Survival of Escherichia coli O157:H7 and Listeria monocytogenes on Spinach and Blueberries Treated With Aqueous Chlorine Dioxide and Muscadine (Vitis rotundifolia) Extract

IF 2.8 4区 农林科学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Angelica Abdallah , Juan L. Silva , Wes Schilling , Eric T. Stafne , Shecoya B. White
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Abstract

The antimicrobial effect of various concentrations of chlorine dioxide (ClO2) and muscadine extract (ME) was investigated on Escherichia coli O157:H7 and Listeria monocytogenes under in vitro conditions and on treated spinach and blueberries. Tryptic soy broth (TSB) and produce were inoculated with a 3-strain cocktail of each pathogen. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined using either 96-well plates incubated in a microplate reader for ClO2 or test tubes incubated in a conventional incubator at 37 °C for 24 h for the ME. Pathogen reduction on inoculated produce (inoculation levels were 5.6–7.0 log CFU/g for spinach and 4.5–5.1 log CFU/g for blueberries) was evaluated after exposure to various antimicrobial treatments for 10 min + 30–45 min dry time + storage at 8 °C for up to six days. Under in vitro, L. monocytogenes was more susceptible than E. coli O157:H7 to ClO2 and ME. On spinach, 300 mg/ml ME and 3 ppm ClO2 + 300 mg/ml ME treatments resulted in the maximum reduction of E. coli O157:H7 (4.6 log CFU/g reduction at day 1) and L. monocytogenes (5.6 log CFU/g reduction at day 2), respectively. On blueberries, all the treatments significantly decreased E. coli O157:H7 counts (≤1.7 log CFU/g), and no differences (P > 0.05) were detected from day 1 to day 6. The treatment 3 ppm ClO2 + 300 mg/ml ME led to nondetectable (P ≤ 0.05) L. monocytogenes levels on blueberries at days 1, 2, 4, and 6, leading to surface reductions >4.1 log CFU/g. Based on the study, ME combined with ClO2 could be a potential candidate as postharvest treatment to reduce the presence of E. coli O157:H7 and L. monocytogenes on blueberries. Both pathogens were less susceptible to these combined treatments on spinach.
用二氧化氯水溶液和麝香碱提取物处理菠菜和蓝莓后,大肠杆菌O157:H7和单核增生李斯特菌的存活。
研究了不同浓度二氧化氯(ClO2)和麝香碱提取物(ME)在体外条件下对大肠杆菌O157:H7和单核增生李斯特菌的抑菌效果,以及对处理过的菠菜和蓝莓的抑菌效果。用每种病原体的3株鸡尾酒接种胰蛋白酶肉汤(TSB)和农产品。最小抑菌浓度(MIC)和最小杀菌浓度(MBC)分别用96孔板在微孔板读本仪中培养ClO2或试管在常规培养箱中37°C孵育24 h来测定ME。在不同的抗菌剂处理10分钟+ 30-45分钟干燥时间+ 8°C保存6天后,对接种过的产品(菠菜接种量为5.6-7.0 log CFU/g,蓝莓接种量为4.5-5.1 log CFU/g)的致病菌减少情况进行了评估。在体外,单核增生乳杆菌比大肠杆菌O157:H7对ClO2和ME更敏感。在菠菜上,300 mg/ml ME和3 ppm ClO2 + 300 mg/ml ME处理分别最大限度地减少了大肠杆菌O157:H7(第1天减少4.6 log CFU/g)和单核细胞增多杆菌(第2天减少5.6 log CFU/g)。在蓝莓上,所有处理均显著降低大肠杆菌O157:H7计数(≤1.7 log CFU/g),第1 ~ 6天无显著差异(P < 0.05)。在3 ppm ClO2 + 300 mg/ml ME处理下,蓝莓在第1、2、4和6天的单核细胞增生L.细胞水平均未检测到(P≤0.05),导致蓝莓表面减少>.1 log CFU/g。基于该研究,ME联合ClO2可能是一种潜在的采后处理方法,可以减少蓝莓上大肠杆菌O157:H7和单核细胞增生乳杆菌的存在。这两种病原体对菠菜的联合处理不那么敏感。
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来源期刊
Journal of food protection
Journal of food protection 工程技术-生物工程与应用微生物
CiteScore
4.20
自引率
5.00%
发文量
296
审稿时长
2.5 months
期刊介绍: The Journal of Food Protection® (JFP) is an international, monthly scientific journal in the English language published by the International Association for Food Protection (IAFP). JFP publishes research and review articles on all aspects of food protection and safety. Major emphases of JFP are placed on studies dealing with: Tracking, detecting (including traditional, molecular, and real-time), inactivating, and controlling food-related hazards, including microorganisms (including antibiotic resistance), microbial (mycotoxins, seafood toxins) and non-microbial toxins (heavy metals, pesticides, veterinary drug residues, migrants from food packaging, and processing contaminants), allergens and pests (insects, rodents) in human food, pet food and animal feed throughout the food chain; Microbiological food quality and traditional/novel methods to assay microbiological food quality; Prevention of food-related hazards and food spoilage through food preservatives and thermal/non-thermal processes, including process validation; Food fermentations and food-related probiotics; Safe food handling practices during pre-harvest, harvest, post-harvest, distribution and consumption, including food safety education for retailers, foodservice, and consumers; Risk assessments for food-related hazards; Economic impact of food-related hazards, foodborne illness, food loss, food spoilage, and adulterated foods; Food fraud, food authentication, food defense, and foodborne disease outbreak investigations.
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