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1.
Drug Test Anal ; 8(5-6): 549-55, 2016 May.
Article in English | MEDLINE | ID: mdl-27443210

ABSTRACT

The widespread use of antibiotics in animals is causing concerns about the growing risk for development and the spread of antibiotic-resistant bacteria. Antibiotic consumption is higher in animals than in humans as reported in a joint publication of EFSA (European Food Safety Agency), ECDC (European Centre for Disease Prevention and Control), and EMA (European Medicines Agency) using data from 2011 and 2012. Both in humans and animals, positive associations between the consumption of antibiotics and resistant bacteria are observed. Responsible use of antibiotics in humans and animals should therefore be promoted. In this paper some general aspects of antibiotic resistance such as microbiological versus clinical resistance, intrinsic versus acquired resistance, resistance mechanisms, and transfer of resistance are briefly introduced. In 2012, the Belgian Center of Expertise on Antimicrobial Consumption and Resistance in Animals (AMCRA) was founded. Its mission is to collect and analyze all data related to antibiotic use and resistance in animals in Belgium and to communicate these findings in a neutral and objective manner. One of AMCRA's 10 objectives is a 50% reduction in antibiotic consumption in veterinary medicine in Belgium by 2020. The aim of this paper is to report on the achievements of this national project. The Institute for Agricultural and Fisheries Research (ILVO, Merelbeke-Melle), in collaboration with Ghent University, is currently working on three nationally funded projects on antibiotic resistance in animal husbandry. In the first project, an in vitro model is used to study the influence of low antibiotic concentrations due to carry-over after production and usage of medicated feed on the development of resistance in the pig gut. Part of that project is to develop a quantitative risk assessment model. A second project focuses on tracking excreted antibiotics used in pig rearing and their influence on the development of antibiotic resistance in pig manure and the environment. In the last project, the relation between the use of biocides in animal husbandry and antibiotic resistance development are being studied. Copyright © 2016 John Wiley & Sons, Ltd.


Subject(s)
Agriculture , Animal Husbandry/methods , Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial , Food Safety , Veterinary Drugs/pharmacology , Agriculture/methods , Animal Feed/analysis , Animals , Anti-Bacterial Agents/administration & dosage , Bacteria/drug effects , Belgium , Disinfectants/administration & dosage , Disinfectants/pharmacology , Fertilizers/analysis , Food Safety/methods , Humans , Risk Assessment , Swine , Veterinary Drugs/administration & dosage
2.
Vet Microbiol ; 171(3-4): 298-306, 2014 Jul 16.
Article in English | MEDLINE | ID: mdl-24598135

ABSTRACT

Using the agar dilution method, antimicrobial susceptibility to human-use antibiotics was determined among Belgian faecal Salmonella isolates from healthy pigs and broiler chickens. Both epidemiological cut-off values and clinical breakpoints were applied for interpretation of the results. Cephalosporin-resistant isolates were examined for the presence of genes encoding CTX-M, SHV, TEM and CMY ß-lactamases. All isolates with decreased quinolone susceptibility were screened for plasmid-borne genes qnr, qepA and aac(6')-Ib-cr. In all, 368 Salmonella isolates were recovered from pigs and 452 from chickens. Clinical resistance to ciprofloxacin was absent in isolates of both host species, and was 1.9 and 13.1% to cefotaxime in pig and poultry isolates, respectively. Decreased susceptibility to cefotaxime amounted to 2.2 and 0.7%, whereas for ciprofloxacin this was 3.0 and 23.0% in pig and poultry isolates, respectively. Ciprofloxacin decreased susceptibility was limited to few serovars, mainly Paratyphi B. Multidrug resistance was markedly higher for pig isolates (39.7%) than for chicken isolates (17.3%). Sixty-six cefotaxime-resistant isolates, 59 from chickens and 7 from pigs, were phenotypically determined as ESBL/AmpC producers; predominantly Paratyphi B and Typhimurium serovars. BlaCTX-M (mostly blaCTXM-1, but also blaCTXM-2 and blaCTXM-9) and blaTEM-52 were the predominant ESBL genes. Only few isolates expressed SHV-12 or an AmpC enzyme (CMY-2). Isolates of four serovars carried qnr genes: Brandenburg and Llandof from pigs, both qnrS; Indiana and Paratyphi B from chickens with qnrB and qnrA. The latter isolate carried blaCTX-M-9 and was the only strain with a plasmid-borne quinolone resistance gene among the ESBL/AmpC producers. This Salmonella survey confirms that the ESBL/AmpC producers are particularly prevalent in chickens (12.8%), and much less in pigs (1.9%). A link between plasmid-borne quinolone resistance genes and ESBLs/AmpC was uncommon.


