Tansirichaiya Supathep, Reynolds Liam J, Cristarella Gianmarco, Wong Li Chin, Rosendahl Kimie, Roberts Adam P
1 Department of Microbial Diseases, UCL Eastman Dental Institute, University College London , London, United Kingdom .
2 Department of Bacteriology, Animal and Plant Health Agency , Addlestone, United Kingdom .
Microb Drug Resist. 2018 Mar;24(2):105-112. doi: 10.1089/mdr.2017.0105. Epub 2017 Jun 12.
Antimicrobial resistance is common in the microbial inhabitants of the human oral cavity. Antimicrobials are commonly encountered by oral microbes as they are present in our diet, both naturally and anthropogenically, and also used in oral healthcare products and amalgam fillings. We aimed to determine the presence of genes in the oral microbiome conferring reduced susceptibility to common antimicrobials. From an Escherichia coli library, 12,277 clones were screened and ten clones with reduced susceptibility to triclosan were identified. The genes responsible for this phenotype were identified as fabI, originating from a variety of different bacteria. The gene fabI encodes an enoyl-acyl carrier protein reductase (ENR), which is essential for fatty acid synthesis in bacteria. Triclosan binds to ENR, preventing fatty acid synthesis. By introducing the inserts containing fabI, ENR is likely overexpressed in E. coli, reducing the inhibitory effect of triclosan. Another clone was found to have reduced susceptibility to cetyltrimethylammonium bromide and cetylpyridinium chloride. This phenotype was conferred by a UDP-glucose 4-epimerase gene, galE, homologous to one from Veillonella parvula. The product of galE is involved in lipopolysaccharide production. Analysis of the E. coli host cell surface showed that the charge was more positive in the presence of galE, which likely reduces the binding of these positively charged antiseptics to the bacteria. This is the first time galE has been shown to confer resistance against quaternary ammonium compounds and represents a novel, epimerase-based, global cell adaptation, which confers resistance to cationic antimicrobials.
抗菌药物耐药性在人类口腔微生物群落中很常见。口腔微生物在我们的饮食中经常接触到抗菌药物,这些抗菌药物既天然存在,也有人为添加,同时还用于口腔保健产品和汞合金填充物中。我们旨在确定口腔微生物组中是否存在赋予对常见抗菌药物敏感性降低的基因。从大肠杆菌文库中筛选了12277个克隆,鉴定出10个对三氯生敏感性降低的克隆。导致这种表型的基因被鉴定为fabI,它来源于多种不同的细菌。基因fabI编码烯酰 - 酰基载体蛋白还原酶(ENR),这是细菌脂肪酸合成所必需的。三氯生与ENR结合,阻止脂肪酸合成。通过引入含有fabI的插入片段,ENR可能在大肠杆菌中过表达,从而降低三氯生的抑制作用。另一个克隆被发现对十六烷基三甲基溴化铵和十六烷基氯化吡啶敏感性降低。这种表型是由一个UDP - 葡萄糖4 - 表异构酶基因galE赋予的,该基因与细小韦荣球菌的一个基因同源。galE的产物参与脂多糖的产生。对大肠杆菌宿主细胞表面的分析表明,在galE存在的情况下,电荷更正,这可能减少了这些带正电荷的防腐剂与细菌的结合。这是首次证明galE赋予对季铵化合物的抗性,代表了一种基于表异构酶基因的新型全局细胞适应性,赋予对阳离子抗菌药物的抗性。