Maximizing rhizosphere populations of fluorescent pseudomonads on potatoes and their effects onErwinia carotovora

Field-grown potato plants were treated withPseudomonas putida andP. fluorescens strains in order to maximize the rhizosphere populations of the pseudomonads and determine their effects on indigenous populations ofErwinia carotovora. Single applications of the pseudomonads to seed pieces at planting resulted in peak populations of approximately 10⁵ colony-forming units (CFU) per gram (fresh weight) of root in July, whereas a second application in June boosted rhizosphere populations 10- to 100-fold higher throughout the remainder of the growing season; they composed nearly 20% of the average total population of rhizosphere bacteria in early July. Although rhizosphere populations of the introduced pseudomonads were high,E. carotovora populations sharply increased from very low numbers to reach populations ranging between 10⁵ and 10⁷ CFU/g by early July. Furthermore, coapplications of pseudomonad strains failed to suppress native populations ofE. carotovora despite the growth and maintenance of high rhizosphere populations of both pseudomonad strains.     

Factors affecting chicken thrombocyte morphology and the relationship with heterophil:lymphocyte ratios

1. Thrombocytes were observed in a haemocytometer chamber and cells were classified into 5 morphological groups which were related to the extent of environmental stress. Thrombocyte morphology scores (TMS) were calculated for each blood sample. 2. Following exposure to social stress, chilling, or the injection of killed Escherichia coli, both TMS and heterophil:lymphocyte (H:L) ratios were increased. From maximum values 1 d after chilling H:L and TMS values returned to normal within 2 and 11 d respectively. 3. The addition of corticosterone (200 mg/kg) to the food resulted in increased H:L ratios whereas TMS were not affected. 4. The injection of an adrenal blocker, 1,1-dichloro-2,2 bis p-choro-phenyl ethane, resulted in decreased H:L values whereas TMS were not affected. 5. Resistance to E. coli challenge infection was not affected by TMS.     

Pharmacodynamics and pharmacokinetics of orally administered bishydroxycoumarin in the goat

Eight goats, 2 nontreated controls and 6 treated, were used to study the pharmacodynamics and pharmacokinetics of bishydroxycoumarin. In 5 of the 6 treated goats, there was a significant relationship between prothrombin times and drug concentrations. Activated clotting times did not change with time in either the controls or the treated goats. Five of 6 treated goats reached a plateau of drug concentration after 24 to 36 hours. Lag times for onset of pharmacologic effect ranged from 12 to 24 hours. The one goat (No. 3) that did not respond in concert with the other 5 was extremely nervous and became anorectic during the period of indoor confinement.     

Lesions of experimental flea bite hypersensitivity in the dog

Hypersensitivity to fleas was induced in flea-naive dogs by controlled challenge exposure to virgin fleas. By week 10 of the investigation, immediate (15 minute) and delayed (24-48 hours) responses could be elicited in the skin by flea bites. Histologically, the immediate response consisted of edema and eosinophils which sometimes overlapped with a delayed inflammatory response comprised of perivascular lymphocytes and fewer histiocytes. These inflammatory patterns correlated with type I or immediate, and type IV or cellular, allergic reactions. The combined immediate and delayed responses to fleas in the dog are as observed by other investigators in man and guinea pigs.     

Environment-genetic influences on immunocompetence

The immunological responses of an animal are changing continually in response to perceived environmental changes. This is because the genetic background, the lifelong environment of animals and their interaction greatly influence immunological responsiveness. An animal's genetic background influences all factors related to immunocompetence. Among these are age of onset of immunocompetence, responsiveness to specific antigens, antibody titers, type of antibody and immune response, as well as the persistence of the responses. Defense by immunity must require considerable resources, because chickens with a high antibody response are smaller and have poorer feed efficiencies than those chickens whose antibody response is lower. An increase in the effectiveness of one defensive factor may result in reduced effectiveness of another factor. For example, chickens selected for a high antibody titer response to antigen have reduced effectiveness of macrophages. Environmental stresses influence the immune response. Stress at the time of the animal's contact with antigen results in a reduced antibody response. After the antibody response begins, stress has little effect. Stress promotes the sensitization of cell-mediated immunity but inhibits its effectiveness. A short-term stressor such as weaning is followed, in about 24 h, by a short period of reduced immunocompetence, even though lymphoid mass may be reduced. Reduced immunocompetence during stressful periods can be reduced by employing adrenal blocking chemicals, or by socializing animals to their handlers.     

