Affiliation:
1. Queensland Institute of Medical Research
2. Australian Centre for International & Tropical Health & Nutrition, Brisbane
3. Menzies School of Health Research, Darwin, Australia
Abstract
ABSTRACT
All isolates of serotype M1 of group A streptococci possess a gene for streptococcal inhibitor of complement (SIC) in the
mga
regulon, which harbors genes for other virulence factors, such as M and M-like proteins, C5a peptidase, and a regulator. In serotype M57 the gene for a protein that is closely related to SIC (
crs57
) is located outside the
mga
regulon. We mapped the location of the
crs57
gene in six strains of
emm57
(gene encoding the M57 protein) sequence types to an intergenic region between the ABC transporter gene (SPy0778) and the gene for a small ribosomal protein (
rpsU
). The noncoding sequences on both sides of
crs57
exhibited high degrees of identity to the corresponding regions of
sic
from M1 strains. This included one of the inverted repeat sequences of IS
1562
but not the insertion element itself. These observations suggest that
crs57
was recently acquired by serotype M57 or its progenitor via horizontal acquisition from serotype M1. The six
emm57
sequence type isolates analyzed in this study belong to two distinct molecular types (vir types VT8 and VT101). Although the
crs57
sequences from VT8 strains had very few substitution mutations, the VT101
crs57
sequence had a large number of such mutations. The CRS57 proteins from these strains are secretory products and have the ability to bind to complement proteins. All these proteins contain several tryptophan-rich repeats designated DWS motifs and internal repeat sequences. In all of these structural and biochemical characteristics CRS57 resembles SIC from M1 strains. Hence, CRS57 has a functional role similar to that of SIC in an M1 strain.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
16 articles.
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