ABSTRACT
ABSTRACT Clostridium perfringens is the causative agent for necrotic enteritis. It secretes the major virulence factors, and α- and NetB-toxins that are responsible for intestinal lesions. The TpeL toxin affects cell morphology by producing myonecrosis, but its role in the pathogenesis of necrotic enteritis is unclear. In this study, the presence of netB and tpeL genes in C. perfringens type A strains isolated from chickens with necrotic enteritis, their cytotoxic effects and role in adhesion and invasion of epithelial cells were evaluated. Six (27.3%) of the 22 C. perfringens type A strains were harboring the tpeL gene and produced morphological alterations in Vero cells after 6 h of incubation. Strains tpeL (-) induced strong cell rounding after 6 h of incubation and produced cell enlargement. None of the 22 strains harbored netB gene. All the six tpeL (+) gene strains were able to adhere to HEp-2 cells; however, only four of them (66.6%) were invasive. Thus, these results suggest that the presence of tpeL gene or TpeL toxin might be required for the adherence of bacteria to HEp-2 cells; however, it could not have any role in the invasion process.
Subject(s)
Humans , Animals , Poultry Diseases/microbiology , Bacterial Adhesion , Clostridium Infections/microbiology , Clostridium Infections/veterinary , Clostridium perfringens/physiology , Epithelial Cells/microbiology , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Vero Cells , Chlorocebus aethiops , Chickens , Clostridium perfringens/isolation & purification , Clostridium perfringens/geneticsABSTRACT
This study aimed to characterize the safety and technological properties of Enterococcus faecium strains isolated from Brazilian Coalho cheeses. High levels of co-aggregation were observed between Enterococcus faecium strains EM485 and EM925 and both Escherichia coli and Clostridium perfringens. Both strains presented low levels of hydrophobicity. E. faecium EM485 and EM925 were both able to grow in the presence of 0.5% of the sodium salts of taurocholic acid (TC), taurodeoxycholic acid (TDC), glycocholic acid (GC), and glycodeoxycholic acid (GDC), although they showed the ability to deconjugate only GDC and TDC. Both strains showed good survival when exposed to conditions simulating the gastro intestinal tract (GIT). When tested for the presence of virulence genes, only tyrosine decarboxylase and vancomycin B generated positive PCR results.
Subject(s)
Cheese/microbiology , Enterococcus faecium/isolation & purification , Enterococcus faecium/physiology , Food Safety , Food Handling/methods , Bacterial Adhesion , Brazil , Chemical Phenomena , Cholic Acids/metabolism , Cholic Acids/toxicity , Clostridium perfringens/chemistry , Clostridium perfringens/physiology , Enterococcus faecium/chemistry , Escherichia coli/chemistry , Escherichia coli/physiology , Gastrointestinal Tract/chemistry , Hydrophobic and Hydrophilic Interactions , Inactivation, Metabolic , Microbial Viability/drug effects , Polymerase Chain Reaction , Virulence Factors/analysis , Virulence Factors/geneticsABSTRACT
One strain (S32) of Clostridium perfringens type A was isolated from a case of catarrhal enteritis of piglets. This strain was able to adhere to HeLa cells showing an adherence index (AI) of 25.15ñ1.26(mean ñ 1 standard error of the mean). Treatment of the bacterial cells with trypsin (025mg/ml) decreased in 70 (per cent)-80 (per cent) the AI and metaperiodate (10mg/ml) abolished completely the adherence, suggesting that the structure responsible for this phenomenon was probably a glycoprotein. Heating of bacterial suspensions (100§C/5 min) before carrying out the adhesion test decreased the AI rendering it equal to the negative controls. Rabbit homologous S32 antiserum inhibited the adherence up to dilutions of 1:640, at least. The piglet ileal loop assay carried out with strains S32 and Jab-1 (negative control) demonstrated that the strain S32 was able to adhere to the intestinal epithelial cells when examined after Gram staining. Transmission electron microscopy (TEM) demonstrated that S32 strain displayed a loose fibrillar material not seen with Jab-1. Stabilization of the bacterial cells with homologous antiserum of strain S32, followed by staining with rhutenium red, revealed loose long fibrillar material on the outer surface of the cells, that sometimes could be seen spreading out from the cells and linking bacterial cells. The question whether this structure might be an adhesin for this strain of Cl. perfringes type A, perhaps playing a role in the pathogenesis of the catarrhal enteritis of piglets, is dependent on further studies.