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多重连接探针扩增技术在临床病原体检测中的应用 被引量:1

MLPA application in clinical diagnosis of pathogen
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摘要 真菌等临床病原体的诊断、基因分型和耐药性检测对于临床诊治十分重要。多重连接探针扩增是一个可以同时定量检测多个基因序列的,简单、有效、快速的方法。其步骤包括待测DNA变性、半探针与待测DNA杂交,半探针的连接、PCR法扩增、凝胶电泳或者毛细管电泳鉴定扩增产物。MLPA已经在临床微生物诊断和研究中有了一定的应用,虽然尚处于起步阶段,但因其操作简便,反应快速,高通量,高敏感性和特异性的特点,拥有良好的应用前景。 As for patients diagnosed with Infectious diseases,favorable prognosis is determined by correct diagnosis and proper treatment.So it is important to diagnose clinical pathogens rapidly.Compared with other clinical test methods,MLPA is a simple,valid,and fast one which can detect several gene sequences in quantity at the same time. The steps include: the degeneration of DNA sample,hybridization,ligation,and PCR amplification.Although being at its first stage,there are already certain applications of MLPA in diagnosing and researching of clinic microorganism,and the peculiarity of easy operation,fast reaction,high pass rate and high sensitivity have reveal bright prospect of MLPA.
出处 《中国真菌学杂志》 CSCD 2015年第5期307-311,共5页 Chinese Journal of Mycology
基金 国家973项目(2013CB531601) 重大传染病防治科技重大专项(2013ZX10004612) 上海市科委专项(14DZ2272900)
关键词 多重连接探针扩增 病原体 诊断 multiplex ligation-dependent probe amplification pathogen diagnosis
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  • 1Armour, J.A., Sismani, C., Patsalis, P,C., and Cross, G. (2000). Measurement of locus copy number by hybridisation with amplifiable probes. Nucleic Acids Res. 28: 605-609.
  • 2Armour, J.A., Barton, D.E., Cockburn, D.J., and Taylor, G.R. (2002). The detection of large deletions or duplications in genomic DNA. Hum. Mutat. 20: 325-337.
  • 3Bunyan, D.J., Skinner, A.C., Ashton, E.J, Sillibourne, J., Brown, T., Collins, A.L., Cross, N.C., Harvey, J.F., and Robinson, D.O. (2007). Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene. Mol. Biotechnol. 35: 135-140.
  • 4Casilli, F., Di Rocco, Z.C., Gad, S., Tournier, 1., Stoppa-Lyonnet, D., Frebourg, T., and Tosi, M. (2002). Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments. Hum. Mutat. 20: 218-226.
  • 5Chudoba, I, Plesch, A., Lorch, T., Lemke, J., Claussen, U., and Senger, G. (1999). High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes. Cytogenet. Cell Genet. 84: 156-160.
  • 6Eldering, E., Spek, C.A., Aberson, H.L., Grummeis, A., Derks, I.A., de Vos, A.F., McElgunn, CJ., and Schouten, J.P. (2003). Expression profiling via novel multiplex assay allows rapid assessment of gene regulation in defined signalling pathways. Nucleic Acids Res. 31: e153.
  • 7Gibbons, B., Datta, P., Wu, Y., Chan, A., and AI Armour, J. (2006). Microarray MAPH: Accurate array-based detection of relative copy number in genomic DNA. BMC Genomics 7: 163.
  • 8Ginzinger, D.G. (2002). Gene quantification using real-time quantitative PCR: An emerging technology hits the mainstream. Exp. Hematol. 30: 503-512.
  • 9Gouas, L., Goumy, C., Veronese, L., Tchirkov, A., and Vago, P. (2008). Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities. Pathol. Biol. (Paris) 56: 345-353.
  • 10Heath, K.E., Day, I.N., and Humphries, S.E. (2000). Universal primer quantitative fluorescent multiplex (UPQFM) PCR: A method to detect major and minor rearrangements of the low density lipoprotein recep- tor gene. J. Med. Genet. 37: 272-280.

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