Detailed Information on Publication Record
2021
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms
BEZDÍČEK, Matěj, Marketa NYKRYNOVA, Karel SEDLAR, Stanislava KRÁLOVÁ, Jana HANSLIKOVA et. al.Basic information
Original name
Rapid high-resolution melting genotyping scheme for Escherichia coli based on MLST derived single nucleotide polymorphisms
Authors
BEZDÍČEK, Matěj (203 Czech Republic, belonging to the institution), Marketa NYKRYNOVA (203 Czech Republic), Karel SEDLAR (203 Czech Republic), Stanislava KRÁLOVÁ (703 Slovakia, belonging to the institution), Jana HANSLIKOVA (203 Czech Republic), Aja KOMPRDOVA (203 Czech Republic), Helena SKUTKOVA (203 Czech Republic), Iva KOCMANOVA (203 Czech Republic), Jiří MAYER (203 Czech Republic) and Martina LENGEROVÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Scientific Reports, London, Nature Research, 2021, 2045-2322
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10606 Microbiology
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.996
RIV identification code
RIV/00216224:14110/21:00122323
Organization unit
Faculty of Medicine
UT WoS
000686663200027
Keywords in English
Bacteriology; Clinical microbiology; Infectious-disease epidemiology
Tags
International impact, Reviewed
Změněno: 24/7/2023 12:55, Mgr. Tereza Miškechová
Abstract
V originále
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'.
Links
MUNI/A/1595/2020, interní kód MU |
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