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Serological reactivity to Anaplasma phagocytophilum in neoehrlichiosis patients
Authors:Linda Wass  Anna Grankvist  Mattias Mattsson  Helena Gustafsson  Karen Krogfelt  Björn Olsen  Kenneth Nilsson  Andreas Mårtensson  Hanne Quarsten  Anna J. Henningsson  Christine Wennerås
Affiliation:1.Department of Infectious Diseases, Sahlgrenska Academy,University of Gothenburg,G?teborg,Sweden;2.Department of Hematology,Uppsala University Hospital,Uppsala,Sweden;3.Department of Hematology,G?vle Hospital,G?vle,Sweden;4.Department of Bacteria, Parasites and Fungi,Statens Serum Institut,Copenhagen,Denmark;5.Section of Clinical Microbiology and Infectious Diseases, Department of Medical Sciences,Uppsala University,Uppsala,Sweden;6.Department of Women’s and Children’s Health, International Maternal and Child Health,Uppsala University,Uppsala,Sweden;7.Department of Medical Microbiology,S?rlandet Hospital Health Enterprise,Kristiansand,Norway;8.Department of Clinical Microbiology,County Hospital Ryhov,J?nk?ping,Sweden;9.Department of Clinical Microbiology,Sahlgrenska University Hospital,G?teborg,Sweden
Abstract:
The tick-borne bacterium Candidatus (Ca.) Neoehrlichia (N.) mikurensis is a cause of “fever of unknown origin” because this strict intracellular pathogen escapes detection by routine blood cultures. Case reports suggest that neoehrlichiosis patients may display serological reactivity to Anaplasma (A.) phagocytophilum. Since Anaplasma serology is part of the diagnostic work-up of undetermined fever in European tick-exposed patients, we wanted to investigate (1) the prevalence of A. phagocytophilum seropositivity among neoehrlichiosis patients, (2) the frequency of misdiagnosed neoehrlichiosis patients among A. phagocytophilum seropositive patients, and (3) the frequency of A. phagocytophilum and Ca. N. mikurensis co-infections. Neoehrlichiosis patients (n?=?18) were analyzed for A. phagocytophilum IgM and IgG serum antibodies by indirect immunofluorescence assay. Serum samples from suspected anaplasmosis patients (n?=?101) were analyzed for bacterial DNA contents by singleplex PCR specific for A. phagocytophilum and Ca. N. mikurensis, respectively. One fifth of the neoehrlichiosis patients (4/18) were seropositive for IgM and/or IgG to A. phagocytophilum at the time of diagnosis. Among the patients with suspected anaplasmosis, 2% (2/101) were positive for Ca. N. mikurensis by PCR whereas none (0/101) had detectable A. phagocytophilum DNA in the serum. To conclude, patients with suspected anaplasmosis may in fact have neoehrlichiosis. We found no evidence of A. phagocytophilum and Ca. N. mikurensis co-infections in humans with suspected anaplasmosis or confirmed neoehrlichiosis.
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