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Mungo bean sprout microbiome and changes associated with culture based enrichment protocols used in detection of Gram-negative foodborne pathogens

机译:Mungo Bean Sprout Microbiome和与培养基富集协议相关的变化,用于检测革兰氏阴性食物载体病原体

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Background Fresh sprouted seeds have been associated with a number of large outbreaks caused by Salmonella and Shiga toxin-producing E. coli . However, the high number of commensal bacteria found on sprouted seeds hampers the detection of these pathogens. Knowledge about the composition of the sprout microbiome is limited. In this study, the microbiome of mungo bean sprouts and the impact of buffered peptone water (BPW) and Enterobacteriaceae enrichment broth (EE-broth)-based enrichment protocols on this microbiome were investigated. Results Assessments based on aerobic mesophilic colony counts showed similar increases in mungo bean sprout background flora levels independent of the enrichment protocol used. 16S rRNA sequencing revealed a mungo bean sprout microbiome dominated by Proteobacteria and Bacteroidetes . EE-broth enrichment of such samples preserved and increased Proteobacteria dominance while reducing Bacteroidetes and Firmicutes relative abundances. BPW enrichment, however, increased Firmicutes relative abundance while decreasing Proteobacteria and Bacteroidetes levels. Both enrichments also lead to various genus level changes within the Protobacteria and Firmicutes phyla. Conclusions New insights into the microbiome associated with mungo bean sprout and how it is influenced through BPW and EE-broth-based enrichment strategies used for detecting Gram-negative pathogens were generated. BPW enrichment leads to Firmicutes and Proteobacteria dominance, whereas EE-broth enrichment preserves Proteobacteria dominance in the mungo bean sprout samples. By increasing the relative abundance of Firmicutes , BPW also increases the abundance of Gram-positive organisms including some that might inhibit recovery of Gram-negative pathogens. The use of EE-broth, although preserving and increasing the dominance of Proteobacteria , can also hamper the detection of lowly abundant Gram-negative target pathogens due to outgrowth of such organisms by the highly abundant non-target Proteobacteria genera comprising the mungo bean sprout associated background flora.
机译:背景技术新鲜发芽的种子已与由沙门氏菌和滋阴毒素的大肠杆菌引起的许多大爆发有关。然而,在发芽的种子上发现的高分性细菌妨碍了这些病原体的检测。关于发芽微生物组成的构成的知识是有限的。在这项研究中,研究了Mungo豆芽的微生物组和缓冲蛋白水(BPW)和肠杆菌菌富集肉汤(EE-BROTH)的基于该微生物组的富集方案的影响。结果基于好氧嗜苯胺菌落计数的评估显示Mungo Bean Sprout背景植物群的相似增加,与所使用的富集方案无关。 16S RRNA测序揭示了由植物和细菌的Mumgo Bean Sprout Microbiome。 EE-BROTH富集这些样品保存并增加了噬菌体菌群的优势,同时减少了细菌和迫使相对丰富。然而,BPW富集在减少植物体外和菌体水平的同时增加了相对丰富的富裕。两种富集也会导致血糖细菌内的各种属级变化,并使PHYLA更加变化。结论产生了与Mungo Bean Sprout相关的微生物组的新见解,以及如何通过BPW和EE-肉汤的富集策略影响用于检测革兰阴性病原体的浓缩策略。 BPW富集导致迫切和植物的优势,而EE-BROTH浓缩保留MUNGO豆芽样本中的植物菌群。通过增加对压实的相对丰富,BPW还增加了革兰氏阳性生物的丰度,包括一些可能抑制革兰氏阴性病原体的恢复。 ee-brooth的使用虽然保留和增加植物的主导地位,但也可以阻碍由于这种生物体的高度的非靶蛋白属属,并且包括Mungo Bean Sprout相关的生物的生长,妨碍了劣质革兰氏阴性靶病原体背景植物群。

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