Assuntos
Clindamicina/uso terapêutico , Proteinose Alveolar Pulmonar/tratamento farmacológico , Idoso , Idoso de 80 Anos ou mais , Animais , Cobaias , Humanos , Imunocompetência , Pneumopatias/complicações , Masculino , Proteinose Alveolar Pulmonar/complicações , Recidiva , Infecções Estreptocócicas/complicaçõesRESUMO
The influence of normal microbial flora on cell proliferation in mouse colonic crypts was assessed by a comparison of conventional and germ-free animals. The following characteristics of the crypts were measured: length, diameter in the middle, number of columns, number of cell per one column, percentage of goblet cells, mitotic and labelling index distribution and average cell cycle time for the proliferative compartment. It has been found that the crypts in conventional mice are longer than in their germ-free counterparts, while their diameter and percentage of goblet cells were similar in both animal groups. The mitotic index was lower in germ-free mice, as well as the labelling index. The average cell cycle time was about 1.7-fold shorter in conventional animals than in germ-free animals. This result was verified using computer simulation model; it turned out that the change in average cell cycle time could be solely responsible for all the observed differences between germ-free and conventional animals. It seems therefore that normal microbial flora stimulates cell proliferation in mouse colon, most probably due to shortening of the average cell cycle.
Assuntos
Colo/microbiologia , Colo/patologia , Vida Livre de Germes , Animais , Divisão Celular/fisiologia , Masculino , Camundongos , Camundongos Endogâmicos BALB CRESUMO
Blood agar medium with dialysis membrane mounted between two layers of agar was applied to study the haemolytic activity of 28 strains of Serratia marcescens. Two kinds of lytic substances differing with their ability to pass through dialysis membrane were found. Haemolytic activity was not detected in cell-free filtrates from liquid cultures. The discrepancies between haemolytic activity in blood agar media and activity of liquid cultures were observed. Stable attachment of bacterial cells to the erythrocytes was not necessary to lysis. The possibility of extracellular haemolysin is discussed.