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Radiolabeled Borrelia burgdorferi, the etiologic agent of Lyme disease, injected intravenously into rats are cleared from the vasculature within 1 h of injection. One low passage isolate showed trafficking between the circulation and possibly the vessel walls for the first 2 h after injection. All strains used were resistant to the effects of normal and heat-inactivated rat serum. During the first 2 h after injection, B. burgdorferi can be visualized in, and recovered from, the platelet-rich plasma. B. burgdorferi can adhere to both human and rat platelets in in vitro assays, but an in vivo association with these cells was not apparent. Similarly, none of the strains of B. burgdorferi used induced platelet aggregation. Removal from the circulation into the organs was measured in perfused rats by polymerase chain reaction and autoradiography and in non-perfused rats by organ cultures. These organisms invade organs (heart, kidneys, bladder, liver, spleen, brain) within 1-6 h after injection. Invasion of organs occurred in an apparent random manner; a large amount of radiolabel but no live organisms was excreted in the urine during the first 24 h, suggesting degradation of the inoculum.

The house mouse (laboratory strain), Mus musculus (L.), the cotton mouse, Peromyscus gossypinus (LeConte), the broad-headed skink, Eumeces laticeps (Schneider), and the guinea pig, Cavia porcellus (L.), were successively infested five times with larvae of the blacklegged tick, Ixodes scapularis Say. Tick feeding success, engorgement weight, and subsequent molting success were measured after each infestation. A greater percentage of ticks (P less than 0.05) fed on M. musculus and E. laticeps than on P. gossypinus or C. porcellus. P. gossypinus expressed a transitory partial resistance, measured in percentage of ticks feeding, during the third infestation but showed increased tolerance during the fourth and fifth infestations. Ticks fed on E. laticeps were heavier than those fed on any other host (P less than 0.05). Those fed on M. musculus were heavier than those fed on P. gossypinus, but the difference was not statistically significant. On C. porcellus, only 1.6% of larvae from the third infestation and none thereafter engorged; weights of larvae from first and second infestations were higher (P less than 0.05) than those fed on M. musculus and P. gossypinus and lower (P less than 0.05) than those fed on E. laticeps. A greater percentage of larvae from E. latticeps and M. musculus (P less than 0.05) molted to nymphs compared with those from P. gossypinus and C. porcellus. Molting success was the same for ticks fed on P. gossypinus and on C. porcellus during the first and second infestations. M. musculus, P. gossypinus, and E. laticeps expressed no resistance (measured as percentage feeding, engorgement weight, and molting) to feeding by I. scapularis larvae after five infestations. Host serum was tested using an ELISA for detection of antibodies against I. scapularis salivary gland antigens before and after each infestation. Antibodies were detected after the second infestation and thereafter in C. porcellus, the only species to show antibodies or to express and maintain an acquired resistance to tick feeding throughout five infestations.

Background: The characteristics of a Spanish strain of Borrelia burgdorferi, the spirochete which causes Lyme's disease, and which, up to the present, has not been isolated in Spain, are described., Methods: The organism was obtained from ticks (Ixodes ricinus) from the northern part of Spain. It was studied in culture by dark field microscopy and the internal structure observed by electron transmission. The antigenic composition was analyzed under polyacrylamide electrophoresis, immunoblot and reactivity against monoclonal antibodies. Plasmid analysis was carried out by Southern blot., Results: In culture the length of the organism is somewhat shorter than normal. It grows slowly and tends to autoagglutinate. It has 6-13 periplasmic flagella. The antigenic analysis of this microorganism through immunoblot and reactivity against different monoclonal antibodies showed differences with regards to other North American strains, with the most significant being the composition of certain proteins of the surface of the organism. These differences may have clinical repercussion. DNA analysis by Southern blot demonstrated slight differences in regard to the composition of plasmids compared to other strains analyzed., Conclusions: Borrelia burgdorferi exists in Spain. The isolated strain shows peculiar characteristics with respect to others analyzed. The availability of an autochthonous strain may allow more reliable serological diagnosis in Spain.