scholarly journals Virulence of Vibrio harveyi ORM4 toward the European abalone Haliotis tuberculata involves both quorum sensing and a type III secretion system

Author(s):  
Amandine Morot ◽  
Sahar El Fekih ◽  
Adeline Bidault ◽  
Alizée Le Ferrand ◽  
Albane Jouault ◽  
...  
PLoS ONE ◽  
2015 ◽  
Vol 10 (12) ◽  
pp. e0143935 ◽  
Author(s):  
H. A. Darshanee Ruwandeepika ◽  
Indrani Karunasagar ◽  
Peter Bossier ◽  
Tom Defoirdt

2009 ◽  
Vol 22 (8) ◽  
pp. 964-976 ◽  
Author(s):  
Xin Deng ◽  
Yanmei Xiao ◽  
Lefu Lan ◽  
Jian-Min Zhou ◽  
Xiaoyan Tang

Pseudomonas syringae bacteria utilize the type III secretion system (T3SS) to deliver effector proteins into host cells. The T3SS and T3 effector genes (together called the T3 genes hereafter) are repressed in nutrient-rich medium but rapidly induced after the bacteria are transferred into minimal medium or infiltrated into plants. The induction of the T3 genes is mediated by HrpL, an alternative sigma factor that recognizes the conserved hrp box motif in the T3 gene promoters. The induction of hrpL is mediated by HrpR and HrpS, two homologous proteins that bind the hrpL promoter. To identify additional genes involved in regulation of the T3 genes, we screened for the P. syringae pv. phaseolicola NPS3121 transposon-tagged mutants with reduced induction of avrPto-luc and hrpL-luc, reporter genes for promoters of effector gene avrPto and hrpL, respectively. Determination of the transposon-insertion sites revealed genes with putative functions in signal transduction and transcriptional regulation, protein synthesis, and basic metabolism. A transcriptional regulator (AefRNPS3121) was identified in our screen that is homologous to AefR of P. syringae pv. syringae strain B728a, a regulator of the quorum-sensing signal and epiphytic traits, but was not known to regulate the T3 genes. AefRNPS3121 in P. syringae pv. phaseolicola NPS3121 and AefR in P. syringae pv. syringae B728a behave similarly in regulating the quorum-sensing signal in liquid medium but differ in regulating the epiphytic traits, including swarming motility, leaf entry, and epiphytic survival.


2007 ◽  
Vol 15 (2) ◽  
pp. 308-313 ◽  
Author(s):  
Olivier Epaulard ◽  
Madiha Derouazi ◽  
Carole Margerit ◽  
Raphaël Marlu ◽  
Didier Filopon ◽  
...  

ABSTRACT During the last few years, the use of type III secretion system-based bacterial vectors for immunotherapy purposes has been assessed in various applications. We showed that a type III secretion-based Pseudomonas aeruginosa vector delivering the ovalbumin (OVA) antigen induced an efficient specific CD8+ T-lymphocyte immune response against OVA-expressing cells. Because of the intrinsic toxicity of the vector, further virulence attenuation was needed. Therefore, we explored the effects of the deletion of quorum-sensing genes and the aroA gene toward toxicity and efficiency of the vector strain. The aroA mutation in our strain (making the strain auxotrophic for aromatic amino acids) conferred a strikingly reduced toxicity, with the bacterial lethal dose being more than 100 times higher than that of the parental strain. The quorum-sensing gene mutation alone was associated with a slightly reduced toxicity. In a prophylactic OVA-expressing melanoma mouse model, an OVA-delivering aroA-deficient mutant was the most efficient at a low dose (105), but dose enhancement was not associated with a greater immune response. The quorum-sensing-deficient strain was the most efficient at a mild dose (106), but this dose was close to the toxic dose. Combination of both mutations conferred the highest efficiency at an elevated dose (107), in agreement with the known negative effects of quorum-sensing molecules upon T-cell activation. In conclusion, we have obtained a promising immunotherapy vector regarding toxicity and efficiency for further developments in both antitumor and anti-infectious strategies.


2006 ◽  
Vol 31 (4) ◽  
pp. 297-306 ◽  
Author(s):  
Hua Zhu ◽  
Tim C.R. Conibear ◽  
Rani Bandara ◽  
Yulina Aliwarga ◽  
Fiona Stapleton ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document