Paliwal Sanjhi, Shanker Daya, Sudan Vikrant, Kumar Sanjeev, Srivastava Mukesh, Gupta Kapil Kumar
U P Pandit Deen Dayal Upadhyaya Pashu Chikitsa Vigyan Vishwavidyalaya Evam Go Anusandhan Sansthan (DUVASU), Mathura, 281001, India.
U P Pandit Deen Dayal Upadhyaya Pashu Chikitsa Vigyan Vishwavidyalaya Evam Go Anusandhan Sansthan (DUVASU), Mathura, 281001, India.
Biologicals. 2019 Jan;57:50-54. doi: 10.1016/j.biologicals.2018.12.004. Epub 2018 Dec 12.
The polymorphic nature of Theileria annulata merozoite surface antigen (TAMS 1) attributes to limitation in PCR based detection of various T. annulata genotypes present in different geographical domains across the globe. Multiple reports of failure of detection of tropical theileriosis using classical N516/517 primer set in the studied area were noticed. Hence, three single PCR protocols using N516/517, TAMS F/R and NTA F/R primer sets encoding different portions of TAMS 1 gene and two nested protocols, using combinations of these three primers, were compared to find out the most suitable primer set for diagnosis of calf theileriosis in studied area. The studied area constitutes the semi-arid theileriosis endemic area of Northern India. The various PCR protocols were tested on 75 clinically confirmed cases of calf theileriosis. Alongside, 25 confirmed theileriosis negative blood samples and DNA of other haemoprotozoa were also tested for specificity of these primer sets. Results revealed that the primer set NTA F/R to be more suitable in detecting the circulating T. annulata genotypes in the studied area in comparison to the classical N516/517 primer set. None of the primers gave false positive amplification with negative samples and/or DNA of other haemoprotozoa.
环形泰勒虫裂殖子表面抗原(TAMS 1)的多态性导致基于PCR检测全球不同地理区域存在的各种环形泰勒虫基因型受到限制。在研究区域,有多项报告指出使用经典的N516/517引物组未能检测到热带泰勒虫病。因此,比较了使用编码TAMS 1基因不同部分的N516/517、TAMS F/R和NTA F/R引物组的三种单重PCR方案,以及使用这三种引物组合的两种巢式PCR方案,以找出研究区域犊牛泰勒虫病诊断最合适的引物组。研究区域为印度北部半干旱泰勒虫病流行区。对75例临床确诊的犊牛泰勒虫病病例进行了各种PCR方案的检测。此外,还对25份确诊为泰勒虫病阴性的血样以及其他血液原虫的DNA进行检测,以验证这些引物组的特异性。结果显示,与经典的N516/517引物组相比,引物组NTA F/R在检测研究区域循环的环形泰勒虫基因型方面更合适。所有引物对阴性样本和/或其他血液原虫的DNA均未产生假阳性扩增。