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开发一种简单且高度灵敏的病毒粒子浓缩方法以检测唾液中的新型冠状病毒 2 型。

Development of a simple and highly sensitive virion concentration method to detect SARS-CoV-2 in saliva.

作者信息

Yamazaki Yasuko, Alonso Uxía Alonso, Galay Remil L, Yamazaki Wataru

机构信息

Center for Southeast Asian Studies, Kyoto University, 46 Shimoadachi-cho, Yoshida, Sakyo-ku, Kyoto, 606-8501, Japan.

Animal Medicine and Health at Institut de Recerca i Tecnologia Agroalimentàries (IRTA) - Centre de Recerca en Sanitat Animal (CReSA), Spain.

出版信息

Heliyon. 2024 Jun 15;10(12):e33168. doi: 10.1016/j.heliyon.2024.e33168. eCollection 2024 Jun 30.

Abstract

BACKGROUND

Controlling novel coronavirus pandemic infection (COVID-19) is a global challenge, and highly sensitive testing is essential for effective control. The saliva is a promising sample for high-sensitivity testing because it is easier to collect than nasopharyngeal swab samples and allows large-volume testing.

RESULTS

We developed a simple SARS-CoV-2 concentration method from saliva samples that can be completed in less than 60 min. We performed a spike test using 12 ml of saliva samples obtained from healthy volunteer people, and the developed method performance was evaluated by comparison using a combination of automatic nucleic acid extraction followed by RT-qPCR detection. In saliva spike tests using a 10-fold dilution series of SARS-CoV-2, the developed method was consistently 100-fold more sensitive than the conventional method.

CONCLUSIONS

The developed method can improve the analytical sensitivity of the SARS-CoV-2 test using saliva and speed up and save labor in screening tests by pooling many samples. Furthermore, the developed method has the potential to contribute to the highly sensitive detection of various human and animal viral pathogens from the saliva and various clinical samples.

摘要

背景

控制新型冠状病毒大流行感染(COVID-19)是一项全球挑战,高灵敏度检测对于有效控制至关重要。唾液是高灵敏度检测的一种有前景的样本,因为它比鼻咽拭子样本更容易采集,并且允许进行大容量检测。

结果

我们开发了一种从唾液样本中简单的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)浓缩方法,该方法可在不到60分钟内完成。我们使用从健康志愿者获得的12毫升唾液样本进行了加标测试,并通过结合自动核酸提取后进行逆转录定量聚合酶链反应(RT-qPCR)检测的比较来评估所开发方法的性能。在使用SARS-CoV-2 10倍稀释系列的唾液加标测试中,所开发的方法始终比传统方法灵敏100倍。

结论

所开发的方法可以提高使用唾液进行SARS-CoV-2检测的分析灵敏度,并通过合并许多样本在筛查测试中加快速度并节省劳动力。此外,所开发的方法有可能有助于从唾液和各种临床样本中高度灵敏地检测各种人类和动物病毒病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/144a/11238118/606d22a22d65/gr1.jpg

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