Background: A marked genotype shift among vancomycin-resistant Enterococcus faecium (VREfm) from vanB to vanA in Australia between 2011 and 2015 is a well-known phenomenon. It is hypothesized that this was caused by multiple independent clones emerging simultaneously in different settings and/or regions.
Objectives: To gain insights into the circumstances surrounding the shift from vanB to vanA VREfm in one Australian hospital.
Methods: The genomes of 69 vanA VREfm isolates from St George Hospital collected between 2009 and 2018 were studied. An expansion of ST80 vanA VREfm was noted following a single introduction. ST80 isolates were thus further characterized using hybrid sequencing and contextualized through comparisons with other published Australian ST80 isolates. Phylogenies were constructed with plasmid sequences compared with the index isolate.
Results: The 2011 expansion of ST80 vanA VREfm isolates in our institution originated from the 2009 index isolate, from a patient transferred from overseas. Phylogenetic analysis with other Australian ST80 vanA VREfm isolates showed that the 2011 expansion event was unique, with limited spread to adjacent local health districts. Plasmid analysis showed multiple variants, which can also be traced back to the 2009 isolate, consistent with ongoing plasmid adaptation over time.
Conclusions: These findings confirm an expansion event following a VREfm introduction event leading to a sustained clonal and plasmid outbreak over several years. Moreover, it demonstrates the complexity of countrywide replacement events. This study also highlights the use of hybrid sequencing in establishing an epidemiological relationship to the index isolate that was initially inapparent.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1093/jac/dkab379 | DOI Listing |
Int J Antimicrob Agents
December 2024
State Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, NO. 28 Qiaozhong Middle Rd, Liwan District, Guangzhou, China. Electronic address:
Objectives: The detection rate of vancomycin-resistant Enterococcus faecium (VREfm) displayed a dramatically increase in Guangdong, China from 2021 to 2023, for which the molecular epidemiology and genomic characteristics remain largely unexplored. In this study, we investigated the genetic features and epidemiology of VREfm isolates in Guangdong.
Methods: A total of 54 Guangdong VREfm isolates were collected from three tertiary hospitals in Guangdong.
J Glob Antimicrob Resist
November 2024
School of Food and Drug, Shenzhen Polytechnic University, Shenzhen, Guangdong, China. Electronic address:
Objective: To investigate the prevalence and characteristics of vancomycin-resistant Enterococcus (VRE) isolates in a Chinese tertiary hospital in Shenzhen.
Methods: A hospital-based retrospective epidemiological survey of Enterococcus was conducted over a 6.5-y period, from January 2018 to June 2024.
J Hosp Infect
January 2025
Laboratory for Medical Microbiology and Medical Immunology, Meander Medical Centre, Amersfoort, The Netherlands.
Objectives: The study institute was challenged with an outbreak of different vancomycin-resistant Enterococcus faecium (VREfm), including vanA- and/or vanB-containing isolates. Remarkably, screening overnight enriched specimens using a vanA and vanB real-time polymerase chain reaction (PCR) gave positive results for vanB with very low cycle threshold values, whereas VREfm-specific enrichment cultures remained negative. This paper describes the analysis of the diagnostic results leading to adaptation of the diagnostic algorithm.
View Article and Find Full Text PDFmSphere
October 2024
Institute of Clinical Oncology, Lianyungang Hospital Affiliated to Kangda College of Nanjing Medical University, Lianyungang, China.
Unlabelled: The objective of this study was to establish a rapid visual diagnosis method for vancomycin-resistant (VREFm) based on multienzyme isothermal rapid amplification (MIRA) combined with lateral flow strips (LFSs). The MIRA primers and probes were specifically designed to maintain the sequence of the VanA gene of VREFm. We optimized the reaction time and temperature and thoroughly assessed the specificity and sensitivity of the MIRA-LFS system.
View Article and Find Full Text PDFJ Appl Microbiol
September 2024
Laboratory Ward, National Bone Marrow Transplant Center, Tunis 1006, Tunisia.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!