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Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate
BACKGROUND: Lactobacillus species are used as probiotics and play an important role in fermented food production. However, use of 16S rRNA gene sequences as standard markers for the differentiation of Lactobacillus species offers a very limited scope, as several species of Lactobacillus share simila...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160897/ https://www.ncbi.nlm.nih.gov/pubmed/32295530 http://dx.doi.org/10.1186/s12866-020-01781-z |
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author | Kim, Eiseul Yang, Seung-Min Lim, Bora Park, Si Hong Rackerby, Bryna Kim, Hae-Yeong |
author_facet | Kim, Eiseul Yang, Seung-Min Lim, Bora Park, Si Hong Rackerby, Bryna Kim, Hae-Yeong |
author_sort | Kim, Eiseul |
collection | PubMed |
description | BACKGROUND: Lactobacillus species are used as probiotics and play an important role in fermented food production. However, use of 16S rRNA gene sequences as standard markers for the differentiation of Lactobacillus species offers a very limited scope, as several species of Lactobacillus share similar 16S rRNA gene sequences. In this study, we developed a rapid and accurate method based on comparative genomic analysis for the identification of 37 Lactobacillus species that are commonly used in probiotics and fermented foods. RESULTS: To select species-specific sequences or genes, a total of 180 Lactobacillus genome sequences were compared using Python scripts. In 14 out of 37 species, species-specific sequences could not be found due to the similarity of the 16S–23S rRNA gene. Selected unique genes were obtained using comparative genomic analysis and all genes were confirmed to be specific for 52,478,804 genomes via in silico analysis; they were found not to be strain-specific, but to exist in all strains of the same species. Species-specific primer pairs were designed from the selected 16S–23S rRNA gene sequences or unique genes of species. The specificity of the species-specific primer pairs was confirmed using reference strains, and the accuracy and efficiency of the polymerase chain reaction (PCR) with the standard curve were confirmed. The PCR method developed in this study is able to accurately differentiate species that were not distinguishable using the 16S rRNA gene alone. This PCR assays were designed to detect and identify 37 Lactobacillus species. The developed method was then applied in the monitoring of 19 probiotics and 12 dairy products. The applied tests confirmed that the species detected in 17 products matched those indicated on their labels, whereas the remaining products contained species other than those appearing on the label. CONCLUSIONS: The method developed in this study is able to rapidly and accurately distinguish different species of Lactobacillus, and can be used to monitor specific Lactobacillus species in foods such as probiotics and dairy products. |
format | Online Article Text |
id | pubmed-7160897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71608972020-04-21 Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate Kim, Eiseul Yang, Seung-Min Lim, Bora Park, Si Hong Rackerby, Bryna Kim, Hae-Yeong BMC Microbiol Research Article BACKGROUND: Lactobacillus species are used as probiotics and play an important role in fermented food production. However, use of 16S rRNA gene sequences as standard markers for the differentiation of Lactobacillus species offers a very limited scope, as several species of Lactobacillus share similar 16S rRNA gene sequences. In this study, we developed a rapid and accurate method based on comparative genomic analysis for the identification of 37 Lactobacillus species that are commonly used in probiotics and fermented foods. RESULTS: To select species-specific sequences or genes, a total of 180 Lactobacillus genome sequences were compared using Python scripts. In 14 out of 37 species, species-specific sequences could not be found due to the similarity of the 16S–23S rRNA gene. Selected unique genes were obtained using comparative genomic analysis and all genes were confirmed to be specific for 52,478,804 genomes via in silico analysis; they were found not to be strain-specific, but to exist in all strains of the same species. Species-specific primer pairs were designed from the selected 16S–23S rRNA gene sequences or unique genes of species. The specificity of the species-specific primer pairs was confirmed using reference strains, and the accuracy and efficiency of the polymerase chain reaction (PCR) with the standard curve were confirmed. The PCR method developed in this study is able to accurately differentiate species that were not distinguishable using the 16S rRNA gene alone. This PCR assays were designed to detect and identify 37 Lactobacillus species. The developed method was then applied in the monitoring of 19 probiotics and 12 dairy products. The applied tests confirmed that the species detected in 17 products matched those indicated on their labels, whereas the remaining products contained species other than those appearing on the label. CONCLUSIONS: The method developed in this study is able to rapidly and accurately distinguish different species of Lactobacillus, and can be used to monitor specific Lactobacillus species in foods such as probiotics and dairy products. BioMed Central 2020-04-15 /pmc/articles/PMC7160897/ /pubmed/32295530 http://dx.doi.org/10.1186/s12866-020-01781-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Kim, Eiseul Yang, Seung-Min Lim, Bora Park, Si Hong Rackerby, Bryna Kim, Hae-Yeong Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title | Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title_full | Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title_fullStr | Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title_full_unstemmed | Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title_short | Design of PCR assays to specifically detect and identify 37 Lactobacillus species in a single 96 well plate |
title_sort | design of pcr assays to specifically detect and identify 37 lactobacillus species in a single 96 well plate |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160897/ https://www.ncbi.nlm.nih.gov/pubmed/32295530 http://dx.doi.org/10.1186/s12866-020-01781-z |
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