Association of multilocus sequence typing, MSH2 gene mutations, and antifungal resistance in Candida glabrata: implications for clinical outcomes in Chinese hospitals.

IF 4.6 2区 医学 Q1 MICROBIOLOGY
Guanyi Zhang, Yisheng Chen, Jia Chen, Dongting Yao
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引用次数: 0

Abstract

Background: Candida glabrata is the second most common cause of invasive candidiasis worldwide. In this study, we determined the clinical characteristics and drug sensitivity of C. glabrata isolates and investigated the associations between MSH2 gene mutations, sequence types (ST), and drug resistance.

Methods: A total of 154 C. glabrata isolates were collected from patients being treated in three hospitals in China. The antifungal sensitivity of the strains was assessed using the broth microdilution method. Multilocus sequence typing (MLST) was also performed, followed by MSH2 sequencing. The clinical features and outcomes of C. glabrata infection were analysed for a total of 49 strains, which were collected from patients with invasive Candida infection at Longhua Hospital.

Results: All 154 isolates were found to be susceptible to amphotericin, 5-fluorocytosine, anidulafungin, caspofungin, and micafungin, whereas 11.7% were fluconazole-resistant, 18.8% were itraconazole non-wild type, and 35.7% were voriconazole non-wild type. ST7 (62.34%) was the most common ST genotype, followed by ST10 (16.88%) and ST15 (7.79%). The total azole resistance rates for all isolates, ST7, ST10, and other STs were 36.4, 42.7, 34.6, and 18.8%, respectively. The ST7 and ST10 isolates were characterised by a higher drug resistance rate than the other minor ST isolates. Moreover, 59.09% of isolates had one or more MSH2 non-synonymous mutations, with V239L being the most commonly detected mutation. The frequency of MSH2 mutations was significantly higher in azole-resistant isolates than in other isolates, whereas P6L or L87P mutations were associated with the highest azole resistance rates of up to 87.5% and 80%, respectively. Our results indicated that ST7 and ST15 are independent predictors of mortality caused by C. glabrata infection and revealed a higher 30-day mortality in patients infected with these strains than in those infected with other ST isolates.

Conclusions: Our findings revealed the relationships between MLST, MSH2 gene mutations, and drug resistance in the common pathogenic fungus C. glabrata, and thereby enabled us to identify strains that are associated with higher rates of mortality. These findings will contribute to enhancing our understanding of the pathogenesis of C. glabrata infection.

多焦点序列分型、MSH2 基因突变与白色念珠菌抗真菌耐药性的关联:对中国医院临床结果的影响。
背景:全球侵袭性念珠菌病的第二大常见病因是白色念珠菌。在这项研究中,我们测定了分离出的白色念珠菌的临床特征和药物敏感性,并研究了 MSH2 基因突变、序列类型(ST)和耐药性之间的关联:方法:研究人员从中国三家医院接受治疗的患者中采集了 154 株玻璃疽杆菌。采用肉汤微稀释法评估菌株的抗真菌敏感性。此外,还进行了多焦点序列分型(MLST)和 MSH2 测序。对从龙华医院侵袭性念珠菌感染患者中采集的共 49 株菌株的临床特征和感染结果进行了分析:结果:154株分离菌株均对两性霉素、5-氟胞嘧啶、阿尼芬净、卡泊芬净和米卡芬净敏感,11.7%对氟康唑耐药,18.8%为非野生型伊曲康唑,35.7%为非野生型伏立康唑。ST7(62.34%)是最常见的ST基因型,其次是ST10(16.88%)和ST15(7.79%)。所有分离物、ST7、ST10 和其他 ST 的总唑抗性率分别为 36.4%、42.7%、34.6% 和 18.8%。ST7 和 ST10 分离物的耐药率高于其他小 ST 分离物。此外,59.09%的分离株有一个或多个MSH2非同义突变,其中V239L是最常检测到的突变。MSH2突变在耐唑分离物中的频率明显高于其他分离物,而P6L或L87P突变与最高的耐唑率有关,分别高达87.5%和80%。我们的研究结果表明,ST7 和 ST15 可独立预测玻璃疽杆菌感染导致的死亡率,并显示感染这些菌株的患者的 30 天死亡率高于感染其他 ST 分离物的患者:我们的研究结果揭示了常见致病真菌草履蛆中多态性差异、MSH2 基因突变和耐药性之间的关系,从而使我们能够确定与较高死亡率相关的菌株。这些发现将有助于加深我们对克林霉素感染发病机理的了解。
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来源期刊
CiteScore
8.60
自引率
0.00%
发文量
49
审稿时长
>12 weeks
期刊介绍: Annals of Clinical Microbiology and Antimicrobials considers good quality, novel and international research of more than regional relevance. Research must include epidemiological and/or clinical information about isolates, and the journal covers the clinical microbiology of bacteria, viruses and fungi, as well as antimicrobial treatment of infectious diseases. Annals of Clinical Microbiology and Antimicrobials is an open access, peer-reviewed journal focusing on information concerning clinical microbiology, infectious diseases and antimicrobials. The management of infectious disease is dependent on correct diagnosis and appropriate antimicrobial treatment, and with this in mind, the journal aims to improve the communication between laboratory and clinical science in the field of clinical microbiology and antimicrobial treatment. Furthermore, the journal has no restrictions on space or access; this ensures that the journal can reach the widest possible audience.
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