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Development of a heptaplex PCR assay for identification of Staphylococcus aureus and CoNS with simultaneous detection of virulence and antibiotic resistance genes

机译:用于鉴定金黄色葡萄球菌和CoNS的同时检测毒力和抗生素抗性基因的七重PCR检测方法的开发

摘要

BackgroundudStaphylococcal toxicity and antibiotic resistance (STAAR) have been menacing public health. Although vancomycin-resistant Staphylococcus aureus (VRSA) is currently not as widespread as methicillin-resistant S. aureus (MRSA), genome evolution of MRSA into VRSA, including strains engineered within the same patient under anti-staphylococcal therapy, may build up to future public health concern. To further complicate diagnosis, infection control and anti-microbial chemotherapy, non-sterile sites such as the nares and the skin could contain both S. aureus and coagulase-negative staphylococci (CoNS), either of which could harbour mecA the gene driving staphylococcal methicillin-resistance and required for MRSA-VRSA evolution.ududResultsudA new heptaplex PCR assay has been developed which simultaneously detects seven markers for: i) eubacteria (16S rRNA), ii) Staphylococcus genus (tuf), iii) Staphylococcus aureus (spa), iv) CoNS (cns), v) Panton-Valentine leukocidin (pvl), vi) methicillin resistance (mecA), and vii) vancomycin resistance (vanA). Following successful validation using 255 reference bacterial strains, applicability to analyse clinical samples was evaluated by direct amplification in spiked blood cultures (n = 89) which returned 100 % specificity, negative and positive predictive values. The new assay has LoD of 1.0x103 CFU/mL for the 16S rRNA marker and 1.0x104 CFU/mL for six other markers and completes cycling in less than one hour.ududConclusionudThe speed, sensitivity (100 %), NPV (100 %) and PPV (100 %) suggest the new heptaplex PCR assay could be easily integrated into a routine diagnostic microbiology workflow. Detection of the cns marker allows for unique identification of CoNS in mono-microbial and in poly-microbial samples containing mixtures of CoNS and S. aureus without recourse to the conventional elimination approach which is ambiguous. In addition to the SA-CoNS differential diagnostic essence of the new assay, inclusion of vanA primers will allow microbiology laboratories to stay ahead of the emerging MRSA-VRSA evolution. To the best of our knowledge, the new heptaplex PCR assay is the most multiplexed among similar PCR-based assays for simultaneous detection of STAAR.
机译:背景葡萄球菌毒性和抗生素耐药性(STAAR)一直威胁着公众健康。尽管目前耐万古霉素的金黄色葡萄球菌(VRSA)不如耐甲氧西林的金黄色葡萄球菌(MRSA)广泛,但MRSA的基因组进化为VRSA,包括在同一患者体内进行抗葡萄球菌治疗的菌株,可能会持续发展公共卫生问题。为了进一步使诊断,感染控制和抗微生物化学疗法复杂化,非消毒部位(如鼻孔和皮肤)可能同时含有金黄色葡萄球菌和凝固酶阴性葡萄球菌(CoNS),这两个部位均可能包含驱动葡萄球菌甲氧西林基因的mecA耐药性,是MRSA-VRSA进化所必需的。 (spa),iv)CoNS(cns),v)Panton-Valentine leukocidin(pvl),vi)耐甲氧西林(mecA)和vii)耐万古霉素(vanA)。在使用255个参考细菌菌株成功验证之后,通过在加标血培养物中直接扩增(n = 89)来评估分析临床样品的适用性,该培养物返回100%的特异性,阴性和阳性预测值。新测定法的16S rRNA标记的LoD为1.0x103 CFU / mL,其他六个标记的LoD为1.0x104 CFU / mL,并在不到一小时的时间内完成了循环。 ud ud结论 ud速度,灵敏度(100%),NPV (100%)和PPV(100%)表明,新的heptaplex PCR分析法可以轻​​松地整合到常规诊断微生物学工作流程中。 cns标记的检测可在含有CoNS和金黄色葡萄球菌混合物的单微生物和多微生物样品中对CoNS进行唯一鉴定,而无需采用模棱两可的常规消除方法。除了新测定法的SA-CoNS鉴别诊断要点外,vanA引物的加入将使微生物实验室在新兴的MRSA-VRSA进化方面保持领先地位。据我们所知,在同时进行STAAR检测的类似基于PCR的检测中,新的heptaplex PCR检测是最复杂的。

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