Yan Linlin, Tang Chong, Cai Yu, Nong Jinqing, Zhang Ke, Zhu Linlin, Wang Pengfei, Wu Lei, Zhao Fan, Hu Shoukui
Department of Clinical Laboratory, Peking University Shougang Hospital, Beijing, 100144, China.
Department of Orthopaedic Surgery, Peking University Shougang Hospital, Beijing, 100144, China.
Anal Biochem. 2022 Oct 1;654:114740. doi: 10.1016/j.ab.2022.114740. Epub 2022 May 24.
Meningococcal disease caused by Neisseria meningitidis remains a major global public health concern. Serogroup A, B, C and W135 were the major disease-causing serogroups. It is vital to timely and efficiently detect and differentiate these four serogroups. Herein, we developed multiple cross displacement amplification-lateral flow biosensor (MCDA-LFB) assays targeting ctrA, sacB, siaD, siaD and synG gene respectively for detection and subtyping of four N. meningitidis serogroups. This assay utilizes LFB to detect FITC and biotin-labeled target amplicons produced by MCDA through double antibody sandwich principle, to allow sensitive and specific detection under a constant temperature. The detection limit was as low as 10 fg or 100 fg genomic DNA in pure cultures and 5.5 CFUs or 36 CFUs in spiked cerebrospinal fluid (CSF) specimens, which were overall 100 to 1000-fold more sensitive than conventional PCR. High specificity of these assays was also validated through type strains and clinical isolates, with no cross-reactions. MCDA-LFB testing procedure can be finished within 1 h. In conclusion, the N. meningitidis- and serogroup-MCDA-LFB assays established in this study are simple, rapid and efficient, providing valuable molecular methods for diagnosis and surveillance of meningococcal disease, especially in resource-limited regions and when specimen culture fails.
由脑膜炎奈瑟菌引起的脑膜炎球菌病仍然是全球主要的公共卫生问题。A、B、C和W135血清群是主要的致病血清群。及时、高效地检测和区分这四个血清群至关重要。在此,我们分别针对ctrA、sacB、siaD、siaD和synG基因开发了多重交叉置换扩增-侧向流动生物传感器(MCDA-LFB)检测方法,用于检测和分型四种脑膜炎奈瑟菌血清群。该检测方法利用LFB通过双抗体夹心原理检测MCDA产生的异硫氰酸荧光素(FITC)和生物素标记的目标扩增子,以便在恒温下进行灵敏且特异的检测。在纯培养物中,检测限低至10 fg或100 fg基因组DNA,在加标的脑脊液(CSF)标本中为5.5 CFU或36 CFU,总体比传统PCR灵敏100至1000倍。这些检测方法的高特异性也通过标准菌株和临床分离株得到验证,无交叉反应。MCDA-LFB检测程序可在1小时内完成。总之,本研究建立的脑膜炎奈瑟菌和血清群MCDA-LFB检测方法简单、快速且高效,为脑膜炎球菌病的诊断和监测提供了有价值的分子方法,特别是在资源有限的地区以及标本培养失败时。