Sau S, Lee C Y
Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, 66160, USA.
J Bacteriol. 1996 Apr;178(7):2118-26. doi: 10.1128/jb.178.7.2118-2126.1996.
Eleven serotypes of capsular polysaccharide from Staphylococcus aureus have been reported. We have previously cloned a cluster of type 1 capsule (cap1) genes responsible for type 1 capsular polysaccharide biosynthesis in S. aureus M. To clone the type 8 capsule (cap8) genes, a plasmid library of type 8 strain Becker was screened with a labelled DNA fragment containing the cap1 genes under low-stringency conditions. One recombinant plasmid containing a 14-kb insert was chosen for further study and found to complement 14 of the 18 type 8 capsule-negative (Cap8-) mutants used in the study. Additional library screening, subcloning, and complementation experiments showed that all of the 18 Cap8- mutants were complemented by DNA fragments derived from a 20.5-kb contiguous region of the Becker chromosome. The mutants were mapped into six complementation groups, indicating that the cap8 genes are clustered. By Southern hybridization analyses under high-stringency conditions, we found that DNA fragments containing the cap8 gene cluster show extensive homology with all 17 strains tested, including type 1 strains. By further Southern analyses and cloning of the cap8-related homolog from strain M, we show that strain M carries an additional capsule gene cluster different from the cap1 gene cluster. In addition, by using DNA fragments containing different regions of the cap8 gene cluster as probes to hybridize DNA from different strains, we found that the central region of the cap8 gene cluster hybridizes only to DNAs from certain strains tested whereas the flanking regions hybridize to DNAs of all strains tested. Thus, the cap8 gene clusters and its closely related homologs are likely to have organizations similar to those of the encapsulation genes of other bacterial systems.
已报道了金黄色葡萄球菌的11种荚膜多糖血清型。我们之前克隆了一组负责金黄色葡萄球菌M型1荚膜多糖生物合成的1型荚膜(cap1)基因。为了克隆8型荚膜(cap8)基因,在低严谨条件下,用含有cap1基因的标记DNA片段筛选8型菌株贝克尔的质粒文库。选择了一个含有14 kb插入片段的重组质粒进行进一步研究,发现它能互补该研究中使用的18个8型荚膜阴性(Cap8-)突变体中的14个。额外的文库筛选、亚克隆和互补实验表明,所有18个Cap8-突变体都被来自贝克尔染色体20.5 kb连续区域的DNA片段互补。这些突变体被定位到6个互补组,表明cap8基因是成簇的。通过高严谨条件下的Southern杂交分析,我们发现含有cap8基因簇的DNA片段与所有测试的17个菌株,包括1型菌株,都有广泛的同源性。通过进一步的Southern分析和从菌株M克隆cap8相关同源物,我们表明菌株M携带一个不同于cap1基因簇的额外荚膜基因簇。此外,通过使用含有cap8基因簇不同区域的DNA片段作为探针与不同菌株的DNA杂交,我们发现cap8基因簇的中心区域仅与某些测试菌株的DNA杂交,而侧翼区域与所有测试菌株的DNA杂交。因此,cap8基因簇及其密切相关的同源物可能具有与其他细菌系统的荚膜化基因相似的组织形式。