JAC Advance Access originally published online on July 1, 2006
Journal of Antimicrobial Chemotherapy 2006 58(3):537-542; doi:10.1093/jac/dkl273
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
High prevalence of OXA-51-type class D ß-lactamases among ceftazidime-resistant clinical isolates of Acinetobacter spp.: co-existence with OXA-58 in multiple centres
1 Enfeksiyon Hast. & Klin Mikrobiyoloji AD, Kocaeli Universitesi Kocaeli, Turkey 2 Mikrobiyoloji. & Klin Mikrobiyoloji AD, Kocaeli Universitesi Kocaeli, Turkey 3 Tibbi Biyoloji AD, Kocaeli Universitesi Kocaeli, Turkey 4 Biofizik AD, Kocaeli Universitesi Kocaeli, Turkey 5 Mikrobiyoloji. & Klin Mikrobiyoloji AD, Ondokuzmayis Universitesi Samsun, Turkey
Received 29 March 2006; returned 3 May 2006; revised 15 May 2006; accepted 1 June 2006
*Correspondence address. Kocaeli Tip Fakultesi, Umuttepe Kampusu, 41300, Kocaeli, Turkey. Tel: +90-262-3037560; Fax: +90-262-3037002; E-mail: vahabo{at}hotmail.com
Objectives: This study was designed to demonstrate the prevalence of the newly discovered carbapenem-hydrolysing class D enzymes, OXA-51-type and OXA-58, among clinical isolates of Acinetobacter spp.
Methods: A total of 72 isolates from six centres were studied. Isolates were screened by PCR with specific primers for blaOXA-51-type and blaOXA-58. PCR products were sequence-analysed. Plasmids were digested with EcoRV and genomic DNAs were digested with PvuII. Hybridization experiments were done with digoxigenin-labelled specific probes. Macro-restriction analysis was done on SmaI-digested genomic DNAs.
Results: A total of 56 (77.8%) isolates were positive for blaOXA-51-type genes. Sequence analysis of the products from 23 selected isolates revealed the occurrence of multiple alleles in all contributing centres. The blaOXA-58 gene was detected among 10 isolates from five centres. All were also positive for blaOXA-51-type genes. Among the blaOXA-58-positive isolates, two from the same centre were positive for a novel OXA-51 allele (OXA-86). Southern hybridization of plasmids and of genomic DNAs suggested that blaOXA-51-type genes are located on chromosomes whereas blaOXA-58 genes are plasmid borne in these 10 isolates. Plasmid profiles and pulsed-field gel electrophoresis patterns indicated the spread of the blaOXA-58 gene among multiple clones. The blaOXA-51-type and blaOXA-58 co-carrier strains were mostly associated with a pandrug-resistant phenotype.
Conclusions: This study indicated that blaOXA-58-bearing plasmids are readily spreading among multiple clones of the blaOXA-51-type-bearing clinical isolates of Acinetobacter spp. Since these isolates are highly resistant to antibiotics this finding indicates the existence of a significant problem in Turkish hospitals.
Keywords: oxacillinases , carbapenemases , pandrug resistance
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Giannouli, F. Tomasone, A. Agodi, H. Vahaboglu, Z. Daoud, M. Triassi, A. Tsakris, and R. Zarrilli Molecular epidemiology of carbapenem-resistant Acinetobacter baumannii strains in intensive care units of multiple Mediterranean hospitals J. Antimicrob. Chemother., April 1, 2009; 63(4): 828 - 830. [Full Text] [PDF] |
||||
![]() |
D. Gur, V. Korten, S. Unal, L. M. Deshpande, and M. Castanheira Increasing carbapenem resistance due to the clonal dissemination of oxacillinase (OXA-23 and OXA-58)-producing Acinetobacter baumannii: report from the Turkish SENTRY Program sites J. Med. Microbiol., December 1, 2008; 57(12): 1529 - 1532. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Bratu, D. Landman, D. A. Martin, C. Georgescu, and J. Quale Correlation of Antimicrobial Resistance with {beta}-Lactamases, the OmpA-Like Porin, and Efflux Pumps in Clinical Isolates of Acinetobacter baumannii Endemic to New York City Antimicrob. Agents Chemother., September 1, 2008; 52(9): 2999 - 3005. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Marti, J. Sanchez-Cespedes, M. D. Blasco, M. Ruiz, P. Espinal, V. Alba, F. Fernandez-Cuenca, A. Pascual, and J. Vila Characterization of the Carbapenem-Hydrolyzing Oxacillinase Oxa-58 in an Acinetobacter Genospecies 3 Clinical Isolate Antimicrob. Agents Chemother., August 1, 2008; 52(8): 2955 - 2958. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Y. Peleg, H. Seifert, and D. L. Paterson Acinetobacter baumannii: Emergence of a Successful Pathogen Clin. Microbiol. Rev., July 1, 2008; 21(3): 538 - 582. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. E. Karageorgopoulos, T. Kelesidis, I. Kelesidis, and M. E. Falagas Tigecycline for the treatment of multidrug-resistant (including carbapenem-resistant) Acinetobacter infections: a review of the scientific evidence J. Antimicrob. Chemother., July 1, 2008; 62(1): 45 - 55. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Wang, P. Guo, H. Sun, H. Wang, Q. Yang, M. Chen, Y. Xu, and Y. Zhu Molecular Epidemiology of Clinical Isolates of Carbapenem-Resistant Acinetobacter spp. from Chinese Hospitals Antimicrob. Agents Chemother., November 1, 2007; 51(11): 4022 - 4028. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Queenan and K. Bush Carbapenemases: the Versatile {beta}-Lactamases Clin. Microbiol. Rev., July 1, 2007; 20(3): 440 - 458. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. H. Lee, C. H. Choi, H. Y. Kang, J. Y. Lee, J. Kim, Y. C. Lee, S. Y. Seol, D. T. Cho, K. W. Kim, D. Y. Song, et al. Differences in phenotypic and genotypic traits against antimicrobial agents between Acinetobacter baumannii and Acinetobacter genomic species 13TU J. Antimicrob. Chemother., April 1, 2007; 59(4): 633 - 639. [Abstract] [Full Text] [PDF] |
||||



