Fei Hong, Naqvi Muhammad Ali-Ul-Husnain, Naqvi Sana Zahra, Xu Lixin, Song Xiaokai, Li Xiangrui, Yan Ruofeng
MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China.
PLoS Negl Trop Dis. 2021 Nov 30;15(11):e0009958. doi: 10.1371/journal.pntd.0009958. eCollection 2021 Nov.
Trichinella spiralis is mammalian skeletal muscles parasite which may cause trichinellosis in animals and humans. Gamma interferon inducible lysosomal thiol reductase (GILT) is a widespread superfamily which plays key role in processing and presentation of MHC class II restricted antigen by catalyzing disulfide bond reduction. There are no reports about GILT in T. spiralis. In present study, GILT from T. spiralis (Tsp-GILT) was cloned, analyzed by multiple-sequence alignment, and predicted by 3D structure model. Recombinant Tsp-GILT (about 46 kDa) was efficiently expressed in Escherichia coli and thiol reductase activity suggested that in acidic environment the addition of a reducing agent is needed. Soaking method was used to knockdown expression of Tsp-GILT using small interference RNA (siRNA). Immunofluorescence assay confirmed the transformation of siRNA into muscle larva (ML) and new born larva (NBL). Quantitative real time-PCR (QRT-PCR) analysis revealed that transcription level of Tsp-GILT mRNA can be up-regulated by stimulation of mouse IFN-γ and down-regulated by siRNA2 in vitro. NBLs soaked with siRNA2 showed 32.3% reduction in the generation of MLs. MLs soaked with siRNA2 showed 26.2% reduction in the next generation of MLs, but no significant effect was observed on adult worms or NBLs. These findings concluded that GILT may play important roles in the development of T. spiralis parasite.
旋毛虫是寄生于哺乳动物骨骼肌的寄生虫,可导致动物和人类患旋毛虫病。γ干扰素诱导溶酶体巯基还原酶(GILT)是一个广泛存在的超家族,通过催化二硫键还原在MHC II类限制性抗原的加工和呈递中起关键作用。目前尚无关于旋毛虫中GILT的报道。在本研究中,克隆了旋毛虫的GILT(Tsp-GILT),进行了多序列比对分析,并通过三维结构模型进行了预测。重组Tsp-GILT(约46 kDa)在大肠杆菌中高效表达,其巯基还原酶活性表明在酸性环境中需要添加还原剂。采用浸泡法利用小干扰RNA(siRNA)敲低Tsp-GILT的表达。免疫荧光分析证实了siRNA可进入肌幼虫(ML)和新生幼虫(NBL)。定量实时PCR(QRT-PCR)分析显示,体外经小鼠IFN-γ刺激可上调Tsp-GILT mRNA的转录水平,而siRNA2可使其下调。用siRNA2浸泡的NBL产生的ML减少了32.3%。用siRNA2浸泡的ML产生的下一代ML减少了26.2%,但对成虫或NBL未观察到显著影响。这些结果表明,GILT可能在旋毛虫的发育中起重要作用。