-
Je něco špatně v tomto záznamu ?
Genomic insights into the spread of vancomycin- and tigecycline-resistant Enterococcus faecium ST117
M. Brajerova, O. Nyc, P. Drevinek, M. Krutova
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
No 197323
Univerzita Karlova v Praze
LX22NPO5103
European Commission
00064203
Ministerstvo Zdravotnictví Ceské Republiky
NLK
BioMedCentral
od 2002-01-01
BioMedCentral Open Access
od 2002
Directory of Open Access Journals
od 2002
Free Medical Journals
od 2002
PubMed Central
od 2002
Europe PubMed Central
od 2002
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2002-01-01
Open Access Digital Library
od 2002-09-01
Open Access Digital Library
od 2002-01-01
Medline Complete (EBSCOhost)
od 2002-09-16
Health & Medicine (ProQuest)
od 2009-01-01
Public Health Database (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2002
Springer Nature OA/Free Journals
od 2002-01-01
- MeSH
- antibakteriální látky * farmakologie MeSH
- bakteriální proteiny genetika MeSH
- Enterococcus faecium * genetika účinky léků izolace a purifikace klasifikace MeSH
- enterokoky rezistentní vůči vankomycinu * genetika účinky léků izolace a purifikace MeSH
- genom bakteriální MeSH
- grampozitivní bakteriální infekce * mikrobiologie epidemiologie MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- mnohočetná bakteriální léková rezistence genetika MeSH
- multilokusová sekvenční typizace MeSH
- rezistence na vankomycin genetika MeSH
- sekvenování celého genomu MeSH
- tigecyklin * farmakologie MeSH
- vankomycin * farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
BACKGROUND: Since the incidence of vancomycin-resistant enterococci (VRE) is increasing and treatment options remain limited, we aimed to investigate the epidemiology of vancomycin- and tigecycline-resistant enterococci in a university hospital using whole genome sequencing (WGS). METHODS: Between April and December 2021, 102 VRE isolates were collected from a single tertiary care hospital in the Czech Republic. Forty selected isolates underwent antimicrobial susceptibility testing and WGS (Illumina short reads and long reads with MinION in selected isolates). RESULTS: All Enterococcus faecium isolates were resistant to ampicillin, carrying the PBP5_Met485Ala, PBP5_Glu629Val, and fluoroquinolones carrying the GyrA_Ser83Ile and ParC_Ser80Ile substitutions. The vanA operon was found on pELF2-like plasmids and plasmids carrying rep17 and/or rep18b genes. The novel Tn1546 structural variants were identified in vanA-carrying isolates. The vanB operon was located on the chromosome within a Tn1549 structural variant. Linezolid resistance was detected in one isolate carrying the 23S rDNA_G2576T substitution. Twenty-two isolates were resistant to tigecycline (tet(L), tet(M) and rpsJ_del 155-166 or RpsJ_Lys57Arg). Discrepancies between phenotypic and genotypic resistance profiles were observed for daptomycin (RpoB_Ser491Phe), trimethoprim/sulfamethoxazole (dfrG gene), nitrofurantoin (NmrA_Gln48Lys substitution without the EF0404 and EF0648 genes) and tetracycline (truncated TetM). The two multilocus sequence typing (MLST) schemes identified different numbers of STs: 5 STs, with ST117 as the predominant one (n = 32, 80%), versus 10 STs, with ST138 (27.5%), ST136 (25%), and ST1067 (20%) being the most frequent, respectively. The whole genome MLST revealed clonal clustering (0-7 allele differences) among isolates of the same ST. When comparing ST117 isolates from our study with 2,204 ST117 isolates from 15 countries, only one Czech isolate clustered closely with strains from Germany and the Netherlands, differing by just 16 alleles. CONCLUSIONS: The spread of E. faecium isolates ST117 resistant to vancomycin and tigecycline was identified. The discrepancies between resistance genotypes and phenotypes highlight the importance of combining molecular and phenotypic surveillance in antimicrobial resistance monitoring.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25015325
- 003
- CZ-PrNML
- 005
- 20250731090920.0
- 007
- ta
- 008
- 250708s2025 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s12941-025-00806-7 $2 doi
- 035 __
- $a (PubMed)40500694
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Brajerova, Marie $u Department of Medical Microbiology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic
- 245 10
- $a Genomic insights into the spread of vancomycin- and tigecycline-resistant Enterococcus faecium ST117 / $c M. Brajerova, O. Nyc, P. Drevinek, M. Krutova
- 520 9_
