Identification of a novel insertion sequence element in Streptococcus agalactiae. bspeller@imib.rwth-aachen.de
- PMID: 10607898
- DOI: 10.1016/s0378-1119(99)00469-2
Identification of a novel insertion sequence element in Streptococcus agalactiae. bspeller@imib.rwth-aachen.de
Abstract
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.
Similar articles
-
Identification of genetic determinants for the hemolytic activity of Streptococcus agalactiae by ISS1 transposition.J Bacteriol. 1999 May;181(10):3212-9. doi: 10.1128/JB.181.10.3212-3219.1999. J Bacteriol. 1999. PMID: 10322024 Free PMC article.
-
ISSa4-based differentiation of Streptococcus agalactiae strains and identification of multiple target sites for ISSa4 insertions.J Bacteriol. 2004 Feb;186(4):1106-9. doi: 10.1128/JB.186.4.1106-1109.2004. J Bacteriol. 2004. PMID: 14762005 Free PMC article.
-
ISSag1 in streptococcal strains of human and animal origin.Int J Med Microbiol. 2004 Oct;294(4):247-54. doi: 10.1016/j.ijmm.2004.04.002. Int J Med Microbiol. 2004. PMID: 15532982
-
Physiological impact of transposable elements encoding DDE transposases in the environmental adaptation of Streptococcus agalactiae.Microbiology (Reading). 2014 Jul;160(Pt 7):1298-1315. doi: 10.1099/mic.0.077628-0. Epub 2014 Apr 23. Microbiology (Reading). 2014. PMID: 24760965 Review.
-
IS982 and kin: new insights into an old IS family.Mob DNA. 2020 Jul 4;11:24. doi: 10.1186/s13100-020-00221-z. eCollection 2020. Mob DNA. 2020. PMID: 32641975 Free PMC article. Review.
Cited by
-
Natural Mutations in Streptococcus agalactiae Resulting in Abrogation of β Antigen Production.PLoS One. 2015 Jun 5;10(6):e0128426. doi: 10.1371/journal.pone.0128426. eCollection 2015. PLoS One. 2015. PMID: 26047354 Free PMC article.
-
Comparative genomics and the role of lateral gene transfer in the evolution of bovine adapted Streptococcus agalactiae.Infect Genet Evol. 2011 Aug;11(6):1263-75. doi: 10.1016/j.meegid.2011.04.019. Epub 2011 Apr 22. Infect Genet Evol. 2011. PMID: 21536150 Free PMC article.
-
Acquisition of insertion sequences and the GBSi1 intron by Streptococcus agalactiae isolates correlates with the evolution of the species.J Bacteriol. 2005 Sep;187(17):6248-52. doi: 10.1128/JB.187.17.6248-6252.2005. J Bacteriol. 2005. PMID: 16109968 Free PMC article.
-
Group B streptococcal haemolysin and pigment, a tale of twins.FEMS Microbiol Rev. 2014 Sep;38(5):932-46. doi: 10.1111/1574-6976.12071. Epub 2014 Apr 4. FEMS Microbiol Rev. 2014. PMID: 24617549 Free PMC article. Review.
-
Group B streptococcal infections in pregnancy and early life.Clin Microbiol Rev. 2025 Mar 13;38(1):e0015422. doi: 10.1128/cmr.00154-22. Epub 2024 Nov 25. Clin Microbiol Rev. 2025. PMID: 39584819 Review.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources