Antimicrobial metabolites from Probiotics, Pleurotus ostreatus and their co-cultures against foodborne pathogens isolated from ready-to-eat foods

IF 3 4区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Oluwaferanmi Esther Bamisi, Clement Olusola Ogidi, Bamidele Juliet Akinyele
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引用次数: 0

Abstract

The incidence of foodborne pathogens in ready- to-eat (RTE) can be attributed to various foodborne diseases. Most of the isolated microorganisms from RTE foods are resistant to common antibiotics and thus, resulted to treatment failure when commercially available antibiotics are administered. However, the secondary metabolites secreted by microorganisms can serve as alternative therapy that are reliable and safe. Secondary metabolites obtained from mono- and co-culture microorganisms can inhibit the growth of antibiotic-resistant microorganisms. Bioactive compounds in the secreted metabolites can be identified and utilized as sources of new antibiotics. In this study, antimicrobial activity of secondary metabolites from Lactobacillus fermentum, Saccharomyces cerevisiae, Pleurotus ostreatus, and their co-cultures were tested against foodborne pathogens isolated from RTE foods using agar well diffusion. The bioactive compounds in the metabolites were identified using gas chromatography-mass spectrometry. From a total of 100 RTE foods examined, Salmonella enterica, Shigella dysenteriae, Escherichia coli, Klebsiella pneumoniae (subsp ozaenae), Pseudomonas fluorescens, Clostridium perfringes, Bacillus cereus, Listeria monocytogens, and Staphylococcus aureus, Penicillium chrysogenum, Aspergillus flavus, and Aspergillus niger were isolated and displayed multiple antibiotic resistance. The secondary metabolites secreted by co-culture of L. fermentum + P. ostreatus + S. cerevisiae, and co-culture of P. ostreatus + S. cerevisiae have the highest (P ≤ 0.05) zones of inhibition (23.70 mm) and (21.10 mm) against E. coli, respectively. Metabolites from mono-cultured L. fermentum, P. ostreatus, and S. cerevisiae showed zones of inhibition against indicator microorganisms with values ranging from 8.80 to 11.70 mm, 9.00 to 14.30 mm, and 9.30 to 13.00 mm, respectively. Some of the bioactive compounds found in the metabolites of co-cultured microorganisms were alpha-linolenic acid (25.71%), acetic acid 3-methylbutyl ester (13.83%), trans-squalene (12.39%), pentadecylic acid (11.68%), 3- phenyllactic acid (30.13%), linolelaidic acid methyl ester (15.63%), and 4-O-methylmannose (53.74%). RTE foods contain multiple antibiotics resistance pathogens. The pronounced antimicrobial activity of the secondary metabolites against microorganisms from RTE foods could be attributed to the presence of bioactive compounds in the metabolites. These metabolites can be exploited as alternative food preservatives, biopharmaceuticals and can be used towards better health delivering systems.
益生菌、牛肝菌及其共培养物对从即食食品中分离出的食源性致病菌的抗菌代谢产物
即食食品中的食源性病原体可导致各种食源性疾病。从即食食品中分离出的大多数微生物对普通抗生素具有抗药性,因此,使用市售抗生素治疗时会导致治疗失败。然而,微生物分泌的次级代谢物可作为可靠、安全的替代疗法。从单培养和共培养微生物中获得的次生代谢物可以抑制抗生素耐药微生物的生长。分泌代谢物中的生物活性化合物可被鉴定并用作新抗生素的来源。本研究采用琼脂井扩散法测试了发酵乳杆菌、酿酒酵母、牡蛎及其共培养物的次生代谢物对从即食食品中分离出的食源性致病菌的抗菌活性。代谢物中的生物活性化合物采用气相色谱-质谱法进行鉴定。在检测的 100 种即食性食品中,分离出了肠炎沙门氏菌、痢疾志贺氏菌、大肠埃希氏菌、肺炎克雷伯菌(大肠杆菌亚种)、荧光假单胞菌、产气荚膜梭菌、蜡样芽孢杆菌、单核细胞李斯特菌、金黄色葡萄球菌、金黄色青霉、黄曲霉和黑曲霉,并显示出多种抗生素耐药性。L. fermentum + P. ostreatus + S. cerevisiae 共培养物和 P. ostreatus + S. cerevisiae 共培养物分泌的次生代谢物对大肠杆菌的抑菌作用分别为(23.70 毫米)和(21.10 毫米),抑菌面积最大(P ≤ 0.05)。单培养 L. fermentum、P. ostreatus 和 S. cerevisiae 的代谢物对指示微生物的抑制区分别为 8.80 至 11.70 毫米、9.00 至 14.30 毫米和 9.30 至 13.00 毫米。在共培养微生物的代谢产物中发现的一些生物活性化合物有:α-亚麻酸(25.71%)、乙酸 3-甲基丁酯(13.83%)、反式角鲨烯(12.39%)、十五烷酸(11.68%)、3-苯基乳酸(30.13%)、亚油酸甲酯(15.63%)和 4-O-甲基甘露糖(53.74%)。即食食品中含有多种抗生素耐药性病原体。次生代谢物对来自即食食品的微生物具有明显的抗菌活性,这可能是因为代谢物中含有生物活性化合物。这些代谢物可用作替代食品防腐剂和生物制药,并可用于改善健康服务系统。
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来源期刊
Annals of Microbiology
Annals of Microbiology 生物-生物工程与应用微生物
CiteScore
6.40
自引率
0.00%
发文量
41
审稿时长
3.2 months
期刊介绍: Annals of Microbiology covers these fields of fundamental and applied microbiology: general, environmental, food, agricultural, industrial, ecology, soil, water, air and biodeterioration. The journal’s scope does not include medical microbiology or phytopathological microbiology. Papers reporting work on bacteria, fungi, microalgae, and bacteriophages are welcome. Annals of Microbiology publishes Review Articles, Original Articles, Short Communications, and Editorials. Originally founded as Annali Di Microbiologia Ed Enzimologia in 1940, Annals of Microbiology is an official journal of the University of Milan.
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