292 results on '"Ferran, Aude"'
Search Results
2. Antimicrobial combinations against Helicobacter pylori including benzoxadiazol-based flavodoxin inhibitors: in vitro characterization
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Ministerio de Ciencia e Innovación (España), Gobierno de Aragón, Beyria, Lilha [0000-0002-1862-5637], #NODATA#, Salillas, Sandra [0000-0003-0195-5434], Díaz de Villegas, María Dolores [0000-0001-9033-8459], Aínsa, José Antonio [0000-0003-2076-844X], Sancho, Javier [0000-0002-2879-9200], Bousquet-Mélou, Alain [0000-0002-7661-4311], Ferran, Aude A. [0000-0002-6629-1088], Beyria, Lilha, Gourbeyre, Ophelie, Salillas, Sandra, Mahía, Alejandro, Díaz de Villegas, María Dolores, Aínsa, José Antonio, Sancho, Javier, Bousquet-Mélou, Alain, Ferran, Aude A., Ministerio de Ciencia e Innovación (España), Gobierno de Aragón, Beyria, Lilha [0000-0002-1862-5637], #NODATA#, Salillas, Sandra [0000-0003-0195-5434], Díaz de Villegas, María Dolores [0000-0001-9033-8459], Aínsa, José Antonio [0000-0003-2076-844X], Sancho, Javier [0000-0002-2879-9200], Bousquet-Mélou, Alain [0000-0002-7661-4311], Ferran, Aude A. [0000-0002-6629-1088], Beyria, Lilha, Gourbeyre, Ophelie, Salillas, Sandra, Mahía, Alejandro, Díaz de Villegas, María Dolores, Aínsa, José Antonio, Sancho, Javier, Bousquet-Mélou, Alain, and Ferran, Aude A.
- Abstract
The antimicrobial resistance of Helicobacter pylori (Hp) currently poses a threat to available treatment regimens. Developing antimicrobial drugs targeting new bacterial targets is crucial, and one such class of drugs includes Hp-flavodoxin (Hp-fld) inhibitors that target an essential metabolic pathway in Hp. Our study demonstrated that combining these new drugs with conventional antibiotics used for Hp infection treatment prevented the regrowth observed with drugs used alone. Hp-fld inhibitors show promise as new drugs to be incorporated into the treatment of Hp infection, potentially reducing the development of resistance and shortening the treatment duration.
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- 2024
3. Supplemental material for Antimicrobial combinations against Helicobacter pylori including benzoxadiazol-based flavodoxin inhibitors: in vitro characterization
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Beyria, Lilha, Gourbeyre, Ophelie, Salillas, Sandra, Mahía, Alejandro, Díaz de Villegas, María D., Aínsa, José Antonio, Sancho, Javier, Bousquet-Mélou, Alain, Ferran, Aude A., Beyria, Lilha, Gourbeyre, Ophelie, Salillas, Sandra, Mahía, Alejandro, Díaz de Villegas, María D., Aínsa, José Antonio, Sancho, Javier, Bousquet-Mélou, Alain, and Ferran, Aude A.
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- 2024
4. Development of an in vitro biofilm model for the study of the impact of fluoroquinolones on sewer biofilm microbiota
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Naudin, Sarah A., primary, Ferran, Aude A., additional, Imazaki, Pedro Henrique, additional, Arpaillange, Nathalie, additional, Marcuzzo, Camille, additional, Vienne, Maïna, additional, Demmou, Sofia, additional, Bousquet-Mélou, Alain, additional, Ramon-Portugal, Felipe, additional, Lacroix, Marlene Z., additional, Hoede, Claire, additional, Barret, Maialen, additional, Dupouy, Véronique, additional, and Bibbal, Delphine, additional
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- 2024
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5. Why Were More Than 200 Subjects Required to Demonstrate the Bioequivalence of a New Formulation of Levothyroxine with an Old One?
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2020
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6. Dynamic interactions between cephalexin and macrophages on different Staphylococcus aureus inoculum sizes: a tripartite in vitro model
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Lallemand, Elodie Anne, Zemirline, Claudine, Toutain, Pierre-Louis, Bousquet-Melou, Alain, Ferran, Aude A., and Boullier, Séverine
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- 2021
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7. Destruction of Staphylococcus aureus biofilms by combining an antibiotic with subtilisin A or calcium gluconate
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Liu, JingJing, Madec, Jean-Yves, Bousquet-Mélou, Alain, Haenni, Marisa, and Ferran, Aude A.
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- 2021
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8. The sub-MIC selective window decreases along the digestive tract: determination of the minimal selective concentration of oxytetracycline in sterilised intestinal contents.
