4.1 Article

SEASONAL PREVALENCE OF SERUM ANTIBODIES TO WHOLE CELL AND RECOMBINANT ANTIGENS OF BORRELIA BURGDORFERI AND ANAPLASMA PHAGOCYTOPHILUM IN WHITE-TAILED DEER IN CONNECTICUT

Journal

JOURNAL OF WILDLIFE DISEASES
Volume 46, Issue 3, Pages 781-790

Publisher

WILDLIFE DISEASE ASSOC, INC
DOI: 10.7589/0090-3558-46.3.781

Keywords

Anaplasma phagocytophilum; antibodies; Borrelia burgdorferi; ELISA; Odocoileus virginianus

Funding

  1. United States Department of Agriculture

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Whole-blood samples were obtained from 214 white-tailed deer (Odocoileus virginianus) representing 44 sites in Connecticut (USA) during 1992, 1993, 1996, 1999, and 2000 through 2006 Sera were analyzed for total antibodies to whole-cell or recombinant antigens of Borrelia burgdorferi sensu strict and Anaplasma phagocytophilum, the respective causative agents of Lyme borreliosis and human granulocytic anaplasmosis Deer sent contained antibodies to both bacteria (hiring different seasons and throughout the 11-yr study Of the 224 sera tested, 141 (63%) contained antibodies to whole-cell B burgdorferi in a polyvalent enzyme-linked immunosorbent assay, whereas 124 (55%) were positive to whole-cell A phagocytophilum by indirect fluorescent antibody staining Use of highly specific recombinant antigens (VIsE of B burgdorferi and protein 44 of A phagocytophilum) provided strong confirmatory results of past or current in There was coexistence of antibodies to whole-cell or recombinant antigens of both agents in 72 (32%) sera Analyses of 18 sera from eight deer that were marked, released, and recaptured, showed minimal changes in antibody titer over sampling tune Intervals ranging from 17 clays to 5.1 yr. Relatively high antibody prevalences fir both bacterial agents in different seasons and years reaffirm that there are well-established foci for both tick-borne infections and probably reflect frequent exposure of deer to infected Ixodes scapularis ticks November and December is a suitable: period to obtain blood samples from deer to conduct serosurveillance for both bacteria.

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