Development and application of polymerase chain reaction (PCR) tests for the detection of subgroup J avian leukosis virus

被引:263
作者
Smith, LM
Brown, SR
Howes, K
McLeod, S
Arshad, SS
Barron, GS
Venugopal, K [1 ]
McKay, JC
Payne, LN
机构
[1] Inst Anim Hlth, Compton RG20 7NN, Berks, England
[2] Ross Breeders Ltd, Newbridge EH28 8SZ, Midlothian, Scotland
关键词
PCR; avian leukosis virus; Env gene retrovirus;
D O I
10.1016/S0168-1702(98)00022-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Subgroup J avian leukosis virus (ALV) is a recently identified avian retrovirus associated with myeloid leukosis in meat-type chickens. The env gene of the HPRS-103 strain of ALV, the prototype of this subgroup, differs considerably from that of other subgroups, but shows close homology to the env-like sequences of members of the EAV family of endogenous retroviruses. Polymerase chain reaction (PCR) tests using two sets of primers were developed for the specific detection of the members of this new subgroup along with another pair of primers for detecting other subgroup viruses. The specificity and sensitivity of this detection system was compared with the conventional detection methods in experimentally and naturally infected samples. The use of PCR was found to be rapid, specific and more sensitive than the conventional diagnostic tests for the detection of ALV. Moreover, the two subgroup J ALV-specific PCR tests were found to be capable of differentiating between 'prototype-like' viruses and more recent isolates which show extensive antigenic and sequence variations. The use of this test as a rapid and sensitive method of detection of viruses in epidemiological studies and eradication programs is discussed. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:87 / 98
页数:12
相关论文
共 18 条
[1]   DETECTION OF RETICULOENDOTHELIOSIS VIRUS-INFECTION USING THE POLYMERASE CHAIN-REACTION [J].
ALY, MM ;
SMITH, EJ ;
FADLY, AM .
AVIAN PATHOLOGY, 1993, 22 (03) :543-554
[2]   Tissue tropism of the HPRS-103 strain of J subgroup avian leukosis virus and of a derivative acutely transforming virus [J].
Arshad, SS ;
Howes, K ;
Barron, GS ;
Smith, LM ;
Russell, PH ;
Payne, LN .
VETERINARY PATHOLOGY, 1997, 34 (02) :127-137
[3]   SEQUENCE OF HOST-RANGE DETERMINANTS IN THE ENV GENE OF A FULL-LENGTH, INFECTIOUS PROVIRAL CLONE OF EXOGENOUS AVIAN-LEUKOSIS VIRUS HPRS-103 CONFIRMS THAT IT REPRESENTS A NEW SUBGROUP (DESIGNATED J) [J].
BAI, J ;
HOWES, K ;
PAYNE, LN ;
SKINNER, MA .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :181-187
[4]   HPRS-103 (EXOGENOUS AVIAN-LEUKOSIS VIRUS, SUBGROUP-J) HAS AN ENV GENE-RELATED TO THOSE OF ENDOGENOUS ELEMENTS EAV-0 AND E51 AND AN E-ELEMENT FOUND PREVIOUSLY ONLY IN SARCOMA-VIRUSES [J].
BAI, J ;
PAYNE, LN ;
SKINNER, MA .
JOURNAL OF VIROLOGY, 1995, 69 (02) :779-784
[5]   GENETIC-ANALYSIS OF THE ROUS-SARCOMA VIRUS SUBGROUP-D ENV GENE - MAMMAL TROPISM CORRELATES WITH TEMPERATURE SENSITIVITY OF GP85 [J].
BOVAHILL, C ;
OLSEN, JC ;
SWANSTROM, R .
JOURNAL OF VIROLOGY, 1991, 65 (04) :2073-2080
[6]   DETECTION OF AVIAN ONCOVIRUS GROUP-SPECIFIC ANTIGENS BY THE ENZYME-LINKED IMMUNOSORBENT-ASSAY [J].
CLARK, DP ;
DOUGHERTY, RM .
JOURNAL OF GENERAL VIROLOGY, 1980, 47 (APR) :283-291
[7]   A COMPARISON OF TEST MATERIALS FOR DIFFERENTIATING AVIAN-LEUKOSIS VIRUS GROUP-SPECIFIC ANTIGENS OF EXOGENOUS AND ENDOGENOUS ORIGIN [J].
CRITTENDEN, LB ;
SMITH, EJ .
AVIAN DISEASES, 1984, 28 (04) :1057-1070
[8]   TOUCHDOWN PCR TO CIRCUMVENT SPURIOUS PRIMING DURING GENE AMPLIFICATION [J].
DON, RH ;
COX, PT ;
WAINWRIGHT, BJ ;
BAKER, K ;
MATTICK, JS .
NUCLEIC ACIDS RESEARCH, 1991, 19 (14) :4008-4008
[9]  
FADLY A. M, 1989, LAB MANUAL ISOLATION, P135
[10]   Use of reverse transcriptase polymerase chain reaction for detection of vaccine contamination by avian leukosis virus [J].
Hauptli, D ;
Bruckner, L ;
Ottiger, HP .
JOURNAL OF VIROLOGICAL METHODS, 1997, 66 (01) :71-81