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评估 Gambeya lacourtiana(De Wild)Aubr. & Pellegr 次生代谢产物的抗群体感应和抗生物膜作用对选定病原体的影响。

Evaluation of anti-quorum sensing and antibiofilm effects of secondary metabolites from Gambeya lacourtiana (De Wild) Aubr. & Pellegr against selected pathogens.

机构信息

Department of Organic Chemistry, Faculty of Science, The University of Yaoundé 1, P.O. Box 812, Yaoundé, Cameroon.

Department of Chemistry, Higher Teacher Training C ollege, The University of Yaoundé 1, P.O. Box 47, Yaoundé, Cameroon.

出版信息

BMC Complement Med Ther. 2023 Aug 24;23(1):300. doi: 10.1186/s12906-023-04115-4.

Abstract

BACKGROUND

Microbial infections cause serious health problems especially with the rising antibiotic resistance which accounts for about 700,000 human deaths annually. Antibiotics which target bacterial death encounter microbial resistance with time, hence, there is an urgent need for the search of antimicrobial substances which target disruption of virulence factors such as biofilm and quorum sensing (QS) with selective pressure on the pathogens so as to avoid resistance.

METHODS

Natural products are suitable leads for antimicrobial drugs that can inhibit bacterial biofilms and QS. Twenty compounds isolated from the medicinal plant Gambeya lacourtiana were evaluated for their antibiofilm and anti-quorum sensing effects against selected pathogenic bacteria.

RESULTS

Most of the compounds inhibited violacein production in Chromobacterium violaceum CV12472 and the most active compound, Epicatechin had 100% inhibition at MIC (Minimal Inhibitory Concentration) and was the only compound to inhibit violacein production at MIC/8 with percentage inhibition of 17.2 ± 0.9%. Since the bacteria C. violaceum produces violacein while growing, the inhibition of the production of this pigment reflects the inhibition of signal production. Equally, some compounds inhibited violacein production by C. violaceum CV026 in the midst of an externally supplied acylhomoserine lactone, indicating that they disrupted signal molecule reception. Most of the compounds exhibited biofilm inhibition on Staphyloccocus aureus, Escherichia coli and Candida albicans and it was observed that the Gram-positive bacteria biofilm was most susceptible. The triterpenoids bearing carboxylic acid group, the ceramide and epicatechin were the most active compounds compared to others.

CONCLUSION

Since some of the compounds disrupted QS mediated processes in bacteria, it indicates that this plant is a source of antibiotics drugs that can reduce microbial resistance.

摘要

背景

微生物感染会导致严重的健康问题,尤其是抗生素耐药性的不断上升,每年导致约 70 万人死亡。针对细菌死亡的抗生素随着时间的推移会遇到微生物耐药性,因此,迫切需要寻找针对生物膜和群体感应(QS)等毒力因子的抗菌物质,对病原体施加选择性压力,以避免耐药性。

方法

天然产物是抑制细菌生物膜和 QS 的抗菌药物的合适先导物。从药用植物 Gambeya lacourtiana 中分离出的 20 种化合物被评估了其对选定致病菌的抗生物膜和抗群体感应作用。

结果

大多数化合物抑制 Chromobacterium violaceum CV12472 产生紫色素,最活跃的化合物表儿茶素在 MIC(最小抑菌浓度)下具有 100%的抑制作用,并且是唯一一种在 MIC/8 下抑制紫色素产生的化合物,抑制率为 17.2±0.9%。由于细菌 C. violaceum 在生长过程中产生紫色素,因此该色素的产生抑制反映了信号产生的抑制。同样,一些化合物在外部供应酰基高丝氨酸内酯的情况下抑制 C. violaceum CV026 产生紫色素,表明它们破坏了信号分子的接收。大多数化合物对金黄色葡萄球菌、大肠杆菌和白色念珠菌表现出生物膜抑制作用,并且观察到革兰氏阳性菌生物膜最敏感。与其他化合物相比,具有羧基的三萜类化合物、神经酰胺和表儿茶素是最活跃的化合物。

结论

由于一些化合物破坏了细菌中 QS 介导的过程,这表明该植物是一种可以减少微生物耐药性的抗生素药物的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/076f/10464238/5ac17b06d800/12906_2023_4115_Fig1_HTML.jpg

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