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Imazaki, Pedro Henrique, Voisin, Bertille, Arpaillange, Nathalie, Roques, Béatrice B., Dordet-Frisoni, Emilie, Dupouy, Véronique, Ferran, Aude A., Bousquet-Mélou, Alain, and Bibbal, Delphine
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GASTROINTESTINAL contents ,ALIMENTARY canal ,OXYTETRACYCLINE ,DRUG resistance in microorganisms ,CECUM - Abstract
Introduction: The administration of antibiotics can expose the digestive microbiota of humans and animals to sub-inhibitory concentrations, potentially favouring the selection of resistant bacteria. The minimal selective concentration (MSC) is a key indicator to understand this process. The MSC is defined as the lowest concentration of an antibiotic that promotes the growth of a resistant strain over a susceptible isogenic strain. It represents the lower limit of the sub-minimal inhibitory concentration (MIC) selective window, where resistant mutants can be selected. Previous studies focused on determining the MSC under standard culture conditions, whereas our research aimed to determine the MSC in a model that approximates in vivo conditions. Methods: We investigated the MSC of oxytetracycline (OTC) in Mueller-Hinton broth (MHB) and sterilised intestinal contents (SIC) from the jejunum, caecum and rectum (faeces) of pigs, using two isogenic strains of Escherichia coli (one susceptible and one resistant to OTC). Additionally, the MIC of OTC against the susceptible strain was determined to assess the upper limit of the sub-MIC selective window. Results: Our study took a novel approach, and the results indicated that MIC and MSC values were lower in MHB than in SIC. In the latter, these values varied depending on the intestinal segment, with distal compartments exhibiting higher MIC and MSC values. Moreover, the sub-MIC selective window of OTC in SIC narrowed from the jejunum to the rectum, with a significantly closer MSC to MIC in faecal SIC. Discussion: The results suggest that OTC binds to digestive contents, reducing the fraction of free OTC. However, binding alone does not fully explain our results, and interactions between bacteria and intestinal contents may play a role. Furthermore, our findings provide initial estimates of low concentrations facilitating resistance selection in the gut. Finally, this research enhances the understanding of antimicrobial resistance selection, emphasising the intricate interplay between antibiotics and intestinal content composition in assessing the risk of resistance development in the gut. [ABSTRACT FROM AUTHOR]
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- 2024
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9. Predicted efficacy and tolerance of different dosage regimens of benzylpenicillin in horses based on a pharmacokinetic study with three IM formulations and one IV formulation.
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Ferran, Aude A., Roques, Béatrice B., Chapuis, Laura, Taisuke Kuroda, Lacroix, Marlène Z., Toutain, Pierre-Louis, Bousquet-Melou, Alain, and Lallemand, Elodie A.
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PENICILLIN G ,HORSES ,CLINICAL chemistry ,STREPTOCOCCUS equi ,INTRAMUSCULAR injections - Abstract
Introduction: Benzylpenicillin (BP) is a first-line antibiotic in horses but there are discrepancies between manufacturers and literature recommendations regarding dosing regimen. Objectives of this study were to evaluate pharmacokinetics and local tolerance of four different formulations of BP in adult horses, and to suggest optimized dosing regimen according to the formulation. Methods: A cross-over design was used in 3 phases for the intramuscular injection of three different products: procaine BP alone, procaine BP/benzathine BP combination or penethamate hydriodide were administered IM in the gluteal muscles of 6 horses for 3 days. Single IV administration of sodium BP was performed to the same horses with a dose of 22,000 IU BP/kg bwt 39 weeks after last IM injection. BP plasma concentrations were determined by UPLC assay coupled with mass spectrometry and a PK/PD analysis was conducted to predict the efficacy of various dosing regimens by estimating values of the fT>MIC index for different minimum inhibitory concentrations (MIC). Tolerance at the site of IM injection was monitored by creatine kinase activity quantified with a validated chemistry system and clinical scorings. Results and discussion: Except one neurological reaction following one administration of penethamate hydriodide, the tolerance was good. Procaine BP alone, procaine BP/benzathine BP combination or penethamate hydriodide intramuscular administrations at a dosage of 22,000 IU BP/kg bwt q24h for 5 days would yield plasma concentrations that should be effective against bacteria with MIC of ≤0.256, 0.125 or 0.064 mg/L respectively. Of all the tested treatments, the use of a sodium BP by IV Constant Rate Infusion (CRI) for 10 hours a day was deemed to be the most efficient. All the formulations tested in this study are adequate to treat infections with susceptible Streptococcus equi. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Antimicrobial combinations against Helicobacter pylori including benzoxadiazol-based flavodoxin inhibitors: in vitro characterization
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Beyria, Lilha, primary, Gourbeyre, Ophelie, additional, Salillas, Sandra, additional, Mahía, Alejandro, additional, Díaz de Villegas, María Dolores, additional, Aínsa, José Antonio, additional, Sancho, Javier, additional, Bousquet-Mélou, Alain, additional, and Ferran, Aude A., additional
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- 2023
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11. Pharmacokinetic–pharmacodynamic cutoff values for benzylpenicillin in horses to support the establishment of clinical breakpoints for benzylpenicillin antimicrobial susceptibility testing in horses
