Defining the Mga regulon: comparative transcriptome analysis reveals both direct and indirect regulation by Mga in the group A streptococcus

被引:89
作者
Ribardo, Deborah A. [1 ]
McIver, Kevin S. [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
关键词
D O I
10.1111/j.1365-2958.2006.05381.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The regulator Mga in the group A streptococcus (GAS) is known to directly activate several virulence genes important for colonization and immune evasion. Transcriptome analysis comparing two mga-1 serotypes (M1 SF370, M6 JRS4) and one mga-2 serotype (M4 GA40634) against their isogenic mga-inactivated strains uncovered a broader Mga regulon profile containing both activated and repressed genes with predicted functions primarily related to sugar metabolism. This was reflected in the altered abilities of M1 and M4 Mga mutants to grow in chemically defined media with a single sugar source compared with their wild-type counterparts. Although the M1 and M4 Mga profiles were similar, the M6 JRS4 was clearly distinct, even from other M6 strains. Real-time RT-PCR and Northern blots confirmed that established core Mga regulon genes directly activated by Mga (emm, scpA, sof, fba) exhibited the highest activation levels across all strains tested. Spy2036 encoding a cytosolic hypothetical protein was highly activated in all three serotypes and was called gene regulated by Mga (grm). Mga bound directly to Pgrm, which overlaps the Mga-regulated Psof in OF+ strains, suggesting that grm is part of the core Mga regulon and Mga is able to activate divergently transcribed genes from a single site. Furthermore, Mga activated speB when detectable in the wild-type strain, although direct binding of Mga to PspeB could not be demonstrated. Thus, Mga is able to both directly and indirectly regulate genes shown to be important for virulence and the metabolic homeostasis of GAS.
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页码:491 / 508
页数:18
相关论文
共 49 条
[1]   Protein SIC, a novel extracellular protein of Streptococcus pyogenes interfering with complement function [J].
Akesson, P ;
Sjoholm, AG ;
Bjorck, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (02) :1081-1088
[2]   Mga is sufficient to activate transcription in vitro of sof-sfbX and other Mga-regulated virulence genes in the group A streptococcus [J].
Almengor, AC ;
Walters, MS ;
McIver, KS .
JOURNAL OF BACTERIOLOGY, 2006, 188 (06) :2038-2047
[3]   Transcriptional activation of sclA by Mga requires a distal binding site in Streptococcus pyogenes [J].
Almengor, AC ;
McIver, KS .
JOURNAL OF BACTERIOLOGY, 2004, 186 (23) :7847-7857
[4]   Complementation of divergent mga genes in group A Streptococcus [J].
Andersson, G ;
McIver, K ;
Heden, LO ;
Scott, JR .
GENE, 1996, 175 (1-2) :77-81
[5]   Group A streptococcal rofA gene is involved in the control of several virulence genes and eukaryotic cell attachment and internalization [J].
Beckert, S ;
Kreikemeyer, B ;
Podbielski, A .
INFECTION AND IMMUNITY, 2001, 69 (01) :534-537
[6]   EVIDENCE FOR 2 DISTINCT CLASSES OF STREPTOCOCCAL M-PROTEIN AND THEIR RELATIONSHIP TO RHEUMATIC-FEVER [J].
BESSEN, D ;
JONES, KF ;
FISCHETTI, VA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (01) :269-283
[7]   Genomic localization of a T serotype locus to a recombinatorial zone encoding extracellular matrix-binding proteins in Streptococcus pyogenes [J].
Bessen, DE ;
Kalia, A .
INFECTION AND IMMUNITY, 2002, 70 (03) :1159-1167
[8]   Analysis of the growth phase-associated transcriptome of Streptococcus pyogenes [J].
Beyer-Sehlmeyer, G ;
Kreikemeyer, B ;
Hörster, A ;
Podbielski, A .
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 295 (03) :161-177
[9]  
Brent, 1997, SHORT PROTOCOLS MOL
[10]   GENTLE METHOD FOR LYSIS OF ORAL STREPTOCOCCI [J].
CHASSY, BM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1976, 68 (02) :603-608