Sozzi M, Crosatti M, Kim S K, Romero J, Blaser M J
Division of Gastroenterology and Digestive Endoscopy, CRO, Via Pedemontana Occidentale 12, 33081 Aviano, Italy.
FEMS Microbiol Lett. 2001 Sep 11;203(1):109-14. doi: 10.1111/j.1574-6968.2001.tb10828.x.
Our aim was to assess whether the Helicobacter pylori population recovered from experimentally infected mice show heterogeneity in cag genotypes. Wild-type FVB/N mice were challenged with strain Hp1 and sacrificed 8 weeks later. Direct PCR on gastric tissue was performed using primers for glmM and cagA, and for these two genes and for cagE and virB11 using DNA from the infecting and the emerging strains. The gastric tissues of two of five mice were PCR+ for glmM but not cagA. For the infecting strain, the PCRs for all four genes studied were strongly positive, but the sweeps from the emerging strains from both mice gave weaker signals for cagA and cagE. Examination of single colonies showed reduced or absent signals for cagA and cagE in relation to glmM and virB11. Serial dilution PCR of sweep isolates from the mice showed a 10- to 100-fold decrease in cagA signal compared to the infecting strain. The decrease of cagA and cagE, but not virB11, amplification and lack of cagA hybridization in Southern blots indicates a selective loss of the right half of the cag island during murine infection. This phenomenon is consistent with host-induced adaptive changes of cag genotype in the population of colonizing H. pylori cells.
我们的目的是评估从实验感染小鼠体内分离出的幽门螺杆菌群体在cag基因型上是否存在异质性。将野生型FVB/N小鼠用Hp1菌株感染,8周后处死。使用针对glmM和cagA的引物对胃组织进行直接PCR,并使用感染菌株和新出现菌株的DNA对这两个基因以及cagE和virB11进行PCR。五只小鼠中有两只的胃组织glmM PCR呈阳性,但cagA PCR呈阴性。对于感染菌株,所研究的所有四个基因的PCR均呈强阳性,但来自这两只小鼠新出现菌株的样本中cagA和cagE的信号较弱。对单个菌落的检测显示,与glmM和virB11相比,cagA和cagE的信号减弱或缺失。对小鼠样本分离株进行系列稀释PCR显示,与感染菌株相比,cagA信号下降了10至100倍。cagA和cagE的扩增减少,但virB11没有减少,并且Southern印迹中缺乏cagA杂交,这表明在小鼠感染期间cag岛右半部分发生了选择性缺失。这种现象与宿主诱导的定殖幽门螺杆菌群体中cag基因型的适应性变化一致。