CAJ | 학술논문

v、牛分枝杆菌和非洲分枝杆菌为阳性,24株非MTB均为阴性;mpt64基因扩增的结果与ELISA法检测结果完全相符.ELISA法检测MTB临床分离株的敏感度为97.3%(110/113),57株非MTB均未检出MPT64蛋白,检测特异度为100.0%.基因扩增MTB中2株为阴性,非MTB均为阴性.结论采用ELISA法检测分泌蛋白MPT64来鉴定MTB复合群,是一种准确、快速和简便的方法,值得临床推广应用.
v、우분지간균화비주분지간균위양성,24주비MTB균위음성;mpt64기인확증적결과여ELISA법검측결과완전상부.ELISA법검측MTB림상분리주적민감도위97.3%(110/113),57주비MTB균미검출MPT64단백,검측특이도위100.0%.기인확증MTB중2주위음성,비MTB균위음성.결론 채용ELISA법검측분비단백MPT64래감정MTB복합군,시일충준학、쾌속화간편적방법,치득림상추엄응용.
non-tuberculosis mycobacterium strains. Conclusion Identification of the Mycobacterium tuberculosis complex by detecting secretory protein MPT64 is rapid, sensitive, and specific, which can be used routinely in clinical laboratories.