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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
1991-8-29
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pubmed:abstractText |
Minimal inhibitory concentrations (MICs) of the oral cephalosporin BAY v 3522, and of cephprozyl, cefaclor, cefixime, cefuroxime, cefetamet, cefpodoxime and cefotaxime were determined against Gram-positive and Gram-negative clinical isolates with the NCCLS agar dilution procedures. BAY was the most active drug against Gram-positive organisms. MICs ranged from 0.01 mg/l against group A streptococci to 16 mg/l against S. faecium. Although mean MICs of BAY against methicillin-resistant S. aureus and S. epidermidis were between 0.9-1.8 mg/l, respectively, such strains showed typical heteroresistance in population studies. In addition, the biochemical correlate of methicillin-resistance, the PBP-2', showed similar low affinity to BAY as methicillin. beta-lactamase-producing H. influenzae and B. catarrhalis were inhibited by 2-8 and 0.25-2 mg/l, respectively, whereas non-producers were inhibited by 0.25-2 and 0.12-1 mg/l of the drug. The activity of BAY against enterobacteriaceae was rather low. Ampicillin-susceptible E. coli strains were inhibited by 2-8 and resistant strains by 8-32 mg/l. The mean MIC against cephalothin-susceptible K. pneumoniae strains was 2.8, and that against resistant strains 27.4 mg/l. MICs against beta-lactamase-producing enterobacteriaceae determined in broth dilution were 4-8 times higher than those determined in agar dilution. Bactericidal activity was measured in killing-curve experiments at 4 times the MIC. BAY killed equally well as standard control drugs.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Bay v 3522,
http://linkedlifedata.com/resource/pubmed/chemical/Benzothiazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Cephalosporins,
http://linkedlifedata.com/resource/pubmed/chemical/Hexosyltransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Muramoylpentapeptide...,
http://linkedlifedata.com/resource/pubmed/chemical/Penicillin-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Peptidyl Transferases
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pubmed:status |
MEDLINE
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pubmed:issn |
0378-6501
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
515-25
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2100734-Administration, Oral,
pubmed-meshheading:2100734-Bacterial Proteins,
pubmed-meshheading:2100734-Benzothiazoles,
pubmed-meshheading:2100734-Carrier Proteins,
pubmed-meshheading:2100734-Cephalosporins,
pubmed-meshheading:2100734-Colony Count, Microbial,
pubmed-meshheading:2100734-Gram-Negative Bacteria,
pubmed-meshheading:2100734-Gram-Positive Bacteria,
pubmed-meshheading:2100734-Hexosyltransferases,
pubmed-meshheading:2100734-Methicillin Resistance,
pubmed-meshheading:2100734-Microbial Sensitivity Tests,
pubmed-meshheading:2100734-Muramoylpentapeptide Carboxypeptidase,
pubmed-meshheading:2100734-Penicillin-Binding Proteins,
pubmed-meshheading:2100734-Peptidyl Transferases
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pubmed:year |
1990
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pubmed:articleTitle |
In vitro activity of oral cephalosporin BAY v 3522 compared with other oral cephalosporins.
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pubmed:affiliation |
Institute of Medical Microbiology, University of Zürich, Switzerland.
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pubmed:publicationType |
Journal Article,
Comparative Study
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