Nejvíce citovaný článek - PubMed ID 9232429
Early consequences of macrophage-Francisella tularensis interaction under the influence of different genetic background in mice
There remains to this day a great gap in understanding as to the role of B cells and their products-antibodies and cytokines-in mediating the protective response to Francisella tularensis, a Gram-negative coccobacillus belonging to the group of facultative intracellular bacterial pathogens. We previously have demonstrated that Francisella interacts directly with peritoneal B-1a cells. Here, we demonstrate that, as early as 12 h postinfection, germ-free mice infected with Francisella tularensis produce infection-induced antibody clones reacting with Francisella tularensis proteins having orthologs or analogs in eukaryotic cells. Production of some individual clones was limited in time and was influenced by virulence of the Francisella strain used. The phylogenetically stabilized defense mechanism can utilize these early infection-induced antibodies both to recognize components of the invading pathogens and to eliminate molecular residues of infection-damaged self cells.
- MeSH
- B-lymfocyty imunologie metabolismus MeSH
- cytokiny metabolismus MeSH
- Francisella tularensis patogenita MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- tularemie imunologie mikrobiologie MeSH
- tvorba protilátek MeSH
- virulence MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytokiny MeSH
The implication of the Bcg locus in the control of natural resistance to infection with a live vaccine strain (LVS) of the intracellular pathogen Francisella tularensis was studied. Analysis of phenotypic expression of natural resistance and susceptibility was performed using mouse strains congenic at the Bcg locus. Comparison of the kinetics of bacterial colonization of spleen showed that B10.A.Bcg(r) mice were extremely susceptible during early phases of primary sublethal infection, while their congenic C57BL/10N [Bcg(s)] counterparts could be classified as resistant to F. tularensis LVS infection according to the 2-log-lower bacterial CFU within the tissue as long as 5 days after infection. Different phenotypes of Bcg congenic mice were associated with differential expression of the cytokines tumor necrosis factor alpha, interleukin-10, and gamma interferon and production of reactive oxygen intermediates. These results strongly suggest that the Bcg locus, which is close or identical to the Nramp1 gene, controls natural resistance to infection by F. tularensis and that its effect is the opposite of that observed for other Bcg-controlled pathogens.
- MeSH
- cytokiny biosyntéza MeSH
- dusitany metabolismus MeSH
- kultivované buňky MeSH
- mapování chromozomů * MeSH
- membránové proteiny genetika MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- přirozená imunita MeSH
- proteiny přenášející kationty * MeSH
- reaktivní formy kyslíku MeSH
- slezina mikrobiologie MeSH
- transportní proteiny genetika MeSH
- tularemie imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytokiny MeSH
- dusitany MeSH
- membránové proteiny MeSH
- natural resistance-associated macrophage protein 1 MeSH Prohlížeč
- proteiny přenášející kationty * MeSH
- reaktivní formy kyslíku MeSH
- transportní proteiny MeSH