Τίτλος:
Mouse respiratory epithelial cells support efficient replication of human rhinovirus
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Human rhinoviruses (HRV) are responsible for the majority of virus infections of the upper respiratory tract. Furthermore, HRV infection is associated with acute exacerbation of asthma and other chronic respiratory diseases of the lower respiratory tract. A small animal model of HRV-induced disease is required for the development of new therapies. However, existing mouse models of HRV infection are difficult to work with and until recently mouse cell lines were thought to be generally non-permissive for HRV replication in vitro. In this report we demonstrate that a virus of the minor receptor group, HRV1B, can infect and replicate in a mouse respiratory epithelial cell line (LA-4) more efficiently than in a mouse fibroblast cell line (L). The major receptor group virus HRV16 requires human intercellular adhesion molecule-1 (ICAM-1) for cell entry and therefore cannot infect LA-4 cells. However, transfection of in vitro-transcribed HRV16 RNA resulted in the replication of viral RNA and production of infectious virus. Expression of a chimeric ICAM-1 molecule, comprising mouse ICAM-1 with extracellular domains 1 and 2 replaced by the equivalent human domains, rendered the otherwise non-permissive mouse respiratory epithelial cell line susceptible to entry and efficient replication of HRV16. These observations suggest that the development of mouse models of respiratory tract infection by major as well as minor group HRV should be pursued.
Συγγραφείς:
Tuthill, T.J.
Papadopoulos, N.G.
Jourdan, P.
Challinor, L.J.
Sharp, N.A.
Plumpton, C.
Shah, K.
Barnard, S.
Dash, L.
Burnet, J.
Killington, R.A.
Rowlands, D.J.
Clarke, N.J.
Blair, E.D.
Johnston, S.L.
Περιοδικό:
Journal of General Virology
Λέξεις-κλειδιά:
intercellular adhesion molecule 1; virus receptor; virus RNA, animal cell; article; cell line; controlled study; epithelium cell; fibroblast culture; genetic transfection; human; human cell; Human rhinovirus; in vitro study; infection sensitivity; mouse; nonhuman; nucleotide sequence; priority journal; protein domain; protein expression; respiratory epithelium; respiratory tract infection; virus replication, Animals; Cell Line; Cytopathogenic Effect, Viral; Epithelial Cells; Hela Cells; Humans; Intercellular Adhesion Molecule-1; Mice; Recombinant Fusion Proteins; Respiratory System; Rhinovirus; RNA, Viral; Transfection; Virus Replication, Animalia; Human rhinovirus sp.; Rhinovirus; RNA viruses
DOI:
10.1099/vir.0.19109-0
