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甲真菌病体外模型中红色毛癣菌几丁质合酶的表达 被引量:1

Genes Expression of Chitin Synthase from Trichophyton Rubrum in Vitro Onychomycosis Model
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摘要 目的探讨红色毛癣菌几丁质合酶(chitin synthase,CHS)m RNA在甲真菌病体外模型中的改变及其在致病中的作用。方法构建甲真菌病体外模型,随机分为实验组和对照组(未加甲板),分别于培养的第0,1,3,5,7,14和20天提取红色毛癣菌总RNA,采用实时荧光定量PCR检测不同时间点CHS m RNA的表达水平,并进行统计学分析。结果对照组CHS m RNA表达水平极低,实验组在红色毛癣菌感染甲板1d,3d,5d表达升高,7d表达达高峰,此后渐渐下降,但仍高于对照组。各时间点与对照组相比,除CHS 3d外,其余差异均有统计学意义(P<0.05)。结论 CHS m RNA在甲真菌病体外模型中有较高表达,在甲真菌病的致病中可能起重要作用。 Objective To investigate the expression and pathological role of CHS m RNA in vitro onychomycosis model.Methods Total RNA of Trichophyton rubrum in the treated group and control group( non-infected nails)was extracted from cultured onychomycosis model at different time points(0d,1d,3d,5d,7d,14 d and 20d).The expression of CHS m RNA at different time points were detected by real-time fluorescence quantitative PCR method,respectively,and performed statistical analysis. Results The expression of CHS m RNA was very low in control group. In treated group,the expression of CHS m RNA increased at 1d,3d and 5d,and reached a peak at 7d. Then the expression decreased gradually,but still higher than control group. Compared to the control group,the expression levels of CHS m RNA at each time points were significantly higher than the treated group with the exception of 3d( P 〈0. 05). Conclusion In vitro onychomycosis model,the expression levels of CHS m RNA are higher in cultured keratin from nail. CHS may play an important role in the pathogenesis of onychomycosis.
出处 《中国皮肤性病学杂志》 CAS CSCD 北大核心 2016年第3期233-235,256,共4页 The Chinese Journal of Dermatovenereology
基金 解放军南京军区医学科技创新课题(09MA065)
关键词 红色毛癣菌 几丁质合酶 实时荧光定量PCR Trichophyton rubrum Chitin synthase Real-time fluorescence quantitative PCR
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  • 1Nenoff P, Kruger C, Ginter-Hanselmayer G, et al. Mycology-an update. Part 1 : Dermatomycoses: causative agents, epidemiology and pathogen- esis [ J]. J Dtsch Dermatol Ges ,2014,12 (3) : 188 - 209. 被引量:1
  • 2Scher RK, Rich P, Pariser D, et al. The epidemiology, etiology, and pathophysiology of onychomycosis [ J ]. Semin Cutan Med Surg,2013,32 (2 Suppl 1 ) : S2 - 4. 被引量:1
  • 3Monod M. Secreted pmteases from dermatophytes [ J ] . Mycopathologia,2008, 166(5-6) :285 -294. 被引量:1
  • 4Chen J,Yi J, Liu L, et al. Substrate adaptation of Trichophyton rubrum secreted endoproteases [ J ]. Microbial Pathog,2010,48 ( 2 ) : 57 - 61. 被引量:1
  • 5胡婵,朱红梅,谭宏月,李平,赵瑾,陈力,温海,宋维芳.甲真菌病体外模型研究[J].中国真菌学杂志,2013,8(5):265-268. 被引量:1
  • 6Frans MK, Pieternella M, Klaas H, et al. Dynamics of cell wall struc- ture in Saccharomyces cerevisiae [J]. FEMS Microbiology Reviews, 2002, 26(3) : 239 -256. 被引量:1
  • 7Soulie MC, Perino C, Piffeteau A, et al. Botrytis cinerea virulence is drastically reduced after disruption of chitin synthase class III gene ( Bcchs3a ) [J]. Cellular Microbiology,2006, 8 ( 8 ) : 1310 - 1321. 被引量:1
  • 8Munro CA, Winter K, Buchan A, et al. Chsl of Candida albicans is an essential chitin synthase required for synthesis of the septum and for cell integrity[ J]. Mol Microbiol,2001, 39 (5) : 1414 - 1426. 被引量:1
  • 9Kano R, Okabayashi K, Nakamuka Y, et al. Differences among chitin synthase I gene sequences in trichophyton rubrum and t. violaceum[J]. Med Mycology ,2000,38 ( 1 ) :47 - 50. 被引量:1
  • 10Kano R,Aihara S,Nakamuka Y,et al. Chitin synthase 1 (Chsl) gene sequences of Microsporum equinum and Trichophyton equinum [ J ]. Veterinary Microbiology,2001, 78 ( 1 ) : 85 - 90. 被引量:1

二级参考文献32

  • 1闻玉梅,陆德源,何丽芳.现代医学微生物学.上海:上海医科大学出版社.2000.677—728 被引量:1
  • 2Borkovich K A, Alex L A, Yarden O, et al. Lessons from the genome sequence of Neurospora crassa: Tracing the path from genomic blueprint to multicellular organism. Microbiol Mol Biol Rev, 2004, 68 (1): 1-108 被引量:1
  • 3Galagan J E, Calvo S E, Cuomo C, et al. Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature, 2005, 438:1105-1115 被引量:1
  • 4Chambergo F S, Bonaccorsi E D, Ferreira A J S, et al. Elucidation of the metabolic fate of glucose in the filamentous fungus Trichoderma reesei using expressed sequence tag (EST) analysis and cDNA microarrays, J Biol Chem, 2002, 277(16): 13983-13988 被引量:1
  • 5Schena M, Shalon D, Davis R W, et al. Quantitative monitoring of gene expression patterns with a complementary DNA microarray. Science, 1995, 270 (5235): 467-470 被引量:1
  • 6Kanehisa M, Goto S, Kawashima S, et al. The KEGG resource for deciphering the genome. Nucleic Acids Res, 2004, 32 (Database issue): 277-280 被引量:1
  • 7Peng J P, Zhang X B, Yang J, et al. The use of comparative genomic hybridization to characterize genome dynamics and diversity among the serotypes of Shigella. BMC Genomics, 2006, 7:218 被引量:1
  • 8Kasuga T, Townsend J P, Tian C G, et al. Long-oligomer microarray profiling in Neurospora crassa reveals the transcriptional program underlying biochemical and physiological events of conidial germination. Nucleic Acids Res, 2005, 33 (20): 6469-6485 被引量:1
  • 9Galagan J E, Calvo S E, Borkovich K A, et al. The genome sequence of the filamentous fungus Neurospora crassa. Nature, 2003, 422: 859-868 被引量:1
  • 10Lengeler K B, Davidson R C, Souza C D, et al. Signal transduction cascades regulating fungal development and virulence. Microbiol Mol Biol Rev, 2000, 64 (4): 746-785 被引量:1

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