1985
DOI: 10.1128/iai.50.2.555-559.1985
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Mycobacterium bovis BCG vaccine fails to protect protein-deficient guinea pigs against respiratory challenge with virulent Mycobacterium tuberculosis

Abstract: Specific-pathogen-free Hartley guinea pigs were maintained on isocaloric-purified diets either adequate (30%) or moderately deficient (10%) in protein. Half of each diet group was vaccinated with viable Mycobacterium bovis BCG. Six weeks later, all animals were challenged by the respiratory route with virulent Mycobacterium tuberculosis H37Rv. At intervals of 1, 2, and 3 weeks postchallenge, guinea pigs from each diet and vaccination group were skin tested with tuberculin and sacrificed. Protein deficiency res… Show more

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Cited by 54 publications
(34 citation statements)
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“…tuberculosis H37Rv in the guinea pig model (2,12,13,21). Successful vaccination minimizes hematogenous dissemination of tubercle bacilli to distal organs such as the spleen, may modulate resulting in significant reductions in the mycobacterial load Ivith pulmonary in that organ (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…tuberculosis H37Rv in the guinea pig model (2,12,13,21). Successful vaccination minimizes hematogenous dissemination of tubercle bacilli to distal organs such as the spleen, may modulate resulting in significant reductions in the mycobacterial load Ivith pulmonary in that organ (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Proteasome is a multisubunit complex that degrades various cellular proteins, and the degradation in this complex requires a specific signal: attachment of a multiubiquitin chain to the target protein. It has been reported that protease inhibitors induce overexpression of factors such as heat‐shock proteins, 16 , 17 ATF3, GADD153 and MAD1; 18 however, regulation of cytokine production in vascular endothelial cells by the protease system has not been known.…”
Section: Discussionmentioning
confidence: 99%
“…To prepare these suspensions, the bacterial cells were dispersed by sonication for 30 s and filtered through an 8 µm filter. The mice were infected via the respiratory route using an aerosol chamber that produces droplet nuclei of the size appropriate for entry into alveolar spaces 15 , 16 . The concentration of viable M. bovis in the nebulizer fluid was empirically adjusted to result in the inhalation and retention of approximately 10 viable organisms per mouse.…”
Section: Methodsmentioning
confidence: 99%