The Replicase Gene of Avian Coronavirus Infectious Bronchitis Virus Is a Determinant of Pathogenicity

被引:109
作者
Armesto, Maria
Cavanagh, Dave
Britton, Paul
机构
[1] Division of Microbiology, Institute for Animal Health, Compton Laboratory, Newbury, Berkshire, Compton
来源
PLOS ONE | 2009年 / 4卷 / 10期
基金
英国生物技术与生命科学研究理事会;
关键词
MOUSE HEPATITIS-VIRUS; DEFECTIVE RNAS; SPIKE PROTEIN; SEQUENCE; STRAINS; GENOME; EXPRESSION; IDENTIFICATION; PATHOGENESIS; BEAUDETTE;
D O I
10.1371/journal.pone.0007384
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have previously demonstrated that the replacement of the S gene from an avirulent strain (Beaudette) of infectious bronchitis virus (IBV) with an S gene from a virulent strain (M41) resulted in a recombinant virus (BeauR-M41(S)) with the in vitro cell tropism of the virulent virus but that was still avirulent. In order to investigate whether any of the other structural or accessory genes played a role in pathogenicity we have now replaced these from the Beaudette strain with those from M41. The recombinant IBV was in effect a chimaeric virus with the replicase gene derived from Beaudette and the rest of the genome from M41. This demonstrated that it is possible to exchange a large region of the IBV genome, approximately 8.4 kb, using our transient dominant selection method. Recovery of a viable recombinant IBV also demonstrated that it is possible to interchange a complete replicase gene as we had in effect replaced the M41 replicase gene with the Beaudette derived gene. Analysis of the chimaeric virus showed that it was avirulent indicating that none of the structural or accessory genes derived from a virulent isolate of IBV were able to restore virulence and that therefore, the loss of virulence associated with the Beaudette strain resides in the replicase gene.
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页数:11
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共 51 条
[1]   Identification of sequence changes responsible for the attenuation of avian infectious bronchitis virus strain Arkansas DPI [J].
Ammayappan, Arun ;
Upadhyay, Chitra ;
Gelb, Jack, Jr. ;
Vakharia, Vikram N. .
ARCHIVES OF VIROLOGY, 2009, 154 (03) :495-499
[2]  
[Anonymous], VIRUS TAXONOMY
[3]  
Armesto Maria, 2008, V454, P255, DOI 10.1007/978-1-59745-181-9_19
[4]   Development and use of the H strain of avian infectious bronchitis virus from the Netherlands as a vaccine: a review [J].
Bijlenga, G ;
Cook, JKA ;
Gelb, J ;
de Wit, JJ .
AVIAN PATHOLOGY, 2004, 33 (06) :550-557
[5]   A new DNA sequence assembly program [J].
Bonfield, JK ;
Smith, KF ;
Staden, R .
NUCLEIC ACIDS RESEARCH, 1995, 23 (24) :4992-4999
[6]   COMPLETION OF THE SEQUENCE OF THE GENOME OF THE CORONAVIRUS AVIAN INFECTIOUS-BRONCHITIS VIRUS [J].
BOURSNELL, MEG ;
BROWN, TDK ;
FOULDS, IJ ;
GREEN, PF ;
TOMLEY, FM ;
BINNS, MM .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :57-77
[7]   SEQUENCES OF THE NUCLEOCAPSID GENES FROM 2 STRAINS OF AVIAN INFECTIOUS-BRONCHITIS VIRUS [J].
BOURSNELL, MEG ;
BINNS, MM ;
FOULDS, IJ ;
BROWN, TDK .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 (MAR) :573-580
[8]   Generation of a recombinant avian coronavirus infectious bronchitis virus using transient dominant selection [J].
Britton, P ;
Evans, S ;
Dove, B ;
Davies, M ;
Casais, R ;
Cavanagh, D .
JOURNAL OF VIROLOGICAL METHODS, 2005, 123 (02) :203-211
[9]   Expression of bacteriophage T7 RNA polymerase in avian and mammalian cells by a recombinant fowlpox virus [J].
Britton, P ;
Green, P ;
Kottier, S ;
Mawditt, KL ;
Penzes, Z ;
Cavanagh, D ;
Skinner, MA .
JOURNAL OF GENERAL VIROLOGY, 1996, 77 :963-967
[10]  
Britton P, 2008, NIDOVIRUSES, P29