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Lallemand, Elodie A., primary, Bousquet-Mélou, Alain, additional, Chapuis, Laura, additional, Davis, Jennifer, additional, Ferran, Aude A., additional, Kukanich, Butch, additional, Kuroda, Taisuke, additional, Lacroix, Marlène Z., additional, Minamijima, Yohei, additional, Olsén, Lena, additional, Pelligand, Ludovic, additional, Portugal, Felipe Ramon, additional, Roques, Béatrice B., additional, Santschi, Elizabeth M., additional, Wilson, Katherine E., additional, and Toutain, Pierre-Louis, additional
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- 2023
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12. Authors’ Reply to Yu et al.: “Levothyrox® New and Old Formulations: Are They Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2020
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13. Authors’ Reply to Nicolas: “Why Were More than 200 Subjects Required to Demonstrate the Bioequivalence of a New Formulation of Levothyroxine with an Old One?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2020
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14. Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude, and Toutain, Pierre-Louis
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- 2019
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15. Authors’ Reply to Castello-Bridoux et al.: “Comment on Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2019
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16. Authors’ Reply to Nicolas: “Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2019
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17. Biased computation of probability of target attainment for antimicrobial drugs
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Toutain, Pierre‐Louis, primary, Gandia, Peggy, additional, Pelligand, Ludovic, additional, Ferran, Aude A., additional, Lees, Peter, additional, Bousquet‐Mélou, Alain, additional, and Concordet, Didier, additional
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- 2023
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18. Pharmacokinetic-pharmacodynamic cutoff values for benzylpenicillin in horses to support the establishment of clinical breakpoints for benzylpenicillin antimicrobial susceptibility testing in horses
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Lallemand, Elodie A., Bousquet-Melou, Alain, Chapuis, Laura, Davis, Jennifer L., Ferran, Aude A., Kukanich, Butch, Kuroda, Taisuke, Lacroix, Marlene Z., Minamijima, Yohei, Olsen, Lena, Pelligand, Ludovic, Portugal, Felipe Ramon, Roques, Beatrice B., Santschi, Elizabeth M., Wilson, Katherine E., Toutain, Pierre-Louis, Lallemand, Elodie A., Bousquet-Melou, Alain, Chapuis, Laura, Davis, Jennifer L., Ferran, Aude A., Kukanich, Butch, Kuroda, Taisuke, Lacroix, Marlene Z., Minamijima, Yohei, Olsen, Lena, Pelligand, Ludovic, Portugal, Felipe Ramon, Roques, Beatrice B., Santschi, Elizabeth M., Wilson, Katherine E., and Toutain, Pierre-Louis
- Abstract
Introduction: The aim of this international project was to establish a species-specific Clinical Breakpoint for interpretation of Antimicrobial Susceptibility Testing of benzylpenicillin (BP) in horses. Methods: A population pharmacokinetic model of BP disposition was developed to compute PK/PD cutoff values of BP for different formulations that are commonly used in equine medicine around the world (France, Sweden, USA and Japan). Investigated substances were potassium BP, sodium BP, procaine BP, a combination of procaine BP and benzathine BP and penethamate, a prodrug of BP. Data were collected from 40 horses that provided 63 rich profiles of BP corresponding to a total of 1022 individual BP plasma concentrations. Results: A 3-compartment disposition model was selected. For each of these formulations, the PK/PD cutoff was estimated for different dosage regimens using Monte Carlo simulations. The fAUC/MIC or fT>MIC were calculated with a free BP fraction set at 0.4. For fAUC/MIC, a target value of 72 h (for a 72h treatment) was considered. For fT>MIC, efficacy was assumed when free plasma concentrations were above the explored MIC (0.0625-2 mg/L) for 30 or 40 % of the dosing interval. For continuous infusion, a fT>MIC of 90 % was considered. It was shown that a PK/PD cutoff of 0.25 mg/L can be achieved in 90 % of horses with routine regimen (typically 22,000 IU/kg or 12.4 mg/kg per day) with IM procaine BP once a day (France, Japan, Sweden but not USA1) and with IM sodium BP at 14.07 mg/kg, twice a day or IV sodium BP infusion of 12.4 mg/kg per day. In contrast, penethamate and the combination of procaine BP and benzathine BP were unable to achieve this PK/PD cutoff not even an MIC of 0.125 mg/L. Discussion: The PK/PD cutoff of 0.25 mg/L is one dilution lower than the clinical breakpoint released by the CLSI (0.5 mg/ L). From our simulations, the CLSI clinical breakpoint can be achieved with IM procaine BP twice a day at 22,000 IU i.e. 12.4 mg/kg.
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- 2023
19. The Selection of Antibiotic- and Bacteriophage-Resistant Pseudomonas aeruginosa Is Prevented by Their Combination
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Ferran, Aude A., primary, Lacroix, Marlène Z., additional, Gourbeyre, Ophélie, additional, Huesca, Alicia, additional, Gaborieau, Baptiste, additional, Debarbieux, Laurent, additional, and Bousquet-Mélou, Alain, additional
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- 2022
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20. Species Differences in Pharmacokinetics and Pharmacodynamics
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Toutain, Pierre-Louis, Ferran, Aude, Bousquet-Mélou, Alain, Cunningham, Fiona, editor, Elliott, Jonathan, editor, and Lees, Peter, editor
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- 2010
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21. Authors’ Reply to Lechat et al.: “Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2019
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22. Authors’ Reply to Coste et al.: “Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2019
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23. Author’s Reply to Trechot: “Comment on Levothyrox® New and Old Formulations: Are they Switchable for Millions of Patients?”
