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吉尔吉斯斯坦细粒棘球绦虫和多房棘球绦虫的遗传多样性:A2 基因型是感染人类的主要多房棘球绦虫变体。

Genetic diversity of Echinococcus multilocularis and Echinococcus granulosus sensu lato in Kyrgyzstan: The A2 haplotype of E. multilocularis is the predominant variant infecting humans.

机构信息

Institute of Parasitology, Vetsuisse and Medical Faculty, University of Zürich, Zürich, Switzerland.

City Clinical Hospital #1, Surgical Department, Faculty of Surgery of the Kyrgyz State Medical Academy, Bishkek, Kyrgyzstan.

出版信息

PLoS Negl Trop Dis. 2020 May 13;14(5):e0008242. doi: 10.1371/journal.pntd.0008242. eCollection 2020 May.

Abstract

Alveolar and cystic echinococcosis (AE, CE) caused by E. multilocularis and E. granulosus s.l., respectively, are considered emerging zoonotic diseases in Kyrgyzstan with some of the world highest regional incidences. Little is known regarding the molecular variability of both species in Kyrgyzstan. In this study we provide molecular data from a total of 72 parasite isolates derived from humans (52 AE and 20 CE patients) and 43 samples from dogs (23 infected with E. multilocularis and 20 with E. granulosus s.l.).Genetic variability in E. multilocularis was studied using the concatenated complete sequences of the cob, nad2 and cox1 mitochondrial genes adding a total of 3,558bp per isolate. The cob/nad2/cox1 A2 haplotype was identified in 63.4% of the human and in 65.2% of the dog samples. This haplotype was originally described in samples from Kazakhstan and St. Lawrence Island (Alaska, USA). We also describe here 16 non-previously defined variants of E. multilocularis (called A11-A26). All haplotypes cluster together within the Asian group in the haplotype network. Based on Fst values, low level of genetic differentiation was found between the populations of E. multilocularis isolated from different regions within the country. However, high degree of differentiation was found when all the concatenated sequences from Kyrgyzstan are considered as a single population and compared with the population of the parasite from the neighbouring country China. In the case of E. granulosus s.l. the analysis was based in 1,609bp of the cox1 gene. One isolate from a dog was identified as E. equinus, while all the other sequences were identified belonging to E. granulosus s.s. In total, 24 cox1 haplotypes of E. granulosus s.s. were identified including the already described variants: Eg01 (in 6 samples), Eg33 (in 4 samples), EgCl04 (in 2 samples), Eg03 (in 1 sample) and Eg32 (in 1 sample). From the twenty-five other isolates of E. granulosus s.s. a total of 19 non-previously described cox1 haplotypes were identified and named as EgKyr1 to EgKyr19. The most common haplotype infecting human is the EgKyr1 which was found in 5 isolates.The cob/nad2/cox1 A2 haplotype of E. multilocularis is responsible for the majority of human infections in Kyrgyzstan and is also found in the majority of dogs included in this study. Further similar studies in different parts of Asia could elucidate if it is also the most common variant infecting humans in other countries. It remains unknown if this particular haplotype presents differences in virulence which could have contributed to the emergency of alveolar echinococcosis in Kyrgyzstan. In the case of E. granulosus s.s. it seems that there is no dominant haplotype infecting humans in Kyrgzstan. Further characterization of biological or antigenic features of dominant mitochondrial haplotypes could help to elucidate if they present differences which could be relevant in the diagnostic, pathogenicity or in the host/parasite interaction when infecting humans.

摘要

泡型包虫病(AE)和细粒棘球蚴病(CE)分别由多房棘球绦虫和细粒棘球绦虫引起,在吉尔吉斯斯坦被认为是新兴的人畜共患疾病,其局部发病率在世界上处于较高水平。关于这两种寄生虫在吉尔吉斯斯坦的分子变异性,人们知之甚少。在本研究中,我们提供了总共 72 个寄生虫分离株的分子数据,这些寄生虫分离株来自人类(52 例 AE 和 20 例 CE 患者)和 43 个来自狗的样本(23 例感染多房棘球绦虫,20 例感染细粒棘球绦虫)。使用 cob、nad2 和 cox1 线粒体基因的完整串联序列研究了多房棘球绦虫的遗传变异性,每个分离株的总长度为 3558bp。在 63.4%的人类和 65.2%的狗样本中发现了 cob/nad2/cox1 A2 单倍型。该单倍型最初在哈萨克斯坦和圣劳伦斯岛(美国阿拉斯加)的样本中描述。我们还在这里描述了 16 种以前未定义的多房棘球绦虫变异体(称为 A11-A26)。所有单倍型在单倍型网络中聚集在亚洲组内。基于 Fst 值,发现来自该国不同地区的多房棘球绦虫种群之间遗传分化程度较低。然而,当将来自吉尔吉斯斯坦的所有串联序列视为一个单一种群并与来自邻国中国的寄生虫种群进行比较时,发现了高度的分化。在细粒棘球绦虫的情况下,分析基于 cox1 基因的 1609bp。从一只狗中分离出的一个分离株被鉴定为马圆棘球绦虫,而其他所有序列均被鉴定为细粒棘球绦虫。总共鉴定出 24 种细粒棘球绦虫 cox1 单倍型,包括已经描述的变体:Eg01(在 6 个样本中)、Eg33(在 4 个样本中)、EgCl04(在 2 个样本中)、Eg03(在 1 个样本中)和 Eg32(在 1 个样本中)。从其他 25 个细粒棘球绦虫分离株中总共鉴定出 19 种以前未描述的 cox1 单倍型,并命名为 EgKyr1 至 EgKyr19。感染人类最常见的单倍型是 EgKyr1,在 5 个分离株中发现。多房棘球绦虫的 cob/nad2/cox1 A2 单倍型是导致吉尔吉斯斯坦大多数人类感染的原因,在本研究中包括的大多数狗中也发现了该单倍型。在亚洲其他地区进行类似的进一步研究可以阐明它是否也是感染其他国家人类的最常见变体。尚不清楚这种特定的单倍型是否在毒力方面存在差异,这可能导致了吉尔吉斯斯坦泡型包虫病的爆发。在细粒棘球绦虫的情况下,似乎没有一种优势单倍型感染吉尔吉斯斯坦的人类。进一步表征优势线粒体单倍型的生物学或抗原特征可以帮助阐明它们是否存在差异,这些差异可能与感染人类时的诊断、致病性或宿主/寄生虫相互作用有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f64/7219741/64d8bac56a31/pntd.0008242.g001.jpg

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