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Detection molecular typing and phylogenetic analysis of Leishmania isolated from cases of leishmaniasis among Syrian refugees in Lebanon

机译:从黎巴嫩叙利亚难民的利什曼病病例中分离出的利什曼原虫的检测分子分型和系统发育分析

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摘要

Leishmania is a parasitic protozoan with more than two-dozen species causing the disease leishmaniasis. It is transmitted to humans through the bite of an infected female phlebotomine sand-fly vector. In the past two years the incidence of leishmaniasis has been drastically increasing in Lebanon. This was in parallel with the deterioration of the security in Syria forcing thousands to flee and seek shelter in poorly maintained refugee camps and collective shelters. Cutaneous leishmaniasis (CL) is now considered a public health problem, but its epidemiology has not been fully elucidated. To our knowledge, this is the first study comparing two different molecular methods for the detection and identification of Leishmania tropica in Lebanon.Two molecular typing methods of 39 FFPE Leishmania isolates were used: the ITS1-PCR RFLP and the nested ITS1-5.8S rDNA gene amplification followed by sequencing and phylogenetic analysis. The efficiency of these two techniques in Leishmania identification was compared and the phylogenetic relationships among these isolates were illustrated based on the neighbor-joining (NJ) method. The results were statistically correlated with the parasitic index (PI). The DNA storage in formalin-fixed paraffin embedded (FFPE) tissues was assessed as well. The parasites identified were all L. tropica as determined by both techniques. ITS1-5.8S rDNA gene based typing proved to be more sensitive in the detection of parasites (positive in 69.2% of the isolates) as opposed to the ITS1-PCR RFLP method that was successful in identifying L. tropica in only 43.6% of the isolates. Sequencing and phylogenetic analysis revealed high levels of heterogeneity. A statistically significant correlation was observed between PI and the results of the nested ITS1-5.8S rDNA gene PCR. Genotyping at the species level is essential for monitoring the relative frequency of CL in the Mediterranean area that is correlated to three different Leishmania species (Leishmania infantum, Leishmania major and L. tropica), each characterized by distinct epidemiological features. The obtained results highlight the need to find a universally accepted diagnostic tool for Leishmania typing.
机译:利什曼原虫是一种寄生的原生动物,有超过两种导致利什曼原虫病的物种。它通过被感染的雌性白屈沙蝇媒介的叮咬传播给人类。在过去的两年中,黎巴嫩的利什曼病发病率急剧上升。与此同时,叙利亚的安全状况恶化,迫使成千上万的人逃离并在维护不良的难民营和集体收容所中寻求庇护。皮肤利什曼病(CL)现在被认为是公共卫生问题,但是其流行病学尚未得到充分阐明。据我们所知,这是首次比较两种检测和鉴定黎巴嫩热带利什曼原虫的分子方法。使用39种FFPE利什曼原虫分离株的两种分子分型方法:ITS1-PCR RFLP和巢式ITS1-5.8S rDNA基因扩增,然后进行测序和系统发育分析。比较了这两种技术在利什曼原虫鉴定中的效率,并基于邻居连接(NJ)方法说明了这些分离株之间的系统发育关系。结果与寄生指数(PI)在统计上相关。还评估了福尔马林固定石蜡包埋(FFPE)组织中的DNA储存。通过两种技术测定,鉴定出的寄生虫均为热带劳氏乳杆菌。事实证明,基于ITS1-5.8S rDNA基因的分型对寄生虫的检测更为敏感(在分离株中为69.2%呈阳性),而与ITS1-PCR RFLP方法仅在43.6%的情况下成功地鉴定了热带疟原虫的方法相反。隔离株。测序和系统发育分析表明高度异质性。 PI与嵌套ITS1-5.8S rDNA基因PCR结果之间存在统计学意义的相关性。在物种水平上进行基因分型对于监测地中海地区CL的相对频率至关重要,该频率与三种不同的利什曼原虫物种(婴儿利什曼原虫,大利什曼原虫和热带麻风杆菌)相关,每种特征均具有独特的流行病学特征。获得的结果突出表明需要找到一种普遍接受的利什曼原虫分型诊断工具。

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