Characterization and immunoprotective effect of SjIrV1, a 66 kDa calcium-binding protein from Schistosoma japonicum.
- Author:
Meimei WEI
1
;
Yanian XIONG
;
Yang HONG
;
Lini HUANG
;
Peipei MENG
;
Dezhou AI
;
Min ZHANG
;
Zhiqiang FU
;
Shengfa LIU
;
Jiaojiao LIN
Author Information
1. Key Laboratory of Animal Parasitology, Ministry of Agriculture of China, Shanghai Veterinary Research, Chinese Academy of Agricultural Science, Shanghai 200241, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Antibodies, Helminth;
blood;
Calcium-Binding Proteins;
genetics;
metabolism;
Cloning, Molecular;
Escherichia coli;
metabolism;
Female;
Genetic Vectors;
Helminth Proteins;
genetics;
metabolism;
Male;
Mice;
Recombinant Proteins;
genetics;
metabolism;
Schistosoma japonicum;
genetics;
metabolism
- From:
Chinese Journal of Biotechnology
2013;29(7):891-903
- CountryChina
- Language:Chinese
-
Abstract:
Calcium-binding protein is an indispensable protein which performs extensive and important functions in the growth of Schistosoma japonicum. Based on our primary study on tegument surface proteins of S. japonicun, a cDNA encoding a 66 kDa calcium-binding protein of S. japonicum (Chinese strain) was cloned, sequence analysis revealed that it was identical with that of SjIrV1 of Philippines strains S. japonicum. The expression of SjIrV1 were detected by Real-time PCR, using cDNA templates isolated from 7, 14, 21, 28, 35 and 42 days worms and the results revealed that the gene was expressed in all investigated stages, and the mRNA level of SjIrV1 is much higher in 42 d female worms than that in 42 d male worms. The cDNA containing the open reading frame of IrV1 was subcloned into a pET28a (+) vector and transformed into competent Escherichia coli BL21 for expression. The recombinant protein was purified using a Ni-NTA purification system, and confirmed by high performance liquid chromatography (RP-HPLC) and tandem mass spectrometry (MS/MS). Western blotting analysis showed that recombinant SjIrV1 (rSjIrV1) could be recognized by the S. japonicum infected mouse serum and the mouse serum specific to rSjIrV1, respectively. Immunofluorescence observation exhibited that SjIrV1 was mainly distributed on the tegument of the 35-day adult worms. ELISA test revealed that IgG, IgG1 and IgG2a antibodies are significantly increased in the serum of rSjIrV1 vaccinated mice. The study suggested that rSjIrV1 might play an important role in the development of S. japonicum.
