Affiliation:
1. Department of Clinical Bacteriology, Umeå University, S-901 85 Umeå, Sweden,1 and
2. Centre de Génétique Moléculaire du CNRS, 91190 Gif-sur-Yvette, France2
Abstract
ABSTRACT
The present study shows that active, self-splicing group II intron GBSi1 is located downstream of the C5a-peptidase gene,
scpB
, in some group B streptococcus (GBS) isolates that lack insertion sequence IS
1548
. IS
1548
was previously reported to be often present at the
scpB
locus in GBS isolated in association with endocarditis. Since none of 67 GBS isolates examined, 40 of which were of serotype III, harbored both IS
1548
and GBSi1, these two elements are suggested to be markers for different genetic lineages in GBS serotype III. The DNA region downstream of
scpB
in GBS isolates harboring either GBSi1, IS1548, or none of these mobile elements was found to encode the laminin binding protein, Lmb, which shows sequence similarities to a family of streptococcal adhesins. IS
1548
is inserted 9 bp upstream of the putative promoter for
lmb
, while the insertion site for GBSi1 is located 88 bp further upstream. Sequences highly similar to GBSi1 exist also in
Streptococcus pneumoniae
. An inverted repeat sequence, with features typical of transcription terminators, was identified immediately upstream of the insertion site for the group II intron both in the GBS and
S. pneumoniae
sequences. This motif is suggested to constitute a target for the GBS intron as well as for rather closely related introns in
Bacillus halodurans, Pseudomonas alcaligenes
, and
Pseudomonas putida
. When transcripts containing the GBSi1 intron were incubated at high concentrations of ammonium and magnesium, a major product with the expected length and sequence for the ligated exons was generated. Unlike, however, all members of group II investigated so far, the excised intron was in linear, rather than in a branched (lariat), form.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology