Research Topics
| J A TriccasSummaryAffiliation: Institut Pasteur Country: France Publications
| Collaborators
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Detail Information
Publications
Specific serological diagnosis of leprosy with a recombinant Mycobacterium leprae protein purified from a rapidly growing mycobacterial hostJ A Triccas
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia
J Clin Microbiol 36:2363-5. 1998..The assay proved highly specific (97.5%) and sensitive (90%) and compared favorably with two other established methods routinely utilized for leprosy serodiagnosis...
An inducible expression system permitting the efficient purification of a recombinant antigen from Mycobacterium smegmatisJ A Triccas
Unite de Genetique Mycobacterienne, Institut Pasteur, Paris, France
FEMS Microbiol Lett 167:151-6. 1998....
DNA encoding a single mycobacterial antigen protects against leprosy infectionE Martin
Centenary Institute of Cancer Medicine and Cell Biology, Locked Bag No. 6, NSW 2042, Newtown, Australia
Vaccine 19:1391-6. 2001..Therefore, DNA immunization with the 35 kDa antigen is effective against M. leprae infection and genetic immunization with a combination of antigens holds the potential for an improved vaccine against leprosy...
A 35-kilodalton protein is a major target of the human immune response to Mycobacterium lepraeJ A Triccas
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia
Infect Immun 64:5171-7. 1996..leprae 35-kDa protein appears to be a major and relatively specific target of the human immune response to M. leprae and is a potential component of a diagnostic test to detect exposure to leprosy or a vaccine to combat the disease...
Molecular and immunological analyses of the Mycobacterium avium homolog of the immunodominant Mycobacterium leprae 35-kilodalton proteinJ A Triccas
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales 2042, Australia
Infect Immun 66:2684-90. 1998..Strong delayed-type hypersensitivity was elicited by the protein in guinea pigs sensitized with M. avium...
Protection against virulent Mycobacterium avium infection following DNA vaccination with the 35-kilodalton antigen is accompanied by induction of gamma interferon-secreting CD4(+) T cellsE Martin
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales 2042, Australia
Infect Immun 68:3090-6. 2000..These results illustrate the importance of the 35-kDa protein in the protective response to M. avium infection and indicate that DNA vaccination successfully promotes a sustained level of protection during chronic M. avium infection...
Comparative protective effects of recombinant DNA and Mycobacterium bovis bacille Calmette-Guérin vaccines against M. avium infectionE Martin
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, NSW, Australia
Clin Exp Immunol 126:482-7. 2001..Therefore, recombinant BCG-35 and BCG induced similar levels of protection in this model, and maximal protection against M. avium infection was attained by immunization with DNA encoding the 35 kDa protein...
Isolation of strong expression signals of Mycobacterium tuberculosisJ A Triccas
Unite de Genetique Mycobacterienne, Institut Pasteur, 25 rue du Dr Roux, 75724 Paris Cedex 15, France
Microbiology 147:1253-8. 2001..Furthermore, this study demonstrated that FACS provides a sensitive and efficient technique to measure and select strong mycobacterial expression signals...
Inactivation of the Mycobacterium tuberculosis fadB4 gene results in increased virulence in host cell and miceG M Scandurra
Centenary Institute of Cancer Medicine and Cell Biology, University of Sydney, NSW 2006, Australia
Microbes Infect 10:38-44. 2008..tuberculosis lacking the fadB4 gene. Therefore fadB4 is part of the family of genes whose expression serves to regulate the virulence of M. tuberculosis within the host...
Analysis of the phthiocerol dimycocerosate locus of Mycobacterium tuberculosis. Evidence that this lipid is involved in the cell wall permeability barrierL R Camacho
, Institut Pasteur, 25 rue du Dr. Roux, 75725 Paris Cedex 15, France
J Biol Chem 276:19845-54. 2001..tuberculosis play a role in the cell envelope architecture and permeability. This function may represent one of the molecular mechanisms by which DIMs are involved in the virulence of M. tuberculosis...
Life on the inside: probing mycobacterium tuberculosis gene expression during infectionJ A Triccas
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia
Immunol Cell Biol 78:311-7. 2000..This information is expected to provide new strategies to prevent tuberculosis infection, new targets for antimicrobial therapy and new insights into the infectious process...
Analysis of stress- and host cell-induced expression of the Mycobacterium tuberculosis inorganic pyrophosphataseJ A Triccas
Unite de Genetique Mycobacterienne, Institut Pasteur, 25 rue du Dr, Roux, 75724 Paris Cedex 15, France
BMC Microbiol 1:3. 2001..The causative agent of tuberculosis, Mycobacterium tuberculosis, contains a well conserved copy of PPase. We sought to determine if expression of the M. tuberculosis PPase is regulated by the intracellular environment...
Characterization of the gene encoding the immunodominant 35 kDa protein of Mycobacterium lepraeN Winter
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, New South Wales, Australia
Mol Microbiol 16:865-76. 1995..smegmatis. The availability of the recombinant 35 kDa protein will permit dissection of both antibody- and T-cell-mediated immune responses in leprosy patients...
Effect of phthiocerol dimycocerosate deficiency on the transcriptional response of human macrophages to Mycobacterium tuberculosisG M Scandurra
Mycobacterial Research Group, Centenary Institute of Cancer Medicine and Cell Biology, Locked Bag No 6, Newtown, NSW 2042, Australia
Microbes Infect 9:87-95. 2007..Therefore, although fadD26 deficiency is responsible for the early attenuation of the growth of M. tuberculosis in vivo, this effect is not associated with differences in the initial macrophage transcriptional response...
