Lares-Jiménez Luis Fernando, Booton Gregory C, Lares-Villa Fernando, Velázquez-Contreras Carlos Arturo, Fuerst Paul A
Programa de Doctorado en Ciencias en Biotecnología, Instituto Tecnológico de Sonora, Ciudad Obregón, Son., Mexico.
Department of Molecular Genetics, The Ohio State University, Columbus, OH, USA.
Exp Parasitol. 2014 Nov;145 Suppl:S57-61. doi: 10.1016/j.exppara.2014.07.007. Epub 2014 Jul 27.
Since the first report of Balamuthia mandrillaris as a causative agent of granulomatous amoebic encephalitis in humans, the environmental niche of this amoeba was assumed to be restricted to soil and dust. A single isolation from water was recently made independently by us from Northern Mexico. Now we report the isolation of 8 new strains of B. mandrillaris from Mexico. This continues the pattern of an excess of isolates from North America, compared to other parts of the world. All of the new isolates are environmental isolates, 7 from water samples and one from soil. The identity of each isolate was confirmed by PCR and by examining the sequences of the mitochondrial 16S-like rRNA gene. Success in amplification was determined using comparisons of amplifications of DNA from the strain CDC: V039 and the water strain (ITSON-BM1) as positive controls. The DNA sequences of the new isolates were compared to older strains from clinical cases using phylogenetic analysis, showing very high sequence similarity. The similarity among the new isolates and with previous clinical and environmental isolates of B. mandrillaris was also examined using biochemical and immunological studies. High homogeneity of total protein products, and similarity in antigenic moiety among the eight new isolates and two controls was found. Taken together, the molecular and biochemical studies indicate very low levels of genetic variation within B. mandrillaris.
自从首次报道曼氏巴兰姆希阿米巴(Balamuthia mandrillaris)作为人类肉芽肿性阿米巴脑炎的病原体以来,人们一直认为这种阿米巴的环境生态位仅限于土壤和灰尘。最近我们在墨西哥北部独立地从水中分离出了一株该阿米巴。现在我们报告从墨西哥分离出8株新的曼氏巴兰姆希阿米巴菌株。与世界其他地区相比,北美分离株数量过多的这种模式仍在持续。所有新分离株均来自环境,7株来自水样,1株来自土壤。通过PCR以及检测线粒体16S样rRNA基因序列来确认每个分离株的身份。使用来自CDC菌株V039和水株(ITSON - BM1)的DNA扩增作为阳性对照,通过比较扩增情况来确定扩增是否成功。利用系统发育分析将新分离株的DNA序列与临床病例中的较老菌株进行比较,结果显示序列相似性非常高。还通过生化和免疫学研究检查了新分离株之间以及与曼氏巴兰姆希阿米巴先前临床和环境分离株之间的相似性。发现8株新分离株和两个对照的总蛋白产物具有高度同质性,抗原部分也相似。综合来看,分子和生化研究表明曼氏巴兰姆希阿米巴内部的遗传变异水平非常低。