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1.
New Microbiol ; 32(3): 303-10, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19845114

RESUMEN

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.


Asunto(s)
Infecciones Relacionadas con Catéteres/microbiología , Infecciones por Bacterias Gramnegativas/microbiología , Unidades de Cuidado Intensivo Neonatal , Infecciones Estafilocócicas/microbiología , Infecciones Relacionadas con Catéteres/epidemiología , Estudios de Cohortes , Infección Hospitalaria/epidemiología , Infección Hospitalaria/microbiología , Contaminación de Equipos , Femenino , Bacterias Gramnegativas/aislamiento & purificación , Infecciones por Bacterias Gramnegativas/epidemiología , Humanos , Lactante , Recién Nacido , Masculino , Infecciones Estafilocócicas/epidemiología , Staphylococcus/aislamiento & purificación
2.
J Med Microbiol ; 53(Pt 2): 87-91, 2004 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-14729926

RESUMEN

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.


Asunto(s)
Antibacterianos/farmacología , Lactoferrina/análogos & derivados , Lactoferrina/farmacología , Listeria monocytogenes/efectos de los fármacos , Listeria monocytogenes/patogenicidad , Macrófagos/microbiología , Animales , Bovinos , Línea Celular , Humanos , Recién Nacido , Listeriosis/microbiología , Pruebas de Sensibilidad Microbiana , Péptidos/farmacología
3.
Infect Immun ; 70(8): 4369-78, 2002 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12117947

RESUMEN

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.


Asunto(s)
Adaptación Fisiológica/genética , Toxinas Bacterianas , Regulación Bacteriana de la Expresión Génica , Listeria monocytogenes/genética , Proteínas Bacterianas/genética , Células CACO-2 , Línea Celular , Medios de Cultivo , Proteínas de Escherichia coli , Regulación Bacteriana de la Expresión Génica/efectos de los fármacos , Glutamato Descarboxilasa/genética , Proteínas de Choque Térmico/genética , Proteínas Hemolisinas , Humanos , Concentración de Iones de Hidrógeno , Interferón gamma/farmacología , Líquido Intracelular/microbiología , Ácido Láctico/farmacología , Listeria monocytogenes/efectos de los fármacos , Listeria monocytogenes/crecimiento & desarrollo , Listeria monocytogenes/fisiología , Activación de Macrófagos , Macrófagos/citología , Macrófagos/efectos de los fármacos , Macrófagos/inmunología , Macrófagos/microbiología , Proteínas de la Membrana/genética , Factores de Terminación de Péptidos , Fosfatidilinositol Diacilglicerol-Liasa , Superóxido Dismutasa/genética , Transactivadores/genética , Transcripción Genética/efectos de los fármacos , Fosfolipasas de Tipo C/genética , Virulencia
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