A Note on a Greenhouse Evaluation of Wild Arachis Species for Resistance to Athelia rolfsii

Athelia rolfsii (Curzi) C.C. Tu & Kimbr. is the one of the most damaging pathogens of cultivated peanut, causing the soilborne disease known regionally as white mold, stem rot, or southern blight. Because the genetic base for cultivated peanut is narrow, wild Arachis species may possess novel sources of disease resistance. We evaluated 18 accessions representing 15 Arachis species ( batizocoi , benensis , cardenasii , correntina , cruziana , diogoi , duranensis , herzogii , hoehnei , kempff - mercadoi , kuhlmannii , microsperma , monticola , simpsonii , williamsii ) in the greenhouse for resistance to At. rolfsii . Assays were conducted on intact plants propagated from rooted cuttings inoculated with mycelial plugs, and lesion length and mycelial growth were measured at 4, 6, 10, and 12 days after inoculation. For lesion length, Arachis batizocoi (PI 468326 and PI 468327), and A. kuhlmannii PI 468159 were the most susceptible entries with a mean lesion length >50 mm at 12 days after inoculation. Arachis microsperma (PI 666096 and PI 674407) and A. diogoi PI 468354 had the shortest lesions with mean lengths ≤16 mm at 12 days after inoculation. Arachis cruziana PI 476003 and the two A. batizocoi PIs had the highest mean area under the disease progress curves (AUDPCs), and the lowest AUDPC was obtained from the A. microsperma PI 674407. Mycelial growth was correlated with lesion length in most species except A. monticola PI 497260 . These results may be useful to peanut geneticists seeking additional sources of resistance to Athelia rolfsii .

Greenhouse Evaluation of Clubroot Resistant-Brassica napus cv. Mendel and Its Efficacy Concerning Virulence and Soil Inoculum Levels of Plasmodiophora brassicae

Clubroot resistance of oilseed rape (OSR) cultivars frequently relies on a major resistance gene originating from cv. Mendel. The efficacy of this resistance was studied in greenhouse experiments using two Plasmodiophora brassicae isolates, which were either virulent (P1(+)) or avirulent (P1) on Mendel. Seeds of clubroot-susceptible cultivar Visby and clubroot-resistant cultivar Mendel were sown in soil mixtures inoculated with different concentrations of resting spores (101, 103, 105, and 107 resting spores/g soil). Clubroot severity, plant height, shoot and root weight as well as resting spore propagation were assessed for each isolate and cultivar separately at four dates after sowing. The OSR cultivars behaved significantly different in the measured parameters. The threshold of inoculum density to cause disease depended strongly on the virulence of the pathogen and susceptibility of the host plant. In Visby grown in soil infested with P1, clubroot symptoms and increases in root weight and the number of propagated resting spores occurred at inoculum levels of 101 resting spores and higher, whereas Mendel was not affected in soils under the three lowest inoculum densities. In contrast, the P1(+) isolate led to earlier and more severe symptoms, heavier galls, and a significantly higher number of new resting spores in both cultivars.

Field Screen and Genotyping of Phaseolus vulgaris against Two Begomoviruses in Georgia, USA

The production and quality of Phaseolusvulgaris (snap bean) have been negatively impacted by leaf crumple disease caused by two whitefly-transmitted begomoviruses: cucurbit leaf crumple virus (CuLCrV) and sida golden mosaic Florida virus (SiGMFV), which often appear as a mixed infection in Georgia. Host resistance is the most economical management strategy against whitefly-transmitted viruses. Currently, information is not available with respect to resistance to these two viruses in commercial cultivars. In two field seasons (2018 and 2019), we screened Phaseolus spp. genotypes (n = 84 in 2018; n = 80 in 2019; most of the genotypes were common in both years with a few exceptions) for resistance against CuLCrV and/or SiGMFV. We also included two commonly grown Lima bean (Phaseolus lunatus) varieties in our field screening. Twenty Phaseolus spp. genotypes with high to moderate-levels of resistance (disease severity ranging from 5%–50%) to CuLCrV and/or SiGMFV were identified. Twenty-one Phaseolus spp. genotypes were found to be highly susceptible with a disease severity of ≥66%. Furthermore, based on the greenhouse evaluation with two genotypes-each (two susceptible and two resistant; identified in field screen) exposed to viruliferous whiteflies infected with CuLCrV and SiGMFV, we observed that the susceptible genotypes accumulated higher copy numbers of both viruses and displayed severe crumple severity compared to the resistant genotypes, indicating that resistance might potentially be against the virus complex rather than against the whiteflies. Adult whitefly counts differed significantly among Phaseolus genotypes in both years. The whole genome of these Phaseolus spp. [snap bean (n = 82); Lima bean (n = 2)] genotypes was sequenced and genetic variability among them was identified. Over 900 giga-base (Gb) of filtered data were generated and >88% of the resulting data were mapped to the reference genome, and SNP and Indel variants in Phaseolus spp. genotypes were obtained. A total of 645,729 SNPs and 68,713 Indels, including 30,169 insertions and 38,543 deletions, were identified, which were distributed in 11 chromosomes with chromosome 02 harboring the maximum number of variants. This phenotypic and genotypic information will be helpful in genome-wide association studies that will aid in identifying the genetic basis of resistance to these begomoviruses in Phaseolus spp.