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大肠杆菌暴露于DNA甲基化剂会通过下调N - 乙酰神经氨酸裂解酶NanA来损害生物膜形成和真核细胞侵袭。

Exposure of E. coli to DNA-Methylating Agents Impairs Biofilm Formation and Invasion of Eukaryotic Cells via Down Regulation of the N-Acetylneuraminate Lyase NanA.

作者信息

Di Pasquale Pamela, Caterino Marianna, Di Somma Angela, Squillace Marta, Rossi Elio, Landini Paolo, Iebba Valerio, Schippa Serena, Papa Rosanna, Selan Laura, Artini Marco, Palamara Anna Teresa, Duilio Angela

机构信息

Department of Chemical Sciences, University of Naples "Federico II" Naples, Italy.

Department of Molecular Medicine and Medical Biotechnology, University of Naples "Federico II" Naples, Italy.

出版信息

Front Microbiol. 2016 Feb 11;7:147. doi: 10.3389/fmicb.2016.00147. eCollection 2016.

Abstract

DNA methylation damage can be induced by endogenous and exogenous chemical agents, which has led every living organism to develop suitable response strategies. We investigated protein expression profiles of Escherichia coli upon exposure to the alkylating agent methyl-methane sulfonate (MMS) by differential proteomics. Quantitative proteomic data showed a massive downregulation of enzymes belonging to the glycolytic pathway and fatty acids degradation, strongly suggesting a decrease of energy production. A strong reduction in the expression of the N-acetylneuraminate lyases (NanA) involved in the sialic acid metabolism was also observed. Using a null NanA mutant and DANA, a substrate analog acting as competitive inhibitor, we demonstrated that down regulation of NanA affects biofilm formation and adhesion properties of E. coli MV1161. Exposure to alkylating agents also decreased biofilm formation and bacterial adhesion to Caco-2 eukaryotic cell line by the adherent invasive E. coli (AIEC) strain LF82. Our data showed that methylation stress impairs E. coli adhesion properties and suggest a possible role of NanA in biofilm formation and bacteria host interactions.

摘要

DNA甲基化损伤可由内源性和外源性化学物质诱导产生,这使得每个生物体都发展出了合适的应对策略。我们通过差异蛋白质组学研究了大肠杆菌在暴露于烷基化剂甲磺酸甲酯(MMS)时的蛋白质表达谱。定量蛋白质组学数据显示,属于糖酵解途径和脂肪酸降解的酶大量下调,强烈表明能量产生减少。还观察到参与唾液酸代谢的N-乙酰神经氨酸裂解酶(NanA)的表达大幅降低。使用NanA基因缺失突变体和作为竞争性抑制剂的底物类似物DANA,我们证明NanA的下调会影响大肠杆菌MV1161的生物膜形成和黏附特性。暴露于烷基化剂还会降低黏附侵袭性大肠杆菌(AIEC)菌株LF82的生物膜形成以及细菌对Caco-2真核细胞系的黏附。我们的数据表明甲基化应激会损害大肠杆菌的黏附特性,并提示NanA在生物膜形成和细菌与宿主相互作用中可能发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34f3/4749703/db5397c6a7e7/fmicb-07-00147-g0001.jpg

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