TY - JOUR
T1 - Variation in M protein production among Streptococcus pyogenes strains according to emm genotype
AU - Matsumoto, Masakado
AU - Suzuki, Masahiro
AU - Hirose, Kaoru
AU - Hiramatsu, Reiji
AU - Minagawa, Hiroko
AU - Minami, Masaaki
AU - Tatsuno, Ichiro
AU - Okamoto, Akira
AU - Ohta, Michio
AU - Hasegawa, Tadao
PY - 2011/6
Y1 - 2011/6
N2 - M protein is an important virulence determinant in Streptococcus pyogenes, but the amounts of M protein in various strains of the species remain to be elucidated. To assess the amount of M protein in strains of each emm genotype, dot blot analysis was performed on 141 clinically isolated strains. Among the cell membrane-associated proteins, M protein was present in greater quantities in the emm1, 3, and 6 strains than in the other emm strains. In addition three strains, one each of the emm1, 3, and 6 types, showed prolific M protein production (M protein-high producers). These three emm genotypes are frequently isolated in clinical practice. Sequencing of the csrRS gene, one of the two-component signal transduction systems implicated in virulence, was performed on 25 strains bearing different amounts of M protein. CsrS mutations, in contrast to CsrR protein, were detected in 11 strains. The M protein-high producer strain of emm1 type carried two amino acid substitutions, whereas the other three emm1 strains carried only one substitution each. The M protein-high producer expressed its emm gene more strongly than the corresponding M protein-low producer did according to TaqMan RT-PCR. These observations suggest that the accumulation of amino acid substitutions in CsrS protein may contribute, at least in part, to the large amount of M protein production seen in several emm genotypes.
AB - M protein is an important virulence determinant in Streptococcus pyogenes, but the amounts of M protein in various strains of the species remain to be elucidated. To assess the amount of M protein in strains of each emm genotype, dot blot analysis was performed on 141 clinically isolated strains. Among the cell membrane-associated proteins, M protein was present in greater quantities in the emm1, 3, and 6 strains than in the other emm strains. In addition three strains, one each of the emm1, 3, and 6 types, showed prolific M protein production (M protein-high producers). These three emm genotypes are frequently isolated in clinical practice. Sequencing of the csrRS gene, one of the two-component signal transduction systems implicated in virulence, was performed on 25 strains bearing different amounts of M protein. CsrS mutations, in contrast to CsrR protein, were detected in 11 strains. The M protein-high producer strain of emm1 type carried two amino acid substitutions, whereas the other three emm1 strains carried only one substitution each. The M protein-high producer expressed its emm gene more strongly than the corresponding M protein-low producer did according to TaqMan RT-PCR. These observations suggest that the accumulation of amino acid substitutions in CsrS protein may contribute, at least in part, to the large amount of M protein production seen in several emm genotypes.
UR - http://www.scopus.com/inward/record.url?scp=79957599731&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79957599731&partnerID=8YFLogxK
U2 - 10.1111/j.1348-0421.2011.00329.x
DO - 10.1111/j.1348-0421.2011.00329.x
M3 - Article
C2 - 21371090
AN - SCOPUS:79957599731
SN - 0385-5600
VL - 55
SP - 379
EP - 387
JO - MICROBIOLOGY and IMMUNOLOGY
JF - MICROBIOLOGY and IMMUNOLOGY
IS - 6
ER -