<p>Antimicrobial resistance is a public health threat associated with increased morbidity, mortality and financial burden in nursing homes and other healthcare settings<sup><CitationRef CitationID="CR1">1</CitationRef></sup>. Residents of nursing homes are at increased risk of pathogen colonization and infection owing to antimicrobial-resistant bacteria and fungi. Nursing homes act as reservoirs, amplifiers and disseminators of antimicrobial resistance in healthcare networks and across geographical regions<sup><CitationRef CitationID="CR2">2</CitationRef></sup>. Here we investigate the genomic epidemiology of the emerging, multidrug-resistant human fungal pathogen <i>Candida auris</i> in a ventilator-capable nursing home. Coupling&#xa0;strain-resolved metagenomics with isolate sequencing, we report skin&#xa0;colonization and clonal spread of <i>C.</i> <i>auris</i> on the skin of nursing home residents and&#xa0;throughout a metropolitan region. We also report that&#xa0;most <i>Enterococcus faecium</i>, <i>Staphylococcus aureus</i>, <i>Klebsiella pneumoniae</i>, <i>Acinetobacter baumannii</i>, <i>Pseudomonas aeruginosa</i> and <i>Entobacter</i> species (ESKAPE) pathogens and other high-priority pathogens (including <i>Escherichia coli</i>, <i>Providencia stuartii</i>, <i>Proteus mirabilis</i> and <i>Morganella morganii</i>) are shared in a nursing home. Integrating microbiome and clinical microbiology data, we detect carbapenemase genes at multiple skin sites on residents identified as carriers of these genes. We analyse publicly available shotgun metagenomic samples (stool and skin) collected from residents with varying medical conditions living in seven other nursing homes and provide additional evidence of previously unappreciated bacterial strain sharing. Taken together, our data suggest that skin is a reservoir for colonization by <i>C.</i> <i>auris</i> and ESKAPE pathogens and their associated antimicrobial-resistance genes.</p>

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Clonal Candida auris and ESKAPE pathogens on the skin of residents of nursing homes

  • Diana M. Proctor,
  • Sarah E. Sansom,
  • Clay Deming,
  • Sean Conlan,
  • Ryan A. Blaustein,
  • Thomas K. Atkins,
  • Jim Mullikin,
  • Jim Thomas,
  • Alice Young,
  • Gerry Bouffard,
  • Betty Barnabas,
  • Shelise Brooks,
  • Joel Han,
  • Chlöe Buchter,
  • Shi-ling Ho,
  • Juyun Crawford,
  • Richelle Legaspi,
  • Quino Maduro,
  • Holly Marfani,
  • Casandra Montemayor,
  • Nancy Riebow,
  • Karen Schandler,
  • Brian Schmidt,
  • Christina Sison,
  • Mal Stantripop,
  • Sean Black,
  • Mila Dekhtyar,
  • Cathy Masiello,
  • Jenny McDowell,
  • Morgan Park,
  • Pam Thomas,
  • Meg Vemulapalli,
  • Thelma Dangana,
  • Christine Fukuda,
  • Lahari Thotapalli,
  • Heidi H. Kong,
  • Michael Y. Lin,
  • Mary K. Hayden,
  • Julia A. Segre

摘要

Antimicrobial resistance is a public health threat associated with increased morbidity, mortality and financial burden in nursing homes and other healthcare settings1. Residents of nursing homes are at increased risk of pathogen colonization and infection owing to antimicrobial-resistant bacteria and fungi. Nursing homes act as reservoirs, amplifiers and disseminators of antimicrobial resistance in healthcare networks and across geographical regions2. Here we investigate the genomic epidemiology of the emerging, multidrug-resistant human fungal pathogen Candida auris in a ventilator-capable nursing home. Coupling strain-resolved metagenomics with isolate sequencing, we report skin colonization and clonal spread of C.auris on the skin of nursing home residents and throughout a metropolitan region. We also report that most Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Entobacter species (ESKAPE) pathogens and other high-priority pathogens (including Escherichia coli, Providencia stuartii, Proteus mirabilis and Morganella morganii) are shared in a nursing home. Integrating microbiome and clinical microbiology data, we detect carbapenemase genes at multiple skin sites on residents identified as carriers of these genes. We analyse publicly available shotgun metagenomic samples (stool and skin) collected from residents with varying medical conditions living in seven other nursing homes and provide additional evidence of previously unappreciated bacterial strain sharing. Taken together, our data suggest that skin is a reservoir for colonization by C.auris and ESKAPE pathogens and their associated antimicrobial-resistance genes.