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中国生物工程杂志

China Biotechnology
China Biotechnology  2013, Vol. 33 Issue (4): 92-100    DOI:
    
Detection of Individualized Treatment and Test of Helicobacter pylori Infection through Visualized Gene Chip Technology
YAO Xue1, LIU Qi-qi2, ZHAO Qing1, CHEN Su-hong2
1. Guangzhou Medical College, Guangzhou 510182, China;
2. Beijing Institute of Radiation Medicine, Beijing 100038, China
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Abstract  Objective: To establish a method of visualized gene chip detection that can simultaneously measure the gene polymorphism of CYP2C19 that is related to clarithromycin and quinolones resistance mutation in Helicobacter pylori infection and to the metabolism of proton pump inhibitor. Method: Through analysis the sequence of human CYP2C19*2, CYP2C19*3 and the targets related to resistance to clarithromycin and quinolone, a gene chip to test the resistence of Helicobacter Pylori was established. The specificity, sensitivity and repeatability of the gene chip was evaluated in the optimized PCR system, with hybridization reaction and visualized detection. Result: The results of detection of 196 clinical samples using gene chips were consistent with that by sequencing. The detection sensitivity of the chip for Hp was 103CFU/ml, and that for human genomic DNA was 2ng/μl.Conclusion: This method was quick, highly specific, sensitive, and economic. With its clinical application potential, it is promising in providing medication guidance for Hp elimination in clinical use and individualized treatment.

Key wordsDrug resistance of Helicobacter pylori      Gene polymorphism of CYP2C19      Individualized treatment      Gene chip      Visual detection method     
Received: 07 January 2013      Published: 25 April 2013
ZTFLH:  Q819  
Cite this article:

YAO Xue, LIU Qi-qi, ZHAO Qing, CHEN Su-hong. Detection of Individualized Treatment and Test of Helicobacter pylori Infection through Visualized Gene Chip Technology. China Biotechnology, 2013, 33(4): 92-100.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2013/V33/I4/92

[1] 张万岱,姚永莉. 幽门螺杆菌的研究现状与展望.医学与哲学(临床决策论坛版),2007,06(28):8-16. Zhang W D, Yao Y L. The progress of Helicobacter pylori infection. Medicine & Philosophy (Clinical Decision Making Forum Edition),2007,06(28):8-16.
[2] 刘国栋,张建中.幽门螺杆菌致病因子研究进展.现代消化及介入诊疗,2010,01(15):33-38. Liu G D, Zhang J Z. The progress of Helicobacter pylori virulence factor.Modern Digestion & Intervention, 2010,01(15):33-38.
[3] 赵媛,吴康智.胃粘膜相关淋巴组织淋巴瘤研究进展.青海医学院学报,2004,2(25):142-144. Zhao Y,Wu K Z. Gastric mucosa-associated lymphoid tissue lymphoma research progress. Journal of Qinghai Medical College, 2004,2(25):142-144.
[4] 欧阳颖. 幽门螺杆菌相关性溃疡的发病原因及治疗进展. 新疆医科大学学报,2005,28(5):487-489. OuYang Y. The causes of Helicobacter pylori-related ulcers and the treatment progress. Journal of Xinjiang Medical University,2005,28(5):487-489.
[5] Shaohua Chen, Youming Li, Chaohui Yu. Oligonucleotide microarray: A new rapid method for screening the 23S rRNA gene of Helicobacter pylori for single nucleotide polymorphisms associated with clarithromycin resistance. Journal of Gastroenterology and Hepatology,2008,23: 126-131.
[6] Baik S C, Kim K M, Song S M, et al. Proteomic analysis of the sarcosineinsoluble outer membrane fraction of Helicobacter pylori strain 26695. J Bacteriol,2004,186(4):949-955.
[7] Tiwari S K, Khan A A, Manoj G,et al. A simple multiplex PCR assay for diagnosing virulent Helicobacter pylori infection in human gastric biopsy specimens from subjects with gastric carcinoma and other gasto-duodenal diseases.J Appe Microboe,2007,103 (6):2353-2360.
[8] Taylor D E, Ge Z, Purych D, et al. Cloning and sequence analysis of two copies of a 23S rRNA gene from Helicobacter pylori and association of clarithromycin resistance with 23S rRNA mutations. Antimicrob Agents Chemother,1997,41(12):2621-2628.
[9] 喻海忠,许国莹.幽门螺杆菌耐药的分子机理研究进展.右江民族医学院学报,2007,1:113-115. Yu H Z, Xu G Y. Molecular mechanisms of Helicobacter pylori resistant.Journal of Youjiang Medical College, 2007,1:113-115.
[10] 周学琴,段丽芳.CYP2C19基因多态性对奥美拉唑临床疗效的研究进展.中国药物应用与监测,2010,1(7):55-57. Zhou X Q, Duan L F. Advance of CYP2C19 polymorphism on clinical efficacy of omeprazole. Chinese Journal of Drug Application and Monitoring,2010,1(7):55-57.
[11] de Jonge R, Durrani Z, Rijpkema S G, et al. Role of the Helicobacter pylori orter-membrane proteins AlpA and AlpB in colonization of the guinea pig stomach. J Med Microbiol,2004,53(Pt5):375-379.
[12] Snelling W J, Moran A P, Ryan K A, et al. HorB(HP0127) is a gastric epithelial cell adhesion. Helicobacter,2007,12(3):200-209.
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