García-Sorribes Soraya, Lara-Hernández Francisco, Manzano-Blasco Iris, Abadía-Otero Jessica, Albert Eliseo, Mulet Alba, Briongos-Figuero Laisa Socorro, Gabella-Martín Miriam, Torres Ignacio, Signes-Costa Jaime, Navarro David, Martín-Escudero Juan-Carlos, García-García Ana-Bárbara, Chaves Felipe Javier
Genomic and Diabetes Unit, INCLIVA Biomedical Research Institute, 46010 Valencia, Spain.
Internal Medicine Service, Rio Hortega University Hospital, 47012 Valladolid, Spain.
Biology (Basel). 2023 Jun 23;12(7):900. doi: 10.3390/biology12070900.
The SARS-CoV-2 coronavirus is responsible for the COVID-19 pandemic resulting in a global health emergency. Given its rapid spread and high number of infected individuals, a diagnostic tool for a rapid, simple, and cost-effective detection was essential. In this work, we developed a COVID-19 diagnostic test, that incorporates a human internal control, based on the Reverse Transcription Loop-Mediated Isothermal Amplification (RT-LAMP). When working with synthetic SARS-CoV-2 RNA, the optimized RT-LAMP assay has a sensitivity of 10 viral copies and can be detected by fluorescence in less than 15 min or by the naked eye in 25 min using colorimetric RT-LAMP. To avoid the RNA extraction step, a pre-treatment of the sample was optimized. Subsequently, a validation was performed on 268 trypsin treated samples (including nasopharyngeal, buccal, and nasal exudates) and amplified with colorimetric RT-LAMP to evaluate its sensitivity and specificity in comparison with RT-qPCR of extracted samples. The validation results showed a sensitivity and specificity of 100% for samples with Ct ≤ 30. The rapid, simple, and inexpensive RT-LAMP SARS-CoV-2 extraction-free procedure developed may be an alternative test that could be applied for the detection of SARS-CoV-2 or adapted to detect other viruses present in saliva or nasopharyngeal samples with higher sensitivity and specificity of the antibody test.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发了新冠疫情,导致全球卫生紧急状况。鉴于其传播迅速且感染人数众多,一种快速、简便且经济高效的诊断工具至关重要。在这项工作中,我们开发了一种基于逆转录环介导等温扩增(RT-LAMP)的新冠诊断测试,该测试纳入了人类内部对照。使用合成的SARS-CoV-2 RNA时,优化后的RT-LAMP检测法灵敏度为10个病毒拷贝,采用荧光法可在不到15分钟内检测到,采用比色RT-LAMP法则可在25分钟内肉眼检测到。为避免RNA提取步骤,对样品预处理进行了优化。随后,对268份经胰蛋白酶处理的样品(包括鼻咽、颊部和鼻腔分泌物)进行了验证,并采用比色RT-LAMP进行扩增,以评估其与提取样品的RT-qPCR相比的灵敏度和特异性。验证结果显示,对于Ct值≤30的样品,灵敏度和特异性均为100%。所开发的快速、简便且廉价的无需提取SARS-CoV-2的RT-LAMP程序可能是一种替代检测方法,可用于检测SARS-CoV-2,或经调整后以更高的抗体检测灵敏度和特异性检测唾液或鼻咽样品中存在的其他病毒。