DUFKOVÁ, Kristýna, Matěj BEZDÍČEK, Markéta NYKRÝNOVÁ, Iva KOCMANOVÁ, Petra KUBÁČKOVÁ, Jana HANSLIKOVA, Karolina FEJKOVA, Jiří MAYER and Martina LENGEROVÁ. Rapid Identification of Pseudomonas aeruginosa International High-Risk Clones Based on High-Resolution Melting Analysis. Microbiology Spectrum. WASHINGTON: AMER SOC MICROBIOLOGY, 2023, vol. 11, No 1, p. 1-9. ISSN 2165-0497. Available from: https://dx.doi.org/10.1128/spectrum.03571-22.
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Basic information
Original name Rapid Identification of Pseudomonas aeruginosa International High-Risk Clones Based on High-Resolution Melting Analysis
Authors DUFKOVÁ, Kristýna (203 Czech Republic, belonging to the institution), Matěj BEZDÍČEK (203 Czech Republic), Markéta NYKRÝNOVÁ (203 Czech Republic), Iva KOCMANOVÁ (203 Czech Republic), Petra KUBÁČKOVÁ (203 Czech Republic), Jana HANSLIKOVA (203 Czech Republic), Karolina FEJKOVA (203 Czech Republic), Jiří MAYER (203 Czech Republic, belonging to the institution) and Martina LENGEROVÁ (203 Czech Republic, guarantor, belonging to the institution).
Edition Microbiology Spectrum, WASHINGTON, AMER SOC MICROBIOLOGY, 2023, 2165-0497.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10606 Microbiology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.700 in 2022
RIV identification code RIV/00216224:14110/23:00131013
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1128/spectrum.03571-22
UT WoS 000911842300001
Keywords in English Pseudomonas aeruginosa; high-resolution melting; mini-MLST; molecular epidemiology; strain typing
Tags 14110212, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 30/1/2024 12:48.
Abstract
The Pseudomonas aeruginosa population has a nonclonal epidemic structure. It is generally composed of a limited number of widespread clones selected from a background of many rare and unrelated genotypes recombining at high frequency. Due to the increasing prevalence of nosocomial infections caused by multidrug-resistant/extensively drug-resistant (MDR/XDR) strains, it is advisable to implement infection control measures. Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) are considered the gold standard methods in bacterial typing, despite being limited by cost, staff, and instrumental demands. Here, we present a novel mini-MLST scheme for P. aeruginosa rapid genotyping based on high-resolution melting analysis. Using the proposed mini-MLST scheme, 3,955 existing sequence types (STs) were converted into 701 melting types (MelTs), resulting in a discriminatory power of D = 0.993 (95% confidence interval [CI], 0.992 to 0.994). Whole-genome sequencing of 18 clinical isolates was performed to support the newly designed mini-MLST scheme. The clonal analysis of STs belonging to MelTs associated with international high-risk clones (HRCs) performed by goeBURST software revealed that a high proportion of the included STs are highly related to HRCs and have also been witnessed as responsible for serious infections. Therefore, mini-MLST provides a clear warning for the potential spread of P. aeruginosa clones recognized as MDR/XDR strains with possible serious outcomes.IMPORTANCE In this study, we designed a novel mini-MLST typing scheme for Pseudomonas aeruginosa. Its great discriminatory power, together with ease of performance and short processing time, makes this approach attractive for prospective typing of large isolate sets. Integrating the novel P. aeruginosa molecular typing scheme enables the development and spread of MDR/XDR high-risk clones to be investigated. In this study, we designed a novel mini-MLST typing scheme for Pseudomonas aeruginosa. Its great discriminatory power, together with ease of performance and short processing time, makes this approach attractive for prospective typing of large isolate sets. Integrating the novel P. aeruginosa molecular typing scheme enables the development and spread of MDR/XDR high-risk clones to be investigated.
Links
MUNI/A/1224/2022, interní kód MUName: Nové přístupy ve výzkumu, diagnostice a terapii hematologických malignit X
Investor: Masaryk University
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