4.5 Article

Quantifying acquisition and transmission of Enterococcus faecium using genomic surveillance

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NATURE MICROBIOLOGY
卷 6, 期 1, 页码 103-+

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NATURE PORTFOLIO
DOI: 10.1038/s41564-020-00806-7

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资金

  1. Department of Health [WT098600, HICF-T5-342]
  2. Wellcome Trust [WT098600, HICF-T5-342, 103387/Z/13/Z, 201344/Z/16/Z, 110243/Z/15/Z]
  3. Academy of Medical Sciences
  4. Health Foundation
  5. National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre
  6. Wellcome Trust [201344/Z/16/Z, 110243/Z/15/Z, 103387/Z/13/Z] Funding Source: Wellcome Trust
  7. MRC [MR/N029399/1] Funding Source: UKRI

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Longitudinal genomic surveillance of Enterococcus faecium carriage, environmental contamination, and transmission within a defined patient cohort revealed high endemicity of a hospital-adapted E. faecium lineage.
Nosocomial acquisition and transmission of vancomycin-resistant Enterococcus faecium (VREfm) is the driver for E. faecium carriage in hospitalized patients, which, in turn, is a risk factor for invasive infection in immunocompromised patients. In the present study, we provide a comprehensive picture of E. faecium transmission in an entire sampled patient population using a sequence-driven approach. We prospectively identified and followed 149 haematology patients admitted to a hospital in England for 6 months. Patient stools (n = 376) and environmental swabs (n = 922) were taken at intervals and cultured for E. faecium. We sequenced 1,560 isolates (1,001 stool, 559 environment) and focused our genomic analyses on 1,477 isolates (95%) in the hospital-adapted clade A1. Of 101 patients who provided two or more stool samples, 40 (40%) developed E. faecium carriage after admission based on culture, compared with 64 patients (63%) based on genomic analysis (73% VREfm). Half of 922 environmental swabs (447, 48%) were positive for VREfm. Network analysis showed that, of 111 patients positive for the A1 clade, 67 had strong epidemiological and genomic links with at least one other patient and/or their direct environment, supporting nosocomial transmission. Six patients (3.4%) developed an invasive E. faecium infection from their own gut-colonizing strain, which was preceded by nosocomial acquisition of the infecting isolate in half of these. Two informatics approaches (subtype categorization to define phylogenetic clusters and the development of an SNP cut-off for transmission) were central to our analyses, both of which will inform the future translation of E. faecium sequencing into routine outbreak detection and investigation. In conclusion, we showed that carriage and environmental contamination by the hospital-adapted E. faecium lineage were hyperendemic in our study population and that improved infection control measures will be needed to reduce hospital acquisition rates. A longitudinal genomic surveillance of Enterococcus faecium carriage, environmental contamination and transmission in a defined patient cohort shows that a hospital-adapted E. faecium lineage was hyperendemic.

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