Sanitizer Resistance and Persistence of Listeria monocytogenes Isolates in Tree Fruit Packing Facilities

IF 2.1 4区 农林科学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
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Abstract

The foodborne pathogen Listeria monocytogenes can persist in produce processing environments, which increases the risk for food contamination. Increased resistance to antimicrobials commonly used in cleaning and sanitizing procedures may contribute to L. monocytogenes’ persistence in these environments. This study aimed to evaluate sanitizer resistance in L. monocytogenes isolates collected from three tree fruit packing facilities (F1, F2, and F3) during packing seasons 2020–2021 (Y1) and 2021–2022 (Y2), and to assess evidence of persistence based on the genomic similarity of isolates to historical isolates collected in previous years. L. monocytogenes isolates collected in 2020–2022 (n = 44) were tested for resistance to peroxyacetic acid (PAA) and a proprietary biofilm−removing agent using a broth microdilution assay. Further, L. monocytogenes isolates were whole genome sequenced and screened for the presence of antimicrobial resistance and virulence genes, as well as to assess the genomic similarity of isolates using the CFSAN SNP bioinformatic pipeline. Over half (57%) of the tested isolates had a PAA minimum inhibitory concentration (MIC) of 250 ppm, which was similar to the applied concentration of the PAA sanitizer in the three facilities (230 ppm). In contrast, 80% of tested isolates had a biofilm remover MIC of 0.13 ppm, which was substantially below the concentration applied in the facilities (137 ppm). Genomes of all tested isolates carried antimicrobial resistance (fosX, lin, mdrL, mprF, and norB) and virulence (inlA, inlB, plcA, plcB, prfA, hly, mpl, and iap) genes. L. monocytogenes isolates collected between 2020 and 2022 belonged to three distinct lineages, with 22 multilocus sequence types (MLSTs) belonging to 22 different clonal complexes. Genomic similarity analysis with historical isolates collected from the same facilities in 2016–2017 demonstrated a 5-year persistence of the genotypes ST 1003 and ST 554 in F2, which were no longer detected in 2022. Overall, our results highlight the need to re-evaluate sanitizer concentrations to effectively control persistent L. monocytogenes strains in tree fruit packing facilities.

果树包装设施中单核细胞增生李斯特菌分离物的抗消毒剂性和持久性。
食源性病原体单核细胞增生李斯特菌可在农产品加工环境中持续存在,这增加了食品污染的风险。对清洁和消毒程序中常用抗菌剂的耐药性增加可能是导致单核细胞增生李斯特氏菌在这些环境中持续存在的原因。本研究旨在评估在 2020-2021 年(Y1)和 2021-2022 年(Y2)包装季节从三个林果包装设施(F1、F2 和 F3)中收集到的单核细胞增生奈氏菌分离物对消毒剂的耐药性,并根据分离物与往年收集到的历史分离物的基因组相似性评估其持久性的证据。采用肉汤微量稀释法检测 2020-2022 年收集的单核细胞增多症 L. 分离物(n = 44)对过氧乙酸 (PAA) 和专有生物膜去除剂的耐药性。此外,还对单核细胞增生症分离物进行了全基因组测序,筛查是否存在抗菌药耐药性和毒力基因,并使用 CFSAN SNP 生物信息学管道评估分离物的基因组相似性。半数以上(57%)的受测分离物的 PAA 最低抑菌浓度(MIC)为 250 ppm,与这三个设施中使用的 PAA 消毒剂浓度(230 ppm)相近。相比之下,80%的受测分离物的生物膜去除剂 MIC 为 0.13 ppm,大大低于设施中使用的浓度(137 ppm)。所有受测分离物的基因组都带有抗菌药耐药性基因(fosX、lin、mdrL、mprF 和 norB)和毒力基因(inlA、inlB、plcA、plcB、prfA、hly、mpl 和 iap)。2020-2022 年间收集的单核细胞增生性酵母菌分离物属于三个不同的品系,22 个多焦点序列类型(MLST)属于 22 个不同的克隆复合体。基因组相似性分析表明,2016-2017 年从相同设施中采集的历史分离物在 F2 中的基因型 ST 1003 和 ST 554 持续存在了 5 年,而在 2022 年已不再检测到。总之,我们的研究结果突出表明,有必要重新评估消毒剂的浓度,以有效控制林果包装设施中持续存在的单核细胞增多症菌株。
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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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