Department of Infectious Diseases, Austin Health, Heidelberg, Australia.
Department of Microbiology, Austin Health, Heidelberg, Australia.
Am J Trop Med Hyg. 2020 Nov;103(5):1930-1933. doi: 10.4269/ajtmh.19-0841.
There has been increased interest in using metagenomic next-generation sequencing as an unbiased approach for diagnosing infectious diseases. We describe a 61-year-old man on fingolimod therapy for multiple sclerosis with an extensive travel history who presented with 7 months of fevers, night sweats, and weight loss. Peripheral blood tests showed pancytopenia and abnormal acute phase reactants. A bone marrow aspirate showed the presence of numerous intracellular and extracellular amastigotes consistent with visceral leishmaniasis (VL). Metagenomic sequencing of the bone marrow aspirate confirmed , a species widely reported in the Mediterranean region. This correlated with acquisition of VL infection during the patient's most recent epidemiological exposure in southern Italy 12 months prior. This case demonstrates the potential application of metagenomic sequencing for identification and speciation of in cases of VL; however, further assessment is required using other more readily obtained clinical samples such as blood.
人们越来越感兴趣地使用宏基因组下一代测序作为一种用于诊断传染病的无偏方法。我们描述了一名 61 岁的多发性硬化症患者,他接受了 fingolimod 治疗,并有广泛的旅行史,他出现了 7 个月的发热、盗汗和体重减轻。外周血检查显示全血细胞减少和异常的急性期反应物。骨髓抽吸显示存在大量细胞内和细胞外无鞭毛体,符合内脏利什曼病(VL)。骨髓抽吸物的宏基因组测序证实了 ,这是在地中海地区广泛报道的物种。这与患者在 12 个月前最近在意大利南部的流行病学暴露期间获得的 VL 感染有关。该病例证明了宏基因组测序在 VL 病例中用于鉴定和种属鉴定的潜在应用;然而,需要使用其他更容易获得的临床样本(如血液)进行进一步评估。
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