Henriksen A Z, Maeland J A
Department of Microbiology, Faculty of Medicine, University of Trondheim, Norway.
J Clin Microbiol. 1987 Nov;25(11):2181-8. doi: 10.1128/jcm.25.11.2181-2188.1987.
Antibodies to Escherichia coli outer membrane proteins in sera from healthy persons and from patients bacteremic with various enteric or nonenteric bacteria were measured by an enzyme-linked immunosorbent assay (ELISA). Outer membranes were prepared from E. coli O55. Serum was absorbed with E. coli O55 lipopolysaccharide and diluted 1:100 for immunoglobulin A (IgA) or IgM and 1:1,000 for IgG antibodies. Paired serum specimens were obtained from the 56 patients included in the study (the first specimen on the day of positive blood culture and the second specimen 8 to 12 days later) and compared with sera from blood donors (n = 50) as controls. On an average, the patients bacteremic with enterobacteria (n = 40) showed increased levels of antibodies of all three immunoglobulin classes in the first serum specimens and significantly higher levels in the second specimens compared with the controls, although with considerable case-to-case variation. Increased levels of IgG antibodies showed the best combination of diagnostic specificity (100%) and sensitivity (53%) for bacteremia caused by enteric bacilli. Mostly, the antibody response was directed against the major E. coli O55 outer membrane proteins at 81,000, 38,500, 33,500, and 7,500 molecular weights as shown by Western blot (immunoblot) analysis. Some of the patients bacteremic with nonenteric bacteria showed increased levels of IgA antibodies, but not of IgG or IgM antibodies. Cross-reactivity of the nonenteric blood culture isolates with the E. coli outer membrane preparation was not demonstrated. The cross-reactivity of the E. coli O55 outer membrane proteins with those of enteric bacilli of other genera was examined by absorption experiments. Western blots with serum absorbed with live E. coli O55 provided evidence that the epitopes of the outer membrane protein at 7,500 molecular weight were available for antibody binding at the bacterial surface, and that at least some of the epitopes of the 38,500- and 33,500-molecular -weight proteins were accessible to antibodies. The results suggest that an ELISA for the measurement of antibodies against cross-reactive outer membrane proteins from enteric bacilli may be useful in the diagnosis of serious infections caused by members of the family Enterobacteriaceae, and that antibodies to the major outer membrane proteins may have an immunobiological function.
采用酶联免疫吸附测定法(ELISA)检测健康人以及患有各种肠道或非肠道细菌血症患者血清中针对大肠杆菌外膜蛋白的抗体。大肠杆菌O55外膜制备物用于检测。血清用大肠杆菌O55脂多糖吸收,免疫球蛋白A(IgA)或IgM抗体检测时稀释1:100,IgG抗体检测时稀释1:1000。从纳入研究的56例患者中获取配对血清标本(第一份标本在血培养阳性当天采集,第二份标本在8至12天后采集),并与作为对照的献血者血清(n = 50)进行比较。平均而言,患有肠杆菌血症的患者(n = 40)在第一份血清标本中显示所有三种免疫球蛋白类别的抗体水平升高,与对照组相比,第二份标本中的抗体水平显著更高,尽管病例之间存在相当大的差异。IgG抗体水平升高对肠道杆菌引起的菌血症显示出最佳的诊断特异性(100%)和敏感性(53%)组合。如蛋白质印迹(免疫印迹)分析所示,大多数抗体反应针对分子量为81,000、38,500、33,500和7,500的主要大肠杆菌O55外膜蛋白。一些患有非肠道细菌血症的患者显示IgA抗体水平升高,但IgG或IgM抗体水平未升高。未证实非肠道血培养分离株与大肠杆菌外膜制备物存在交叉反应性。通过吸收实验检测了大肠杆菌O55外膜蛋白与其他属肠道杆菌外膜蛋白的交叉反应性。用活的大肠杆菌O55吸收血清进行蛋白质印迹分析表明,分子量为7,500的外膜蛋白表位可用于在细菌表面结合抗体,并且分子量为38,500和33,500的蛋白的至少一些表位可被抗体识别。结果表明,用于检测针对肠道杆菌交叉反应性外膜蛋白抗体的ELISA可能有助于诊断由肠杆菌科成员引起的严重感染,并且主要外膜蛋白的抗体可能具有免疫生物学功能。