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携带核酸水解3D8单链抗体片段的副干酪乳杆菌作为预防小鼠诺如病毒感染的益生菌的开发。

Development of Lactobacillus paracasei harboring nucleic acid-hydrolyzing 3D8 scFv as a preventive probiotic against murine norovirus infection.

作者信息

Hoang Phuong Mai, Cho Seungchan, Kim Kee Eun, Byun Sung June, Lee Taek-Kyun, Lee Sukchan

机构信息

Department of Genetic Engineering, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, 440-746, Korea.

出版信息

Appl Microbiol Biotechnol. 2015 Mar;99(6):2793-803. doi: 10.1007/s00253-014-6257-7. Epub 2014 Dec 9.

Abstract

The protein 3D8 single-chain variable fragment (3D8 scFv) has potential anti-viral activity due to its ability to penetrate into cells and hydrolyze nucleic acids. Probiotic Lactobacillus paracasei engineered to secrete 3D8 scFv for oral administration was used to test the anti-viral effects of 3D8 scFv against gastrointestinal virus infections. We found that injection of 3D8 scFv into the intestinal lumen resulted in the penetration of 3D8 scFv into the intestinal villi and lamina propria. 3D8 scFv secreted from engineered L. paracasei retained its cell-penetrating and nucleic acid-hydrolyzing activities, which were previously shown with 3D8 scFv expressed in Escherichia coli. Pretreatment of RAW264.7 cells with 3D8 scFv purified from L. paracasei prevented apoptosis induction by murine norovirus infection and decreased messenger RNA (mRNA) expression of the viral capsid protein VP1. In a mouse model, oral administration of the engineered L. paracasei prior to murine norovirus infection reduced the expression level of mRNA encoding viral polymerase. Taken together, these results suggest that L. paracasei secreting 3D8 scFv provides a basis for the development of ingestible anti-viral probiotics active against gastrointestinal viral infection.

摘要

蛋白质3D8单链可变片段(3D8 scFv)因其能够穿透细胞并水解核酸而具有潜在的抗病毒活性。经基因工程改造以分泌用于口服给药的3D8 scFv的益生菌副干酪乳杆菌被用于测试3D8 scFv对胃肠道病毒感染的抗病毒作用。我们发现,将3D8 scFv注入肠腔会导致其穿透肠绒毛和固有层。经基因工程改造的副干酪乳杆菌分泌的3D8 scFv保留了其细胞穿透和核酸水解活性,这与之前在大肠杆菌中表达的3D8 scFv所显示的活性相同。用从副干酪乳杆菌中纯化的3D8 scFv预处理RAW264.7细胞可防止小鼠诺如病毒感染诱导的细胞凋亡,并降低病毒衣壳蛋白VP1的信使核糖核酸(mRNA)表达。在小鼠模型中,在小鼠诺如病毒感染之前口服经基因工程改造的副干酪乳杆菌可降低编码病毒聚合酶的mRNA的表达水平。综上所述,这些结果表明,分泌3D8 scFv的副干酪乳杆菌为开发对胃肠道病毒感染具有活性的可食用抗病毒益生菌提供了基础。

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