Development of a High-Resolution Single-Nucleotide Polymorphism Strain-Typing Assay Using Whole Genome-Based Analyses for the Lactobacillus acidophilus Probiotic Strain

被引:4
|
作者
Huang, Chien-Hsun [1 ]
Chen, Chih-Chieh [2 ,3 ]
Chiu, Shih-Hau [1 ]
Liou, Jong-Shian [1 ]
Lin, Yu-Chun [4 ]
Lin, Jin-Seng [5 ]
Huang, Lina [1 ]
Watanabe, Koichi [1 ,5 ,6 ]
机构
[1] Food Ind Res & Dev Inst, Bioresource Collect & Res Ctr, 331 Shih Pin Rd, Hsinchu 30062, Taiwan
[2] Natl Sun Yat Sen Univ, Inst Med Sci & Technol, Kaohsiung 80424, Taiwan
[3] Natl Sun Yat Sen Univ, Rapid Screening Res Ctr Toxicol & Biomed, Kaohsiung 80424, Taiwan
[4] Execut Yuan, Council Agr, Livestock Res Inst, Tainan 71246, Taiwan
[5] Synbio Tech Inc, Culture Collect & Res Inst, Kaohsiung 82151, Taiwan
[6] Natl Taiwan Univ, Coll Bioresources & Agr, Dept Anim Sci & Technol, 50,Ln 155,Sec 3,Keelung Rd, Taipei 10673, Taiwan
关键词
whole genome sequences; core genome MLST; Strain-Specific Identification; monophyletic bacterium; Lactobacillus acidophilus; HUMAN FECES; IDENTIFICATION; PRIMERS; PCR; QUANTIFICATION; SURVEILLANCE; STRATEGIES; SOFTWARE; TAXONOMY; MEMBERS;
D O I
10.3390/microorganisms8091445
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lactobacillus acidophilus is one of the most commonly used industrial products worldwide. Since its probiotic efficacy is strain-specific, the identification of probiotics at both the species and strain levels is necessary. However, neither phenotypic nor conventional genotypic methods have enabled the effective differentiation of L. acidophilus strains. In this study, a whole-genome sequence-based analysis was carried out to establish high-resolution strain typing of 41 L. acidophilus strains (including commercial isolates and reference strains) using the cano-wgMLST_BacCompare analytics platform; consequently, a strain-specific discrimination method for the probiotic strain LA1063 was developed. Using a core-genome multilocus sequence-typing (cgMLST) scheme based on 1390 highly conserved genes, 41 strains could be assigned to 34 sequence types. Subsequently, we screened a set of 92 loci with a discriminatory power equal to that of the 1390 loci cgMLST scheme. A strain-specific polymerase chain reaction combined with a multiplex minisequencing method was developed based on four (phoU, secY, tilS, and uvrA_1) out of 21 loci, which could be discriminated between LA1063 and other L. acidophilus strains using the cgMLST data. We confirmed that the strain-specific single-nucleotide polymorphisms method could be used to quickly and accurately identify the L. acidophilus probiotic strain LA1063 in commercial products.
引用
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页码:1 / 22
页数:18
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