Effect of miR-17 onpolysaccharide against transmissible gastroenteritis virus.

Abstract

Transmissible gastroenteritis virus (TGEV) could cause diarrhea, vomiting, dehydration and even death in piglets, miRNA played an important role in the interaction between virus and cell. The study aimed to investigate the impact of miR-17 on the polysaccharide of Polygonum Cillinerve (PCP) in combating TGEV. miR-17 was screened and transfection validation was performed by Real-time PCR. The function of miR-17 on PK15 cells infected with TGEV and treated with PCP was investigated by DCFH-DA loading probe, JC-1 staining and Hoechst fluorescence staining. Furthermore, the effect of miR-17 on PCP inhibiting TGEV replication and apoptosis signaling pathways during PCP against TGEV infection was measured through Real-time PCR and Western blot. The results showed that miR-17 mimic and inhibitor could be transferred into PK15 cells and the expression of miR-17 significantly increased and decreased respectively compared with miR-17 mimic and inhibitor (< 0.05). A total 250 &#x3bc;g/mL of PCP could inhibit cells apoptosis after transfection with miR-17. PCP (250 &#x3bc;g/mL and 125 &#x3bc;g/mL) significantly inhibited the decrease in mitochondrial membrane potential induced by TGEV after transfection with miR-17 (< 0.05). After transfection of miR-17 mimic, PCP at concentrations of 250 &#x3bc;g/mL and 125 &#x3bc;g/mL significantly promoted the mRNA expression of P53, cyt C and caspase 9 (< 0.05). Compared with the control group, the replication of TGEV gRNA and gene N was significantly inhibited by PCP at concentrations of 250 &#x3bc;g/mL and 125 &#x3bc;g/mL after transfection of both miR-17 mimic and inhibitor (< 0.05). PCP at 62.5 &#x3bc;g/mL significantly inhibited the replication of gene S following transfection with miR-17 inhibitor (< 0.05). These results suggested that PCP could inhibit the replication of TGEV and apoptosis induced by TGEV by regulating miR-17.