Noormohammadi Amir H, Markham Philip F, Markham Jillian F, Whithear Kevin G, Browning Glenn F
Microbiology (Reading). 1999 Aug;145 ( Pt 8):2087-2094. doi: 10.1099/13500872-145-8-2087.
Mycoplasma synoviae is a poultry pathogen causing respiratory disease and synovitis. A number of serological assays have been developed for diagnosis of M. synoviae infection; however, they lack sensitivity and/or are prone to false-positive reactions. Using a combination of PCR and expression cloning, four overlapping regions (regions 1-4) of the surface antigen MSPB of M. synoviae WVU-1853 were expressed in a bacterial expression system. Immunostaining of the resultant polypeptides with chicken sera raised against different M. synoviae strains, or Mycoplasma gallisepticum S6, suggested that region 4 contained a highly antigenic and species-specific domain (amino acids 212-317) [corrected] of MSPB. A fusion protein of region 4 was expressed in the pMAL expression system and purified from cold-osmotic-shock fluids of Escherichia coli cells for use in an indirect ELISA. The potential of the purified antigen for detection of M. synoviae antibodies was assessed with sera obtained from chickens experimentally infected with different strains of M. synoviae or M. gallisepticum, or from uninoculated chickens. All the sera from M. synoviae-inoculated chickens provided higher absorbance values than those from M. gallisepticum-inoculated or uninoculated chickens. Chickens inoculated with M. synoviae 86079/7NS had detectable increases of serum anti-MSPB immunoglobulins at day 7 after inoculation. These studies have identified the most antigenic region of one of the major species-specific surface proteins of M. synoviae, and shown the potential of this protein as a serodiagnostic reagent.
滑膜支原体是一种引起家禽呼吸道疾病和滑膜炎的病原体。已经开发了多种血清学检测方法用于诊断滑膜支原体感染;然而,它们缺乏敏感性和/或容易出现假阳性反应。通过聚合酶链反应(PCR)和表达克隆相结合的方法,滑膜支原体WVU-1853表面抗原MSPB的四个重叠区域(区域1-4)在细菌表达系统中得以表达。用针对不同滑膜支原体菌株或鸡毒支原体S6制备的鸡血清对所得多肽进行免疫染色,结果表明区域4包含MSPB的一个高度抗原性且种特异性的结构域(氨基酸212-317)[已校正]。区域4的融合蛋白在pMAL表达系统中表达,并从大肠杆菌细胞的冷渗透休克液中纯化,用于间接酶联免疫吸附测定(ELISA)。用从实验感染不同菌株的滑膜支原体或鸡毒支原体的鸡或未接种鸡获得的血清评估纯化抗原检测滑膜支原体抗体的潜力。所有接种滑膜支原体的鸡的血清所提供的吸光度值均高于接种鸡毒支原体或未接种鸡的血清。接种滑膜支原体86079/NS的鸡在接种后第7天血清抗MSPB免疫球蛋白有可检测到的增加。这些研究确定了滑膜支原体主要种特异性表面蛋白之一的最具抗原性的区域,并表明该蛋白作为血清学诊断试剂的潜力。