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Changes in specific cleavability of the Sendai virus fusion protein: implications for pathogenicity in mice

¹ Department of Virology, Jichi Medical School, Minami-Kawachi, Tochigi 329-04, Japan
² Department of Microbiology, California State University, Los Angeles, Los Angeles, California 90032-8205, U.S.A.
³ Institut für Virologie and Institut für Mikrobiologie und Molekularbiologie, Justut-Liebig-Universität Giessen, D-6300 Giessen
and⁴ Institut für Virologie, Philipps-Universität Marburg, D-3550 Marburg, Germany

Sendai virus mutants, KDe-21 and KDe-62, which had undergone multiple cycles of replication in Madin Darby canine kidney (MDCK) cells in the absence of exogenous proteases were isolated. The fusion (F) protein of the mutants regained proteolytic cleavability in MDCK cells and chick embryos, but the F protein remained non-cleavable in other cell lines. Unlike the F protein of wild-type (wt) virus, the mutant F was resistant to trypsin but was sensitive to elastase and, to a lesser extent, to chymotrypsin. Sequence analyses of the F gene and the F protein revealed an amino acid substitution at the cleavage site, Arg(116) to Ile, which conferred trypsin resistance and enhanced cleavability at Ile(116) by elastase and host proteases present in MDCK cells and in chicken embryos. In contrast to the pneumopathogenicity in mice of wt Sendai virus, the KDe mutants were non-pathogenic; cleavage activation of the F protein did not occur in the lungs and thereby infection was terminated after an initial cycle of replication.

Received 9 October 1991; accepted 28 January 1992.