Evaluation of methods for detection of Campylobacter in raw milk: A multi-country study

IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY International journal of food microbiology Pub Date : 2024-10-12 DOI:10.1016/j.ijfoodmicro.2024.110938
Ásgeir Ástvaldsson , Gunnar Andersson , Linda Svensson , Karin Bruckner , Martine Denis , Sevinc Ferrari , Olwen Golden , Janine Heise , Moa Lavander , Elisabeth Repérant , Hilde M. Riedel , Kerstin Stingl , Hanna Skarin
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Abstract

Raw milk is considered a high-risk source of Campylobacter due to faecal contamination from healthy cattle and farm environments, thus linking raw milk consumption to global outbreaks. Detection of Campylobacter in raw milk poses challenges due to low contamination levels and antibacterial properties of the milk. Culture-based protocols for Campylobacter detection in milk vary, mainly with regard to pH adjustment and the choice of enrichment broth.
This European collaborative study was organised by the EU Reference Laboratory (EURL) for Campylobacter together with eight EU National Reference Laboratories (NRL) for Campylobacter with the purpose to evaluate methods for culture-based detection of Campylobacter in raw cow's milk. The study was divided into two parts, an interlaboratory part and an intralaboratory part, both organised around the same two protocols. The aim of protocol 1 was to evaluate the impact of pH adjustment and storage of the milk on the culturability of Campylobacter over time. Aliquots of the spiked milk were adjusted either to pH 7.0 or pH 7.6 or left unadjusted. The milk was stored up to 48 h at refrigerated temperature and Campylobacter was quantified according to ISO 10272-2 on day 0, 1 and 2. The aim of protocol 2 was to evaluate which enrichment broth, Bolton broth (BB) or Preston broth (PB), showed highest sensitivity in detection of Campylobacter. The spiked milk was enriched in BB and PB as described in ISO 10272-1:2017 or ISO 10272-1:2017/Amd1.2023. In the interlaboratory part, each milk batch was collected locally by each participating NRL/EURL and inoculated with the same Campylobacter strain. In the follow-up intralaboratory part, the EURL-Campylobacter repeated the tests in protocol 1 and 2 but used different Campylobacter strains and strains subjected to thermal stress prior to inoculation.
The results show that pH adjustment of raw milk has a negligible impact on culture-based detection of Campylobacter, regardless of strain and level of environmental stress. The composition of milk and properties of the inoculated strain influence culture-based detection of Campylobacter over storage time, and strains subjected to additional stress prior to inoculation in milk are reduced in culturability much faster than the same strains prepared under normal conditions.
Finally, the study showed that PB without Campylobacter growth supplement is less effective than BB in detecting Campylobacter in raw milk.
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评估检测生奶中弯曲杆菌的方法:多国研究。
由于来自健康牛和农场环境的粪便污染,生奶被认为是弯曲杆菌的高风险来源,因此生奶消费与全球疫情爆发有关。由于污染水平低和牛奶的抗菌特性,检测生牛奶中的弯曲杆菌是一项挑战。基于培养的牛奶弯曲杆菌检测方案各不相同,主要涉及 pH 值调整和富集肉汤的选择。这项欧洲合作研究由欧盟弯曲杆菌参考实验室(EURL)与八个欧盟国家弯曲杆菌参考实验室(NRL)共同组织,目的是评估基于培养基检测生牛乳中弯曲杆菌的方法。研究分为两部分,即实验室间部分和实验室内部分,均围绕相同的两个方案进行。方案 1 的目的是评估牛奶的 pH 值调整和储存对弯曲杆菌长期培养的影响。将等分的加标牛奶调节至 pH 7.0 或 pH 7.6,或不作任何调节。牛奶在冷藏温度下储存 48 小时,在第 0、1 和 2 天按照 ISO 10272-2 标准对弯曲菌进行定量。方案 2 的目的是评估博尔顿肉汤(BB)和普雷斯顿肉汤(PB)哪种富集肉汤在检测弯曲杆菌方面灵敏度最高。根据 ISO 10272-1:2017 或 ISO 10272-1:2017/Amd1.2023,在 BB 和 PB 中富集加标牛奶。在实验室间部分,每个参与的 NRL/EURL 在当地收集每批牛奶,并接种相同的弯曲杆菌菌株。在后续的实验室内部分,EURL-弯曲菌实验室重复了方案 1 和 2 中的试验,但使用了不同的弯曲菌菌株,并在接种前对菌株进行了热压处理。结果表明,无论菌株和环境应激水平如何,调整生乳的 pH 值对弯曲杆菌的培养基检测影响微乎其微。牛奶的成分和接种菌株的特性会影响弯曲菌在贮存时间内的培养基检测,在牛奶中接种前受到额外压力的菌株比在正常条件下制备的相同菌株的可培养性降低得更快。最后,研究表明,在检测生乳中弯曲菌方面,不添加弯曲菌生长补充剂的 PB 不如 BB 有效。
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来源期刊
International journal of food microbiology
International journal of food microbiology 工程技术-食品科技
CiteScore
10.40
自引率
5.60%
发文量
322
审稿时长
65 days
期刊介绍: The International Journal of Food Microbiology publishes papers dealing with all aspects of food microbiology. Articles must present information that is novel, has high impact and interest, and is of high scientific quality. They should provide scientific or technological advancement in the specific field of interest of the journal and enhance its strong international reputation. Preliminary or confirmatory results as well as contributions not strictly related to food microbiology will not be considered for publication.
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