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3-吲哚乙腈可降低大肠杆菌 O157:H7 生物膜的形成和铜绿假单胞菌的毒力。

3-indolylacetonitrile decreases Escherichia coli O157:H7 biofilm formation and Pseudomonas aeruginosa virulence.

机构信息

School of Display and Chemical Engineering, Yeungnam University, Gyeongsan-si, Gyeongsangbuk-do 712-749, Korea.

出版信息

Environ Microbiol. 2011 Jan;13(1):62-73. doi: 10.1111/j.1462-2920.2010.02308.x.

Abstract

Intercellular signal indole and its derivative hydroxyindoles inhibit Escherichia coli biofilm and diminish Pseudomonas aeruginosa virulence. However, indole and bacterial indole derivatives are unstable in the microbial community because they are quickly degraded by diverse bacterial oxygenases. Hence, this work sought to identify novel, non-toxic, stable and potent indole derivatives from plant sources for inhibiting the biofilm formation of E. coli O157:H7 and P. aeruginosa. Here, plant auxin 3-indolylacetonitrile (IAN) was found to inhibit the biofilm formation of both E. coli O157:H7 and P. aeruginosa without affecting its growth. IAN more effectively inhibited biofilms than indole for the two pathogenic bacteria. Additionally, IAN decreased the production of virulence factors including 2-heptyl-3-hydroxy-4(1H)-quinolone (PQS), pyocyanin and pyoverdine in P. aeruginosa. DNA microarray analysis indicated that IAN repressed genes involved in curli formation and glycerol metabolism, whereas IAN induced indole-related genes and prophage genes in E. coli O157:H7. It appeared that IAN inhibited the biofilm formation of E. coli by reducing curli formation and inducing indole production. Also, corroborating phenotypic results of P. aeruginosa, whole-transcriptomic data showed that IAN repressed virulence-related genes and motility-related genes, while IAN induced several small molecule transport genes. Furthermore, unlike bacterial indole derivatives, plant-originated IAN was stable in the presence of either E. coli or P. aeruginosa. Additionally, indole-3-carboxyaldehyde was another natural biofilm inhibitor for both E. coli and P. aeruginosa.

摘要

细胞间信号吲哚及其衍生物羟基吲哚抑制大肠杆菌生物膜形成并降低铜绿假单胞菌毒力。然而,由于吲哚和细菌吲哚衍生物在微生物群落中不稳定,它们会被多种细菌加氧酶迅速降解。因此,本研究旨在从植物来源中鉴定新型、无毒、稳定且有效的吲哚衍生物,以抑制大肠杆菌 O157:H7 和铜绿假单胞菌的生物膜形成。研究发现,植物生长素 3-吲哚乙腈 (IAN) 可抑制大肠杆菌 O157:H7 和铜绿假单胞菌的生物膜形成,而不影响其生长。IAN 比吲哚更有效地抑制这两种致病菌的生物膜形成。此外,IAN 降低了铜绿假单胞菌中包括 2-庚基-3-羟基-4(1H)-喹啉 (PQS)、绿脓菌素和吡咯并菌素在内的毒力因子的产生。DNA 微阵列分析表明,IAN 抑制了卷曲形成和甘油代谢相关基因的表达,而在大肠杆菌 O157:H7 中,IAN 诱导了吲哚相关基因和噬菌体基因的表达。IAN 似乎通过减少卷曲形成和诱导吲哚产生来抑制大肠杆菌生物膜的形成。此外,与细菌吲哚衍生物相反,植物来源的 IAN 在存在大肠杆菌或铜绿假单胞菌时稳定。此外,吲哚-3-羧酸醛也是另一种天然生物膜抑制剂,可抑制大肠杆菌和铜绿假单胞菌的生物膜形成。

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