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Concordet, Didier, Gandia, Peggy, Montastruc, Jean-Louis, Bousquet-Mélou, Alain, Lees, Peter, Ferran, Aude A., and Toutain, Pierre-Louis
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- 2019
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24. Pharmacokinetic/pharmacodynamic assessment of the effects of parenteral administration of a fluoroquinolone on the intestinal microbiota: Comparison of bactericidal activity at the gut versus the systemic level in a pig model
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Ferran, Aude A., Bibbal, Delphine, Pellet, Terence, Laurentie, Michel, Gicquel-Bruneau, Mireille, Sanders, Pascal, Schneider, Marc, Toutain, Pierre-Louis, and Bousquet-Melou, Alain
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- 2013
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25. The selection of antibiotic- and bacteriophage-resistant Pseudomonas aeruginosa is prevented by their combination
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Ferran, Aude A, primary, Lacroix, Marlène Z., additional, Gourbeyre, Ophélie, additional, Huesca, Alicia, additional, Gaborieau, Baptiste, additional, Debarbieux, Laurent, additional, and Bousquet-Mélou, Alain, additional
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- 2022
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26. Les inhalations chez le cheval
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Ferran, Aude A., Lallemand, Elodie, and Baures, Simone
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[SDV] Life Sciences [q-bio] - Published
- 2022
27. Pour limiter l'exposition de l'environnement aux antibiotiques lors de traitements en médecine vétérinaire
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Millemann, Yves, Ferran, Aude A., Hugnet, Christophe, Berny, Philippe, Perrot, Sébastien, Bouchard, Damien S., Faucon, Jean-Christophe, and Chiffoleau, Emmanuelle
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médicament vétérinaire ,sustainable development ,ecotoxicity ,Antibiotic resistance ,[SDV.BA.MVSA] Life Sciences [q-bio]/Animal biology/Veterinary medicine and animal Health ,veterinary drug ,environnement ,ecotoxicology ,antibiotique ,veterinary medicine ,écotoxicité ,antibiotic ,développement durable ,pollution ,médecine vétérinaire ,environment ,écotoxicologie ,Résistance Aux Médicaments - Abstract
Les antibiotiques jouent un rôle central dans la gestion des maladies infectieuses chez l'homme, les animaux de compagnie, le bétail et en aquaculture.Les antibiotiques sont produits, consommés et libérés dans l'environnement à grande échelle, ce qui suscite des inquiétudes quant à l'impact négatif de la présence de résidus d'antibiotiques sur les écosystèmes aquatiques et terrestres (Brandt et al. 2015).Plusieurs rapports récents font état de la contamination de l'environnement par des antibiotiques, des bactéries résistantes aux antibiotiques (naturellement ou par pression de sélection liée aux activités anthropiques) et des supports génétiques de la résistance (Anses 2021, EFSA 2021).La contribution de l'environnement à l'émergence, la sélection et/ou la dissémination de résistances aux antibiotiques à l'homme et à l'animal devrait être à l'avenir prise en compte dans l'évaluation de la sécurité des médicaments vétérinaires (CVMP, 2018 ; Règlement 2019/6).
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- 2022
28. Impact of early versus later fluoroquinolone treatment on the clinical; microbiological and resistance outcomes in a mouse-lung model of Pasteurella multocida infection
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Ferran, Aude A., Toutain, Pierre-Louis, and Bousquet-Mélou, Alain
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- 2011
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29. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 9: Polymyxins: colistin
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I., Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Indústries Alimentàries, Funcionalitat i Seguretat Alimentària, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., and Peixe L.
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663/664 ,medicine.drug_class ,Veterinary (miscellaneous) ,Polymyxin ,Growth promotion ,TP1-1185 ,Plant Science ,Biology ,Microbiology ,Non target ,Antibiotic resistance ,growth promotion ,medicine ,TX341-641 ,antimicrobial resistance ,colistin ,yield increase ,Animal health ,Nutrition. Foods and food supply ,business.industry ,Chemical technology ,sub-inhibitory concentration ,sub‐inhibitory concentration ,Contamination ,Feed Antimicrobial Resistance Selection Concentration (FARSC) ,Antimicrobial ,food-producing animal ,Biotechnology ,Colistin ,Animal Science and Zoology ,Parasitology ,business ,Food Science ,medicine.drug - Abstract
The specific concentrations of colistin in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels of colistin in feed that showed to have an effect on growth promotion/increased yield were reported. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these antimicrobials. info:eu-repo/semantics/publishedVersion
- Published
- 2021
30. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 13: Diaminopyrimidines: trimethoprim
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I., Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Indústries Alimentàries, Funcionalitat i Seguretat Alimentària, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., and Peixe L.
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Complete data ,663/664 ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Biology ,Microbiology ,Trimethoprim ,Non target ,Antibiotic resistance ,growth promotion ,medicine ,TX341-641 ,antimicrobial resistance ,yield increase ,Animal health ,Nutrition. Foods and food supply ,business.industry ,Chemical technology ,sub-inhibitory concentration ,food-producing animals ,Biol5012 ,food‐producing animals ,sub‐inhibitory concentration ,Contamination ,Feed Antimicrobial Resistance Selection Concentration (FARSC) ,Antimicrobial ,food-producing animal ,Biotechnology ,Scientific Opinion ,Animal Science and Zoology ,Parasitology ,business ,Food Science ,medicine.drug - Abstract
The specific concentrations of trimethoprim in non-target feed for food-producing animals below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. The FARSC for trimethoprim was estimated. Uncertainties and data gaps associated to the levels reported were addressed. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. No suitable data for the assessment were available. It was recommended to perform further studies to supply more diverse and complete data related to the requirements for calculation of the FARSC for trimethoprim. info:eu-repo/semantics/publishedVersion
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- 2021
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31. Maximum levels of cross‐contamination for 24 antimicrobial active substances in non‐target feed. Part 12: Tetracyclines: tetracycline, chlortetracycline, oxytetracycline, and doxycycline
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Indústries Alimentàries, Funcionalitat i Seguretat Alimentària, Koutsoumanis K., Allende A., Alvarez-Ordonez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., and Peixe L.
