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39例足癣复发后病原菌核糖体基因序列变化

The changes of DNA sequence of pathogen after relapse in athlete's foot
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摘要 目的:检测红色毛癣菌足癣复发后致病菌株基因型的变化。方法:对39例红色毛癣菌足癣复发后进行红色毛癣菌核糖体保守区(部分5.8s和ITS-2)和非转录间隔区(NTS)内的两个重复亚单位(TRS-1,TRS-2)进行PCR扩增,基因序列测定。结果:39株红色毛癣菌复发前后和标准株保守区基因序列测定比较,同源性均达99%,均为红色毛癣菌;(NTS)内的两个重复亚单位(TRS-1,TRS-2)基因序列测定比较,其中3株菌TRS-1区存在个别碱基突变,3株TRS-1区存在重复序列拷贝数变异,1株菌TRS-2区存在个别碱基突变。结论:复发后的红色毛癣菌基因型基本稳定,说明足癣复发大部分与原浅表真菌复燃有关。 Objective:To determine the changes of DNA sequence of Trichophytin rubrum after relapse in athlete's foot. Methods:Two epetition subunits( TRS-1,TRS-2) of Trichophyton rubrum ribosomal non-conservertive region NTS were amplified by PCR and followed by gene sequencing in 39 patients with relapsed athlete's foot. Results:The Trichophyton rubrum ribosomal non-conservative region NTS in the first and the second isolates of tinea pedis was very close ( the isogeny was 99%) . Individual base mutation happened in TRS-1 region of 3 cases or TRS-2 region of 1 case. Copy number of gene duplication sequence in TRS-1 region of ribosomal non-conservative region was seen in 3 cases. Conclusion: The genotype of Trichophyton rubrum is stable in the isolates of the patients with relapsed tinea pedis. Recurrence of tinea pedis was most likely caused by the existing fungi rather than new infections with other stains of fungi.
出处 《中国麻风皮肤病杂志》 2014年第4期208-210,共3页 China Journal of Leprosy and Skin Diseases
基金 福建中医药大学校管科研课题(编号:XB2012039)
关键词 足癣 红色毛癣菌 核糖体非保守区 基因序列测序 tinea pedis Trichophyton rubrum ribosomal non-conservative region gene sequencing
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参考文献6

  • 1CURTIS JW. The two foot-one hand disease. Bull Assoc milit Dermatol, 1964,13 : 1.
  • 2李筱芳,陈辉,崔凡,吕桂霞,沈永年,刘维达.浅部真菌病临床标本致病菌DNA提取方法的初步研究[J].医学研究杂志,2006,35(3):18-20. 被引量:4
  • 3Jackson C J, Barton RC, Evans EG. Species identification and strain differentiation of dematophyte fungi by analysis of riboso- mal DNA intergenic spacer regions. J Clin Microbiol, 1999,37 (4) :931-936.
  • 4Jackson C J, Barton RC, Kelly SL, et al. Strain identification of Trichophyton rubum by specific amplification of subrepeat ele- ments in the ribosomal DNA nontranscribed spacer. J Clin Mi- crobio1,2000,38(12) :4527-4534.
  • 5Loeffler J, Stevens DA. Antifungal drug resistance. Clin Infect Dis ,2003,36( Suppl 1 ) :3-41.
  • 6Jousson O, Lechenne B, Bontems O, et al. Secreted subtilisin gene family inTrichophyton rubrum. Gene, 2004,339 : 79- 88.

二级参考文献6

  • 1王辉,陈民钧.加强临床微生物室在感染性疾病诊治中的作用[J].中华检验医学杂志,2005,28(1):2-4. 被引量:41
  • 2卢圣栋.现代分子生物学技术.第2版.北京:中国协和医科大学出版社,2001.464—465.
  • 3Makimura K, et al. Phylogenetic classification and species identification of dermatophyte strains based on DNA sequences of nuclear ribosomal internal transcribed spacer 1 regions. J Clin Microbiol, 1999, 37: 920-924.
  • 4Arca E, et al. Polymerase chain reaction in the diagnosis of onychomycosis. Eur J Dermatol, 2004, 14: 52-55.
  • 5Machouart - Dubach M, et al. Rapid discrimination among dermatophytes,Scytalidium spp., and other fungi with a PCR - restriction fragment length polymorphism ribotyping method. J Clin Microbiol, 2001, 39:685 -690.
  • 6Iwen PC, et al. Utilization of the internal transcribed spacer regions as molecular targets to detect and identify human fungal pathogens. Med Mycol, 2002, 40: 87-109.

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