Department of Microbiology, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.
Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Mycoses. 2022 Dec;65(12):1137-1145. doi: 10.1111/myc.13504. Epub 2022 Aug 10.
The accurate occurrence rate of C. auris infections is still not clear, mainly due to the defects in detection and identification tools routinely used. In this study, we used conventional PCR and real-time PCR assays for sensitive and specific detection/identification of C. auris from either yeast isolates or clinical specimens collected from various patients in different parts of Iran. Our survey is the first large-scale study rating the incidence of C. auris infections in Iran.
A total of 439 yeast isolates and 590 clinical specimens were screened by specific C. auris-PCR, targeting the ITS region. The validity of positive samples was assessed by sequencing.
Four out of 590 clinical specimens (0.68%) were positive by conventional PCR, while in real-time PCR performed on 100 clinical samples, including those four samples positive in conventional samples, 6 samples were positive. A complete agreement of the identification of positive cases with sequencing results was documented. Among 439 culture isolates, none was positive for C. auris. After following up and resampling of the patients with positive PCR, only one specimen showed positive culture for C. auris, which was confirmed by sequencing.
C. auris is not a common cause of systemic or superficial fungal infections in Iran, and a few detected positive cases can be considered as a commensal, coloniser or infecting yeast which may potentially emerge in some clinical and therapeutical conditions. Mycological and phenotypical assays are not sensitive approaches for isolation/identification of C. auris, unless a specific and sensitive molecular-based method is applied.
由于常规检测和鉴定工具的缺陷,C. 耳念珠菌感染的准确发生率尚不清楚。在这项研究中,我们使用常规 PCR 和实时 PCR 检测/鉴定方法,从伊朗不同地区的各种患者采集的酵母分离株或临床标本中,对 C. 耳念珠菌进行敏感和特异性检测/鉴定。我们的调查是首次对伊朗 C. 耳念珠菌感染发生率进行的大规模研究。
我们用特异性 C. 耳念珠菌 PCR 检测 ITS 区,对 439 株酵母分离株和 590 份临床标本进行筛查。通过测序评估阳性样本的有效性。
4 份临床标本(0.68%)经常规 PCR 阳性,100 份临床样本进行实时 PCR 时,包括在常规样本中检测到的 4 份阳性样本,有 6 份阳性。测序结果与阳性病例的鉴定完全一致。在 439 株培养分离株中,均未检测到 C. 耳念珠菌。对 PCR 阳性患者进行随访和再次采样后,只有 1 份标本的 C. 耳念珠菌培养阳性,测序结果证实了这一点。
C. 耳念珠菌不是伊朗系统性或浅部真菌感染的常见原因,少数检测到的阳性病例可能被视为共生菌、定殖菌或潜在感染的酵母,在某些临床和治疗条件下可能会出现。除非应用特异性和敏感的分子基础方法,否则微生物学和表型鉴定方法对 C. 耳念珠菌的分离/鉴定并不敏感。