Staphylococcus xylosus, Staphylococcus equorum, and Staphylococcus epidermidis strains were isolated from Bryndza cheese and identified using PCR method. The antimicrobial susceptibility of these strains was assessed using disc diffusion method and broth microdilution method. The highest percentage of resistance was detected for ampicillin and oxacillin, and in contrary, isolates were susceptible or intermediate resistant to ciprofloxacin and chloramphenicol. Fourteen of the S. xylosus isolates (45%) and eleven of the S. equorum isolates (41%) exhibited multidrug resistance. None of the S. epidermidis isolate was multiresistant. The phenotypic resistance to oxacillin was verified by PCR amplification of the gene mecA.

• MeSH
• Anti-Bacterial Agents pharmacology   MeSH
• Drug Resistance, Bacterial * MeSH
• Microbial Sensitivity Tests MeSH
• Food Microbiology * MeSH
• Methicillin Resistance MeSH
• Staphylococcus classification   drug effects   isolation & purification   MeSH
• Cheese microbiology   MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Anti-Bacterial Agents MeSH

Strains identified in ovine cheese and bryndza by matrix-assisted laser desorption/ionization time-of-flight analysis belonged to ten species of non-enterococcal lactic acid bacteria and included Lactobacillus casei/Lactobacillus paracasei, Lactobacillus plantarum, Lactobacillus rhamnosus, Lactobacillus helveticus, Lactobacillus delbrueckii, Lactobacillus fermentum, Lactobacillus brevis, Lactococcus lactis, Pediococcus pentosaceus and Pediococcus acidilactici. The susceptibility toward antibiotics was determined in lactobacilli, lactococci and pediococci and also in Escherichia coli for comparison. Analysis of L. fermentum and pediococci revealed the presence of non-wild-type epidemiological cut-offs in streptomycin, clindamycin or gentamicin. E. coli were resistant to ampicillin, tetracycline, enrofloxacin and florfenicol. No extended spectrum β-lactamases were detected.

• MeSH
• Anti-Bacterial Agents pharmacology   MeSH
• Bacteria drug effects   genetics   isolation & purification   MeSH
• Microbial Sensitivity Tests MeSH
• Sheep MeSH
• Cheese microbiology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Anti-Bacterial Agents MeSH

An occurrence of resistance to tetracycline (TET) and erythromycin (ERY) was ascertained in 82 isolates of Enterococcus spp. of animal and environmental origin. Using E test, 33 isolates were resistant to TET and three isolates to ERY. Using polymerase chain reaction (PCR; single and multiplex), the TET determinants tet(M) and tet(L) were detected in 35 and 13 isolates, respectively. Twelve isolates carried both tet(M) and tet(L) genes. Eight isolates possessed ermB gene associated with ERY resistance. Multiplex PCR was shown to be a suitable method for simultaneous determination of all three resistance determinants that occurred most frequently in bacteria isolated from poultry. This study also demonstrates that gastrointestinal tract of broilers may be a reservoir of enterococci with acquired resistance to both TET and ERY that can be transferred to humans via food chain.

• MeSH
• Anti-Bacterial Agents pharmacology   MeSH
• Genes, Bacterial drug effects   MeSH
• DNA, Bacterial analysis   MeSH
• Poultry microbiology   MeSH
• Enterococcus drug effects   genetics   isolation & purification   MeSH
• Gastrointestinal Tract microbiology   MeSH
• Macrolides pharmacology   MeSH
• Microbial Sensitivity Tests MeSH
• Drug Resistance, Multiple, Bacterial genetics   MeSH
• Polymerase Chain Reaction MeSH
• Tetracycline pharmacology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Anti-Bacterial Agents MeSH
• DNA, Bacterial MeSH
• Macrolides MeSH
• Tetracycline MeSH

The development of resistance to quinolones (nalidixic acid, ciprofloxacin and enrofloxacin) in 2006-2008 was evaluated in 317 strains of Escherichia coli isolated from healthy chicken broilers from various farms. The isolates (2006/2007/2008) showed a high resistance to nalidixic acid (87/85/67 %), ciprofloxacin (CIP) (49/54/29 %) and enrofloxacin (ENR) (52/42/22 %). Nalidixic acid-resistant isolates with low level of MIC for CIP and ENR represented a single mutation; intermediary MIC for CIP and ENR were related to two mutations and high level resistance MIC for CIP (> or =4 mg/L) and ENR (> or =16 mg/L) represented three mutations (two in gyrA and one in parC). There was a correlation between the phenotype reading of high-level resistance and mutations in gyrA (Ser83Leu, Asp87Tyr or Asp87Asn) and parC (Ser80Ile) gene. Plasmid-mediated quinolone-resistance qnrS gene was detected in one Escherichia coli strain with a high level of ciprofloxacin resistance. Our results demonstrate the increase in occurrence of multiresistant E. coli strains with a high level of chromosomal and plasmid resistance to fluoroquinolones.

