Biofilm eradication ability of phage cocktail against Listeria monocytogenes biofilms formed on food contact materials and effect on virulence-related genes and biofilm structure

被引:25
作者
Byun, Kye-Hwan [1 ]
Ha Han, Sang [1 ]
Choi, Min Woo [1 ]
Kim, Byoung-Hu [1 ]
Park, Si Hong [1 ,2 ]
Ha, Sang -Do [1 ,3 ]
机构
[1] Chung Ang Univ, Dept Food Sci & Technol, Adv Food Safety Res Grp, Nae Ri,Daeduk Myun, Ansun 17546, Kyunggido, South Korea
[2] Oregon State Univ, Food Sci & Technol, Corvallis, OR USA
[3] Chung Ang Univ, Dept Food Sci & Technol, Daeduk myun, 72-1 Nae Ri,Daeduk Myun, Ansung 17546, Kyunggido, South Korea
基金
新加坡国家研究基金会;
关键词
Listeria monocytogenes; FCMs; Biofilms; Bacteriophage; Virulence-related genes; BACTERIOPHAGE; EXPRESSION; BIOCONTROL; RESISTANCE; EVOLUTION; PRODUCTS; SALMON;
D O I
10.1016/j.foodres.2022.111367
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
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 degrees 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/cm2 of the young biofilms, and approximately 1 log CFU/cm2 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.
引用
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页数:11
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