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Two species of Bartonella, a novel Bartonella clarridgeiae-like bacterium and B. vinsonii subsp. berkhoffii, were isolated from rural dogs and gray foxes in northern California. A novel B. clarridgeiae-like species was isolated from 3 (1.7%) of 182 dogs and 22 (42%) of 53 gray foxes, while B. vinsonii subsp. berkhoffii was isolated from 1 dog (0.5%) and 5 gray foxes (9.4%). PCR and DNA sequence analyses of the citrate synthase (gltA) gene and the 16S-23S intergenic spacer region suggested that strains infecting dogs and gray foxes were identical. Fifty-four dogs (29%) and 48 gray foxes (89%) had reciprocal titers of antibodies against Bartonella spp. of >64. The high prevalence of bacteremia and seroreactivity to Bartonella spp. in gray foxes suggests that they may act as a reservoir species for the B. clarridgeiae-like species in this region. Domestic dogs were also tested for other arthropod-borne infectious agents. Fifty-one dogs (28%) were positive for Dirofilaria immitis antigen, seventyfour (40%) were seroreactive to Anaplasma phagocytophilum, and five (2.7%) were seropositive for Yersinia pestis. Fourteen dogs (7.6%) were PCR positive for A. phagocytophilum. Polytomous logistic regression models were used to assess the association of Bartonella antibody titer categories with potential risk factors and the presence of other vector-borne agents in domestic dogs. Older dogs were more likely to be seroreactive to Bartonella spp. There was no association between the exposure of dogs to Bartonella and the exposure of dogs to A. phagocytophilum in this study.

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Livers from 4,501 deer mice (Peromyscus maniculatus) collected from a weedy habitat in northeastern California during 48 consecutive monthly samplings were examined microscopically for Taenia taeniaeformis larva. Although there were pronounced seasonal fluctuations in host density, there were no significant annual or season-related differences in cestode intensities in adult deer mice. There were no significant differences in prevalences associated with sex of the host, nor were there significant changes in level of reproduction noted between infected and non-infected hosts. There were, however, significant differences in prevalences between young (1.2%) and adult (4.2%) hosts. Plausible mechanisms for this age-related difference in prevalence rates include (1) differential susceptibility due to the activity pattern of adult mice and/or (2) passive immunity in neonates as a result of colostrum- and/or transplacentally-transferred immunoglobulins and (3) capture of subadult animals before they had completed the period of highest susceptibility to T. taeniaeformis. Density of larvae per mouse liver was determined during a 21 mo consecutive period. The intensity of T. taeniaeformis larvae was not significantly different between the sexes of the adult mice. The larval stage showed an overdispersion pattern within the adult population. These results suggest that determinations of T. taeniaeformis abundances can be accurately made, at least in this P. maniculatus population, at any time of the year provided adjustment is made for the relative age structure of the host population.

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