期刊文献+

感染组学(infectomics)——对感染性疾病的总体性和综合性研究 被引量:1

Infectomics: The Global and Integrative Study of Infectious Diseases
在线阅读 下载PDF
导出
摘要 在感染性疾病的范畴内,目前急需一个能有效地、精确地和综合性地研究微生物感染的结构性和功能性基因组学和蛋白质组学(感染组学) 的全面方法. 新的方法(如DNA和蛋白质微阵列) 和传统方法(如分子克隆、PCR、基因敲除,加进(knockin) 和反义术等) 的结合将有助于克服今天的困难. 在感染时,微生物及其宿主的全部表型改变(感染组) 均由微生物病原体及其宿主的基因组所编码,并在特异的微生物-宿主相互作用时的某些环境条件下表达. 微生物及其宿主的全部药物反应(药理组) 可用基因组或蛋白质组的方法检出. 分析基因型和表型或表达形式的全基因组方法将最终导致对微生物的发病机理、感染性疾病的快速诊断和控制感染的新策略的全面研究. 感染性疾病中最基本的问题是,如何全面地和综合性地应用感染组学,来了解微生物病原体及其宿主的相互作用. In the field of infectious diseases there is an urgent need for global researches that can efficiently, precisely and integratively study structural and functional genomics and proteomics of microbial infection (infectomics). The combination of new (e.g. DNA and protein microarrays) and traditional approaches (e.g. cloning, PCR, gene knockin and knockout, and antisense) will help overcome the challenges we are facing today. It was assumed that the global phenotypic changes (infectomes) in microbes and their host during infections are encoded by the genomes of microbial pathogens and their hosts, expressed in certain environmental conditions devoted to specific microbe-host interactions. Global drug responses (pharmacomes) in microbes and their host can be detected by genomic and proteomic approaches. Genome-wide approaches to genotyping and phenotyping or expression profiling will eventually lead to global dissection of microbial pathogenesis, efficient and rapid diagnosis of infectious diseases, and the development of novel strategies to control infections. The key fundamental issue of infectious diseases is how to globally and integratively understand the interactions between microbial pathogens and their hosts by using infectomics.
作者 黄胜和 徐钤
出处 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2005年第4期304-309,共6页 Progress In Biochemistry and Biophysics
  • 相关文献

参考文献20

  • 1Fauci A S. Infectious diseases: consideration for the twenty-first century. Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America, 2001, 32 (5): 675~685.
  • 2McClane B A, Mietzner T A. Microbial pathogenesis: A Principles-Orientated Approach. Frence: Fence Creek Publishing.1999. 1~5.
  • 3Huang S H, Triche T, Jong A Y. Infectomics: genomics and proteomics of microbial infections. Functional Integrative Genomics. 2002, 1 (6): 331~344.
  • 4Cummings C A, Relman D A. Using DNA microarrays to study host-microbe interactions. Emerging Infectious Diseases, 2000, 6(5): 513~525.
  • 5Wang D, Liu S, Trummer B J, et al. Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells. Nature Biotechnology, 2002, 20 (3): 275~281.
  • 6Walter G, Bussow K, Lucking A, et al. High throughput protein arrays, prospects for molecular diagnostics. Trends in Molecular Medicine. 2002, 8 (6): 250~253.
  • 7Ochman H, Moran N A. Genes lost and genes found: evolution of bacterial pathogenesis and symbiosis. Science, 2000, 292(5519):1096~1099.
  • 8Huang S H, Jong A. Cellular mechanisms of microbial proteins contributing to invasion of the blood brain barrier. Cell Microbiol,2001, 3 (5): 277~287.
  • 9Maurelli A T, Fernandez R E, Bloch C A, et al. "Black holes" and bacterial pathogenicity: a large genomic deletion that enhances the virulence ofShigella spp. and enteroinvasive Escherichia coli.Proc Natl Acad Sci USA, 1998, 95 (7): 3943~3948.
  • 10Sokurenko E V, Chesnokova V, Dykhuizen D E, et al. Pathogenicadaptation of Escherichia coli by natural variation of the FimH adhesion. Proc Natl Acad Sci USA, 1998, 95:8922~8926.

二级参考文献10

  • 1Duggan D J,Nature Genetics,1999年,21卷,10页
  • 2Cheng J,Anal Biochem,1998年,257卷,101页
  • 3Cheng J,Anal Chem,1998年,70卷,2321页
  • 4Cheng J,Nature Biotechnol,1998年,16卷,541页
  • 5Cheng J,A special vohume in Topics in Gurrent Chemistry Springer,1998年
  • 6Lockhart D J,Nature Biotechnol,1996年,14卷,1675页
  • 7Cheng J,Nucleic Acids Res,1996年,24卷,380页
  • 8Chee M,Science,1996年,274卷,610页
  • 9Kricka L J,Clinical Chemistry,1994年,41卷,1211页
  • 10Markx G H,Microbiology,1994年,140卷,585页

共引文献20

同被引文献25

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