Department of Food Science and Technology, Advanced Food Safety Research Group, Chung-Ang University, Nae-ri, Daeduk-myun, Ansung, Kyunggido 17546, Republic of Korea.
Food Science and Technology, Oregon State University, Corvallis, OR, United States.
Food Res Int. 2022 Jul;157:111367. doi: 10.1016/j.foodres.2022.111367. Epub 2022 May 20.
Listeria monocytogenes is a foodborne pathogen that can form biofilms in food processing facilities even under unfavorable growth environment. This study aimed to evaluate the biofilm eradication ability of Listeria-specific bacteriophage (phage) cocktail (LMPC01+02+03) against L. monocytogenes young (1 day) and mature (3 days) biofilms formed on food contact materials (FCMs: polyethylene, polypropylene, and stainless steel) at 4, 15, and 30 °C. In addition, virulence-related genes and biofilm structure parameters of the phage-treated biofilms were investigated. The biofilm eradication ability of the phage cocktail was evaluated on 96 well and MBEC plate, and the results revealed that a multiplicity-of-infection (MOI) 100 of the phage cocktail exhibited the ability of eradicate biofilms. Using MOI 100, the phage cocktail treatment on the biofilms formed on FCMs for 8 h reduced over 2 log CFU/cm of the young biofilms, and approximately 1 log CFU/cm of the mature biofilms. In addition, the phage treatment against the biofilms resulted in a significant up-regulation of two genes (flaA and motB), and up/down-regulation or no changes in three genes (hlyA, prfA, and actA). Confocal and scanning electron microscopy images revealed the loss of the biofilm matrix after the phage treatment, and quantitative analysis revealed a reduction in the structural parameters of the biofilm, except the microcolonies at the substratum level, which increased. These results suggested that MOI 100 of the phage cocktail (LMPC01+02+03) was an effective tool for eradicating L. monocytogenes biofilms formed on FCMs, and it is essential to develop a countermeasure to eradicate the biofilm remaining after phage treatment.
李斯特菌是一种食源性病原体,即使在不利的生长环境下,也能在食品加工设施中形成生物膜。本研究旨在评估李斯特菌特异性噬菌体(噬菌体)鸡尾酒(LMPC01+02+03)对在食品接触材料(FCM:聚乙烯、聚丙烯和不锈钢)上形成的年轻(1 天)和成熟(3 天)生物膜的清除能力,温度分别为 4、15 和 30°C。此外,还研究了噬菌体处理生物膜的毒力相关基因和生物膜结构参数。通过 96 孔板和 MBEC 板评估噬菌体鸡尾酒的生物膜清除能力,结果表明噬菌体鸡尾酒的感染复数(MOI)为 100 时具有清除生物膜的能力。使用 MOI 100,噬菌体鸡尾酒处理在 FCM 上形成的生物膜 8 小时后,可减少年轻生物膜超过 2 个对数 CFU/cm,成熟生物膜减少约 1 个对数 CFU/cm。此外,噬菌体处理对生物膜的处理导致两个基因(flaA 和 motB)的显著上调,以及三个基因(hlyA、prfA 和 actA)的上调/下调或无变化。共聚焦和扫描电子显微镜图像显示,噬菌体处理后生物膜基质丢失,定量分析显示生物膜结构参数减少,除了基质水平的微菌落增加外。这些结果表明,噬菌体鸡尾酒(LMPC01+02+03)的 MOI 100 是清除 FCM 上形成的李斯特菌生物膜的有效工具,开发一种清除噬菌体处理后残留生物膜的对策至关重要。