26例热带念珠菌血流感染的临床及分子流行病学特征。

IF 2.9 3区 生物学 Q2 MYCOLOGY
Weihong Lin, Qianyue Yang, Zhiwei Lin, Shuang Liu, Liangyan Zhang, Yueting Jiang, Jingchun Fang, Yaqin Peng, Penghao Guo
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引用次数: 0

摘要

目的:探讨热带念珠菌血流感染的临床和分子流行病学特征。方法:回顾性分析2020年1月至2022年12月诊断为热带衣原体血流感染患者的临床资料。进行抗真菌药敏试验。采用多位点序列分型(Multilocus sequence typing, MLST)分析菌株同源性,并进行ERG11 (azole resistance-associated)和FKS1 (echinocandin resistance-associated)基因突变分析。结果:26例热带弓形虫血流感染中,血液系统恶性肿瘤是最常见的基础疾病,总死亡率为38.5%。对伏立康唑和氟康唑的耐药率为30.8%,对刺白菌素类药物和两性霉素b的敏感性较高。所有氟康唑耐药菌株均含有ERG11基因突变,其中Y132F和S154F是最常见的突变位点。氟康唑耐药患者的死亡率(37.5%)与敏感或剂量依赖性敏感患者的死亡率(38.8%)相似。在26株菌株中共鉴定出20种不同的序列类型(DSTs),这些序列类型均为已知,表明具有显著的遗传多样性。最多的是DST376型。结论:血液恶性肿瘤是热带弓形虫血流感染最常见的基础疾病。分离菌株表现出显著的遗传多样性和对氟康唑的高水平抗性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical and Molecular Epidemiological Characteristics of 26 Bloodstream Infection Cases Caused by Candida tropicalis.

Clinical and Molecular Epidemiological Characteristics of 26 Bloodstream Infection Cases Caused by Candida tropicalis.

Clinical and Molecular Epidemiological Characteristics of 26 Bloodstream Infection Cases Caused by Candida tropicalis.

Purpose: This study aims to investigate the clinical and molecular epidemiological characteristics of bloodstream infections caused by Candida tropicalis.

Methods: This retrospective study analyzed the clinical data of patients diagnosed with C. tropicalis bloodstream infections from January 2020 to December 2022. Antifungal susceptibility testing was performed. Multilocus sequence typing (MLST) was used to analyze strain homology, and mutation analysis of the ERG11 (azole resistance-associated) and FKS1 (echinocandin resistance-associated) genes was conducted.

Results: Among the 26 cases of C. tropicalis bloodstream infections, hematologic malignancies were the most common underlying condition, with an overall mortality rate of 38.5%. Resistance rates to voriconazole and fluconazole were 30.8%, while the isolates exhibited high susceptibility to echinocandin drugs and amphotericin B. All fluconazole-resistant strains contained mutations in the ERG11 gene, with Y132F and S154F being the most frequent mutation sites. The mortality rate in fluconazole-resistant patients (37.5%) was similar to that of susceptible or dose-dependently susceptible patients (38.8%). A total of 20 distinct sequence types (DSTs) were identified among the 26 strains, all of which were previously known, indicating significant genetic diversity. The most abundant type was DST376.

Conclusion: Hematologic malignancies are the most common underlying disease of C. tropicalis bloodstream infections. The isolated strains demonstrate significant genetic diversity and a high level resistance to fluconazole.

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来源期刊
Mycopathologia
Mycopathologia 生物-真菌学
CiteScore
6.80
自引率
3.60%
发文量
76
审稿时长
3 months
期刊介绍: Mycopathologia is an official journal of the International Union of Microbiological Societies (IUMS). Mycopathologia was founded in 1938 with the mission to ‘diffuse the understanding of fungal diseases in man and animals among mycologists’. Many of the milestones discoveries in the field of medical mycology have been communicated through the pages of this journal. Mycopathologia covers a diverse, interdisciplinary range of topics that is unique in breadth and depth. The journal publishes peer-reviewed, original articles highlighting important developments concerning medically important fungi and fungal diseases. The journal highlights important developments in fungal systematics and taxonomy, laboratory diagnosis of fungal infections, antifungal drugs, clinical presentation and treatment, and epidemiology of fungal diseases globally. Timely opinion articles, mini-reviews, and other communications are usually invited at the discretion of the editorial board. Unique case reports highlighting unprecedented progress in the diagnosis and treatment of fungal infections, are published in every issue of the journal. MycopathologiaIMAGE is another regular feature for a brief clinical report of potential interest to a mixed audience of physicians and laboratory scientists. MycopathologiaGENOME is designed for the rapid publication of new genomes of human and animal pathogenic fungi using a checklist-based, standardized format.
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