4.7 Article

Determinants of fluconazole resistance and echinocandin tolerance in C. parapsilosis isolates causing a large clonal candidemia outbreak among COVID-19 patients in a Brazilian ICU

期刊

EMERGING MICROBES & INFECTIONS
卷 11, 期 1, 页码 2264-2274

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/22221751.2022.2117093

关键词

Candida parapsilosis; outbreak; candidemia; fluconazole resistance; echinocandin tolerance

资金

  1. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [FAPESP 2017/022037]
  2. Science Foundation Ireland [19/FFP/6668]
  3. NIH [R01AI109025]
  4. Center for Discovery and Innovation

向作者/读者索取更多资源

Patients with severe COVID-19 are at risk of acquiring COVID-19-associated candidemia (CAC), often caused by drug-resistant C. parapsilosis. This study reports the largest outbreak of CAC caused by fluconazole-resistant and echinocandin-tolerant C. parapsilosis. The findings underscore the importance of antifungal stewardship and infection control strategies.
Patients presenting with severe COVID-19 are predisposed to acquire secondary fungal infections such as COVID-19-associated candidemia (CAC), which are associated with poor clinical outcomes despite antifungal treatment. The extreme burden imposed on clinical facilities during the COVID-19 pandemic has provided a permissive environment for the emergence of clonal outbreaks of multiple Candida species, including C. auris and C. parapsilosis. Here we report the largest clonal CAC outbreak to date caused by fluconazole resistant (FLZR) and echinocandin tolerant (ECT) C. parapsilosis. Sixty C. parapsilosis strains were obtained from 57 patients at a tertiary care hospital in Brazil, 90% of them were FLZR and ECT. Although only 35.8% of FLZR isolates contained an ERG11 mutation, all of them contained the TAC1(L518F) mutation and significantly overexpressed CDR1. Introduction of TAC1(L518F) into a susceptible background increased the MIC of fluconazole and voriconazole 8-fold and resulted in significant basal overexpression of CDR1. Additionally, FLZR isolates exclusively harboured E1939G outside of Fks1 hotspot-2, which did not confer echinocandin resistance, but significantly increased ECT. Multilocus microsatellite typing showed that 51/60 (85%) of the FLZR isolates belonged to the same cluster, while the susceptible isolates each represented a distinct lineage. Finally, biofilm production in FLZR isolates was significantly lower than in susceptible counterparts Suggesting that it may not be an outbreak determinant. In summary, we show that TAC1(L518F) and FKS1(E1393G) confer FLZR and ECT, respectively, in CAC-associated C. parapsilosis. Our study underscores the importance of antifungal stewardship and effective infection control strategies to mitigate clonal C. parapsilosis outbreaks.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据