Spellerberg B, Martin S, Franken C, Berner R, Lütticken R
Institute of Medical Microbiology and National Reference Center for Streptococci, University Hospital Aachen, Pauwelsstrasse 30, D-52057, Aachen, Germany.
Gene. 2000 Jan 4;241(1):51-6. doi: 10.1016/s0378-1119(99)00469-2.
Gain and loss of bacterial pathogenicity is often associated with mobile genetic elements. A novel insertion sequence (IS) element designated ISSa4 was identified in Streptococcus agalactiae (group B streptococci). The 963bp IS element is flanked by 25bp perfect inverted repeats and led to the duplication of a 9bp target sequence at the insertion site. ISSa4 contains one open reading frame coding for a putative transposase of 287 aa and exhibits closest similarities to insertion elements of the IS982 family which has previously not been identified in streptococci. Analysis of different S. agalactiae strains showed that the copy number of ISSa4 in S. agalactiae varies significantly between strains. The S. agalactiae strain with the highest copy number of ISSa4 was nonhemolytic and harbored one copy inserted in cylB, which encodes the membrane-spanning domain of the putative hemolysin transporter (Spellerberg et al., 1999. Identification of genetic determinants for the hemolytic activity of Streptococcus agalactiae by ISS1 transposition. J. Bacteriol. 181, 3212-3219). Determination of the distribution of ISSa4 in different S. agalactiae strains revealed that ISSa4 could be detected only in strains isolated after 1996, which might indicate a recent acquisition of this novel insertion element by S. agalactiae.
细菌致病性的获得与丧失通常与可移动遗传元件相关。在无乳链球菌(B族链球菌)中鉴定出一种新的插入序列(IS)元件,命名为ISSa4。这个963bp的IS元件两侧是25bp的完美反向重复序列,并导致插入位点处9bp靶序列的重复。ISSa4包含一个开放阅读框,编码一个287个氨基酸的假定转座酶,与IS982家族的插入元件具有最密切的相似性,而该家族此前尚未在链球菌中被鉴定出来。对不同无乳链球菌菌株的分析表明,ISSa4在无乳链球菌中的拷贝数在不同菌株间差异显著。ISSa4拷贝数最高的无乳链球菌菌株不溶血,在编码假定溶血素转运蛋白跨膜结构域的cylB中插入了一个拷贝(Spellerberg等人,1999年。通过IS1转座鉴定无乳链球菌溶血活性的遗传决定因素。《细菌学杂志》181,3212 - 3219)。对ISSa4在不同无乳链球菌菌株中的分布进行测定,结果显示仅在1996年之后分离的菌株中能检测到ISSa4,这可能表明无乳链球菌最近获得了这种新的插入元件。