乳酸菌和腐败菌:它们在食品接触表面的大肠杆菌 O157:H7 生物膜中的相互作用及其对牛肉污染的影响

IF 1.9 4区 农林科学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yuchen Nan, Argenis Rodas-Gonzalez, Kim Stanford, Celine Nadon, Xianqin Yang, Tim McAllister, Claudia Narváez-Bravo
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引用次数: 0

摘要

本研究探讨了产志贺毒素大肠杆菌(STEC)O157:H7 与牛肉加工环境中常见的细菌种类(特别是卡诺杆菌、乳酸杆菌、科莫纳菌、拉乌尔特氏菌和假单胞菌)之间的相互作用。该研究调查了各种环境条件如何影响生物膜的形成以及 O157:H7 从多菌种生物膜转移到牛肉表面的能力。为此,将乳酸菌(LAB)、腐败菌(106 CFU/mL)和大肠杆菌 O157(103 CFU/mL)的混合物组合如下:乳酸菌(T1):鲤鱼杆菌(T1):鲤鱼杆菌 + 保加利亚乳杆菌 + O157:H7;腐败菌(T2):韩国鲤鱼杆菌 + 保加利亚乳杆菌 + O157:H7:腐败菌(T3):铜绿假单胞菌 + O157:H7:铜绿假单胞菌 + 韩国酵母菌菌株 + O157:H7 和仅以 O157:H7 为对照(T4)。多菌种生物膜在热塑性聚氨酯(TPU)和不锈钢(SS)试样上形成,分别在 10 和 25 摄氏度条件下培养 6 天,然后在湿润(60%-90% 相对湿度)和干燥(20%-50% 相对湿度)条件下清洗并储存 6、30 和 60 天。为了评估 O157:H7 的转移情况,将牛肉块(3 × 3 × 1 厘米)放在砧板上,然后施加 50 克的重量(7.35 千帕)。每种菌株组合重复实验三次,每次一式三份。结果表明,与 25°C 的生物膜相比,10°C 下形成的生物膜普遍较弱(生物量较少)。无论温度如何,从 TPU 表面潮湿的生物膜转移到牛肉上的 O157:H7 活细胞都更多。在 25°C 时,T3 生物膜向牛肉转移的 O157:H7 细胞最少,为 1.44 log10 CFU/cm2(p <0.01)。在 10°C 时,多菌种生物膜(T1-T3)都不会影响牛肉中 O157:H7 的转移数量(p >0.05)。值得注意的是,在 30 天和 60 天的干生物膜(T1-T4)中,食品接触表面未检测到 O157:H7。通过富集,从多菌种生物膜 T1、T2 和 T3 中回收了大肠杆菌 O157:H7。这项研究的结果表明,多菌种生物膜有助于 O157:H7 在干燥条件下的存活,而与温度无关。这些结果凸显了多种环境因素(包括表面类型、生物膜年龄、湿度、温度和其他细菌物种的存在)对生物膜导致的牛肉污染风险的复杂影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lactic acid bacteria and spoilage bacteria: Their interactions in Escherichia coli O157:H7 biofilms on food contact surfaces and implications for beef contamination

Lactic acid bacteria and spoilage bacteria: Their interactions in Escherichia coli O157:H7 biofilms on food contact surfaces and implications for beef contamination

This research explores the interaction between Shiga toxin-producing Escherichia coli (STEC) O157:H7 and bacteria species commonly found in beef processing environments, specifically Carnobacterium, Lactobacillus, Comamonas, Raoultella, and Pseudomonas. The study investigated how various environmental conditions impact the formation of biofilms and the ability of O157:H7 to transfer from multispecies biofilm onto beef surfaces. For this purpose, a mixture of lactic acid bacteria (LAB), spoilage bacteria (106 CFU/mL), and E. coli O157 (103 CFU/mL) were combined as follows: LAB (T1): Carnobacterium piscicola + Lactobacillus bulgaricus + O157:H7, an spoilage bacteria (T2): Comamonas koreensis + Raoultella terrigena + O157:H7, an spoilage bacteria (T3): Pseudomonas aeruginosa + C. koreensis strain + O157:H7 and only O157:H7 as control (T4). Multispecies biofilms were developed on thermoplastic polyurethane (TPU) and stainless steel (SS) coupons at 10 and 25°C for 6 days, washed and stored for 6, 30, and 60 days at wet (60%–90% RH) and dry (20%–50%, RH) conditions. To evaluate O157:H7 transfer, beef cubes (3 × 3 × 1 cm) were placed on the coupons, followed by a 50-g weight (7.35 kPa). The experiment was repeated three times in triplicate for each strain combination. Results demonstrate that biofilms formed at 10°C were generally weaker (less biomass) than those at 25°C. Regardless of temperature, more viable O157:H7 cells were transferred to beef from moist biofilms on TPU surfaces. At 25°C, T3 biofilm exhibited the lowest O157:H7 transfer to beef by 1.44 log10 CFU/cm2 (p < 0.01). At 10°C, none of the multispecies biofilm (T1–T3) affected the number of O157:H7 transfers to beef (p > 0.05). Notably, O157:H7 was not detected on food contact surfaces with 30 and 60-day-old dry biofilms (T1–T4). Through enrichment, E. coli O157:H7 was recovered from multispecies biofilms T1, T2, and T3. Findings from this study imply that multispecies biofilms contribute to the persistence of O157:H7 under dry conditions, regardless of temperature. These results underscore the intricate influence of multiple environmental factors—including surface type, biofilm age, humidity, temperature, and the presence of other bacterial species—on the risk of beef contamination facilitated by biofilms.

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来源期刊
Journal of Food Safety
Journal of Food Safety 工程技术-生物工程与应用微生物
CiteScore
5.30
自引率
0.00%
发文量
69
审稿时长
1 months
期刊介绍: The Journal of Food Safety emphasizes mechanistic studies involving inhibition, injury, and metabolism of food poisoning microorganisms, as well as the regulation of growth and toxin production in both model systems and complex food substrates. It also focuses on pathogens which cause food-borne illness, helping readers understand the factors affecting the initial detection of parasites, their development, transmission, and methods of control and destruction.
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