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      Molecular mechanisms of acquired antifungal drug resistance in principal fungal pathogens and EUCAST guidance for their laboratory detection and clinical implications

      review-article
      , , , , , Subcommittee on Antifungal Susceptibility Testing (AFST) of the ESCMID European Committee for Antimicrobial Susceptibility Testing (EUCAST)
      Journal of Antimicrobial Chemotherapy
      Oxford University Press

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          Abstract

          The increasing incidence and changing epidemiology of invasive fungal infections continue to present many challenges to their effective management. The repertoire of antifungal drugs available for treatment is still limited although there are new antifungals on the horizon. Successful treatment of invasive mycoses is dependent on a mix of pathogen-, host- and antifungal drug-related factors. Laboratories need to be adept at detection of fungal pathogens in clinical samples in order to effectively guide treatment by identifying isolates with acquired drug resistance. While there are international guidelines on how to conduct in vitro antifungal susceptibility testing, these are not performed as widely as for bacterial pathogens. Furthermore, fungi generally are recovered in cultures more slowly than bacteria, and often cannot be cultured in the laboratory. Therefore, non-culture-based methods, including molecular tests, to detect fungi in clinical specimens are increasingly important in patient management and are becoming more reliable as technology improves. Molecular methods can also be used for detection of target gene mutations or other mechanisms that predict antifungal drug resistance. This review addresses acquired antifungal drug resistance in the principal human fungal pathogens and describes known resistance mechanisms and what in-house and commercial tools are available for their detection. It is emphasized that this approach should be complementary to culture-based susceptibility testing, given the range of mutations, resistance mechanisms and target genes that may be present in clinical isolates, but may not be included in current molecular assays.

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          Most cited references270

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          Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of america.

          Cryptococcosis is a global invasive mycosis associated with significant morbidity and mortality. These guidelines for its management have been built on the previous Infectious Diseases Society of America guidelines from 2000 and include new sections. There is a discussion of the management of cryptococcal meningoencephalitis in 3 risk groups: (1) human immunodeficiency virus (HIV)-infected individuals, (2) organ transplant recipients, and (3) non-HIV-infected and nontransplant hosts. There are specific recommendations for other unique risk populations, such as children, pregnant women, persons in resource-limited environments, and those with Cryptococcus gattii infection. Recommendations for management also include other sites of infection, including strategies for pulmonary cryptococcosis. Emphasis has been placed on potential complications in management of cryptococcal infection, including increased intracranial pressure, immune reconstitution inflammatory syndrome (IRIS), drug resistance, and cryptococcomas. Three key management principles have been articulated: (1) induction therapy for meningoencephalitis using fungicidal regimens, such as a polyene and flucytosine, followed by suppressive regimens using fluconazole; (2) importance of early recognition and treatment of increased intracranial pressure and/or IRIS; and (3) the use of lipid formulations of amphotericin B regimens in patients with renal impairment. Cryptococcosis remains a challenging management issue, with little new drug development or recent definitive studies. However, if the diagnosis is made early, if clinicians adhere to the basic principles of these guidelines, and if the underlying disease is controlled, then cryptococcosis can be managed successfully in the vast majority of patients.
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            Clinical Practice Guideline for the Management of Candidiasis: 2016 Update by the Infectious Diseases Society of America.

            It is important to realize that guidelines cannot always account for individual variation among patients. They are not intended to supplant physician judgment with respect to particular patients or special clinical situations. IDSA considers adherence to these guidelines to be voluntary, with the ultimate determination regarding their application to be made by the physician in the light of each patient's individual circumstances.
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              Global burden of disease of HIV-associated cryptococcal meningitis: an updated analysis.

              Cryptococcus is the most common cause of meningitis in adults living with HIV in sub-Saharan Africa. Global burden estimates are crucial to guide prevention strategies and to determine treatment needs, and we aimed to provide an updated estimate of global incidence of HIV-associated cryptococcal disease.
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                Author and article information

                Contributors
                Journal
                J Antimicrob Chemother
                J Antimicrob Chemother
                jac
                Journal of Antimicrobial Chemotherapy
                Oxford University Press
                0305-7453
                1460-2091
                August 2022
                15 June 2022
                15 June 2022
                : 77
                : 8
                : 2053-2073
                Affiliations
                Department of Clinical Microbiology, Trinity College Dublin, St James’s Hospital Campus , Dublin 8, Ireland
                Department of Medical Microbiology, Radboud University Medical Center , Nijmegen, The Netherlands
                Center of Expertise in Mycology, Radboud umc/CWZ , Nijmegen, The Netherlands
                JMI Laboratories, North Liberty , IA, USA
                Unité de parasitologie-mycologie, service de microbiologie, hôpital européen Georges-Pompidou, AP-HP , Paris, France
                Faculté de médecine, université de Paris , ParisFrance
                Public Health Wales Microbiology Cardiff, UHW , Cardiff, UK
                Unit of Mycology , Statens Serum Institut, Copenhagen, Denmark
                Department of Clinical Microbiology, Rigshospitalet , Copenhagen, Denmark
                Department of Clinical Medicine, University of Copenhagen , Copenhagen, Denmark
                Author notes
                Corresponding author. E-mail: rogerstr@ 123456tcd.ie

                Paul E. Verweij, Catherijne A.J. Knibbe, Eric Dannaoui and P. Lewis White Contributed equally.

                Author information
                https://orcid.org/0000-0003-4336-7729
                https://orcid.org/0000-0002-8600-9860
                https://orcid.org/0000-0003-0126-1782
                https://orcid.org/0000-0002-4747-0144
                Article
                dkac161
                10.1093/jac/dkac161
                9333407
                35703391
                68bbcbda-e861-4330-a839-3e4aca85fcfc
                © The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                Page count
                Pages: 21
                Categories
                Review
                AcademicSubjects/MED00740
                AcademicSubjects/MED00290
                AcademicSubjects/MED00230

                Oncology & Radiotherapy
                Oncology & Radiotherapy

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