Mikita Kei, Tajima Moe, Haque Anwarul, Kato Yasuyuki, Iwata Satoshi, Suzuki Koichi, Hasegawa Naoki, Yano Hisakazu, Matsumoto Tetsuya
Department of Infectious Diseases, Keio University School of Medicine, Tokyo 160-8582, Japan.
Department of Infectious Diseases, Graduate School of Medicine, International University of Health and Welfare, Narita 286-8520, Japan.
Diagnostics (Basel). 2024 May 16;14(10):1027. doi: 10.3390/diagnostics14101027.
Infections by carbapenemase-producing constitute a global public health threat. The rapid and efficient diagnosis of infection is critical for prompt treatment and infection control, especially in hospital settings. We developed a novel loop-mediated isothermal amplification (LAMP) method combined with DNA chromatography to identify five major groups of carbapenemase-producing genes (, , , , and ). This method uses DNA-DNA hybridization-based detection in which LAMP products can be easily visualized as colored lines. No specific technical expertise, expensive equipment, or special facilities are required for this method, allowing its broad application. Here, 73 bacteria collections including strains with carbapenemase-producing genes were tested. Compared to sequencing results, LAMP DNA chromatography for five carbapenemase-producing genes had a sensitivity and specificity of 100% and >97%, respectively. This newly developed method can be a valuable rapid diagnostic test to guide appropriate treatments and infection control measures, especially in resource-limited settings.
产碳青霉烯酶的细菌感染构成了全球公共卫生威胁。对产碳青霉烯酶细菌感染进行快速有效的诊断对于及时治疗和感染控制至关重要,尤其是在医院环境中。我们开发了一种结合DNA色谱法的新型环介导等温扩增(LAMP)方法,以鉴定产碳青霉烯酶基因的五个主要类别(blaKPC、blaNDM、blaOXA-48、blaVIM和blaIMP)。该方法采用基于DNA-DNA杂交的检测,其中LAMP产物可轻松可视化为彩色条带。此方法不需要特定的技术专长、昂贵的设备或特殊设施,因而可广泛应用。在此,对73个细菌样本集进行了检测,其中包括带有产碳青霉烯酶基因的菌株。与测序结果相比,针对五个产碳青霉烯酶基因的LAMP DNA色谱法的灵敏度和特异性分别为100%和>97%。这种新开发的方法可以成为一种有价值的快速诊断测试,以指导适当的治疗和感染控制措施,尤其是在资源有限的环境中。