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Antimicrobial Agents and Chemotherapy, February 2008, p. 745-747, Vol. 52, No. 2
0066-4804/08/$08.00+0 doi:10.1128/AAC.01095-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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Université Pierre et Marie Curie-Paris 6, EA1541, Paris F-75013, France,1 Laboratoire de Bactériologie-Virologie-Hygiène, AP-HP, Groupe Hospitalier Albert Chenevier-Henri Mondor, Créteil F-94000, France,2 Université Paris 12, IFR10, Créteil F-94000, France,3 Service Bactériologie, AP-HP, Groupe hospitalier Pitié-Salpêtrière, Paris F-75013, France4
Received 21 August 2007/ Returned for modification 1 November 2007/ Accepted 26 November 2007
Mycobacterium leprae DNA gyrases carrying various mutations, previously described in clinical strains, were investigated for quinolone susceptibility by inhibition of supercoiling and DNA cleavage promotion. We demonstrated that the gyrA mutations leading to G89C or A91V confer fluoroquinolone resistance whereas the gyrB mutation leading to D205N does not.
Published ahead of print on 10 December 2007.
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