Haghighi Ali, Kobayashi Seiki, Takeuchi Tsutomu, Thammapalerd Nitaya, Nozaki Tomoyoshi
Department of Parasitology, National Institute of Infectious Diseases, Keio University School of Medicine, Shinjuku-ku, Japan.
J Clin Microbiol. 2003 Aug;41(8):3748-56. doi: 10.1128/JCM.41.8.3748-3756.2003.
It has been known that only 5 to 10% of those infected with Entamoeba histolytica develop symptomatic disease. However, the parasite and the host factors that determine the onset of disease remain undetermined. Molecular typing by using polymorphic genetic loci has been proven to aid in the close examination of the population structure of E. histolytica field isolates in nature. In the present study, we analyzed the genetic polymorphisms of two noncoding loci (locus 1-2 and locus 5-6) and two protein-coding loci (chitinase and serine-rich E. histolytica protein [SREHP]) among 79 isolates obtained from different geographic regions, mainly Japan, Thailand, and Bangladesh. When the genotypes of the four loci were combined for all isolates that we have analyzed so far (overlapping isolates from mass infection events were excluded), a total of 53 different genotypes were observed among 63 isolates. The most remarkable and extensive variations among the four loci was found in the SREHP locus; i.e., 34 different genotypes were observed among 52 isolates. These results demonstrate that E. histolytica has an extremely complex genetic structure independent of geographic location. Our results also show that, despite the proposed transmission of other sexually transmitted diseases, including human immunodeficiency virus infection, from Thailand to Japan, the spectra of the genotypes of the E. histolytica isolates from these two countries are distinct, suggesting that the major E. histolytica strains prevalent in Japan at present were likely introduced from countries other than Thailand. Although the genetic polymorphism of the SREHP locus was previously suggested to be closely associated with the clinical presentation, e.g., colitis or dysentery and liver abscess, no association between the clinical presentation and the SREHP genotype at either the nucleotide or the predicted amino acid level was demonstrated.
已知感染溶组织内阿米巴的人群中只有5%至10%会出现症状性疾病。然而,决定疾病发作的寄生虫和宿主因素仍未确定。利用多态性基因座进行分子分型已被证明有助于仔细研究自然界中溶组织内阿米巴野外分离株的种群结构。在本研究中,我们分析了从不同地理区域(主要是日本、泰国和孟加拉国)获得的79株分离株中两个非编码基因座(基因座1-2和基因座5-6)以及两个蛋白质编码基因座(几丁质酶和富含丝氨酸的溶组织内阿米巴蛋白[SREHP])的基因多态性。当将我们目前分析的所有分离株(排除大规模感染事件中的重叠分离株)的四个基因座的基因型组合在一起时,在63株分离株中总共观察到53种不同的基因型。在四个基因座中,SREHP基因座存在最显著和广泛的变异;即52株分离株中观察到34种不同的基因型。这些结果表明,溶组织内阿米巴具有极其复杂的遗传结构,与地理位置无关。我们的结果还表明,尽管有人提出包括人类免疫缺陷病毒感染在内的其他性传播疾病从泰国传播到日本,但这两个国家的溶组织内阿米巴分离株的基因型谱是不同的,这表明目前在日本流行的主要溶组织内阿米巴菌株可能是从泰国以外的国家引入的。尽管先前有人认为SREHP基因座的基因多态性与临床表现密切相关,例如结肠炎或痢疾以及肝脓肿,但在核苷酸或预测氨基酸水平上均未证明临床表现与SREHP基因型之间存在关联。