{"title":"幽门螺杆菌溶血磷脂相对含量高介导溃疡疾病的风险增加","authors":"Tone Tannaes , Ida K. Bukholm , Geir Bukholm","doi":"10.1016/j.femsim.2004.10.003","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Helicobacter pylori</span></span><span><span><span> phospholipase A<span><span> (OMPLA) degrades bacterial membrane phospholipids to </span>lysophospholipids. High levels of lysophospholipids are associated with higher </span></span>hemolytic activity, increased release of </span>urease and vacA and better adherence to epithelial cells in vitro. The phospholipase A gene (</span><em>pldA</em><span>) displays phase variation due to a slippage in a homopolymeric tract. The aim of this study was to determine if the relative amount of lysophospholipids in the cell wall is associated with ulcer disease, and to further investigate the significance of </span><em>pldA</em> phase variation. <em>H. pylori</em> isolates of 40 patients were examined. The relative lysophospholipid content of each isolate was determined and the <em>pldA</em> gene was sequenced. The study indicated that <em>H. pylori</em> can regulate its OMPLA activity by phase variation in the <em>pldA</em> gene or by protein level regulation among phase variants in the <em>pldA</em> ‘ON’ status. We found a significant difference between the relative amount of lysophospholipids of the ulcer group and the non-ulcer group (<em>p</em> <!-->=<!--> <!-->0.022). When the lysophospholipid/phospholipid ratios were compared with outcome, the OR for ulcer disease was 9.0 (95% CI 1.6–49.4; <em>p</em> <!-->=<!--> <!-->0.014). Isolates with a high OMPLA activity are significantly associated with patients with ulcer disease.</p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":"44 1","pages":"Pages 17-23"},"PeriodicalIF":0.0000,"publicationDate":"2005-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2004.10.003","citationCount":"36","resultStr":"{\"title\":\"High relative content of lysophospholipids of Helicobacter pylori mediates increased risk for ulcer disease\",\"authors\":\"Tone Tannaes , Ida K. Bukholm , Geir Bukholm\",\"doi\":\"10.1016/j.femsim.2004.10.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Helicobacter pylori</span></span><span><span><span> phospholipase A<span><span> (OMPLA) degrades bacterial membrane phospholipids to </span>lysophospholipids. High levels of lysophospholipids are associated with higher </span></span>hemolytic activity, increased release of </span>urease and vacA and better adherence to epithelial cells in vitro. The phospholipase A gene (</span><em>pldA</em><span>) displays phase variation due to a slippage in a homopolymeric tract. The aim of this study was to determine if the relative amount of lysophospholipids in the cell wall is associated with ulcer disease, and to further investigate the significance of </span><em>pldA</em> phase variation. <em>H. pylori</em> isolates of 40 patients were examined. The relative lysophospholipid content of each isolate was determined and the <em>pldA</em> gene was sequenced. The study indicated that <em>H. pylori</em> can regulate its OMPLA activity by phase variation in the <em>pldA</em> gene or by protein level regulation among phase variants in the <em>pldA</em> ‘ON’ status. We found a significant difference between the relative amount of lysophospholipids of the ulcer group and the non-ulcer group (<em>p</em> <!-->=<!--> <!-->0.022). When the lysophospholipid/phospholipid ratios were compared with outcome, the OR for ulcer disease was 9.0 (95% CI 1.6–49.4; <em>p</em> <!-->=<!--> <!-->0.014). Isolates with a high OMPLA activity are significantly associated with patients with ulcer disease.</p></div>\",\"PeriodicalId\":12220,\"journal\":{\"name\":\"FEMS immunology and medical microbiology\",\"volume\":\"44 1\",\"pages\":\"Pages 17-23\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.femsim.2004.10.003\",\"citationCount\":\"36\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FEMS immunology and medical microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0928824404002147\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS immunology and medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928824404002147","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 36
摘要
幽门螺杆菌磷脂酶A (OMPLA)将细菌膜磷脂降解为溶血磷脂。在体外,高水平的溶血磷脂与更高的溶血活性、脲酶和vacA释放增加以及更好地粘附上皮细胞有关。磷脂酶A基因(pldA)由于在同聚体通道中的滑移而显示相位变化。本研究的目的是确定细胞壁中溶血磷脂的相对含量是否与溃疡疾病有关,并进一步探讨pldA期变化的意义。对40例患者的幽门螺杆菌进行了检测。测定各分离物的相对溶血磷脂含量,并对pldA基因进行测序。研究表明,幽门螺杆菌可以通过pldA基因的期变或pldA“ON”状态期变之间的蛋白水平调控其OMPLA活性。我们发现溃疡组和非溃疡组溶血磷脂的相对量有显著差异(p = 0.022)。当溶血磷脂/磷脂比率与结果进行比较时,溃疡疾病的OR为9.0 (95% CI 1.6-49.4;p = 0.014)。具有高OMPLA活性的分离株与溃疡疾病患者显著相关。
High relative content of lysophospholipids of Helicobacter pylori mediates increased risk for ulcer disease
Helicobacter pylori phospholipase A (OMPLA) degrades bacterial membrane phospholipids to lysophospholipids. High levels of lysophospholipids are associated with higher hemolytic activity, increased release of urease and vacA and better adherence to epithelial cells in vitro. The phospholipase A gene (pldA) displays phase variation due to a slippage in a homopolymeric tract. The aim of this study was to determine if the relative amount of lysophospholipids in the cell wall is associated with ulcer disease, and to further investigate the significance of pldA phase variation. H. pylori isolates of 40 patients were examined. The relative lysophospholipid content of each isolate was determined and the pldA gene was sequenced. The study indicated that H. pylori can regulate its OMPLA activity by phase variation in the pldA gene or by protein level regulation among phase variants in the pldA ‘ON’ status. We found a significant difference between the relative amount of lysophospholipids of the ulcer group and the non-ulcer group (p = 0.022). When the lysophospholipid/phospholipid ratios were compared with outcome, the OR for ulcer disease was 9.0 (95% CI 1.6–49.4; p = 0.014). Isolates with a high OMPLA activity are significantly associated with patients with ulcer disease.