Characterization of a recombinant canine coronavirus with a distinct receptor-binding (S1) domain

被引:43
作者
Regan, Andrew D. [1 ]
Millet, Jean K. [1 ]
Tse, Long Ping V. [1 ]
Chillag, Zach [1 ]
Rinaldi, Vera D. [1 ]
Licitra, Beth N. [1 ]
Dubovi, Edward J. [2 ]
Town, Christopher D. [3 ]
Whittaker, Gary R. [1 ]
机构
[1] Cornell Univ, Dept Microbiol & Immunol, Ctr Vet Med, Ithaca, NY 14853 USA
[2] Cornell Univ, Anim Hlth Diagnost Ctr, Coll Vet Med, Ithaca, NY 14853 USA
[3] J Craig Venter Sequencing Ctr, Rockville, MD USA
基金
美国国家卫生研究院;
关键词
Canine coronavirus; Spike protein; Receptor binding domain; Recombination; INFECTIOUS PERITONITIS VIRUS; MOLECULAR CHARACTERIZATION; AMINOPEPTIDASE-N; FELINE CORONAVIRUS; DIVERGENT; ENTRY; DETERMINANTS; PORCINE; DOG;
D O I
10.1016/j.virol.2012.04.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Canine alphacoronaviruses (CCoV) exist in two serotypes, type I and II, both of which can cause severe gastroenteritis. Here, we characterize a canine alphacoronavirus, designated CCoV-A76, first isolated in 1976. Serological studies show that CCoV-A76 is distinct from other CCoVs, such as the prototype CCoV-1-71. Efficient replication of CCoV-A76 is restricted to canine cell lines, in contrast to the prototypical type II strain CCoV-1-71 that more efficiently replicates in feline cells. CCoV-A76 can use canine aminopeptidase N (cAPN) receptor for infection of cells, but was unable to use feline APN (fAPN). In contrast, CCoV-1-71 can utilize both. Genomic analysis shows that CCoV-A76 possesses a distinct spike, which is the result of a recombination between type I and type II CCoV, that occurred between the N- and C-terminal domains (NTD and C-domain) of the Si subunit. These data suggest that CCoV-A76 represents a recombinant coronavirus form, with distinct host cell tropism. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:90 / 99
页数:10
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