Hoover T A, Culp D W, Vodkin M H, Williams J C, Thompson H A
Bacteriology Division, USAMRIID, Ft. Detrick, Frederick, Maryland 21701, USA.
Infect Immun. 2002 Dec;70(12):6726-33. doi: 10.1128/IAI.70.12.6726-2733.2002.
After repeated passages through embyronated eggs, the Nine Mile strain of Coxiella burnetii exhibits antigenic variation, a loss of virulence characteristics, and transition to a truncated lipopolysaccharide (LPS) structure. In two independently derived strains, Nine Mile phase II and RSA 514, these phenotypic changes were accompanied by a large chromosomal deletion (M. H. Vodkin and J. C. Williams, J. Gen. Microbiol. 132:2587-2594, 1986). In the work reported here, additional screening of a cosmid bank prepared from the wild-type strain was used to map the deletion termini of both mutant strains and to accumulate all the segments of DNA that comprise the two deletions. The corresponding DNAs were then sequenced and annotated. The Nine Mile phase II deletion was completely nested within the deletion of the RSA 514 strain. Basic alignment and homology studies indicated that a large group of LPS biosynthetic genes, arranged in an apparent O-antigen cluster, was deleted in both variants. Database homologies identified, in particular, mannose pathway genes and genes encoding sugar methylases and nucleotide sugar epimerase-dehydratase proteins. Candidate genes for addition of sugar units to the core oligosaccharide for synthesis of the rare sugar 6-deoxy-3-C-methylgulose (virenose) were identified in the deleted region. Repeats, redundancies, paralogous genes, and two regions with reduced G+C contents were found within the deletions.
经鸡胚卵反复传代后,伯纳特柯克斯体九英里株表现出抗原变异、毒力特性丧失以及向截短的脂多糖(LPS)结构转变。在两个独立衍生的菌株九英里II期菌株和RSA 514中,这些表型变化伴随着一个大的染色体缺失(M. H. Vodkin和J. C. Williams,《普通微生物学杂志》132:2587 - 2594,1986年)。在本文报道的研究中,对从野生型菌株制备的黏粒文库进行了额外筛选,以绘制两个突变菌株的缺失末端图谱,并积累构成这两个缺失的所有DNA片段。然后对相应的DNA进行测序和注释。九英里II期菌株的缺失完全嵌套在RSA 514菌株的缺失范围内。基本比对和同源性研究表明,在两个变体中,一大组LPS生物合成基因(排列成一个明显的O抗原簇)被删除。数据库同源性分析特别鉴定出了甘露糖途径基因以及编码糖甲基化酶和核苷酸糖表异构酶 - 脱水酶蛋白的基因。在缺失区域鉴定出了用于向核心寡糖添加糖单元以合成稀有糖6 - 脱氧 - 3 - C - 甲基古洛糖(病毒糖)的候选基因。在缺失区域内发现了重复序列、冗余序列、旁系同源基因以及两个G + C含量降低的区域。