infection with live RSV, followed a time-course parallel to viral loads assessed in the respiratory tract and was significantly correlated with RSV-induced airway disease. BioMed Central 2010 2010-09-15 /pmc/articles/PMC2946301/ /pubmed/20843364 http://dx.doi.org/10.1186/1465-9921-11-125 Text en Copyright ©2010 Torres 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 cited. |
spellingShingle | Research Torres, Juan Pablo Gomez, Ana M Khokhar, Shama Bhoj, Vijay G Tagliabue, Claudia Chang, Michael L Kiener, Peter A Revell, Paula A Ramilo, Octavio Mejias, Asuncion Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title | Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title_full | Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title_fullStr | Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title_full_unstemmed | Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title_short | Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice |
title_sort | respiratory syncytial virus (rsv) rna loads in peripheral blood correlates with disease severity in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946301/ https://www.ncbi.nlm.nih.gov/pubmed/20843364 http://dx.doi.org/10.1186/1465-9921-11-125 |
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