๐ Spike protein fusion peptide and feline coronavirus virulence
Coronaviruses are well known for their potential to change their host or tissue tropism, resulting in unpredictable new diseases and changes in pathogenicity; severe acute respiratory syndrome and feline coronaviruses, respectively, are the most recognized examples. Feline coronaviruses occur as 2 pathotypes: nonvirulent feline enteric coronaviruses (FECVs), which replicate in intestinal epithelium cells, and lethal feline infectious peritonitis viruses (FIPVs), which replicate in macrophages. Evidence indicates that FIPV originates from FECV by mutation, but consistent distinguishing differences have not been established. We sequenced the full genome of 11 viruses of each pathotype and then focused on the single most distinctive site by additionally sequencing hundreds of viruses in that region. As a result, we identifi ed 2 alternative amino acid differences in the putative fusion peptide of the spike protein that together distinguish FIPV from FECV in >95% of cases. By these and perhaps other mutations, the virus apparently acquires its macrophage tropism and spreads systemically.
keywords
๐ severe acute (1373)
๐ spike protein (353)
๐ amino acid (454)
๐ infectious peritonitis (181)
๐ peritonitis virus (67)
๐ feline infectious (145)
๐ enteric coronavirus (111)
๐ feline coronavirus (148)
๐ respiratory syndrome (2004)
๐ acute respiratory (1734)
author
๐ค Chang, Hui Wen
๐ค Egberink, Herman F.
๐ค Halpin, Rebecca
๐ค Spiro, David J.
๐ค Rottie, Peter J.M.
year
โฐ 2012
issn
๐ 10806040 10806059
volume
18
number
7
page
1089-1095
citedbycount
66
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