与传统显微镜相比,多重qPCR技术对肠道原生动物诊断的改善:一项对3500份粪便样本为期3年的前瞻性研究

IF 6.1 2区 医学 Q1 MICROBIOLOGY
Journal of Clinical Microbiology Pub Date : 2025-05-14 Epub Date: 2025-03-31 DOI:10.1128/jcm.01610-24
Florence Robert-Gangneux, Xavier Duval, Clément Cazala, Sorya Belaz, Anne Dupuis, Hélène Guegan, Brice Autier, Jean-Pierre Gangneux
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引用次数: 0

摘要

商业多重实时聚合酶链式反应(qPCR)目前广泛用于肠道原生动物感染的诊断,但很少有前瞻性研究评估其在大型患者队列中的表现。我们从信息系统中提取了2021年1月1日至2024年3月15日的数据,并纳入了常规分析的所有粪便样本。采用多重PCR (AllPlex胃肠道面板试验,Seegene)和镜检两种浓缩方法进行寄生虫搜索。当特别要求隐孢子虫检测时,进行抗酸染色。总共分析了来自2127名患者的3495个粪便。经多重qPCR检测,分别在45份(1.28%)、30份(0.85%)、9份(0.25%)、310份(8.86%)、673份(19.25%)样本中检出肠贾第虫、隐孢子虫、溶组织内阿米巴、脆弱地阿米巴和囊胚虫中检出单株(n = 909)。在绝大多数情况下,PCR在第一个粪便样本上检测到一种原生动物。镜检结果分别为25份(0.7%)、8份(0.23%)、24份(0.68%)、22份(0.63%)、229份(6.55%),分别为肠道隐孢子虫、溶组织内阿米巴和囊虫。大肠弧菌、隐孢子虫和溶组织弧菌均未检出PCR-/显微镜+,而脆弱弧菌和囊胚弧菌分别在6份和20份样品中检出。显微镜下可以检测到未被多重靶板靶向的寄生虫(5个囊虫异孢子虫,331个非致病性原生动物样本,68个蠕虫样本)。总的来说,多重PCR被证明对检测原生动物寄生虫更有效,但当怀疑感染了贝利梭菌(hiv感染者)或蠕虫(迁移者和旅行者)时,应该采用显微技术。在越来越多地使用多重PCR检测板诊断肠道原生动物感染的时代,对这些检测在实验室工作流程中的定位形成意见是很重要的。本研究分析了3年来通过显微镜和商业多重PCR获得的常规结果,并表明该方法符合临床实验室检测医学感兴趣的原生动物寄生虫的期望。这是回顾belli囊异孢子虫不是目标的多重试验,显微镜仍然是必要的,以检测蠕虫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improvement of the diagnosis of intestinal protozoa using a multiplex qPCR strategy compared to classical microscopy: a prospective study on 3,500 stool samples over 3 years.

Commercial multiplex real-time PCR (qPCR assays) are now widely used for the diagnosis of intestinal protozoan infections, but few prospective studies evaluated their performances on large patient cohorts. We extracted data from our information system from 1 January 2021 to 15 March 2024 and included all stool samples analyzed in routine. Parasites were searched using a multiplex PCR (AllPlex Gastrointestinal Panel assay, Seegene) and microscopic examination with two concentration methods. Acid-fast staining was performed when Cryptosporidium detection was specifically requested. In total, 3,495 stools were analyzed from 2,127 patients. Giardia intestinalis, Cryptosporidium spp., Entamoeba histolytica, Dientamoeba fragilis, and Blastocystis spp. were found by multiplex qPCR in 45 (1.28%), 30 (0.85%), 9 (0.25%), 310 (8.86%), and 673 (19.25%) samples, respectively, alone or in combination (n = 909). In the vast majority of cases, PCR detected a protozoan on the first stool sample. Microscopy was positive for G. intestinalis, Cryptosporidium spp., Entamoeba histolytica/dispar, D. fragilis, and Blastocystis spp. in 25 (0.7%), 8 (0.23%), 24 (0.68%), 22 (0.63%), and 229 (6.55%), samples, respectively, alone or in combination (n = 286 samples). No samples were PCR-/Microscopy+ for G. intestinalis, Cryptosporidium spp., and E. histolytica, while D. fragilis and Blastocystis spp. were detected only with microscopy in 6 and 20 samples, respectively. Microscopy allowed the detection of parasites not targeted by the multiplex panel (5 Cystoisospora belli, 331 samples with non-pathogenic protozoa, and 68 samples with helminths). Overall, the multiplex PCR proved more efficient to detect protozoan parasites, but a microscopic technique should be performed when infection with C. belli (HIV-infected patients) or helminths is suspected (migrants and travelers).IMPORTANCEIn the era of increasing use of multiplex PCR panels for the diagnosis of intestinal protozoan infections, it is important to form an opinion on the positioning of those assays within a lab workflow. This study analyzes routine results obtained prospectively by microscopy and a commercial multiplex PCR over 3 years, and shows that the assay meets the expectations of a clinical laboratory for the detection of protozoan parasites of medical interest. It is recalled that Cystoisospora belli is not targeted by the multiplex assay, and that microscopy still remains necessary to detect helminths.

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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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