School of Biological Sciences, UM-DAE Centre for Excellence in Basic Sciences, University of Mumbai, Kalina Campus, Vidyanagari, Mumbai, 400098, India.
Appl Biochem Biotechnol. 2022 Feb;194(2):671-693. doi: 10.1007/s12010-021-03632-7. Epub 2021 Aug 27.
The growth of respiratory diseases, as witnessed through the SARS and COVID-19 outbreaks, and antimicrobial-resistance together pose a serious threat to humanity. One reason for antimicrobial resistance is formation of bacterial biofilms. In this study the sulphated polysaccharides from green algae Chlamydomonas reinhardtii (Cr-SPs) is tested for its antibacterial and antibiofilm potential against Klebsiella pneumoniae and Serratia marcescens. Agar cup assay clearly indicated the antibacterial potential of Cr-SPs. Minimum inhibitory concentration (MIC) of Cr-SPs against Klebsiella pneumoniae was found to be 850 µg/ml, and it is 800 µg/ml in Serratia marcescens. Time-kill and colony-forming ability assays suggest the concentration-dependent bactericidal potential of Cr-SPs. Cr-SPs showed 74-100% decrease in biofilm formation in a concentration-dependent manner by modifying the cell surface hydrophobic properties of these bacteria. Cr-SPs have also distorted preformed-biofilms by their ability to interact and destroy the extra polymeric substance and eDNA of the matured biofilm. Scanning electron microscopy analysis showed that Cr-SPs effectively altered the morphology of these bacterial cells and distorted the bacterial biofilms. Furthermore reduced protease, urease and prodigiosin pigment production suggest that Cr-SPs interferes the quorum sensing mechanism in these bacteria. The current study paves way towards developing Cr-SPs as a control strategy for treatment of respiratory tract infections.
呼吸道疾病的增长,如 SARS 和 COVID-19 爆发所见证的那样,以及抗微生物药物耐药性一起对人类构成了严重威胁。抗微生物药物耐药性的一个原因是细菌生物膜的形成。在这项研究中,绿藻莱茵衣藻(Cr-SPs)的硫酸多糖被测试其对肺炎克雷伯菌和粘质沙雷氏菌的抗菌和抗生物膜潜力。琼脂杯测定清楚地表明了 Cr-SPs 的抗菌潜力。Cr-SPs 对肺炎克雷伯菌的最小抑菌浓度(MIC)为 850 µg/ml,对粘质沙雷氏菌为 800 µg/ml。时间杀灭和菌落形成能力测定表明 Cr-SPs 具有浓度依赖性的杀菌潜力。Cr-SPs 通过改变这些细菌的细胞表面疏水性,以浓度依赖的方式使生物膜形成减少了 74-100%。Cr-SPs 还通过其与成熟生物膜的外多聚物物质和 eDNA 相互作用和破坏的能力,扭曲了预先形成的生物膜。扫描电子显微镜分析表明,Cr-SPs 有效地改变了这些细菌细胞的形态,并扭曲了细菌生物膜。此外,蛋白酶、脲酶和灵菌红素产量的减少表明,Cr-SPs 干扰了这些细菌的群体感应机制。本研究为开发 Cr-SPs 作为治疗呼吸道感染的控制策略铺平了道路。