Kim Hye Jin, Kim Yu Jin, Yong Dong Eun, Lee Kyungwon, Park Jeon Han, Lee Jae Myun, Yoon Sang Sun
Department of Microbiology and Immunology, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Laboratory Medicine and Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, Republic of Korea.
J Microbiol Methods. 2014 Sep;104:61-6. doi: 10.1016/j.mimet.2014.05.021. Epub 2014 Jun 10.
Vancomycin-resistant enterococci (VRE) are one of the leading causes of nosocomial infection at intensive care unit (ICU). A rapid and sensitive detection of VRE infection is in high demand for timely and suitable antibiotic treatment. Here, we optimized a distinct DNA-based diagnostic technique, loop-mediated isothermal amplification (LAMP) for a rapid detection of the presence of vanA gene, a critical component of the gene cluster required for vancomycin resistance. Amplification efficiency was optimal at 62°C and with 2mM MgSO4. The detection limit of the DNA template was 80pg and LAMP amplicons were detected within 40min; thereby suggesting a potential applicability of LAMP as a sensitive and urgent diagnostic method. Furthermore, positive LAMP reaction was directly detected with the naked-eye by monitoring the formation of a white precipitate or the color change induced by hydroxy naphthol blue (HNB) dye. Finally, 56 clinical isolates were successfully tested for the presence of vanA gene by LAMP, which was determined to be more sensitive than PCR. Together, our results clearly demonstrate the usefulness of LAMP for the diagnosis of VRE infection.
耐万古霉素肠球菌(VRE)是重症监护病房(ICU)医院感染的主要原因之一。快速、灵敏地检测VRE感染对于及时、合理地使用抗生素治疗至关重要。在此,我们优化了一种独特的基于DNA的诊断技术——环介导等温扩增技术(LAMP),用于快速检测vanA基因的存在,vanA基因是耐万古霉素基因簇的关键组成部分。在62°C和2mM MgSO4条件下扩增效率最佳。DNA模板的检测限为80pg,40分钟内可检测到LAMP扩增产物;这表明LAMP作为一种灵敏且快速的诊断方法具有潜在的适用性。此外,通过监测白色沉淀的形成或羟基萘酚蓝(HNB)染料引起的颜色变化,可直接用肉眼检测LAMP阳性反应。最后,通过LAMP成功检测了56株临床分离株中vanA基因的存在,结果表明LAMP比PCR更灵敏。总之,我们的结果清楚地证明了LAMP在诊断VRE感染方面的实用性。