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拭子混合对用于严重急性呼吸综合征冠状病毒2(SARS-CoV-2)检测的Accula即时检测逆转录聚合酶链反应(RT-PCR)的影响。

Effect of swab pooling on the Accula point-of-care RT-PCR for SARS-CoV-2 detection.

作者信息

Lancelot Moira, Fibben Kirby, Sullivan Julie, O'Sick William, McLendon Kaleb, Wu Huixia, Rao Anuradha, Bassit Leda C, Greenleaf Morgan, Miller Pamela, Krull Wolfgang, Tyburski Erika, Roback John D, Lam Wilbur A, Damhorst Gregory L

机构信息

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, United States.

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, United States.

出版信息

Front Microbiol. 2023 Aug 7;14:1219214. doi: 10.3389/fmicb.2023.1219214. eCollection 2023.

Abstract

INTRODUCTION

Swab pooling may allow for more efficient use of point-of-care assays for SARS-CoV-2 detection in settings where widespread testing is warranted, but the effects of pooling on assay performance are not well described.

METHODS

We tested the Thermo-Fisher Accula rapid point-of-care RT-PCR platform with contrived pooled nasal swab specimens.

RESULTS

We observed a higher limit of detection of 3,750 copies/swab in pooled specimens compared to 2,250 copies/swab in individual specimens. Assay performance appeared worse in a specimen with visible nasal mucous and debris, although performance was improved when using a standard laboratory mechanical pipette compared to the transfer pipette included in the assay kit.

CONCLUSION

Clinicians and public health officials overseeing mass testing efforts must understand limitations and benefits of swab or sample pooling, including reduced assay performance from pooled specimens. We conclude that the Accula RT-PCR platform remains an attractive candidate assay for pooling strategies owing to the superior analytical sensitivity compared to most home use and point-of-care tests despite the inhibitory effects of pooled specimens we characterized.

摘要

引言

在有必要进行广泛检测的情况下,拭子混合检测可能有助于更有效地利用即时检测方法来检测严重急性呼吸综合征冠状病毒2(SARS-CoV-2),但混合检测对检测性能的影响尚未得到充分描述。

方法

我们使用人工合成的混合鼻拭子样本对赛默飞世尔Accula快速即时逆转录聚合酶链反应(RT-PCR)平台进行了测试。

结果

我们观察到,混合样本的检测下限为每拭子3750个拷贝,高于单个样本的每拭子2250个拷贝。在含有可见鼻黏液和碎屑的样本中,检测性能似乎较差,不过与检测试剂盒中包含的移液管相比,使用标准实验室机械移液器时性能有所改善。

结论

监督大规模检测工作的临床医生和公共卫生官员必须了解拭子或样本混合检测的局限性和益处,包括混合样本检测性能的降低。我们得出结论,尽管我们发现混合样本具有抑制作用,但与大多数家用和即时检测相比,Accula RT-PCR平台具有更高的分析灵敏度,因此仍是混合检测策略的一个有吸引力的候选检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19b7/10440424/c317754a12ac/fmicb-14-1219214-g001.jpg

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