Orosz Erika, Farkas Ágnes, Kucsera István
1 Department of Parasitology, National Center for Epidemiology , Budapest, Hungary.
2 Division of Virology, National Center for Epidemiology , Budapest, Hungary.
Acta Microbiol Immunol Hung. 2016 Sep;63(3):293-299. doi: 10.1556/030.63.2016.004. Epub 2016 Aug 31.
Acanthamoeba species are free-living amebae that can be found in almost every range of environments. Within this genus, numerous species are recognized as human pathogens, potentially causing Acanthamoeba keratitis (AK). AK is a corneal disease that is predominantly associated with contact lens use, the epidemiology of which is related to the specific genotype of Acanthamoeba. This study reports seven (7/16; 43.75%) positive cases. Detection of Acanthamoeba in corneal scrapings is based on cultivation and polymerase chain reaction (PCR) combined with the molecular taxonomic identification method. By PCR, seven samples were positive; cultivation was successful for five samples, probably because of the low quantity of samples. Genotype identification was carried out with a real-time fluorescence resonance energy transfer PCR assay based on sequence analysis of the 18S rRNA gene, and sensitivity and specificity were evaluated in comparison with traditional parasitological techniques. All seven detected Acanthamoeba strains belonged to the T4 genotype, the main AK-related genotype worldwide. These results confirmed the importance of a complete diagnostic protocol, including a PCR assay, for the clinical diagnosis of AK from human samples. Genotyping allowed the identification of all isolates in the T4 group, thus demonstrating the prevalence of this genotype in Hungary.
棘阿米巴属是自由生活的阿米巴原虫,几乎在各种环境中都能找到。在该属中,许多物种被认为是人类病原体,有可能导致棘阿米巴角膜炎(AK)。AK是一种主要与隐形眼镜使用相关的角膜疾病,其流行病学与棘阿米巴的特定基因型有关。本研究报告了7例(7/16;43.75%)阳性病例。角膜刮片中棘阿米巴的检测基于培养、聚合酶链反应(PCR)以及分子分类鉴定方法。通过PCR,7个样本呈阳性;5个样本培养成功,可能是因为样本量较少。基于18S rRNA基因序列分析,采用实时荧光共振能量转移PCR检测法进行基因型鉴定,并与传统寄生虫学技术比较评估其敏感性和特异性。所有7株检测到的棘阿米巴菌株均属于T4基因型,这是全球与AK相关的主要基因型。这些结果证实了包括PCR检测在内的完整诊断方案对于从人类样本中临床诊断AK的重要性。基因分型能够鉴定出T4组中的所有分离株,从而证明了该基因型在匈牙利的流行情况。