A protocol for the bacteriophage amplification technique was developed for quantitative detection of viable Listeria monocytogenes cells using the A511 listeriophage with plaque formation as the end-point assay. Laser and toluidine blue O (TBO) were employed as selective virucidal treatment for destruction of exogenous bacteriophage. Laser and TBO can bring a total reduction in titer phage (ca. 10(8) pfu/mL) without affecting the viability of L. monocytogenes cells. Artificially inoculated skimmed milk revealed mean populations of the bacteria as low as between 13 cfu/mL (1.11 log cfu/mL), after a 10-h assay duration. Virucidal laser treatment demonstrated better protection of Listeria cells than the other agents previously tested. The protocol was faster and easier to perform than standard procedures. This protocol constitutes an alternative for rapid, sensitive and quantitative detection of L. monocytogenes.

In a previous study we demonstrated that the incidence of fibroblast colony-forming units (CFU-F) was very low in bone marrow primary cultures from the majority of untreated advanced non-small lung cancer patients (LCP) compared to normal controls (NC). For this reason, we studied the ability of bone marrow stromal cells to achieve confluence in primary cultures and their proliferative capacity following four continuous subcultures in consecutive untreated LCP and NC. We also evaluated the production of interleukin-1ß (IL-1ß) and prostaglandin E2 (PGE2) by pure fibroblasts. Bone marrow was obtained from 20 LCP and 20 NC. A CFU-F assay was used to investigate the proliferative and confluence capacity. Levels of IL-1ß and PGE2 in conditioned medium (CM) of pure fibroblast cultures were measured with an ELISA kit and RIA kit, respectively. Only fibroblasts from 6/13 (46%) LCP confluent primary cultures had the capacity to proliferate following four subcultures (NC = 100%). Levels of spontaneously released IL-1ß were below 10 pg/ml in the CM of LCP, while NC had a mean value of 1,217 ± 74 pg/ml. In contrast, levels of PGE2 in these CM of LCP were higher (77.5 ± 23.6 pg/ml) compared to NC (18.5 ± 0.9 pg/ml). In conclusion, bone marrow fibroblasts from LCP presented a defective proliferative and confluence capacity, and this deficiency may be associated with the alteration of IL-1ß and PGE2 production.

Thermophilic campylobacters were isolated from three sewage plants in Rio de Janeiro, RJ, Brazil and identified. Laboratory analysis of 390 sewage samples showed the presence of 169 thermophilic strains. The results demonstrated that human and animal pathogenic biotypes could be isolated from activated sludge during the initial processing steps. The aeration tank could be considered a barrier to Campylobacter survival. C. jejuni was the prevalent species isolated (40.8%).The most common biotypes were C. jejuni biotype I (21.3%), C. coli biotype I (16%) and C. jejuni biotype II ( 14.8%).

Strains of Vibrio parahaemolyticus, Vibrio fluvialis and Vibrio mimicus isolated from seafood and seawater were examined for characteristics related to infectivity, such as enzymatic activity and animal assays. All strains hydrolysed DNA, starch, gelatin and chitin. Variable results were obtained with the haemolysin, chondroitin, collagen, elastin and lecithin tests. Production of thermostable direct haemolysin by V. parahaemolyticus was detected in 7.1% strains derived from seafood and 2%from seawater. In the animal assays, strains of V. fluvialis showed positive results at skin PF (75%), mouse lethality (100%), but no fluid accumulation in the suckling mice model was noted. Concerning V. mimicus, results showed skin PF (100%), mouse lethality (100%) and fluid accumulation in suckling mice (66.6%).

Foi investigada a presençaa de L. monocytogenes em 20 amostras de solos da superficie, oriundas de diferentes áreas ecológicas do Estado do Rio de Janeiro (perímetro urbano, pasto, mata e horta). A análise bacteriológica evidenciou 32 amostras do microrganismo, revelando maior incidencia no solo não cultivado (mata) que representou 56,25% dos isolamentos, ficando em segundo plano a area urbana com 25%. No levantamento, destacam-se os sorotipos L1/2b (46,87%), L4b (25%) e L1/2a (18,75%) como os mais frequentes, embora incidindo de mameira heterogenea em relação as áreas analisadas. Entre os vários aspectos estudados, salienta-se que 50% das amostras se comportaram como patogenicas, em decorrencia da producao de ceratoconjuntivite em cobaia, detalhe este intimamente relacionado com a atividade hemolitica "in vitro". Confirma-se que tanto as formas virulenta e avirulenta de L. monocytogenes sobrevivem as condicoes impostas pelo solo, sendo provavelmente a causa primária desta contaminação os dejetos eliminados por diferentes espécies de animais portadores, corroborada pela presença de coliformes fecais nas áreas analisadas.

Was investigated the presence of L. monocytogenes in 20 samples from surface soils, from different ecological areas of Rio de Janeiro State (urban, pasture, forest and plantation areas). The bacteriological analysis revealed 32 samples showing more incidence in the non cultivated soil which represented 56.25% of the isolations: the urban area contributed with 25.0%. In the survey destached the serotypes L1/2b (46.87%), L4b (25.0%) and L1/2a (18.75%) as more frequent although the incidence was heterogeneous in relation to the analysed areas. Amongst the several studied aspects must be emphasized that 50.0% of the samples showed to be pathogenic due to the production of ceratoconjuntivites in guinea pigs which is very much related with hemolitic activity "in vitro". Therefore the virulent and non virulent strains of l. monocytogenes can survive under the conditions imposed by the soil being probably the primary motive of this contamination the stools eliminated by different species of harbouring animals, confirmed by the presence of fecal coliforms in the analised areas.