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LIAISON PLEX酵母血培养检测法在血培养中鉴定16种侵袭性真菌病原体的性能。

Performance of the LIAISON PLEX yeast blood culture assay for identifying 16 invasive fungal pathogens in blood cultures.

作者信息

Emery Christopher L, Dhiman Neelam, Chow Siu-Kei, Peterson Gwyn, Granato Paul, Bernier Brian, Farhang Janet

机构信息

Indiana University Health, Indianapolis, Indiana, USA.

Quest Diagnostics, Lewisville, Texas, USA.

出版信息

J Clin Microbiol. 2025 Jul 9;63(7):e0036225. doi: 10.1128/jcm.00362-25. Epub 2025 Jun 2.

Abstract

UNLABELLED

Fungi frequently cause potentially life-threatening bloodstream infections, particularly in immunocompromised and hospitalized individuals. Molecular methods can allow earlier pathogen identification for faster optimization of appropriate therapy. This multisite study evaluated the analytical and clinical performance of the automated multiplex LIAISON PLEX Yeast Blood Culture nucleic acid assay (Luminex Corporation, Northbrook, IL), which detects and identifies 14 and 2 pathogens from positive blood cultures. Samples included 69 prospectively collected specimens, 63 pre-selected samples, and 829 contrived specimens. The assay demonstrated 100% positivity in detecting target fungal pathogens and 0% positivity in negative blood cultures. All 13 tested bottle/matrix types gave 100% detection of six evaluated pathogens. Limits of detection ranged from 7.77 × 10 CFU/mL () to 2.83 × 10 CFU/mL (). The assay identified five strains tested for each of the 16 target species, indicating good inclusivity. No cross-reactivity occurred with 40 bacterial strains. Cross-reactivity with 2 of 37 off-target fungi ( [] and ) was predicted by sequence analyses. Low concentrations of on-panel fungi were detectable alongside high concentrations of potential fungal and bacterial confounders. Reproducibility was 100% within-lab and 99.7% across sites. For combined prospective plus pre-selected specimens, sensitivity/positive percent agreement (PPA) was 100% for detected fungal pathogens, and specificity/negative percent agreement (NPA) was 97.6%‒100.0%. Common pathogens in prospective samples were (36%) and (25%). Contrived specimen PPA was 100%, and NPA was ≥99.6%. The LIAISON PLEX Yeast Blood Culture assay provides outstanding sensitivity and specificity for rapidly identifying and differentiating fungal pathogens in positive blood culture specimens.

IMPORTANCE

Bloodstream fungal infections have serious risks of illness and death. Optimal treatment requires early pathogen identification so appropriate antifungal therapy can be immediately started. Blood culture is standard for confirming fungal infection but takes several days for results and may not provide detailed pathogen information. The LIAISON PLEX Yeast Blood Culture assay quickly analyzes fungus-positive blood cultures to identify 16 pathogenic fungi, including multiple spp. that are common causes of bloodstream infection. This study demonstrated a high degree of test accuracy and reliability in rapidly identifying the infective pathogen in blood cultures from 132 patients with demonstrated culture-positive fungal infections. Assay performance was confirmed in 829 contrived samples, whereby samples were spiked with different fungal pathogens.

摘要

未标记

真菌经常引起潜在的危及生命的血流感染,特别是在免疫功能低下和住院患者中。分子方法可以更早地鉴定病原体,以便更快地优化适当的治疗方案。这项多中心研究评估了自动化多重LIAISON PLEX酵母血培养核酸检测法(Luminex公司,伊利诺伊州诺斯布鲁克)的分析和临床性能,该检测法可从阳性血培养物中检测和鉴定14种和2种病原体。样本包括69份前瞻性收集的标本、63份预先选择的样本和829份人工合成标本。该检测法在检测目标真菌病原体时显示出100%的阳性率,在阴性血培养物中显示出0%的阳性率。所有13种测试的瓶/基质类型对6种评估的病原体的检测率均为100%。检测限范围为7.77×10 CFU/mL()至2.83×10 CFU/mL()。该检测法对16种目标菌种中的每一种都检测了5株菌株,显示出良好的包容性。与40株细菌菌株未发生交叉反应。通过序列分析预测与37种非目标真菌中的2种([]和)发生交叉反应。在高浓度的潜在真菌和细菌混杂因素存在的情况下,仍可检测到低浓度的板上真菌。实验室内的重复性为100%,不同地点间的重复性为99.7%。对于前瞻性和预先选择的标本组合,检测到的真菌病原体的敏感性/阳性百分一致性(PPA)为100%,特异性/阴性百分一致性(NPA)为97.6% - 100.0%。前瞻性样本中的常见病原体为(36%)和(25%)。人工合成标本的PPA为100%,NPA≥99.6%。LIAISON PLEX酵母血培养检测法在快速鉴定和区分阳性血培养标本中的真菌病原体方面具有出色的敏感性和特异性。

重要性

血流真菌感染有严重的发病和死亡风险。最佳治疗需要早期鉴定病原体,以便立即开始适当的抗真菌治疗。血培养是确认真菌感染的标准方法,但结果需要几天时间,且可能无法提供详细的病原体信息。LIAISON PLEX酵母血培养检测法可快速分析真菌阳性血培养物,以鉴定16种致病真菌,包括多种是血流感染常见原因的菌种。这项研究在快速鉴定132例已证实培养阳性真菌感染患者的血培养中的感染病原体方面显示出高度的检测准确性和可靠性。在829份人工合成样本中证实了检测性能,这些样本中添加了不同的真菌病原体。

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