吉林大学学报(医学版) ›› 2023, Vol. 49 ›› Issue (1): 222-230.doi: 10.13481/j.1671-587X.20230130

• 方法学 • 上一篇    

呼吸道真菌感染核酸胶体金试纸条快速检测方法的建立和评价

姜菲菲1,宋伶俐2,潘蓓珍1,王岳峰1,李昊宇3,孙丽媛1()   

  1. 1.北华大学医学技术学院分子生物教研室,吉林 吉林 132013
    2.北华大学附属医院检验科,吉林 吉林 132011
    3.中国铁路沈阳局集团有限公司吉林疾病预防控制所,吉林 吉林 132001
  • 收稿日期:2022-03-09 出版日期:2023-01-28 发布日期:2023-02-03
  • 通讯作者: 孙丽媛 E-mail:jlsunliyuan@163.com
  • 作者简介:姜菲菲(1996-),女,山东省青岛市人,在读硕士研究生,主要从事临床微生物检测方面的研究。
  • 基金资助:
    吉林省科技厅科技发展计划项目(20190304115YY);吉林省教育厅“十三五”科学技术项目(JJKH20190657KJ);北华大学校级科研项目(BH001)

Establishment and evaluation of nucleic acid colloidal gold test strip for rapid detection of respiratory tract fungal infection

Feifei JIANG1,Lingli SONG2,Beizhen PAN1,Yuefeng WANG1,Haoyu LI3,Liyuan SUN1()   

  1. 1.Department of Molecular Biology,School of Medical Technology,Beihua University,Jilin 132013,China
    2.Department of Laboratory,Affiliated Hospital,Beihua University,Jilin 132011,China
    3.Jilin Institute for Disease Control and Prevention,China Railway Shenyang Bureau Group Co. ,Ltd. ,Jilin 132001,China
  • Received:2022-03-09 Online:2023-01-28 Published:2023-02-03
  • Contact: Liyuan SUN E-mail:jlsunliyuan@163.com

摘要:

目的 采用聚合酶链式反应(PCR)技术和胶体金技术建立一种呼吸道真菌感染核酸胶体金试纸条检测方法,并对其检测效果进行评价。 方法 根据GenBank数据库选择真菌内转录间隔区(ITS)基因片段作为靶基因,应用DNAMAN软件对真菌ITS基因片段进行分析,并分别在真菌通用引物5'端用生物素(Biotin)和异硫氰酸荧光素(FITC)进行修饰标记;建立PCR体系,进行体系的最佳条件优化;确定胶体金免疫层析试纸条标记链霉亲和素的最佳标记量和质控线及检测线最佳包被物浓度,组装核酸胶体金试纸条,对试纸条的特异度、灵敏度、重复性和稳定性进行验证。 结果 水煮法提取白假丝酵母菌、新生隐球菌和毛霉菌DNA,浓度为180 μg·L-1以上,纯度为1.60~2.10;在pH 7.0条件下,每100 μL胶体金溶液中制备胶体金标记链霉亲和素最佳标记量为 3.3 μg,质控线包被Biotin化牛血清白蛋白(BSA-Biotin)浓度为2.00 g·L-1,检测线包被抗FITC抗体浓度为1.00 g·L-1。核酸试纸条的特异度与电泳结果一致,仅白假丝酵母菌、新生隐球菌和毛霉菌出现阳性结果,与金黄色葡萄球菌、肺炎链球菌、乙型溶血性链球菌、铜绿假单胞菌、肺炎克雷伯菌、鲍曼不动杆菌和大肠埃希菌等常见呼吸道感染细菌无交叉反应。灵敏度检测,白假丝酵母菌、新生隐球菌和毛霉菌的DNA浓度分别为10-4、10-2和10-3 mg·L-1时核酸试纸条仍可准确检出,而普通PCR电泳结果显示白假丝酵母菌、新生隐球菌和毛霉菌最低检测浓度分别为0.01、1.00和0.10 mg·L-1;重复性检测,在不同实验室不同操作人员对核酸试纸条进行验证,结果一致,重复性良好;稳定性检测,核酸试纸条在第6、9和12个月进行检测,结果符合预期,稳定性良好。 结论 本研究建立的呼吸道真菌感染核酸胶体金试纸条可以检测白假丝酵母菌、新生隐球菌和毛霉菌等真菌,特异度和灵敏度均较高,操作简便且快速。

关键词: 呼吸道感染, 真菌, 胶体金, 核酸试纸条

Abstract:

Objective To establish a method of nucleic acid colloidal gold strip for rapid detection of respiratory tract fungal infection with polymerase chain reaction (PCR) technique and colloidal gold technique, and to evaluate the detection effect. Methods The fungal internal transcribed spacer(ITS) gene fragment was selected as the target gene according to GenBank database, and the fungal ITS gene fragment was analyzed by DNAMAN software, and labeled with Biotin and fluorescein isothiocyanate (FITC) at the 5' end of fungal universal primers, respectively; the PCR system was established and the optimal conditions of the systerm were optimized. The best labeling amount of colloidal gold test strips to label streptavidin and the best coating concentration of quality control line and detection line were comfirmed, the nucleic acid colloidal gold test strip was assembled, and the specificity, sensitivity, repeatability and stability of the colloidal gold test strip were verified. Results The DNA of Candida albicansCryptococcus neoformans and Mucor was extracted by boiling method, the concentrations were more than 180 μg·L-1,and the purities were 1.60-2.10. Under the condition of pH 7.0, the optimal labeling amount of colloidal gold- labeled streptavidin was 3.3 μg in 100 μL of colloidal gold-solution, the concentration of biotinylated bovine serum albumin (BSA-Biotin) coated by quality control line was 2.00 g·L-1, and the concentration of anti-FITC antibody coated by detection line was 1.00 g·L-1. The specificity of nucleic acid test strip was consistent with the results of electrophoresis, and only Candida albicansCryptococcus neoformans and Mucor showed positive results. There were no cross reactions with Staphylococcus aureusStreptococcus pneumoniaeType B Hemolytic streptococcusPseudomonas aeruginosaKlebsiella pneumoniaeAcinetobacter baumanniiEscherichia coli and other common respiratory tract infection bacteria. The sensitivity detection results showed that the nucleic acid test strips could still accurately detect the DNA of Candida albicansCryptococcus neoformans and Mucor when the DNA concentrations were of 10-4, 10-2 and 10-3 μg·L-1, respectively. The results of ordinary PCR electrophoresis showed that the lowest detection concentrations of Candida albicansCryptococcus neoformans and Mucor were 0.01, 1.00,and 0.10μg·L-1, respectively.In repeatability test, nucleic acid test strips were verified by different operators in different laboratories, the results were consistent, and the reproducibility was good; in stability test, nucleic acid test strips were tested in 6, 9 and 12 months and the results were as expected with good stability. Conclusion The established method of nucleic acid colloidal gold test strip for respiratory tract fungal infection in this study can be used to detect Candida albicansCryptococcus neoformansMucor and other fungi with high specificity, sensitivity, simple and rapid operation.

Key words: Respiratory tract infection, Fungi, Colloidal gold, Nucleic acid test strip

中图分类号: 

  • R446