Department of Microbiology, Faculty of Medicine, Kuwait University, Safat, Kuwait.
Microbiology Department, Ibn Sina Hospital, Shuwaikh, Kuwait.
Mycoses. 2022 Mar;65(3):331-343. doi: 10.1111/myc.13419. Epub 2022 Jan 3.
Candida auris is an emerging, potentially multidrug-resistant pathogen that exhibits clade-specific resistance to fluconazole and also develops resistance to echinocandins and amphotericin B easily. This study analysed 49 C auris isolates for alterations in hotspot-1 and hotspot-2 of FKS1 for the detection of mutations conferring reduced susceptibility to echinocandins.
C auris isolates (n = 49) obtained from 18 immunocompromised patients during June 2016-December 2018 were analysed. Antifungal susceptibility testing was performed by Etest and broth microdilution-based MICRONAUT-AM assay. Mutations in hotspot-1 and hotspot-2 regions of FKS1 were detected by PCR sequencing and fingerprinting of the isolates was done by short tandem repeat typing.
The patients had multiple comorbidities/risk factors for Candida spp. infection including cancer/leukaemia/lymphoma/myeloma (n = 16), arterial/central line (n = 17), urinary catheter (n = 17), mechanical ventilation (n = 14) and major surgery (n = 9) and received antifungal drugs as prophylaxis and/or empiric treatment. Seven patients developed C auris candidemia/breakthrough candidemia, nine patients had candiduria with/without candidemia and four patients developed surgical site/respiratory infection. Resistance to fluconazole and amphotericin B was detected in 44 and four isolates, respectively. Twelve C auris isolates from eight patients showed reduced susceptibility to echinocandins. Seven isolates contained hostspot-1 mutations and three isolates from a candidemia patient contained R1354H mutation in hotspot-2 of FKS1. Ten patients died, five were cured, two were lost to follow-up and treatment details for one patient were not available.
Our findings describe development of a novel mutation in FKS1 conferring reduced susceptibility to echinocandins in one patient during treatment and unfavourable clinical outcome for many C auris-infected patients.
耳念珠菌是一种新兴的、潜在的多药耐药病原体,对氟康唑具有特定的谱系耐药性,而且很容易对棘白菌素类药物和两性霉素 B 产生耐药性。本研究分析了 49 株耳念珠菌分离株中 FKS1 的热点 1 和热点 2 区域的改变,以检测对棘白菌素类药物敏感性降低的突变。
分析了 2016 年 6 月至 2018 年 12 月期间 18 名免疫功能低下患者的 49 株耳念珠菌分离株。采用 Etest 和微量肉汤稀释法 MICRONAUT-AM 测定法进行抗真菌药敏试验。通过 PCR 测序检测 FKS1 热点 1 和热点 2 区的突变,并通过短串联重复分型对分离株进行指纹图谱分析。
这些患者患有多种念珠菌感染的合并症/危险因素,包括癌症/白血病/淋巴瘤/骨髓瘤(n=16)、动静脉/中央静脉导管(n=17)、导尿管(n=17)、机械通气(n=14)和大手术(n=9),并接受了抗真菌药物的预防和/或经验性治疗。7 名患者发生耳念珠菌血症/突破性念珠菌血症,9 名患者发生念珠菌尿伴/不伴念珠菌血症,4 名患者发生手术部位/呼吸道感染。44 株和 4 株分离株分别对氟康唑和两性霉素 B 耐药。12 株耳念珠菌分离株来自 8 名患者,对棘白菌素类药物的敏感性降低。7 株分离株含有热点 1 突变,1 株来自念珠菌血症患者的分离株含有 FKS1 热点 2 中的 R1354H 突变。10 名患者死亡,5 名患者治愈,2 名患者失访,1 名患者的治疗细节不详。
我们的研究结果描述了在 1 名患者治疗过程中 FKS1 中出现新的突变,导致对棘白菌素类药物敏感性降低,以及许多感染耳念珠菌的患者临床预后不良。