Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Int J Immunopathol Pharmacol ; 24(4): 1057-68, 2011.
Article in English | MEDLINE | ID: mdl-22230411

ABSTRACT

In cystic fibrosis (CF) high iron concentration in airway secretion plays a pivotal role in bacterial multiplication and biofilm formation as well as in inflammatory response. Burkholderia cenocepacia, an opportunistic facultative pathogen responsible for chronic lung infections and cepacia syndrome, recurrently infects CF patients. Lactoferrin (Lf), an iron binding multifunctional glycoprotein synthesized by exocrine glands and neutrophils, has been found at higher concentration in the airway secretions of infected CF patients than in healthy subjects. Here the influence of milk derivative bovine lactoferrin (bLf), an emerging important regulator of iron and inflammatory homeostasis, on invasiveness of B. cenocepacia iron-modulated biofilm, as well as on inflammatory response by infected CF bronchial (IB3-1) cells, is reported. bLf did not significantly affect invasion efficacy by biofilmforming B. cenocepacia clinical strains. Conversely, the addition of bLf to cell monolayers during infection significantly decreased the pro-inflammatory Interleukin (IL)-1beta and increased the anti-inflammatory IL-11 expression compared to that observed in cells infected in the absence of bLf. The bLf ability to modulate genes expressed following B. cenocepacia infection seems related to its localization to the nucleus of infected IB3-1 cells. These results provide evidence for a role of bLf in the protection of infected CF cells from inflammation-related damage, thus extending the therapeutic potential of this multifunctional natural protein.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Biofilms/drug effects , Bronchi/drug effects , Burkholderia cenocepacia/drug effects , Cystic Fibrosis/microbiology , Inflammation Mediators/metabolism , Iron/metabolism , Lactoferrin/pharmacology , Animals , Anti-Inflammatory Agents/isolation & purification , Biofilms/growth & development , Bronchi/immunology , Bronchi/metabolism , Bronchi/microbiology , Burkholderia cenocepacia/growth & development , Burkholderia cenocepacia/metabolism , Cattle , Cell Line , Cystic Fibrosis/genetics , Cystic Fibrosis/immunology , Cystic Fibrosis/metabolism , Gene Expression Regulation/drug effects , Humans , Interleukin-11/metabolism , Interleukin-1beta/metabolism , Lactoferrin/isolation & purification , Milk/chemistry
2.
Int J Immunopathol Pharmacol ; 23(4): 1253-60, 2010.
Article in English | MEDLINE | ID: mdl-21244775

ABSTRACT

Streptococcus mutans and Streptococcus sobrinus, the principal etiologic agents of caries decay of teeth, are generally acquired in oral cavity at the moment of tooth eruption. However, as S. mutans has been detected in oral cavity of predentate children, the eruption of teeth seems not to be a necessary prerequisite, suggesting that this species may be not confined to dental plaque. Here, we evaluate the ability of S. mutans and S. sobrinus in planktonic and biofilm lifestyle to adhere, invade and survive within human gingival fibroblast (HGF-1) cells. Planktonic and biofilm streptococci adhered and invaded host cells to different extents, showing higher efficiencies of biofilm than planktonic counterparts. Moreover, planktonic and biofilm streptococci showed the same percentage of survival within host cells. Transmission electron and confocal microscopy observations confirmed intracellular localization of planktonic and biofilm bacteria. The adhesion, invasion and survival abilities within human oral cells may be considered S. mutans and S. sobrinus virulence mechanisms to colonize and persist in the oral cavity in the absence of tooth surface.


Subject(s)
Bacterial Adhesion , Gingiva/microbiology , Streptococcus mutans/pathogenicity , Streptococcus sobrinus/pathogenicity , Biofilms , Cell Line , Fibroblasts/microbiology , Gingiva/cytology , Humans , Plankton
3.
Int J Immunopathol Pharmacol ; 21(1): 51-9, 2008.
Article in English | MEDLINE | ID: mdl-18336731

ABSTRACT

Pseudomonas aeruginosa and Burkholderia cenocepacia are two important opportunistic respiratory pathogens of cystic fibrosis (CF) patients. Infections caused by these microorganisms are particularly difficult to eradicate because they are usually highly resistant to several currently available broad-spectrum antibiotics. Lactoferrin (Lf), a glycoprotein found in physiological fluids of mammals and present at high concentrations in infected and inflamed tissues, plays an important role in the natural defence mechanism against pathogens and in immune regulation. In the present study, we evaluate the ability of bovine lactoferrin (bLf) to influence P. aeruginosa PAO1 and B. cenocepacia PV1 adhesiveness and invasiveness, using the A549 human bronchial cell line. Three different iron-induced morphological forms of bacteria (free-living, aggregates and biofilm) were assayed. The addition of bLf to cells just before infection had little influence on adhesion efficiency for all three of the morphological forms of B. cenocepacia PV1, while a slight increase in adhesion efficiency by P. aeruginosa PAO1 was noticed. Conversely, invasion of all three morphological forms of both P. aeruginosa and B. cenocepacia was strongly inhibited by the presence of bLf, independently of its degree of iron-binding activity. This is the first report demonstrating an anti-invasive property of bLf for strains of P. aeruginosa and B. cenocepacia.


Subject(s)
Burkholderia cepacia/drug effects , Iron/metabolism , Lactoferrin/pharmacology , Lung/microbiology , Pseudomonas aeruginosa/drug effects , Animals , Bacterial Adhesion/drug effects , Biofilms , Burkholderia cepacia/physiology , Cattle , Cell Line, Tumor , Cystic Fibrosis/microbiology , Humans , Lung/ultrastructure , Microscopy, Electron, Transmission , Pseudomonas aeruginosa/physiology
SELECTION OF CITATIONS
SEARCH DETAIL
...