Folsom James P, Frank Joseph F
Department of Food Science and Technology, University of Georgia, Athens, Georgia 30602-7610, USA.
J Food Prot. 2007 May;70(5):1129-36. doi: 10.4315/0362-028x-70.5.1129.
Following exposure of Listeria monocytogenes Scott A (SA) to hypochlorous acid, rough colony variants were identified that were tolerant of hypochlorous acid and produced increased amounts of biofilm. A derivative of one of these variants was smooth, produced even more biofilm, and exhibited greater biofilm chlorine resistance. The objective of this research was to compare the protein expression of a cultural variant to SA and to identify proteins that might be associated with biofilm production and chlorine tolerance. Suspension chlorine tolerance for several cultural variants (SAR, SAR5, and SBS) was determined by exposure to 60 to 120 ppm of hypochlorous acid for 5 min. Hypochlorous acid tolerance of biofilms was determined after growing biofilms on stainless steel and then exposing them to 200 ppm of hypochlorous acid for 5 min. All cultural variants were able to survive 120 ppm of hypochlorous acid in suspension. There was little difference in the hypochlorous acid tolerance of the cultural variant planktonic cells. The cultural variants produced greater amounts of biofilm than the common form of L. monocytogenes and were more tolerant of hypochlorous acid. The SBS variant was selected for proteomic comparison because it was the variant that produced the most biofilm and was the most tolerant of hypochlorous acid when grown as a biofilm. Protein expression of planktonic and biofilm cells of SBS was compared to SA by two-dimensional difference gel electrophoresis. The 50s ribosomal protein, L10, was down-regulated in biofilm SBS. Other proteins down-regulated in planktonic SBS were the peroxide resistance protein (Dpr) and a sugar-binding protein (LMO0181). This sugar-binding protein was also up-regulated in biofilm SBS. One protein spot down-regulated in planktonic SBS contained both 50s ribosomal protein L7/L12 and an unknown protein (LM01888).
将单核细胞增生李斯特菌斯科特A株(SA)暴露于次氯酸后,鉴定出了粗糙菌落变体,这些变体对次氯酸具有耐受性,并产生了更多的生物膜。其中一个变体的衍生物是光滑的,产生了更多的生物膜,并且表现出更高的生物膜耐氯性。本研究的目的是比较一种培养变体与SA的蛋白质表达,并鉴定可能与生物膜产生和耐氯性相关的蛋白质。通过将几种培养变体(SAR、SAR5和SBS)暴露于60至120 ppm的次氯酸中5分钟来测定其悬浮液耐氯性。在不锈钢上培养生物膜,然后将其暴露于200 ppm的次氯酸中5分钟后,测定生物膜的耐次氯酸能力。所有培养变体在悬浮液中都能在120 ppm的次氯酸中存活。培养变体浮游细胞的耐次氯酸能力差异不大。培养变体比单核细胞增生李斯特菌的常见形式产生更多的生物膜,并且对次氯酸更具耐受性。选择SBS变体进行蛋白质组学比较,因为它是产生生物膜最多的变体,并且在作为生物膜生长时对次氯酸的耐受性最强。通过二维差异凝胶电泳将SBS浮游细胞和生物膜细胞的蛋白质表达与SA进行比较。50S核糖体蛋白L10在生物膜SBS中表达下调。在浮游SBS中表达下调的其他蛋白质是过氧化物抗性蛋白(Dpr)和一种糖结合蛋白(LMO0181)。这种糖结合蛋白在生物膜SBS中也上调。在浮游SBS中表达下调的一个蛋白点同时包含50S核糖体蛋白L7/L12和一种未知蛋白(LM01888)。