Pinchon Elena, Henry Steven, Leon Fanny, Fournier-Wirth Chantal, Foulongne Vincent, Cantaloube Jean-François
Pathogénèse et Contrôle des Infections Chroniques et Emergentes, Etablissement Français du Sang, Université de Montpellier, Inserm, 34184 Montpellier, France.
Diagnostics (Basel). 2024 Feb 29;14(5):517. doi: 10.3390/diagnostics14050517.
The measles virus is highly contagious, and efforts to simplify its diagnosis are essential. A reverse transcriptase/recombinase polymerase amplification assay coupled with CRISPR/Cas12a and an immunochromatographic lateral flow detection (RT-RPA-CRISPR-LFD) was developed for the simple visual detection of measles virus. The assay was performed in less than 1 h at an optimal temperature of 42 °C. The detection limit of the assay was 31 copies of an RNA standard in the reaction tube. The diagnostic performances were evaluated on a panel of 27 measles virus RT-PCR-positive samples alongside 29 measles virus negative saliva samples. The sensitivity and specificity were 96% (95% CI, 81-99%) and 100% (95% CI, 88-100%), respectively, corresponding to an accuracy of 98% (95% CI, 94-100%; < 0.0001). This method will open new perspectives in the development of the point-of-care testing diagnosis of measles.
麻疹病毒具有高度传染性,因此简化其诊断方法至关重要。我们开发了一种逆转录酶/重组酶聚合酶扩增检测法,并结合CRISPR/Cas12a和免疫层析侧向流动检测(RT-RPA-CRISPR-LFD),用于简单直观地检测麻疹病毒。该检测在42℃的最佳温度下不到1小时即可完成。该检测方法在反应管中的RNA标准检测限为31个拷贝。在27份麻疹病毒RT-PCR阳性样本和29份麻疹病毒阴性唾液样本中评估了该诊断方法的性能。敏感性和特异性分别为96%(95%CI,81-99%)和100%(95%CI,88-100%),相应的准确率为98%(95%CI,94-100%;<0.0001)。该方法将为麻疹即时检测诊断的发展开辟新的前景。