开发新型广谱泛属 PCR 检测方法,用于检测 Tropheryma 物种。

Florian Tagini, Mhedi Belkoniene, Katia Jaton, Onya Opota, Gilbert Greub
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摘要

简介Tropheryma whipplei 是经典惠普尔病的元凶。最近,在一名患有胸膜炎的比利时免疫力低下患者身上发现了一种新的Tropheryma。目前还没有一种特异性分子诊断测试能检测出除惠普尔病热带真菌以外的其他热带真菌。开发并验证两种可同时检测白喉螺菌和新螺菌的广谱螺菌属 PCR。根据比利时受试者肺组织活检的枪弹测序数据,我们设计了两种针对 23S rRNA 和 rnpB 基因的 PCR。2019年1月至2022年11月期间,我们使用T. whipplei特异性PCR和两种Tropheryma广谱PCR对申请进行了前瞻性检测。共有 2605 份样本同时使用泛 Tropheryma 23S rRNA PCR 和 T. whipplei 特异性 PCR 进行了检测。此外,2605 个样本中还有 833 个样本也使用了全托博氏菌 rnpB PCR 进行了检测。与物种特异性 T. whipplei PCR 相比,23S rRNA 和 rnpB PCR 的灵敏度分别为 78.8%和 79.7%。23S rRNA 和 rnpB PCR 的特异性分别为 99.9% 和 99.7%。我们发现一名患者的支气管肺泡灌洗液经两种广谱 PCR 检测呈阳性,拷贝数大于 105 ml-1。特异性 T. whipplei PCR 呈阴性。这名 49 岁的男性因患泛葡萄膜炎而复发眼部炎症,CT 扫描显示多发性纵隔-肺泡坏死性腺病。多西环素(1 年)、羟氯喹(1 年)和联合三唑醇(1 个月)治疗后,患者病情好转。特异性 T. whipplei PCR 的灵敏度高于泛螺旋体 PCR。然而,这两种广谱丙种球蛋白PCR都表现出极好的特异性,在确定另一物种感染丙种球蛋白的新病例中发挥了关键作用。
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Development of novel broad-range pan-genus PCR assays for the detection of Tropheryma species.

Introduction. Tropheryma whipplei is responsible for the classical Whipple's disease. Recently, a new Tropheryma species was described in a Belgian immunocompromised patient with pleuritis.Gap Statement. There is currently no specific molecular diagnostic test detecting other Tropheryma species than Tropheryma whipplei.Aim. To develop and validate two broad-range pan-Tropheryma genus PCRs detecting both T. whipplei and new Tropheryma species.Methodology. From shotgun sequencing data of the lung tissue biopsy of the Belgian subject, we designed two PCRs targeting the 23S rRNA and rnpB genes. Prospectively, requests for T. whipplei PCR were tested with T. whipplei-specific PCRs and the two Tropheryma broad-range PCRs from January 2019 to November 2022.Results. In total, 2605 samples were tested using both the pan-Tropheryma 23S rRNA PCR and the T. whipplei-specific PCR. In addition, 833 of the 2605 samples were also tested using the pan-Tropheryma rnpB PCRs. Sensitivity was 78.8% and 79.7% for 23S rRNA and rnpB PCRs, as compared with the species-specific T. whipplei PCR. Specificity was 99.9% and 99.7% for the 23S rRNA and the rnpB PCRs, respectively. We identified a patient whose bronchoalveolar lavage tested positive with the two broad-range PCRs with >105 copies ml-1. Specific T. whipplei PCRs were negative. Known for panuveitis, this 49-year-old male presented with an eye inflammation recurrence, and a CT scan showed multiple mediastino-hilar necrotic adenopathies. Doxycyclin (1 year), hydroxychloroquin (1 year) and co-trimoxazol (1 month) treatments led to a favourable outcome.Conclusion. Specific T. whipplei PCR exhibited better sensitivity than the pan-Tropheryma PCRs. However, both broad-range pan-Tropheryma PCRs demonstrated excellent specificity and were pivotal to identifying a new probable case of Tropheryma infection due to another species-level lineage.

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