Western immunoblot analysis of the antigens of Haemobartonella felis with sera from experimentally infected cats

Cats were experimentally infected with a Florida isolate of Haemobartonella felis in order to collect organisms and evaluate the immune response to H. felis. Cryopreserved organisms were thawed and injected intravenously into nonsplenectomized and splenectomized cats. Splenectomized animals H ere gi, en 10 mg of methylprednisolone per mi at the time of inoculation. Blood firms were evaluated daily for I week prior to infection and for up to 60 days postinfection (p.i.). Blood for H. felis purification was repeatedly collected from splenectomized animals at periods of peak parasitemias. Organisms were purified from infected blood by differential centrifugation, separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. and transferred to nitrocellulose membranes for immunoblot analysis. Serum was collected from nonsplenectomized animals prior to and for up to 60 days p.i. and was used on immunoblots to identify antigens. The combination of splenectomy and corticosteroid treatment resulted in marked? cyclic parasitemias without concurrent severe anemia, providing an opportunity to harvest organisms in a manner that Has not lethal to the animals. Several antigens (150, 52, 47, 45, and IJ kDa) were identified. An antigen with a molecular mass of approximately 14 kDa appeared to be one of the most immunodominant and was consistently recognized by immune sera collected at various times during the course of infection. These data suggest that one or more of these antigens might be useful for the serologic diagnosis of H. felis infections in cats.