» Articles » PMID: 15215087

Diversity and Evolution of the Class A Chromosomal Beta-lactamase Gene in Klebsiella Pneumoniae

Overview
Specialty Pharmacology
Date 2004 Jun 25
PMID 15215087
Citations 70
Authors
Affiliations
Soon will be listed here.
Abstract

We investigated the diversity of the chromosomal class A beta-lactamase gene in Klebsiella pneumoniae in order to study the evolution of the gene. A 789-bp portion was sequenced in a panel of 28 strains, representative of three phylogenetic groups, KpI, KpII, and KpIII, recently identified in K. pneumoniae and of different chromosomal beta-lactamase variants previously identified. Three groups of sequences were found, two of them corresponding to the families SHV (pI 7.6) and LEN (pI 7.1), respectively, and one, more heterogeneous, corresponding to a new family that we named OKP (for other K. pneumoniae beta-lactamase). Levels of susceptibility to ampicillin, cefuroxime, cefotaxime, ceftazidime, and aztreonam and inhibition by clavulanic acid were similar in the three groups. One new SHV variant, seven new LEN variants, and four OKP variants were identified. The OKP variants formed two subgroups based on nucleotide sequences, one with pIs of 7.8 and 8.1 and the other with pIs of 6.5 and 7.0. The nucleotide sequences of the housekeeping genes gyrA, coding for subunit A of gyrase, and mdh, coding for malate dehydrogenase, were also determined. Phylogenetic analysis of the three genes studied revealed parallel evolution, with the SHV, OKP, and LEN beta-lactamase families corresponding to the phylogenetic groups KpI, KpII, and KpIII, respectively. This correspondence was fully confirmed for 34 additional strains in PCR assays specific for the three beta-lactamase families. We estimated the time since divergence of the phylogenetic groups KpI and KpIII at between 6 and 28 million years, confirming the ancient presence of the beta-lactamase gene in the genome of K. pneumoniae.

Citing Articles

the impact of stakeholder decision-making on antimicrobial resistance evolution.

Ashfield T, Cooray M, Jimenez-Acha I, Riaz Z, Gifford D, Lagator M Microbiology (Reading). 2025; 171(2).

PMID: 40008972 PMC: 11865498. DOI: 10.1099/mic.0.001534.


Genomic and phenotypic characterization of ST2012 clinical Klebsiella quasipneumoniae subsp. similipneumoniae harboring bla in China.

Liu Y, Liu X, Xu H, Zhang X, Liu R, Chen M BMC Microbiol. 2024; 24(1):506.

PMID: 39614148 PMC: 11606014. DOI: 10.1186/s12866-024-03637-2.


Multidrug-resistant ESBL-producing Klebsiella pneumoniae complex in Czech hospitals, wastewaters and surface waters.

Davidova-Gerzova L, Lausova J, Sukkar I, Nechutna L, Kubackova P, Krutova M Antimicrob Resist Infect Control. 2024; 13(1):141.

PMID: 39593189 PMC: 11590221. DOI: 10.1186/s13756-024-01496-0.


Diversity, functional classification and genotyping of SHV β-lactamases in .

Tsang K, Lam M, Wick R, Wyres K, Bachman M, Baker S Microb Genom. 2024; 10(10).

PMID: 39432416 PMC: 11493186. DOI: 10.1099/mgen.0.001294.


The Impact of Bamboo Consumption on the Spread of Antibiotic Resistance Genes in Giant Pandas.

Yan Z, He X, Ayala J, Xu Q, Yu X, Hou R Vet Sci. 2023; 10(11).

PMID: 37999453 PMC: 10675626. DOI: 10.3390/vetsci10110630.


References
1.
Bradford P . Extended-spectrum beta-lactamases in the 21st century: characterization, epidemiology, and detection of this important resistance threat. Clin Microbiol Rev. 2001; 14(4):933-51, table of contents. PMC: 89009. DOI: 10.1128/CMR.14.4.933-951.2001. View

2.
Arakawa Y, Ohta M, Kido N, Fujii Y, Komatsu T, Kato N . Close evolutionary relationship between the chromosomally encoded beta-lactamase gene of Klebsiella pneumoniae and the TEM beta-lactamase gene mediated by R plasmids. FEBS Lett. 1986; 207(1):69-74. DOI: 10.1016/0014-5793(86)80014-x. View

3.
Barlow M, Hall B . Origin and evolution of the AmpC beta-lactamases of Citrobacter freundii. Antimicrob Agents Chemother. 2002; 46(5):1190-8. PMC: 127158. DOI: 10.1128/AAC.46.5.1190-1198.2002. View

4.
Vogel R, Entian K, Mecke D . Cloning and sequence of the mdh structural gene of Escherichia coli coding for malate dehydrogenase. Arch Microbiol. 1987; 149(1):36-42. DOI: 10.1007/BF00423133. View

5.
Ochman H, Wilson A . Evolution in bacteria: evidence for a universal substitution rate in cellular genomes. J Mol Evol. 1987; 26(1-2):74-86. DOI: 10.1007/BF02111283. View