Büyüktanir Ozlem, Yildirim Tuba, Yakicier Cengiz, Genç Oktay, Yurdusev Nevzat
Ondokuz Mayis University, Faculty of Veterinary Medicine, Department of Microbiology, 55139 Kurupelit, Samsun, Turkey.
Vet Microbiol. 2008 May 25;129(1-2):139-49. doi: 10.1016/j.vetmic.2007.11.028. Epub 2007 Dec 4.
Mycoplasma gallisepticum is the primary agent of chronic respiratory disease causing important economic losses in the poultry industry. Serological monitoring is essential to maintain mycoplasma-free breeder flocks and often complicated by the cross-reactions between different mycoplasma species. To overcome serological cross-reactions, a large fragment of the M. gallisepticum PvpA cytadhesin, species-specific surface-exposed protein, was produced in E. coli as a recombinant protein (rPvpA336) and used as a potential diagnostic antigen. The rPvpA336 protein possesses 336 mycoplasma-specific amino acids with relative molecular weight of 44 kDa. A deletion region of 37 amino acids was identified when compared to the wild-type PvpA protein. Immunoreactivity of the rPvpA336 protein has been demonstrated by Western blot analysis with M. gallisepticum-positive and -negative chicken sera. Furthermore, an enzymatic rapid immunofiltration assay (ERIFA) prototype based on the rPvpA336 protein has been developed and its species-specific detection capability has been demonstrated by using M. gallisepticum and/or M. synoviae-positive and -negative chicken sera. In addition to its species-specificity, the ERIFA prototype presents certain advantages such as rapidity, field-applicability and cost-effectiveness. Therefore, these advantages would make the prototype a species-specific rapid diagnostic tool of choice in the field and limited laboratory conditions for screening M. gallisepticum infections.
鸡毒支原体是慢性呼吸道疾病的主要病原体,给家禽业造成了重大经济损失。血清学监测对于维持无支原体种鸡群至关重要,但常因不同支原体物种之间的交叉反应而变得复杂。为了克服血清学交叉反应,鸡毒支原体PvpA细胞粘附素(一种物种特异性表面暴露蛋白)的大片段在大肠杆菌中作为重组蛋白(rPvpA336)产生,并用作潜在的诊断抗原。rPvpA336蛋白含有336个支原体特异性氨基酸,相对分子质量为44 kDa。与野生型PvpA蛋白相比,确定了一个37个氨基酸的缺失区域。通过用鸡毒支原体阳性和阴性鸡血清进行蛋白质印迹分析,证明了rPvpA336蛋白的免疫反应性。此外,还开发了一种基于rPvpA336蛋白的酶促快速免疫过滤测定(ERIFA)原型,并通过使用鸡毒支原体和/或滑膜支原体阳性和阴性鸡血清证明了其物种特异性检测能力。除了具有物种特异性外,ERIFA原型还具有快速、现场适用性和成本效益等优点。因此,这些优点将使该原型成为在现场和有限实验室条件下筛查鸡毒支原体感染的物种特异性快速诊断工具的首选。