pubmed-article:10639363 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0001699 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0025252 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C1167331 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0007559 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0370215 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0250480 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0683598 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0392747 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C2700640 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0106041 | lld:lifeskim |
pubmed-article:10639363 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:10639363 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:10639363 | pubmed:dateCreated | 2000-3-23 | lld:pubmed |
pubmed-article:10639363 | pubmed:abstractText | We describe Klebsiella pneumoniae 15571, a clinical isolate resistant to ceftazidime MIC = 32 microg/ml) and piperacillin-tazobactam (MICs = 1,024 and 128 microg/ml). K. pneumoniae 15571 expresses a single beta-lactamase with a pI of 7.6. However, when cloned in a high-copy-number vector in Escherichia coli, this bla(SHV-1) gene did not confer resistance to ceftazidime, a spectrum consistent with the nucleotide sequence, which was nearly identical to those of previously described bla(SHV-1) genes. Outer membrane protein (OMP) analysis of K. pneumoniae 15571 revealed a decrease in the quantity of a minor 45-kDa OMP in comparison to that in K. pneumoniae 44NR, a low-level ampicillin-resistant strain that also expresses a chromosomally determined bla(SHV-1). Crude beta-lactamase enzyme extracts from K. pneumoniae 15571 produced roughly 200-fold more beta-lactamase activity than K. pneumoniae 44NR. Northern hybridization analysis revealed that this difference was explainable by quantifiable differences in transcription of the bla(SHV-1) gene in the two strains. Primer extension analysis of bla(SHV-1) mRNA from K. pneumoniae 15571 and 44NR indicated that the transcriptional start sites were identical in the two strains. DNA sequencing of the promoter regions upstream of the of bla(SHV-1) open reading frames in the two K. pneumoniae strains revealed an A-->C change in the second position of the -10 region in K. pneumoniae 44NR compared to that in 15571. Site-directed mutagenesis of the cloned K. pneumoniae 15571 bla(SHV-1), in which the A in the second position of the 15571 -10 region was changed to a C, resulted in a substantial lowering of the MIC of ampicillin. When the levels of beta-lactamase enzyme expression in E. coli were compared, the bla(SHV-1) downstream of the altered -10 region produced 17-fold less beta-lactamase enzyme. These results indicate that elevated levels of ceftazidime resistance can result from a combination of increased enzyme production and minor OMP changes and that levels of chromosomally encoded SHV-1 beta-lactamase production can vary substantially with a single-base-pair change in promoter sequence. | lld:pubmed |
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pubmed-article:10639363 | pubmed:language | eng | lld:pubmed |
pubmed-article:10639363 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10639363 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:10639363 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10639363 | pubmed:month | Feb | lld:pubmed |
pubmed-article:10639363 | pubmed:issn | 0066-4804 | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:HuttonRR | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:HoyerGG | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:RiceL BLB | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:BonomoR ARA | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:CariasL LLL | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:HujerA MAM | lld:pubmed |
pubmed-article:10639363 | pubmed:author | pubmed-author:BonafedeMM | lld:pubmed |
pubmed-article:10639363 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10639363 | pubmed:volume | 44 | lld:pubmed |
pubmed-article:10639363 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10639363 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10639363 | pubmed:pagination | 362-7 | lld:pubmed |
pubmed-article:10639363 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:10639363 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10639363 | pubmed:articleTitle | High-level expression of chromosomally encoded SHV-1 beta-lactamase and an outer membrane protein change confer resistance to ceftazidime and piperacillin-tazobactam in a clinical isolate of Klebsiella pneumoniae. | lld:pubmed |
pubmed-article:10639363 | pubmed:affiliation | Medical Service, Department of Veterans Affairs Medical Center, Cleveland, OH 44106, USA. louis.rice@med.va.gov | lld:pubmed |
pubmed-article:10639363 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10639363 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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