基于基因组的副乳杆菌 NY1301 安全特性评估以及作为益生菌上市的近缘菌株的基因组差异。

IF 2.5 Q3 MICROBIOLOGY Bioscience of microbiota, food and health Pub Date : 2024-01-01 Epub Date: 2024-01-24 DOI:10.12938/bmfh.2023-072
Masanori Fukao, Atsushi Oki, Shuichi Segawa
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引用次数: 0

摘要

对副酸乳杆菌 NY1301 的益生特性进行了全面描述,并利用基因组工具对密切相关的 LcA(Actimel)和 LcY(养乐多)益生菌株进行了比较。所有菌株都表现出高度的遗传相似性,很可能具有共同的祖先;差异主要表现为染色体的轻微重排、替换、插入和缺失。与 LcY 相比,NY1301 表现出 125 个单核苷酸多态性。NY1301 缺乏毒力因子、抗生素抗性基因和与抗生素抗性相关的突变,并有一个 46 kbp 的雌球菌。这种噬菌体可在低水平下自发诱导,并在标准培养条件下保持非裂解状态。观察到的因果适应性突变很可能与各自实验室内的生态位适应或菌株维持过程中的生产工艺有关。然而,这些基因组差异的表型效应仍不清楚。为了验证 NY1301 的安全性,我们进行了一项开放标签试验,健康参与者每天摄入过量 NY1301(3.0 × 1011 cfu),持续 28 天。这项试验的结果和其他体内研究的结果,加上人类长期食用NY1301而未对人体造成风险的事实,为证实NY1301的安全性提供了强有力的证据。
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Genome-based assessment of safety characteristics of Lacticaseibacillus paracasei NY1301 and genomic differences in closely related strains marketed as probiotics.

The probiotic attributes of Lacticaseibacillus paracasei NY1301 were comprehensively characterized, and a comparison between the closely related LcA (Actimel) and LcY (Yakult) probiotic strains was conducted using genomic tools. All strains exhibited high genetic similarity and likely shared a common ancestor; differences were primarily expressed as minor chromosomal re-arrangements, substitutions, insertions, and deletions. Compared with LcY, NY1301 exhibited 125 single-nucleotide polymorphisms. NY1301 lacked virulence factors, antibiotic resistance genes, and mutations associated with antibiotic resistance and had a 46-kbp prophage. This prophage is spontaneously induced at low levels and remains in a non-lytic state under standard culture conditions. The observed causal adaptive mutations were likely related to niche adaptation within the respective laboratory or manufacturing processes that occurred during the maintenance of the strains. However, the phenotypic effects of these genomic differences remain unclear. To validate the safety of NY1301, we conducted an open-label trial with healthy participants who consumed excessive amounts of NY1301 (3.0 × 1011 cfu) daily for 28 days. The results of this trial and those of other in vivo studies, coupled with the long history of human consumption without established risks to humans, provide strong evidence confirming the safety of NY1301.

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