AbstractsBiology & Animal Science

Characterization of the Oxidative Stress Response and the Type II Secretion System for the Phytopathogen, <italic>Xylella</italic> <italic>fastidiosa</italic>

by Peng Wang




Institution: University of California – Riverside
Department: Plant Pathology
Year: 2014
Keywords: Plant pathology
Record ID: 2036844
Full text PDF: http://www.escholarship.org/uc/item/5bn8r2xx


Abstract

<italic>Xylella</italic> <italic>fastidiosa</italic> (<italic>Xf</italic>), a xylem-limited fastidious bacterium, is the causal agent of Pierce's Disease (PD) of grapevine. <italic>Xf</italic> has a very broad host range, including grapevine, citrus, almond, oleander, peach and maple. PD is a lethal disease of grapevine and understanding the disease from the perspective of molecular interactions between <italic>Xf</italic> and grapevine is very important. Pathogens often encounter reactive oxygen species (ROS) from a variety of sources during the infection process. These ROS can be toxic to the pathogen and correspondingly, the pathogen has evolved several tightly regulated mechanisms to cope with this stress. OxyR is a redox-responsive transcription factor that regulates expression of antioxidant enzymes. Interestingly. OxyR is the only known oxidative stress regulator in the <italic>Xf</italic> genome leading us to speculate that it plays a vital role in adaptation to the host environment. We constructed an <italic>oxyR</italic> mutant and found it was significantly more sensitive to H<sub>2</sub>O<sub>2</sub> than wild type <italic>Xf</italic>. In addition, we found that the <italic>Xf</italic> <italic>oxyR</italic> mutant was reduced in surface attachment, cell-cell aggregation and mature biofilm formation. <italic>In</italic> <italic>planta</italic> tests indicated that the <italic>oxyR</italic> mutant was significantly compromised in the ability to colonize the host xylem, but, interestingly, no difference in virulence was observed when compared with wild type <italic>Xf</italic>.The Type II secretion system (T2SS) is an important protein secretion system in plant pathogenic bacteria. The repertoire of proteins secreted by this system are largely involved in nutrition and include plant cell wall degrading enzymes (CWDEs). <italic>Xf</italic> employs CWDEs to degrade xylem pit membranes to facilitate systematic movement within the xylem. The majority of the demonstrated and putative CWDEs are predicted to be secreted by the T2SS. By knocking out a T2SS structure gene <italic>xpsE</italic>, which encodes a putative ATPase that provides the energy that drives the T2SS, I demonstrated that <italic>Xf</italic> requires XpsE for full virulence and establishment in the xylem vessels indicating that the T2SS is an important factor employed during the infection process.