The multidrug-resistant Candida auris, Candida haemulonii complex and phylogenetic related species: Insights into antifungal resistance mechanisms

IF 5.8 Q1 MICROBIOLOGY Current Research in Microbial Sciences Pub Date : 2025-01-01 Epub Date: 2025-01-28 DOI:10.1016/j.crmicr.2025.100354
Lívia S. Ramos , Pedro F. Barbosa , Carolline M.A. Lorentino , Joice C. Lima , Antonio L. Braga , Raquel V. Lima , Lucas Giovanini , Ana Lúcia Casemiro , Nahyara L.M. Siqueira , Stefanie C. Costa , Célia F. Rodrigues , Maryam Roudbary , Marta H. Branquinha , André L.S. Santos
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Abstract

The rise of multidrug-resistant (MDR) fungal pathogens poses a serious global threat to human health. Of particular concern are Candida auris, the Candida haemulonii complex (which includes C. haemulonii sensu stricto, C. duobushaemulonii and C. haemulonii var. vulnera), and phylogenetically related species, including C. pseudohaemulonii and C. vulturna. These emerging, widespread, and opportunistic pathogens have drawn significant attention due to their reduced susceptibility to commonly used antifungal agents, particularly azoles and polyenes, and, in some cases, therapy-induced resistance to echinocandins. Notably, C. auris is classified in the critical priority group on the World Health Organization's fungal priority pathogens list, which highlights fungal species capable of causing systemic infections with significant mortality and morbidity risks as well as the challenges posed by their MDR profiles, limited treatment and management options. The mechanisms underlying antifungal resistance within these emerging fungal species is still being explored, but some advances have been achieved in the past few years. In this review, we compile current literature on the distribution of susceptible and resistant clinical strains of C. auris, C. haemulonii complex, C. pseudohaemulonii and C. vulturna across various antifungal classes, including azoles (fluconazole, voriconazole, itraconazole), polyenes (amphotericin B), echinocandins (caspofungin, micafungin, anidulafungin), and pyrimidine analogues (flucytosine). We also outline the main antifungal resistance mechanisms identified in planktonic cells of these yeast species. Finally, we explore the impact of biofilm formation, a classical virulence attribute of fungi, on antifungal resistance, highlighting the resistance mechanisms associated with this complex microbial structure that have been uncovered to date.

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多重耐药耳念珠菌、haemulonii念珠菌复合体和系统发育相关物种:抗真菌耐药机制的见解
耐多药真菌病原体的兴起对人类健康构成了严重的全球性威胁。特别值得关注的是耳念珠菌、haemulonii念珠菌复合体(包括C. haemulonii狭义念珠菌、C. duobushaemulonii和C. haemulonii变种),以及系统发育相关的物种,包括C. pseudohaemulonii和C. vulturna。这些新出现的、广泛存在的机会致病菌引起了人们的极大关注,因为它们对常用的抗真菌药物,特别是唑类和多烯类药物的易感性降低,并且在某些情况下,对棘白菌素产生了治疗性耐药性。值得注意的是,在世界卫生组织的真菌优先病原体清单中,金黄色葡萄球菌被列为关键优先群体,该清单突出了能够引起系统性感染的真菌物种,具有显著的死亡率和发病率风险,以及它们的耐多药概况、有限的治疗和管理选择所带来的挑战。这些新出现的真菌物种的抗真菌抗性机制仍在探索中,但在过去几年中取得了一些进展。在这篇综述中,我们收集了目前关于耳念珠菌、haemulonii复合物、假haemulonii和秃鹫念珠菌的临床敏感和耐药菌株分布的文献,包括各种抗真菌类药物,包括唑类药物(氟康唑、伏立康唑、伊曲康唑)、多烯类药物(两性霉素B)、棘白菌素(caspofungin、micafungin、anidulafungin)和嘧啶类似物(氟胞嘧啶)。我们还概述了在这些酵母种类的浮游细胞中鉴定的主要抗真菌抗性机制。最后,我们探讨了生物膜形成(真菌的经典毒力属性)对抗真菌耐药性的影响,强调了迄今为止发现的与这种复杂微生物结构相关的耐药机制。
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来源期刊
Current Research in Microbial Sciences
Current Research in Microbial Sciences Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
7.90
自引率
0.00%
发文量
81
审稿时长
66 days
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