Whang H Y, Mayer H, Schmidt G, Neter E
Infect Immun. 1972 Oct;6(4):533-9. doi: 10.1128/iai.6.4.533-539.1972.
Enterobacteriaceae share a common antigen (CA). This antigen exists as a powerful immunogen, when produced by Escherichia coli O14, and as a minimally effective immunogen, when present in cultures of most other smooth strains. The present study was directed toward the assessment of immunogenicity of this antigen produced by various rough mutants and their parent strains as well as that of viable and nonviable bacterial suspensions. Rabbits were immunized intravenously, and the passive hemagglutination test was used for the quantitation of CA antibodies. The following results were obtained. (i) Immunization of rabbits with viable or heat-killed (1 hr, 100 C) suspensions of smooth parent strains resulted in only slight or insignificant antibody production. Of seven additional smooth strains of Enterobacteriaceae tested, none induced CA antibodies upon immunization with killed (1 hr, 100 C) suspensions, and only two engendered antibodies in moderate titers when viable suspensions were used, possibly due to the presence of undetected R mutant cells. (ii) In contrast, administration of viable suspensions of the corresponding mutant strains, regardless of core types, including E. coli R1, R2, R3, and Salmonella Ra types, caused a significant antibody response. (iii) The immunogenicity of R mutants differed strikingly, inasmuch as mutants with the R1 core [E. coli O8(-):K27(-)(R) and Shigella boydii type 3(-)(R)] engendered CA antibodies when heated suspensions were administered, in contrast to heated suspensions of mutants with the R2, R3, and Ra cores. (iv) Viability per se is not an abolute requirement for immunogenicity of R2 mutants, since CA antibodies were engendered by suspensions killed at 60 C or by merthiolate or formaldehyde. (v) Ethanol fractionation revealed that immunogenic CA of the R1 mutant is ethanol-insoluble and that of the parental smooth strain is ethanol-soluble; thus, CA of R1 mutants resembles that of E. coli O14 in both immunogenicity and ethanol insolubility.
肠杆菌科细菌有共同抗原(CA)。当由大肠杆菌O14产生时,这种抗原作为一种强大的免疫原存在;而当存在于大多数其他光滑菌株的培养物中时,它作为一种效果甚微的免疫原存在。本研究旨在评估各种粗糙突变体及其亲本菌株产生的这种抗原以及活细菌悬液和非活细菌悬液的免疫原性。给兔子静脉注射免疫,并用被动血凝试验定量CA抗体。得到了以下结果。(i)用光滑亲本菌株的活悬液或热灭活(1小时,100℃)悬液免疫兔子,仅产生轻微或不显著的抗体。在另外测试的7种肠杆菌科光滑菌株中,用灭活(1小时,100℃)悬液免疫时,没有一种诱导产生CA抗体,当使用活悬液时,只有两种产生了中等滴度的抗体,这可能是由于存在未检测到的R突变细胞。(ii)相反,给予相应突变菌株的活悬液,无论其核心类型如何,包括大肠杆菌R1、R2、R3和沙门氏菌Ra型,都会引起显著的抗体反应。(iii)R突变体的免疫原性差异显著,因为具有R1核心的突变体[大肠杆菌O8(-):K27(-)(R)和鲍氏志贺菌3型(-)(R)]在给予加热悬液时会产生CA抗体,这与具有R2、R3和Ra核心的突变体的加热悬液形成对比。(iv)活力本身并非R2突变体免疫原性的绝对必要条件,因为在60℃下杀死的悬液或硫柳汞或甲醛处理的悬液会产生CA抗体。(v)乙醇分级分离显示,R1突变体的免疫原性CA不溶于乙醇,而亲本光滑菌株的则溶于乙醇;因此,R1突变体的CA在免疫原性和乙醇不溶性方面都与大肠杆菌O14的相似。