Previous Article | Next Article 
Antimicrobial Agents and Chemotherapy, September 2005, p. 3948-3951, Vol. 49, No. 9
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.9.3948-3951.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Cloning and Characterization of a Novel Trimethoprim-Resistant Dihydrofolate Reductase from a Nosocomial Isolate of Staphylococcus aureus CM.S2 (IMCJ1454)
Jun-ichiro Sekiguchi,1
Prasit Tharavichitkul,3
Tohru Miyoshi-Akiyama,1
Vena Chupia,3
Tomoko Fujino,1
Minako Araake,1
Atsushi Irie,1
Koji Morita,4
Tadatoshi Kuratsuji,2,5 and
Teruo Kirikae1*
Department of Infectious Diseases,1
Research Institute, International Medical Center of Japan, Shinjuku, Tokyo 162-8655, Japan,2
Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand,3
Department of Microbiology, Kyorin University School of Health Sciences, Hachioji, Tokyo 192-8508, Japan,4
National Research Institute for Child Health and Development, Setagaya, Tokyo 157-8535, Japan5
Received 16 March 2005/
Returned for modification 24 April 2005/
Accepted 14 June 2005
A novel gene, dfrG, encoding a trimethoprim (TMP)-resistant dihydrofolate reductase (DHFR, designated S3DHFR) was cloned from a clinical isolate of methicillin-resistant Staphylococcus aureus. Escherichia coli expressing dfrG was highly resistant to TMP. Recombinant S3DHFR exhibited DHFR activity that was not inhibited by TMP.
* Corresponding author. Mailing address: Department of Infectious Diseases, Research Institute, International Medical Center of Japan, 1-21-1 Toyama, Shinjuku, Tokyo 162-8655, Japan. Phone: (81) 3 3202 7181, ext. 2838. Fax: (81) 3 3202 7364. E-mail:
tkirikae{at}ri.imcj.go.jp.
Antimicrobial Agents and Chemotherapy, September 2005, p. 3948-3951, Vol. 49, No. 9
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.9.3948-3951.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Kadlec, K., Ehricht, R., Monecke, S., Steinacker, U., Kaspar, H., Mankertz, J., Schwarz, S.
(2009). Diversity of antimicrobial resistance pheno- and genotypes of methicillin-resistant Staphylococcus aureus ST398 from diseased swine. J Antimicrob Chemother
64: 1156-1164
[Abstract]
[Full Text]
-
Vickers, A. A., Potter, N. J., Fishwick, C. W. G., Chopra, I., O'Neill, A. J.
(2009). Analysis of mutational resistance to trimethoprim in Staphylococcus aureus by genetic and structural modelling techniques. J Antimicrob Chemother
63: 1112-1117
[Abstract]
[Full Text]
-
Oefner, C., Bandera, M., Haldimann, A., Laue, H., Schulz, H., Mukhija, S., Parisi, S., Weiss, L., Lociuro, S., Dale, G. E.
(2009). Increased hydrophobic interactions of iclaprim with Staphylococcus aureus dihydrofolate reductase are responsible for the increase in affinity and antibacterial activity. J Antimicrob Chemother
63: 687-698
[Abstract]
[Full Text]
-
Clark, C., Ednie, L. M., Lin, G., Smith, K., Kosowska-Shick, K., McGhee, P., Dewasse, B., Beachel, L., Caspers, P., Gaucher, B., Mert, G., Shapiro, S., Appelbaum, P. C.
(2009). Antistaphylococcal Activity of Dihydrophthalazine Antifolates, a Family of Novel Antibacterial Drugs. Antimicrob. Agents Chemother.
53: 1353-1361
[Abstract]
[Full Text]
-
Kadlec, K., Schwarz, S.
(2009). Identification of a Novel Trimethoprim Resistance Gene, dfrK, in a Methicillin-Resistant Staphylococcus aureus ST398 Strain and Its Physical Linkage to the Tetracycline Resistance Gene tet(L). Antimicrob. Agents Chemother.
53: 776-778
[Abstract]
[Full Text]