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      In vitro characterization and molecular epidemiology of Cryptococcus spp. isolates from non-HIV patients in Guangdong, China

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          Abstract

          Background

          The burden of cryptococcosis in mainland China is enormous. However, the in vitro characterization and molecular epidemiology in Guangdong, a key region with a high incidence of fungal infection in China, are not clear.

          Methods

          From January 1, 2010, to March 31, 2019, clinical strains of Cryptococcus were collected from six medical centres in Guangdong. The clinical information and characteristics of the strains were analysed. Furthermore, molecular types were determined.

          Results

          A total of 84 strains were collected, mostly from male and young or middle-aged adult patients. Pulmonary and cerebral infections (82.1%) were most common. All strains were Cryptococcus neoformans, grew well at 37°C and had capsules around their cells. One melanin- and urea- and one melanin+ and urea- variants were found. Although most strains exhibited a low minimum inhibitory concentration (MIC) value for voriconazole (mean: 0.04 μg/mL) and posaconazole (mean: 0.12 μg/mL), the results for these isolates showed a high degree of variation in the MIC values of fluconazole and 5-fluorocytosine, and resistance was observed for 4 out of 6 drugs. A significant proportion of these strains had MIC values near the ECV values, particularly in the case of amphotericin B. The proportion of strains near the clinical breakpoints was as follows: fluconazole: 3.66%; voriconazole: 3.66%; itraconazole: 6.10%; posaconazole: 13.41%; amphotericin B: 84.15%; 5-fluorocytosine: 2.44%. These strains were highly homogeneous and were dominated by the Grubii variant (95.2%), VNI (94.0%), α mating (100%), and ST5 (89.3%) genotypes. Other rare types, including ST4, 31, 278, 7, 57 and 106, were also found.

          Conclusion

          Phenotypically variant and non-wild-type strains were found in Guangdong, and a significant proportion of these strains had MIC values near the ECV values towards the 6 antifungal drugs, and resistance was observed for 4 out of 6 drugs. The molecular type was highly homogeneous but compositionally diverse, with rare types found. Enhanced surveillance of the aetiology and evolution and continuous monitoring of antifungal susceptibility are needed to provide references for decision-making in the health sector and optimization of disease prevention and control.

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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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            Cryptococcus: from environmental saprophyte to global pathogen.

            Cryptococcosis is a globally distributed invasive fungal infection that is caused by species within the genus Cryptococcus which presents substantial therapeutic challenges. Although natural human-to-human transmission has never been observed, recent work has identified multiple virulence mechanisms that enable cryptococci to infect, disseminate within and ultimately kill their human host. In this Review, we describe these recent discoveries that illustrate the intricacy of host-pathogen interactions and reveal new details about the host immune responses that either help to protect against disease or increase host susceptibility. In addition, we discuss how this improved understanding of both the host and the pathogen informs potential new avenues for therapeutic development.
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              Echinocandin antifungal drugs.

              The echinocandins are large lipopeptide molecules that are inhibitors of beta-(1,3)-glucan synthesis, an action that damages fungal cell walls. In vitro and in vivo, the echinocandins are rapidly fungicidal against most Candida spp and fungistatic against Aspergillus spp. They are not active at clinically relevant concentrations against Zygomycetes, Cryptococcus neoformans, or Fusarium spp. No drug target is present in mammalian cells. The first of the class to be licensed was caspofungin, for refractory invasive aspergillosis (about 40% response rate) and the second was micafungin. Adverse events are generally mild, including (for caspofungin) local phlebitis, fever, abnormal liver function tests, and mild haemolysis. Poor absorption after oral administration limits use to the intravenous route. Dosing is once daily and drug interactions are few. The echinocandins are widely distributed in the body, and are metabolised by the liver. Results of studies of caspofungin in candidaemia and invasive candidiasis suggest equivalent efficacy to amphotericin B, with substantially fewer toxic effects. Absence of antagonism in combination with other antifungal drugs suggests that combination antifungal therapy could become a general feature of the echinocandins, particularly for invasive aspergillosis.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2509428/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/2510070/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1537994/overviewRole: Role: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/432852/overviewRole: Role: Role: Role:
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                URI : https://loop.frontiersin.org/people/1319224/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                15 January 2024
                2023
                : 14
                : 1295363
                Affiliations
                [1] 1State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, National Center for Respiratory Medicine , Guangzhou, China
                [2] 2Department of Respiratory Medicine, Longgang Central Hospital , Shenzhen, China
                [3] 3Microscopy Core Facility, Biomedical Research Core Facilities, Westlake University , Hangzhou, China
                [4] 4Intensive Care Unit, Guangzhou First People’s Hospital , Guangzhou, China
                [5] 5Department of Hematology Oncology, Jieyang City People's Hospital , Jieyang, China
                [6] 6Clinical Medicine Laboratory, Foshan City First People's Hospital , Foshan, China
                [7] 7Clinical Medicine Laboratory, Southern Military Region General Hospital , Guangzhou, China
                [8] 8Clinical Medicine Laboratory, Sun Yat-sen University First Affiliated Hospital , Guangzhou, China
                Author notes

                Edited by: Renátó Kovács, University of Debrecen, Hungary

                Reviewed by: Jayapradha R., SASTRA University, India; Sueli Fumie Yamada-Ogatta, State University of Londrina, Brazil

                *Correspondence: Feng Ye, tu276025@ 123456gird.cn

                These authors have contributed equally to this work

                Article
                10.3389/fmicb.2023.1295363
                10823435
                38287960
                9a85552f-272e-4b41-971d-2ad4ad9d7ce3
                Copyright © 2024 Wang, Li, Gao, Tang, Zheng, Wu, Wang, Guo and Ye.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 16 September 2023
                : 27 December 2023
                Page count
                Figures: 4, Tables: 3, Equations: 0, References: 56, Pages: 12, Words: 8011
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the Natural Science Foundation of Guangdong Province (2022A1515010089) and the Open Fund of the State Key Laboratory of Respiratory Diseases (SKLRD-OP-202210).
                Categories
                Microbiology
                Original Research
                Custom metadata
                Antimicrobials, Resistance and Chemotherapy

                Microbiology & Virology
                cryptococcus,virulence factor,molecular epidemiology,antifungal susceptibility test,genetic evolution analysis

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