基础医学与临床 ›› 2022, Vol. 42 ›› Issue (6): 883-889.doi: 10.16352/j.issn.1001-6325.2022.06.007

• 研究论文 • 上一篇    下一篇

葡聚糖结合蛋白的原核表达及检测深部真菌感染的应用

朱李茹1, 黄友明2, 章宏祥2, 周发友2, 唐晓磊2*   

  1. 1.湖北文理学院附属医院 襄阳市中心医院 医学检验部, 湖北 襄阳 441021;
    2.皖南医学院第二附属医院 转化医学中心, 安徽 芜湖 241000
  • 收稿日期:2020-07-27 修回日期:2022-04-11 出版日期:2022-06-05 发布日期:2022-06-02
  • 通讯作者: * 278471655@qq.com
  • 基金资助:
    国家自然科学基金(81601806)

Prokaryotic expression of glucans binding protein and application for detecting invasive fungal infection

ZHU Li-ru1, HUANG You-ming2, ZHANG Hong-xiang2, ZHOU Fa-you2, TANG Xiao-lei2*   

  1. 1. Department of Clinical Laboratory, Xiangyang Central Hospital, the Affiliated Hospital of Hubei College of Arts and Sciences, Xiangyang 441021;
    2. Centre for Translational Medicine, the Second Affiliated Hospital of Wannan Medical College, Wuhu 241000, China
  • Received:2020-07-27 Revised:2022-04-11 Online:2022-06-05 Published:2022-06-02
  • Contact: * 278471655@qq.com

摘要: 目的 验证葡聚糖特异性的结合蛋白用于检测深部真菌感染(IFI)患者血清中(1,3)-β-D-葡聚糖的应用价值。方法 通过构建美洲鲎葡聚糖结合蛋白(GBP)252位氨基酸至668位氨基酸活性区域表达质粒——pET30a-GBP252-668,表达并纯化获得GBP252-668重组蛋白。随后通过棋盘法构建双GBP252-668夹心法,并以此检测IFI患者血清中(1,3)-β- D-葡聚糖。同时与G试验(G-Test)进行检测性能的比对。 结果 成功纯化获得分子质量约为46 ku的GBP252-668重组蛋白,并确定最佳包被浓度和检测浓度分别为8和16 g/L,以此构建了GBP252-668夹心法。对48名深部真菌感染患者和48名健康人血清进行检测,根据受试者工作特征曲线(ROC)可得其灵敏度为 91.67%,特异度为89.58%。其灵敏度与G-Test相当,特异性高于同批次G-Test(79.17%)。结论 本研究构建的双GBP夹心法是一种极具潜力检测侵袭性真菌的方法,其灵敏度与G-Test相当,特异性高于同批次G-Test。

关键词: 深部真菌感染, 葡聚糖结合蛋白, 夹心法, 临床应用

Abstract: Objective To explore the potential application of glucans binding protein (GBP) in the detection of soluble glucans from serum sampled from patients with invasive fungal infection (IFI). Methods The prokaryotic plasmid pET30a-GBP252-668 coding for 252 to 668 amino acid in GBP as an active domain of GBP of Limulus polyphemus was constructed. The recombinant GBP252-668 was expressed and purified.Then a double GBP252-668 sandwich method was developed to detect (1,3)-β-D-glucans in the serum of patients with IFI. Meanwhile, the results were compared with G-test. Results Recombinant GBP252-668 (molecular weight is about 46 ku) was obtained and the double GBP252-668 sandwich method was established and optimized via chessboard method, the concentrations of GBP252-668 were 8 and 16 g/L for coating and detection respectively. The serum sampled from 48 patients with IFI and from 48 healthy donors were examined.and results were analysed. The sensitivity and specificity of double GBP252-668 sandwich method were 91.67% and 89.58% respectively and the sensitivity was non-inferior to G-test, and specificity of double GBP252-668 sandwich method was even higher than that of G-test (79.17%). Conclusions The GBP252-668 sandwich method is a potential detection method for IFI diagnosis. The method is non-inferior to G-test and its specificity is even higher than G-test. It is expected to be a new commercially available kit for IFI detection.

Key words: invasive fungal infection(IFI), glucans binding protein, sandwich method, clinical application

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