通过一种新的基于探针的多重实时PCR系统快速准确地诊断败血症。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Marco Favaro, Christian Fini, Maurizio Capannari, Ivano Petriccione, Claudia Rotondo, Assunta Navarra, Chiara Stellitano, Chiara De Giuli, Antonella Vulcano, Carla Fontana
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引用次数: 0

摘要

脓毒症是一种严重的临床急症,需要及时诊断和干预。由于人口老龄化和抗生素耐药性的增加,其患病率有所增加。早期识别和使用创新技术对于改善患者预后至关重要。需要现代方法来最大限度地缩短诊断周转时间并改善结果。快速诊断测试和多重PCR是有效的,但在识别一系列病原体和靶基因方面存在局限性。我们的研究评估了两种新的基于探针的多重实时PCR系统:SEPSI ID和SEPSI DR面板。这些系统可以快速识别细菌和真菌病原体,以及抗生素抗性基因。检测涵盖29种微生物(革兰氏阴性菌、革兰氏阳性菌、酵母菌和霉菌),以及23种耐药基因和4种毒力因子。简化的工作流程使用阳性血培养(BCs)的2µL肉汤,无需核酸提取,大约1小时即可提供结果。我们对228个BCs和22个分离株进行了全基因组测序评估。与参考方法相比,SEPSI ID面板的灵敏度为96.88%,特异性为100%,PPV为100%,而SEPSI DR面板的灵敏度为97.8%,PPV为89.7%,特异性为96.7%。两个小组还确定了常规方法未检测到的其他病原体和耐药性相关靶点。这种检测方法有望快速准确地诊断败血症。未来的研究应验证其在各种临床环境中的表现,以加强败血症管理并改善患者预后。我们提出了一种新的诊断方法,可以快速准确地从阳性血培养中鉴定病原体和耐药基因,从而消除了核酸提取的需要。该技术也可用于新鲜病原菌培养。它有可能极大地改善治疗方案,导致更好的患者结果,更负责任的抗生素使用,以及更有效的医疗资源管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid and accurate sepsis diagnostics via a novel probe-based multiplex real-time PCR system.

Sepsis is a critical clinical emergency that requires prompt diagnosis and intervention. Its prevalence has increased due to the aging population and increased antibiotic resistance. Early identification and the use of innovative technologies are crucial for improving patient outcomes. Modern methodologies are needed to minimize the turnaround time for diagnosis and improve outcomes. Rapid diagnostic tests and multiplex PCR are effective but have limitations in identifying a range of pathogens and target genes. Our study evaluated two novel probe-based multiplex real-time PCR systems: the SEPSI ID and SEPSI DR panels. These systems can quickly identify bacterial and fungal pathogens, alongside antibiotic resistance genes. The assays cover 29 microorganisms (gram-negative bacteria, gram-positive bacteria, yeast, and mold species), alongside 23 resistance genes and four virulence factors. A streamlined workflow uses 2 µL of broth from positive blood cultures (BCs) without nucleic acid extraction and provides results in approximately 1 h. We present the results from an evaluation of 228 BCs and 22 isolates previously characterized by whole-genome sequencing. In comparison to the reference methods, the SEPSI ID panel demonstrated a sensitivity of 96.88%, a specificity of 100%, and a PPV of 100%, whereas the SEPSI DR panel showed a sensitivity of 97.8%, a PPV of 89.7%, and a specificity of 96.7%. Both panels also identified additional pathogens and resistance-related targets not detected by conventional methods. This assay shows promise for rapidly and accurately diagnosing sepsis. Future studies should validate its performance in various clinical settings to enhance sepsis management and improve patient outcomes.IMPORTANCEWe present a new diagnostic method that enables the quick and precise identification of pathogens and resistance genes from positive blood cultures, eliminating the need for nucleic acid extraction. This technique can also be used on fresh pathogen cultures. It has the potential to greatly improve treatment protocols, leading to better patient outcomes, more responsible antibiotic use, and more efficient management of healthcare resources.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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