Insight into the molecular mechanism of miR-192 regulating Escherichia coli resistance in piglets
Author(s) -
Li Sun,
Sen Wu,
Chaohui Dai,
Shouyong Sun,
Guoqiang Zhu,
Shenglong Wu,
Wenbin Bao
Publication year - 2018
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20171160
Subject(s) - biology , alcam , escherichia coli , transcription activator like effector nuclease , effector , nuclease , gene , gene knockout , microrna , microbiology and biotechnology , genetics , genome , genome editing
MicroRNAs (miRNAs) have important roles in many cellular processes, including cell proliferation, growth and development, and disease control. Previous study demonstrated that the expression of two highly homologous miRNAs (miR-192 and miR-215) was up-regulated in weaned piglets with Escherichia coli F18 infection. However, the potential molecular mechanism of miR-192 in regulating E. coli infection remains unclear in pigs. In the present study, we analyzed the relationship between level of miR-192 and degree of E. coli resistance using transcription activator-like effector nuclease (TALEN), in vitro bacterial adhesion assays, and target genes research. A TALEN expression vector that specifically recognizes the pig miR-192 was constructed and then monoclonal epithelial cells defective in miR-192 were established. We found that miR-192 knockout led to enhance the adhesion ability of the E. coli strains F18ab, F18ac and K88ac, meanwhile increase the expression of target genes ( DLG5 and ALCAM ) by qPCR and Western blotting analysis. The results suggested that miR-192 and its key target genes ( DLG5 and ALCAM ) could have a key role in E. coli infection. Based on our findings, we propose that further investigation of miR-192 function is likely to lead to insights into the molecular mechanisms of E. coli infection.
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