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Antimicrobial Agents and Chemotherapy, August 2001, p. 2224-2228, Vol. 45, No. 8
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.8.2224-2228.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Metallo-
-Lactamases in Clinical
Pseudomonas Isolates in Taiwan and Identification of VIM-3,
a Novel Variant of the VIM-2 Enzyme
Jing-Jou
Yan,1
Po-Ren
Hsueh,2
Wen-Chien
Ko,3
Kwen-Tay
Luh,2
Shu-Huei
Tsai,1
Hsiu-Mei
Wu,4 and
Jiunn-Jong
Wu4,*
Department of Pathology, National Cheng Kung
University Medical Center,1 and
Departments of Medicine3 and
Medical Technology,4 National Cheng Kung
University Medical College, Tainan, Department of
Laboratory Medicine, National Taiwan University Hospital,
Taipei,2 Taiwan
Received 9 October 2000/Returned for modification 29 January
2001/Accepted 4 May 2001
A total of 209 clinical isolates of Pseudomonas (193 Pseudomonas aeruginosa, 10 P. putida, 4 P. stutzeri, and 2 P. fluorescens isolates) with reduced susceptibilities to imipenem and/or
ceftazidime were subjected to PCR assays with primers specific for
blaIMP-1, blaIMP-2,
blaVIM-1, and blaVIM-2
and sequence analysis to identify the metallo-
-lactamases (MBLs)
prevalent among these organisms in Taiwan; and 21 isolates gave
positive results. Five isolates including two P. putida and
three P. stutzeri isolates were found to carry
blaIMP-1, and six isolates including five
P. putida and one P. stutzeri isolates harbored
blaVIM-2. The remaining 10 isolates were
P. aeruginosa, and all were found to carry a novel variant of blaVIM-2, designated
blaVIM-3. There are only two nucleotide differences between blaVIM-2 and
blaVIM-3, leading to two amino acid
alterations. Our findings indicate that VIM-2 and its variant have
become the most prevalent metalloenzymes in Pseudomonas in Taiwan. Southern hybridization with the
blaVIM-2-, blaVIM-3-, and blaIMP-1 -specific probes revealed that
only two VIM-2-producing P. putida isolates appeared to
carry the MBL gene on plasmids. Pulsed-field gel electrophoresis showed
that six VIM-3-producing P. aeruginosa isolates and two
IMP-1-producing P. stutzeri isolates were genetically
related, suggesting that the spread of these MBL genes in Taiwan could
be due to clonal dissemination as well as genetic exchange between
different clones.
*
Corresponding author. Mailing address: Department of
Medical Technology, National Cheng Kung University Medical College, No. 1 University Rd., Tainan, Taiwan 70101. Phone: 886-6-2353535, ext.
5775. Fax: 886-6-2363956. E-mail:
jjwu{at}mail.ncku.edu.tw.
Antimicrobial Agents and Chemotherapy, August 2001, p. 2224-2228, Vol. 45, No. 8
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.8.2224-2228.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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