Subject(s)
Anti-Infective Agents/pharmacology , Cephalosporins/pharmacology , Chickens/microbiology , Ciprofloxacin/pharmacology , Drug Resistance, Multiple, Bacterial/genetics , Salmonella/drug effects , Sus scrofa/microbiology , Animals , Bacterial Proteins/genetics , Belgium , Chickens/genetics , Feces/microbiology , Humans , Microbial Sensitivity Tests/statistics & numerical data , Microbial Sensitivity Tests/veterinary , Salmonella/genetics , Salmonella/isolation & purification , Species Specificity , Sus scrofa/genetics , Swine , beta-Lactamases/genetics
3.
Int J Syst Evol Microbiol ; 55(Pt 5): 2177-2182, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16166728

ABSTRACT

The taxonomic position of strain LMG 13590(T), originally isolated from dog faeces and classified as Enterococcus dispar in the BCCM/LMG Bacteria Catalogue, was reinvestigated. This strain and 12 recent isolates from faecal samples of healthy dogs occupied a clearly separate position when investigated with multilocus sequence analysis (MLSA) of the genes encoding the alpha subunit of ATP synthase (atpA), RNA polymerase alpha subunit (rpoA) and phenylalanyl-tRNA synthase alpha subunit (pheS). The 16S rRNA gene sequence of one representative strain showed highest similarities of 98-99% with E. dispar LMG 13521(T), Enterococcus canis LMG 12316(T) and Enterococcus asini LMG 18727(T). A further polyphasic taxonomic study based on whole-cell protein fingerprinting, DNA-DNA hybridization and biochemical features demonstrated that the 13 enterococcal dog faecal strains represent a single, novel Enterococcus species for which the name Enterococcus canintestini sp. nov. is proposed. The type strain is LMG 13590(T) (=CCM 7285(T)).


Subject(s)
Dogs/microbiology , Enterococcus/classification , Feces/microbiology , Animals , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Typing Techniques , DNA, Bacterial/analysis , DNA, Ribosomal/analysis , Enterococcus/genetics , Enterococcus/isolation & purification , Genes, rRNA , Molecular Sequence Data , Nucleic Acid Hybridization , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
4.
Int J Syst Evol Microbiol ; 55(Pt 4): 1569-1573, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16014483

ABSTRACT

Four staphylococcal isolates from clinical and necropsy specimens from a cat, a dog, a horse and a parrot (Psittacus erithacus timneh) were found to constitute a distinct taxon. 16S rRNA gene sequence analysis revealed that its closest phylogenetic relatives are Staphylococcus intermedius and Staphylococcus delphini. Growth characteristics, biochemical features and DNA-DNA hybridizations demonstrated that the strains differ from these and other known species and that they represent a single, novel Staphylococcus species for which the name Staphylococcus pseudintermedius sp. nov. is proposed. The novel species is commonly confused with S. intermedius in routine diagnostic veterinary bacteriology. Although the strains described were isolated from lesions and show several characteristics typical of pathogenic staphylococci, such as coagulase, DNase and beta-haemolysin production, the pathogenic significance of the novel species remains unclear. The type strain, LMG 22219(T) (=ON 86(T)=CCUG 49543(T)), was isolated from lung tissue of a cat.


Subject(s)
Cats/microbiology , Coagulase/metabolism , Dogs/microbiology , Horses/microbiology , Parrots/microbiology , Staphylococcus/classification , Animals , DNA, Bacterial/analysis , DNA, Ribosomal/analysis , Genes, rRNA , Molecular Sequence Data , Nucleic Acid Hybridization , Phenotype , RNA, Ribosomal, 16S , Sequence Analysis, DNA , Species Specificity , Staphylococcus/enzymology , Staphylococcus/genetics , Staphylococcus/growth & development
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