Echinocandin Resistance in Candida Species Isolates from Liver Transplant Recipients

Author:

Prigent Gwénolé1,Aït-Ammar Nawel12,Levesque Eric3,Fekkar Arnaud4,Costa Jean-Marc25,El Anbassi Sarra1,Foulet Françoise1,Duvoux Christophe6,Merle Jean-Claude3,Dannaoui Eric27ORCID,Botterel Françoise12

Affiliation:

1. Unité de Parasitologie-Mycologie, Département de Virologie, Bactériologie-Hygiène, Parasitologie-Mycologie, DHU VIC, CHU Henri Mondor, AP-HP, Créteil, France

2. EA Dynamyc UPEC, ENVA, Faculté de Médecine, Créteil, France

3. Réanimation Digestive et Hépato-Biliaire, Service d'Anesthésie et des Réanimations Chirurgicales, CHU Henri Mondor, AP-HP, Créteil, France

4. Service de Parasitologie-Mycologie, CHU La Pitié-Salpêtrière, AP-HP, Paris, France

5. Laboratoire Cerba, Saint-Ouen-l'Aumône, France

6. Service d'Hépatologie, CHU Henri Mondor, AP-HP, Créteil, France

7. Unité de Parasitologie-Mycologie, Service de Microbiologie, Université Paris-Descartes, Faculté de Médecine, Hôpital Européen Georges Pompidou, AP-HP, Paris, France

Abstract

ABSTRACT Liver transplant recipients are at risk of invasive fungal infections, especially candidiasis. Echinocandin is recommended as prophylactic treatment but is increasingly associated with resistance. Our aim was to assess echinocandin drug resistance in Candida spp. isolated from liver transplant recipients treated with this antifungal class. For this, all liver-transplanted patients in a University Hospital (Créteil, France) between January and June of 2013 and 2015 were included. Susceptibilities of Candida isolates to echinocandins were tested by Etest and the EUCAST reference method. Isolates were analyzed by FKS sequencing and genotyped based on microsatellites or multilocus sequence typing (MLST) profiles. Ninety-four patients were included, and 39 patients were colonized or infected and treated with echinocandin. Echinocandin resistance appeared in 3 (8%) of the treated patients within 1 month of treatment. One patient was colonized by resistant Candida glabrata , one by resistant Candida dubliniensis , and one by resistant Candida albicans . Molecular analysis found three mutations in FKS2 HS1 (F659S, S663A, and D666E) for C. glabrata and one mutation in FKS1 HS1 (S645P) for C. dubliniensis and C. albicans . Susceptible and resistant isolates belonged to the same genotype. To our knowledge, this is the first study on echinocandin resistance in Candida spp. in a liver transplant population. Most resistant isolates were found around/in digestive sites, perhaps due to lower diffusion of echinocandin in these sites. This work documents the risk of emergence of resistance to echinocandin, even after short-term treatment.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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