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dc.rights.licenseopenen_US
dc.contributor.authorLEVAST, Benoit
dc.contributor.authorBENECH, Nicolas
dc.contributor.authorGASC, Cyrielle
dc.contributor.authorBATAILLER, Cecile
dc.contributor.authorSENNEVILLE, Eric
dc.contributor.authorLUSTIG, Sebastien
dc.contributor.authorPOUDEROUX, Cecile
dc.contributor.authorBOUTOILLE, David
dc.contributor.authorBOUCINHA, Lilia
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDAUCHY, Frederic-Antoine
dc.contributor.authorZELLER, Valerie
dc.contributor.authorMAYNARD, Marianne
dc.contributor.authorCAZANAVE, Charles
dc.contributor.authorLE THI, Thanh-Thuy
dc.contributor.authorJOSSE, Jerome
dc.contributor.authorDORE, Joel
dc.contributor.authorLAURENT, Frederic
dc.contributor.authorFERRY, Tristan
dc.date.accessioned2021-05-10T09:01:49Z
dc.date.available2021-05-10T09:01:49Z
dc.date.issued2021-03-05
dc.identifier.issn2296-858X (Print) 2296-858X (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/27220
dc.description.abstractEnThere is a growing interest in the potentially deleterious impact of antibiotics on gut microbiota. Patients with bone and joint infection (BJI) require prolonged treatment that may impact significantly the gut microbiota. We collected samples from patients with BJI at baseline, end of antibiotics (EOT), and 2 weeks after antibiotic withdrawal (follow-up, FU) in a multicenter prospective cohort in France. Microbiota composition was determined by shotgun metagenomic sequencing. Fecal markers of gut permeability and inflammation as well as multi-drug-resistant bacteria (MDRB) and Clostridioides difficile carriage were assessed at each time point. Sixty-two patients were enrolled: 27 native BJI, 14 osteosynthesis-related BJI, and 21 prosthetic joint infections (PJI). At EOT, there was a significant loss of alpha-diversity that recovered at FU in patients with native BJI and PJI, but not in patients with osteosynthesis-related BJI. At EOT, we observed an increase of Proteobacteria and Bacteroidetes that partially recovered at FU. The principal component analysis (PCoA) of the Bray–Curtis distance showed a significant change of the gut microbiota at the end of treatment compared to baseline that only partially recover at FU. Microbiota composition at FU does not differ significantly at the genus level when comparing patients treated for 6 weeks vs. those treated for 12 weeks. The use of fluoroquinolones was not associated with a lower Shannon index at the end of treatment; however, the PCoA of the Bray–Curtis distance showed a significant change at EOT, compared to baseline, that fully recovered at FU. Levels of fecal neopterin were negatively correlated with the Shannon index along with the follow-up (r2 = 0.17; p < 0.0001). The PCoA analysis of the Bray–Curtis distance shows that patients with an elevated plasma level of C-reactive protein (≥5 mg/L) at EOT had a distinct gut microbial composition compared to others. MDRB and C. difficile acquisition at EOT and FU represented 20% (7/35) and 37.1% (13/35) of all MDRB/C. difficile-free patients at the beginning of the study, respectively. In patients with BJI, antibiotics altered the gut microbiota diversity and composition with only partial recovery, mucosal inflammation, and permeability and acquisition of MDRB carriage. Microbiome interventions should be explored in patients with BJI to address these issues.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enGut microbiota
dc.subject.enAntimicrobial therapy
dc.subject.enAntibiotics
dc.subject.enBone and joint infection
dc.subject.enDysbiosis
dc.title.enImpact on the Gut Microbiota of Intensive and Prolonged Antimicrobial Therapy in Patients With Bone and Joint Infection
dc.typeArticle de revueen_US
dc.identifier.doi10.3389/fmed.2021.586875en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed33748154en_US
bordeaux.journalFrontiers in Medicineen_US
bordeaux.page586875en_US
bordeaux.volume8en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamMORPH3Eusen_US
bordeaux.teamHEALTHY_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03222293
hal.version1
hal.date.transferred2021-05-10T09:01:55Z
hal.exporttrue
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