Feng Jintao, Xu Rui, Zhang Xin, Han Yu, He Chuanchuan, Lu Chao, Hong Yang, Lu Ke, Li Hao, Jin Yamei, Lin Jiaojiao, Liu Jinming
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Animal Parasitology, Ministry of Agriculture, Shanghai 200241, PR China.
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Animal Parasitology, Ministry of Agriculture, Shanghai 200241, PR China; Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious and Zoonosea, Yangzhou, Jiangsu Province 225009, PR China.
Vet Parasitol. 2017 Aug 30;243:242-247. doi: 10.1016/j.vetpar.2017.06.015. Epub 2017 Jun 20.
Domestic animals infected with Schistosoma japonicum are a major source of infection and play an important role in transmission to humans. A key strategy for the elimination of schistosomiasis is to control the sources of infection. In the present study, we identified a candidate diagnostic antigen-encoding gene, SjMRP1, the putative multidrug resistance protein 1 gene, by screening a cDNA phage display library from 44-day-old S. japonicum worms using IgGs from goat, cattle, and buffalo infected with S. japonicum. We cloned and expressed the fragment of SjMRP1 and subsequently evaluated the diagnostic potential of the recombinant protein rSjMRP1. In the enzyme-linked immunosorbent assay of rSjMRP1 (rSjMRP1-ELISA), the sensitivity in goat, cattle, and buffalo was 95.6% (86/90), 100% (22/22), and 90% (81/90), respectively, and the specificity was 100% (30/30) in goat and cattle and 96.67% (29/30) in buffalo. These results were not significantly different from soluble egg antigen (SEA)-ELISA results. Notably, rSjMRP1-ELISA has no cross reaction with Haemonchus contortus, a most common nematode seen in goat and bovine in China, in 13 infected goats, and with Orientobilhazia turkestanica, which is genetically under Schistosoma, in 36 infected goats; whereas SEA-ELISA showed false positive rate of 15.38% and 83.33% in the two respective animal groups. The results obtained here suggest that rSjMRP1 may be used for diagnosis of S. japonicum infection of domestic animals.
感染日本血吸虫的家畜是主要传染源,在传播给人类的过程中起重要作用。消除血吸虫病的一项关键策略是控制传染源。在本研究中,我们从44日龄日本血吸虫虫体构建的cDNA噬菌体展示文库中,利用感染日本血吸虫的山羊、牛和水牛的IgG筛选出一个候选诊断抗原编码基因SjMRP1,即推定的多药耐药蛋白1基因。我们克隆并表达了SjMRP1片段,随后评估了重组蛋白rSjMRP1的诊断潜力。在rSjMRP1的酶联免疫吸附测定(rSjMRP1-ELISA)中,山羊、牛和水牛的敏感性分别为95.6%(86/90)、100%(22/22)和90%(81/90),山羊和牛的特异性为100%(30/30),水牛的特异性为96.67%(29/30)。这些结果与可溶性虫卵抗原(SEA)-ELISA结果无显著差异。值得注意的是,rSjMRP1-ELISA在13只感染山羊中与中国山羊和牛中最常见的线虫捻转血矛线虫无交叉反应,在36只感染山羊中与属于血吸虫属的土耳其东毕吸虫无交叉反应;而SEA-ELISA在这两组动物中分别显示出15.38%和83.33%的假阳性率。此处获得的结果表明,rSjMRP1可用于家畜日本血吸虫感染的诊断。