Effects of dietary corticosterone in young Leghorn and meat-type cockerels

1. Cockerels from meat-type (MT) and Leghorn (LG) stocks were fed on diets containing 0, 20, or 30 mg corticosterone/kg from 1 to 22 d after hatching. 2. Within MT and within LG stocks, responses to dietary corticosterone inclusion rates were similar; however, patterns differed between these major classes resulting in stock X diet interactions. 3. Traits responding to different inclusion rates of corticosterone in a dissimilar manner for MT and LG chickens included: immunoresponsiveness, body weight, efficiency of food utilisation, feathering; relative weights of liver, spleen, bursa, testes, breast and abdominal fat pad, as well as the proportion of liver lipid. 4. No differential responses occurred for relative adrenal weight, plasma xanthophyll concentrations, proportion of breast lipid and abdominal fat, or surface and cloacal temperatures. 5. Results indicated genetic differences in thresholds for response to corticosterone and in degree of response once thresholds were reached. Within populations, sensitivities varied between target organs.     

Effect of ascorbic acid on the disease caused by Escherichia coli challenge infection

In a series of experiments, leghorn-type chickens were fed diets containing from 0 to 880 mg of ascorbic acid/kg of feed beginning 1 day before air-sac challenge with Escherichia coli. Infection occurred in 46/60 (76%) of the controls and in 12/63 (19%) of those given feed containing 330 mg of ascorbic acid/kg. Levels of ascorbic acid above and below 330 mg/kg feed were less effective.     

Adrenal cortex reactivity in dairy cows differs between lactational stages and between different feeding levels

Changes in ACTH challenge test characteristics in dairy cows changing their physiological status at different lactational stages and different feeding levels were not investigated in terms of repeatability yet. In 23 multiparous Holstein cows (10 cows fed a sole fresh herbage diet without concentrate, 13 cows fed with concentrate), three ACTH challenge tests were performed: once during pregnancy shortly prior to drying off ( T1 ), and in week 3 ( T2 ) and 8 ( T3 ) after parturition. Test characteristics were correlated to performance and metabolic parameters: DMI, BW, energy balance (EB), plasma concentrations of free fatty acids (NEFA) and beta‐hydroxybutyrate (BHB). Basal plasma cortisol concentrations were higher at T1 compared with T2 and T3 (p < .05). The adrenal cortex sensitivity (expressed as total AUC (AUC_t) of cortisol response after ACTH application) was lowest at T2 compared with T1 and T3 (p < .05). Ranking of the individual animals’ responses was not repeatable between time points of the ACTH tests. Enhancing the energy deficiency during early lactation by omission of concentrate did not affect baseline cortisol concentrations in plasma, but decreased peak height at T2 (p < .05). Baseline plasma cortisol concentrations were positively correlated with cortisol peak values after ACTH application, previous lactation performance, milk yield and BW (p < .05). The AUC_t was positively correlated with baseline cortisol concentrations, EB and DMI. Cortisol release after ACTH injection was lower in animals with high plasma concentrations of NEFA, BHB and with higher contents of fat and free fatty acids in milk (p < .05). Cortisol peak height after ACTH administration was higher in cows with a more positive EB, higher DMI and lower plasma concentrations of NEFA and BHB. In summary, cortisol responses to ACTH challenges in this study were not repeatable in dairy cows changing their physiological status.