Sagar Pankaj Kumar, Sharma Poonam, Singh Rambir
Department of Microbiology, Bundelkhand University, Jhansi-284128, Uttar Pradesh, India.
Department of Zoology, Indira Gandhi National Tribal University (A Central University), Amarkantak-484886, Madhya Pradesh, India.
Avicenna J Med Biotechnol. 2024 Jan-Mar;16(1):49-56. doi: 10.18502/ajmb.v16i1.14171.
The aim of this study was to determination of Anti-Quorum Sensing (AQS) and anti-biofilm potential of the methanol extract of ginger () rhizomes against multidrug-resistant clinical isolates of ().
The AQS activity of ginger was determined against () ATCC 12472 (CV12472), a biosensor strain, in qualitative manner using the agar well diffusion method. The violacein pigment inhibition was assessed to confirm AQS activity of ginger. The AQS potential of sub-minimum Inhibitory Concentrations (sub-MICs) of the ginger extract was determined by targeting different QS regulated virulence factors, including swarming motility (using swarm diameter measurement method), pyocyanin pigment (using chloroform extraction method), Exopolysaccharide (EPS) (using phenol-sulphuric acid method), and biofilm formation (using microtiter plate assay), against clinical isolates (CIs 2, 3, and 4) and standard reference strain of (PA01).
The AQS activity of methanol extract of ginger was confirmed against (CV12472) as inhibition of violacein pigment formation without effecting the growth of CIs and PA01 of . The ginger extract exhibited concentration-dependent inhibition of virulence factors and biofilm formation. The maximum reduction was found in swarming motility, pyocyanin, EPS and biofilm formation against PA01 (51.38%), CI3 (57.91%), PA01 (63.29%) and CI2 (64.37%), respectively at 1/2 MIC of ginger extract.
The results of present study revealed the effective AQS and anti-biofilm potential of rhizome methanol extract at a reduced dose (sub-MICs). The extract may be explored as an agent of antimicrobial compounds having AQS and anti-biofilm activity for controlling microbial infection and also for reducing the chances of emergence of resistance in
本研究旨在测定生姜根茎甲醇提取物对多重耐药临床分离株铜绿假单胞菌的抗群体感应(AQS)和抗生物膜潜力。
采用琼脂孔扩散法,以定性方式测定生姜对生物传感器菌株铜绿假单胞菌ATCC 12472(CV12472)的AQS活性。通过评估紫菌素色素抑制来确认生姜的AQS活性。通过针对不同的群体感应调节毒力因子,包括群游运动性(使用群游直径测量法)、绿脓菌素色素(使用氯仿萃取法)、胞外多糖(EPS)(使用苯酚-硫酸法)以及生物膜形成(使用微量滴定板测定法),测定生姜提取物亚最小抑菌浓度(亚MICs)的AQS潜力,针对临床分离株(CIs 2、3和4)以及铜绿假单胞菌的标准参考菌株(PA01)。
生姜甲醇提取物对铜绿假单胞菌(CV12472)的AQS活性得到确认,表现为抑制紫菌素色素形成,而不影响铜绿假单胞菌临床分离株和PA01的生长。生姜提取物对毒力因子和生物膜形成呈现浓度依赖性抑制。在生姜提取物的1/2 MIC时,针对PA01的群游运动性、绿脓菌素、EPS和生物膜形成的最大减少分别为51.38%、CI3为57.91%、PA01为63.29%以及CI2为64.37%。
本研究结果揭示了生姜根茎甲醇提取物在降低剂量(亚MICs)时有效的AQS和抗生物膜潜力。该提取物可作为具有AQS和抗生物膜活性的抗菌化合物制剂进行探索,用于控制微生物感染以及降低耐药性出现的几率。