Nasal carriage of methicillin-resistant Staphylococcus aureus in university students

In a study of university students, the percentage nasal carriage of Staphylococcus aureus was 40.8 percent (102/250). Of the isolates, MIC50 of methicillin was 0.5 µg/mL and MIC90 was 1 µg/mL. Six (5.8 percent) isolates were methicillin-resistant and carried the mecA gene. These results suggest that community-associated methicillin-resistant S. aureus may be spreading in Brazil.

Lack of association between genotypes and virulence factors in C. albicans strains isolated from vaginal secretion

The physiopathogenesis of vulvovaginal candidiasis (VVC) is still not completely elucidated. The objective of this study was to evaluate if there is a relationship between the different genotypes of Candida albicans, their main agent and the virulence of this yeast in vaginal isolates, and to check if there are laboratorial markers that can predict the ability of each isolate to develop VVC independently of symptoms. The production of exoenzymes protease, phospholipase and haemolysin, resistance to hydrogen peroxide, and the genotype were determined. Genotype A was predominant (75 percent), protease, phospholipase and haemolytic activity were highly expressed, and the majority of the yeasts were sensitive to H2O2 in 1 and 2 hours of exposure, suggesting that these factors are important in the virulence of vaginal isolates. However they did not have any correlation with the genotypes. The different isolates expressed similar virulence potential, suggesting that other factors relating to the yeasts and the host must participate in the development of the clinical disease.

A fisiopatogenia da candidíase vulvovaginal (CVV) não está completamente elucidada até o presente momento. O objetivo deste estudo foi avaliar se exite relação entre os diferentes genótipos de Candida albicans, seu principal agente, e a virulência desta levedura em isolados vaginais, e checar se existem marcadores laboratoriais que possam predizer a habilidade de cada isolado para desenvolver CVV independentemente dos sintomas. Foram determinados a produção de exoenzimas protease, fosfolipase and hemolisina, resistência ao peróxido de hidrogêncio, e genótipo. O genótipo A foi predominante (75 por cento), protease, fosfolipase e atividade hemolítica foram alevadamente expressos, e a maioria das leveduras foram sensíveis ao H2O2 em 1 e 2 horas de exposição, sugerindo que estes fatores são importantes na virulênciae de isolados vaginais. Entretanto, não houve nenhuma correlação com os genótipos. Os diferentes isolados expressaram potencial de virulência similares, sugerindo que outros fatores relacionados às leveduras e ao hospedeiro devem participar no desenvolvimento da doença clínica.

Differential gene expression during Trypanosoma cruzi metacyclogenesis

The transformation of epimastigotes into metacyclic trypomastigotes involves changes in the pattern of expressed genes, resulting in important morphological and functional differences between these developmental forms of Trypanosoma cruzi. In order to identify and characterize genes involved in triggering the metacyclogenesis process and in conferring to metacyclic trypomastigotes their stage specific biological properties, we have developed a method allowing the isolation of genes specifically expressed when comparing two close related cell populations (representation of differential expression or RDE). The method is based on the PCR amplification of gene sequences selected by hybridizing and subtracting the populations in such a way that after some cycles of hybridization-amplification genes specific to a given population are highly enriched. The use of this method in the analysis of differential gene expression during T. cruzi metacyclogenesis (6 hr and 24 hr of differentiation and metacyclic trypomastigotes) resulted in the isolation of several clones from each time point. Northern blot analysis showed that some genes are transiently expressed (6 hr and 24 hr differentiating cells), while others are present in differentiating cells and in metacyclic trypomastigotes. Nucleotide sequencing of six clones characterized so far showed that they do not display any homology to gene sequences available in the GeneBank.