Using Genomics To Investigate an Outbreak of Vancomycin-Resistant Enterococcus faecium ST78 at a Large Tertiary Hospital in Queensland

被引:7
作者
Permana, Budi [1 ,2 ,8 ]
Harris, Patrick N. A. [3 ,4 ,5 ]
Runnegar, Naomi [6 ,7 ]
Lindsay, Margaret [7 ]
Henderson, Belinda C. [7 ]
Playford, E. G. [7 ]
Paterson, David L. [4 ]
Beatson, Scott A. [1 ,2 ,3 ]
Forde, Brian M. [3 ,4 ]
机构
[1] Univ Queensland, Fac Sci, Sch Chem & Mol Biosci, Brisbane, Qld, Australia
[2] Univ Queensland, Australian Ctr Ecogen, Brisbane, Qld, Australia
[3] Univ Queensland, Fac Sci, Australian Infect Dis Res Ctr, Brisbane, Qld, Australia
[4] Univ Queensland, Ctr Clin Res, Fac Med, Brisbane, Qld, Australia
[5] Pathol Queensland, Cent Lab, Brisbane, Qld, Australia
[6] Univ Queensland, Fac Med, Princess Alexandra Southside Clin Sch, Brisbane, Qld, Australia
[7] Princess Alexandra Hosp, Infect Management Serv, Brisbane, Qld, Australia
[8] Metro North Hlth, Herston Infect Dis Inst, Brisbane, Qld, Australia
关键词
vancomycin resistance; Enterococcus faecium; VRE; ST78; whole-genome sequencing; genomic epidemiology; surveillance; Enterococcus; epidemiology; genomics; outbreak; transmission; GLYCOPEPTIDE RESISTANCE; GENE; INFECTION; DISCOVERY; UPDATE; TOOL;
D O I
10.1128/spectrum.04204-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of health care-associated infections (HAIs) globally. In Australia, the spread of hospital-adapted VREfm is largely driven by a single clonal group (clonal complex [CC]), CC17, to which the lineage ST78 belongs. To investigate an outbreak of vancomycin-resistant Enterococcus faecium (VREfm) sequence type 78 (ST78) in a large tertiary Australian hospital. A collection of 63 VREfm ST78 isolates, identified during a routine genomic surveillance program, were subjected to genomic epidemiological analysis based on whole-genome sequencing (WGS) data. The population structure was reconstructed using phylogenetic analysis, and a collection of publicly available VREfm ST78 genomes were used to provide global context. Core genome single nucleotide polymorphism (SNP) distances and available clinical metadata were used to characterize outbreak clusters and reconstruct transmission events. In silico genotyping confirmed that all study isolates were vanB-type VREfm carrying virulence characteristics of the hospital-associated E. faecium. Phylogenetic analysis identified two distinct phylogenetic clades, only one of which was responsible for a hospital outbreak. Four outbreak subtypes could be defined with examples of recent transmissions. Inference on transmission trees suggested complex transmission routes with unknown environmental reservoirs mediating the outbreak. WGS-based cluster analysis with publicly available genomes identified closely related Australian ST78 and ST203 isolates, highlighting the capacity for WGS to resolve complex clonal relationships between the VREfm lineages. Whole genome-based analysis has provided a high-resolution description of an outbreak of vanB-type VREfm ST78 in a Queensland hospital. Combined routine genomic surveillance and epidemiological analysis have facilitated better understanding of the local epidemiology of this endemic strain, providing valuable insight for better targeted control of VREfm.IMPORTANCE Vancomycin-resistant Enterococcus faecium (VREfm) is a leading cause of health care-associated infections (HAIs) globally. In Australia, the spread of hospital-adapted VREfm is largely driven by a single clonal group (clonal complex [CC]), CC17, to which the lineage ST78 belongs. While implementing a genomic surveillance program in Queensland, we observed increased incidence of ST78 colonizations and infections among patients. Here, we demonstrate the use of real-time genomic surveillance as a tool to support and enhance infection control (IC) practices. Our results show that real-time whole-genome sequencing (WGS) can efficiently disrupt outbreaks by identifying transmission routes that in turn can be targeted using resource-limited interventions. Additionally, we demonstrate that by placing local outbreaks in a global context, high-risk clones can be identified and targeted prior to them becoming established within clinical environments. Finally, the persistence of these organism within the hospital highlights the need for routine genomic surveillance as a management tool to control VRE transmission.
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页数:10
相关论文
共 77 条
[51]  
Permana B., HAIVIZ HEALTHCARE AS
[52]  
Permana B., GRAPHSNP GRAPH BASED
[53]   Macrolide resistance genes in Enterococcus spp. [J].
Portillo, A ;
Ruiz-Larrea, F ;
Zarazaga, M ;
Alonso, A ;
Martinez, JL ;
Torres, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (04) :967-971
[54]   Characterization of Tn1547, a composite transposon flanked by the IS16 and IS256-like elements, that confers vancomycin resistance in Enterococcus faecalis BM4281 [J].
Quintiliani, R ;
Courvalin, P .
GENE, 1996, 172 (01) :1-8
[55]   Complex Routes of Nosocomial Vancomycin-Resistant Enterococcus faecium Transmission Revealed by Genome Sequencing` [J].
Raven, Kathy E. ;
Gouliouris, Theodore ;
Brodrick, Hayley ;
Coll, Francesc ;
Brown, Nicholas M. ;
Reynolds, Rosy ;
Reuter, Sandra ;
Toeroek, M. Estee ;
Parkhill, Julian ;
Peacock, Sharon J. .
CLINICAL INFECTIOUS DISEASES, 2017, 64 (07) :886-893
[56]   A decade of genomic history for healthcare-associated Enterococcus faecium in the United Kingdom and Ireland [J].
Raven, Kathy E. ;
Reuter, Sandra ;
Reynolds, Rosy ;
Brodrick, Hayley J. ;
Russell, Julie E. ;
Torok, M. Estee ;
Parkhill, Julian ;
Peacock, Sharon J. .
GENOME RESEARCH, 2016, 26 (10) :1388-1396
[57]   PulseNet: Entering the Age of Next-Generation Sequencing [J].
Ribot, Efrain M. ;
Freeman, Molly ;
Hise, Kelley B. ;
Gerner-Smidt, Peter .
FOODBORNE PATHOGENS AND DISEASE, 2019, 16 (07) :451-456
[58]   A potential virulence gene, hylEfm, predominates in Enterococcus faecium of clinical origin [J].
Rice, LB ;
Carias, L ;
Rudin, S ;
Vael, C ;
Goossens, H ;
Konstabel, C ;
Klare, I ;
Nallapareddy, SR ;
Huang, WX ;
Murray, BE .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (03) :508-512
[59]   Update on acquired tetracycline resistance genes [J].
Roberts, MC .
FEMS MICROBIOLOGY LETTERS, 2005, 245 (02) :195-203
[60]  
Sayers EW, 2020, NUCLEIC ACIDS RES, V48, pD9, DOI [10.1093/nar/gkz899, 10.1093/nar/gkab1112, 10.1093/nar/gkv1290, 10.1093/nar/gkaa892]