Detection of avian leukosis virus subgroup J using the polymerase chain reaction

被引:60
|
作者
Smith, EJ [1 ]
Williams, SM [1 ]
Fadly, AM [1 ]
机构
[1] ARS, USDA, Avian Dis & Oncol Lab, E Lansing, MI 48823 USA
关键词
myeloid leukosis; primers; amplification; infection; avian leukosis virus;
D O I
10.2307/1592488
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
A polymerase chain reaction (PCR) assay was developed for the detection of avian leukosis virus strain J (ALV-J) in chickens. Primers were based in the E element and the 3' terminus of the long terminal repeat of proviral ALV-J. PCR products were amplified from genomic DNA extracted from chicken embryo fibroblasts (CEF) infected with either strain HPRS-103, the prototype of ALV-J, or field isolates of ALV-J obtained from broiler breeder hocks in the United States that exhibited myeloid leukosis. The newly developed PCR detected ALV-J in DNA prepared from CEF inoculated with ALV-J but not from CEF inoculated with subgroup A, B, C, D, or E. The PCR also detected ALV-J in DNA prepared from blood, combs, and toes obtained from chickens experimentally infected with ALV-J and in DNA obtained from peripheral blood monocytes from naturally infected broiler breeder chickens. The PCR described here offers a specific and sensitive alternative to conventional virus isolation tests for ALV-J.
引用
收藏
页码:375 / 380
页数:6
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