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华西医学  2012 

幽门螺杆菌NCTC11637株Hp1501基因序列的测定与生物信息学分析

DOI: CNKI:51-1356/R.20120115.1546.013, PP. 58-62

Keywords: 幽门螺杆菌,Hp1501基因,序列测定,生物信息学分析

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Abstract:

目的 幽门螺杆菌NCTC11637菌株Hp1501基因进行序列测定,并运用生物信息学软件对其进行分析。方法 用聚合酶链反应方法从幽门螺杆菌NCTC11637菌株基因组DNA扩增Hp1501基因,T-A克隆,鉴定后测序,将基因序列向GeneBank提交并申请登录号,用生物信息学软件分析其生物学特性。结果 成功获取幽门螺杆菌NCTC11637株Hp1501基因序列,获得GeneBank登录号JF820815。软件分析表明,序列全长为1164bp,与幽门螺杆菌国际标准株26695和J99的基因序列一致性为96%~97%,氨基酸序列一致性为97%~98%;软件预测其编码的前59个氨基酸为信号肽,其编码的核心肽为幽门螺杆菌外膜蛋白。结论 成功测定幽门螺杆菌NCTC11637菌株Hp1501基因序列并预测出其生物学特性,为进一步研究其功能,阐明其致病机制奠定了基础。Objective TodeterminethesequenceofHp1501genefromH.pyloriNCTC11637andanalyzethesequencewithbioinformaticssoftware.Methods Polymerasechainreaction(PCR)wasusedtoamplifytheHp1501genefromchromosomalDNAofH.pyloriNCTC11637.AfterT-Aclone,theamplifiedDNAsequencewasdeterminedandthegenesequencewassenttoGeneBankforanalysiswithbioinformaticssoftware.Results Hp1501genefromH.pyloriNCTC11637wassuccessfullyattained,andtheloggingnumberforGeneBankwasJF820815.Theanalysisshowedthatthegenesequencewas1164bpinlength,96%-97%identicalinDNAsequenceand97%-98%identicalinaminoacidsequencecomparedwithstandardstrain26695andJ99.Theforward59aminoacidsweresignalpeptideandthecorepeptidewasoutermembraneproteinofH.pyloribasedonthesoftwareprediction.Conclusions ThesequenceandbionomicsofHp1501genefromH.pyloriNCTC11637hasbeendeterminedsuccessfully.ItprovidesasolidbaseforthefurtherresearchofthebiologicalfunctionandpathogenicitymechanismofH.pylori.

References

[1]   胡伏莲. 幽门螺杆菌感染相关疾病――幽门螺杆菌感染的流行病学[J]. 中国医刊, 2007, 42(2): 17-18.
[2]   杨小东, 沈朝东, 蒋叙川. 雷贝拉唑与奥美拉唑治疗幽门螺杆菌阳性消化性溃疡的临床比较[J]. 华西医学, 2010, 25(10): 1871-1872.
[3]   邹全明. 幽门螺杆菌疫苗的研究进展[J]. 胃肠病学, 2007, 12(9): 567-570.
[4]   Axsen WS, Styer CM, Solnick JV. Inhibition of heat shock protein expression by Helicobacter pylori[J]. Microb Pathog, 2009, 47(4): 231-236.
[5]   Fujimoto S, Olaniyi Ojo O, Arnqvist A, et al. Helicobacter pylori BabA expression, gastric mucosal injury, and clinical outcome[J]. Clin Gastroenterol Hepatol, 2007, 5(1): 49-58.
[6]   López-Vidal Y, Ponce-de-León S, Castillo-Rojas G, et al. High diversity of vacA and cagA Helicobacter pylori genotypes in patients with and without gastric cancer[J]. PLoS One, 2008, 3(12): e3849.
[7]   Suzuki M, Mimuro H, Kiga K, et al. Helicobacter pylori CagA phosphorylation-independent function in epithelial proliferation and inflammation[J]. Cell Host Microbe, 2009, 22, 5(1): 23-34.
[8]   Alm RA, Bina J, Andrews BM, et al. Comparative genomics of Helicobacter pylori: analysis of the outer membrane protein families[J]. Infect Immun, 2000, 68(7): 4155-4168.
[9]   Yamaoka Y, Ojo O, Fujimoto S, et al. Helicobacter pylori outer membrane proteins and gastroduodenal disease[J]. Gut, 2006, 55(6): 775-781.
[10]   Dossumbekova A, Prinz C, Mages J, et al. Helicobacter pylori HopH (OipA) and bacterial pathogenicity: genetic and functional genomic analysis of hopH gene polymorphisms[J]. J Infect Dis, 2006, 194(10): 1346-1355.
[11]   Zhang XP, Wang WH, Tian Y, et al. Aspirin increases susceptibility of Helicobacter pylori to metronidazole by augmenting endocellular concentrations of antimicrobials[J]. World J Gastroenterol, 2009, 15(8): 919-926.
[12]   葛迪, 郭刚, 毛旭虎, 等. 幽门螺杆菌UreB414-OMP18-LTB融合蛋白的构建及免疫原性初步研究[J]. 第三军医大学学报, 2008, 30(12): 1107-1110.
[13]   黄学勇, 李永红, 段广才, 等. 幽门螺杆菌外膜蛋白基因omp22克隆、表达和鉴定[J]. 广西医科大学学报, 2010, 27(5): 678-680.
[14]   王华, 邵世和. 幽门螺杆菌OipA、HopX、HopW基因的检测及序列分析[J]. 世界华人消化杂志, 2007, 15(35): 3710-3714.
[15]   Peck B, Ortkamp M, Nau U, et al. Characterization of four members of a multigene family encoding outer membrane proteins of Helicobacter pylori and their potential for vaccination[J]. Microbes Infect, 2001, 3(3): 171-179.
[16]   杨宪武,赵逵,张晓博. 根除幽门螺杆菌失败33例相关因素分析[J]. 华西医学. 2010, 25(5): 837-839.
[17]   杨杰, 吕锐, 李丽滨, 等. 铋剂四联方案根除幽门螺杆菌的比较研究[J]. 临床消化病杂志, 2010, 22(5): 277-281.

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