par Glineur, Stéphanie 
;Renshaw, Randall RW;Percopo, Caroline CM;Dyer, Kimberly KD;Dubovi, Edward EJ;Domachowske, Joseph JB;Rosenberg, Helene F.
Référence Virology, 443, 2, page (257-264)
Publication Publié, 2013-09
;Renshaw, Randall RW;Percopo, Caroline CM;Dyer, Kimberly KD;Dubovi, Edward EJ;Domachowske, Joseph JB;Rosenberg, Helene F.Référence Virology, 443, 2, page (257-264)
Publication Publié, 2013-09
Article révisé par les pairs
| Résumé : | A previous report of a novel pneumovirus (PnV) isolated from the respiratory tract of a dog described its significant homology to the rodent pathogen, pneumonia virus of mice (PVM). The original PnV-Ane4 pathogen replicated in and could be re-isolated in infectious state from mouse lung but elicited minimal mortality compared to PVM strain J3666. Here we assess phylogeny and physiologic responses to 10 new PnV isolates. The G/glycoprotein sequences of all PnVs include elongated amino-termini when compared to the characterized PVMs, and suggest division into groups A and B. While we observed significant differences in cytokine production and neutrophil recruitment to the lungs of BALB/c mice in response to survival doses (50 TCID50 units) of representative group A (114378-10-29-KY-F) and group B (7968-11-OK) PnVs, we observed no evidence for positive selection (dN > dS) among the PnV/PnV, PVM/PnV or PVM/PVM G/glycoprotein or F/fusion protein sequence pairs. |
