An accurate multiplex antibiotic susceptibility test using a high-resolution CE-SSCP-based stuffer-free multiplex ligation-dependent probe amplification system

被引:4
作者
Chung, Boram [1 ]
Shin, Gi Won [2 ]
Choi, Woong [1 ]
Hwang, Hee Sung [1 ]
Oh, Mi-Hwa [3 ]
Jung, Gyoo Yeol [1 ,4 ]
机构
[1] Pohang Univ Sci & Technol, Sch Interdisciplinary Biosci & Bioengn, Pohang 790784, Gyeongbuk, South Korea
[2] Pohang Univ Sci & Technol, Inst Environm & Energy Technol, Pohang 790784, Gyeongbuk, South Korea
[3] Natl Inst Anim Sci, Rural Dev Adm, Suwon, Gyeonggi, South Korea
[4] Pohang Univ Sci & Technol, Dept Chem Engn, Pohang 790784, Gyeongbuk, South Korea
关键词
Antibiotic susceptibility test; High-resolution CE-SSCP; Multiplex detection; Stuffer-free multiplex ligation-dependent probe amplification; REAL-TIME PCR; CAPILLARY-ELECTROPHORESIS; INFECTIONS; ASSAY; QUANTIFICATION; BACTEREMIA; COMMUNITY; THERAPY; DNA;
D O I
10.1002/elps.201200372
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The success of antimicrobial therapy depends on effective prescription of antibiotics. Assessment of clinical isolates using rapid antimicrobial susceptibility tests allows effective microbiological therapy to be commenced in a timely manner. However, conventional antimicrobial susceptibility testing is time-consuming and laborious. In the present study, we employed stuffer-free multiplex ligation-dependent probe amplification (MLPA) coupled with analysis of single-strand conformation polymorphisms, via high-resolution CE, to develop a multiplex antibiotic susceptibility test. Using this method, parallel analysis of specific genetic markers was employed to determine minimal inhibitory concentration values. The values derived using the stuffer-free MLPA method agreed with those estimated using a conventional broth dilution method. These findings indicate that the stuffer-free MLPA-based approach is a viable alternative to the conventional method.
引用
收藏
页码:284 / 288
页数:5
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