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在模拟食品加工环境中,单核细胞增生李斯特菌生物被膜对消毒剂的抗性。

Resistance of Listeria monocytogenes biofilms to sanitizing agents in a simulated food processing environment.

作者信息

Pan Y, Breidt F, Kathariou S

机构信息

North Carolina Agricultural Research Service, Department of Food Science, North Carolina State University, Raleigh, NC 27695-7624, USA.

出版信息

Appl Environ Microbiol. 2006 Dec;72(12):7711-7. doi: 10.1128/AEM.01065-06. Epub 2006 Sep 29.

Abstract

The objective of this study was to evaluate the resistance of biofilms of Listeria monocytogenes to sanitizing agents under laboratory conditions simulating a food processing environment. Biofilms were initially formed on stainless steel and Teflon coupons using a five-strain mixture of L. monocytogenes. The coupons were then subjected to repeated 24-h daily cycles. Each cycle consisted of three sequential steps: (i) a brief (60 s) exposure of the coupons to a sanitizing agent (a mixture of peroxides) or saline as a control treatment, (ii) storage of the coupons in sterile plastic tubes without any nutrients or water for 15 h, (iii) and incubation of the coupons in diluted growth medium for 8 h. This regimen was repeated daily for up to 3 weeks and was designed to represent stresses encountered by bacteria in a food processing environment. The bacteria on the coupons were reduced in number during the first week of the simulated food processing (SFP) regimen, but then adapted to the stressful conditions and increased in number. Biofilms repeatedly exposed the peroxide sanitizer in the SFP regimen developed resistance to the peroxide sanitizer as well as other sanitizers (quaternary ammonium compounds and chlorine). Interestingly, cells that were removed from the biofilms on peroxide-treated and control coupons were not significantly different in their resistance to sanitizing agents. These data suggest that the resistance of the treated biofilms to sanitizing agents may be due to attributes of extracellular polymeric substances and is not an intrinsic attribute of the cells in the biofilm.

摘要

本研究的目的是在模拟食品加工环境的实验室条件下,评估单核细胞增生李斯特菌生物膜对消毒剂的抗性。使用单核细胞增生李斯特菌的五菌株混合物在不锈钢和聚四氟乙烯试片上初步形成生物膜。然后将试片每天进行24小时的重复循环处理。每个循环包括三个连续步骤:(i) 将试片短暂(60秒)暴露于消毒剂(过氧化物混合物)或作为对照处理的盐水中,(ii) 将试片在没有任何营养物或水的无菌塑料管中储存15小时,(iii) 将试片在稀释的生长培养基中孵育8小时。该方案每天重复进行,最长持续3周,旨在模拟食品加工环境中细菌所遇到的压力。在模拟食品加工(SFP)方案的第一周,试片上的细菌数量减少,但随后适应了压力条件并数量增加。在SFP方案中反复暴露于过氧化物消毒剂的生物膜对过氧化物消毒剂以及其他消毒剂(季铵化合物和氯)产生了抗性。有趣的是,从用过氧化物处理的试片和对照试片上的生物膜中去除的细胞对消毒剂的抗性没有显著差异。这些数据表明,经处理的生物膜对消毒剂的抗性可能归因于细胞外聚合物的特性,而不是生物膜中细胞的固有特性。

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