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Publication : Osteopontin plays a pivotal role in increasing severity of respiratory syncytial virus infection.

First Author  Sampayo-Escobar V Year  2018
Journal  PLoS One Volume  13
Issue  4 Pages  e0192709
PubMed ID  29677209 Mgi Jnum  J:336826
Mgi Id  MGI:6154721 Doi  10.1371/journal.pone.0192709
Citation  Sampayo-Escobar V, et al. (2018) Osteopontin plays a pivotal role in increasing severity of respiratory syncytial virus infection. PLoS One 13(4):e0192709
abstractText  The molecular mechanisms underlying susceptibility to severe respiratory syncytial virus (RSV) infection remain poorly understood. Herein, we report on the role of osteopontin (OPN) in regulation of RSV infection in human epithelial cells and how interleukin-1 beta (IL-1beta), a cytokine secreted soon after RSV infection, when persistently expressed can induce OPN expression leading to increased viral infection. We first compared OPN expression in two human epithelial cell lines: HEK-293 and HEp-2. In contrast to HEp-2, HEK-293 expresses low levels of pro-caspase-1 resulting in decreased IL-1beta expression in response to RSV infection. We found a correlation between low IL-1beta levels and a delay in induction of OPN expression in RSV-infected HEK-293 cells compared to HEp-2. This phenomenon could partially explain the high susceptibility of HEp-2 cells to RSV infection versus the moderate susceptibility of HEK-293 cells. Also, HEK-293 cells expressing low levels of pro-caspase-1 exhibit decreased IL-1beta expression and delayed OPN expression in response to RSV infection. HEK-293 cells incubated with human rIL-1beta showed a dose-dependent increase in OPN expression upon RSV infection. Also, incubation with rOPN increased RSV viral load. Moreover, HEp-2 cells or mice infected with a mucogenic RSV strain RSV-L19F showed elevated levels of OPN in contrast to mice infected with the laboratory RSV strain rA2. This correlated with elevated levels of OPN following infection with RSV-L19F compared to rA2. Together, these results demonstrate that increased OPN expression is regulated in part by IL-1beta, and the interplay between IL-1beta and OPN signaling may play a pivotal role in the spread of RSV infection.
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