12 research outputs found
Regulation of Cell Wall-Bound Invertase in Pepper Leaves by <em>Xanthomonas campestris</em> pv. <em>vesicatoria</em> Type Three Effectors
<div><p><em>Xanthomonas campestris</em> pv. <em>vesicatoria (Xcv)</em> possess a type 3 secretion system (T3SS) to deliver effector proteins into its <em>Solanaceous</em> host plants. These proteins are involved in suppression of plant defense and in reprogramming of plant metabolism to favour bacterial propagation. There is increasing evidence that hexoses contribute to defense responses. They act as substrates for metabolic processes and as metabolic semaphores to regulate gene expression. Especially an increase in the apoplastic hexose-to-sucrose ratio has been suggested to strengthen plant defense. This shift is brought about by the activity of cell wall-bound invertase (cw-Inv). We examined the possibility that <em>Xcv</em> may employ type 3 effector (T3E) proteins to suppress cw-Inv activity during infection. Indeed, pepper leaves infected with a T3SS-deficient <em>Xcv</em> strain showed a higher level of cw-Inv mRNA and enzyme activity relative to <em>Xcv</em> wild type infected leaves. Higher cw-Inv activity was paralleled by an increase in hexoses and mRNA abundance for the <em>pathogenesis-related</em> gene <em>PRQ.</em> These results suggest that <em>Xcv</em> suppresses cw-Inv activity in a T3SS-dependent manner, most likely to prevent sugar-mediated defense signals. To identify <em>Xcv</em> T3Es that regulate cw-Inv activity, a screen was performed with eighteen <em>Xcv</em> strains, each deficient in an individual T3E. Seven <em>Xcv</em> T3E deletion strains caused a significant change in cw-Inv activity compared to <em>Xcv</em> wild type. Among them, <em>Xcv</em> lacking the <em>xopB</em> gene (<em>Xcv</em> Δ<em>xopB</em>) caused the most prominent increase in cw-Inv activity. Deletion of <em>xopB</em> increased the mRNA abundance of <em>PRQ</em> in <em>Xcv</em> Δ<em>xopB-</em>infected pepper leaves, but not of <em>Pti5</em> and <em>Acre31,</em> two PAMP-triggered immunity markers. Inducible expression of XopB in transgenic tobacco inhibited <em>Xcv</em>-mediated induction of cw-Inv activity observed in wild type plants and resulted in severe developmental phenotypes. Together, these data suggest that XopB interferes with cw-Inv activity <em>in planta</em> to suppress sugar-enhanced defense responses during <em>Xcv</em> infection.</p> </div
Content of soluble sugars in susceptible pepper leaves after infection with <i>Xcv</i> wild type or with the TTSS<i>-</i>deficient <i>Xcv</i> Δ<i>hrpB1</i> strain.
<p>Contents of glucose, fructose and sucrose were determined following inoculation of pepper leaves with <i>Xcv</i> wild type (wt) or the <i>Xcv</i> Δ<i>hrpB1</i> using a concentration of 5×10<sup>8</sup> cfu ml<sup>−1</sup> and compared to 10 mM MgCl<sub>2</sub> infiltrated control leaves. Samples were taken before (0 h), 24 and 48 hours post infection (hpi). Each value represents the mean ± SE of four different experiments each with four to six individual samples. Statistically significant differences to Mock-inoculated control plants were determined using two-tailed t-test assuming normal distribution and are indicated by asterisks (*p<0.05).</p
Expression of <i>cw-Inv</i>, <i>PRQ</i> and <i>RbcS</i> in susceptible pepper leaves in response to infection with <i>Xcv</i> Δ<i>xopB</i>.
<p>Leaves of pepper plants were infected with the <i>Xcv</i> wild type (wt), <i>Xcv</i> Δ<i>hrpB1</i>, <i>Xcv</i> Δ<i>xopB</i> using a concentration of 10<sup>9</sup> cfu ml<sup>−1</sup>, and as control with 10 mM MgCl<sub>2</sub>.Total RNA was isolated from pepper leaves before (0), and 1, 2, 3 days post infection (dpi). Twenty five µg of total RNA was separated per each lane. Northern blots were hybridized with <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0051763#pone.0051763-Dean1" target="_blank">[<sup>32</sup>]</a>P dCTP-labelled cDNA fragments of <i>cw-Inv</i>, <i>PRQ</i> and <i>RbcS.</i> A representative experiment is shown. Similar results were obtained in two other experiments.</p
Inducible <i>xopB</i> expression in transgenic tobacco leaves suppresses cw-Inv activity during <i>Xcv</i> infection.
<p>Control plants and two selected transgenic tobacco lines with inducible <i>xopB</i> expression (#22, #71) were watered with 1% ethanol. After 24 h, plantlets were inoculated with a 10<sup>9</sup> cfu ml<sup>−1</sup> suspension of <i>Xcv</i> wild type. Samples were taken directly before inoculation and 1 and 2 days post inoculation (1dpi +EtOH; 2dpi <i>Xcv</i>+ EtOH). Non-ethanol watered plants were also inoculated with <i>Xcv</i> and samples were taken accordingly (1dpi -EtOH; 2dpi -EtOH). For control purposes ethanol-treated and non-treated plants were inoculated with 10 mM MgCl<sub>2</sub>. Cw-Inv activity was determined from four independent samples and fold changes ± SD were calculated for each sample relative to values obtained before <i>Xcv</i> inoculation. The experiment was repeated with similar results.</p
Expression of PTI marker genes <i>Pti5</i> and <i>Acre31</i> in susceptible pepper leaves after infection with different <i>Xcv</i> strains.
