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  • Gharizadeh, BabackStanford Univ, Stanford Genome Technol Ctr (author)

Detection of gyrA mutations associated with ciprofloxacin resistance in Neisseria gonorrhoeae by rapid and reliable pre-programmed short DNA sequencing

  • Article/chapterEnglish2005

Publisher, publication year, extent ...

  • Elsevier BV,2005
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:kth-8159
  • https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-8159URI
  • https://doi.org/10.1016/j.ijantimicag.2005.08.017DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:115987776URI

Supplementary language notes

  • Language:English
  • Summary in:English

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Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • QC 20100624
  • Quinolone resistance is rapidly increasing in Neisseria gonorrhoeae and is posing a significant public health threat that requires constant surveillance. A rapid and reliable mutation detection assay has been developed. The assay is based on pre-programmed short DNA sequencing and is designed to detect point mutations in the gyrA gene that are highly related to ciprofloxacin resistance, i.e. in codons 91 and 95. By developing an assay based on pyrosequencing and exploiting the pre-programmed nucleotide dispensation capability of this technology, the sequence comprising the mutations will be analysed and promptly reveal whether the N. gonorrhoeae pathogen carries resistance to ciprofloxacin. A panel of 40 N. gonorrhoeae clinical isolates, of which 27 phenotypically displayed decreased susceptibility or resistance to ciprofloxacin, was used in the present study. All point mutations in the short stretch of the N. gonorrhoeae gyrA gene were easily discriminated, and the genotypic results obtained by pre-programmed sequencing were mainly in agreement with the phenotypically identified decreased susceptibility or resistance to ciprofloxacin. The new method used in the present study has the potential for rapid and reliable identification of known as well as previously unknown drug resistance mutations.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Akhras, MichaelKTH,Skolan för bioteknologi (BIO)(Swepub:kth)u1oz2y6y (author)
  • Unemo, MagnusÖrebro Univ Hosp, Dept Clin Microbiol (author)
  • Wretlind, BengtKarolinska Inst, Dept Lab Med (author)
  • Nyrén, PålKTH,Skolan för bioteknologi (BIO)(Swepub:kth)u134qr82 (author)
  • Pourmand, NaderStanford Univ, Stanford Genome Technol Ctr (author)
  • Stanford Univ, Stanford Genome Technol CtrSkolan för bioteknologi (BIO) (creator_code:org_t)

Related titles

  • In:International Journal of Antimicrobial Agents: Elsevier BV26:6, s. 486-4900924-85791872-7913

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