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Biofilm Formation and Whole Genome Analysis of MDR Klebsiella Pneumoniae Strains Isolated from Hospital Acquired Infections in Tertiary Hospitals in Dakar, Senegal

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  • Additional Information
    • Contributors:
      Du gène à l'écosystème (MIVEGEC-GeneSys); Pathogènes, Environnement, Santé Humaine (EPATH); Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC); Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD Occitanie )-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD Occitanie )-Université de Montpellier (UM)-Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC); Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD Occitanie )-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD Occitanie )-Université de Montpellier (UM); Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD Occitanie )-Université de Montpellier (UM)
    • Publication Information:
      CCSD
      Austin Publishing Group
    • Publication Date:
      2024
    • Collection:
      Université de Montpellier: HAL
    • Abstract:
      International audience ; Klebsiella pneumoniae is widely recognized as an opportunistic pathogen in both hospital and community settings. It is a key member of the ESKAPE group, which comprises priority microorganisms of major concern owing to their antibiotic resistance. The resistance of K. pneumoniae, particularly related to Extended-Spectrum β-Lactamases (ESBLs), poses a significant global public health challenge. The combination of its Multidrug Resistance (MDR) phenotype and various pathogenicity factors increases its potential to cause severe clinical infections. Biofilm formation was assessed via a semiquantitative microtiter technique. We employed various bioinformatics tools to analyze the Antimicrobial Resistance (AMR), virulence factors, plasmid replicons, and genomic diversity of the CRKP isolates. Overall, among the 24 K. pneumoniae isolates, most produced strong biofilms (n = 21), with some exhibiting moderate (n = 1) or weak (n = 2) biofilm production. An alarming level of resistance to multiple classes of antibiotics was correlated with the presence of various resistance genes, including those for β-lactams (bla OXA-48 , bla OXA-181 , bla CTX-M15 , bla TEM and bla SHV ), aminoglycosides (aph(6)-Id, aac(3)-IIe, aadA2, ant(3'')-IIa, aph(3')-Ia and aac(6')-Ib-cr), and quinolones (qnrA, qnrB, qnrS, CRP, and emrR). Various efflux pumps, such as KpnGH, oqxAB, acrAB, acrD, and KpnEF, are ubiquitously distributed across MDR K. pneumoniae strains. Several virulenceassociated genes encoding type 1 fimbriae (fimH), type 3 fimbriae (mrkA), efflux pumps (acrAB, oqxAB), enterobactin (entA, entB, fepC), and yersiniabactin (irp1, irp2, ytbA, ybtE, ybtP, ybtQ, ytbT, ytbU, ytbX) have been identified. Genetically, the isolates presented high diversity, with 18 Sequence Types (STs) and an average of 70.1% accessory genes. On the basis of SNP distance and pairwise ANI analysis, the majority of K. pneumoniae isolates were grouped into one clade. The high plasticity of K. pneumoniae in the acquisition of an MDR ...
    • Relation:
      IRD: fdi:010093061
    • Online Access:
      https://hal.science/hal-04943312
      https://hal.science/hal-04943312v1/document
      https://hal.science/hal-04943312v1/file/A29_NDiaye_JBM2024.pdf
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • Accession Number:
      edsbas.29CA89F6