Establishing bioequivalence of veterinary premixes (Type A medicated articles)

a) Key issues concerning Premix (Type A medicated articles) Bioequivalence evaluations: 1) This is a complex issue concerning both route of administration and formulation. 2) If the animal is not at the bunk/trough, the animal is not self-administering (eating medicated feed), thus there can be no drug absorption. b) Differing opinions among scientists and regulatory authorities/expert bodies regarding: 1) No harmonization on how to design, conduct, and interpret in vivo studies. 2) Applicability of biowaivers to Type A (premix) products. 3) Why are topdress and complete feed considered differently? Are they different formulations or different routes of administration? 4) Single dose vs. multi-dose studies. 5) What is the final formulation? c) What are the next steps: 1) Harmonize current bioequivalence guidelines through the VICH process. 2) Determine the applicability/non-applicability of the Biopharmaceutical Classification System (BCS). 3) Establish the Total Mixed Ration (i.e. formulation) effects. 4) Define the test subject (individual, pen, etc.).     

Experimental infection in pigs with encephalomyocarditis virus

Non-suppurative myocarditis in pigs that were experimentally infected with encephalomyocarditis (EMC) virus is reported. Two of the four pigs that were infected with the virus died suddenly from myocardial failure, and all four had gross and microscopic changes consistent with EMC infection. This confirms the pathogenic potential of some strains of EMC virus for young pigs.     

Experimental infections with fowl pox in chickens

Seven groups of chickens were challenged with a field isolate of fowl pox virus at 18 weeks old. The birds in the groups that had been vaccinated 3 weeks previously with fowl pox vaccinates showed no signs of disease. Birds which had not been vaccinated against fowl pox developed upper respiratory disease after challenge, and some birds had diphtheritic tracheitis and laryngitis which appeared identical to that commonly seen under field conditions. Seven days after challenge, fowl pox virus was recovered from the tracheas of unvaccinated birds, but not from the vaccinated ones.

Intercurrent Mycoplasma gallisepticum infection appeared to extend slightly the period of respiratory disease but was not essential for development of the diphtheritic lesion.     

Parainfluenza type 3 virus in cattle with upper respiratory disease

Abstract

Extract

Parainfluenza type 3(Pl₃) virus has been associated with upper respiratory disease of cattle in many countries (Hoerlein et al., 1959 Bögel, K. 1961. Virologische Undersuchungsbefunde bei Kalbern mit respiratoris-chem Syndrom unter besonderer Berucksichtigung der Parainfluenza 3 Myxovirus. Mh. Tierheilk, 13: 129–129. 162. [Cited by Jolly, R. D., (1967), N.Z. vet. J., 15: 43–4.] [Google Scholar]; Bögel, 1961 Campbell, R. S. F. 1972. “Virus diseases of cattle. Virology and Virus Disease”. In Proc. No. 16 of Course for Veterinarians, 132–132. University of Sydney.  [Google Scholar]; Reisinger, 1962 Carter, Margery E. and Hunter, R. 1970. Isolation of parainfluenza type 3 virus from sheep in New Zealand. N.Z. vet. J., 18: 226–227. [Taylor &; Francis Online] , [Google Scholar]; Jolly and Ditchfield, 1965 Curtis, R. A. and Sutton, R. H. 1972. Chronic granular rhinitis (nasal catarrh) of cattle. N.Z. vet. J., 20: 125–125. [Taylor &; Francis Online] , [Google Scholar]). However, PI₃ virus has not been isolated from cattle with respiratory disease in New Zealand although a serological study found that 89.3% of cows had significant levels of antibody against PI₃ virus (Pastier and Hansen, 1966). In most cases infections are subclinical, and there is little evidence to suggest that PI₃ virus is an important cause of disease in New Zealand cattle (Jolly, 1967 Fastier, L. B. and Hansen, N. F. 1966. The occurrence of antibodies to bovine virus diarrhoea, infectious bovine rhinotracheitis and parainfluenza 3 viruses in sera from New Zealand cattle. N.Z. vet J., 14: 27–32. [Taylor &; Francis Online] , [Google Scholar]). This communication records an outbreak of upper respiratory disease in cattle from which PI₃ virus was isolated.     

Morphological characteristics of blood cells in monitor lizards: is erythrocyte size linked to actual body size?

Blood cell morphology and count are not uniform across species. Recently, between‐species comparisons revealed that the size of red blood cells is associated with body size in some lizard taxa, and this finding was interpreted in the context of the metabolic theory. In the present study, we examined the numbers and the size of blood cells in 2 species of monitor lizards, the mangrove‐dwelling monitor (Varanus indicus) and the savannah monitor (V. exanthematicus), and we compared these traits in individuals of different body size. The results revealed that during the course of ontogeny, the size of red blood cells increases with body mass. Because the mass‐specific metabolic rate decreases with body size and the cell volume‐to‐surface ratio decreases with the cell size, changes in the erythrocyte size might be the result of oxygen transport adjustment.     

Cellular and cytokine responses in feathers of chickens vaccinated against Marek's disease

In Marek's disease virus infection, feather follicle epithelium (FFE) constitutes the site of formation of infectious virus particles and virus shedding. The objective of this study was to characterize cellular and cytokine responses as indicators of cell-mediated immune response in FFE and associated feather pulp following immunization against Marek's disease. Analysis of feather tips collected between 4 and 28 days post-immunization (d.p.i.) from chickens vaccinated post-hatch with either CVI988/Rispens or herpesvirus of turkeys revealed that replication of these vaccine viruses started at 7d.p.i., peaked by 21d.p.i., and subsequently, showed a declining trend. This pattern of viral replication, which led to viral genome accumulation in feather tips, was associated with infiltration of T cell subsets particularly CD8+ T cells into the feather pulp area and the expression of cytokine genes such as interferon-gamma, which is an indication of elicitation of cell-mediated immune responses at the site of virus shedding.     

Detection of Chlamydiaceae in ocular swabs from Australian pre‐export feedlot sheep

Infectious Ovine Keratoconjunctivitis (IOK) is a contagious ocular disease of sheep. A range of organisms have been observed as the aetiological agents of IOK. In this study, the presence of chlamydial pathogens (C. pecorum, C. abortus, C. psittaci) in conjunctival swabs was tested for. The swabs were collected from sheep with varying grades of IOK in an Australian pre‐export feedlot. The sheep had been rejected from a shipment because of the eye disease. The relative contribution of chlamydial pathogens to IOK and the rejection of animals was evaluated. In total, 149 conjunctival swabs were taken from rejected sheep (IOK Grades 1 to 6; n = 126) as well as those with healthy eyes (Grade 0; n = 23). Screening for chlamydial pathogens was done using species–specific qPCR assays. Chlamydial DNA was detected in 35.6% (53/149) of conjunctival samples. C. pecorum was the most predominant species with an overall prevalence of 28.9% (43/149). C. psittaci prevalence was 6.7% (10/149). Both organisms were detected in healthy as well as IOK‐affected eyes. All swabs tested negative for C. abortus. The results from this study demonstrate that Chlamydia spp can be readily detected in sheep presenting with IOK. The zoonotic C. abortus was not detected in any of the samples in this study, providing further evidence to the suggestion that this pathogen remains absent from Australia. Although the exact contribution of Chlamydia spp in the IOK pathogenesis is unclear, such studies are anticipated to be of benefit to Australian domestic and live export production systems.