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An Assessment of Whole Blood and Fractions by Nested PCR as a DNA Source for Diagnosing Canine Ehrlichiosis and Anaplasmosis
Author(s) -
Tereza Emmanuelle de Farias Rotondano,
Alzira Maria Paiva de Almeida,
Elane Maria Camboim Lustosa,
Aline Antas Cordeiro,
Expedito K. A. Camboim,
Sérgio Santos de Azevêdo,
Paulo Andrade,
Márcia Almeida de Melo
Publication year - 2012
Publication title -
the scientific world journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.453
H-Index - 93
eISSN - 2356-6140
pISSN - 1537-744X
DOI - 10.1100/2012/605743
Subject(s) - ehrlichiosis , anaplasmosis , anaplasma , ehrlichia , buffy coat , nested polymerase chain reaction , ehrlichia canis , canis , anaplasma phagocytophilum , biology , virology , whole blood , babesiosis , tick borne disease , babesia , peripheral blood mononuclear cell , polymerase chain reaction , microbiology and biotechnology , immunology , tick , gene , paleontology , biochemistry , serology , borrelia burgdorferi , antibody , in vitro
Ehrlichiosis and anaplasmosis are tick-borne diseases. Ehrlichia canis and Anaplasma platys infect mainly white cells and platelets, respectively. The main DNA source for PCR is peripheral blood, but the potential of blood cell fractions has not been extensively investigated. This study aims at assessment of whole blood (WB) and blood fractions potential in nested PCR (nPCR) to diagnose canine ehrlichiosis and anaplasmosis. The 16S rRNA gene was amplified in 71.4, 17.8, 31.57, and 30% of the WB, granulocyte (G), mononuclear cells (M), and buffy coat (BC) samples. Compared to the WB, the sensitivity of the PCR was 42.86% for the M, and BC fractions, 21.43% for the G, and 33.33% for the blood clot (C). There was fair agreement between the WB and M, BC and C, and slight with the G. Fair agreement occurred between the nPCR and morulae in the blood smear. One animal was coinfected with A. platys and E. canis . This study provided the first evidence of A. platys infection in dogs in Paraíba, Brazil, and demonstrated that WB is a better DNA source than blood fractions to detect Ehrlichia and Anaplasma by nPCR, probably because of the plasma bacterial concentration following host cell lysis.

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