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[Pathogenicity of hp jhp947 gene to C57BL/6 mice] Wei sheng wu xue bao = Acta microbiologica Sinica [Wei Sheng Wu Xue Bao] Journal article

 
Title[Pathogenicity of hp jhp947 gene to C57BL/6 mice]
Author(s)Sun G, She F, Li N, Chen H 
InstitutionResearch Center of Microbiology, Fujian Medical University, Fuzhou 350004, China. sungeqing@yahoo.com.cn
SourceWei Sheng Wu Xue Bao 2009 Aug 4; 49(8):1109-14.
AbstractOBJECTIVE: To study the effects of Helicobacter pylori jhp947 gene on the pathogenesis of epithelial cells and gene express pattern by animal studies.
METHODS: Twenty-seven special pathogen free (SPF) C57BL/6 mice were divided equally into 3 groups, and challenged with Helicobacter pylori J99, Helicobacter pylori deltaJ99-947 and phosphate buffer (PBS) respectively, at a dose of 10(9) colony formine unit (CFU) at 0, 2, and 4 days. Mice were sacrificed 4 weeks after the last challenge, and went through rapid urease test, culture of Hp, histological examination, immunofluorescent histochemistry and semiquantitative reverse transcription PCR (RT-PCR) of gastric mucosa.
RESULTS: The result of rapid urease test and culture of Hp indicated that the positive rates in J99 and deltaJ99-947 group were both 100% while 0% in PBS group. The result of histology examination indicated that garstric mucosa is all normal in PBS group; in J99 group, 33.3% (3/9) had slightly anabrosis, 66.7% (6/9) had seriously anabrosis; in deltaJ99-947 group, 22.2% (2/9) is normal, 77.8% (7/9) had slightly anabrosis. The degree of anabrosis seems to be more severe in J99 than in deltaJ99-947. The result of immunofluorescent histochemistry and semiquantitative RT-PCR of gastric mucosa indicated that the expression level of ets homologous factor, N-myc downstream regulated gene 1, methylthioadenosine phosphorylase is significantly lower in J99 than in deltaJ99-947 group (P < 0.05).
CONCLUSION: The degree of anabrosis seems to be more severe in Hp with jhp947 gene than in Hp without jhp947 gene. In vivo, jhp947 may induce tumorigenesis by inhibiting anti-oncogenes (N-myc downstream regulated gene 1 and methylthioadenosine phosphorylase).
Languagechi
Pub Type(s)English Abstract
Journal Article
Research Support, Non-U.S. Gov't
PubMed ID19835175
  
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