Mapping polygenes for tuber resistance to late blight in a diploid Solanum phureja × S. stenotomum hybrid population

Potato tuber blight is a disease caused by the oomycete Phytophthora infestans (Mont.) de Bary. Due to the significant economic impact of this disease, introgression of durable resistance into the cultivated potato is one of the top priorities of breeding programmes worldwide. Though numerous resistance loci against this devastating disease have already been mapped, most of the detected loci are contributing towards foliar resistance while specific information on tuber resistance is limited. To identify the genetic components of tuber resistance and its relationship to foliar resistance and plant maturity we have investigated the host‐pathogen interaction in a segregating diploid hybrid Solanum phureja × S. stenotomum family. Mature tubers from this mapping family were inoculated with a sporangial suspension of P. infestans (US‐8 clonal lineage) and evaluated for lesion expansion. No significant correlation was detected between late blight resistance in foliage and tubers, and between plant maturity and tuber resistance. Four chromosomal regions were significantly associated with tuber resistance to the disease. The largest effect was detected near the marker locus PSC (LOD 10.7) located on chromosome 10. This locus explained about 63% of the total phenotypic variation of the trait. The other three resistance‐related loci were mapped on chromosomes 8 (GP1282, LOD 4.4), 6 (CP18, LOD 4.0) and 2 (CP157, LOD 3.8). None of the four tuber resistance loci coincides with the foliage resistance loci detected in this same family. Tuber blight resistance quantitative trait loci (QTL) on chromosomes 2, 8 and 10 are distinct from the maturity QTLs and have an additive effect on tuber resistance. These results indicate that different genes are involved in foliar and tuber resistance to P. infestans in the present family and that some of the resistance genes might be associated with late maturity.     

Late blight resistance in a diploid full-sib potato family

Late blight, caused by Phytophthora infestans (Mont.) de Bary, is the most destructive disease of potato worldwide. As this pathogen can rapidly overcome major race‐specific resistance genes, identifying the basis for enhanced quantitative resistance has become a crucial element for implementing advanced breeding strategies. A population of 230 full‐sib progeny derived from a cross between two diploid hybrid Solanum phureja × S. stenotomum clones was evaluated for foliage resistance against late blight in replicated trials at multiple locations in Pennsylvania between 1999 and 2002. In field experiments, plants were evaluated visually for per cent defoliation, and area under the disease progress curve (AUDPC) was determined. The two parents and three control cultivars (‘Atlantic’, ‘Kennebec’ and ‘Katahdin’) were included in all trials. In all three experiments, the presence of a significant number of clones exhibiting transgressive segregation were observed. There were significant differences among environments as well as among clones, and the clone × environment interaction was also significant. Stability analysis revealed that 37 clones made a significant contribution to the overall environment × clone interaction. Broad‐sense heritability for resistance, measured as AUDPC, was estimated as 0.67. The overall results indicate the presence in this potato family of a high level of field resistance against late blight. This segregating diploid family appears to be a good candidate for quantitative trait loci mapping to identify and characterize the genetic components of partial late blight resistance.     

Barley yield and soil microbial and enzyme activities as affected by contamination of two soils with lead, zinc or copper

The effects of increasing rates of Pb, Zn and Cu on extractable heavy metal levels, barley yields, basal respiration and the activities of catalase, urease, invertase and acid phosphatase were investigated in two soils in a 2-year greenhouse experiment. In the first year, barley yields were decreased by increasing additions of Pb, Zn and Cu. In the second year, increased yields were recorded at lower rates of addition of all three metals in both the chestnut and chernozem soils. Yield depressions were most marked for added Cu and least marked for Pb but, in contrast, accumulation of heavy metals in grain, in excess of recommended limits, was most pronounced for Pb and did not occur for Cu. Increasing rates of all three metals caused a decrease in basal respiration; the degree of inhibition was generally greater in the second than in the first year. After 1 year of incubation, increasing rates of addition of metals reduced all tested enzyme activities. However, after 2 years, the pattern of response was more complex, with increases in enzyme activities being noted at lower rates of addition of all three metals. In general, invertase and urease activities were more markedly inhibited by heavy metal contamination than those of catalase and phosphatase. Ammonium acetate-extractable heavy metal concentrations in soils were less after 2 years than 1 years reaction time due to their transformation into less labile forms. Significant negative correlations between grain yield, basal respiration and enzyme activities were observed in both years.     

