冠状病毒病COVID-19大流行导致苏格兰人类隐孢子虫病病例分子谱的变化

IF 2.7 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY British Journal of Biomedical Science Pub Date : 2023-01-01 DOI:10.3389/bjbs.2023.11462
Ross Bacchetti, Lisa Connelly, Lynda Browning, Claire L Alexander
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引用次数: 1

摘要

隐孢子虫是苏格兰最常见的寄生虫,会引起胃肠道疾病,导致腹泻、恶心和痉挛。大多数病例由两种细菌引起:人隐孢子虫(隐孢子虫)和细小隐孢子虫(隐孢子虫)。传播发生口粪,通过摄入受污染的食物和水,或直接接触粪便。2020年,COVID-19大流行导致全球限制措施,包括国家封锁以限制病毒传播。这些干预措施导致社会混合减少,减少或没有本地和国际旅行,这些都是与隐孢子虫病等多种传染病传播有关的因素。本报告评估了大流行对苏格兰隐孢子虫病病例的影响,并确定了隐孢子虫物种循环分子变异的变化。对2018- 2022年报告的实验室确诊隐孢子虫病病例进行实时PCR和GP60巢式PCR分析。格拉斯哥的苏格兰微生物参考实验室(SMiRL)在2018-22年期间收到了774份隐孢子虫阳性粪便,其中486份样本成功分型。在这段时间内,人原锥虫(n = 155;21%)和小弧菌(n = 572;77%)是最常检出的种类。与2020年前后两年的病例数相比,受大流行严重影响的2020年期间的病例总数明显减少。在2020年之前检测到的最占优势的人族是Ib家族,在2022年转移到Ie家族。2018- 2022年期间,最常见的小梭菌变体是IIa家族,但IId家族的数量有所增加(2018年n = 6, 2022年n = 25)。在2018-19年占71%的占优势的人原体亚型IbA10G2,到2022年被3个罕见亚型IeA11G3T3 (n = 15)、IdA16 (n = 8)和IbA9G3 (n = 3)所取代。2018-19年度报告较多的小恙虫亚型为IIaA15G2R1和IIaA17G1R1,占小恙虫亚型总数的59%。到2022年,IIaA15G2R1仍然是最常见的(n = 28),但在苏格兰出现了三种不寻常的亚型:IIdA24G1 (n = 7), IIaA16G3R1 (n = 7)和IIaA15G1R2 (n = 7)。大流行后持续监测隐孢子虫变异对于探索毒力改变的菌株的进一步变化和出现至关重要。
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Changing Molecular Profiles of Human Cryptosporidiosis Cases in Scotland as a Result of the Coronavirus Disease, COVID-19 Pandemic.

Cryptosporidium, the most frequently reported parasite in Scotland, causes gastrointestinal illness resulting in diarrhoea, nausea and cramps. Two species are responsible for most cases: Cryptosporidium hominis (C. hominis) and Cryptosporidium parvum (C. parvum). Transmission occurs faecal-orally, through ingestion of contaminated food and water, or direct contact with faeces. In 2020, the COVID-19 pandemic led to global restrictions, including national lockdowns to limit viral transmission. Such interventions led to decreased social mixing, and reduced/no local and international travel, which are factors associated with transmission of multiple communicable diseases, including cryptosporidiosis. This report assessed the impact of the pandemic on Scottish cryptosporidiosis cases, and identified changes in circulating molecular variants of Cryptosporidium species. Molecular data generated using real time PCR and GP60 nested-PCR assays on laboratory-confirmed cryptosporidiosis cases reported during 2018-22 were analysed. The Scottish Microbiology Reference Laboratories (SMiRL), Glasgow, received 774 Cryptosporidium-positive faeces during 2018-22, of which 486 samples were successfully subtyped. During this time period, C. hominis (n = 155; 21%) and C. parvum (n = 572; 77%) were the most commonly detected species. The total number of cases during 2020, which was greatly affected by the pandemic, was markedly lower in comparison to case numbers in the 2 years before and after 2020. The most predominant C. hominis family detected prior to 2020 was the Ib family which shifted to the Ie family during 2022. The most common C. parvum variant during 2018-22 was the IIa family, however a rise in the IId family was observed (n = 6 in 2018 to n = 25 in 2022). The dominant C. hominis subtype IbA10G2, which accounted for 71% of C. hominis subtypes in 2018-19 was superseded by three rare subtypes: IeA11G3T3 (n = 15), IdA16 (n = 8) and IbA9G3 (n = 3) by 2022. Frequently reported C. parvum subtypes in 2018-19 were IIaA15G2R1 and IIaA17G1R1, accounting for 59% of total C. parvum subtypes. By 2022, IIaA15G2R1 remained the most common (n = 28), however three unusual subtypes in Scotland emerged: IIdA24G1 (n = 7), IIaA16G3R1 (n = 7) and IIaA15G1R2 (n = 7). Continuous monitoring of Cryptosporidium variants following the pandemic will be essential to explore further changes and emergence of strains with altered virulence.

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来源期刊
British Journal of Biomedical Science
British Journal of Biomedical Science 医学-医学实验技术
CiteScore
4.40
自引率
15.80%
发文量
29
审稿时长
>12 weeks
期刊介绍: The British Journal of Biomedical Science is committed to publishing high quality original research that represents a clear advance in the practice of biomedical science, and reviews that summarise recent advances in the field of biomedical science. The overall aim of the Journal is to provide a platform for the dissemination of new and innovative information on the diagnosis and management of disease that is valuable to the practicing laboratory scientist.
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