Korman S H, Le Blancq S M, Deckelbaum R J, Van der Ploeg L H
Department of Genetics and Development, College of Physicians and Surgeons, Columbia University, New York 10032.
J Clin Invest. 1992 Jun;89(6):1725-33. doi: 10.1172/JCI115774.
The patterns of transmission of Giardia lamblia and the potential contribution of strain differences to pathogenicity of infection is poorly understood. We used pulsed field gradient gel electrophoresis (PFGE) to separate chromosome-sized DNA molecules of 22 stocks of G. lamblia isolated from 13 individuals (6 symptomatic, 7 asymptomatic) living in Jerusalem. PGFE gels run under a variety of conditions revealed up to nine ethidium bromide-stained bands per isolate ranging in size from 0.7 to greater than 3 megabasepairs. Relative staining intensities indicated that some bands contained multiple chromosomes. Major differences in the number, size, and intensity of bands allowed a clear differentiation of the karyotypes of isolates from each of the different individuals. This is in contrast to previous studies where the karyotype of different isolates have been strikingly homogeneous. Hybridization of Southern blots with surface antigen, beta-tubulin, and ribosomal RNA genes revealed that these gene families were distributed to different sized chromosomes amongst the different isolates. PFGE thus revealed major differences in the karyotypes of different G. lamblia isolates that were obtained over a short period of time from a relatively confined geographic area. In contrast, karyotypes of isolates established either by direct cultivation of duodenal trophozoites or by excystation of stool cysts from the same individuals were almost identical. Also, isolates from the same individuals obtained over a prolonged period of time revealed only minor differences in their karyotype, suggesting that recurrent infection can be caused by genetically similar organisms. We conclude that chronic giardiasis can result from recurrence of occult infection or reinfection from a common source.
蓝氏贾第鞭毛虫的传播模式以及菌株差异对感染致病性的潜在影响目前还知之甚少。我们使用脉冲场梯度凝胶电泳(PFGE)来分离从居住在耶路撒冷的13个人(6个有症状,7个无症状)中分离出的22株蓝氏贾第鞭毛虫的染色体大小的DNA分子。在各种条件下运行的PGFE凝胶显示,每个分离株最多有9条溴化乙锭染色带,大小从0.7到大于3兆碱基对不等。相对染色强度表明,一些条带包含多条染色体。条带数量、大小和强度的主要差异使得能够清楚地区分来自不同个体的分离株的核型。这与之前不同分离株核型非常一致的研究形成了对比。用表面抗原、β-微管蛋白和核糖体RNA基因对Southern印迹进行杂交,结果显示这些基因家族分布在不同分离株的不同大小的染色体上。因此,PFGE揭示了在短时间内从相对有限的地理区域获得的不同蓝氏贾第鞭毛虫分离株核型的主要差异。相比之下,通过直接培养十二指肠滋养体或从同一个体的粪便包囊中脱囊建立的分离株核型几乎相同。此外,从同一个体在较长时间内获得的分离株在核型上仅显示出微小差异,这表明反复感染可能由基因相似的生物体引起。我们得出结论,慢性贾第虫病可能是由隐匿感染的复发或来自共同来源的再感染引起的。