- Subjects
Chlortetracycline ,663/664 ,Tetracycline ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Oxytetracycline ,Biology ,Microbiology ,Antibiotic resistance ,growth promotion ,medicine ,TX341-641 ,antimicrobial resistance ,Food science ,chlortetracycline ,tetracycline ,Doxycycline ,doxycycline ,Nutrition. Foods and food supply ,Chemical technology ,food-producing animals ,Contamination ,Antimicrobial ,food-producing animal ,Animal Science and Zoology ,Parasitology ,oxytetracycline ,Food Science ,medicine.drug - Abstract
The specific concentrations of tetracycline, chlortetracycline, oxytetracycline and doxycycline in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. The FARSC for these four tetracyclines was estimated. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for tetracycline, chlortetracycline, oxytetracycline, whilst for doxycycline no suitable data for the assessment were available. Uncertainties and data gaps associated with the levels reported were addressed. It was recommended to perform further studies to supply more diverse and complete data related to the requirements for calculation of the FARSC for these antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
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32. Maximum levels of cross‐contamination for 24 antimicrobial active substances in non‐target feed. Part 10: Quinolones: flumequine and oxolinic acid
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., Peixe L., Indústries Alimentàries, and Funcionalitat i Seguretat Alimentària
- Subjects
663/664 ,Veterinary (miscellaneous) ,Growth promotion ,flumequine ,TP1-1185 ,Plant Science ,Microbiology ,Non target ,Antibiotic resistance ,growth promotion ,oxolinic acid ,Oxolinic acid ,medicine ,TX341-641 ,Food science ,antimicrobial resistance ,Food8822 ,yield increase ,Animal health ,Nutrition. Foods and food supply ,Chemical technology ,sub-inhibitory concentration ,food-producing animals ,food‐producing animals ,Contamination ,sub‐inhibitory concentration ,Antimicrobial ,food-producing animal ,Scientific Opinion ,Flumequine ,Environmental science ,Animal Science and Zoology ,Parasitology ,Food Science ,medicine.drug - Abstract
The specific concentrations of flumequine and oxolinic acid in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data are available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. No suitable data for the assessment were available. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
- View/download PDF
33. Maximum levels of cross‐contamination for 24 antimicrobial active substances in non‐target feed. Part 4: β‐Lactams: amoxicillin and penicillin V
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Indústries Alimentàries, Funcionalitat i Seguretat Alimentària, Koutso111umanis K., Allende A., Alvarez-Ordonez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., and Peixe L.
- Subjects
663/664 ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Biology ,Microbiology ,Antibiotic resistance ,Non target ,growth promotion ,β lactams ,medicine ,TX341-641 ,antimicrobial resistance ,Food science ,yield increase ,amoxicillin ,Nutrition. Foods and food supply ,sub-inhibitory concentration ,Chemical technology ,food-producing animals ,Biol5012 ,food‐producing animals ,sub‐inhibitory concentration ,Contamination ,Amoxicillin ,penicillin V ,Antimicrobial ,food-producing animal ,Penicillin ,Scientific Opinion ,Animal Science and Zoology ,Parasitology ,Food Science ,medicine.drug - Abstract
The specific concentrations of amoxicillin and penicillin V in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for amoxicillin, whilst for penicillin V no suitable data for the assessment were available. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these two antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
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- View/download PDF
34. Maximum levels of cross‐contamination for 24 antimicrobial active substances in non‐target feed. Part 6: Macrolides: tilmicosin, tylosin and tylvalosin
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., Peixe L., Indústries Alimentàries, and Funcionalitat i Seguretat Alimentària
- Subjects
663/664 ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Tylosin ,Biology ,tilmicosin ,Microbiology ,chemistry.chemical_compound ,Antibiotic resistance ,Non target ,growth promotion ,TX341-641 ,antimicrobial resistance ,Food science ,Tilmicosin ,yield increase ,tylosin ,Nutrition. Foods and food supply ,Chemical technology ,food-producing animals ,tylvalosin ,Contamination ,Antimicrobial ,food-producing animal ,chemistry ,Animal Science and Zoology ,Parasitology ,Tylvalosin ,Food Science - Abstract
The specific concentrations of tilmicosin, tylosin and tylvalosin in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield, were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for tilmicosin and tylosin, whilst for tylvalosin no suitable data for the assessment were available. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these three antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
- View/download PDF
35. Maximum levels of cross‐contamination for 24 antimicrobial active substances in non‐target feed. Part 11: Sulfonamides
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I., Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., Peixe L., Indústries Alimentàries, and Funcionalitat i Seguretat Alimentària
- Subjects
Sulfamerazine ,663/664 ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Sulfonamide ,Microbiology ,Antibiotic resistance ,Non target ,growth promotion ,medicine ,TX341-641 ,antimicrobial resistance ,Food science ,yield increase ,Sulfonamides ,Animal health ,Nutrition. Foods and food supply ,Chemical technology ,sub-inhibitory concentration ,food‐producing animals ,food-producing animals ,sub‐inhibitory concentration ,Contamination ,Antimicrobial ,food-producing animal ,Sulfathiazole ,Environmental science ,Animal Science and Zoology ,Parasitology ,Food Science ,medicine.drug - Abstract
The specific concentrations of sulfonamides in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data are available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were identified for three sulfonamides: sulfamethazine, sulfathiazole and sulfamerazine. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
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36. Prediction of Minocycline Activity in the Gut From a Pig Preclinical Model Using a Pharmacokinetic -Pharmacodynamic Approach
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Vallé, Quentin, primary, Roques, Béatrice B., additional, Bousquet-Mélou, Alain, additional, Dahlhaus, David, additional, Ramon-Portugal, Felipe, additional, Dupouy, Véronique, additional, Bibbal, Delphine, additional, and Ferran, Aude A., additional
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- 2021
- Full Text
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37. Additional file 1 of Dynamic interactions between cephalexin and macrophages on different Staphylococcus aureus inoculum sizes: a tripartite in vitro model
- Author
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Lallemand, Elodie Anne, Zemirline, Claudine, Pierre-Louis Toutain, Bousquet-Melou, Alain, Ferran, Aude A., and Boullier, Séverine
- Abstract
Additional file 1 S1 Text. Detailed calculation of indexes.
