Margot H, Tasara T, Zwietering M H, Joosten H, Stephan R
Institute for Food Safety and Hygiene, Vetsuisse Faculty University of Zurich, CH-8057 Zurich, Switzerland.
Laboratory of Food Microbiology, Wageningen University, 6700 AA Wageningen, the Netherlands.
Int J Food Microbiol. 2016 Sep 2;232:26-34. doi: 10.1016/j.ijfoodmicro.2016.05.005. Epub 2016 May 7.
Sprouted seeds have been implicated in a number of serious outbreaks caused by Salmonella and Shiga toxin-producing Escherichia coli. Sprouts pose a very complex challenge to bacterial pathogen enrichment and detection since they naturally contain high levels of background microflora including members of the Enterobacteriaceae. As such, the currently used method cannot ensure reliable detection of STEC in sprouts. In this study, we compared different media for the enrichment of Enterobacteriaceae in their ability to promote the growth of stressed STEC at 37°C and 42°C. Mung bean sprouts were spiked with low levels of STEC and their growth was recorded over time. In addition, the microbiome of mung bean sprouts was analysed before and after enrichment. Our results indicate that the growth of dry-stressed STEC is comparable in all of the tested enrichment media except for mTSB+Novobiocin and not influenced by the incubation temperature. Low levels of STEC spiked into the sprouts resuspended in media only grew to levels of around 4logcfu/ml during enrichment, which could reduce the probability of detection. Proteobacteria was the dominant phylum detected within the microbiome of non-enriched mung bean sprouts. During enrichment in EE-broth, Proteobacteria remained the most abundant phylum. In contrast, during enrichment in BPW the relative abundance of Proteobacteria decreased whereas Firmicutes increased when compared to the non-enriched mung bean sprout microbiome. The microbiome composition was not significantly influenced by the incubation temperature during enrichment in both BPW and EE-broth. This is the first study to examine the microbiome on sprouted mung bean seeds during BPW and EE enrichment and relates the bacterial community composition changes to the enrichment of pathogens.
发芽种子与由沙门氏菌和产志贺毒素大肠杆菌引起的一些严重疫情有关。豆芽对细菌病原体的富集和检测构成了非常复杂的挑战,因为它们天然含有高水平的背景微生物群,包括肠杆菌科成员。因此,目前使用的方法不能确保可靠地检测豆芽中的产志贺毒素大肠杆菌。在本研究中,我们比较了不同培养基在37°C和42°C下富集肠杆菌科细菌以促进应激产志贺毒素大肠杆菌生长的能力。在绿豆芽中加入低水平的产志贺毒素大肠杆菌,并随时间记录其生长情况。此外,在富集前后分析了绿豆芽的微生物群。我们的结果表明,除了mTSB+新生霉素外,在所有测试的富集培养基中,干旱应激产志贺毒素大肠杆菌的生长情况相当,且不受培养温度的影响。加入到培养基中重悬的豆芽中的低水平产志贺毒素大肠杆菌在富集过程中仅生长到约4logcfu/ml的水平,这可能会降低检测概率。变形菌门是未富集绿豆芽微生物群中检测到的主要门类。在EE肉汤中富集期间,变形菌门仍然是最丰富的门类。相比之下,在BPW中富集时,与未富集的绿豆芽微生物群相比,变形菌门的相对丰度下降,而厚壁菌门增加。在BPW和EE肉汤中富集期间,微生物群组成不受培养温度的显著影响。这是第一项研究在BPW和EE富集过程中绿豆芽发芽种子上的微生物群,并将细菌群落组成变化与病原体富集相关联的研究。