Migliaccio Antonella, Esposito Eliana Pia, Bagattini Maria, Berisio Rita, Triassi Maria, De Gregorio Eliana, Zarrilli Raffaele
Department of Public Health, University of Naples Federico II, Naples, Italy.
Institute of Biostructures and Bioimaging, National Research Council, Naples, Italy.
Front Microbiol. 2022 Feb 7;12:790263. doi: 10.3389/fmicb.2021.790263. eCollection 2021.
The management of infections caused by is hindered by its intrinsic tolerance to a wide variety of biocides. The aim of the study was to analyze the role of different efflux pumps (EPs) in tolerance to chlorhexidine (CHX) and benzalkonium (BZK) and identify non-toxic compounds, which can restore susceptibility to CHX and BZK in . ATCC 19606 strain was tolerant to both CHX and BZK with MIC and MBC value of 32 mg/L. CHX subMIC concentrations increased the expression of and (RND superfamily), (PACE family) and (MFS superfamily) EP genes. The values of CHX MIC and MBC decreased by eightfold in Δ and twofold in Δ or Δ mutants, respectively, while not affected in Δ mutant; EPs double and triple deletion mutants showed an additive effect on CHX MIC. CHX susceptibility was restored in double and triple deletion mutants with inactivation of gene. BZK MIC was decreased by fourfold in Δ mutant, and twofold in Δ and Δ mutants, respectively; EPs double and triple deletion mutants showed an additive effect on BZK MIC. BZK susceptibility was recovered in Δ Δ Δ and Δ Δ Δ triple mutants. The structural comparison of AdeB and AdeJ protomers showed a more negatively charged entrance binding site and F-loop in AdeB, which may favor the transport of CHX. The carbonyl cyanide m-chlorophenylhydrazine protonophore (CCCP) EP inhibitor reduced dose-dependently CHX MIC in ATCC 19606 and in Δ, Δ, or Δ mutants, but not in Δ mutant. Either piperine (PIP) or resveratrol (RV) at non-toxic concentrations inhibited CHX MIC in ATCC 19606 parental strain and EPs gene deletion mutants, and CHX-induced EP gene expression. Also, RV inhibited BZK MIC and EP genes expression in ATCC 19606 parental strain and EPs mutants. These results demonstrate that tolerance to CHX and BZK in is mediated by the activation of AdeB, AceI and AmvA EPs, AdeB playing a major role. Importantly, inhibition of EP genes expression by RV restores CHX and BZK susceptibility in
因其对多种杀菌剂具有内在耐受性,导致由其引起的感染难以控制。本研究旨在分析不同外排泵(EPs)在对洗必泰(CHX)和苯扎氯铵(BZK)耐受性中的作用,并鉴定可恢复其对CHX和BZK敏感性的无毒化合物。ATCC 19606菌株对CHX和BZK均耐受,MIC和MBC值为32 mg/L。CHX亚MIC浓度增加了adeB和adeJ(RND超家族)、acmE(PACE家族)和amiE(MFS超家族)外排泵基因的表达。在ΔadeB突变体中,CHX的MIC和MBC值分别降低了八倍,在ΔacmE或ΔamiE突变体中降低了两倍,而在ΔadeJ突变体中未受影响;外排泵双缺失和三缺失突变体对CHX的MIC显示出累加效应。通过使adeJ基因失活,双缺失和三缺失突变体恢复了对CHX的敏感性。在ΔacmE突变体中,BZK的MIC降低了四倍,在ΔadeB和ΔamiE突变体中分别降低了两倍;外排泵双缺失和三缺失突变体对BZK的MIC显示出累加效应。在ΔadeBΔacmEΔamiE三突变体中恢复了对BZK的敏感性。AdeB和AdeJ原体的结构比较显示,AdeB中的入口结合位点和F环带更多负电荷,这可能有利于CHX的转运。羰基氰化物间氯苯腙质子载体(CCCP)外排泵抑制剂可剂量依赖性地降低ATCC 19606菌株以及ΔadeB、ΔacmE或ΔamiE突变体中CHX的MIC,但对ΔadeJ突变体无效。无毒浓度的胡椒碱(PIP)或白藜芦醇(RV)均可抑制ATCC 19606亲本菌株和外排泵基因缺失突变体中CHX的MIC以及CHX诱导的外排泵基因表达。此外,RV还可抑制ATCC 19606亲本菌株和外排泵突变体中BZK的MIC和外排泵基因表达。这些结果表明,对CHX和BZK的耐受性是由AdeB、AceI和AmvA外排泵的激活介导的,其中AdeB起主要作用。重要的是,RV对外排泵基因表达的抑制恢复了其对CHX和BZK的敏感性