Homogeneity of characteristics of Pasteurella multocida isolated from turkeys and wildlife in California, 1985-88

Five hundred twenty isolates of Pasteurella multocida, collected in California from September 1985 to November 1988, were characterized in the laboratory. Characteristics examined included serotype, capsular type, biotype (subspecies), and possession of plasmid DNA. Three hundred thirty-three isolates recovered from turkeys dying from fowl cholera, 88 isolates from liver turkeys in flocks with fowl cholera outbreaks in the recent past, and 99 isolates from wildlife captured on fowl cholera-outbreak and non-outbreak turkey premises were studied in this manner. Characteristics were fairly homogeneous among isolates, especially those obtained from turkeys. The majority of isolates were serotype 3,4, capsular type A, subspecies multocida, and lacked plasmid DNA. Common serotypes of isolates from turkeys and wildlife sampled on the same premises were noted in eight of 13 cases examined.     

Morphology, gas exchange, and chlorophyll content of longleaf pine seedlings in response to rooting volume, copper root pruning, and nitrogen supply in a container nursery

Few pine species develop a seedling grass stage; this growth phase, characterized by strong, carrot-like taproots and a stem-less nature, poses unique challenges during nursery production. Fertilization levels beyond optimum could result in excessive diameter growth that reduces seedling quality as measured by the root bound index (RBI). We grew longleaf pine (Pinus palustris), a grass stage species, in containers of four different volumes (60–336 ml) either coated with copper oxychloride or left untreated and fertilized at low, medium, or high levels of nitrogen (N). In general, N concentration of tissues rose as N rate increased, with larger changes in concentration occurring between low and medium levels than between medium and high levels. N rate influenced root tissue N concentration less than it did stems and needles. Subtle needle color differences caused by N rate were significant, suggesting its potential utility during nursery production. As expected, seedlings grew larger as container volume increased and as N rate increased. Copper treatment, which we posited could influence the RBI, tended to increase root-collar diameter and tap root biomass and decrease total root volume. Chlorophyll abundance was affected more by N rate than by container volume or copper treatment, but photosynthesis was affected more by copper treatment than N rate or container size. Although RBI was 25 % greater for seedlings grown in small containers with high N rates than those grown in large containers with low N rates, RBI ranged only from 11 to 15 %, well below the critical 27 % threshold.     

Experimental infection of domestic cats with passaged genotype I Bartonella henselae

The influence of in vitro passage on Bartonella henselae pathogenesis in cats has not been thoroughly evaluated. Our objective was to examine the bacterial kinetics and humoral immune responses in cats experimentally infected with three different in vitro passages of B. henselae F1, a genotype I strain of feline origin. The F1 strain was in vitro passaged 20 and 40 times, and each was inoculated into a group of 5 cats. The kinetics of bacteremia and the feline humoral immune response to bacterial antigens were compared to a previous study involving a group of six cats inoculated with the original F1 strain. Among the three groups of cats, the kinetics of bacteremia profiles and the humoral immune responses to B. henselae lysates were similar. The influence of passage on bacterial membrane proteins was examined. In vitro passage altered the expression of 4/17 (23.5%) bacterial membrane proteins and 6/15 (40%) bacterial membrane antigens. An association between poor seroreactivity to three lysate antigens (15-, 18- and 45kDa), prolonged bacteremia and decreased serum bactericidal activity was noted. Our data show that in vitro passage of B. henselae did not alter the kinetics of bacteremia, including the occurrence of relapsing bacteremia, in experimentally infected cats. This suggests that highly passaged strains may not be suitable for future vaccination studies. Furthermore, in vitro passage results in phenotypic and antigenic changes in the bacterial membrane protein profile, which warrants caution in the interpretation of studies involving passaged B. henselae strains.     

Experimental infection of dogs with various Bartonella species or subspecies isolated from their natural reservoir

Dogs can be infected by a wide variety of Bartonella species. However, limited data is available on experimental infection of dogs with Bartonella strains isolated from domestic animals or wildlife. We report the inoculation of six dogs with Bartonella henselae (feline strain 94022, 16S rRNA type II) in three sets of two dogs, each receiving a different inoculum dose), four dogs inoculated with B. vinsonii subsp. berkhoffii type I (ATCC strain, one mongrel dog) or type II (coyote strain, two beagles and one mongrel) and B. rochalimae (coyote strain, two beagles). None of the dogs inoculated with B. henselae became bacteremic, as detected by classical blood culture. However, several dogs developed severe necrotic lesions at the inoculation site and all six dogs seroconverted within one to two weeks. All dogs inoculated with the B. v. berkhoffii and B. rochalimae strains became bacteremic at levels comparable to previous experimental infections with either a dog isolate or a human isolate. Our data support that dogs are likely accidental hosts for B. henselae, just like humans, and are efficient reservoirs for both B. v. berkhoffii and B. rochalimae.     

Combined effects of pre-hardening and fall fertilization on nitrogen translocation and storage in Quercus variabilis seedlings

Maintaining proper seedling nitrogen status is important for outplanting success. Fall fertilization of evergreen conifer seedlings is a well-known technique for averting nitrogen (N) dilution caused by continued seedling growth during hardening. For deciduous seedlings, this technique is much less understood, and regardless of foliage type, the interaction of N status prior to fall fertilization and the rate of fall fertilization have yet to be fully explored. Therefore, we fertilized Quercus variabilis container seedlings with either 25, 100, or 150 mg total N seedling^?1, applied exponentially, during a 23-week pre-hardening regime, followed by either 0, 12, or 24 mg total N seedling^?1 applied during hardening (i.e., fall fertilization) in equal aliquots for 4 weeks. For seedlings without supplemental N during hardening, N concentration in stems and roots increased significantly despite substantial growth. The absence of N dilution was attributed to N translocation from foliage to these tissues, which was independent of pre-hardening N status. Overall, 32 % of foliar N was translocated and accounted for 75 % of the total N increase in stems and roots. Final stem N status was a function of pre-hardening fertilization, whereas root N concentration was affected by the interaction of pre-hardening and fall fertilization. Roots appear to be the main site of N storage, and root N content was significantly affected by pre-hardening and fall fertilization, but not their interaction. A combination of pre-hardening and fall fertilizer at a rate of 100 and 24 mg total N seedling^?1, respectively, yielded seedlings with the largest root systems.     

Spatial Response of Mammals to Late Quaternary Environmental Fluctuations

Analyses of fossil mammal faunas from 2945 localities in the United States demonstrate that the geographic ranges of individual species shifted at different times, in different directions, and at different rates in response to late Quaternary environmental fluctuations. The geographic pattern of faunal provinces was similar for the late Pleistocene and late Holocene, but differing environmental gradients resulted in dissimilar species composition for these biogeographic regions. Modern community patterns emerged only in the last few thousand years, and many late Pleistocene communities do not have modern analogs. Faunal heterogeneity was greater in the late Pleistocene.