Nixon Julie E J, Wang Amy, Field Jessica, Morrison Hilary G, McArthur Andrew G, Sogin Mitchell L, Loftus Brendan J, Samuelson John
Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Eukaryot Cell. 2002 Apr;1(2):181-90. doi: 10.1128/EC.1.2.181-190.2002.
Giardia lamblia and Entamoeba histolytica are amitochondriate, microaerophilic protists which use fermentation enzymes like those of bacteria to survive anaerobic conditions within the intestinal lumen. Genes encoding fermentation enzymes and related electron transport peptides (e.g., ferredoxins) in giardia organisms and amebae are hypothesized to be derived from either an ancient anaerobic eukaryote (amitochondriate fossil hypothesis), a mitochondrial endosymbiont (hydrogen hypothesis), or anaerobic bacteria (lateral transfer hypothesis). The goals here were to complete the molecular characterization of giardial and amebic fermentation enzymes and to determine the origins of the genes encoding them, when possible. A putative giardia [2Fe-2S]ferredoxin which had a hypothetical organelle-targeting sequence at its N terminus showed similarity to mitochondrial ferredoxins and the hydrogenosomal ferredoxin of Trichomonas vaginalis (another luminal protist). However, phylogenetic trees were star shaped, with weak bootstrap support, so we were unable to confirm or rule out the endosymbiotic origin of the giardia [2Fe-2S]ferredoxin gene. Putative giardial and amebic 6-kDa ferredoxins, ferredoxin-nitroreductase fusion proteins, and oxygen-insensitive nitroreductases each tentatively supported the lateral transfer hypothesis. Although there were not enough sequences to perform meaningful phylogenetic analyses, the unique common occurrence of these peptides and enzymes in giardia organisms, amebae, and the few anaerobic prokaryotes suggests the possibility of lateral transfer. In contrast, there was more robust phylogenetic evidence for the lateral transfer of G. lamblia genes encoding an NADH oxidase from a gram-positive coccus and a microbial group 3 alcohol dehydrogenase from thermoanaerobic prokaryotes. In further support of lateral transfer, the G. lamblia NADH oxidase and adh3 genes appeared to have an evolutionary history distinct from those of E. histolytica.
贾第虫和溶组织内阿米巴是无线粒体的微需氧原生生物,它们利用类似于细菌的发酵酶在肠腔内的厌氧条件下生存。贾第虫生物和阿米巴中编码发酵酶及相关电子传递肽(如铁氧化还原蛋白)的基因被推测来源于古代厌氧真核生物(无线粒体化石假说)、线粒体共生体(氢假说)或厌氧细菌(横向转移假说)。这里的目标是完成贾第虫和阿米巴发酵酶的分子特征分析,并在可能的情况下确定编码这些酶的基因的起源。一种假定的贾第虫[2Fe-2S]铁氧化还原蛋白在其N端有一个假定的细胞器靶向序列,与线粒体铁氧化还原蛋白和阴道毛滴虫(另一种腔内生原生生物)的氢化酶体铁氧化还原蛋白相似。然而,系统发育树呈星形,自展支持度较弱,因此我们无法证实或排除贾第虫[2Fe-2S]铁氧化还原蛋白基因的内共生起源。假定的贾第虫和阿米巴6 kDa铁氧化还原蛋白、铁氧化还原蛋白-硝基还原酶融合蛋白和氧不敏感硝基还原酶均初步支持横向转移假说。尽管没有足够的序列进行有意义的系统发育分析,但这些肽和酶在贾第虫生物、阿米巴和少数厌氧原核生物中的独特共同出现表明了横向转移可能。相比之下,有更强有力的系统发育证据表明,贾第虫编码NADH氧化酶的基因从革兰氏阳性球菌横向转移而来,编码微生物群3醇脱氢酶的基因从嗜热厌氧原核生物横向转移而来。为进一步支持横向转移,贾第虫NADH氧化酶和adh3基因的进化历史似乎与溶组织内阿米巴的不同。