Kenji M. Cunnion, E. Stephen Buescher, Pamela S. Hair
{"title":"血清补体因子I降低金黄色葡萄球菌的吞噬作用","authors":"Kenji M. Cunnion, E. Stephen Buescher, Pamela S. Hair","doi":"10.1016/j.lab.2005.07.001","DOIUrl":null,"url":null,"abstract":"<div><p>Complement-mediated opsonization of <em>Staphylococcus aureus</em> is a critical host defense in animal models. Specifically, C3b and CD35 play important roles in effective opsonophagocytosis of <em>S. aureus</em>. We have shown that complement control protein factor I mediates cleavage of the complement opsonin C3b bound to the <em>S. aureus</em> surface. In this study, we examined the physiologic relevance of this observation by determining whether factor I-mediated cleavage of <em>S. aureus</em>-bound C3b decreased phagocytosis of <em>S. aureus</em> by neutrophils. Compared with controls, anti-factor I antibody inhibited C3b-cleavage on the <em>S. aureus</em> surface by >83% (as measured by iC3b generation) and increased phagocytosis of <em>S. aureus</em> by >100%. Treatment of C3b-coated <em>S. aureus</em> with factor I increased generation of iC3b (75%), decreased the total amount of C3-fragments bound to the <em>S. aureus</em> surface (58%), and decreased the number of bacteria phagocytosed (40%). Testing specifically for C3-fragments shed from the <em>S. aureus</em> surface, we found that factor I increased shedding (43%). Notably, these factor I-mediated effects were of the same magnitude regardless of whether factor H, a known cofactor for factor I, was present. These findings indicate that <em>S. aureus</em> benefits from, and possibly manipulates, the normally host-protective activity of factor I cleavage of C3b, which results in bacterial escape from complement-mediated opsonophagocytosis. Because escaping opsonophagocytosis-mediated destruction is a necessary mechanism for bacterial survival resulting in human disease, preventing cleavage of C3b on the <em>S. aureus</em> surface, and thereby enhancing opsonophagocytosis, is a promising potential target for therapeutic intervention.</p></div>","PeriodicalId":16273,"journal":{"name":"Journal of Laboratory and Clinical Medicine","volume":"146 5","pages":"Pages 279-286"},"PeriodicalIF":0.0000,"publicationDate":"2005-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.lab.2005.07.001","citationCount":"22","resultStr":"{\"title\":\"Serum complement factor I decreases Staphylococcus aureus phagocytosis\",\"authors\":\"Kenji M. Cunnion, E. Stephen Buescher, Pamela S. Hair\",\"doi\":\"10.1016/j.lab.2005.07.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Complement-mediated opsonization of <em>Staphylococcus aureus</em> is a critical host defense in animal models. Specifically, C3b and CD35 play important roles in effective opsonophagocytosis of <em>S. aureus</em>. We have shown that complement control protein factor I mediates cleavage of the complement opsonin C3b bound to the <em>S. aureus</em> surface. In this study, we examined the physiologic relevance of this observation by determining whether factor I-mediated cleavage of <em>S. aureus</em>-bound C3b decreased phagocytosis of <em>S. aureus</em> by neutrophils. Compared with controls, anti-factor I antibody inhibited C3b-cleavage on the <em>S. aureus</em> surface by >83% (as measured by iC3b generation) and increased phagocytosis of <em>S. aureus</em> by >100%. Treatment of C3b-coated <em>S. aureus</em> with factor I increased generation of iC3b (75%), decreased the total amount of C3-fragments bound to the <em>S. aureus</em> surface (58%), and decreased the number of bacteria phagocytosed (40%). Testing specifically for C3-fragments shed from the <em>S. aureus</em> surface, we found that factor I increased shedding (43%). Notably, these factor I-mediated effects were of the same magnitude regardless of whether factor H, a known cofactor for factor I, was present. These findings indicate that <em>S. aureus</em> benefits from, and possibly manipulates, the normally host-protective activity of factor I cleavage of C3b, which results in bacterial escape from complement-mediated opsonophagocytosis. Because escaping opsonophagocytosis-mediated destruction is a necessary mechanism for bacterial survival resulting in human disease, preventing cleavage of C3b on the <em>S. aureus</em> surface, and thereby enhancing opsonophagocytosis, is a promising potential target for therapeutic intervention.</p></div>\",\"PeriodicalId\":16273,\"journal\":{\"name\":\"Journal of Laboratory and Clinical Medicine\",\"volume\":\"146 5\",\"pages\":\"Pages 279-286\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.lab.2005.07.001\",\"citationCount\":\"22\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Laboratory and Clinical Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022214305002477\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Laboratory and Clinical Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022214305002477","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Serum complement factor I decreases Staphylococcus aureus phagocytosis
Complement-mediated opsonization of Staphylococcus aureus is a critical host defense in animal models. Specifically, C3b and CD35 play important roles in effective opsonophagocytosis of S. aureus. We have shown that complement control protein factor I mediates cleavage of the complement opsonin C3b bound to the S. aureus surface. In this study, we examined the physiologic relevance of this observation by determining whether factor I-mediated cleavage of S. aureus-bound C3b decreased phagocytosis of S. aureus by neutrophils. Compared with controls, anti-factor I antibody inhibited C3b-cleavage on the S. aureus surface by >83% (as measured by iC3b generation) and increased phagocytosis of S. aureus by >100%. Treatment of C3b-coated S. aureus with factor I increased generation of iC3b (75%), decreased the total amount of C3-fragments bound to the S. aureus surface (58%), and decreased the number of bacteria phagocytosed (40%). Testing specifically for C3-fragments shed from the S. aureus surface, we found that factor I increased shedding (43%). Notably, these factor I-mediated effects were of the same magnitude regardless of whether factor H, a known cofactor for factor I, was present. These findings indicate that S. aureus benefits from, and possibly manipulates, the normally host-protective activity of factor I cleavage of C3b, which results in bacterial escape from complement-mediated opsonophagocytosis. Because escaping opsonophagocytosis-mediated destruction is a necessary mechanism for bacterial survival resulting in human disease, preventing cleavage of C3b on the S. aureus surface, and thereby enhancing opsonophagocytosis, is a promising potential target for therapeutic intervention.