The bacterial signal molecule, ppGpp, regulates Salmonella virulence gene expression

被引:113
作者
Pizarro-Cerdá, J
Tedin, K
机构
[1] Free Univ Berlin, Inst Mikrobiol & Tierseuchen, D-10115 Berlin, Germany
[2] Inst Pasteur, Unite Interact Bacteries Cellules, F-75724 Paris 15, France
关键词
D O I
10.1111/j.1365-2958.2004.04122.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
Numerous, overlapping global regulatory systems mediate the environmental signalling controlling the virulence of Salmonella typhimurium. With both extra- and intracellular lifestyles, unravelling the mechanisms involved in regulating Salmonella pathogenesis has been complex. Here, we report a factor co-ordinating environmental signals with global regulators involved in pathogenesis. An S. typhimuriumDeltarelADeltaspoT strain deficient in guanosine tetraphosphate (ppGpp) synthesis was found to be highly attenuated in vivo and non-invasive in vitro. The DeltarelADeltaspoT strain exhibited severely reduced expression of hilA and invF, encoding major transcriptional activators required for Salmonella pathogenicity island 1 (SPI-1) gene expression and at least two other pathogenicity islands. None of the growth conditions intended to mimic the intestinal milieu was capable of inducing hilA expression in the absence of ppGpp. However, the expression of global regulators of Salmonella virulence, RpoS and PhoP/Q, and RpoS- and PhoP/Q-dependent, non-virulence-related genes was not significantly different from the wild-type strain. The results indicate that ppGpp plays a central role as a regulator of virulence gene expression in S. typhimurium and implicates ppGpp as a major factor in the environmental and host-dependent regulation of Salmonella pathogenesis.
引用
收藏
页码:1827 / 1844
页数:18
相关论文
共 118 条
[1]   REGULATION OF SPVR GENE-EXPRESSION OF SALMONELLA VIRULENCE PLASMID PKDSC50 IN SALMONELLA-CHOLERAESUIS SEROVAR CHOLERAESUIS [J].
ABE, A ;
MATSUI, H ;
DANBARA, H ;
TANAKA, K ;
TAKAHASHI, H ;
KAWAHARA, K .
MOLECULAR MICROBIOLOGY, 1994, 12 (05) :779-787
[2]   GROWTH-RATE PARADOX OF SALMONELLA-TYPHIMURIUM WITHIN HOST MACROPHAGES [J].
ABSHIRE, KZ ;
NEIDHARDT, FC .
JOURNAL OF BACTERIOLOGY, 1993, 175 (12) :3744-3748
[3]   Salmonella SirA is a global regulator of genes mediating enteropathogenesis [J].
Ahmer, BMM ;
van Reeuwijk, J ;
Watson, PR ;
Wallis, TS ;
Heffron, F .
MOLECULAR MICROBIOLOGY, 1999, 31 (03) :971-982
[4]   AraC/XylS family members, HilD and HilC, directly activate virulence gene expression independently of HilA in Salmonella typhimurium [J].
Akbar, S ;
Schechter, LM ;
Lostroh, CP ;
Lee, CA .
MOLECULAR MICROBIOLOGY, 2003, 47 (03) :715-728
[5]   Characterization of two novel regulatory genes affecting Salmonella invasion gene expression [J].
Altier, C ;
Suyemoto, M ;
Ruiz, AI ;
Burnham, KD ;
Maurer, R .
MOLECULAR MICROBIOLOGY, 2000, 35 (03) :635-646
[6]   The RcsB-RcsC regulatory system of Salmonella typhi differentially modulates the expression of invasion proteins, flagellin and Vi antigen in response to osmolarity [J].
Arricau, N ;
Hermant, D ;
Waxin, H ;
Ecobichon, C ;
Duffey, PS ;
Popoff, MY .
MOLECULAR MICROBIOLOGY, 1998, 29 (03) :835-850
[7]   EXPRESSION OF THE GENES-CODING FOR THE ESCHERICHIA-COLI INTEGRATION HOST FACTOR ARE CONTROLLED BY GROWTH-PHASE, RPOS, PPGPP AND BY AUTOREGULATION [J].
AVIV, M ;
GILADI, H ;
SCHREIBER, G ;
OPPENHEIM, AB ;
GLASER, G .
MOLECULAR MICROBIOLOGY, 1994, 14 (05) :1021-1031
[8]   Growth phase-dependent variation in protein composition of the Escherichia coli nucleoid [J].
Azam, TA ;
Iwata, A ;
Nishimura, A ;
Ueda, S ;
Ishihama, A .
JOURNAL OF BACTERIOLOGY, 1999, 181 (20) :6361-6370
[9]   hilA is a novel ompR/toxR family member that activates the expression of Salmonella typhimurium invasion genes [J].
Bajaj, V ;
Hwang, C ;
Lee, CA .
MOLECULAR MICROBIOLOGY, 1995, 18 (04) :715-727
[10]   Co-ordinate regulation of Salmonella typhimurium invasion genes by environmental and regulatory factors is mediated by control of hilA expression [J].
Bajaj, V ;
Lucas, RL ;
Hwang, C ;
Lee, CA .
MOLECULAR MICROBIOLOGY, 1996, 22 (04) :703-714