Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms
Abstract Routinely used typing methods including MLST, rep-PCR and whole genome sequencing (WGS) are time-consuming, costly, and often low throughput. Here, we describe a novel mini-MLST scheme for Eschericha coli as an alternative method for rapid genotyping. Using the proposed mini-MLST scheme, 10...
Guardado en:
Autores principales: | , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f40d483413004e129df96d4cdd5a08fe |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:f40d483413004e129df96d4cdd5a08fe |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:f40d483413004e129df96d4cdd5a08fe2021-12-02T16:45:54ZRapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms10.1038/s41598-021-96148-32045-2322https://doaj.org/article/f40d483413004e129df96d4cdd5a08fe2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-96148-3https://doaj.org/toc/2045-2322Abstract Routinely used typing methods including MLST, rep-PCR and whole genome sequencing (WGS) are time-consuming, costly, and often low throughput. Here, we describe a novel mini-MLST scheme for Eschericha coli as an alternative method for rapid genotyping. Using the proposed mini-MLST scheme, 10,946 existing STs were converted into 1,038 Melting Types (MelTs). To validate the new mini-MLST scheme, in silico analysis was performed on 73,704 strains retrieved from EnteroBase resulting in discriminatory power D = 0.9465 (CI 95% 0.9726–0.9736) for mini-MLST and D = 0.9731 (CI 95% 0.9726–0.9736) for MLST. Moreover, validation on clinical isolates was conducted with a significant concordance between MLST, rep-PCR and WGS. To conclude, the great portability, efficient processing, cost-effectiveness, and high throughput of mini-MLST represents immense benefits, even when accompanied with a slightly lower discriminatory power than other typing methods. This study proved mini-MLST is an ideal method to screen and subgroup large sets of isolates and/or quick strain typing during outbreaks. In addition, our results clearly showed its suitability for prospective surveillance monitoring of emergent and high-risk E. coli clones’.Matej BezdicekMarketa NykrynovaKarel SedlarStanislava KralovaJana HanslikovaAja KomprdovaHelena SkutkovaIva KocmanovaJiri MayerMartina LengerovaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Matej Bezdicek Marketa Nykrynova Karel Sedlar Stanislava Kralova Jana Hanslikova Aja Komprdova Helena Skutkova Iva Kocmanova Jiri Mayer Martina Lengerova Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
description |
Abstract Routinely used typing methods including MLST, rep-PCR and whole genome sequencing (WGS) are time-consuming, costly, and often low throughput. Here, we describe a novel mini-MLST scheme for Eschericha coli as an alternative method for rapid genotyping. Using the proposed mini-MLST scheme, 10,946 existing STs were converted into 1,038 Melting Types (MelTs). To validate the new mini-MLST scheme, in silico analysis was performed on 73,704 strains retrieved from EnteroBase resulting in discriminatory power D = 0.9465 (CI 95% 0.9726–0.9736) for mini-MLST and D = 0.9731 (CI 95% 0.9726–0.9736) for MLST. Moreover, validation on clinical isolates was conducted with a significant concordance between MLST, rep-PCR and WGS. To conclude, the great portability, efficient processing, cost-effectiveness, and high throughput of mini-MLST represents immense benefits, even when accompanied with a slightly lower discriminatory power than other typing methods. This study proved mini-MLST is an ideal method to screen and subgroup large sets of isolates and/or quick strain typing during outbreaks. In addition, our results clearly showed its suitability for prospective surveillance monitoring of emergent and high-risk E. coli clones’. |
format |
article |
author |
Matej Bezdicek Marketa Nykrynova Karel Sedlar Stanislava Kralova Jana Hanslikova Aja Komprdova Helena Skutkova Iva Kocmanova Jiri Mayer Martina Lengerova |
author_facet |
Matej Bezdicek Marketa Nykrynova Karel Sedlar Stanislava Kralova Jana Hanslikova Aja Komprdova Helena Skutkova Iva Kocmanova Jiri Mayer Martina Lengerova |
author_sort |
Matej Bezdicek |
title |
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
title_short |
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
title_full |
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
title_fullStr |
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
title_full_unstemmed |
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms |
title_sort |
rapid high-resolution melting genotyping scheme for escherichia coli based on mlst derived single nucleotide polymorphisms |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/f40d483413004e129df96d4cdd5a08fe |
work_keys_str_mv |
AT matejbezdicek rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT marketanykrynova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT karelsedlar rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT stanislavakralova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT janahanslikova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT ajakomprdova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT helenaskutkova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT ivakocmanova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT jirimayer rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms AT martinalengerova rapidhighresolutionmeltinggenotypingschemeforescherichiacolibasedonmlstderivedsinglenucleotidepolymorphisms |
_version_ |
1718383491025993728 |