Samuelson J, Ayala P, Orozco E, Whirth D
Department of Tropical Public Health, Harvard School of Public Health, Boston, MA.
Arch Invest Med (Mex). 1990;21 Suppl 1:183-9.
Although drug therapy is critical for control of amoebiasis, little is known about mechanisms of drug resistance by E. histolytica parasites. Here we tested the hypothesis that multidrug resistant (mdr) amoeba mutants, similar to mdr tumor cells, are drug resistant based upon overexpression of a P-glycoprotein pump that effluxes drugs from the cells. Using primers to conserved regions of the human P-glycoprotein and the polymerase chain reaction (PCR), we identified multiple 344 base par segments of amoeba DNA similar to the mammalian P glycoprotein. The amino acid sequences of amoeba mdr-like PCR products were from 53 to 97 identical with each other, 55 to identical to human mdr1 sequences, and 41-44% identical with P. falciparum mdr-like sequences. On northern blots, the mdr-like PCR products identified amoeba mRNAs 4.5-5 kilobases long, similar to the 5 kilobase mRNAs reported for the mammalian mdr gene. These mRNAs were increased at least seven times in emetine resistant mutant clone C2 amoebae versus wild-type clone A parasites. Further, the expression of the mdr-like mRNAs was increased three to four times when clone C2 mutants were grown under drug pressure versus the same parasites grown without emetine. In contrast, the number of genomic copies of the mdr-like DNA segments was not increased in the mutant clone C2 versus the wild-type clone A amoebae, and no rearrangements of the mdr-like DNA segments by the mutant were identified on Southern blots. In conclusion there appears to be a family of mdr-like genes in E. histolytica, which may be involved in drug resistance by the parasite.
尽管药物治疗对于控制阿米巴病至关重要,但对于溶组织内阿米巴寄生虫的耐药机制却知之甚少。在此,我们检验了这样一个假设:多药耐药(mdr)的阿米巴突变体,类似于mdr肿瘤细胞,其耐药性是基于一种能将药物从细胞中排出的P-糖蛋白泵的过表达。我们使用针对人类P-糖蛋白保守区域的引物和聚合酶链反应(PCR),鉴定出多个与哺乳动物P-糖蛋白相似的344个碱基对的阿米巴DNA片段。阿米巴mdr样PCR产物的氨基酸序列彼此间有53%至97%的同一性,与人类mdr1序列有55%的同一性,与恶性疟原虫mdr样序列有41%-44%的同一性。在Northern印迹分析中,mdr样PCR产物鉴定出长度为4.5 - 5千碱基的阿米巴mRNA,类似于报道的哺乳动物mdr基因的5千碱基mRNA。与野生型克隆A寄生虫相比,在抗吐根碱突变体克隆C2阿米巴中,这些mRNA至少增加了7倍。此外,当克隆C2突变体在药物压力下生长时,与在无吐根碱条件下生长的相同寄生虫相比,mdr样mRNA的表达增加了3至4倍。相比之下,与野生型克隆A阿米巴相比,突变体克隆C2中mdr样DNA片段的基因组拷贝数并未增加,并且在Southern印迹分析中未发现突变体对mdr样DNA片段的重排。总之,溶组织内阿米巴似乎存在一个mdr样基因家族,这可能与该寄生虫的耐药性有关。