Antifungal Resistance in Cryptococcal Infections

Author:

Melhem Marcia S. C.123ORCID,Leite Júnior Diniz Pereira1ORCID,Takahashi Juliana P. F.24,Macioni Milena Bronze1,Oliveira Lidiane de5,de Araújo Lisandra Siufi26,Fava Wellington S.2ORCID,Bonfietti Lucas X.6,Paniago Anamaria M. M.2ORCID,Venturini James2ORCID,Espinel-Ingroff Ana78

Affiliation:

1. Graduate Program in Sciences, Secretary of Health, São Paulo 01246-002, SP, Brazil

2. Graduate Program in Infectious and Parasitic Diseases, Federal University of Mato Grosso do Sul, Campo Grande 79070-900, MS, Brazil

3. Graduate Program in Tropical Diseases, State University of São Paulo, Botucatu 18618-687, SP, Brazil

4. Pathology Division, Adolfo Lutz Institute, São Paulo 01246-002, SP, Brazil

5. Grupo Fleury Laboratories, São Paulo 04701-200, SP, Brazil

6. Central Public Health Laboratory-LACEN, Mycology Unit, Adolfo Lutz Institut, São Paulo 01246-002, SP, Brazil

7. Central Public Health Laboratory-LACEN, Campo Grande 79074-460, MS, Brazil

8. VCU Medical Center, Richmond, VA 23284, USA

Abstract

Antifungal therapy, especially with the azoles, could promote the incidence of less susceptible isolates of Cryptococcus neoformans and C. gattii species complexes (SC), mostly in developing countries. Given that these species affect mostly the immunocompromised host, the infections are severe and difficult to treat. This review encompasses the following topics: 1. infecting species and their virulence, 2. treatment, 3. antifungal susceptibility methods and available categorical endpoints, 4. genetic mechanisms of resistance, 5. clinical resistance, 6. fluconazole minimal inhibitory concentrations (MICs), clinical outcome, 7. environmental influences, and 8. the relevance of host factors, including pharmacokinetic/pharmacodynamic (PK/PD) parameters, in predicting the clinical outcome to therapy. As of now, epidemiologic cutoff endpoints (ECVs/ECOFFs) are the most reliable antifungal resistance detectors for these species, as only one clinical breakpoint (amphotericin B and C. neoformans VNI) is available.

Funder

National Council for Scientific and Technological Development (CNPq), the Ministry of Science and Technology of Brazil

Ministry of Science, Technology, and Innovation (MCTI), Brazil

São Paulo Research Foundation

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

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