Zhao Yanan, Nagasaki Yoji, Kordalewska Milena, Press Ellen G, Shields Ryan K, Nguyen M Hong, Clancy Cornelius J, Perlin David S
Public Health Research Institute, New Jersey Medical School-Rutgers Biomedical and Health Sciences, Newark, New Jersey, USA
Public Health Research Institute, New Jersey Medical School-Rutgers Biomedical and Health Sciences, Newark, New Jersey, USA.
Antimicrob Agents Chemother. 2016 Oct 21;60(11):6573-6577. doi: 10.1128/AAC.01574-16. Print 2016 Nov.
A novel and highly accurate diagnostic assay platform was established for rapid identification of FKS mutations associated with echinocandin resistance in Candida glabrata The assay platform uses allele-specific molecular beacon and DNA melt analysis following asymmetric PCR. A dual assay for FKS1 and FKS2 was developed to identify within 3 h the most common and clinically relevant resistance-associated mutations, including 8 FKS1 HS1 (wild type [WT], S629P, F625S, D632Y, D632E [T1896G], D632E [T1896A], I634V, and F625F) and 7 FKS2 HS1 (WT, F659del, F659S, F659V, F659L, S663P, and S663F) genotypes. A blinded panel of 188 C. glabrata clinical isolates was tested by both assays. The molecular diagnostic results from the dual assay were 100% concordant with data obtained from DNA sequencing. This platform has the potential to overcome the deficiencies of existing in vitro susceptibility-based assays to identify echinocandin-resistant C. glabrata and holds promise as a surrogate diagnostic method to better direct echinocandin therapy.
建立了一种新型且高度准确的诊断检测平台,用于快速鉴定光滑念珠菌中与棘白菌素耐药性相关的FKS突变。该检测平台在不对称PCR后使用等位基因特异性分子信标和DNA熔解分析。开发了一种针对FKS1和FKS2的双重检测方法,可在3小时内鉴定出最常见且与临床相关的耐药性相关突变,包括8种FKS1 HS1(野生型[WT]、S629P、F625S、D632Y、D632E[T1896G]、D632E[T1896A]、I634V和F625F)和7种FKS2 HS1(WT、F659del、F659S、F659V、F659L、S663P和S663F)基因型。通过这两种检测方法对188株光滑念珠菌临床分离株的盲样进行了检测。双重检测的分子诊断结果与DNA测序获得的数据100%一致。该平台有可能克服现有基于体外药敏试验的检测方法在鉴定棘白菌素耐药性光滑念珠菌方面的不足,并有望作为一种替代诊断方法,更好地指导棘白菌素治疗。