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J Brownlie

Publications and source records attributed to J Brownlie.

80 records · Page 5Linked to original sources

The virulence of T-mycoplasmas, isolated from various animal species, assayed by intramammary inoculation in cattle.

The virulence of T-mycoplasmas for cattle was tested by examining their ability to produce mastitis in cows. It was found that both virulent and avirulent strains of T-mycoplasmas can be isolated from cattle. All of four strains from pneumonic calf lungs and a strain from a case of bovine kerato-conjunctivitis caused mastitis but only two of four strains isolated from the urogenital tract of cows were virulent. None of the human, simian or canine T-mycoplasmas examined were able to cause mastitis in cattle. However, a bovine strain was found to be capable of causing mastitis in goats. Virulent and avirulent strains from the same and different species contain common antigens detected by the metabolic inhibition test. Pathogenicity could not be shown to be characteristic of any particular serotype. The possibility is raised of some species barrier being responsible for the inability of non-bovine strains to infect cattle.

Animals↗

The production of mastitis in cows by the intramammary inoculation of T-mycoplasmas.

Six milking cows were inoculated with bovine and human T-mycoplasmas and control materials into the udder via the teat canal. Control materials produced only a slight transient cell response in the milk. Bovine T-mycoplasmas produced clinical mastitis in nine out of ten quarters inoculated. Seven developed clinical mastitis together with visible changes in the milk, excretion of T-mycoplasmas and greatly increased cell counts in the milk. In three of these quarters, in two different cows, milk secretion ceased completely. Two quarters in a different cow showed visible milk changes, excretion of T-mycoplasmas and increased cell counts. Two quarters were inoculated with human T-mycoplasmas and neither produced any signs of mastitis.Infection of the udder with T-mycoplasmas did not stimulate high-titre serum antibody levels as measured by the metabolic inhibition test, but whey samples gave high titres in two of the cows that were able to control and resolve the infection.

Animals↗

The antimicrobial activity of cationic proteins isolated from the cells in bulk milk samples.

Cationic proteins isolated from the cells in bulk milk samples were shown to inhibit the growth of two pathogenic strains of staphylococci and also Streptococcus agalactiae S 13. Polyacrylamide gel disk electrophoresis studies on these proteins revealed the presence of at least 9 components some of which had isoelectric pH's between 7.0 and 9.0. Trace amounts of the isolated protein had isoelectric pH's greater than 9.0. Staphylococci incubated with milk-cell cationic proteins absorbed the protein, thereby allowing the organism to be stained with the anionic dye Fast Green FCF. Protein-treated staphylococci in isotonic solutions autoagglutinated. This autoagglutination was more marked in hypo- and hypertonic solutions. Lysozyme was not demonstrated in the isolated protein fractions in assays involving incubation with Micrococcus lysodeikticus for 90 min. The antimicrobial activity of the cationic proteins isolated from the bulk milk samples was not destroyed after heating to temperatures up to 70 degrees C for 30 min., whereas at higher temperatures the activity diminished and was almost completely lost at 100 degrees C.

Agglutination↗

Investigation of the cellular tropism of bovine immunodeficiency-like virus.

Bovine immunodeficiency-like virus (BIV) was first isolated from an animal showing transient leucocytosis, lymphadenopathy, lesions in the central nervous system and progressive weakness and emaciation. Similar signs are observed in other immunosuppressive lentiviral infections. BIV, like other lentiviruses, has been isolated from peripheral blood mononuclear cells and lymphoid tissue of infected animals. However, the in vivo cellular tropism of BIV remains unclear although initial studies indicate that BIV may be pantropic, infecting T cells, B cells and monocytes similar to some of the immunodeficiency-causing lentiviruses. PCR, Southern blot hybridisation, cell culture and reverse transcriptase assays were used to demonstrate the presence of BIV proviral DNA and the production of infectious virus in CD2+, WC1+, B cells and monocytes during the acute stages of infection. Western immunoblot assays were used to assess the development of antibody responses towards the virus.

Animals↗