Infectious and Tropical Diseases Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Parasitology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Parasit Vectors. 2024 Jan 16;17(1):21. doi: 10.1186/s13071-023-06103-6.
Strongyloidiasis is a neglected tropical disease (NTD) that is caused mainly by Strongyloides stercoralis, with an estimated 600 million people infected worldwide, and in fewer cases by Strongyloides fuelleborni fuelleborni and Strongyloides fuelleborni kellyi. A number of studies have been conducted on the genetic diversity of S. stercoralis in East and Southeast Asia; however, there is very limited corresponding information from West Asian countries, including Iran.
For Strongyloides worms collected from patients in southwestern Iran, the hypervariable regions I (HVR-I) and IV (HVR-IV) of the nuclear 18S ribosomal DNA (rDNA) locus (SSU) and a fragment of the subunit 1 mitochondrial cytochrome c oxidase gene (cox-1) were sequenced. For a subset of the worms, whole-genome sequencing data were generated.
The cox-1 sequences of 136 worms isolated from 23 patients indicated that all isolates were S. stercoralis. Among the cox-1 sequences, 33 polymorphic sites and 13 haplotypes were found. The phylogenetic analysis demonstrated that some sequences clustered fairly closely with sequences from humans and dogs from other parts of the world, while others formed a separate, Iran-specific group. Among 64 S. stercoralis analyzed, we found three of the previously described SSU HVR-I haplotypes, with haplotype II being the most frequent haplotype. In contrast to Southeast Asia, where S. stercoralis heterozygous for different haplotypes at the HVR-I locus are rare, we found 20 worms to be heterozygous for two different HVR-I haplotypes, 18 of which fell into the Iran-specific cox-1 cluster. SSU-heterozygous worms also showed elevated heterozygosity at the whole-genome level.
We conclude that the S. stercoralis population from the Khuzestan province shares much of the genetic diversity with the population in Southeast Asia, but there is an indication of additional genetic input. There appears to be some population structure with different subpopulations, which however do interbreed at least occasionally.
旋毛虫病是一种被忽视的热带病(NTD),主要由粪类圆线虫引起,全球估计有 6 亿人感染,在较少情况下由福勒线虫福勒亚种和福勒线虫凯利亚种引起。已经有许多关于东亚和东南亚粪类圆线虫遗传多样性的研究;然而,来自西亚国家,包括伊朗的相应信息非常有限。
对来自伊朗西南部患者的旋毛虫进行研究,对核 18S 核糖体 DNA(SSU)的高变区 I(HVR-I)和 IV(HVR-IV)以及亚单位 1 线粒体细胞色素 c 氧化酶基因(cox-1)的片段进行测序。对一部分蠕虫进行了全基因组测序。
从 23 名患者中分离出的 136 条蠕虫的 cox-1 序列表明,所有分离株均为粪类圆线虫。在 cox-1 序列中,发现了 33 个多态性位点和 13 个单倍型。系统发育分析表明,一些序列与来自世界其他地区的人类和狗的序列聚类非常紧密,而其他序列则形成了一个单独的、伊朗特有的群体。在分析的 64 条粪类圆线虫中,我们发现了之前描述的三种 SSU HVR-I 单倍型,其中单倍型 II 是最常见的单倍型。与东南亚不同,那里的粪类圆线虫在 HVR-I 基因座上异质的不同单倍型很少见,我们发现有 20 条蠕虫是两种不同 HVR-I 单倍型的杂合体,其中 18 条属于伊朗特有的 cox-1 聚类。SSU 杂合子蠕虫在全基因组水平上也表现出较高的杂合度。
我们的结论是,来自胡齐斯坦省的粪类圆线虫种群与东南亚的种群具有许多遗传多样性,但存在额外遗传输入的迹象。似乎存在一些种群结构,不同的亚种群存在,但它们至少偶尔会杂交。