Consejo Nacional de Investigaciones Científicas y Tecnológicas, Buenos Aires, Argentina, 1425.
Consejo Nacional de Investigaciones Científicas y Tecnológicas, Buenos Aires, Argentina, 1425; Instituto Nacional de Tecnología Agropecuaria, Instituto de Virología, Buenos Aires, Argentina, 1686.
J Dairy Sci. 2018 Jul;101(7):6366-6374. doi: 10.3168/jds.2017-14253. Epub 2018 Apr 11.
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.
牛白血病病毒(BLV)前病毒 DNA 的检测是确定动物是否感染 BLV 的重要工具。与血清学检测相比,实时 PCR 具有更高的灵敏度,可作为澄清不确定或不一致的血清学检测结果的确证性检测。然而,实时 PCR 检测的高成本限制了它们在 BLV 监测和根除计划中的系统纳入。本研究的目的是验证一种低成本的定量实时 PCR。有趣的是,通过使用 SYBR Green 检测染料,与大多数基于荧光探针(即 TaqMan 技术)的常见检测相比,我们能够将单个反应的成本降低 5 倍。这种方法允许从纯化的外周血白细胞和牛奶基质中高度敏感和特异性地检测和定量 BLV 前病毒 DNA。由于其简单性和低成本,我们的内部 BLV SYBR 定量实时 PCR 可以用作 BLV 控制计划中的筛选或确证性检测。