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MDR1 过度表达与 ERG11 突变联合导致热带假丝酵母临床分离株产生高水平氟康唑耐药性。

MDR1 overexpression combined with ERG11 mutations induce high-level fluconazole resistance in Candida tropicalis clinical isolates.

机构信息

Department of Clinical Laboratory, Peking University People's Hospital, No. 11 Xizhimen South Street, Xicheng District, Beijing, 100044, People's Republic of China.

International Curriculum Center, The High School Affiliated to the Renmin University of China, Beijing, 100080, China.

出版信息

BMC Infect Dis. 2018 Apr 10;18(1):162. doi: 10.1186/s12879-018-3082-0.

Abstract

BACKGROUND

Marked increases in fluconazole resistance in Candida tropicalis have been recently reported. In this study, the molecular mechanisms behind fluconazole resistance were investigated.

METHODS

Twenty-two C. tropicalis clinical isolates, including 12 fluconazole-resistant isolates and 10 fluconazole-susceptible isolates, were collected from a tertiary care teaching hospital in Beijing between 2013 and 2017. Antifungal susceptibility testing, multilocus sequence typing, ERG11 amplification and sequencing, quantitative real-time reverse transcription-polymerase chain reaction (ERG11, UPC2, MDR1, and CDR1), and clinical data collection were performed for all C. tropicalis isolates.

RESULTS

Multilocus sequence typing revealed that the 10 fluconazole-susceptible isolates and 12 fluconazole-resistant isolates were divided into nine and seven diploid sequence types, respectively. Of the 12 patients with fluconazole-resistant isolates, six had been previously exposed to azole and four had a fatal outcome. Y132F and S154F amino acid substitutions in Erg11p were found in all fluconazole-resistant isolates except one. MDR1 gene overexpression was identified in fluconazole-resistant isolates. In particular, seven high-level fluconazole resistant isolates (minimum inhibitory concentration ≥ 128 mg/L) and three pan-azole resistant isolates were identified. CDR1, ERG11, and UPC2 gene expression levels in fluconazole-resistant isolates were not significantly different from the control isolates (P = 0.262, P = 0.598, P = 0.114, respectively).

CONCLUSIONS

This study provides evidence that the combination of MDR1 gene overexpression and ERG11 missense mutations is responsible for high-level fluconazole resistance and pan-azole resistance in C. tropicalis clinical isolates. To the best of our knowledge, this is the first study investigating the relationship between MDR1 gene overexpression and increased fluconazole resistance.

摘要

背景

最近有报道称,热带念珠菌对氟康唑的耐药性显著增加。在这项研究中,我们研究了氟康唑耐药性的分子机制。

方法

2013 年至 2017 年,我们从北京一家三级教学医院收集了 22 株热带念珠菌临床分离株,包括 12 株氟康唑耐药株和 10 株氟康唑敏感株。对所有热带念珠菌分离株进行抗真菌药敏试验、多位点序列分型、ERG11 扩增和测序、实时定量逆转录聚合酶链反应(ERG11、UPC2、MDR1 和 CDR1)和临床数据收集。

结果

多位点序列分型显示,10 株氟康唑敏感株和 12 株氟康唑耐药株分别分为 9 种和 7 种二倍体序列类型。在 12 例氟康唑耐药株患者中,6 例曾接触过唑类药物,4 例死亡。除 1 株外,所有氟康唑耐药株均发现 erg11p 中的 Y132F 和 S154F 氨基酸取代。鉴定出氟康唑耐药株中 MDR1 基因过表达。特别是,鉴定出 7 株高水平氟康唑耐药株(最低抑菌浓度≥128mg/L)和 3 株泛唑耐药株。氟康唑耐药株与对照株相比,CDR1、ERG11 和 UPC2 基因表达水平无显著差异(P=0.262,P=0.598,P=0.114)。

结论

本研究提供了证据表明,MDR1 基因过表达和 ERG11 错义突变的组合导致了热带念珠菌临床分离株的高水平氟康唑耐药和泛唑耐药。据我们所知,这是第一项研究 MDR1 基因过表达与氟康唑耐药性增加之间关系的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/685c/5891969/e7eab5a1a9f4/12879_2018_3082_Fig1_HTML.jpg

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