Peptide extract from Hexaplex trunculus: A promising antimicrobial agent with inhibitory effects on quorum sensing and biofilm formation

Kofi Junior Osei , De-youngster Wereko Brobbey , Jennifer Tetteh , Michael Konney Laryea , Godfred Darko , Lawrence Sheringham Borquaye
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Abstract

Purpose

Infectious diseases are a global concern and antimicrobial resistance is a major cause of their prevalence. Antimicrobial peptides (AMPs), which are key components of the innate immune system of marine invertebrates, provide a rapid and immediate response against invading microbes. They possess remarkable antimicrobial activities and slower rates of resistance acquisition, making them an attractive target for new antimicrobial therapeutics. This work seeks to extract peptides from the marine mollusc, Hexaplex trunculus, and explore their antimicrobial activity.

Methods

Peptides were precipitated from the body tissue of H. trunculus, and the peptides were characterized using spectroscopic methods such as FTIR and UV. The broth dilution technique was used to determine the peptides' minimum inhibitory concentrations (MICs). The peptide extract was tested against Escherichia coli, Enterococcus faecalis, Staphylococcus aureus, Candida albicans, and Pseudomonas aeruginosa. The study also evaluated the effect of the peptide extracts on quorum sensing-mediated processes in Pseudomonas aeruginosa.

Results

The MIC values obtained against the various microorganisms ranged between 0.50 mg/mL and 0.25 mg/mL. Minimum bactericidal concentration (MBC) determination showed that the peptide extract at 0.50 mg/mL and 0.25 mg/mL had bacteriostatic effects. The results showed that the crude peptide extract inhibited biofilm formation in Pseudomonas aeruginosa. The expression of pyocyanin and pyoverdine, which are mediated by cell-to-cell communication, was inhibited by 88% and 66%, respectively, at 1/2 MIC of the peptide extract.

Conclusion

These findings suggest that crude peptide extract from Hexaplex trunculus may serve as a potential source of new antimicrobial agents to combat infectious diseases.
六轴草肽提取物:具有群体感应和生物膜形成抑制作用的抗菌药物
目的传染病是全球关注的问题,抗微生物药物耐药性是其流行的主要原因。抗菌肽(Antimicrobial peptides, AMPs)是海洋无脊椎动物先天免疫系统的重要组成部分,能够对入侵的微生物做出快速、即时的反应。它们具有显著的抗菌活性和较慢的耐药性获得率,使其成为新的抗菌治疗的有吸引力的目标。本研究旨在从海洋软体动物(Hexaplex trunculus)中提取肽,并探索其抗菌活性。方法采用紫外光谱和傅里叶红外光谱等方法对提取的多肽进行表征。采用肉汤稀释法测定肽的最低抑制浓度(mic)。对肽提取物进行了抗大肠杆菌、粪肠球菌、金黄色葡萄球菌、白色念珠菌和铜绿假单胞菌的实验。该研究还评估了肽提取物对铜绿假单胞菌群体感应介导过程的影响。结果对不同微生物的MIC值在0.50 ~ 0.25 mg/mL之间。最小杀菌浓度(MBC)测定表明,0.50 mg/mL和0.25 mg/mL的肽提取物具有抑菌作用。结果表明,粗肽提取物对铜绿假单胞菌生物膜的形成具有抑制作用。通过细胞间通讯介导的pyocyanin和pyoverdine的表达在1/2 MIC时分别被抑制了88%和66%。结论六轴藤肽粗提物具有开发新型抗菌药物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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