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Detection of Ehrlichia spp. and Anaplasma phagocytophilum in whole blood specimens using a duplex real-time PCR assay on the ARIES instrument
Institution:1. EPIA, UMR 0346, Epidémiologie des maladies Animales et zoonotiques, INRA, VetAgroSup, Route de Theix, F-63122 Saint Genes Champanelle, France;2. Evolutionary Ecology Group, Department of Biology, University of Antwerp, Universiteitsplein 1, 2610, Wilrijk, Belgium;3. CEFS, UR0035, Comportement et Ecologie de la Faune Sauvage, Université de Toulouse, INRA, 24 chemin de Borde-Rouge, F-31326 Castanet-Tolosan, France;4. BIOEPAR, UMR 1300, Biologie, Epidemiologie et Analyse de Risque, INRA, UNAM Université, Oniris, Ecole Nationale Vétérinaire, Agroalimentaire et de l''Alimentation Nantes-Atlantique, Atlanpôle, la Chantrerie, F-44307, Nantes, France;5. MIVEGEC (UMR 5290), Maladie Infectieuses et Vecteurs: Ecologie, Génétique Evolution et Contrôle, Centre National de la Recherche Scientifique, Université de Montpellier, Institut de Recherche pour le Développement (UR224), 911 Avenue d''Agropolis, BP 64501, F-34394 Cedex 5, Montpellier, France
Abstract:Cases of tick-borne diseases are increasing in the United States, and new tick-borne pathogen species causing human illness are being discovered. The specific etiology is generally difficult to diagnose based on clinical signs and symptoms alone, because of their generalized nature and often lack of a known tick bite. For some infections, such as Lyme disease and spotted fever group rickettsioses, serology remains the most appropriate laboratory diagnostic tool, but for others such as anaplasmosis, ehrlichiosis, and babesiosis, direct detection in the blood is preferred for rapid diagnosis. In Kentucky, USA, the area served by our laboratory, the most commonly reported tick-borne illnesses include spotted fever group rickettsiosis, ehrlichiosis and Lyme disease, but of these three diseases, only ehrlichiosis is well-suited for direct detection using PCR methods during the acute stage of illness. We report here the validation of a duplex real-time PCR assay using whole blood specimens on the Luminex ARIES® instrument, combining DNA extraction, amplification and detection into a one-step process. This method allows for rapid and sensitive detection of acute infections with Ehrlichia spp. and Anaplasma phagocytophilum using whole blood specimens. We included A. phagocytophilum to monitor emergence of this pathogen in Kentucky, since surrounding states have reported many more cases than Kentucky.
Keywords:real-time PCR  Ehrlichiosis  Anaplasmosis  Closed-system  Whole blood
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