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Development and Clinical Validation of a Multiplex Real-Time Quantitative PCR Assay for Human Infection by Anaplasma phagocytophilum and Ehrlichia chaffeensis

机译:噬菌体和查菲埃里希氏菌感染人类的​​多重实时定量PCR分析方法的开发和临床验证

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摘要

Background: Human granulocytic anaplasmosis (HGA), caused by Anaplasma phagocytophilum, and human monocytic ehrlichiosis (HME), caused by Ehrlichia chaffeensis, often present as undifferentiated fever but are not treated by typical empiric regimens for acute febrile illness. Their role as agents of vector-borne febrile disease in tropical regions is more poorly studied than for other rickettsial infections. Limitations in diagnosis have impaired epidemiologic and clinical research and needless morbidity and mortality occur due to untreated illness. Methods: We designed and clinically validated a multiplex real-time quantitative PCR assay for Anaplasma phagocytophilum and Ehrlichia chaffeensis using samples confirmed by multiple gold-standard methods. Results: Clinical sensitivity and specificity for A. phagocytophilum were 100% (39/39) and 100% (143/143), respectively, and for E. chaffeensis 95% (20/21) and 99% (159/161), respectively. Conclusions: These assays could support early diagnosis and treatment as well as the high-throughput testing required for large epidemiologic studies.
机译:背景:由吞噬性无浆细胞引起的人粒细胞无性病(HGA)和由恰菲埃里希氏菌引起的人单核细胞埃希氏菌病(HME)通常表现为未分化的发热,但未经典型的急性发热疾病的经验疗法治疗。在热带地区,它们作为媒介传播的高热病病原体的作用比对其他立克次氏体感染的研究更差。诊断的局限性削弱了流行病学和临床研究,并且由于未治疗的疾病而导致不必要的发病率和死亡率。方法:我们使用多种金标准方法确认的样品,设计并临床验证了吞噬性无胞浆菌和恰菲埃里希氏菌的多重实时定量PCR检测方法。结果:对吞噬链球菌的临床敏感性和特异性分别为100%(39/39)和100%(143/143),而对恰菲大肠杆菌的95%(20/21)和99%(159/161),分别。结论:这些检测方法可以支持早期诊断和治疗以及大型流行病学研究所需的高通量检测。

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