Faculty of Pharmacy, Department of Microbiology and Immunology, Helwan University, P.O. Box 11795, Ain-Helwan, Cairo, Egypt.
Department of Microbiology and Immunology, Faculty of Pharmacy, Modern University for Technology, and Information (MTI), Cairo, Egypt.
BMC Microbiol. 2024 Aug 24;24(1):312. doi: 10.1186/s12866-024-03443-w.
More than a century has passed since it was discovered that many bacteria produce indole, but research into the actual biological roles of this molecule is just now beginning. The influence of indole on bacterial virulence was extensively investigated in indole-producing bacteria like Escherichia coli. To gain a deeper comprehension of its functional role, this study investigated how indole at concentrations of 0.5-1.0 mM found in the supernatant of Escherichia coli stationary phase culture was able to alter the virulence of non-indole-producing bacteria, such as Pseudomonas aeruginosa, Proteus mirabilis, and Klebsiella pneumoniae, which are naturally exposed to indole in mixed infections with Escherichia coli.
Biofilm formation, antimicrobial susceptibility, and efflux pump activity were the three phenotypic tests that were assessed. Indole was found to influence antibiotic susceptibly of Pseudomonas aeruginosa, Proteus mirabilis and Klebsiella pneumoniae to ciprofloxacin, imipenem, ceftriaxone, ceftazidime, and amikacin through significant reduction in MIC with fold change ranged from 4 to 16. Biofilm production was partially abrogated in both 32/45 Pseudomonas aeruginosa and all eight Proteus mirabilis, while induced biofilm production was observed in 30/40 Klebsiella pneumoniae. Moreover, acrAB and oqxAB, which encode four genes responsible for resistance-nodulation-division multidrug efflux pumps in five isolates of Klebsiella pneumoniae were investigated genotypically using quantitative real-time (qRT)-PCR. This revealed that all four genes exhibited reduced expression indicated by 2^-ΔΔCT < 1 in indole-treated isolates compared to control group.
The outcomes of qRT-PCR investigation of efflux pump expression have established a novel clear correlation of the molecular mechanism that lies beneath the influence of indole on bacterial antibiotic tolerance. This research provides novel perspectives on the various mechanisms and diverse biological functions of indole signaling and how it impacts the pathogenicity of non-indole-producing bacteria.
自一个多世纪前发现许多细菌会产生吲哚以来,人们对这种分子的实际生物学作用的研究才刚刚开始。在产吲哚细菌如大肠杆菌中,吲哚对细菌毒力的影响已得到广泛研究。为了更深入地了解其功能作用,本研究调查了在大肠杆菌静止期培养物上清液中浓度为 0.5-1.0 mM 的吲哚如何改变非产吲哚细菌(如铜绿假单胞菌、奇异变形杆菌和肺炎克雷伯菌)的毒力,这些细菌在与大肠杆菌的混合感染中自然会接触到吲哚。
评估了三种表型测试,即生物膜形成、抗生素敏感性和外排泵活性。吲哚被发现通过降低铜绿假单胞菌、奇异变形杆菌和肺炎克雷伯菌对环丙沙星、亚胺培南、头孢曲松、头孢他啶和阿米卡星的 MIC,显著影响其抗生素敏感性,变化倍数为 4 至 16 倍。在 32/45 株铜绿假单胞菌和所有 8 株奇异变形杆菌中部分阻断生物膜形成,而在 30/40 株肺炎克雷伯菌中观察到诱导生物膜形成。此外,通过定量实时 (qRT)-PCR 对编码五个肺炎克雷伯菌中负责抗性-结节-分裂多药外排泵的四个基因 acrAB 和 oqxAB 的基因进行了基因型研究。结果表明,与对照组相比,吲哚处理的分离株中所有四个基因的表达均降低,2^-ΔΔCT < 1。
qRT-PCR 对外排泵表达的研究结果建立了吲哚对细菌抗生素耐受性影响的分子机制的新的明确关联。本研究为吲哚信号的各种机制和不同生物学功能以及它们如何影响非产吲哚细菌的致病性提供了新的视角。