Ng Sally, Tan Chai Yuin, Yah Jing Yan, Osman Nur A'tikah Binte, Chew Ka Lip
Department of Laboratory Medicine, National University Hospital, , Singapore.
J Clin Microbiol. 2024 Dec 11;62(12):e0116924. doi: 10.1128/jcm.01169-24. Epub 2024 Nov 6.
Rapid multiplex PCR kits have been used for rapid identification of blood culture isolates and prediction of antimicrobial resistance. We performed an evaluation of the QIAstat-Dx BCID GN and GPF research use only (RUO) kits on positive blood culture bottles using routine laboratory testing as the reference standard. Positive blood culture bottles between November 2023 and January 2024 were tested with QIAstat-Dx BCID GN and GPF kits based on initial Gram stain results and compared against routine identification and phenotypic susceptibility testing. A total of 174 monomicrobial blood cultures were included in the final analysis. The 174 monomicrobial blood cultures composed of 129 BCID GN tests and 45 BCID GPF tests. The majority of on-target Gram-negative organisms in monomicrobial cultures were identified. One isolate was not identified as such, although the pan-Enterobacterales target was positive. All on-target Gram-positive organisms in monomicrobial cultures were identified. Overall sensitivity and specificity of for detection of aminopenicillin resistance in was 94.7% (18/19) and 95.8% (23/24). The presence/absence of and had 100% sensitivity and specificity for identification of third-generation cephalosporin resistance in and . The combination of and gene detection was fully predictive of phenotypic susceptibility results to penicillin and cloxacillin for . Overall, the QIAstat-Dx BCID GN and GPF kits were able to identify on-target pathogens. Detected resistance mechanisms were highly predictive of β-lactam resistance. Prediction of resistance for non-β-lactam antimicrobial was more variable.
This is one of the first evaluations of the QIAstat BCID kit and demonstrates high levels of correlation for both identification and antimicrobial resistance prediction.
快速多重PCR试剂盒已用于血液培养分离株的快速鉴定和抗菌药物耐药性预测。我们以常规实验室检测作为参考标准,对仅用于研究的QIAstat-Dx BCID GN和GPF试剂盒在阳性血培养瓶上进行了评估。根据初始革兰氏染色结果,使用QIAstat-Dx BCID GN和GPF试剂盒对2023年11月至2024年1月期间的阳性血培养瓶进行检测,并与常规鉴定和表型药敏试验进行比较。最终分析共纳入174份单微生物血培养。这174份单微生物血培养包括129次BCID GN检测和45次BCID GPF检测。单微生物培养中大多数目标革兰氏阴性菌被鉴定出来。有一株分离株未被正确鉴定,尽管泛肠杆菌科目标呈阳性。单微生物培养中所有目标革兰氏阳性菌均被鉴定出来。检测氨基青霉素耐药性的总体敏感性和特异性分别为94.7%(18/19)和95.8%(23/24)。blaCTX-M和blaKPC的存在与否对肺炎克雷伯菌和大肠埃希菌中第三代头孢菌素耐药性的鉴定具有100%的敏感性和特异性。blaTEM和blaOXA基因检测的组合对青霉素和氯唑西林的表型药敏结果具有完全预测性。总体而言,QIAstat-Dx BCID GN和GPF试剂盒能够鉴定目标病原体。检测到的耐药机制对β-内酰胺耐药性具有高度预测性。非β-内酰胺抗菌药物耐药性的预测则更具变异性。
这是对QIAstat BCID试剂盒的首批评估之一,证明了在鉴定和抗菌药物耐药性预测方面都具有高度相关性。