TTSS;
T3SS1;
Vibrio parahaemolyticus;
Pseudomonas aeruginosa;
THERMOSTABLE DIRECT HEMOLYSIN;
FOOD-RELATED ILLNESS;
PROTEIN SECRETION;
UNITED-STATES;
IDENTIFICATION;
MECHANISM;
VECTORS;
TRANSLOCATION;
COLONIZATION;
INFECTIONS;
D O I:
10.4161/viru.1.4.12318
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Vibrio parahaemolyticus ExsA is the transcriptional regulator for type III secretion system 1 (T3SS 1) while ExsD blocks T3SS 1 expression. Herein we show that deletion of exsC from V. parahaemolyticus blocked synthesis of T3SS 1-dependent proteins under inducing conditions (contact with HeLa cells), while in trans complementation of the Delta exsC strain with wild-type exsC restored protein synthesis. Under non-inducing conditions (Luria broth plus salt), in trans expression of exsC in a wild-type strain resulted in synthesis and secretion of T3SS 1-dependent proteins. Deletion of exsC does not affect the synthesis of ExsA while expression of T3SS 1 genes is independent of ExsC in the absence of ExsD. Co-expression of recombinant proteins with different antigenic tags demonstrated that ExsC binds ExsD and that the N-terminal amino acids of ExsC (positions 7 to 12) are required for binding. Co-expression and purification of antigentically tagged ExsA and ExsD demonstrated that ExsD directly binds ExsA and presumably prevents ExsA from binding promoter regions of T3SS 1 genes. Collectively these data demonstrate that ExsD binds ExsA to block expression of T3SS 1 genes, while ExsC binds ExsD to permit expression of T3SS 1 genes. ExsA, ExsC and ExsD from V. parahaemolyticus appear to be functional orthologues of their Pseudomonas aeruginosa counterparts.