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- 2021
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38. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 5: Lincosamides: lincomycin
- Author
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Indústries Alimentàries, Funcionalitat i Seguretat Alimentària, Koutsoumanis K., Allende A., Alvarez-Ordonez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., and Peixe L.
- Subjects
663/664 ,medicine.drug_class ,Veterinary (miscellaneous) ,Growth promotion ,Plant Science ,TP1-1185 ,Biology ,Microbiology ,Antibiotic resistance ,Non target ,growth promotion ,medicine ,TX341-641 ,Food science ,antimicrobial resistance ,yield increase ,Lincosamides ,Animal health ,Nutrition. Foods and food supply ,sub-inhibitory concentration ,Chemical technology ,Biol5012 ,food‐producing animals ,food-producing animals ,Contamination ,sub‐inhibitory concentration ,Antimicrobial ,Feed Antimicrobial Resistance Selection Concentration (FARSC) ,food-producing animal ,Lincomycin ,Scientific Opinion ,Animal Science and Zoology ,Parasitology ,lincomycin ,Food Science ,medicine.drug - Abstract
The specific concentrations of lincomycin in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels of lincomycin in feed that showed to have an effect on growth promotion/increased yield were reported. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for lincomycin. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
- View/download PDF
39. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 2: Aminoglycosides/aminocyclitols: apramycin, paromomycin, neomycin and spectinomycin
- Author
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EFSA Panel on Biological Hazards (BIOHAZ), Allende, Ana, Koutsoumanis, Konstantinos, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Allende A., Koutsoumanis K., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., Peixe L., Indústries Alimentàries, and Funcionalitat i Seguretat Alimentària
- Subjects
Spectinomycin ,663/664 ,spectinomycin ,Veterinary (miscellaneous) ,Growth promotion ,Paromomycin ,TP1-1185 ,Plant Science ,Biology ,Apramycin ,Microbiology ,Antibiotic resistance ,growth promotion ,medicine ,TX341-641 ,Food science ,antimicrobial resistance ,Nutrition. Foods and food supply ,Chemical technology ,neomycin ,food-producing animals ,Neomycin ,Contamination ,Antimicrobial ,food-producing animal ,Animal Science and Zoology ,Parasitology ,paromomycin ,Food Science ,medicine.drug ,apramycin - Abstract
The specific concentrations of apramycin, paromomycin, neomycin and spectinomycin in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield, were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC for these antimicrobials, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for apramycin and neomycin, whilst for paromomycin and spectinomycin, no suitable data for the assessment were available. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these four antimicrobials. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
- View/download PDF
40. Determination of the minimal selective concentration (MSC) of oxytetracycline in sterilised intestinal contents from pigs
- Author
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Imazaki, Pedro Henrique, Voisin, Bertille, Bousquet-Melou, Alain, Ferran, Aude, and Bibbal, Delphine
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- 2021
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- View/download PDF
41. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 3: Amprolium
- Author
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, Koutsoumanis K., Allende A., Alvarez-Ordoñez A., Bolton D., Bover-Cid S., Chemaly M., Davies R., De Cesare A., Herman L., Hilbert F., Lindqvist R., Nauta M., Ru G., Simmons M., Skandamis P., Suffredini E., Andersson D.I., Bampidis V., Bengtsson-Palme J., Bouchard D., Ferran A., Kouba M., Lopez Puente S., Lopez-Alonso M., Nielsen S.S., Pechova A., Petkova M., Girault S., Broglia A., Guerra B., Innocenti M.L., Liebana E., Lopez-Galvez G., Manini P., Stella P., Peixe L., Indústries Alimentàries, and Funcionalitat i Seguretat Alimentària
- Subjects
663/664 ,Veterinary (miscellaneous) ,Growth promotion ,TP1-1185 ,Plant Science ,Biology ,Microbiology ,chemistry.chemical_compound ,Antibiotic resistance ,Non target ,Amprolium ,growth promotion ,TX341-641 ,Food science ,antimicrobial resistance ,yield increase ,Animal health ,Nutrition. Foods and food supply ,Chemical technology ,Biol5012 ,food‐producing animals ,food-producing animals ,Feed Antimicrobial Resistance Selection Concentration (FARSC), growth promotion ,Contamination ,Antimicrobial ,Feed Antimicrobial Resistance Selection Concentration (FARSC) ,food-producing animal ,Scientific Opinion ,subinhibitory concentration ,chemistry ,Animal Science and Zoology ,Parasitology ,Food Science ,amprolium - Abstract
The specific concentrations of amprolium in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC for amprolium, it was not possible to conclude the assessment. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels of amprolium in feed that showed to have an effect on growth promotion/increased yield were reported. The lack of antibacterial activity at clinically relevant concentrations for amprolium suggests that further studies relating to bacterial resistance are not a priority. info:eu-repo/semantics/publishedVersion
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- 2021
- Full Text
- View/download PDF
42. Additional file 2 of Dynamic interactions between cephalexin and macrophages on different Staphylococcus aureus inoculum sizes: a tripartite in vitro model
- Author
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Lallemand, Elodie Anne, Zemirline, Claudine, Pierre-Louis Toutain, Bousquet-Melou, Alain, Ferran, Aude A., and Boullier, Séverine
- Abstract
Additional file 2 S2 Figure.
