Department of Parasitology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Parasit Vectors. 2012 Sep 4;5:187. doi: 10.1186/1756-3305-5-187.
In this study, a total of 426 human faecal samples were examined for the presence of Entamoeba histolytica, Entamoeba dispar, Entamoeba moshkovskii infection via a combination of microscopic examination and nested polymerase chain reaction (PCR) targeting 16S ribosomal RNA of Entamoeba species.
Faecal sample were collected from 426 participants in five rural villages in Peninsular Malaysia. The faecal samples were processed by direct wet smear and formalin ethyl acetate concentration technique followed by iodine staining and examined via microscopy for the presence of Entamoeba species and other intestinal parasites. Microscopically positive samples for Entamoeba species cysts were further characterized using a Nested Polymerase Chain Reaction (Nested-PCR) targeting 16S-like ribosomal RNA gene. The data entry and analysis was carried out using the SPSS software (Statistical Package for the Social Sciences) program for Windows version 17 (SPSS, Chicago, IL, USA).
Based on single faecal examination, overall prevalence of Entamoeba infection was 17.6% (75/426). Females (19.1%) were more commonly infected compared to males (15.9%). Comparison by age groups showed that adults (23.9%) had higher infection rates than children (15.3%). The PCR results showed that 52 out of 75 microscopy positive samples successfully generated species-specific amplicons. The infection with E. histolytica (75.0%; 39/52) was the most common, followed by E. dispar (30.8%; 18/52) and E. moshkovskii (5.8%; 3/52). Of these, 33 (63.5%) were shown to contain only E. histolytica, 10 (19.2%) contained E. dispar and 3 (5.8%) contained only E. moshkovskii. Mixed infection with E. histolytica and E. dispar was found in 6 (11.5%) samples.
The present study essentially emphasized the benefit of molecular techniques in discriminating the pathogenic Entamoeba species from the non-pathogenic for accurate diagnosis and better management of amoebiasis. The presence of E. moshkovskii is of great public health concern as it was the first time it has been reported in Malaysia.
本研究通过结合显微镜检查和针对 16S 核糖体 RNA 的巢式聚合酶链反应 (PCR),对来自马来西亚半岛五个农村村庄的 426 名参与者的粪便样本进行了检测,以确定是否存在溶组织内阿米巴、迪斯帕内阿米巴和莫氏内阿米巴感染。
收集来自马来西亚半岛五个农村村庄的 426 名参与者的粪便样本。粪便样本采用直接湿涂片和甲醛-乙酸乙酯浓缩技术处理,然后用碘染色,通过显微镜检查观察是否存在内阿米巴属和其他肠道寄生虫。对显微镜检查发现的内阿米巴属包囊阳性样本进一步采用针对 16S 样核糖体 RNA 基因的巢式聚合酶链反应 (Nested-PCR) 进行鉴定。数据录入和分析使用 Windows 版本 17 的 SPSS 软件 (统计软件包 for the Social Sciences) 程序(SPSS,芝加哥,IL,美国)进行。
基于单次粪便检查,总的内阿米巴属感染率为 17.6%(75/426)。女性(19.1%)的感染率高于男性(15.9%)。按年龄组比较,成年人(23.9%)的感染率高于儿童(15.3%)。PCR 结果显示,75 份显微镜检查阳性样本中有 52 份成功生成了种特异性扩增子。最常见的感染是溶组织内阿米巴(75.0%;39/52),其次是迪斯帕内阿米巴(30.8%;18/52)和莫氏内阿米巴(5.8%;3/52)。其中,33 份(63.5%)仅含有溶组织内阿米巴,10 份(19.2%)含有迪斯帕内阿米巴,3 份(5.8%)仅含有莫氏内阿米巴。6 份(11.5%)样本存在溶组织内阿米巴和迪斯帕内阿米巴混合感染。
本研究强调了分子技术在鉴别致病性内阿米巴属与非致病性内阿米巴属方面的优势,以便进行准确诊断和更好地管理阿米巴病。莫氏内阿米巴的存在引起了极大的公共卫生关注,因为这是它首次在马来西亚被报告。