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- Publisher Website: 10.1093/jac/47.5.655
- Scopus: eid_2-s2.0-0035011959
- PMID: 11328779
- WOS: WOS:000168839000021
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Article: Target site modifications and efflux phenotype in clinical isolates of Streptococcus pneumoniae from Hong Kong with reduced susceptibility to fluoroquinolones
Title | Target site modifications and efflux phenotype in clinical isolates of Streptococcus pneumoniae from Hong Kong with reduced susceptibility to fluoroquinolones |
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Authors | |
Issue Date | 2001 |
Publisher | Oxford University Press. The Journal's web site is located at http://jac.oxfordjournals.org/ |
Citation | Journal Of Antimicrobial Chemotherapy, 2001, v. 47 n. 5, p. 655-658 How to Cite? |
Abstract | Ciprofloxacin-susceptible (n = 7) and -resistant (MIC ≥4 mg/L) (n = 15) clinical isolates of Streptococcus pneumoniae from diverse sources in Hong Kong were studied for target site modifications and efflux phenotype. Reserpine-inhibited efflux of ciprofloxacin and/or levofloxacin was common in both susceptible and non-susceptible isolates. The ParC substitutions K137N and/or S79F or Y were associated with increased ciprofloxacin MICs. The GyrA substitution S81F was only found in isolates with full resistance to ciprofloxacin (MIC ≥ 16 mg/L) and levofloxacin (MIC ≥ 8 mg/L). Among clinical isolates of S. pneumoniae, accumulation of target site mutations in strains with an efflux mechanism was associated with increasing MICs of fluoroquinolones. |
Persistent Identifier | http://hdl.handle.net/10722/79163 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.271 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ho, PL | en_HK |
dc.contributor.author | Yam, WC | en_HK |
dc.contributor.author | Que, TL | en_HK |
dc.contributor.author | Tsang, DNC | en_HK |
dc.contributor.author | Seto, WH | en_HK |
dc.contributor.author | Ng, TK | en_HK |
dc.contributor.author | Ng, WS | en_HK |
dc.date.accessioned | 2010-09-06T07:51:21Z | - |
dc.date.available | 2010-09-06T07:51:21Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Journal Of Antimicrobial Chemotherapy, 2001, v. 47 n. 5, p. 655-658 | en_HK |
dc.identifier.issn | 0305-7453 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/79163 | - |
dc.description.abstract | Ciprofloxacin-susceptible (n = 7) and -resistant (MIC ≥4 mg/L) (n = 15) clinical isolates of Streptococcus pneumoniae from diverse sources in Hong Kong were studied for target site modifications and efflux phenotype. Reserpine-inhibited efflux of ciprofloxacin and/or levofloxacin was common in both susceptible and non-susceptible isolates. The ParC substitutions K137N and/or S79F or Y were associated with increased ciprofloxacin MICs. The GyrA substitution S81F was only found in isolates with full resistance to ciprofloxacin (MIC ≥ 16 mg/L) and levofloxacin (MIC ≥ 8 mg/L). Among clinical isolates of S. pneumoniae, accumulation of target site mutations in strains with an efflux mechanism was associated with increasing MICs of fluoroquinolones. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Oxford University Press. The Journal's web site is located at http://jac.oxfordjournals.org/ | en_HK |
dc.relation.ispartof | Journal of Antimicrobial Chemotherapy | en_HK |
dc.rights | Journal of Antimicrobial Chemotherapy. Copyright © Oxford University Press. | en_HK |
dc.subject.mesh | Amino Acid Substitution | en_HK |
dc.subject.mesh | Anti-Infective Agents - pharmacology | en_HK |
dc.subject.mesh | Bacterial Proteins - genetics | en_HK |
dc.subject.mesh | Biological Transport | en_HK |
dc.subject.mesh | Drug Resistance, Microbial - genetics - physiology | en_HK |
dc.subject.mesh | Fluoroquinolones | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Microbial Sensitivity Tests | en_HK |
dc.subject.mesh | Mutation | en_HK |
dc.subject.mesh | Phenotype | en_HK |
dc.subject.mesh | Streptococcus pneumoniae - drug effects - genetics - metabolism | en_HK |
dc.title | Target site modifications and efflux phenotype in clinical isolates of Streptococcus pneumoniae from Hong Kong with reduced susceptibility to fluoroquinolones | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0305-7453&volume=47&spage=655&epage=658&date=2001&atitle=Target+site+modifications+and+efflux+phenotype+in+clinical+isolates+of+Streptococcus+pneumoniae+from+Hong+Kong+with+reduced+susceptibility+to+fluoroquinolones | en_HK |
dc.identifier.email | Ho, PL:plho@hkucc.hku.hk | en_HK |
dc.identifier.email | Yam, WC:wcyam@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ho, PL=rp00406 | en_HK |
dc.identifier.authority | Yam, WC=rp00313 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1093/jac/47.5.655 | - |
dc.identifier.pmid | 11328779 | - |
dc.identifier.scopus | eid_2-s2.0-0035011959 | en_HK |
dc.identifier.hkuros | 60648 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035011959&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 47 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 655 | en_HK |
dc.identifier.epage | 658 | en_HK |
dc.identifier.isi | WOS:000168839000021 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Ho, PL=7402211363 | en_HK |
dc.identifier.scopusauthorid | Yam, WC=7004281720 | en_HK |
dc.identifier.scopusauthorid | Que, TL=7003786628 | en_HK |
dc.identifier.scopusauthorid | Tsang, DNC=7005609132 | en_HK |
dc.identifier.scopusauthorid | Seto, WH=36950521100 | en_HK |
dc.identifier.scopusauthorid | Ng, TK=7402229817 | en_HK |
dc.identifier.scopusauthorid | Ng, WS=36787042500 | en_HK |
dc.identifier.issnl | 0305-7453 | - |