Buysse J M, Hartman A B, Strockbine N, Venkatesan M
Department of Bacterial Immunology, Walter Reed Army Medical Center, Washington, D.C., 20307-5100, USA.
Microb Pathog. 1995 Nov;19(5):335-49. doi: 10.1016/s0882-4010(96)80005-2.
The ipaH loci comprise a multicopy antigen gene family unique to Shigella species and enteroinvasive Escherichia coli (EIEC). DNA probes derived from the Shigella flexneri serotype 5 ipaH7.8 gene were used to compare the molecular arrangement of ipaH alleles in a variety of Shigella and EIEC strains. Multiple copies of ipaH-homologous sequences were detected in all invasion plasmids examined. Oligonucleotide probes covering discrete 24 bp segments of the ipaH7.8 gene and sequences flanking the ipaH4.5 (probe H25) and ipaH2.5 (probe H24) loci were used to define the extent of homology among invasion plasmid copies of ipaH in S. flexneri serotypes 1, 2 and 5 and in S. sonnei. IpaH alleles carried by these invasion plasmids were not structurally equivalent and showed sequence divergence at their amino- and carboxy-terminal ends. The H25 probe was shown to correspond to an IS629 sequence genetically linked to the ipaH alleles, while the H24 probe defined a DNA sequence found only in Shigella invasion plasmids. Chromosomal DNA from invasion plasmid-cured S. flexneri and S. sonnei strains hybridized a core ipaH7.8 gene segment, indicating that portions of the ipaH7.8 structural gene were reiterated and contained within the shigellae chromosomes. Based on the specificity of the ipaH7.8 core probe and the detection of ipaH sequences on the invasion plasmids and chromosomes of Shigella strains, three polymorphic groups within a collection of forty S. dysenteriae 1 isolates received by the United States Centers for Disease Control in 1988 were identified using this probe. These results suggest that ipaH restriction fragment length polymorphisms may be useful in genetic lineage and epidemiologic studies of virulent shigellae.
ipaH基因座包含一个多拷贝抗原基因家族,这是志贺氏菌属和肠侵袭性大肠杆菌(EIEC)所特有的。源自福氏志贺氏菌5型ipaH7.8基因的DNA探针被用于比较多种志贺氏菌和EIEC菌株中ipaH等位基因的分子排列。在所检测的所有侵袭质粒中均检测到多个ipaH同源序列拷贝。覆盖ipaH7.8基因离散24 bp片段以及ipaH4.5(探针H25)和ipaH2.5(探针H24)基因座侧翼序列的寡核苷酸探针,被用于确定福氏志贺氏菌1型、2型和5型以及宋内志贺氏菌中ipaH侵袭质粒拷贝之间的同源程度。这些侵袭质粒携带的IpaH等位基因在结构上并不等同,并且在其氨基末端和羧基末端表现出序列差异。已证明H25探针对应于与ipaH等位基因遗传连锁的IS629序列,而H24探针则定义了仅在志贺氏菌侵袭质粒中发现的DNA序列。来自侵袭质粒消除的福氏志贺氏菌和宋内志贺氏菌菌株的染色体DNA与ipaH7.8基因核心片段杂交,表明ipaH7.8结构基因的部分序列是重复的,并包含在志贺氏菌染色体中。基于ipaH7.8核心探针的特异性以及在志贺氏菌菌株侵袭质粒和染色体上检测到的ipaH序列,使用该探针鉴定了1988年美国疾病控制中心收到的40株痢疾志贺氏菌1型分离株中的三个多态性组。这些结果表明,ipaH限制性片段长度多态性可能有助于对致病性志贺氏菌进行遗传谱系和流行病学研究。