Antimicrobial activity of DC-159a, a new fluoroquinolone, against 1,149 recently collected clinical isolates
dc.contributor.author | Jones, Ronald N. | |
dc.contributor.author | Fritsche, Thomas R. | |
dc.contributor.author | Sader, Helio S. [UNIFESP] | |
dc.contributor.institution | JMI Labs | |
dc.contributor.institution | Tufts Univ | |
dc.contributor.institution | Universidade Federal de São Paulo (UNIFESP) | |
dc.date.accessioned | 2016-01-24T13:51:42Z | |
dc.date.available | 2016-01-24T13:51:42Z | |
dc.date.issued | 2008-10-01 | |
dc.description.abstract | The activity of DC-159a, a novel orally administered fluorinated quinolone, was evaluated by reference broth microdilution or agar dilution methods against 1,149 recently collected clinical isolates from five continents. Against pathogens associated with community-acquired respiratory tract infections (CA-RTIs), the MIC(90)s were 0.12 mu g/ml for Streptococcus pneumoniae, 0.015 to 0.03 mu g/ml for Haemophilus influenzae, 0.03 mu g/ml for Moraxella catarrhalis, and 0.12 mu g/ml for beta-hemolytic streptococci. Similarly, DC-59a was potent against various types of staphylococci (MIC90 range, 0.03 to 2 mu g/ml), Enterococcus faecalis (MIC90, 4 mu g/ml), wild-type isolates of the family Enterobacteriaceae (MIC90 range, 0.06 to 2 mu g/ml), wild-type Pseudomonas aeruginosa (MIC90, 2 mu g/ml), and Acinetobacter spp. (MIC90, 0.12 mu g/ml). Fluoroquinolone-nonsusceptible organism subsets usually had elevated DC-159a MICs, but the MICs were often two- to fourfold lower than those of levofloxacin and moxifloxacin. in conclusion, DC-159a appears to possess a balanced broad spectrum of activity that exceeds the activities of the currently marketed fluoroquinolones, especially against pathogens that cause CA-RTIs. | en |
dc.description.affiliation | JMI Labs, N Liberty, IA 52317 USA | |
dc.description.affiliation | Tufts Univ, Sch Med, Boston, MA 02111 USA | |
dc.description.affiliation | Universidade Federal de São Paulo, São Paulo, Brazil | |
dc.description.affiliationUnifesp | Universidade Federal de São Paulo, São Paulo, Brazil | |
dc.description.source | Web of Science | |
dc.description.sponsorship | Daiichi Pharmaceutical Co., Ltd. | |
dc.format.extent | 3763-3775 | |
dc.identifier | http://dx.doi.org/10.1128/AAC.00294-08 | |
dc.identifier.citation | Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 52, n. 10, p. 3763-3775, 2008. | |
dc.identifier.doi | 10.1128/AAC.00294-08 | |
dc.identifier.file | WOS000259480800039.pdf | |
dc.identifier.issn | 0066-4804 | |
dc.identifier.uri | http://repositorio.unifesp.br/handle/11600/30921 | |
dc.identifier.wos | WOS:000259480800039 | |
dc.language.iso | eng | |
dc.publisher | Amer Soc Microbiology | |
dc.relation.ispartof | Antimicrobial Agents and Chemotherapy | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.title | Antimicrobial activity of DC-159a, a new fluoroquinolone, against 1,149 recently collected clinical isolates | en |
dc.type | info:eu-repo/semantics/article |
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