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- 2021
- Full Text
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43. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 7:Amphenicols: florfenicol and thiamphenicol
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, and Peixe, Luisa
- Abstract
The specific concentrations of florfenicol and thiamphenicol in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield, were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. The FARSC for florfenicol was estimated. However, due to the lack of data, the calculation of the FARSC for thiamphenicol was not possible until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for florfenicol, whilst for thiamphenicol no suitable data for the assessment were available. Uncertainties and data gaps associated to the levels reported were addressed. For florfenicol, it was recommended to perform further studies to supply more diverse and complete data related to the requirements for calculation of the FARSC, whereas for thiamphenicol, the recommendation was to generate the data required to fill the gaps which prevented the FARSC calculation.
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- 2021
44. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 1: Methodology, general data gaps and uncertainties
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, and Peixe, Luisa
- Abstract
The European Commission requested EFSA to assess, in collaboration with EMA, the specific concentrations of antimicrobials resulting from cross-contamination in non-target feed for food-producing animals below which there would not be an effect on the emergence of, and/or selection for, resistance in microbial agents relevant for human and animal health, as well as the levels of the antimicrobials which could have a growth promotion/increase yield effect. The assessment was performed for 24 antimicrobial active substances, as specified in the mandate. This scientific opinion describes the methodology used, and the main associated data gaps and uncertainties. To estimate the antimicrobial levels in the non-target feed that would not result in emergence of, and/or selection for, resistance, a model was developed. This ‘Feed Antimicrobial Resistance Selection Concentration’ (FARSC) model is based on the minimal selective concentration (MSC), or the predicted MSC (PMSC) if MSC for the most susceptible bacterial species is unavailable, the fraction of antimicrobial dose available for exposure to microorganisms in the large intestine or rumen (considering pharmacokinetic parameters), the daily faecal output or rumen volume and the daily feed intake. Currently, lack of data prevents the establishment of PMSC and/or FARSC for several antimicrobials and animal species. To address growth promotion, data from an extensive literature search were used. Specific assessments of the different substances grouped by antimicrobial classes are addressed in separate scientific opinions. General conclusions and recommendations were made.
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- 2021
45. Maximum levels of cross-contamination for 24 antimicrobial active substances in non-target feed. Part 8::Pleuromutilins: tiamulin and valnemulin
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EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, Peixe, Luisa, EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis, Konstantinos, Allende, Ana, Alvarez-Ordóñez, Avelino, Bolton, Declan, Bover-Cid, Sara, Chemaly, Marianne, Davies, Robert, De Cesare, Alessandra, Herman, Lieve, Hilbert, Friederike, Lindqvist, Roland, Nauta, Maarten, Ru, Giuseppe, Simmons, Marion, Skandamis, Panagiotis, Suffredini, Elisabetta, Andersson, Dan I, Bampidis, Vasileios, Bengtsson-Palme, Johan, Bouchard, Damien, Ferran, Aude, Kouba, Maryline, López Puente, Secundino, López-Alonso, Marta, Nielsen, Søren Saxmose, Pechová, Alena, Petkova, Mariana, Girault, Sebastien, Broglia, Alessandro, Guerra, Beatriz, Innocenti, Matteo Lorenzo, Liébana, Ernesto, López-Gálvez, Gloria, Manini, Paola, Stella, Pietro, and Peixe, Luisa
- Abstract
The specific concentrations of tiamulin and valnemulin in non-target feed for food-producing animals, below which there would not be an effect on the emergence of, and/or selection for, resistance in bacteria relevant for human and animal health, as well as the specific antimicrobial concentrations in feed which have an effect in terms of growth promotion/increased yield were assessed by EFSA in collaboration with EMA. Details of the methodology used for this assessment, associated data gaps and uncertainties, are presented in a separate document. To address antimicrobial resistance, the Feed Antimicrobial Resistance Selection Concentration (FARSC) model developed specifically for the assessment was applied. However, due to the lack of data on the parameters required to calculate the FARSC, it was not possible to conclude the assessment until further experimental data become available. To address growth promotion, data from scientific publications obtained from an extensive literature review were used. Levels in feed that showed to have an effect on growth promotion/increased yield were reported for tiamulin, while for valnemulin no suitable data for the assessment were available. It was recommended to carry out studies to generate the data that are required to fill the gaps which prevented the calculation of the FARSC for these two antimicrobials.
