Relative expression of the <i>TubB</i> gene in <i>Phytophthora capsici</i> isolates.

a<p>Isolates were only considered resistant (R) when they were able to grow on PDA plates amended with 30 µg ml⁻¹ zoxamide.</p>b<p>The expression of the <i>PcTubB</i> gene was normalized using the <i>PcWS21</i> gene and then calibrated to the normalized <i>PcTubB</i> mRNA value of the HX-1 isolate in the absence of zoxamide. The mean and standard deviation values indicate the average relative expression between two independent biological experiments. The relative expression was determined in isolates subjected to zoxamide for 6 hours prior to mRNA isolation.</p

<i>Phytophthora capsici</i> isolates used in this study.

a<p>RZ4-1, RZ3-5, and RZ13-2 are zoxamide-resistant mutants generated from PCAS1 by UV-mutagenesis. XH38-10 and XH38-13 are zoxamide-resistant mutants generated from HX-1 by zoxamide adaption.</p>b<p>Isolates were only considered resistant (R) when they were able to grow on PDA plates amended with 30 µg ml⁻¹ zoxamide.</p

Frequency distributions of EC₅₀ values (the effective concentration causing 50% inhibition of mycelial growth of <i>Phytophthora melonis</i>) for flumorph, dimethomorph and iprovalicarb.

<p>In total, 80 isolates of <i>P. melonis</i> were collected from areas never exposed to carboxylic acid amide fungicides.</p

Results of the experiments conducted to induce resistance against flumorph, dimethomorph, and iprovalicarb in <i>Phytophthora melonis</i>.

a<p>SM, spontaneous mutation. UV, UV-mutagenesis.</p>b<p>Survival frequency, number of mutants/total number of zoospores used for mutant generation.</p>c<p>EC₅₀, the effective concentration for causing 50% inhibition of mycelial growth inhibition of <i>P. melonis</i>.</p>d<p>Resistance factor  =  EC₅₀ of resistant isolates at the 10^th transfer/EC₅₀ of its parent.</p

Genetic relationships among 15 isolates of <i>Phytophthora melonis</i>.

<p>The denrogram (UPGMA) shows the relationships among the isolates of <i>P. melonis</i> based on randomly amplified polymorphic DNA (RAPD) analysis with 16 decamer primers. Scale at the bottom depicts the genetic distance.</p

Segregation of zoxamide-resistance in the sexual progeny of different <i>Phytophthora capsici</i> isolates.

a<p>Sexual progeny were only considered resistant (R) when they were able to grow on PDA plates amended with 30 µg ml⁻¹ zoxamide.</p

Fitness of CAA-resistant and -sensitive isolates of <i>Phytophthora melonis in vitro</i>.

a<p>Isolates in bold font are parents of the resistant isolates listed under them in regular font. Isolates starting with the letter F, D, and I, are flumorph-resistant mutants, dimethomorph-resistant mutants, and iprovalicarb-resistant mutants, respectively.</p>b<p>For each parent and its resistant progeny, means followed by same letters are not significantly different according to Fisher’s least significance difference (α = 0.05).</p>c<p>CFI (compound fitness index)  =  mycelial growth × zoospore production × lesion area on cucumber leaves.</p

Isolates of <i>Phytophthora melonis</i> used for RAPD analysis and their sensitivities to flumorph, dimethomorph and iprovalicarb.

a<p>One isolate of <i>Phytophthora drechsleri</i> was used as an outgroup control.</p>b<p>EC₅₀ values, the effective concentration for causing 50% inhibition of mycelial growth inhibition of <i>P. melonis</i>.</p>c<p>Number represents a different field in the same district.</p

Overview of the crossing strategy used to determine the segregation of zoxamide-resistance in progeny of <i>P. capsici</i>.

<p>SET, sensitivity test; MTD, mating type determination (A1/A2); OSP, oospore progeny; UV, ultraviolet treatment; AD, adaptation to zoxamide-amended media; CR, cross; SCR, self-cross; S₀, S₁, parental isolates and first generation of isolates from self-cross hybridization, respectively; F₀, F₁, F₂, parental isolates and progeny of sexual hybridization, respectively; BC, backcross.</p

Genotype segregation pattern and expected phenotype of S1, F1, F2 and BC progeny according to the one-gene and two-gene resistance models.

<p>Genotype segregation pattern and expected phenotype of S1, F1, F2 and BC progeny according to the one-gene and two-gene resistance models.</p