Patel Mitesh, Siddiqui Arif Jamal, Ashraf Syed Amir, Surti Malvi, Awadelkareem Amir Mahgoub, Snoussi Mejdi, Hamadou Walid Sabri, Bardakci Fevzi, Jamal Arshad, Jahan Sadaf, Sachidanandan Manojkumar, Adnan Mohd
Department of Biotechnology, Parul Institute of Applied Sciences and Centre of Research for Development, Parul University, Vadodara 391760, India.
Department of Biology, College of Science, University of Hail, Hail P.O. Box 2440, Saudi Arabia.
Microorganisms. 2022 May 13;10(5):1026. doi: 10.3390/microorganisms10051026.
Quorum sensing (QS) controls the expression of diverse biological traits in bacteria, including virulence factors. Any natural bioactive compound that disables the QS system is being considered as a potential strategy to prevent bacterial infection. Various biological activities of biosurfactants have been observed, including anti-QS effects. In the present study, we investigated the effectiveness of a biosurfactant derived from on QS-regulated virulence factors and biofilm formation in and . The structural analogues of the crude biosurfactant were identified using gas chromatography-mass spectrometry (GC-MS). Moreover, the inhibitory prospects of identified structural analogues were assessed with QS-associated CviR, LasA, and LasI ligands via in silico molecular docking analysis. An -derived biosurfactant showed a promising dose-dependent interference with the production of both violacein and acyl homoserine lactone (AHL) in . In , at a sub-MIC concentration (2.5 mg/mL), QS inhibitory activity was also demonstrated by reduction in pyocyanin (66.63%), total protease (60.95%), LasA (56.62%), and LasB elastase (51.33%) activity. The swarming motility and exopolysaccharide production were also significantly reduced in both (61.13%) and (53.11%). When compared with control, biofilm formation was also considerably reduced in (68.12%) and (59.80%). A GC-MS analysis confirmed that the crude biosurfactant derived from was a glycolipid type. Among all, n-hexadecanoic acid, oleic acid, and 1H-indene,1-hexadecyl-2,3-dihydro had a high affinity for CviR, LasI, and LasA, respectively. Thus, our findings suggest that the crude biosurfactant of can be used as a new anti-QS/antibiofilm agent against biofilm-associated pathogenesis, which warrants further investigation to uncover its therapeutic efficacy.
群体感应(QS)控制着细菌中多种生物学特性的表达,包括毒力因子。任何能够使QS系统失活的天然生物活性化合物都被视为预防细菌感染的潜在策略。人们已经观察到生物表面活性剂的各种生物学活性,包括抗群体感应作用。在本研究中,我们调查了一种源自[具体来源未提及]的生物表面活性剂对[具体细菌名称1]和[具体细菌名称2]中群体感应调节的毒力因子及生物膜形成的影响。使用气相色谱 - 质谱联用仪(GC - MS)鉴定了粗制生物表面活性剂的结构类似物。此外,通过计算机模拟分子对接分析,评估了所鉴定结构类似物与群体感应相关的CviR、LasA和LasI配体的抑制前景。一种源自[具体来源未提及]的生物表面活性剂对[具体细菌名称1]中紫罗酮和酰基高丝氨酸内酯(AHL)的产生表现出有前景的剂量依赖性干扰。在[具体细菌名称2]中,在亚最低抑菌浓度(2.5 mg/mL)下,通过降低绿脓菌素(66.63%)、总蛋白酶(60.95%)、LasA(56.62%)和LasB弹性蛋白酶(51.33%)的活性,也证明了群体感应抑制活性。在[具体细菌名称1](61.13%)和[具体细菌名称2](53.11%)中,群体运动性和胞外多糖的产生也显著降低。与对照相比,在[具体细菌名称1](68.12%)和[具体细菌名称2](59.80%)中生物膜形成也明显减少。GC - MS分析证实,源自[具体来源未提及]的粗制生物表面活性剂为糖脂类型。其中,正十六烷酸、油酸和1H - 茚,1 - 十六烷基 - 2,3 - 二氢分别对CviR、LasI和LasA具有高亲和力。因此,我们的研究结果表明,[具体来源未提及]的粗制生物表面活性剂可作为一种新型的抗群体感应/抗生物膜剂用于对抗生物膜相关的发病机制,这值得进一步研究以揭示其治疗效果。