Jimenez Natalia, Canals Rocío, Lacasta Anna, Kondakova Anna N, Lindner Buko, Knirel Yuriy A, Merino Susana, Regué Miguel, Tomás Juan M
Departamento Microbiología, Facultad Biología, Universidad Barcelona, Diagonal 645, 08071 Barcelona, Spain.
J Bacteriol. 2008 May;190(9):3176-84. doi: 10.1128/JB.01874-07. Epub 2008 Feb 29.
By the isolation of three different Aeromonas hydrophila strain AH-3 (serotype O34) mutants with an altered lipopolysaccharide (LPS) migration in gels, three genomic regions encompassing LPS core biosynthesis genes were identified and characterized. When possible, mutants were constructed using each gene from the three regions, containing seven, four, and two genes (regions 1 to 3, respectively). The mutant LPS core structures were elucidated by using mass spectrometry, methylation analysis, and comparison with the full core structure of an O-antigen-lacking AH-3 mutant previously established by us. Combining the gene sequence and complementation test data with the structural data and phenotypic characterization of the mutant LPSs enabled a presumptive assignment of all LPS core biosynthesis gene functions in A. hydrophila AH-3. The three regions and the genes contained are in complete agreement with the recently sequenced genome of A. hydrophila ATCC 7966. The functions of the A. hydrophila genes waaC in region 3 and waaF in region 2 were completely established, allowing the genome annotations of the two heptosyl transferase products not previously assigned. Having the functions of all genes involved with the LPS core biosynthesis and most corresponding single-gene mutants now allows experimental work on the role of the LPS core in the virulence of A. hydrophila.
通过分离三种不同的嗜水气单胞菌菌株AH-3(血清型O34)突变体,这些突变体在凝胶中的脂多糖(LPS)迁移发生改变,从而鉴定并表征了包含LPS核心生物合成基因的三个基因组区域。在可能的情况下,使用来自这三个区域的每个基因构建突变体,这三个区域分别包含七个、四个和两个基因(分别为区域1至3)。通过质谱分析、甲基化分析以及与我们之前建立的缺乏O抗原的AH-3突变体的完整核心结构进行比较,阐明了突变体LPS的核心结构。将基因序列和互补试验数据与突变体LPS的结构数据和表型特征相结合,使得能够对嗜水气单胞菌AH-3中所有LPS核心生物合成基因的功能进行推测性分配。这三个区域及其所含基因与最近测序的嗜水气单胞菌ATCC 7966基因组完全一致。完全确定了嗜水气单胞菌区域3中的基因waaC和区域2中的基因waaF的功能,从而对之前未分配的两种庚糖基转移酶产物进行了基因组注释。现在掌握了所有参与LPS核心生物合成的基因及其大多数相应的单基因突变体的功能,这使得能够开展关于LPS核心在嗜水气单胞菌毒力中作用的实验工作。