| Literature DB >> 32959759 |
Eloise Williams1,2, Nicole S Isles3, Torsten Seemann3, Trevor Kilpatrick4,5,6, Andrew Grigg7, Marcel Leroi2,1, Benjamin P Howden3,1, Jason C Kwong3,1.
Abstract
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 Leishmania infantum, 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 Leishmania in cases of VL; however, further assessment is required using other more readily obtained clinical samples such as blood.Entities:
Mesh:
Year: 2020 PMID: 32959759 PMCID: PMC7646797 DOI: 10.4269/ajtmh.19-0841
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345