Rodríguez-López Pedro, Cabo Marta López
Department of Microbiology and Technology of Marine Products, Instituto de Investigaciones Marinas (IIM-CSIC), Eduardo Cabello 6, 36208 Vigo, Pontevedra, Spain.
Department of Microbiology and Technology of Marine Products, Instituto de Investigaciones Marinas (IIM-CSIC), Eduardo Cabello 6, 36208 Vigo, Pontevedra, Spain.
Food Microbiol. 2017 Oct;67:58-66. doi: 10.1016/j.fm.2017.06.002. Epub 2017 Jun 1.
This study was designed to assess the effects that sublethal exposures to pronase (PRN) and benzalkonium chloride (BAC) combined treatments have on Listeria monocytogenes-Escherichia coli dual-species biofilms grown on stainless steel in terms of tolerance development (TD) to these compounds. Additionally, fluorescence microscopy was used to observe the changes of the biofilm structure. PRN-BAC exposure was carried out using three different approaches and TD was evaluated treating biofilms with a final 100 μg/ml PRN followed by 50 μg/ml BAC combined treatment. Results showed that exposure to PRN-BAC significantly decreased the number of adhered L. monocytogenes (P < 0.05), while E. coli counts remained generally unaltered. It was also demonstrated that the incorporation of recovery periods during sublethal exposures increased the tolerance of both species of the mixed biofilm to the final PRN-BAC treatment. Moreover, control biofilms became more resistant to PRN-BAC if longer incubation periods were used. Regardless of the treatment used, log reduction values were generally lower in L. monocytogenes compared to E. coli. Additionally, microscopy images showed an altered morphology produced by sublethal PRN-BAC in exposed L. monocytogenes-E. coli dual-species biofilms compared to control samples. Results also demonstrated that L. monocytogenes-E. coli dual-species biofilms are able to develop tolerance to PRN-BAC combined treatments depending on way they have been previously exposed. Moreover, they suggest that the generation of bacterial tolerance should be included as a parameter for sanitation procedures design.
本研究旨在评估亚致死剂量的链霉蛋白酶(PRN)和苯扎氯铵(BAC)联合处理对在不锈钢表面生长的单核细胞增生李斯特菌-大肠杆菌双物种生物膜对这些化合物耐受性发展(TD)的影响。此外,还使用荧光显微镜观察生物膜结构的变化。采用三种不同方法进行PRN-BAC处理,并通过用终浓度为100μg/ml的PRN然后50μg/ml的BAC联合处理生物膜来评估TD。结果表明,PRN-BAC处理显著降低了单核细胞增生李斯特菌的附着数量(P<0.05),而大肠杆菌数量总体上保持不变。研究还表明,在亚致死暴露期间加入恢复期可提高混合生物膜中两种细菌对最终PRN-BAC处理的耐受性。此外,如果培养时间更长,对照生物膜对PRN-BAC的抗性会更强。无论采用何种处理方式,单核细胞增生李斯特菌的对数减少值通常低于大肠杆菌。此外,显微镜图像显示,与对照样品相比,亚致死剂量的PRN-BAC使暴露的单核细胞增生李斯特菌-大肠杆菌双物种生物膜的形态发生了改变。结果还表明,单核细胞增生李斯特菌-大肠杆菌双物种生物膜能够根据先前的暴露方式对PRN-BAC联合处理产生耐受性。此外,研究表明细菌耐受性的产生应作为卫生程序设计参数加以考虑。