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- 2021
46. Determination of the pharmacokinetic-pharmacodynamic cut-off values of marbofloxacin in horses to support the establishment of a clinical breakpoint for antimicrobial susceptibility testing
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Bousquet-Mélou, Alain, Schneider, Marc, El Garch, Farid, Broussou, Diane C., Ferran, Aude A., Lallemand, Elodie A., Triboulloy, Cyrielle, Damborg, Peter, Toutain, Pierre Louis, Bousquet-Mélou, Alain, Schneider, Marc, El Garch, Farid, Broussou, Diane C., Ferran, Aude A., Lallemand, Elodie A., Triboulloy, Cyrielle, Damborg, Peter, and Toutain, Pierre Louis
- Abstract
Background: Marbofloxacin (MBX), a fluoroquinolone (FQ), is considered as a critical antibiotic requiring antimicrobial susceptibility testing (AST) for prudent use. No clinical breakpoint (CBP) currently exists to interpret the results of such tests in horses. Objectives: To compute PK/PD cut-offs (PK/PDCO) that is one of the three minimum inhibitory concentrations (MICs) considered establishing a CBP for antimicrobial susceptibility test interpretation. Study design: A meta-analysis conducted by combining five sets of previously published pharmacokinetic data, obtained in clinical and nonclinical settings. Methods: Horses (n = 131) received MBX intravenously at doses of either 2 or 10 mg/kg BW. They were richly sampled (five or six samples per horse). A population model was built to generate a virtual population of 5000 MBX disposition curves by Monte Carlo simulations (MCS) over 24 hours. The selected PK/PD index was the ratio of Area Under the free plasma concentration-time Curve divided by the MIC (fAUC/MIC). The PK/PDCO, which is the highest MIC for which 90% of horses can achieve an a priori selected critical value for the numerical value of the PK/PD index, was established for Gram-positive and Gram-negative bacteria for a dose of 2 mg/kg. Results: The PK/PDCO of MBX in horses was 0.125 mg/L for Gram-positive pathogens and 0.0625 mg/L for Gram-negative pathogens. MBX MICs determined by broth microdilution for 54 Escherichia coli and 189 Streptococcus equi isolates are reported. Main limitation: No clinical data are taken into account in the determination of a PK/PDco. Conclusion: The computed PK/PDco predicts that MBX may be efficacious in horses to treat infections associated with Enterobacteriaceae but unlikely to those involving Staphylococcus aureus or Streptococcus equi.
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- 2021
47. Analyse des associations de prémélanges médicamenteux contenant des antibiotiques
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Ferran, Aude, Millemann, Yves, Sauzéa, Xavier, Barreteau, Sophie, and Chiffoleau, Emmanuelle
- Subjects
médicament vétérinaire ,analysis ,association ,analyse ,[SDV.BA.MVSA] Life Sciences [q-bio]/Animal biology/Veterinary medicine and animal Health ,interaction ,pharmacologie ,veterinary drug ,ruminant ,premix ,antibiotique ,prémélanges médicamenteux ,animaux de rente ,cattle ,antibiotic ,identification ,intéraction ,pharmacology - Abstract
Les associations de premelanges contenant des antibiotiques sont utiles et courantes, sans connaissance pleine et entiere de leurs effets. Depuis deux ans, en raison de l’obligation pour les fabricants d’aliments medicamenteux de declarer les cessions d’antibiotiques, mais aussi grace a une analyse des connaissances actuelles sur les interactions physico-chimiques et pharmacologiques, les prescriptions de ces associations restent pertinentes dans certains cas. Elles doivent neanmoins etre mesurees, en prenant egalement en compte le contexte global d’usage de l’antibiotherapie.
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- 2020
48. Identification et analyse des associations de prémélanges médicamenteux antibiotiques
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Ferran, Aude, Millemann, Yves, Sauzéa, Xavier, Barreteau, Sophie, Ecole Nationale Vétérinaire de Toulouse (ENVT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées, École nationale vétérinaire d'Alfort (ENVA), Ecole Nationale Vétérinaire, Agroalimentaire et de l'alimentation Nantes-Atlantique (ONIRIS), Anses ANMV (Anses ANMV), and Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)
- Subjects
médicament vétérinaire ,[SDV.BA.MVSA]Life Sciences [q-bio]/Animal biology/Veterinary medicine and animal Health ,analysis ,association ,analyse ,interaction ,pharmacologie ,veterinary drug ,ruminant ,premix ,antibiotique ,prémélanges médicamenteux ,animaux de rente ,cattle ,antibiotic ,identification ,intéraction ,pharmacology - Abstract
National audience; Les associations de premelanges contenant des antibiotiques sont utiles et courantes, sans connaissance pleine et entiere de leurs effets. Depuis deux ans, en raison de l’obligation pour les fabricants d’aliments medicamenteux de declarer les cessions d’antibiotiques, mais aussi grace a une analyse des connaissances actuelles sur les interactions physico-chimiques et pharmacologiques, les prescriptions de ces associations restent pertinentes dans certains cas. Elles doivent neanmoins etre mesurees, en prenant egalement en compte le contexte global d’usage de l’antibiotherapie.
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- 2020
49. Species Differences in Pharmacokinetics and Pharmacodynamics
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Toutain, Pierre-Louis, primary, Ferran, Aude, additional, and Bousquet-Mélou, Alain, additional
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- 2010
- Full Text
- View/download PDF
50. Determination of the pharmacokinetic‐pharmacodynamic cut‐off values of marbofloxacin in horses to support the establishment of a clinical breakpoint for antimicrobial susceptibility testing
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Bousquet‐Mélou, Alain, primary, Schneider, Marc, additional, El Garch, Farid, additional, Broussou, Diane C., additional, Ferran, Aude A., additional, Lallemand, Elodie A., additional, Triboulloy, Cyrielle, additional, Damborg, Peter, additional, and Toutain, Pierre‐Louis, additional
- Published
- 2020
- Full Text
- View/download PDF
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