Tachibana Hiroshi, Yanagi Tetsuo, Pandey Kishor, Cheng Xun-Jia, Kobayashi Seiki, Sherchand Jeevan B, Kanbara Hiroji
Department of Infectious Diseases, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.
Mol Biochem Parasitol. 2007 Jun;153(2):107-14. doi: 10.1016/j.molbiopara.2007.02.006. Epub 2007 Mar 1.
An Entamoeba sp. strain, P19-061405, was isolated from a rhesus monkey in Nepal and characterized genetically. The strain was initially identified as Entamoeba histolytica using PCR amplification of peroxiredoxin genes. However, sequence analysis of the 18S rRNA gene showed a 0.8% difference when compared to the reference E. histolytica HM-1:IMSS human strain. Differences were also observed in the 5.8S rRNA gene and the internal transcribed spacer (ITS) regions 1 and 2, and analysis of the serine-rich protein gene from the monkey strain showed unique codon usages compared to E. histolytica isolated from humans. The amino acid sequences of two hexokinases and two glucose phosphate isomerases also differed from those of E. histolytica. Isoenzyme analyses of these enzymes in the monkey strain showed different electrophoretic mobility patterns compared with E. histolytica isolates. Analysis of peroxiredoxin genes indicated the presence of at least seven different types of protein, none of which were identical to proteins in E. histolytica. When the trophozoites from the monkey strain were inoculated into the livers of hamsters, formation of amebic abscesses was observed 7 days after the injection. These results demonstrate that the strain is genetically different from E. histolytica and is virulent. Revival of the name Entamoeba nuttalli is proposed for the organism.
从尼泊尔的一只恒河猴体内分离出一株溶组织内阿米巴样原虫(Entamoeba sp.)菌株P19 - 061405,并对其进行了基因特征分析。最初利用过氧化物还原酶基因的PCR扩增将该菌株鉴定为溶组织内阿米巴(Entamoeba histolytica)。然而,18S rRNA基因的序列分析显示,与参考溶组织内阿米巴HM - 1:IMSS人源菌株相比,存在0.8%的差异。在5.8S rRNA基因以及内部转录间隔区(ITS)区域1和2中也观察到差异,并且对该猴源菌株富含丝氨酸蛋白基因的分析表明,与从人类分离出的溶组织内阿米巴相比,其密码子使用情况独特。两种己糖激酶和两种葡萄糖磷酸异构酶的氨基酸序列也与溶组织内阿米巴不同。对该猴源菌株中这些酶的同工酶分析显示,与溶组织内阿米巴分离株相比,其电泳迁移模式不同。过氧化物还原酶基因分析表明存在至少七种不同类型的蛋白质,其中没有一种与溶组织内阿米巴中的蛋白质相同。当将该猴源菌株的滋养体接种到仓鼠肝脏中时,注射后7天观察到阿米巴脓肿的形成。这些结果表明,该菌株在基因上与溶组织内阿米巴不同且具有毒性。建议将该生物体重新命名为纳氏内阿米巴(Entamoeba nuttalli)。