Quantification of bovine leukemia virus proviral DNA using a low-cost real-time polymerase chain reaction

被引:18
作者
Petersen, M., I [1 ]
Alvarez, I [1 ,2 ]
Trono, K. G. [1 ,2 ]
Jaworski, J. P. [1 ,2 ]
机构
[1] Consejo Nacl Invest Cient & Tecn, RA-1425 Buenos Aires, DF, Argentina
[2] Inst Nacl Tecnol Agr, Inst Virol, RA-1686 Buenos Aires, DF, Argentina
关键词
bovine leukemia virus; proviral DNA; real-time polymerase chain reaction; epidemiology; DAIRY-CATTLE; BLV; BLOOD; PCR;
D O I
10.3168/jds.2017-14253
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The detection of bovine leukemia virus (BLV) proviral DNA is an important tool to address whether an animal is infected with BLV. Compared with serological assays, real-time PCR accounts for greater sensitivity and can serve as a confirmatory test for the clarification of inconclusive or discordant serological test results. However, the high cost related to real-time PCR assays has limited their systematic inclusion in BLV surveillance and eradication programs. The aim of the present study was to validate a low-cost quantitative real-time PCR. Interestingly, by using SYBR Green detection dye, we were able to reduce the cost of a single reaction by a factor of 5 compared with most common assays based on the use of fluorogenic probes (i.e., TaqMan technology). This approach allowed a highly sensitive and specific detection and quantification of BLV proviral DNA from purified peripheral blood leukocytes and a milk matrix. Due to its simplicity and low cost, our in-house BLV SYBR quantitative real-time PCR might be used either as a screening or as a confirmatory test in BLV control programs.
引用
收藏
页码:6366 / 6374
页数:9
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