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猪隐孢子虫 gp60 基因全序列分析揭示一种新型串联重复序列—对监测的启示。

Complete sequencing of the Cryptosporidium suis gp60 gene reveals a novel type of tandem repeats-Implications for surveillance.

机构信息

Sjöbjörnsvägen, (formerly at the Department of Microbiology, Public Health Agency of Sweden, Solna, Sweden), Stockholm, Sweden.

European Programme for Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden; Laboratory of Parasitology, Department of Bacteria, Parasites and Fungi, Statens Serum Institut, Copenhagen S, Denmark.

出版信息

Infect Genet Evol. 2024 Aug;122:105614. doi: 10.1016/j.meegid.2024.105614. Epub 2024 Jun 4.

DOI:10.1016/j.meegid.2024.105614
PMID:38844191
Abstract

Cryptosporidiosis is an infectious enteric disease caused by species (some of them zoonotic) of the genus Cryptosporidium that in many countries are under surveillance. Typing assays critical to the surveillance of cryptosporidiosis typically involve characterization of Cryptosporidium glycoprotein 60 genes (gp60). Here, we characterized the gp60 of Cryptosporidium suis from two samples-a human and a porcine faecal sample-based on which a preliminary typing scheme was developed. A conspicuous feature of the C. suis gp60 was a novel type of tandem repeats located in the 5' end of the gene and that took up 777/1635 bp (48%) of the gene. The C. suis gp60 lacked the classical poly-serine repeats (TCA/TCG/TCT), which is usually subject to major genetic variation, and the length of the tandem repeat made a typing assay incorporating this region based on Sanger sequencing practically unfeasible. We therefore designed a typing assay based on the post-repeat region only and applied it to C. suis-positive samples from suid hosts from Norway, Denmark, and Spain. We were able to distinguish three different subtypes; XXVa-1, XXVa-2, and XXVa-3. Subtype XXVa-1 had a wider geographic distribution than the other subtypes and was also observed in the human sample. We think that the present data will inform future strategies to develop a C. suis typing assay that could be even more informative by including a greater part of the gene, including the tandem repeat region, e.g., by the use of long-read next-generation sequencing.

摘要

隐孢子虫病是一种由隐孢子虫属(其中一些是动物源的)引起的传染性肠道疾病,在许多国家都在进行监测。对隐孢子虫病进行监测的关键分型检测通常涉及到对隐孢子虫糖蛋白 60 基因(gp60)的特征描述。在这里,我们根据从人类和猪粪便样本中分离出的两株隐孢子虫属的 gp60 进行了特征描述,并基于此建立了一个初步的分型方案。猪隐孢子虫 gp60 的一个显著特征是在基因的 5'端存在一种新型串联重复序列,该序列占据了基因的 777/1635bp(48%)。猪隐孢子虫 gp60 缺乏经典的多丝氨酸重复序列(TCA/TCG/TCT),该序列通常会发生较大的遗传变异,而且串联重复序列的长度使得基于 Sanger 测序的该区域的分型检测变得几乎不可行。因此,我们设计了一种仅基于重复后区域的分型检测方法,并将其应用于来自挪威、丹麦和西班牙的猪宿主的隐孢子虫阳性样本。我们能够区分出三种不同的亚型:XXVa-1、XXVa-2 和 XXVa-3。XXVa-1 亚型的地理分布范围比其他亚型更广,也在人类样本中观察到。我们认为,目前的数据将为未来开发更具信息性的猪隐孢子虫分型检测方法提供信息,包括更大部分的基因,例如通过使用长读长下一代测序技术包括串联重复区。

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