Consideration of within-patient diversity highlights transmission pathways and antimicrobial resistance gene variability in vancomycin-resistant Enterococcus faecium

Author:

McHugh Martin P12ORCID,Pettigrew Kerry A1,Taori Surabhi2,Evans Thomas J3ORCID,Leanord Alistair34,Gillespie Stephen H1,Templeton Kate E2,Holden Matthew T G1ORCID

Affiliation:

1. School of Medicine, University of St Andrews , St Andrews , UK

2. Medical Microbiology, Department of Laboratory Medicine, Royal Infirmary of Edinburgh , Edinburgh , UK

3. School of Infection and Immunity, University of Glasgow , Glasgow , UK

4. Scottish Microbiology Reference Laboratories , Glasgow Royal Infirmary, Glasgow , UK

Abstract

Abstract Background WGS is increasingly being applied to healthcare-associated vancomycin-resistant Enterococcus faecium (VREfm) outbreaks. Within-patient diversity could complicate transmission resolution if single colonies are sequenced from identified cases. Objectives Determine the impact of within-patient diversity on transmission resolution of VREfm. Materials and methods Fourteen colonies were collected from VREfm positive rectal screens, single colonies were collected from clinical samples and Illumina WGS was performed. Two isolates were selected for Oxford Nanopore sequencing and hybrid genome assembly to generate lineage-specific reference genomes. Mapping to closely related references was used to identify genetic variations and closely related genomes. A transmission network was inferred for the entire genome set using Phyloscanner. Results and discussion In total, 229 isolates from 11 patients were sequenced. Carriage of two or three sequence types was detected in 27% of patients. Presence of antimicrobial resistance genes and plasmids was variable within genomes from the same patient and sequence type. We identified two dominant sequence types (ST80 and ST1424), with two putative transmission clusters of two patients within ST80, and a single cluster of six patients within ST1424. We found transmission resolution was impaired using fewer than 14 colonies. Conclusions Patients can carry multiple sequence types of VREfm, and even within related lineages the presence of mobile genetic elements and antimicrobial resistance genes can vary. VREfm within-patient diversity could be considered in future to aid accurate resolution of transmission networks.

Funder

Chief Scientist Office

Publisher

Oxford University Press (OUP)

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