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Functional characterization of a glutathione S-transferase in Trichinella spiralis invasion, development and reproduction.
Yang, Da Qi; Liu, Fang; Bai, Ying; Zeng, Jie; Hao, Hui Nan; Yue, Xin; Hu, Chen Xi; Long, Shao Rong; Liu, Ruo Dan; Wang, Zhong Quan; Cui, Jing.
Affiliation
  • Yang DQ; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Liu F; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Bai Y; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Zeng J; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Hao HN; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Yue X; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Hu CX; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Long SR; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Liu RD; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China.
  • Wang ZQ; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China. Electronic address: wangzq@zzu.edu.cn.
  • Cui J; Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou 450052, China. Electronic address: cuij@zzu.edu.cn.
Vet Parasitol ; 297: 109128, 2021 Sep.
Article in En | MEDLINE | ID: mdl-32402492
The purpose of this study was to determine the biological function of a Trichinella spiralis glutathione S-transferase (TsGST) in larval invasion and development by RNA interference (RNAi). The TsGST-specific siRNA 366 was transfected into T. spiralis muscle larvae (ML) via electroporation. At 1 day following transfection, the larval TsGST mRNA and protein expressions were reduced by 40.09 and 65.22 % (P < 0.05), respectively. The enzymatic activity of natural TsGST in siRNA-transfected ML was also suppressed by 45% compared with PBS group (P < 0.05). Silencing of the TsGST significantly inhibited the ability of larvae to invade intestinal epithelium cells (IECs) and isolated intestine. After challenge with siRNA-366-treated ML, the infected mice exhibited a 62.82% reduction of intestinal adult worms, and 65.03 % reduction of muscle larvae compared to the PBS group. Besides, the length of adults, newborn larvae and muscle larvae was significantly shorter than that of control siRNA and PBS group; the female fecundity of siRNA 366 group was lower than those of control siRNA and PBS group (P <  0.05). The results revealed that the specific RNAi significantly reduced the expression and enzymatic activity of TsGST, inhibited the larval invasive and developmental capacity, and impaired the female fecundity. The results further confirmed that TsGST plays a crucial role in the T. spiralis life cycle and it might be a potential molecular target for anti-Trichinella vaccines.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rodent Diseases / Trichinellosis / Trichinella spiralis Limits: Animals Language: En Journal: Vet Parasitol Year: 2021 Document type: Article Affiliation country: China Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rodent Diseases / Trichinellosis / Trichinella spiralis Limits: Animals Language: En Journal: Vet Parasitol Year: 2021 Document type: Article Affiliation country: China Country of publication: Netherlands