Effects of irrigation-induced salinity and sodicity on soil microbial activity

The effects of irrigation-induced salinity and sodicity on the size and activity of the soil microbial biomass in vertic soils on a Zimbabwean sugar estate were investigated. Furrow-irrigated fields were selected which had a gradient of salinity and sugarcane yield ranging from good cane growth at the upper ends to dead and dying cane at the lower ends. Soils were sampled under dead and dying cane, poor, satisfactory and good cane growth and from adjacent undisturbed sites under native vegetation. Electrical conductivity (EC) and sodium adsorption ratio (SAR) of saturation paste extracts was measured, as well as the exchangeable sodium percentage (ESP). There was a significant negative exponential relationship between EC and microbial biomass C, the percentage of organic C present as microbial biomass C, indices of microbial activity (arginine ammonification and fluorescein diacetate hydrolysis rates) and the activities of the exocellular enzymes β-glucosidase, alkaline phosphatase and arylsulphatase but the negative relationships with SAR and ESP were best described by linear functions. By contrast, the metabolic quotient increased with increasing salinity and sodicity, exponentially with EC and linearly with SAR and ESP.Potentially mineralizable N, measured by aerobic incubation, was also negatively correlated with EC, SAR and ESP. These results indicate that increasing salinity and sodicity resulted in a progressively smaller, more stressed microbial community which was less metabolically efficient. The exponential relationships with EC demonstrate the highly detrimental effect that small increases in salinity had on the microbial community. It is concluded that agriculture-induced salinity and sodicity not only influences the chemical and physical characteristics of soils but also greatly affects soil microbial and biochemical properties.     

Self -Compatibility in a Diploid Hybrid Population of <Emphasis Type="Italic">Solanum phureja</Emphasis> – <Emphasis Type="Italic">S. stenotomum</Emphasis>

Recently proposals have been made in both Europe and North America to try to radically change potato breeding strategy from a tetraploid, heterozygous crop to a diploid inbred crop. As part of that effort, clones from the long-day adapted, late blight resistant diploid hybrid Solanum phureja – S. stenotomum population were selfed to begin the process of developing inbred lines. In March of 2016 and 2017, 42 diploid clones from the above-mentioned population were selfed in the greenhouse in Beltsville, MD. In 2016 and 2017, 10 and 13 clones failed to flower, respectively. Among the remaining clones, 716 pollinations were made in 2016, resulting in 57 fruit from 17 clones, and 3742 seeds; 801 pollinations were made in 2017, resulting in 34 fruit from 12 clones, and 1903 seeds. Nine clones were successfully selfed both years. Percent successful selfs was significantly higher in 2016 (7.96%) than in 2017 (4.24%). The most prolific clones in 2016 were BD1241–1 (34% successful selfs, 1090 seed), BD1218–3 (25% successful selfs, 638 seed), BD1215–1 (5% successful selfs, 411 seed), BD1243–1 (23% successful selfs, 232 seed). In contrast, the most prolific clones in 2017 were BD1230–2 (25% successful selfs, 537 seed), BD1203–3 (23% successful selfs, 391 seed), and BD1229–1 (11% successful selfs, 388 seed). These results indicate that there is sufficient self-compatibililty in this population to generate large numbers of inbred individuals, but that genotype x environment interactions are large. Attempts to generate selfed seed should be made over several years to maximize the genetic base of the selfed population.     

Competitive and noncompetitive adsorption of silicate and phosphate by two acid Si-deficient soils and their effects on P and Si extractability

