期刊文献+

微卫星多态性和多位点序列分析技术在光滑念珠菌基因分型中的应用评估 被引量:3

Application evaluation of microsatellite polymorphism and multilocus sequence typing in genotyping of Candida glabrata
下载PDF
导出
摘要 目的评估微卫星多态性分析技术在临床光滑念珠菌基因分型中的作用。方法收集2011年1月至2012年12月仁济医院和东方医院临床分离的光滑念珠菌59株,采用多位点序列分析(MLST)和微卫星多态性分析技术进行基因分型,比较2种基因分型方法的结果和分辨力。结果 59株光滑念珠菌经MLST分型得到6个序列型,其中ST-7型43株、ST-10型7株、ST-15型和ST-55型各3株、ST-3型2株、ST-43型1株,鉴别力指数(DP)为0.456;经微卫星多态性分析方法分为10型,其中A型25株、B型10株、C型8株、D型6株、E型3株、F型和G型各2株、H^J型各1株,DP为0.770。结论微卫星多态性分析方法简便、快速,分辨力高于MLST技术,可作为实验室基因分型的首选方法。 Objective To evaluate the application significance of microsatellite polymorphism in genotyping of Candida glabrata.Methods From January 201 1 to December 201 2,59 isolates of Candida glabrata were collected from Renji Hospital and East Hospital.All the 59 isolates were typed by microsatellite polymorphism and multilocus sequence typing (MLST).The results and discrimination of the 2 genotyping methods were compared.Results By MLST,the 59 isolates belonged to 6 clone sequences,including 43 isolates with ST-7,7 isolates with ST-1 0,3 isolates with ST-1 5,3 isolates with ST-55,2 isolates with ST-3 and 1 isolate with ST-43,and the index of discriminatory power (DP)was 0.456.By microsatellite polymorphism,the 59 isolates were classified into 1 0 genotypes.There were 25 isolates with type A,1 0 isolates with type B,8 isolates with type C,6 isolates with type D,3 isolates with type E,2 isolates with type F,2 isolates with type G,1 isolate with type H,1 isolate with type I and 1 isolate with type J,and the DP was 0.770.Conclusions Microsatellite polymorphism is a simple and rapid method for molecular typing with higher discrimination than MLST.Therefore,microsatellite polymorphism can be the preferred choice in clinical laboratories.
出处 《检验医学》 CAS 2014年第6期593-596,共4页 Laboratory Medicine
关键词 光滑念珠菌 基因分型 多位点序列分析 微卫星多态性分析 Candida glabrata Genotype Multilocus sequence typing Microsatellite polymorphism
  • 相关文献

同被引文献49

  • 1Pfaller MA,Diekema DJ,Gibbs DL, et al. Geographic varia- tion in the frequency of isolation and fluconazole and voricon azole susceptibilities of Candida glabrata : an assessment from the ARTEMIS DISK Global Antifungal Surveillance Program[J]. Diagnostic Microbiology & Infectious Disease, 2010,67 (2) : 162-171.
  • 2Pfaller MA, Diekema DJ, Gibbs DL, et al. Results from the ARTEMIS DISK Global Antifungal Surveillance Study, 1997 to 2007: a 10. 5-year analysis of susceptibilities of Candida Species to flueonazole and voriconazole as determined by CLSI standardized disk diffusion[J]. J Clin Microbial, 2010, 48(4): 1366-1377.
  • 3Khot PD,Ko DL, Fredricks DN. Sequencing and Analysis of Fungal rRNA Operons for Development of Broad-Range Fungal PCR Assays[J]. APPLIED AND ENVIRONMEN- TAL MICROBIOLOGY, 2009,75 (6) : 1559-1565.
  • 4Babiker WM, Merz WG, Merz WG, et al. Evaluation of nucle- ic acid sequencing of the D1/D2 region of the large subunit of the 28S rDNA and the internal transcribed spacer region u sing SmartGene IDNSlcorrected: software for identification of filamentous fungi in a clinical laboratory[J]. J Mol Diagn, 2012,14(6) :634.
  • 5Jang JH, Lee JH, Ki CS, et al. Identification of clinical mold i- solates by sequence analysis of the internal transcribed spacer region, ribosomal large-subunit D1/D2, and β-tubulin[J]. Ann Lab Med,2012,32(2) :126-132.
  • 6Blaalid R, Kumar S, Nilsson RH, et al. ITS1 versus ITS2 as DNA metabarcodes for fungi[J]. Mol Ecol Resour, 2013,13 (2) :218-224.
  • 7Van Burik J A, Myerson D, Schreckhise RW, et al. Panfungal PCR Assay for Detection of Fungal Infection in Human Blood Specimens [J]. J Clin Microbiol, 1998, 36 ( 5), 1169- 1175.
  • 8Sugawara Y, Nakase K, Nakamura A, et al. Clinical Utility of a Panfungal Polymerase Chain Reaction Assay for Invasive Fungal diseases in Patients with Haematologic Disorders[,J]. Eur J Haematol,2013,90(4) ,331-339.
  • 9Mufioz-Cadavid C,Rudd S,Zaki SR,et al. Improving Molecu- lar Detection of Fungal DNA in Formalin-Fixed Paraffin-Em- bedded Tissues:Comparison of Five Tissue DNA Extraction Methods Using Panfungal PCR[J]. J Clin Microbiol, 2010,48 (6) : 2147-2153.
  • 10Heo SM, Sung RS, Scannapieco FA, et al. Genetic relation- ships between Candida albicans strains isolated from dental plaque,trachea, and bronchoalveolar lavage fluid from me- chanically ventilated intensive care unit patients[J]. J Oral Microbiol, 2011,3 : 6362.

引证文献3

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部