Hartman A B, Ruiz M M, Schultz C L
Department of Biologics Research, Walter Reed Army Institute of Research, Washington, D.C. 20307-5100.
J Clin Microbiol. 1991 Jan;29(1):27-32. doi: 10.1128/jcm.29.1.27-32.1991.
The Salmonella typhi-Shigella sonnei hybrid vaccine strain 5076-IC was constructed to express the S. sonnei form I antigen, which may play an important role in producing protective immunity. Three clonal variants which existed in preparations of the vaccine could be distinguished phenotypically by lactose utilization, S. sonnei form I antigen expression, and restriction enzyme analysis of large plasmid DNA. Since expression of the form I antigen was lost in two of the clonal variants, genetic instability of the 120-MDa vaccine plasmid appeared to be a potential problem. To examine the molecular basis of this genetic instability, we hybridized large plasmid DNA isolated from the clonal variants to a variety of DNA probes encoding virulence-associated antigens and to Escherichia coli lacZ DNA. Results indicated that DNA rearrangement accompanied by deletions of plasmid material occurred in the vaccine plasmid. In addition, the vaccine plasmid did not contain some S. sonnei genetic material encoding antigenic polypeptides necessary for virulence.
构建了伤寒沙门氏菌-宋内志贺氏菌杂交疫苗株5076-IC,以表达宋内志贺氏菌I型抗原,该抗原可能在产生保护性免疫中发挥重要作用。疫苗制剂中存在的三种克隆变体可通过乳糖利用、宋内志贺氏菌I型抗原表达以及大质粒DNA的限制性酶切分析进行表型区分。由于两种克隆变体中I型抗原的表达丧失,120-MDa疫苗质粒的遗传不稳定性似乎是一个潜在问题。为了研究这种遗传不稳定性的分子基础,我们将从克隆变体中分离的大质粒DNA与多种编码毒力相关抗原的DNA探针以及大肠杆菌lacZ DNA进行杂交。结果表明,疫苗质粒中发生了伴随质粒物质缺失的DNA重排。此外,疫苗质粒不包含一些编码毒力所需抗原多肽的宋内志贺氏菌遗传物质。