Zhou Yan-ping, Wu Zhong-dao, Yang Lin-lin, Sun Xi, You Xu, Yu Xin-bing, Hu Wei, Zheng Huan-qin, Lv Zhi-yue
Department of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Parasitol Res. 2009 Oct;105(5):1435-44. doi: 10.1007/s00436-009-1575-x. Epub 2009 Jul 29.
Saliva has been suggested as an easily accessible and a noninvasive diagnostic alternative for detection of antibodies. To identify and characterize Schistosoma japonicum (S. japonicum) antigens that are recognized by saliva of infected host, we have used a pool of saliva from infected patients to immunoscreen an egg cDNA library of S. japonicum. The open reading frame of the isolated two clones encodes same protein of 116 amino acids exhibiting 100% identity to an amino acid sequence (AY222893) of S. japonicum in NCBInr database. The protein encoded is inferred a secretory protein with a molecular mass of 13 kDa (Sj13) and shares no homology to any entries in the NCBInr database, demonstrating that Sj13 might be a schistosome-specific protein. Reverse transcriptase polymerase chain reaction, Western blotting, and immunolocalization analysis revealed Sj13 could be detected in cercaria, adult, and egg and was localized to forehead and tegument of cercaria, cell body ("cytons") of adult worm, egg shell, and epidermal plate of miracidium. Furthermore, Sj13 showed a good antigenicity when reacted with saliva or serum from schistosomiasis patients. The recombinant Sj13 (rSj13) expressed and purified from Escherichia coli was applied to detect its specific salivary antibody for schistosomiasis diagnosis by an indirect enzyme linked immunosorbent assay (ELISA). Preliminary laboratory test of 116 subjects, 40 with parasitologically proven S. japonicumm infection, 46 with other infectious diseases, and 30 negative controls exhibited 92.50% sensitivity with saliva/rSj13 and 95.00% with serum/SWAP (P > 0.05). The specificity of the ELISA using saliva/rSj13 was 92.11% versus 85.53% with serum/SWAP (P < 0.05). No direct correlations of anti-Sj13 IgG levels with egg counts in stool were observed in saliva detection. These results suggest that Sj13 specific salivary antibody detection may be useful as an antigen for the salivary diagnosis of schistosomiasis japonica and contribute to epidemiological study of schistosomiasis infection in endemic areas.
唾液已被认为是一种易于获取且非侵入性的抗体检测诊断替代方法。为了鉴定和表征受感染宿主唾液所识别的日本血吸虫抗原,我们使用来自感染患者的唾液池对日本血吸虫卵cDNA文库进行免疫筛选。分离出的两个克隆的开放阅读框编码相同的116个氨基酸的蛋白质,与NCBInr数据库中日本血吸虫的一个氨基酸序列(AY222893)具有100%的同一性。推测所编码的蛋白质是一种分子量为13 kDa的分泌蛋白(Sj13),并且与NCBInr数据库中的任何条目均无同源性,这表明Sj13可能是一种血吸虫特异性蛋白。逆转录聚合酶链反应、蛋白质印迹和免疫定位分析显示,Sj13可在尾蚴、成虫和虫卵中检测到,并定位于尾蚴的头部和体表、成虫的细胞体(“胞体”)、卵壳和毛蚴的表皮板。此外,Sj13与血吸虫病患者的唾液或血清反应时显示出良好的抗原性。从大肠杆菌中表达和纯化的重组Sj13(rSj13)用于通过间接酶联免疫吸附测定(ELISA)检测其针对血吸虫病诊断的特异性唾液抗体。对116名受试者进行的初步实验室检测,其中40名经寄生虫学证实感染日本血吸虫,46名患有其他传染病,30名作为阴性对照,唾液/rSj13检测的敏感性为92.50%,血清/SWAP检测的敏感性为95.00%(P>0.05)。使用唾液/rSj13的ELISA特异性为92.11%,而血清/SWAP为85.53%(P<0.05)。在唾液检测中未观察到抗Sj13 IgG水平与粪便虫卵计数之间的直接相关性。这些结果表明,Sj13特异性唾液抗体检测作为日本血吸虫病唾液诊断的一种抗原可能是有用的,并有助于流行地区血吸虫病感染的流行病学研究。