Loftus Brendan, Anderson Iain, Davies Rob, Alsmark U Cecilia M, Samuelson John, Amedeo Paolo, Roncaglia Paola, Berriman Matt, Hirt Robert P, Mann Barbara J, Nozaki Tomo, Suh Bernard, Pop Mihai, Duchene Michael, Ackers John, Tannich Egbert, Leippe Matthias, Hofer Margit, Bruchhaus Iris, Willhoeft Ute, Bhattacharya Alok, Chillingworth Tracey, Churcher Carol, Hance Zahra, Harris Barbara, Harris David, Jagels Kay, Moule Sharon, Mungall Karen, Ormond Doug, Squares Rob, Whitehead Sally, Quail Michael A, Rabbinowitsch Ester, Norbertczak Halina, Price Claire, Wang Zheng, Guillén Nancy, Gilchrist Carol, Stroup Suzanne E, Bhattacharya Sudha, Lohia Anuradha, Foster Peter G, Sicheritz-Ponten Thomas, Weber Christian, Singh Upinder, Mukherjee Chandrama, El-Sayed Najib M, Petri William A, Clark C Graham, Embley T Martin, Barrell Bart, Fraser Claire M, Hall Neil
TIGR, 9712 Medical Center Drive, Rockville, Maryland 20850, USA.
Nature. 2005 Feb 24;433(7028):865-8. doi: 10.1038/nature03291.
Entamoeba histolytica is an intestinal parasite and the causative agent of amoebiasis, which is a significant source of morbidity and mortality in developing countries. Here we present the genome of E. histolytica, which reveals a variety of metabolic adaptations shared with two other amitochondrial protist pathogens: Giardia lamblia and Trichomonas vaginalis. These adaptations include reduction or elimination of most mitochondrial metabolic pathways and the use of oxidative stress enzymes generally associated with anaerobic prokaryotes. Phylogenomic analysis identifies evidence for lateral gene transfer of bacterial genes into the E. histolytica genome, the effects of which centre on expanding aspects of E. histolytica's metabolic repertoire. The presence of these genes and the potential for novel metabolic pathways in E. histolytica may allow for the development of new chemotherapeutic agents. The genome encodes a large number of novel receptor kinases and contains expansions of a variety of gene families, including those associated with virulence. Additional genome features include an abundance of tandemly repeated transfer-RNA-containing arrays, which may have a structural function in the genome. Analysis of the genome provides new insights into the workings and genome evolution of a major human pathogen.
溶组织内阿米巴是一种肠道寄生虫,也是阿米巴病的病原体,在发展中国家是发病和死亡的重要原因。在此,我们展示了溶组织内阿米巴的基因组,该基因组揭示了与另外两种无线粒体原生生物病原体——蓝氏贾第鞭毛虫和阴道毛滴虫共有的多种代谢适应性。这些适应性包括大多数线粒体代谢途径的减少或消除,以及使用通常与厌氧原核生物相关的氧化应激酶。系统基因组分析确定了细菌基因横向转移到溶组织内阿米巴基因组的证据,其影响集中在扩展溶组织内阿米巴的代谢库方面。这些基因的存在以及溶组织内阿米巴中新代谢途径的可能性可能有助于开发新的化疗药物。该基因组编码大量新型受体激酶,并包含多种基因家族的扩增,包括与毒力相关的基因家族。基因组的其他特征包括大量串联重复的含转运RNA阵列,这可能在基因组中具有结构功能。对该基因组的分析为一种主要人类病原体的运作和基因组进化提供了新的见解。