The effects of pH on the adsorption of silicate and phosphate, either singly or in competition, by two acid soils were investigated. Both soils adsorbed two to three times more P than Si and adsorption isotherms at pH 5.0, 5.5, 6.0 and 6.5 showed that increasing pH greatly increased Si adsorption but decreased that of P. Silicate adsorption was very low below pH 5.0, increased rapidly up to pH 9–10 before decreasing again. Adsorption of P was at a maximum at pH 2.0, decreased slowly up to pH 7.0 and then more rapidly above pH 7.0. When Si and P were added at equimolar concentrations, the presence of P decreased Si adsorption between pH 6.0 and 8.0 while the presence of Si decreased P adsorption in the pH region 6.0 and 11. Addition of calcium silicate at rates equivalent to 300, 600 and 1200 kg Si ha^?1 resulted in a progressive increase in soil pH. Separate samples of soil were treated with Ca(OH)₂ to give the same pH values so that the effect of Si could be identified. The highest rate of Si (1200 kg ha^?1 which gave a pH of 6.5) caused a significant decrease in P adsorption (as determined by adsorption isotherms) and an increase in resin-extractable P but the lower rates had little effect. Addition of P to the soil as calcium phosphate at rates equivalent to 30, 60 and 100 kg P ha^?1 all caused a decrease in Si adsorption capacity and an increase in CaCl₂-extractable Si. It was concluded that the strategy of adding Si to lower P requirements in acid soils is not likely to be effective while addition of fertilizer P may well lower Si adsorption and promote Si desorption and its increased mobility.     

Evaluation of chlorfenapyr for control of the bed bug,Cimex lectularius L.

BACKGROUND: The presence of bed bug populations resistant to pyrethroids demands the development of new control tactics, including the use of insecticides with new modes of action. Insecticides that disrupt oxidative phosphorylation in insect mitochondria can be an option. Laboratory assays were used to measure the toxicity of chlorfenapyr to susceptible strains and two strains highly resistant to pyrethroids. The effectiveness of two chlorfenapyr‐based formulations was compared, and behavioral responses of bed bugs to dry residues of aerosol sprays were evaluated. RESULTS: Chlorfenapyr was effective against all bed bug strains, killing them at a similar rate, regardless of their susceptibility status to pyrethroids. Dry residues aged for 4 months were as toxic as fresh dry residues. The aerosol formulation had contact activity and caused faster mortality than a water‐based formulation. Bed bugs did not avoid resting on surfaces treated with aerosol. CONCLUSION: Chlorfenapyr is an option for controlling pyrethroid‐resistant bed bugs. While it does not cause quick knockdown, its long residual activity and no avoidance behavior of bed bugs to dry residues appear to make this insecticide suitable for bed bug control. A faster insecticidal effect is obtained with the aerosol formulation, suggesting greater bioavailablity of the toxicant. Copyright © 2010 Society of Chemical Industry     

Immunomodulation with killed Propionibacterium acnes in guinea pigs simultaneously vaccinated with Brucella abortus strain 19

Immunomodulation with killed Propionibacterium acnes was attempted in guinea pigs simultaneously vaccinated with Brucella abortus strain 19. Two groups, each comprised of 9 guinea pigs, were injected by different routes (s.c. and or i.v.) with 1.4 mg of P. acnes and 5 X 10(8) CFU of B. abortus, S-19, while 3 other groups each received either P. acnes, B. abortus S-19, or saline (s.c.). The antibody titers to B. abortus measured at 6, 10 and 14 weeks after vaccination indicated no significant (P less than 0.01) response in the 2 groups immunopotentiated with P. acnes concurrent with B. abortus S-19 vaccination. The delayed hypersensitivity response to 3 Brucella antigens conducted 8 weeks after immunization did not show a significant difference between the B. abortus S-19 vaccinated group compared with the 2 groups immunopotentiated and vaccinated. However, the proliferative response of lymphocytes to the B. abortus soluble antigen diluted 1:100 indicated significantly enhanced blastogenesis in the (s.c.) immunopotentiated and immunized guinea pigs compared with the B. abortus S-19 vaccinated group. A slightly enhanced response was also observed in the group immunopotentiated (i.v.) and vaccinated (s.c.). The guinea pigs were challenged with B. abortus strain 2308 and necropsied 4 weeks later. The mean splenic CFU of the Brucella in the group immunopotentiated (i.v.) and vaccinated (s.c.) was significantly decreased when compared with the guinea pigs vaccinated with B. abortus S-19 alone. These findings indicated that P. acnes administered simultaneously with B. abortus S-19 vaccine was able to augment the immune response in guinea pigs. Immunomodulation as evidenced by enhanced clearance of B. abortus from the spleens of immunopotentiated animals was presumably brought about by activated macrophages or a T-cell mediated cytolytic mechanism or both.