Genome stability during serial subculturing in hyperepidemic multidrug-resistant Klebsiella pneumoniae and Escherichia coli

被引:3
|
作者
Moser, Aline I. [1 ]
Campos-Madueno, Edgar I. [1 ,2 ]
Perreten, Vincent [3 ]
Endimiani, Andrea [1 ,4 ]
机构
[1] Univ Bern, Inst Infect Dis, Bern, Switzerland
[2] Univ Bern, Grad Sch Cellular & Biomed Sci, Bern, Switzerland
[3] Univ Bern, Inst Vet Bacteriol, Bern, Switzerland
[4] Univ Bern, Inst Infect Dis, Friedbuhlstr 51, CH-3001 Bern, Switzerland
关键词
SNVs; Genome; Plasmid; Stability; Klebsiella pneumoniae; Escherichia coli; INFECTIONS; INSERTION; ALIGNMENT; CLONES;
D O I
10.1016/j.jgar.2022.08.014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Core-genome single nucleotide variant (cgSNV) analysis represents a powerful tool for epi-demiological investigations of multidrug-resistant (MDR) bacteria. However, cgSNV thresholds to confirm whether isolates are the same clone are not formally defined.Methods: We implemented hybrid whole-genome sequencing to study the genomic changes of four MDR isolates belonging to hyperepidemic sequence types (STs) during 20 propagation steps (T20) on Mac-Conkey and CHROMID(R) ESBL plates. The following strains were analyzed: Klebsiella pneumoniae AE -2247421 (OXA-48/NDM-1-producing, ST101), K. pneumoniae MCL-2017-2 (CTX-M-15-producing, ST307), Escherichia coli Ec-042 (OXA-181-producing, ST410), and E. coli Ec-050 (NDM-5-producing, ST167). The genome assembly at T5 and T20 was compared to that at time point zero (T0) and to two reference genomes.Results: At T20, AE-2247421 lost the IncL blaOXA-48-carrying plasmid when grown on CHROMID(R) ESBL plates, while a large fragment encompassing blaNDM-1 was lost from its IncC plasmid when grown on both plates. In contrast, no structural changes were noted for the other three strains. Regarding the cgSNVs, the following results were obtained at T5 and T20 (ranges considering the different agar plates and reference genomes): AE-2247421 (1-8 and 2-12 cgSNVs), MCL-2017-2 (both 1-2 cgSNVs), Ec-042 (both 0 cgSNVs), and Ec-050 (0-6 and 0-9 cgSNVs).Conclusion: We showed that structural changes and accumulation of cgSNVs can occur in few propagation steps under laboratory conditions. These changes might also arise in the clinical context in a short time, especially under antibiotics treatment. This phenomenon should be carefully considered because it might affect the final interpretation of epidemiological genomic analyses.(c) 2022 The Author(s). Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy.This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ )
引用
收藏
页码:152 / 161
页数:10
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