<p>Leaves of pepper plants were inoculated with <i>Xcv</i> wild type (wt), <i>Xcv</i> Δ<i>hrpB1</i>, <i>Xcv</i> Δ<i>xopB</i> using a concentration of 10<sup>9</sup> cfu ml<sup>−1</sup>, and with 10 mM MgCl<sub>2</sub>. Total RNA was isolated from samples taken before (0 h), 6 h and 24 h after infiltration and reverse transcribed into cDNA. Abundance of <i>Pti5</i> (A.) and <i>Acre31</i> (B.) mRNA was detected by qPCR. Data were analysed using MxPro software v4.1. The expression levels of <i>Pti5</i> and <i>Acre31</i> were normalized with <i>Actin</i> and displayed relative to the expression level at time point 0 h which was set to a value of 1. The average ± SE of three replicates is shown. Similar results were obtained in an independent experiment. White bars, MgCl<sub>2</sub>; light grey, <i>Xcv</i> wild type; black, <i>Xcv</i> Δ<i>hrpB1</i>, dark grey, <i>Xcv</i> Δ<i>xopB</i>.</p
Screening for <i>Xcv</i> T3Es involved in regulation of cw-Inv activity.
<p>Leaves of pepper plants were infiltrated with wild type and mutant <i>Xcv</i> strains at 10<sup>9</sup> cfu ml<sup>−1</sup> and cw-Inv activity was measured 2 and 3 days post infection (dpi) in independent experiments. Graphs represent values calculated relative to the <i>Xcv</i> wild type (wt) response which was set to 100% for each individual experiment. Mean cw-Inv activities after infection with <i>Xcv</i> wild type were 20.96 µmol min<sup>−1</sup> m<sup>−2</sup>±8.43 (100% ±40.2) and 57.57 µmol min<sup>−1</sup> m<sup>−2</sup>±23.92 (100% ±41.6) at 2 and 3 dpi, respectively. The variance of <i>Xcv</i> wild type response (ca. 42%) is illustrated as a dashed line. Values are the mean response (as percentage to <i>Xcv</i> wild type) ± SD from three to nine different experiments. Statistically significant differences from <i>Xcv</i> wild type response were determined using two-tailed t-test assuming normal distribution and are indicated by asterisks (**p<0.01); (***p<0.001).</p
Inducible <i>xopB</i> expression in transgenic tobacco plants causes severe leaf abnormality.
<p>A.) Analysis of <i>xopB</i>-specific transcript accumulation in transgenic tobacco lines. Seven different lines (No. 22, 26, 37, 44, 64, 71, 72) and two control plants (wt) were analysed for <i>xopB</i> expression by Northern blotting. Total RNA was isolated 1 day after watering plants with 1% ethanol to induce <i>xopB</i> expression. Twenty µg of RNA were separated on a formaldehyde-containing agarose gel and analysed by hybridization with a <i>xopB</i>-specific radioactively labelled probe. Ethidium bromide stained rRNA is shown as loading control. B.) Analysis of XopB protein accumulation upon watering with 1% ethanol in selected transgenic lines (#22, #71). XopB migrates at ∼70 kDa, while in tobacco a cross-reactive band appeared at ∼55kDa. Expression of RubisCO as stained by Coomassie Blue is shown as control for protein loading. C.) Phenotypic changes in transgenic tobacco plants caused by <i>xopB</i> expression. Upper panel: symptoms 2 days after ethanol-treatment; lower panel: phenotypic alterations 10 days after induction. Arrows indicate morphological changes of the leaf lamina and cell death of meristematic tissue, respectively. From left to right: control line, lines #22 and #71.</p
Cw-Inv activity of susceptible pepper leaves infected with heat-inactivated and protease-treated preparations of <i>Xcv</i> cells.
<p><i>Xcv</i> wild type (wt) and <i>Xcv</i> Δ<i>hrpB1</i> were grown over night in NYG medium and prepared as described in material and methods. Subsequently, cells were heat-inactivated at 95°C for 20 min. An aliquot was of each cell culture was digested with proteases (proteinase K and trypsin) for 2 h at 60°C. After heat-inactivation for 10 min, cells were pelleted and re-suspended in 10 mM sterile MgCl<sub>2</sub> and adjusted to OD<sub>600</sub> = 1. Heat-inactivated <i>Xcv</i> cells with or without protease treatment were used for inoculation of pepper leaves. Samples were taken before (0 d), 1, 2 and 3 days post infections (dpi) and cw-Inv activity was measured. Values represent the mean of four independent samples ± SD. Similar results were obtained in an independent experiment.</p
<i>Xanthomonas campestris</i> pv. <i>vesicatoria</i> strains used in this study.
<p><i>Xanthomonas campestris</i> pv. <i>vesicatoria</i> strains used in this study.</p
Expression of XopB in <i>Xcv</i> Δ<i>xopB</i> complements the effect on cw-Inv activity.
<p>Susceptible pepper leaves were inoculated with <i>Xcv</i> wild type (wt), <i>Xcv</i> Δ<i>xopB</i> containing both the pBBR1MCS5 vector (EV), or <i>Xcv</i> Δ<i>xopB</i> derivatives in which a genomic fragment was introduced containing the putative <i>xopB</i> promoter and open reading frame in sense (+) or antisense (−) orientation relative to the <i>lac</i> promoter. Samples were taken before (0), 1, 2 and 3 days post infection (dpi). A.) Cw-Inv activity was measured from the infected leaf tissue. Values represent the mean of four independent samples ± SD. B.) Expression of XopB was verified by Western blotting by probing with the anti-XopB antibody. XopB migrates at ∼70 kDa.</p