首页|期刊导航|安徽医科大学学报|采用免疫磁珠捕获念珠菌释放的幽门螺杆菌的研究

采用免疫磁珠捕获念珠菌释放的幽门螺杆菌的研究OA

Study on the capture of Helicobacter pylori released from Candida using immunomagnetic bead

中文摘要英文摘要

目的 探究幽门螺杆菌(H.pylori)特异性基因聚合酶链式反应(PCR)阳性的临床分离的胃念珠菌、阴道念珠菌和大便念珠菌释放H.pylori的能力.方法 复苏实验室从临床分离的4株H.pylori特异性16S rDNA和ureA基因PCR阳性的念珠菌菌株及白念珠菌标准菌株ATCC10231(Ca10231),通过PCR确认5株念珠菌菌株H.pylori ureA基因阳性情况.将上述念珠菌与H.pylori菌株接种于尿素培养基,于37℃恒温培养箱进行培养,逐日观察培养基的颜色变化,若培养基颜色由黄色变为红色,则具有尿素酶活性.使用包被H.pylori抗体的磁珠与上述5株念珠菌菌株及H.pylori菌株分别进行共同孵育,通过生物扫描电子显微镜(SEM)观察磁珠表面H.pylori的吸附情况,采用PCR检测磁珠上H.pylori特异性16S rDNA、ureA基因的阳性情况.结果 通过PCR检测,4株临床来源的念珠菌的ureA基因为阳性,Ca10231的ureA基因为阴性.接种临床来源的4株念珠菌与H.pylori菌株的尿素培养基颜色由黄色变为红色,而接种Ca10231的培养基未变色,表明这4株临床来源的念珠菌菌株具有尿素酶活性,而Ca10231不具有尿素酶活性.通过SEM可观察到,与4株临床来源的念珠菌及H.pylori共同孵育后的磁珠表面都附着有H.pylori,其中与1株阴道念珠菌和1株胃念珠菌及H.pylori共同孵育的磁珠,经PCR检测,H.pylori 16S rDNA、ureA基因均为阳性;与另2株念珠菌共同孵育的磁珠,PCR为阴性.结论 部分H.pylori特异性基因阳性的念珠菌可以释放出H.pylori.

Objective To investigate the ability of clinically isolated,Helicobacter pylori(H.pylori)-specific gene polymerase chain reaction(PCR)-positive gastric,vaginal,and fecal Candida to release H.pylori.Meth-ods Resuscitate 4 strains of H.pylori-specific 16S rDNA and ureA gene PCR-positive Candida strains isolated in laboratory from clinical sources,including 1 strain of gastric Candida,1 strain of fecal Candida,2 strains of vagi-nal Candida and the standard Candida albicans strain ATCC10231(Ca10231).The presence of H.pylori-specific ureA in the 5 strains of Candida isolates was confirmed by PCR.The aforementioned strains of Candida and H.py-lori were inoculated into urea medium and cultured in a constant temperature incubator at 37℃.The color change of the medium was observed daily.A change in the medium's color from yellow to red indicated the presence of ure-ase activity.Then,the five strains of Candida and H.pylori were co-incubated with the magnetic beads coated with H.pylori antibodies respectively.Scanning electron microscopy(SEM)was employed to observe the presence of bacilli adsorbed on the surface of the magnetic beads.PCR was used to detect the presence of H.pylori-specific 16S rDNA and ureA genes on magnetic beads.Results The PCR analysis of the ureA gene in the four Candida iso-lates was positive,whereas the Ca10231 strain tested negative.Upon culturing the four Candida isolates on urea medium,the medium color changed from yellow to red which was determined to be urease positive,while the me-dium containing Ca10231 remained unchanged,which was urease negative.SEM revealed that bacilli could be ob-served on the surface of magnetic beads co-incubated with the 4 strains of Candida of clinical origin and H.pylori isolate.Specifically,PCR testing of the magnetic beads co-incubated with one vaginal Candida,one gastric Can-dida and H.pylori isolate showed positive results for the 16S rDNA and ureA genes of H.pylori;however,the PCR tests for the two genes were negative for the magnetic beads co-incubated with the other two Candida isolate.Con-clusion This study demonstrates that H.pylori-specific genes Candida can release H.pylori.

罗婷婷;孙建超;杨廷秀;许晓丽;崔古贞;罗庆;卓书伟;刘琦;陈峥宏

贵州医科大学附属医院消化内科,贵阳 550004||贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113贵州医科大学附属医院消化内科,贵阳 550004||贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113贵州医科大学附属肿瘤医院检验科,贵阳 550000广东省中医院海南医院临床实验室,海口 570203贵州医科大学附属医院消化内科,贵阳 550004贵州医科大学贵州省微生物组与传染性疾病防控重点实验室,贵州省普通高等学校病原生物学特色重点实验室,贵阳 561113

医药卫生

幽门螺杆菌念珠菌ureA基因免疫磁珠分离法扫描电子显微镜尿素酶

Helicobacter pyloriCandidaureA geneimmunomagnetic separationscanning electron micros-copyurease

《安徽医科大学学报》 2026 (3)

402-408,7

国家自然科学基金项目(编号:82260402)贵州省科技计划项目(编号:黔科合基础-ZK[2022]一般341、黔科合中引地[2025]024、黔科合平台人才-ZDSYS[2023]004)国家科技部及教育部"111计划"项目(编号:D20009) National Natural Science Foundation of China(No.82260402)Scientific and Technological Project of Guizhou Province(Nos.Qiankehe ZK[2022]341,Qiankehe[2025]024,Qiankehe ZDSYS[2023]004)"111 Plan"Project of Ministry of Science and Technology of the People's Republic of China and Ministry of Education of the People's Republic of China(No.D20009)

10.19405/j.cnki.issn1000-1492.2026.03.003

评论