Mapping of the complement C1q binding site on Trichinella spiralis paramyosin

Parasites & Vectors

Chunyue Hao¹  Qinghui Zhuang¹  Zixia Wang¹  Xinping Zhu¹  Jingjing Huang¹  Bin Zhan² 

[1] Department of Medical Microbiology and Parasitology, School of Basic Medical Sciences, Capital Medical University;Department of Pediatrics, National School of Tropical Medicine, Baylor College of Medicine;

关键词: Trichinella spiralis;    Paramyosin;    Immune evasion;    Complement C1q;   

DOI  :  10.1186/s13071-018-3258-x

来源: DOAJ

【 摘 要 】

Abstract Background Trichinella spiralis is a tissue-dwelling parasite has developed the ability to evade the host immune attack to establish parasitism in a host. One of the strategies evolved by the nematode is to produce proteins that immunomodulate the host immune system. TsPmy is a paramyosin secreted by T. spiralis on the surface of larvae and adult worms that can interact with complement components C1q and C8/C9 to compromise their activation and functions. To better understand the mechanism of TsPmy involved in the C1q inactivation and immune evasion, the C1q-binding site on TsPmy was investigated. Methods The TsPmy C1q-binding site was investigated by sequential narrow-down fragment expression in bacteria and peptide binding screening. C1q binding activity was identified by Far-Western blotting and ELISA assays. Results After several runs of sequential fragment expression, the C1q binding site was narrowed down to fragments of N-terminal TsPmy226-280aa and TsPmy231-315aa, suggesting the final C1q binding site is probably located to TsPmy231-280aa. A total of nine peptides covering different amino acid sequences within TsPmy231-280aa were synthesized. The binding assay to C1q determined that only P2 peptide covering TsPmy241-280aa binds to C1q, indicating that the C1q binding domain may need both the linearized sequence and conformational structure required for binding to C1q. The binding of peptide P2 to C1q significantly inhibited both C1q-initiated complement classical activation and C1q-induced macrophage chemotaxis. Conclusions This study identifies the C1q binding site within TsPmy which provides helpful information for developing a vaccine against trichinellosis by targeting the C1q-binding activity of TsPmy.

【 授权许可】

Unknown