通过适体抑制肠产毒素大肠杆菌粘附可防止IPEC-J2细胞感染。

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Zefeng Wang, Tao Xu, Jianxi Tan, Yan Zhou, Qiyi Li, Zhihui Peng
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引用次数: 0

摘要

产肠毒素大肠杆菌(ETEC)是一种众所周知的与断奶后腹泻有关的菌株。因此,预防和抑制ETEC感染的策略至关重要。适配体是单链DNA或RNA序列,具有与靶分子结合的高亲和力和特异性。本研究以肠猪上皮细胞系IPEC-J2为体外模型,证明了两种适体K88- apt A04(一种针对ETEC K88的纤维特异性适体)和K88- apt 37(一种针对ETEC K88的细胞特异性适体)能有效抑制ETEC K88对肠上皮细胞的粘附。我们将IPEC-J2细胞系暴露于ETEC K88,以10次感染的方式建立了ETEC K88-IPEC-J2相互作用模型。我们的研究结果表明,适体以浓度依赖的方式抑制ETEC K88对IPEC-J2细胞的粘附,主要是通过粘附抑制和预防。此外,酶联免疫吸附试验和mRNA表达分析表明,适体减少了ETEC K88感染引发的促炎细胞因子的分泌。综上所述,适体具有降低ETEC k88诱导的IPEC-J2细胞毒性的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibition of Enterotoxigenic Escherichia coli adhesion via aptamers prevents infection in IPEC-J2 cells.

Inhibition of Enterotoxigenic Escherichia coli adhesion via aptamers prevents infection in IPEC-J2 cells.

Inhibition of Enterotoxigenic Escherichia coli adhesion via aptamers prevents infection in IPEC-J2 cells.

Inhibition of Enterotoxigenic Escherichia coli adhesion via aptamers prevents infection in IPEC-J2 cells.

Enterotoxigenic Escherichia coli (ETEC) is a well-known strain associated with post-weaning diarrhea. Consequently, strategies to prevent and inhibit ETEC infections are critically important. Aptamers are single-stranded DNA or RNA sequences that exhibit high affinity and specificity for binding to target molecules. In this study, we used the intestinal porcine epithelial cell line IPEC-J2 as an in vitro model to demonstrate that two aptamers, K88-Apt A04 (a fimbrial-specific aptamer targeting ETEC K88) and K88-Apt 37 (a cell-specific aptamer targeting ETEC K88) effectively inhibited the adhesion of ETEC K88 to intestinal epithelial cells. We established an ETEC K88-IPEC-J2 interaction model by exposing the IPEC-J2 cell line to ETEC K88 at a multiplicity of infection of 10. Our findings revealed that the aptamers inhibited ETEC K88 adhesion to IPEC-J2 cells in a concentration-dependent manner, primarily through adherence inhibition and prevention. Furthermore, enzyme-linked immunosorbent assay and mRNA expression analyses indicated that the aptamers reduced the secretion of pro-inflammatory cytokines triggered by ETEC K88 infection. In conclusion the aptamers demonstrated the ability to reduce ETEC K88-induced cytotoxicity in IPEC-J2 cells in vitro.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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