J Korean Soc Microbiol.
2000 Jun;35(3):263-271.
Involvement of IS26 element in the evolution and dissemination of blaSHV-2a
and blaSHV-12
- Affiliations
-
- 1Department of Microbiology, College of Medicine, Dankook
University, Cheonan, South Korea. dtcho@knu.ac.kr
Abstract
-
A clinical isolate of Klebsiella pneumoniae K7746 produced the
extended-spectrum beta-lactamase (ESBL) SHV-12. A 6.6 kb BamHI fragment
containing the blaSHV-12 gene of K7746 strain was cloned into
pCRScriptCAM vector resulting in the recombinant plasmid p7746-C1. The
restriction map of 3.6 kb inserted DNA and sequences immediately
surrounding blaSHV-12 of p7746-C1 were homologous to plasmid pMPA2a
carrying blaSHV-2a. In addition, both blaSHV-12 and blaSHV-2a were
expressed from a common hybrid promoter made of the -35 region derived
from the left inverted repeat of IS26 and the -10 region from the blaSHV
promoter itself. The results indicate that blaSHV-12 and blaSHV-2a may
have evolved from a common ancestor in the sequential order of blaSHV-2a
first, followed by blaSHV-12. Furthermore, by the PCR mapping method
using primers corresponding to the IS26 and blaSHV, the association
between IS26 and blaSHV was studied in 12 clinical isolates carrying
blaSHV-2a, 27 clinical isolates carrying blaSHV-12, and 5 reference
strains carrying blaSHV-1 to blaSHV-5. All 39 strains carrying blaSHV-2a
or blaSHV-12 were positive by the PCR, providing confirmative evidence
that IS26 has been involved in the evolution and dissemination of
blaSHV-2a and blaSHV-12. But 5 reference strains carrying blaSHV-1 to
blaSHV-5 were negative by the PCR. Therefore, we concluded that the
molecular evolutionary pathway of blaSHV-2a and blaSHV-12 may be
different from that of other blaSHV-ESBL, e.g., blaSHV-2, blaSHV-3,
blaSHV-4, and blaSHV-5.