- $a BACKGROUND: Since the incidence of vancomycin-resistant enterococci (VRE) is increasing and treatment options remain limited, we aimed to investigate the epidemiology of vancomycin- and tigecycline-resistant enterococci in a university hospital using whole genome sequencing (WGS). METHODS: Between April and December 2021, 102 VRE isolates were collected from a single tertiary care hospital in the Czech Republic. Forty selected isolates underwent antimicrobial susceptibility testing and WGS (Illumina short reads and long reads with MinION in selected isolates). RESULTS: All Enterococcus faecium isolates were resistant to ampicillin, carrying the PBP5_Met485Ala, PBP5_Glu629Val, and fluoroquinolones carrying the GyrA_Ser83Ile and ParC_Ser80Ile substitutions. The vanA operon was found on pELF2-like plasmids and plasmids carrying rep17 and/or rep18b genes. The novel Tn1546 structural variants were identified in vanA-carrying isolates. The vanB operon was located on the chromosome within a Tn1549 structural variant. Linezolid resistance was detected in one isolate carrying the 23S rDNA_G2576T substitution. Twenty-two isolates were resistant to tigecycline (tet(L), tet(M) and rpsJ_del 155-166 or RpsJ_Lys57Arg). Discrepancies between phenotypic and genotypic resistance profiles were observed for daptomycin (RpoB_Ser491Phe), trimethoprim/sulfamethoxazole (dfrG gene), nitrofurantoin (NmrA_Gln48Lys substitution without the EF0404 and EF0648 genes) and tetracycline (truncated TetM). The two multilocus sequence typing (MLST) schemes identified different numbers of STs: 5 STs, with ST117 as the predominant one (n = 32, 80%), versus 10 STs, with ST138 (27.5%), ST136 (25%), and ST1067 (20%) being the most frequent, respectively. The whole genome MLST revealed clonal clustering (0-7 allele differences) among isolates of the same ST. When comparing ST117 isolates from our study with 2,204 ST117 isolates from 15 countries, only one Czech isolate clustered closely with strains from Germany and the Netherlands, differing by just 16 alleles. CONCLUSIONS: The spread of E. faecium isolates ST117 resistant to vancomycin and tigecycline was identified. The discrepancies between resistance genotypes and phenotypes highlight the importance of combining molecular and phenotypic surveillance in antimicrobial resistance monitoring.
- 650 12
- $a tigecyklin $x farmakologie $7 D000078304
- 650 12
- $a Enterococcus faecium $x genetika $x účinky léků $x izolace a purifikace $x klasifikace $7 D016984
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a antibakteriální látky $x farmakologie $7 D000900
- 650 12
- $a vankomycin $x farmakologie $7 D014640
- 650 _2
- $a mikrobiální testy citlivosti $7 D008826
- 650 _2
- $a sekvenování celého genomu $7 D000073336
- 650 12
- $a grampozitivní bakteriální infekce $x mikrobiologie $x epidemiologie $7 D016908
- 650 12
- $a enterokoky rezistentní vůči vankomycinu $x genetika $x účinky léků $x izolace a purifikace $7 D065507
- 650 _2
- $a genom bakteriální $7 D016680
- 650 _2
- $a mnohočetná bakteriální léková rezistence $x genetika $7 D024901
- 650 _2
- $a bakteriální proteiny $x genetika $7 D001426
- 650 _2
- $a multilokusová sekvenční typizace $7 D058885
- 650 _2
- $a rezistence na vankomycin $x genetika $7 D020713
- 651 _2
- $a Česká republika $x epidemiologie $7 D018153
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Nyc, Otakar $u Department of Medical Microbiology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic
- 700 1_
- $a Drevinek, Pavel $u Department of Medical Microbiology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic
- 700 1_
- $a Krutova, Marcela $u Department of Medical Microbiology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic. marcela.krutova@lfmotol.cuni.cz $1 https://orcid.org/0000000245119430
- 773 0_
- $w MED00008163 $t Annals of clinical microbiology and antimicrobials $x 1476-0711 $g Roč. 24, č. 1 (2025), s. 36
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40500694 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250708 $b ABA008
- 991 __
- $a 20250731090914 $b ABA008
- 999 __
- $a ok $b bmc $g 2366279 $s 1252450
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 24 $c 1 $d 36 $e 20250611 $i 1476-0711 $m Annals of clinical microbiology and antimicrobials $n Ann Clin Microbiol Antimicrob $x MED00008163
- GRA __
- $a No 197323 $p Univerzita Karlova v Praze
- GRA __
- $a LX22NPO5103 $p European Commission
- GRA __
- $a 00064203 $p Ministerstvo Zdravotnictví Ceské Republiky
- LZP __
- $a Pubmed-20250708