Diagnostic tool for surveillance, detection and monitoring of the high-risk clone K. pneumoniae ST15

被引:2
作者
Gato, E. [1 ,2 ]
Rodino-Janeiro, B. K. [1 ]
Gude, M. J. [4 ]
Fernandez-Cuenca, F. [5 ,6 ,7 ]
Pascual, A. [5 ,6 ,7 ,8 ]
Fernandez, A. [3 ]
Perez, A. [1 ,2 ]
Bou, G. [3 ,8 ]
机构
[1] Inst Biomed Res A Coruna INIB, La Coruna, Spain
[2] Carlos III Hlth Inst ISCIII, Madrid, Spain
[3] Univ Hosp A Coruna HUAC, La Coruna, Spain
[4] Univ Hosp Lucus Augusti HULA, Lugo, Spain
[5] Univ Hosp Virgen Macarena, Seville, Spain
[6] Inst Biomed Sevilla, Seville, Spain
[7] Univ Seville, Seville, Spain
[8] Inst Salud Carlos III, CIBER Enfermedades Infecciosas CIBERINFEC, Madrid, Spain
关键词
Klebsiella pneumoniae; Genomic traits; ST15 high-risk clone; Outbreak; Diagnostic test; KLEBSIELLA-PNEUMONIAE; SECRETION; EMERGENCE; GENES;
D O I
10.1016/j.jhin.2023.09.015
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: The global spread of Klebsiella pneumoniae ST15, causing multi-continental outbreaks, contributes to the movement of resistance genes between clones increasing the antimicrobial resistance crisis. The genomic traits providing it with the ability to outcompete other bacteria and cause epidemics remain unclear. Aim: To identify the specific genomic traits of K. pneumoniae ST15 to develop a diagnostic test.Methods: An outbreak caused by K. pneumoniae occurred in Hospital A Corun similar to a, Spain. Antimicrobial susceptibility analysis and molecular typing (PGFE and MLST) were performed. One isolate of each sequence type was selected for whole-genome sequencing analysis. Comparative analysis of genomes was performed using RAST. BLASTn was used to evaluate the presence of the fhaC and kpiD genes. Two hundred and ninety-four K. pneumoniae from a Spanish nationwide collection were analysed by PCR.Findings: Genotyping showed that 87.5% of the isolates tested belonged to a clone with a unique PFGE pattern which corresponded to ST15. Comparative genomic analysis of the different STs enabled us to determine the specific genomic traits of K. pneumoniae ST15. Two adherence-related systems (Kpi and KpFhaB/FhaC) were specific markers of this clone. Multiplex-PCR analysis with kpiD and fhaC oligonucleotides revealed that K. pneumoniae ST15 is specifically detected with a sensitivity of 100% and a specificity of 97.76%. The PCR results showed 100% concordance with the MLST and whole-genome sequencing data. Conclusion: K. pneumoniae ST15 possesses specific genomic traits that could favour its dissemination. They could be used as targets to detect K. pneumoniae ST15 with high sensitivity and specificity.(c) 2023 The Healthcare Infection Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
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