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Whole-genome analysis of probiotic product isolates reveals the presence of genes related to antimicrobial resistance, virulence factors, and toxic metabolites, posing potential health risks

Authors :
Sebastian Leptihn
Huan Chen
Ying Wang
Chengzhi Liu
Hong Shen
Jin Wei
Hong Li
Hailong Xiao
Shuyan Liu
Chao Liu
Xiaoling Zheng
Qian Liang
Bian Lu
Ya Shi
Source :
BMC Genomics, Vol 22, Iss 1, Pp 1-12 (2021), BMC Genomics
Publication Year :
2021
Publisher :
BMC, 2021.

Abstract

Background Safety issues of probiotic products have been reported frequently in recent years. Ten bacterial strains isolated from seven commercial probiotic products on market were evaluated for their safety, by whole-genome analysis. Results We found that the bacterial species of three probiotic products were incorrectly labeled. Furthermore, six probiotic product isolates (PPS) contained genes for the production of toxic metabolites, while another three strains contained virulence genes, which might pose a potential health risk. In addition, three of them have drug-resistance genes, among which two strains potentially displayed multidrug resistance. One isolate has in silico predicted transferable genes responsible for toxic metabolite production, and they could potentially transfer to human gut microflora or environmental bacteria. Isolates of Lactobacillus rhamnosus and Bifidobacterium animalis subsp. lactis are associated with low risk for human consumption. Based on a comparative genome analysis, we found that the isolated Enterococcus faecium TK-P5D clustered with a well-defined probiotic strain, while E. faecalis TK-P4B clustered with a pathogenic strain. Conclusions Our work clearly illustrates that whole-genome analysis is a useful method to evaluate the quality and safety of probiotic products. Regulatory quality control and stringent regulations on probiotic products are needed to ensure safe consumption and protect human health.

Details

Language :
English
ISSN :
14712164
Volume :
22
Issue :
1
Database :
OpenAIRE
Journal :
BMC Genomics
Accession number :
edsair.doi.dedup.....84d8a488884feab4966c8bf30e5b57ce