Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Eiseul, Yang, Seung-Min, Lim, Bora, Park, Si Hong, Rackerby, Bryna, Kim, Hae-Yeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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
_version_ 1783522843774943232
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
work_keys_str_mv AT kimeiseul designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate
AT yangseungmin designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate
AT limbora designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate
AT parksihong designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate
AT rackerbybryna designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate
AT kimhaeyeong designofpcrassaystospecificallydetectandidentify37lactobacillusspeciesinasingle96wellplate