TY - JOUR
T1 - Simultaneous emergence of multidrug-resistant candida auris on 3 continents confirmed by whole-genome sequencing and epidemiological analyses
AU - Lockhart, Shawn R.
AU - Etienne, Kizee A.
AU - Vallabhaneni, Snigdha
AU - Farooqi, Joveria
AU - Chowdhary, Anuradha
AU - Govender, Nelesh P.
AU - Colombo, Arnaldo Lopes
AU - Calvo, Belinda
AU - Cuomo, Christina A.
AU - Desjardins, Christopher A.
AU - Berkow, Elizabeth L.
AU - Castanheira, Mariana
AU - Magobo, Rindidzani E.
AU - Jabeen, Kauser
AU - Asghar, Rana J.
AU - Meis, Jacques F.
AU - Jackson, Brendan
AU - Chiller, Tom
AU - Litvintseva, Anastasia P.
N1 - Funding Information:
This work was supported by the National Institute of Allergy and Infectious Diseases (grant U19AI110818 to the Broad Institute), United States Agency for International Development (USAID; grant 4-338/PAK-US/HEC/2010/932 to Aga Khan University), and the Advanced Molecular Detection initiative at the CDC.
PY - 2017/1/15
Y1 - 2017/1/15
N2 - Background. Candida auris, a multidrug-resistant yeast that causes invasive infections, was first described in 2009 in Japan and has since been reported from several countries. Methods. To understand the global emergence and epidemiology of C. auris, we obtained isolates from 54 patients with C. auris infection from Pakistan, India, South Africa, and Venezuela during 2012-2015 and the type specimen from Japan. Patient information was available for 41 of the isolates. We conducted antifungal susceptibility testing and whole-genome sequencing (WGS). Results. Available clinical information revealed that 41% of patients had diabetes mellitus, 51% had undergone recent surgery, 73% had a central venous catheter, and 41% were receiving systemic antifungal therapy when C. auris was isolated. The median time from admission to infection was 19 days (interquartile range, 9-36 days), 61% of patients had bloodstream infection, and 59% died. Using stringent break points, 93% of isolates were resistant to fluconazole, 35% to amphotericin B, and 7% to echinocandins; 41% were resistant to 2 antifungal classes and 4% were resistant to 3 classes. WGS demonstrated that isolates were grouped into unique clades by geographic region. Clades were separated by thousands of single-nucleotide polymorphisms, but within each clade isolates were clonal. Different mutations in ERG11 were associated with azole resistance in each geographic clade. Conclusions. C. auris is an emerging healthcare-associated pathogen associated with high mortality. Treatment options are limited, due to antifungal resistance. WGS analysis suggests nearly simultaneous, and recent, independent emergence of different clonal populations on 3 continents. Risk factors and transmission mechanisms need to be elucidated to guide control measures.
AB - Background. Candida auris, a multidrug-resistant yeast that causes invasive infections, was first described in 2009 in Japan and has since been reported from several countries. Methods. To understand the global emergence and epidemiology of C. auris, we obtained isolates from 54 patients with C. auris infection from Pakistan, India, South Africa, and Venezuela during 2012-2015 and the type specimen from Japan. Patient information was available for 41 of the isolates. We conducted antifungal susceptibility testing and whole-genome sequencing (WGS). Results. Available clinical information revealed that 41% of patients had diabetes mellitus, 51% had undergone recent surgery, 73% had a central venous catheter, and 41% were receiving systemic antifungal therapy when C. auris was isolated. The median time from admission to infection was 19 days (interquartile range, 9-36 days), 61% of patients had bloodstream infection, and 59% died. Using stringent break points, 93% of isolates were resistant to fluconazole, 35% to amphotericin B, and 7% to echinocandins; 41% were resistant to 2 antifungal classes and 4% were resistant to 3 classes. WGS demonstrated that isolates were grouped into unique clades by geographic region. Clades were separated by thousands of single-nucleotide polymorphisms, but within each clade isolates were clonal. Different mutations in ERG11 were associated with azole resistance in each geographic clade. Conclusions. C. auris is an emerging healthcare-associated pathogen associated with high mortality. Treatment options are limited, due to antifungal resistance. WGS analysis suggests nearly simultaneous, and recent, independent emergence of different clonal populations on 3 continents. Risk factors and transmission mechanisms need to be elucidated to guide control measures.
KW - Amphotericin b resistance
KW - Candida auris
KW - Candidemia
KW - Fluconazole resistance
KW - Whole genome sequence typing
UR - http://www.scopus.com/inward/record.url?scp=85015249025&partnerID=8YFLogxK
U2 - 10.1093/cid/ciw691
DO - 10.1093/cid/ciw691
M3 - Article
C2 - 27988485
AN - SCOPUS:85015249025
SN - 1058-4838
VL - 64
SP - 134
EP - 140
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 2
ER -