Biofilm formation by Listeria monocytogenes from the meat processing industry environment and the use of different combinations of detergents, sanitizers, and UV-A radiation to control this microorganism in planktonic and sessile forms.

IF 2.1 4区 生物学 Q3 MICROBIOLOGY
Brazilian Journal of Microbiology Pub Date : 2024-09-01 Epub Date: 2024-05-20 DOI:10.1007/s42770-024-01361-7
Larissa Siqueira Lima, Taís Nunzio Müller, Rafaela Ansiliero, Marcia Bär Schuster, Bruna Louise Silva, Itiane Barcellos Jaskulski, Wladimir Padilha da Silva, Liziane Schittler Moroni
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引用次数: 0

Abstract

This study aimed to evaluate the ability of biofilm formation by L. monocytogenes from the meat processing industry environment, as well as the use of different combinations of detergents, sanitizers, and UV-A radiation in the control of this microorganism in the planktonic and sessile forms. Four L. monocytogenes isolates were evaluated and showed moderate ability to form biofilm, as well as carried genes related to biofilm production (agrB, agrD, prfA, actA, cheA, cheY, flaA, sigB), and genes related to tolerance to sanitizers (lde and qacH). The biofilm-forming isolates of L. monocytogenes were susceptible to quaternary ammonium compound (QAC) and peracetic acid (PA) in planktonic form, with minimum inhibitory concentrations of 125 and 75 ppm, respectively, for contact times of 10 and 5 min. These concentrations are lower than those recommended by the manufacturers, which are at least 200 and 300 ppm for QAC and PA, respectively. Biofilms of L. monocytogenes formed from a pool of isolates on stainless steel and polyurethane coupons were subjected to 14 treatments involving acid and enzymatic detergents, QAC and PA sanitizers, and UV-A radiation at varying concentrations and contact times. All treatments reduced L. monocytogenes counts in the biofilm, indicating that the tested detergents, sanitizers, and UV-A radiation exhibited antimicrobial activity against biofilms on both surface types. Notably, the biofilm formed on polyurethane showed greater tolerance to the evaluated compounds than the biofilm on stainless steel, likely due to the material's surface facilitating faster microbial colonization and the development of a more complex structure, as observed by scanning electron microscopy. Listeria monocytogenes isolates from the meat processing industry carry genes associated with biofilm production and can form biofilms on both stainless steel and polyurethane surfaces, which may contribute to their persistence within meat processing lines. Despite carrying sanitizer tolerance genes, QAC and PA effectively controlled these microorganisms in their planktonic form. However, combinations of detergent (AC and ENZ) with sanitizers (QAC and PA) at minimum concentrations of 125 ppm and 300 ppm, respectively, were the most effective.

Abstract Image

肉类加工业环境中单核细胞增生李斯特菌生物膜的形成,以及使用洗涤剂、消毒剂和紫外线-A 辐射的不同组合来控制这种浮游和无柄微生物。
本研究旨在评估肉类加工业环境中的单核细胞增多性酵母菌形成生物膜的能力,以及使用洗涤剂、消毒剂和紫外线-A 辐射的不同组合来控制这种微生物的浮游和无柄形态。对四种单核细胞增多性乳酸杆菌分离物进行了评估,结果表明它们具有中等的形成生物膜的能力,并携带与生物膜产生有关的基因(agrB、agrD、prfA、actA、cheA、cheY、flaA、sigB)和与耐受消毒剂有关的基因(lde 和 qacH)。单核细胞增多性酵母菌的生物膜形成分离物对浮游状态下的季铵化合物(QAC)和过氧乙酸(PA)具有敏感性,接触时间分别为 10 分钟和 5 分钟,最低抑制浓度分别为 125 ppm 和 75 ppm。这些浓度低于制造商推荐的浓度,QAC 和 PA 的推荐浓度分别为至少 200 和 300 ppm。对不锈钢和聚氨酯试样上的单核细胞增多症生物膜进行了 14 种处理,包括不同浓度和接触时间的酸和酶洗涤剂、QAC 和 PA 消毒剂以及紫外线-A 辐射。所有处理方法都降低了生物膜中的单核细胞增生性酵母菌数量,表明所测试的清洁剂、消毒剂和紫外线-A 辐射对这两种表面类型上的生物膜都具有抗菌活性。值得注意的是,与不锈钢上的生物膜相比,聚氨酯上形成的生物膜对评估化合物的耐受性更强,这可能是由于材料表面有利于微生物更快定植并形成更复杂的结构(扫描电子显微镜观察到)。肉类加工业中分离出的单核细胞增生李斯特菌携带与生物膜生成有关的基因,可以在不锈钢和聚氨酯表面形成生物膜,这可能是它们在肉类加工生产线中持久存在的原因。尽管携带耐消毒剂基因,QAC 和 PA 仍能有效控制这些浮游微生物。不过,洗涤剂(AC 和 ENZ)与消毒剂(QAC 和 PA)的组合(最低浓度分别为 125 ppm 和 300 ppm)最为有效。
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来源期刊
Brazilian Journal of Microbiology
Brazilian Journal of Microbiology 生物-微生物学
CiteScore
4.10
自引率
4.50%
发文量
216
审稿时长
1.0 months
期刊介绍: The Brazilian Journal of Microbiology is an international peer reviewed journal that covers a wide-range of research on fundamental and applied aspects of microbiology. The journal considers for publication original research articles, short communications, reviews, and letters to the editor, that may be submitted to the following sections: Biotechnology and Industrial Microbiology, Food Microbiology, Bacterial and Fungal Pathogenesis, Clinical Microbiology, Environmental Microbiology, Veterinary Microbiology, Fungal and Bacterial Physiology, Bacterial, Fungal and Virus Molecular Biology, Education in Microbiology. For more details on each section, please check out the instructions for authors. The journal is the official publication of the Brazilian Society of Microbiology and currently publishes 4 issues per year.
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