Multicenter Candida auris outbreak caused by azole‐susceptible clade IV in Pernambuco, Brazil

Author:

Spruijtenburg Bram12ORCID,Nobrega de Almeida Júnior João34ORCID,Ribeiro Felipe de Camargo34ORCID,Kemmerich Karoline Kristina34ORCID,Baeta Karla5ORCID,Meijer Eelco F. J.12ORCID,de Groot Theun12ORCID,Meis Jacques F.16ORCID,Colombo Arnaldo Lopes34ORCID,

Affiliation:

1. Radboudumc‐CWZ Center of Expertise for Mycology Nijmegen The Netherlands

2. Canisius‐Wilhelmina Hospital (CWZ)/Dicoon Nijmegen The Netherlands

3. Disciplina de Infectologia, Escola Paulista de Medicina Universidade Federal de São Paulo São Paulo Brazil

4. Antimicrobial Resistance Institute of São Paulo‐ARIES São Paulo Brazil

5. Agência Pernambucana de Vigilância Sanitária Recife Brazil

6. Institute of Translational Research, Cologne Excellence Cluster on Cellular Stress Responses in Aging‐Associated Diseases (CECAD) and Excellence Center for Medical Mycology, University of Cologne Cologne Germany

Abstract

AbstractBackgroundCandida auris is an emerging multidrug‐resistant yeast, frequently causing outbreaks in health care facilities. The pathogen persistently colonises human skin and inanimate surfaces such as catheters, aiding to its spread. Moreover, colonisation is a risk factor to develop invasive infection.ObjectivesWe investigated 61 C. auris strains isolated from non‐sterile human body sites (n = 53) and the hospital environment (n = 8), originating from four different centres in a single Brazilian state.Materials and MethodsAntifungal susceptibility testing (AFST) against common antifungals was performed, and resistance‐associated genes were evaluated. Genetic relatedness was investigated with short tandem repeat (STR) genotyping and validated with whole‐genome sequencing (WGS) single nucleotide polymorphism (SNP) analysis.ResultsAntifungal susceptibility testing demonstrated that all isolates were susceptible to azoles, echinocandins and amphotericin B. No mutations were detected in ERG11 and FKS1 genes. With STR typing, isolates were allocated to clade IV and appeared closely related. This was confirmed by WGS SNP analysis of 6 isolates, which demonstrated a maximal difference of only 41 SNPs between these strains. Furthermore, the Brazilian isolates formed a distinct autochthonous branch within clade IV, excluding recent introductions from outside the country. A molecular clock analysis of clade IV isolates from various countries suggests that early in the previous century there was a unique event causing environmental spread of a C. auris ancestor throughout the Latin‐American continent, followed by human introduction during the last decades.ConclusionWe report the emergence of C. auris patient colonisation in multiple centres by fluconazole‐susceptible clade IV close‐related strains in Pernambuco State, Brazil.

Publisher

Wiley

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