B. subtilis |
B. subtilis |
SigB |
See Table 1
|
|
|
B. licheniformis |
|
General stress sigma factor |
Brody et al., 2009 |
|
B. coagulans, B. amyloliquefaciens, B. pumilus, B. clausii |
|
Not reported |
de Been et al., 2011 |
|
Oceanobacillus iheyensis |
|
Not reported |
de Been et al., 2011 |
|
Listeria monocytogenes, L. innocua |
|
Activated in response to nutritional and environmental stresses. |
Wiedmann et al., 1998; Chaturongakul et al., 2008; Toledo-Arana et al., 2009; van der Veen and Abee, 2010; Ondrusch and Kreft, 2011
|
|
|
|
Responsible for swimming motility and invasiveness in the presence of blue light. |
|
|
|
|
Involved in the resistance of both planktonic cells and biofilms to the disinfectants benzalkonium chloride and peracetic acid in L. monocytogenes. |
|
|
|
|
Deletion of sigB attenuated virulence in L. monocytogenes
|
|
|
L. welshimeri |
|
Not reported |
de Been et al., 2011 |
B. cereus |
B. thuringiensis B. cereus B. anthracis B. weihenstephanensis |
SigB |
See Table 1
|
Fouet et al., 2000; van Schaik et al., 2004
|
S. coelicolor |
S. coelicolor |
SigF |
sigF is needed for spore maturation |
Cho et al., 2001; Bentley et al., 2002
|
|
|
SigH |
The sigH operon is controlled by environmental stress (heat, salt, ethanol) and developmental signals. |
|
|
|
|
A strain with a mutated sigH allele is reported to have some abnormalities in spore formation and to be slightly osmosensitive. |
|
|
|
SigB |
sigB is induced by salt and plays a role in osmoprotection and erection of aerial mycelium |
|
|
S. avermitilis, S. griseus |
SigB |
Not reported |
de Been et al., 2011 |
|
Thermobifida fusca |
|
Not reported |
de Been et al., 2011 |
|
Salinispora tropica, S. arenicola |
|
Not reported |
de Been et al., 2011 |
|
Frankia alni, Frankia Ccl3, Frankia EAN1pec |
|
Not reported |
de Been et al., 2011 |
S. aureus |
SigB |
Regulate biosynthesis of staphyloxanthin, a key virulence factor for protecting S. aureus from host-oxidant killing in vivo
|
Wu et al., 1996; Giachino et al., 2001; Bischoff et al., 2004; Chen et al., 2016
|
|
|
Its increased expression always is accompanied by enhanced biofilm formation |
|
|
|
Responsible for antibiotic resistance |
|
Clostridium |
C. difficile |
SigB |
Crucial role in adaptive strategies during gut infection |
Kint et al., 2017, 2019
|
|
C. thermocellum, C. cellulotycum, C. sticklandii, C. sordellii |
SigB |
Not reported |
|
M. tuberculosis |
SigF |
Induced under a variety of stress conditions, most notably antibiotic stress, low oxygen tensions, nutrient depletion, oxidative stress, and during stationary-phase growth |
DeMaio et al., 1996, 1997; Michele et al., 1999; Geiman et al., 2004
|
|
|
Is involved in cell surface modification and virulence factor secretion |
|
Synechocystis sp. |
SigF |
Mutant showed a severe defect in the induction of salt stress proteins |
Bhaya et al., 1999; Huckauf et al., 2000
|
|
|
Required for the biosynthesis of pili and that specific pilA genes |
|