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Sökning: onr:"swepub:oai:DiVA.org:kth-8159" > Detection of gyrA m...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003659naa a2200433 4500
001oai:DiVA.org:kth-8159
003SwePub
008080403s2005 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:115987776
024a https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-81592 URI
024a https://doi.org/10.1016/j.ijantimicag.2005.08.0172 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1159877762 URI
040 a (SwePub)kthd (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Gharizadeh, Babacku Stanford Univ, Stanford Genome Technol Ctr4 aut
2451 0a Detection of gyrA mutations associated with ciprofloxacin resistance in Neisseria gonorrhoeae by rapid and reliable pre-programmed short DNA sequencing
264 1b Elsevier BV,c 2005
338 a print2 rdacarrier
500 a QC 20100624
520 a 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.
650 7a NATURVETENSKAPx Biologix Biokemi och molekylärbiologi0 (SwePub)106022 hsv//swe
650 7a NATURAL SCIENCESx Biological Sciencesx Biochemistry and Molecular Biology0 (SwePub)106022 hsv//eng
653 a DNA sequencing; ciprofloxacin resistance; Neisseria gonorrhoeae; pre-programmed DNA sequencing; pyrosequencing technology; ANTIMICROBIAL RESISTANCE; MECHANISMS; FAILURE; ISOLATE; PARC
653 a Biochemistry
653 a Biokemi
700a Akhras, Michaelu KTH,Skolan för bioteknologi (BIO)4 aut0 (Swepub:kth)u1oz2y6y
700a Unemo, Magnusu Örebro Univ Hosp, Dept Clin Microbiol4 aut
700a Wretlind, Bengtu Karolinska Inst, Dept Lab Med4 aut
700a Nyrén, Pålu KTH,Skolan för bioteknologi (BIO)4 aut0 (Swepub:kth)u134qr82
700a Pourmand, Naderu Stanford Univ, Stanford Genome Technol Ctr4 aut
710a Stanford Univ, Stanford Genome Technol Ctrb Skolan för bioteknologi (BIO)4 org
773t International Journal of Antimicrobial Agentsd : Elsevier BVg 26:6, s. 486-490q 26:6<486-490x 0924-8579x 1872-7913
856u https://europepmc.org/articles/pmc2768773?pdf=render
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-8159
8564 8u https://doi.org/10.1016/j.ijantimicag.2005.08.017
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:115987776

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