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1.
J Antimicrob Chemother ; 75(2): 351-361, 2020 02 01.
Artículo en Inglés | MEDLINE | ID: mdl-31778166

RESUMEN

BACKGROUND: Aminopenicillins with or without a ß-lactamase inhibitor are widely used in both human and veterinary medicine. However, little is known about their differential impact on the gut microbiota and development of antimicrobial resistance. OBJECTIVES: To investigate changes in the faecal microbiota of dogs treated with amoxicillin or amoxicillin/clavulanic acid. METHODS: Faeces collected from 42 dogs (21 per treatment group) immediately before, during and 1 week after termination of oral treatment with amoxicillin or amoxicillin/clavulanic acid were analysed by culture and 16S rRNA gene sequence analysis. RESULTS: In both groups, bacterial counts on ampicillin selective agar revealed an increase in the proportion of ampicillin-resistant Escherichia coli during treatment, and an increased occurrence and proportion of ampicillin-resistant enterococci during and after treatment. 16S rRNA gene analysis showed reductions in microbial richness and diversity during treatment followed by a return to pre-treatment conditions approximately 1 week after cessation of amoxicillin or amoxicillin/clavulanic acid treatment. While no significant differences were observed between the effects of amoxicillin and amoxicillin/clavulanic acid on microbial richness and diversity, treatment with amoxicillin/clavulanic acid reduced the abundance of taxa that are considered part of the beneficial microbiota (such as Roseburia, Dialister and Lachnospiraceae) and enriched Escherichia, although the latter result was not corroborated by phenotypic counts. CONCLUSIONS: Our results suggest a limited effect of clavulanic acid on selection of antimicrobial resistance and microbial richness when administered orally in combination with amoxicillin. However, combination with this ß-lactamase inhibitor appears to broaden the spectrum of amoxicillin, with potential negative consequences on gut health.


Asunto(s)
Combinación Amoxicilina-Clavulanato de Potasio , Amoxicilina , Perros/microbiología , Microbiota , Amoxicilina/farmacología , Amoxicilina/uso terapéutico , Combinación Amoxicilina-Clavulanato de Potasio/farmacología , Combinación Amoxicilina-Clavulanato de Potasio/uso terapéutico , Animales , Antibacterianos/farmacología , Antibacterianos/uso terapéutico , Heces/microbiología , Pruebas de Sensibilidad Microbiana , Microbiota/efectos de los fármacos , ARN Ribosómico 16S/genética , Resistencia betalactámica , beta-Lactamasas/genética
2.
Artículo en Inglés | MEDLINE | ID: mdl-31636067

RESUMEN

Fluoroquinolone treatments induce dysbiosis of the intestinal microbiota, resulting in loss of resistance to colonization by exogenous bacteria such as Clostridioides difficile that may cause severe diarrhea in humans and lethal infection in hamsters. We show here that DAV131A, a charcoal-based adsorbent, decreases the intestinal levels of the fluoroquinolone antibiotics levofloxacin and ciprofloxacin in hamsters, protects their intestinal microbiota, and prevents lethal infection by C. difficile.


Asunto(s)
Carbón Orgánico/administración & dosificación , Clostridioides difficile , Infecciones por Clostridium/prevención & control , Administración Oral , Adsorción , Animales , Antibacterianos/efectos adversos , Antibacterianos/farmacocinética , Ciprofloxacina/efectos adversos , Ciprofloxacina/farmacocinética , Clostridioides difficile/patogenicidad , Modelos Animales de Enfermedad , Disbiosis/inducido químicamente , Disbiosis/metabolismo , Disbiosis/prevención & control , Fluoroquinolonas/efectos adversos , Fluoroquinolonas/farmacocinética , Microbioma Gastrointestinal/efectos de los fármacos , Levofloxacino/efectos adversos , Levofloxacino/farmacocinética , Masculino , Mesocricetus
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