Yamaoka Y, Kwon D H, Graham D Y
Department of Medicine, Veterans Affairs Medical Center and Baylor College of Medicine, 2002 Holcombe Boulevard, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7533-8. doi: 10.1073/pnas.130079797.
The complete genome sequence revealed a family of 32 outer membrane proteins (OMPs) in Helicobacter pylori. We examined the effect of four OMPs (HP0638, HP0796, HP1501, and babA2) on the production of the proinflammatory cytokine, IL-8. Mutants of the four OMPs, as well as cagE and galE from H. pylori from the U.S. and Japan, were constructed by inserting a chloramphenicol-resistant cassette into the gene. Twenty-two pairs of parental and mutant H. pylori strains, as well as 160 clinical isolates (80 from Japanese and 80 from U.S.), were cocultured with gastric cancer cell lines. IL-8 production in the supernatant and adhesion was assayed by ELISA. HP0796, HP1501, babA2, and galE gene knockouts had no significant effect on IL-8 production. Knockout of the HP0638 gene in 81% of cag-positive strains reduced IL-8 production approximately 50%. The three cag-positive strains in which IL-8 levels were unchanged by HP0638 knockout had five or seven CT dinucleotide repeats in the 5' region, resulting in a frame shift and truncation. Strains with naturally inactive HP0638 gene were all from the U.S.; Japanese strains were always "on" and thus, on average, may be more virulent. Although cag-negative isolates produced a limited IL-8 response, cag-negative strains that contained a functional HP0638 gene produced more than 3-fold greater IL-8 than cag-negative nonfunctional HP0638 strains. We hypothesize that functional HP0638 gene may be an important virulence factor in relation to the risk of clinically significant outcomes of H. pylori infection. We denote HP0638 gene as outer inflammatory protein (oipA).
完整的基因组序列显示,幽门螺杆菌中有一个由32种外膜蛋白(OMPs)组成的家族。我们研究了四种OMPs(HP0638、HP0796、HP1501和babA2)对促炎细胞因子白细胞介素-8(IL-8)产生的影响。通过将氯霉素抗性盒插入基因中,构建了这四种OMPs以及来自美国和日本的幽门螺杆菌的cagE和galE的突变体。将22对亲本和突变幽门螺杆菌菌株以及160株临床分离株(80株来自日本,80株来自美国)与胃癌细胞系共培养。通过酶联免疫吸附测定法(ELISA)检测上清液中IL-8的产生和黏附情况。HP0796、HP1501、babA2和galE基因敲除对IL-8的产生没有显著影响。在81%的cag阳性菌株中敲除HP0638基因可使IL-8的产生减少约50%。在HP0638基因敲除后IL-8水平未发生变化的三株cag阳性菌株在5'区域有五个或七个CT二核苷酸重复序列,导致移码和截短。天然无活性HP0638基因的菌株均来自美国;日本菌株总是“开启”状态,因此平均而言可能更具毒性。尽管cag阴性分离株产生的IL-8反应有限,但含有功能性HP0638基因的cag阴性菌株产生的IL-8比cag阴性无功能性HP0638菌株多3倍以上。我们推测功能性HP0638基因可能是与幽门螺杆菌感染临床显著结局风险相关的重要毒力因子。我们将HP0638基因命名为外炎症蛋白(oipA)。