Aziz Ghazal, Zaidi Arsalan, Sullivan Daniel J O '
National Probiotic Laboratory, National Institute for Biotechnology and Genetic Engineering College (NIBGE-C), Punjab, 38000, Faisalabad, Pakistan.
Pakistan Institute of Engineering and Applied Sciences (PIEAS), Nilore, 45650, Islamabad (ICT), Pakistan.
Curr Genet. 2023 Dec;69(4-6):213-234. doi: 10.1007/s00294-023-01271-5. Epub 2023 May 26.
The demand for and acceptance of probiotics is determined by their quality and safety. Illumina NGS sequencing and analytics were used to examine eight marketed probiotics. Up to the species level, sequenced DNA was taxonomically identified, and relative abundances were determined using Kaiju. The genomes were constructed using GTDB and validated through PATRICK and TYGS. A FastTree 2 phylogenetic tree was constructed using several type strain sequences from relevant species. Bacteriocin and ribosomally synthesized polypeptide (RiPP) genes were discovered, and a safety check was performed to test for toxins, antibiotic resistance, and genetic drift genes. Except for two products with unclaimed species, the labeling was taxonomically correct. In three product formulations, Lactobacillus acidophilus, Limosilactobacillus reuteri, Lacticaseibacillus paracasei, and Bifidobacterium animalis exhibited two to three genomic alterations, while Streptococcus equinus was found in one. TYGS and GDTB discovered E. faecium and L. paracasei in distinctly different ways. All the bacteria tested had the genetic repertoire to tolerate GIT transit, although some exhibited antibiotic resistance, and one strain had two virulence genes. Except for Bifidobacterium strains, the others revealed a variety of bacteriocins and ribosomally synthesized polypeptides (RiPP), 92% of which were unique and non-homologous to known ones. Plasmids and mobile genetic elements are present in strains of L. reuteri (NPLps01.et_L.r and NPLps02.uf_L.r), Lactobacillus delbrueckii (NPLps01.et_L.d), Streptococcus thermophilus (NPLps06.ab_S.t), and E. faecium (NPLps07.nf_E.f). Our findings support the use of metagenomics to build better and efficient production and post-production practices for probiotic quality and safety assessment.
益生菌的需求和接受程度取决于其质量和安全性。使用Illumina NGS测序和分析方法对8种市售益生菌进行了检测。在物种水平上,对测序的DNA进行了分类鉴定,并使用Kaiju确定了相对丰度。使用GTDB构建基因组,并通过PATRICK和TYGS进行验证。使用来自相关物种的多个模式菌株序列构建了FastTree 2系统发育树。发现了细菌素和核糖体合成多肽(RiPP)基因,并进行了安全性检查以检测毒素、抗生素抗性和基因漂移基因。除了两种未标明物种的产品外,标签在分类学上是正确的。在三种产品配方中,嗜酸乳杆菌、罗伊氏乳杆菌、副干酪乳杆菌和动物双歧杆菌表现出两到三种基因组改变,而在一种产品中发现了马链球菌。TYGS和GDTB以明显不同的方式发现了屎肠球菌和副干酪乳杆菌。所有测试的细菌都具有耐受胃肠道转运的基因库,尽管有些表现出抗生素抗性,并且一个菌株有两个毒力基因。除双歧杆菌菌株外,其他菌株均显示出多种细菌素和核糖体合成多肽(RiPP),其中92%是独特的,与已知的不同源。罗伊氏乳杆菌(NPLps01.et_L.r和NPLps02.uf_L.r)、德氏乳杆菌(NPLps01.et_L.d)、嗜热链球菌(NPLps06.ab_S.t)和屎肠球菌(NPLps07.nf_E.f)的菌株中存在质粒和移动遗传元件。我们的研究结果支持使用宏基因组学来建立更好、更高效的益生菌质量和安全性评估的生产及产后实践。