棘阿米巴角膜炎:直接从眼组织中分型棘阿米巴

Lisa Connelly , Deepa Anijeet , Derek Tole , Claire L. Alexander
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摘要

本报告探讨了英国患有一种名为棘阿米巴角膜炎(AK)的使人衰弱、威胁视力的角膜疾病的个体的棘阿米巴属的分子特征。2017-2019年间,来自接受AK调查的个人的70份眼部样本被送往格拉斯哥的苏格兰微生物参考实验室(SMiRL),并进行DNA提取,然后使用嵌套PCR/双向测序方法进行深入分子分型。在检测的70个样本中,40个为PCR阳性。其中32个被成功测序,并被分配到23个现有基因型中的两个,即T1至T23。32个样本的分子图谱突出了两种基因型,即T3(n=3)和T4(n=29)。对于被鉴定为T4基因型的29个样本,记录了一个亚基因型(T4A-T4H):T4A(n=18);T4B(n=5);T4C(n=1);T4E(n=4);以及T4F(n=1)。这项研究强调,T4基因型和T4A亚型是导致英国眼病的主要分子变体。深入了解棘阿米巴属的分子特征对于增加我们对这种罕见疾病的感染源、传播途径以及与临床结果的潜在关联的了解至关重要,但可能使人衰弱的眼部疾病。
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Acanthamoeba keratitis: Molecular typing of Acanthamoeba species directly from ocular tissue

This report explores the molecular profiling of Acanthamoeba spp. from individuals in the UK suffering from a debilitating, sight-threatening disease of the cornea known as Acanthamoeba keratitis (AK). Seventy ocular samples from individuals undergoing investigations for AK were sent to the Scottish Microbiology Reference Laboratories (SMiRL), Glasgow during 2017–2019, and subjected to DNA extraction followed by in-depth molecular typing using a nested PCR/bi-directional sequencing approach. Of the 70 samples tested, 40 were PCR-positive. Of these, 32 were successfully sequenced and assigned to two of 23 existing genotypes termed T1 to T23. Molecular profiling of the 32 samples highlighted two genotypes, namely T3 (n = 3) and T4 (n = 29). For those 29 samples identified as the T4 genotype, a sub-genotype (T4A-T4H) was recorded: T4A (n = 18); T4B (n = 5); T4C (n = 1); T4E (n = 4); and T4F (n = 1). This study highlights that the T4 genotype and T4A subtype are the predominant molecular variants to cause ocular disease in the UK. Gaining in-depth information on the molecular profiling of Acanthamoeba spp. is essential to increase our understanding of the source(s) of infection, transmission pathways, and potential associations with clinical outcomes for this rare, yet potentially debilitating ocular disease.

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