期刊文献+

结核分枝杆菌基因敲除的研究进展 被引量:1

原文传递
导出
摘要 结核病仍是世界上致命的传染病之一,2013年约有900万新增患者,150万例死于结核病。结核分枝杆菌(Mycobacterium tuberculosis ,MTB)是结核病主要致病菌,能在宿主巨噬细胞内生长复制,适应、抵抗宿主抗菌免疫。唯一批准用于预防结核病的卡介苗,接种成人或 HIV 阳性新生儿有可能造成 MTB 体内感染播散。因此,亟待改进卡介苗,为免疫缺陷人群提供保护;而耐多药结核病、广泛耐药结核病的发病率逐渐上升,亦急需开发抗结核新药。
出处 《中华传染病杂志》 CAS CSCD 北大核心 2016年第3期190-192,共3页 Chinese Journal of Infectious Diseases
基金 国家自然科学基金(81470001、81170080)
  • 相关文献

参考文献23

  • 1World Health Organization. Global tuberculosis report 2014 [R]. Geneva: World Health Organization,2015.
  • 2Gouzy A, Larrouy-Maumus G, Bottai D,et al. Mycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infection [J/OL]. PLoS Pathog, 2014,10(2) :e1003928 (2014-02-020) [2015-12-13]. http..// journals, plos. org/plospathogens/article? id = 10. 1371/ journal, ppat. 1003928.
  • 3Kraus P, Sivakamasundari V, Xing X,et al. Generating mouse lines {or lineage tracing and knockout studies [J]. Methods Mol Biol, 2014,1194:37-62.
  • 4武晓林,方维焕,俞盈,宋厚辉.结核分枝杆菌同源重组基因敲除系统的构建和应用[J].微生物学报,2012,52(9):1151-1159. 被引量:6
  • 5Gupta RM, Musunuru K. Expanding the genetic editing tool kit: ZFNs, TALENs, and CRISPR-Cas9 [J]. J Clin Invest, 2014,124(10) ..4154-4161.
  • 6Sontheimer EJ, Barrangou R. The Bacterial Origins of the CRISPR Genome-Editing Revolution [J]. Hum Gene Ther, 2015,26(7) :413-424.
  • 7Selle K, Klaenhammer TR, Barrangou R. CRISPR-based screening of genomic island excision events in bacteria [J]. ProcNatl Acad Sci U S A, 2015,112(26):8076-8081.
  • 8Kennedy EM, Cullen BR. Bacterial CRISPR/Cas DNA endonueleases: A revolutionary technology that could dramatically impact viral research and treatment [J]. Virology, 2015, 479-480: 213-220.
  • 9Chen Y, Cao J, Xiong M, et al. Engineering Human Stem Cell Lines with Inducible Gene Knockout using CRISPR/Cas9 [J]. Cell Stem Cell, 2015,17(2):233-244.
  • 10Chen X, Li M, Feng X, et al. Targeted Chromosomal Transloeations and Essential Gene Knockout Using CRISPR/ Cas9 Technology in Caenorhabditis elegans [J]. Genetics, 2015, 201 (4): 1295-1306.

二级参考文献38

  • 1WHO report 2011 global tuberculosis control. 2011: 1- 246.
  • 2Cole ST, Brosch R, Parkhill J, Garnier T, Chureher C, Harris D, Gordon SV, Eiglmeier K, Gas S, Barry CE, 3rd, Tekaia F, Badcock K, Basham D, Brown D, Chillingworth T, Connor R, Davies R, Devlin K, Feltwell T, Gentles S, Hamlin N, Holroyd S, Hornsby T, Jagels K,Barrell BG. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature, 1998, 393 (6685) : 537-544.
  • 3Song H, Wolschendorf F, Niederweis M ( 2008 ) : Construction of unmarked deletion mutants in mycobacteria. In T. Parish, and A. Brown (Eds) : Mycobacteria protocols. Humana Press, Ottawa, pp. 279- 295.
  • 4Song H, Niederweis M. Functional expression of the Flp recombinase in Mycobacterium bovis BCG. Gene, 2007, 399 (2): 112-119.
  • 5Song H, Huff J, Janik K, Walter K, Keller C, Ehlers S, Bossmann SH, Niederweis M. Expression of the ompATb operon accelerates ammonia secretion and adaptation of Mycobacterium tuberculosis Molecular Microbiology, 2011 to acidic environments , 80 (4): 900-918.
  • 6Kessel JC, Hatfull Mycobacterium tuberculosis. (2) : 147-152 GF. Recombineering in Nature Methods, 2007, 4.
  • 7Wolschendorf F, Ackart D, Shrestha TB, Hascall-Dove L, Nolan S, Lamichhane G, Wang Y, Bossmann SH, Basaraba RJ,Niederweis M. Copper resistance is essential for virulence of Mycobacterium tuberculosis. Proceedings of the National Academy of Sciences, 2011, 108 (4) : 1621-1626.
  • 8Guilhot C, Gicquel B, Martin C. Temperature-sensitive mutants of the Mycobacterium pIasmid pAL5000. FEMS Microbiology Letters, 1992, 77 (1-3): 181-186.
  • 9Gavigan JA, Guilhot C, Gicquel B, Martin C. Use of conjugative and thermosensitive cloning vectors for transposon delivery to Myeobacterium smegmatis. FEMS Microbiology Letters, 1995, 127 (1-2):35-39.
  • 10Guilhot C, Otal I, van Rompaey I, Martin C,Gicquel B. Efficient transposition in myeobacteria: construction of Myeobacterium smegmatis insertional mutant libraries. Journal of Bacteriology, 1994, 176 (2): 535-539.

共引文献6

同被引文献4

引证文献1

二级引证文献2

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