ABSTRACT
Unlike the glanders agent, the superficial structures of the melioidosis agent were demonstrated to be responsible for marked was immunosuppressive activity. Some antigenic fractions suppressing the blast transformation of lymphocytes, reducing the count of T helpers and profoundly potentiating the infection in vivo were isolated from P. pseudomallei cells. The immunogenic and immunosuppressive activities of both agents' superficial structures were studied by high performance chromatography. Antigenic complexes that were able to protect immunized laboratory animals against fatal infections and to prevent bacterial carriage due to the activation of T cells and to the bacterial activity of macrophages were identified. A composition comprising several immunogens was found to provide an additive protective action against both causative agents. Therefore, the composition may be considered to be a prototype of a molecular antipseudomonadic vaccine.
Subject(s)
Antigens, Bacterial/immunology , Burkholderia pseudomallei/immunology , Glanders/prevention & control , Melioidosis/prevention & control , Animals , Antigens, Bacterial/isolation & purification , Bacterial Vaccines/administration & dosage , Bacterial Vaccines/immunology , Burkholderia pseudomallei/pathogenicity , Chromatography, High Pressure Liquid , Disease Models, Animal , Glanders/immunology , Lymphocyte Activation , Macrophages/immunology , Melioidosis/immunology , Mice , Rats , T-Lymphocytes/immunology , VirulenceABSTRACT
In Pseudomonas mallei, spontaneous mutants (Tra- mutants) of the plasmids RP4 and R68.45, losing the ability to transfer at conjugation are formed. The plasmids RP4 and R68.45 with Tra(+)-phenotype caused a decrease in P. mallei virulence for laboratory animals. At the same time, Tra- mutants of these plasmids do not affect P. mallei virulence. The insertion of DNA fragment of about 1900 bp into the plasmid transfer gene regions (tra-2-tra-3) gave rise to RP4 and R68.45 tra mutations detectable on examination.
Subject(s)
Burkholderia pseudomallei/genetics , Burkholderia pseudomallei/pathogenicity , R Factors/genetics , Virulence/genetics , Animals , Conjugation, Genetic , Cricetinae , DNA, Bacterial/genetics , Disease Models, Animal , Gene Transfer Techniques , Melioidosis/prevention & control , Mutation , PhenotypeABSTRACT
A highly sensitive latex test system for identification of Legionella in the external medium and clinical materials have been designed. Protein antigens and polysaccharide components of the outer membrane of the agent were analyzed. Proteins having a molecular mass of 45, 29, and 24 kDa, as well as a polysaccharide component of LPS were found to be common for all L. pneumophila species. Highly affinic immunoglobulins to the antigenic components obtained were covalently linked with latex particles. The test system developed does not give cross-reactions with other microorganisms. The sensitivity of the system is 10(4) COE/ml. Testing water and clinical material samples confirmed that the developed system is more sensitive than the bacteriological method and the direct fluorescence test. In addition, the system is simple to use, cost-effective, it requires little time (no more than 5 min).
Subject(s)
Antigens, Bacterial/analysis , Latex Fixation Tests/methods , Legionella pneumophila/immunology , Legionellosis/diagnosis , Animals , Bacterial Outer Membrane Proteins/analysis , Bacteriological Techniques , Fluorescent Antibody Technique, Direct , Humans , Legionellosis/immunology , Microscopy, Fluorescence , Sensitivity and SpecificityABSTRACT
Live attenuated Salmonella vaccines may be used as carriers of heterologous antigens. The optimum expression system for each heterologous antigen requires to be established on an individual basis. This will ensure that the antigen in question is produced at appropriate levels and in the correctly folded conformation. Different techniques for producing stable recombinant Salmonella strains suitable for their use as bivalent vaccines.