“…The sera were assayed by microimmunofluorescence for IgM, IgG and, sometimes, IgA against a large panel of antigens, comprising Rickettsia typhi, C. burnetii, Rickettsia felis, R. helvetica, R. conorii, Rickettsia israeli, R. africae, Rickettsia sibirica mongolotimonae, Rickettsia massiliae, R. slovaca, F. tularensis, Bartonella henselae, and Bartonella quintana, at the WHO Collaborative Centre for Rickettsial Research (Marseille, France), as described previously [9]. When cross-reacting antibodies with a titre > 1:64 prevented identification of the infecting agent, cross-adsorption was performed using either R. helvetica or R. conori antigens.…”