Ulloa Daniel, Núñez Constanza, Matamala Romina, San Martín Aníbal, Páez-De Ávila Dayana, Mercado-Vides Jheyson, Narváez Juan, Aguirre Juan, Effer Brian, Iturrieta-González Isabel
Doctoral Program in Sciences, Mention in Applied Cellular and Molecular Biology, Universidad de La Frontera, Francisco Salazar Ave. 01145, Temuco 4811230, Chile.
Biochemistry Program, Universidad de La Frontera, Francisco Salazar Ave. 01145, Temuco 4811230, Chile.
Int J Mol Sci. 2025 Sep 8;26(17):8732. doi: 10.3390/ijms26178732.
Pneumonia caused by poses a serious threat, particularly to immunocompromised patients such as those with HIV/AIDS, transplant recipients, or individuals undergoing chemotherapy. Its diagnosis is challenging because current methods, such as microscopy and certain molecular tests, have limitations in sensitivity and specificity, and require specialized equipment, which delays treatment initiation. In this context, CRISPR-Cas12-based methods offer a promising alternative: they are rapid, highly specific, sensitive, and low-cost, enabling more timely and accessible detection, even in resource-limited settings. We developed a simple and rapid detection platform based on the CRISPR-Cas12 coupled with lateral flow strips. A guide RNA was designed against , , and genes. The guide corresponding to showed high sensitivity in the detection of to produce a detectable fluorescence signal within the first 20-30 min. In addition, it demonstrated high specificity for when DNA from other microorganisms was used. When coupled with lateral flow strips, high sensitivity and specificity were also observed for detecting positive samples, without the need for genetic amplification. CRISPR-Cas12 successfully detected infection in an initial diagnostic application, demonstrating the potential of this method for integration into public health diagnostic systems, particularly in field, due to its adaptability, speed, and ease of use.
由……引起的肺炎构成严重威胁,尤其对免疫功能低下的患者,如感染艾滋病毒/艾滋病的患者、移植受者或正在接受化疗的个体。其诊断具有挑战性,因为当前方法,如显微镜检查和某些分子检测,在灵敏度和特异性方面存在局限性,且需要专门设备,这会延迟治疗的开始。在这种背景下,基于CRISPR-Cas12的方法提供了一种有前景的替代方案:它们快速、高度特异、灵敏且低成本,即使在资源有限的环境中也能实现更及时和便捷的检测。我们开发了一种基于CRISPR-Cas12与侧流条相结合的简单快速检测平台。针对……、……和……基因设计了引导RNA。对应于……的引导RNA在检测……时显示出高灵敏度,能在最初的20 - 30分钟内产生可检测的荧光信号。此外,当使用来自其他微生物的DNA时,它对……表现出高特异性。当与侧流条结合时,在检测阳性样本时也观察到了高灵敏度和特异性,无需基因扩增。CRISPR-Cas12在初始诊断应用中成功检测到……感染,证明了该方法因其适应性、速度和易用性而有潜力整合到公共卫生诊断系统中,尤其是在现场。 (注:原文中部分内容缺失,用省略号代替,以便更完整呈现逻辑)