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

被引:17
作者
Gharizadeh, B
Akhras, M
Unemo, M
Wretlind, B
Nyrén, P
Pourmand, N
机构
[1] Stanford Univ, Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[2] Royal Inst Technol, Dept Biotechnol, SE-10691 Stockholm, Sweden
[3] Orebro Univ Hosp, Dept Clin Microbiol, Natl Ref Lab Pathogen Neisseria, SE-70185 Orebro, Sweden
[4] Karolinska Univ, Huddinge Hosp, Karolinska Inst, Dept Lab Med,Div Clin Bacteriol, SE-14186 Stockholm, Sweden
关键词
DNA sequencing; ciprofloxacin resistance; Neisseria gonorrhoeae; pre-programmed DNA sequencing; pyrosequencing technology;
D O I
10.1016/j.ijantimicag.2005.08.017
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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. (c) 2005 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:486 / 490
页数:5
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