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1.
New Microbiol ; 32(3): 303-10, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19845114

RESUMO

Newborn babies admitted into the neonatal intensive care unit (NICU) often require many supportive invasive devices and frequently receive antimicrobial therapy. We investigated the microbial flora in NICU patients reporting the distribution of infections in different catheter sites. Results showed that 97% of samples were positive; in particular 11% were positive for two or more microbial agents. Coagulase negative Staphylococci were the most commonly isolated. The detection of Gram-negative bacteria and yeasts suggested that these microorganisms are also involved in infections of hospitalized infants. Finally, no correlation between a specific microbial agent and a particular catheter type was found.


Assuntos
Infecções Relacionadas a Cateter/microbiologia , Infecções por Bactérias Gram-Negativas/microbiologia , Unidades de Terapia Intensiva Neonatal , Infecções Estafilocócicas/microbiologia , Infecções Relacionadas a Cateter/epidemiologia , Estudos de Coortes , Infecção Hospitalar/epidemiologia , Infecção Hospitalar/microbiologia , Contaminação de Equipamentos , Feminino , Bactérias Gram-Negativas/isolamento & purificação , Infecções por Bactérias Gram-Negativas/epidemiologia , Humanos , Lactente , Recém-Nascido , Masculino , Infecções Estafilocócicas/epidemiologia , Staphylococcus/isolamento & purificação
2.
J Med Microbiol ; 53(Pt 2): 87-91, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14729926

RESUMO

Bovine lactoferrin (BLf) and its derivative peptide lactoferricin B (LfcinB) are known for their antimicrobial activity towards several pathogens, including Listeria monocytogenes, a food-borne Gram-positive invasive bacterium that infects a wide variety of host cells, including professional phagocytes. To add further information on the antibacterial effects of these compounds, the influence of BLf, LfcinB and the antimicrobial centre of LfcinB, the hexapeptide LfcinB(4-9), on the invasive behaviour of L. monocytogenes was analysed in IFN-gamma-activated human macrophagic cells (THP-1). Significant inhibition of bacterial entry in THP-1 cells was observed at LfcinB concentrations that were unable to produce any bacteriostatic or bactericidal effect, compared with BLf and LfcinB(4-9) peptide. This inhibition occurred when LfcinB was incubated during the bacterial infection step and was not due only to competition for common glycosaminoglycan receptors. Assays performed through a temperature shift from 4 to 37 degrees C showed that inhibition of invasion took place at an early post-adsorption step, although an effect on a different step of intracellular infection could not be ruled out.


Assuntos
Antibacterianos/farmacologia , Lactoferrina/análogos & derivados , Lactoferrina/farmacologia , Listeria monocytogenes/efeitos dos fármacos , Listeria monocytogenes/patogenicidade , Macrófagos/microbiologia , Animais , Bovinos , Linhagem Celular , Humanos , Recém-Nascido , Listeriose/microbiologia , Testes de Sensibilidade Microbiana , Peptídeos/farmacologia
3.
Infect Immun ; 70(8): 4369-78, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12117947

RESUMO

In Listeria monocytogenes the acid tolerance response (ATR) takes place through a programmed molecular response which ensures cell survival under unfavorable conditions. Much evidence links ATR with virulence, but the molecular determinants involved in the reactivity to low pHs and the behavior of acid-exposed bacteria within host cells are still poorly understood. We have investigated the effect of acid adaptation on the fate of L. monocytogenes in human macrophages. Expression of genes encoding determinants for cell invasion and intracellular survival was tested for acid-exposed bacteria, and invasive behavior in the human myelomonocytic cell line THP-1 activated with gamma interferon was assessed. Functional approaches demonstrated that preexposure to an acidic pH enhances the survival of L. monocytogenes in activated human macrophages and that this effect is associated with an altered pattern of expression of genes involved in acid resistance and cell invasion. Significantly decreased transcription of the plcA gene, encoding a phospholipase C involved in vacuolar escape and cell-to-cell spread, was observed in acid-adapted bacteria. This effect was due to a reduction in the quantity of the bicistronic plcA-prfA transcript, concomitant with an increase in the level(s) of the monocistronic prfA mRNA(s). The transcriptional shift from distal to proximal prfA promoters resulted in equal levels of the prfA transcript (and, as a consequence, of the inlA, hly, and actA transcripts) under neutral and acidic conditions. In contrast, the sodC and gad genes, encoding a cytoplasmic superoxide dismutase and the glutamate-based acid resistance system, respectively, were positively regulated at a low pH. Morphological approaches confirmed the increased intracellular survival and growth of acid-adapted L. monocytogenes cells both in vacuoles and in the cytoplasm of interferon gamma-activated THP-1 macrophages. Our data indicate that preexposure to a low pH has a positive impact on subsequent challenge of L. monocytogenes with macrophagic cells.


Assuntos
Adaptação Fisiológica/genética , Toxinas Bacterianas , Regulação Bacteriana da Expressão Gênica , Listeria monocytogenes/genética , Proteínas de Bactérias/genética , Células CACO-2 , Linhagem Celular , Meios de Cultura , Proteínas de Escherichia coli , Regulação Bacteriana da Expressão Gênica/efeitos dos fármacos , Glutamato Descarboxilase/genética , Proteínas de Choque Térmico/genética , Proteínas Hemolisinas , Humanos , Concentração de Íons de Hidrogênio , Interferon gama/farmacologia , Líquido Intracelular/microbiologia , Ácido Láctico/farmacologia , Listeria monocytogenes/efeitos dos fármacos , Listeria monocytogenes/crescimento & desenvolvimento , Listeria monocytogenes/fisiologia , Ativação de Macrófagos , Macrófagos/citologia , Macrófagos/efeitos dos fármacos , Macrófagos/imunologia , Macrófagos/microbiologia , Proteínas de Membrana/genética , Fatores de Terminação de Peptídeos , Fosfatidilinositol Diacilglicerol-Liase , Superóxido Dismutase/genética , Transativadores/genética , Transcrição Gênica/efeitos dos fármacos , Fosfolipases Tipo C/genética , Virulência
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