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1.
J Appl Microbiol ; 128(5): 1289-1300, 2020 May.
Article in English | MEDLINE | ID: mdl-31840319

ABSTRACT

AIM: The aim of the study was to characterize phenotypically and genotypically Enterococcus faecium strains collected from bovine mastitis milk and to evaluate one of them for its virulence in a murine mastitis model. METHODS AND RESULTS: A total of five E. faecium isolates were collected from cows with subclinical mastitis. EF-7A showed resistance to antibiotics tested, it presented alpha haemolysin and did not present gelatinase activity. It yielded cyA, efafm and gelE1 genes and it could be characterized as a moderate biofilm producer. It was able to internalize in MAC-T cells and 1×108 colony forming unit ml-1 was able to establish an intramammary infection in mice. The strain could be recovered from liver, kidney and blood samples. RAPD profiles showed different bands with respect to the inoculated strain. Histopathology analyses showed different grades of polymorphonuclear neutrophils infiltration in mammary glands. CONCLUSION: This is the first report that studied E. faecium strain in a lactating mouse model of mastitis and showed that the experimental inoculation was able to stimulate an inflammatory response resulting in mastitis. Results contribute to a better understanding of intramammary infections caused by E. faecium. SIGNIFICANCE AND IMPACT OF THE STUDY: This investigation shows that mice represent a valuable model for the study of the mastitis pathogenesis caused by E. faecium considering the high costs of using cows for mastitis research.


Subject(s)
Disease Models, Animal , Enterococcus faecium/isolation & purification , Enterococcus faecium/pathogenicity , Mastitis, Bovine/microbiology , Animals , Biofilms/growth & development , Cattle , Drug Resistance, Bacterial , Enterococcus faecium/genetics , Female , Inflammation , Mastitis, Bovine/pathology , Mice , Milk/microbiology , Virulence
2.
Plant Biol (Stuttg) ; 19(4): 599-607, 2017 Jul.
Article in English | MEDLINE | ID: mdl-28403565

ABSTRACT

Pseudomonas syringae is a phytopathogenic bacterium that causes lesions in leaves during the colonisation process. The damage is associated with production of many virulence factors, such as biofilm and phytotoxins. The essential oils of Thymus vulgaris (thyme) and Origanum vulgare (oregano) have been demonstrated to inhibit P. syringae. The aim of this study was to investigate the effects of T. vulgaris and O. vulgare essential oils on production of virulence factors of phytopathogenic P. syringae strains, including anti-biofilm and anti-toxins activities. The broth microdilution method was used for determination of MIC and biofilm inhibition assays. Coronatine, syringomycin and tabtoxin were pheno- and genotypically evaluated. Both oils showed good inhibitory activity against P. syringae, with MIC values from 1.43 to 11.5 mg·ml-1 for thyme and 5.8 to 11.6 mg·ml-1 for oregano. Biofilm formation, production of coronatine, syringomycin and tabtoxin were inhibited by thyme and oregano essential oil in most strains. The results presented here are promising, demonstrating the bactericidal activity and reduction of virulence factor production after treatment with thyme and oregano oil, providing insight into how they exert their antibacterial activity. These natural products could be considered in the future for the control of diseases caused by P. syringae.


Subject(s)
Oils, Volatile/chemistry , Oils, Volatile/pharmacology , Origanum/chemistry , Plant Extracts/pharmacology , Pseudomonas syringae/drug effects , Pseudomonas syringae/metabolism , Thymus Plant/chemistry , Virulence Factors/metabolism , Amino Acids/metabolism , Bacterial Proteins/metabolism , Dipeptides/metabolism , Indenes/metabolism , Microbial Sensitivity Tests
3.
Biomed Res Int ; 2015: 270973, 2015.
Article in English | MEDLINE | ID: mdl-26078941

ABSTRACT

In this work we extend the toxicological studies of hot aqueous extract of A. satureioides (As-HAE) evaluating cytotoxic and apoptotic effects on human peripheral blood mononuclear cells (PBMCs). We also determine genotoxic action of this extract in vivo. In addition, the extract was chemically characterized. Finally, we established a comparison with previous data of cold aqueous extract. The As-HAE induced cytotoxicity on PBMCs determined by trypan blue dye exclusion (CC50 = 653 µg/mL) and MTT (CC50 = 588 µg/mL) assays being more toxic than cold extract. However, As-HAE as well as cold extract did not induce apoptosis measured by Hoechst 33258 staining, TUNEL assay, and DNA fragmentation analysis. The in vivo micronucleus test showed that As-HAE exerted cytogenotoxic effects on bone marrow of mice, contrary to what was observed with cold extract. The chemical study of As-HAE allowed identifying the flavonoids found in cold extract: luteolin, quercetin, and 3-O-methylquercetin, but at higher concentrations. We suggest that toxic effects induced by As-HAE could be due to high concentrations of these flavonoids. Given that As-HAE is the most used in folkloric medicine, its administration should be controlled in order to prevent potential cell damage.


Subject(s)
Flavonoids/pharmacology , Luteolin/pharmacology , Plant Extracts/pharmacology , Quercetin/analogs & derivatives , Achyrocline/chemistry , Animals , Apoptosis/drug effects , DNA Damage/drug effects , DNA Fragmentation/drug effects , Flavonoids/chemistry , Humans , Leukocytes, Mononuclear/drug effects , Luteolin/isolation & purification , Mice , Plant Extracts/chemistry , Quercetin/isolation & purification , Quercetin/pharmacology
4.
Microbiol Res ; 163(3): 314-22, 2008.
Article in English | MEDLINE | ID: mdl-16930967

ABSTRACT

The aim of the present study was to characterize genotypically 45 Staphylococcus aureus strains isolated from humans, bovine subclinical mastitis and food samples in Argentina by rep-PCR and PCR amplification of virulence genes. Resistances to various antibiotics could be observed for the human S. aureus, less pronounced for the bovine strains, but not for the eight S. aureus isolated from food samples. The strains could be classified genotypically by rep-PCR and by amplification of the genes encoding protein A, coagulase, clumping factor, the collagen adhesin domains A and B, capsular polysaccharide 5 and 8, the accessory gene regulator agr classes I to III, and the S. aureus gene regulator sae. rep-PCR analyses and the different gene patterns revealed that the strains could be divided into seven groups mostly matching with the origin of the isolates. The present study describes genotypic variations of S. aureus strains isolated from different origins in Argentina. The study provides a valuable insight into molecular specificities of this important pathogen.


Subject(s)
DNA, Bacterial/genetics , Food Microbiology , Mastitis, Bovine/microbiology , Staphylococcal Infections/microbiology , Staphylococcus aureus/classification , Staphylococcus aureus/isolation & purification , Animals , Argentina , Bacterial Proteins/genetics , Bacterial Typing Techniques , Cattle , Cluster Analysis , Drug Resistance, Bacterial , Genotype , Humans , Microbial Sensitivity Tests , Molecular Epidemiology , Polymerase Chain Reaction/methods , Staphylococcus aureus/genetics , Virulence Factors/genetics
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