Food Science Department, Food and Agriculture Faculty, Laval University, Quebec, Quebec, Canada.
Faculty of Pharmacy, Laval University and Laboratory of Medicinal Chemistry, CHU de Québec Research Center, Quebec, Quebec, Canada.
Microbiol Spectr. 2022 Feb 23;10(1):e0040621. doi: 10.1128/spectrum.00406-21. Epub 2022 Feb 16.
Bacteria-derived natural antimicrobial compounds such as bacteriocins, reruterin, and organic acids have recently received substantial attention as food preservatives or therapeutic alternatives in human or animal sectors. This study aimed to evaluate the antimicrobial activity of different bacteria-derived antimicrobials, alone or in combination, against a large panel of Gram-negative and Gram-positive bacteria. Bacteriocins, including microcin J25, pediocin PA-1, nisin Z, and reuterin, were investigated alone or in combination with lactic acid and citric acid, using a checkerboard assay. Concentrations were selected based on predetermined MICs against Salmonella enterica subsp. serovar Newport ATCC 6962 and Listeria ivanovii HPB28 as Gram-negative and Gram-positive indicator strains, respectively. The results demonstrated that the combination of microcin J25 + citric acid + lactic acid; microcin J25 + reuterin + citric acid; and microcin J25 + reuterin + lactic acid tested against Newport ATCC 6962 showed synergistic effects (FIC index = 0.5). Moreover, a combination of pediocin PA-1 + citric acid + lactic acid; and reuterin + citric acid + lactic acid against HPB28 showed a partially synergistic interactions (FIC index = 0.75). Nisin Z exerted a partially synergistic effect in combination with acids (FIC index = 0.625 -0.75), whereas when it was combined with reuterin or pediocin PA-1, it showed additive effects (FIC index = 1) against HPB28. The inhibitory activity of synergetic consortia were tested against a large panel of Gram-positive and Gram-negative bacteria. According to our results, combining different antimicrobials with different mechanisms of action led to higher potency and a broad spectrum of inhibition, including multidrug-resistance pathogens. Reuterin and bacteriocins, including microcin J25, pediocin PA-1, nisin were produced and purified with >90% purity. Using the broth-based checkerboard assay the interaction between these compounds (synergetic, additive, or antagonistic) was assessed. By combining different natural antimicrobials with different modes of action and structure (reuteirn, microcin J25, pediocin PA-1, and organic acids), we successfully developed five different synergetic consortia with improved antimicrobial activity and a broad spectrum of inhibition. These consortia were shown to be effective against a large panel of pathogenic and spoilage microorganisms as well as clinically important multidrug-resistance bacteria. Moreover, because the lower concentrations of bacteriocins and reuterin are used in the synergetic consortia, there is a limited risk of toxicity and resistance development for these compounds.
细菌衍生的天然抗菌化合物,如细菌素、雷普汀和有机酸,最近作为食品防腐剂或人类或动物领域的治疗替代品受到了广泛关注。本研究旨在评估不同细菌衍生抗菌剂单独或联合使用对大量革兰氏阴性和革兰氏阳性细菌的抗菌活性。使用棋盘试验单独或组合乳酸和柠檬酸研究了细菌素,包括微菌素 J25、肠球菌素 PA-1、乳链菌肽 Z 和雷普汀。浓度是根据对肠炎沙门氏菌亚种的预定义 MIC 选择的。纽波特 ATCC 6962 和李斯特菌。作为革兰氏阴性和革兰氏阳性指示菌株的 HPB28。结果表明,微菌素 J25+柠檬酸+乳酸;微菌素 J25+雷普汀+柠檬酸;和微菌素 J25+雷普汀+乳酸对纽波特 ATCC 6962 的测试显示协同作用(FIC 指数= 0.5)。此外,肠球菌素 PA-1+柠檬酸+乳酸;和雷普汀+柠檬酸+乳酸对 HPB28 显示部分协同相互作用(FIC 指数= 0.75)。乳链菌肽 Z 与酸联合时表现出部分协同作用(FIC 指数= 0.625-0.75),而与雷普汀或肠球菌素 PA-1 联合时,对 HPB28 显示相加作用(FIC 指数= 1)。协同组合的抑制活性针对一大组革兰氏阳性和革兰氏阴性细菌进行了测试。根据我们的结果,将具有不同作用机制的不同抗菌剂组合使用可提高效力并扩大抑制谱,包括多药耐药病原体。雷普汀和细菌素,包括微菌素 J25、肠球菌素 PA-1、乳链菌肽 Z 被生产和纯化,纯度超过 90%。使用基于肉汤的棋盘试验评估这些化合物之间的相互作用(协同、相加或拮抗)。通过将不同的天然抗菌剂与不同的作用模式和结构(雷普汀、微菌素 J25、肠球菌素 PA-1 和有机酸)结合使用,我们成功开发了五种具有改进的抗菌活性和广泛抑制谱的协同组合。这些组合对多种致病性和腐败微生物以及临床重要的多药耐药菌均有效。此外,由于协同组合中使用的细菌素和雷普汀的浓度较低,因此这些化合物的毒性和耐药性发展的风险有限。