Rouhi Arezou, Falah Fereshteh, Azghandi Marjan, Alizadeh Behbahani Behrooz, Tabatabaei-Yazdi Farideh, Ibrahim Salam A, Dertli Enes, Vasiee Alireza
Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.
Department of Animal Science, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.
Probiotics Antimicrob Proteins. 2024 Jul 4. doi: 10.1007/s12602-024-10318-z.
Listeria monocytogenes is a notable food-borne pathogen that has the ability to create biofilms on different food processing surfaces, making it more resilient to disinfectants and posing a greater risk to human health. This study assessed melittin peptide's anti-biofilm and anti-pathogenicity effects on L. monocytogenes ATCC 19115. Melittin showed minimum inhibitory concenteration (MIC) of 100 μg/mL against this strain and scanning electron microscopy images confirmed its antimicrobial efficacy. The OD measurement demonstrated that melittin exhibited a strong proficiency in inhibiting biofilms and disrupting pre-formed biofilms at concentrations ranging from 1/8MIC to 2MIC and this amount was 92.59 ± 1.01% to 7.17 ± 0.31% and 100% to 11.50 ± 0.53%, respectively. Peptide also reduced hydrophobicity and self-aggregation of L. monocytogenes by 35.25% and 14.38% at MIC. Melittin also significantly reduced adhesion to HT-29 and Caco-2 cells by 61.33% and 59%, and inhibited invasion of HT-29 and Caco-2 cells by 49.33% and 40.66% for L. monocytogenes at the MIC value. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) revealed melittin's impact on gene expression, notably decreasing inlB (44%) and agrA (45%) gene expression in L. monocytogenes. flaA and hly genes also exhibited reduced expression. Also, significant changes were observed in sigB and prfA gene expression. These results underscore melittin's potential in combating bacterial infections and biofilm-related challenges in the food industry.
单核细胞增生李斯特菌是一种著名的食源性病原体,能够在不同的食品加工表面形成生物膜,使其对消毒剂更具抵抗力,并对人类健康构成更大风险。本研究评估了蜂毒肽对单核细胞增生李斯特菌ATCC 19115的抗生物膜和抗致病性作用。蜂毒肽对该菌株的最低抑菌浓度(MIC)为100μg/mL,扫描电子显微镜图像证实了其抗菌效果。OD测量表明,蜂毒肽在浓度范围为1/8MIC至2MIC时,对生物膜的抑制和对已形成生物膜的破坏能力很强,该浓度下生物膜量分别从92.59±1.01%降至7.17±0.31%,以及从100%降至11.50±0.53%。在MIC浓度下,该肽还使单核细胞增生李斯特菌的疏水性和自聚集性分别降低了35.25%和14.38%。蜂毒肽还显著降低了单核细胞增生李斯特菌对HT - 29和Caco - 2细胞的粘附,分别降低了61.33%和59%,并在MIC值下抑制了单核细胞增生李斯特菌对HT - 29和Caco - 2细胞的侵袭,分别为49.33%和40.66%。逆转录定量聚合酶链反应(RT - qPCR)揭示了蜂毒肽对基因表达的影响,显著降低了单核细胞增生李斯特菌中inlB(44%)和agrA(45%)基因的表达。flaA和hly基因的表达也有所降低。此外,还观察到sigB和prfA基因表达的显著变化。这些结果强调了蜂毒肽在对抗食品工业中细菌感染和生物膜相关挑战方面的潜力。