Previous Article | Next Article 
Antimicrobial Agents and Chemotherapy, September 2003, p. 2859-2863, Vol. 47, No. 9
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.9.2859-2863.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Molecular and Biochemical Characterization of OXA-45, an Extended-Spectrum Class 2d' ß-Lactamase in Pseudomonas aeruginosa
Mark A. Toleman,1* Kenneth Rolston,2 Ronald N. Jones,3,4 and Timothy R. Walsh1
Department of Pathology and Microbiology, University of Bristol, Bristol BS8 1TD, United Kingdom,1
Anderson Medical Center, Houston, Texas,2
The JONES Group/JMI Laboratories, North Liberty, Iowa,3
the Tufts University School of Medicine, Boston, Massachusetts4
Received 3 January 2003/
Returned for modification 18 March 2003/
Accepted 20 June 2003
As part of the CANCER Antimicrobial Surveillance Program in North America, a clinical strain of Pseudomonas aeruginosa, strain 07-406, isolated in Texas was found to be resistant to all antimicrobials except polymyxin B. Genetic analysis of this isolate identified two unique extended-spectrum ß-lactamase genes. One, blaVIM-7, encoded a metallo-ß-lactamase (unpublished data), and the other, blaOXA-45, described here, encoded a class D extended-spectrum ß-lactamase. blaOXA-45 was isolated on a Sau3A1 genomic fragment of 1.8 kb and encodes a protein of 264 amino acids with the highest identities to OXA-18 (65.9%), OXA-9 (42.8%), OXA-22 (40.2%), OXA-12 (38.6%), and OXA-29 (35.2%) but weak identities with other class D ß-lactamases. blaOXA-45 was found to be harbored on a 24-kb plasmid in a region that displays high identities with a section of the 43-kb genomic island of Salmonella enterica serovar Typhimurium DT104. Biochemically OXA-45 is most similar to OXA-18 in its substrate profile and inhibition by clavulanic acid and is a member of the 2d' class of ß-lactamases.
* Corresponding author. Mailing address: Department of Pathology and Microbiology, University of Bristol, Bristol BS8 1TD, United Kingdom. Phone: 44 117 9287522. Fax: 44 117 9287896. E-mail:
Mark.Toleman{at}bristol.ac.uk.
Antimicrobial Agents and Chemotherapy, September 2003, p. 2859-2863, Vol. 47, No. 9
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.9.2859-2863.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Li, H., Walsh, T. R., Toleman, M. A.
(2009). Molecular Analysis of the Sequences Surrounding blaOXA-45 Reveals Acquisition of This Gene by Pseudomonas aeruginosa via a Novel ISCR Element, ISCR5. Antimicrob. Agents Chemother.
53: 1248-1251
[Abstract]
[Full Text]
-
Naas, T., Namdari, F., Bogaerts, P., Huang, T.-D., Glupczynski, Y., Nordmann, P.
(2008). Genetic Structure Associated with blaOXA-18, Encoding a Clavulanic Acid-Inhibited Extended-Spectrum Oxacillinase. Antimicrob. Agents Chemother.
52: 3898-3904
[Abstract]
[Full Text]
-
Queenan, A. M., Bush, K.
(2007). Carbapenemases: the Versatile {beta}-Lactamases. Clin. Microbiol. Rev.
20: 440-458
[Abstract]
[Full Text]
-
Doi, Y., de Oliveira Garcia, D., Adams, J., Paterson, D. L.
(2007). Coproduction of Novel 16S rRNA Methylase RmtD and Metallo-{beta}-Lactamase SPM-1 in a Panresistant Pseudomonas aeruginosa Isolate from Brazil. Antimicrob. Agents Chemother.
51: 852-856
[Abstract]
[Full Text]
-
Aboufaycal, H., Sader, H. S., Rolston, K., Deshpande, L. M., Toleman, M., Bodey, G., Raad, I., Jones, R. N.
(2007). blaVIM-2 and blaVIM-7 Carbapenemase-Producing Pseudomonas aeruginosa Isolates Detected in a Tertiary Care Medical Center in the United States: Report from the MYSTIC Program. J. Clin. Microbiol.
45: 614-615
[Abstract]
[Full Text]
-
Moland, E. S., Hanson, N. D., Black, J. A., Hossain, A., Song, W., Thomson, K. S.
(2006). Prevalence of Newer {beta}-Lactamases in Gram-Negative Clinical Isolates Collected in the United States from 2001 to 2002.. J. Clin. Microbiol.
44: 3318-3324
[Abstract]
[Full Text]
-
Toleman, M. A., Bennett, P. M., Walsh, T. R.
(2006). ISCR Elements: Novel Gene-Capturing Systems of the 21st Century?. Microbiol. Mol. Biol. Rev.
70: 296-316
[Abstract]
[Full Text]
-
Paterson, D. L., Bonomo, R. A.
(2005). Extended-Spectrum {beta}-Lactamases: a Clinical Update. Clin. Microbiol. Rev.
18: 657-686
[Abstract]
[Full Text]
-
Lee, S., Park, Y.-J., Kim, M., Lee, H. K., Han, K., Kang, C. S., Kang, M. W.
(2005). Prevalence of Ambler class A and D {beta}-lactamases among clinical isolates of Pseudomonas aeruginosa in Korea. J Antimicrob Chemother
56: 122-127
[Abstract]
[Full Text]
-
Giuliani, F., Docquier, J.-D., Riccio, M. L., Pagani, L., Rossolini, G. M.
(2005). OXA-46, a New Class D {beta}-Lactamase of Narrow Substrate Specificity Encoded by a blaVIM-1-Containing Integron from a Pseudomonas aeruginosa Clinical Isolate. Antimicrob. Agents Chemother.
49: 1973-1980
[Abstract]
[Full Text]
-
Castanheira, M., Toleman, M. A., Jones, R. N., Schmidt, F. J., Walsh, T. R.
(2004). Molecular Characterization of a {beta}-Lactamase Gene, blaGIM-1, Encoding a New Subclass of Metallo-{beta}-Lactamase. Antimicrob. Agents Chemother.
48: 4654-4661
[Abstract]
[Full Text]
-
Mulvey, M. R., Boyd, D. A., Baker, L., Mykytczuk, O., Reis, E. M. F., Asensi, M. D., Rodrigues, D. P., Ng, L.-K.
(2004). Characterization of a Salmonella enterica serovar Agona strain harbouring a class 1 integron containing novel OXA-type {beta}-lactamase (blaOXA-53) and 6'-N-aminoglycoside acetyltransferase genes [aac(6')-I30]. J Antimicrob Chemother
54: 354-359
[Abstract]
[Full Text]