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2019 年和 2020 年西澳大利亚的隐孢子虫病病例的分子分析支持了两起与游泳池相关的暴发的发生,并揭示了一种罕见的 C. hominis IbA12G3 亚型的出现。

Molecular analysis of cryptosporidiosis cases in Western Australia in 2019 and 2020 supports the occurrence of two swimming pool associated outbreaks and reveals the emergence of a rare C. hominis IbA12G3 subtype.

机构信息

Centre for Biosecurity and One Health, Harry Butler Institute, Murdoch University, Perth, Western Australia 6150, Australia.

Centre for Biosecurity and One Health, Harry Butler Institute, Murdoch University, Perth, Western Australia 6150, Australia.

出版信息

Infect Genet Evol. 2021 Aug;92:104859. doi: 10.1016/j.meegid.2021.104859. Epub 2021 Apr 10.

DOI:10.1016/j.meegid.2021.104859
PMID:33848684
Abstract

Cryptosporidium is an important protozoan parasite and due to its resistance to chlorine is a major cause of swimming pool-associated gastroenteritis outbreaks. The present study combined contact tracing and molecular techniques to analyse cryptosporidiosis cases and outbreaks in Western Australia in 2019 and 2020. In the 2019 outbreak, subtyping at the 60 kDa glycoprotein (gp60) gene identified 89.0% (16/18) of samples were caused by the C. hominis IdA15G1 subtype. Amplicon next generation sequencing (NGS) at the gp60 locus identified five C. hominis IdA15G1 subtype samples that also had C. hominis IdA14 subtype DNA, while multi locus sequence typing (MLST) analysis on a subset (n = 14) of C. hominis samples identified three IdA15G1 samples with a 6 bp insertion at the end of the trinucleotide repeat region of the cp47 gene. In 2020, 88.0% (73/83) of samples typed were caused by the relatively rare C. hominis subtype IbA12G3. Four mixed infections were observed by NGS with three IdA15G1/ IdA14 mixtures and one C. parvum IIaA18G3R1 sample mixed with IIaA16G3R1. No genetic diversity using MLST was detected. Epidemiological and molecular data indicates that the outbreaks in 2019 and 2020 were each potentially from swimming pool point sources and a new C. hominis subtype IbA12G3 is emerging in Australia. The findings of the present study are important for understanding the introduction and transmission of rare Cryptosporidium subtypes to vulnerable populations.

摘要

隐孢子虫是一种重要的原生动物寄生虫,由于其对氯的抵抗力,是导致游泳池相关肠胃炎爆发的主要原因。本研究结合接触者追踪和分子技术,分析了 2019 年和 2020 年西澳大利亚的隐孢子虫病病例和爆发。在 2019 年的爆发中,在 60kDa 糖蛋白 (gp60) 基因上的亚分型鉴定出 89.0%(16/18)的样本是由 C. hominis IdA15G1 亚型引起的。在 gp60 基因座上的扩增子下一代测序 (NGS) 鉴定出五个 C. hominis IdA15G1 亚型样本也具有 C. hominis IdA14 亚型 DNA,而在一小部分 (n=14) C. hominis 样本的多基因序列分型 (MLST) 分析中鉴定出三个 IdA15G1 样本在 cp47 基因三核苷酸重复区的末端有 6bp 插入。2020 年,88.0%(73/83)分型的样本是由相对罕见的 C. hominis 亚型 IbA12G3 引起的。通过 NGS 观察到四例混合感染,其中三例为 IdA15G1/IdA14 混合物,一例 C. parvum IIaA18G3R1 样本与 IIaA16G3R1 混合。未检测到 MLST 的遗传多样性。流行病学和分子数据表明,2019 年和 2020 年的爆发均可能来自游泳池的点源,一种新的澳大利亚 C. hominis 亚型 IbA12G3 正在出现。本研究的结果对于了解稀有隐孢子虫亚型对弱势群体的传入和传播非常重要。

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