Transposition of tn125 encoding the ndm-1 carbapenemase in Acinetobacter baumannii
      
      
        
      
      
      
      
        
          
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Bontron, Séverine
  Emerging Antibiotic Resistance Unit, Medical and Molecular Microbiology, Department of Medicine, Faculty of Science, University of Fribourg, Switzerland - INSERM European Unit (LEA Paris, France), University of Fribourg, Switzerland
          
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Nordmann, Patrice
  Emerging Antibiotic Resistance Unit, Medical and Molecular Microbiology, Department of Medicine, Faculty of Science, University of Fribourg, Switzerland - INSERM European Unit (LEA Paris, France), University of Fribourg, Switzerland - University of Lausanne and University Hospital Center, Lausanne, Switzerland
          
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Poirel, Laurent
  Emerging Antibiotic Resistance Unit, Medical and Molecular Microbiology, Department of Medicine, Faculty of Science, University of Fribourg, Switzerland - INSERM European Unit (LEA Paris, France), University of Fribourg, Switzerland
          
 
      
      
      
      
      
      
      
      
      
      
      
      
      
      
      
        
        Published in:
        
          
            
            - Antimicrobial Agents and Chemotherapy. - 2016, vol. 60, no. 12, p. 7245–7251
 
       
      
      
      
       
      
      
      
        
        English
        
        
        
          The blaNDM-1 gene encodes a carbapenemase that confers resistance to almost all  β-lactams, including last-resort carbapenems. This is increasingly reported worldwide  in nosocomial and community-acquired Gram-negative bacteria. Acinetobacter  baumannii is an important opportunistic pathogen that is considered an intermediate  reservoir for the blaNDM-1 gene. In this species, the blaNDM-1 gene is located within  the Tn125 composite transposon. The mechanism driving the mobility of Tn125 has  not yet been elucidated. Here we experimentally demonstrated the transposition of  Tn125 in A. baumannii. Systematic 3-bp duplication of the target site, being the  signature of transposition, was evidenced. The target site consensus sequence for  Tn125 transposition was found to be GC enriched at the duplicated 3 bp and AT rich in  the vicinity. Transposition frequency was not influenced by temperature changes or by  exposure to subinhibitory concentrations of various antibiotics. This work is the first  direct evidence of the functionality of a composite transposon in A. baumannii. It  provides a mechanistic clue for the dissemination of the blaNDM-1 gene in  Acinetobacter spp. and subsequently among Enterobacteriaceae.
        
        
       
      
      
      
        
        
        
        
        
        
        
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- Faculté des sciences et de médecine
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- Médecine 3ème année
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                  Biological sciences
                
              
            
          
        
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          Persistent URL
        
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          https://folia.unifr.ch/unifr/documents/305378
        
 
   
  
  
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