• MeSH
• Anti-Bacterial Agents pharmacology   MeSH
• Chromosomes, Bacterial MeSH
• Drug Resistance, Bacterial * MeSH
• Quinolones pharmacology   MeSH
• DNA Gyrase genetics   MeSH
• DNA Topoisomerase IV genetics   MeSH
• Escherichia coli drug effects   isolation & purification   MeSH
• Chickens microbiology   MeSH
• Microbial Sensitivity Tests MeSH
• Mutation, Missense MeSH
• Molecular Sequence Data MeSH
• Plasmids MeSH
• Escherichia coli Proteins genetics   MeSH
• Amino Acid Sequence MeSH
• Amino Acid Substitution MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Anti-Bacterial Agents MeSH
• Quinolones MeSH
• DNA Gyrase MeSH
• DNA Topoisomerase IV MeSH
• Escherichia coli Proteins MeSH

Enterococci isolated from 28 different commercially available feeds (10-1000 CFU/mL) were identified and their probiotic potential was determined. Species identification of 22 selected strains was performed by intergenic length-polymorphism analysis (tRNA-PCR); PCR products were analyzed using capillary electrophoresis. Six strains were allotted to the species Enterococcus faecium, four to E. faecalis, one to E. hirae; the remaining strains were not classed. The strains were sensitive to vancomycin, ampicillin, tetracycline and rifampicin. They were able to adhere to human as well as canine intestinal mucus. They produced lactic acid (0.99-1.04 mmol/L) and most of them were urease-positive with sufficient survival in 5 % Oxgall-bile. They did not show any inhibitory activity due to antimicrobial substances. Plasmid DNA was detected in 8 strains, the bands responding to small molecular size (10 kbp). Considering all probiotically important properties, E. faecium strain EE3 was suggested as potential feed additive.

• MeSH
• Anti-Bacterial Agents pharmacology   MeSH
• Bacterial Proteins metabolism   MeSH
• Enterococcus chemistry   drug effects   isolation & purification   metabolism   MeSH
• Animal Feed microbiology   MeSH
• Lactic Acid metabolism   MeSH
• Humans MeSH
• Probiotics chemistry   isolation & purification   MeSH
• Dogs MeSH
• Intestines microbiology   MeSH
• Urease metabolism   MeSH
• Animals MeSH
• Check Tag
• Humans MeSH
• Dogs MeSH
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Anti-Bacterial Agents MeSH
• Bacterial Proteins MeSH
• Lactic Acid MeSH
• Urease MeSH

Twelve lactobacilli isolates from mucosa of 3-5-week-old weaned pigs were found to exert good antimicrobial activity against common porcine pathogens (S. aureus, B. cereus, E. coli, C. perfringens). Two of them produced in addition to lactic acid also considerable amounts of acetic acid, and 6 of them produced hydrogen peroxide and metabolites other than organic acids. Isolates 4/26 and 2/25 (identified as L. crispatus or L. amylovorus) were inhibitory against most strains of S. aureus, B. cereus and E. coli, and especially the strain 4/26 survived well in simulated gastric and intestinal juice. Diarrhea-causing E. coli O8K88H9 Ent(+) was successfully inhibited by the growing culture as well as by the catalase-treated and neutralized supernatant of L. reuteri 12/26. Mucin degradation and multiple resistance to antibiotics were not observed.

• MeSH
• Drug Resistance, Microbial MeSH
• Bacillus cereus drug effects   MeSH
• Clostridium perfringens drug effects   MeSH
• Escherichia coli drug effects   MeSH
• Feces microbiology   MeSH
• Ileum microbiology   MeSH
• Culture Media, Conditioned pharmacology   MeSH
• Culture Media chemistry   pharmacology   MeSH
• Lactic Acid pharmacology   MeSH
• Lactobacillus drug effects   isolation & purification   metabolism   MeSH
• Mucins metabolism   MeSH
• Swine Diseases prevention & control   MeSH
• Weaning MeSH
• Hydrogen Peroxide metabolism   MeSH
• Immunity, Innate MeSH
• Probiotics MeSH
• Staphylococcus aureus drug effects   MeSH
• Intestinal Mucosa microbiology   MeSH
• Sus scrofa microbiology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Culture Media, Conditioned MeSH
• Culture Media MeSH
• Lactic Acid MeSH
• Mucins MeSH
• Hydrogen Peroxide MeSH