Respiratory Research (Sep 2010)

Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice

  • Torres Juan,
  • Gomez Ana M,
  • Khokhar Shama,
  • Bhoj Vijay G,
  • Tagliabue Claudia,
  • Chang Michael L,
  • Kiener Peter A,
  • Revell Paula A,
  • Ramilo Octavio,
  • Mejias Asuncion

DOI
https://doi.org/10.1186/1465-9921-11-125
Journal volume & issue
Vol. 11, no. 1
p. 125

Abstract

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Abstract 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.