Shen Jing, Deng Da-Jun, Ke Yang, Zhang Jian-Zhong
Peking University School of Oncology and Beijing Institute for Cancer Research, Beijing 100036, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2008 Feb;29(2):166-72.
To investigate the relationship between point mutation of penicillin-binding protein gene (pbp) and amoxicillin resistance (AMOgamma) of Helicobacter pylori (H. pylori) as well as to compare the protein profiles under proteomic technology to get the candidate resistance-related proteins.
(1) AMOgamma strains were selected from the sensitive H. pylori strain 26695 by serial passage technique in vitro. (2) Point mutations of five putative resistance genes (HP0597, HP1565, HP1542, HP1556, and HP0160) were analyzed by denaturing high-performance liquid chromatography (DHPLC) and DNA sequencing. (3) Proteins samples were separated by two-dimensional electrophoresis (2-DE). Protein profiles were compared between the AMOgamma strain obtained in vitro and its sensitive parent strain 26695. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) was performed to identify the proteins of interest. The proteins were searched by software MASCOT and identified by peptide fingerprint map using the program MS-FIT of Protein Prospect.
(1) An AMOgamma strain (MIC 8 microg/ml) was obtained. Complete loss of the resistant phenotype was observed after cultivation in the absence of AMO or storage at - 80 degrees C. (2) DHPLC and Sequencing result showed no point mutations in five pbp genes in the AMOgamma strain when compared with the corresponding PCR products from its parent strain 26695. (3) Protein profiling showed that eleven protein spots were differently expressed between 26695 and the AMOgamma strain. Of these protein spots in the AMOgamma strain, two new spots (Spot 1 and Spot 2) were observed with one (Spot 3) was up-regulated three-fold and the remained ones (Spot 4-11) were down-regulated.
AMO resistance of H. pylori might be resulted from, unstable phenotype change rather than point mutations of pbp genes. These differentially regulated proteins in AMOgamma strain might play a role in development of resistance to AMO in H. pylori.
探讨幽门螺杆菌青霉素结合蛋白基因(pbp)点突变与阿莫西林耐药性(AMOγ)之间的关系,并通过蛋白质组学技术比较蛋白质图谱以获取候选耐药相关蛋白。
(1)通过体外连续传代技术从敏感幽门螺杆菌菌株26695中筛选出AMOγ菌株。(2)采用变性高效液相色谱(DHPLC)和DNA测序分析5个假定耐药基因(HP0597、HP1565、HP1542、HP1556和HP0160)的点突变。(3)蛋白质样品通过二维电泳(2-DE)进行分离。比较体外获得的AMOγ菌株与其敏感亲本菌株26695之间的蛋白质图谱。采用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)鉴定感兴趣的蛋白质。使用MASCOT软件搜索蛋白质,并使用Protein Prospect的MS-FIT程序通过肽指纹图谱进行鉴定。
(1)获得一株AMOγ菌株(MIC 8μg/ml)。在无AMO培养或-80℃保存后,观察到耐药表型完全丧失。(2)与亲本菌株26695的相应PCR产物相比,DHPLC和测序结果显示AMOγ菌株的5个pbp基因无点突变。(3)蛋白质图谱显示,26695与AMOγ菌株之间有11个蛋白质斑点表达不同。在AMOγ菌株的这些蛋白质斑点中,观察到两个新斑点(斑点1和斑点2),其中一个(斑点3)上调了三倍,其余的(斑点4-11)下调。
幽门螺杆菌的AMO耐药性可能是由于不稳定的表型变化而非pbp基因的点突变所致。AMOγ菌株中这些差异调节的蛋白质可能在幽门螺杆菌对AMO的耐药性形成中起作用。