Unexpected persistence of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the faecal microbiota of hospitalised patients treated with imipenem
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Titre | Unexpected persistence of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the faecal microbiota of hospitalised patients treated with imipenem |
Type de publication | Journal Article |
Year of Publication | 2017 |
Auteurs | Grall N., Lazarevic V., Gaia N., Couffignal C., Laouenan C., Ilic-Habensus E., Wieder I., Plesiat P., Angebault C., Bougnoux M.E, Armand-Lefevre L., Andremont A., Duval X., Schrenzel J. |
Journal | INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS |
Volume | 50 |
Pagination | 81-87 |
Date Published | JUL |
Type of Article | Article |
ISSN | 0924-8579 |
Mots-clés | Antibiotic resistance, ESBL, Extended-spectrum beta-lactamase, Faecal microbiota, Imipenem, Metagenomics |
Résumé | Imipenem is active against extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-E) but favours the intestinal emergence of resistance. The effects of imipenem on intestinal microbiota have been studied using culture-based techniques. In this study, the effects were investigated in patients using culture and metagenomic techniques. Seventeen hospitalised adults receiving imipenem were included in a multicentre study (NCT01703299, http://www.clinicaltrials.gov). Most patients had a history of antibiotic use and/or hospitalisation. Stools were collected before, during and after imipenem treatment. Bacterial and fungal colonisation was assessed by culture, and microbiota changes were assessed using metagenomics. Unexpectedly, high colonisation rates by imipenem-susceptible ESBL-E before treatment (70.6%) remained stable over time, suggesting that imipenem intestinal concentrations were very low. Carriage rates of carbapenem-resistant Gram-negative bacilli (0-25.0%) were also stable over time, whereas those of yeasts (64.7% before treatment) peaked at 76.5% during treatment and decreased thereafter. However, these trends were not statistically significant. Yeasts included highly diverse colonising Candida spp. Metagenomics showed no global effect of imipenem on the bacterial taxonomic profiles at the sequencing depth used but demonstrated specific changes in the microbiota not detected with culture, attributed to factors other than imipenem, including sampling site or treatment with other antibiotics. In conclusion, culture and metagenomics were highly complementary in characterising the faecal microbiota of patients. The changes observed during imipenem treatment were unexpectedly limited, possibly because the microbiota was already disturbed by previous antibiotic exposure or hospitalisation. (C) 2017 Elsevier B.V. and International Society of Chemotherapy. All rights reserved. |
DOI | 10.1016/j.ijantimicag.2017.02.018 |