Genome-wide detection of genetic loci associated with soybean aphid resistance in soybean germplasm PI 603712

Soybean aphid (Aphis glycines Matsumura) has become one of the major pests of soybean [Glycine max (L.) Merr.] in North America since 2000. At least four biotypes of soybean aphid have been confirmed in the United States. Genetic characterization of new sources of soybean aphid resistance will facilitate the expansion of soybean gene pool for soybean aphid resistance and thus will help to develop soybean aphid resistant cultivars. To characterize the genetic basis of soybean aphid resistance in PI 603712, a newly identified resistant germplasm line, 142 F₂ plants derived from the cross ‘Roberts’ × PI 603712 and their parents were evaluated for soybean aphid resistance in the greenhouse, and were genotyped with BARCSoySNP6K Illumina Infinium II BeadChip. A genome-wide molecular linkage map was constructed with 1495 polymorphic SNP markers. QTL analysis revealed that PI 603712 possessed two major loci associated with soybean aphid resistance, located on chromosome 7 and 16, respectively. The locus on chromosome 7 was dominantly expressed and positioned about one Mega-base-pair distant from the previously identified resistance locus Rag1. The locus on chromosome 16 was positioned near the previously identified resistance locus Rag3 and expressed partially dominance or additive effect. Interestingly, two minor loci were also detected on chromosomes 13 and 17 but the alleles from PI 603712 decreased the resistance. In developing soybean aphid resistant cultivars through marker-assisted selection, an appropriate combination of resistance loci should be selected when PI 603712 is used as a donor parent of resistance.     

Mapping genes for grain protein concentration and grain yield on chromosome 5B of Triticum turgidum (L.) var. dicoccoides

Grain protein concentration (GPC) is an important quality factor in durum wheat [Triticum turgidum (L.) var. durum]. Due to the strong environmental influence on GPC, molecular markers linked to quantitative trait loci (QTL) affecting GPC have the potential to be valuable in wheat breeding programs. Various quantitative traits in a population of 133 recombinant inbred chromosome lines were studied in replicated trials at three locations in North Dakota. Segregation for GPC, 1000-kernel weight, gluten strength, heading date, and plant height was observed. By relating phenotypic data to a linkage map obtained from the same population, three QTL affecting GPC, and one affecting yield were identified. The genotypic coefficients of determination for both traits were high.     

Identification and Molecular Mapping of a Gene Conferring Resistance to Pyrenophora tritici-repentis Race 3 in Tetraploid Wheat

ABSTRACT Race 3 of the fungus Pyrenophora tritici-repentis, causal agent of tan spot, induces differential symptoms in tetraploid and hexaploid wheat, causing necrosis and chlorosis, respectively. This study was conducted to examine the genetic control of resistance to necrosis induced by P. tritici-repentis race 3 and to map resistance genes identified in tetraploid wheat (Triticum turgidum). A mapping population of recombinant inbred lines (RILs) was developed from a cross between the resistant genotype T. tur-gidum no. 283 (PI 352519) and the susceptible durum cv. Coulter. Based on the reactions of the Langdon-T. dicoccoides (LDN[DIC]) disomic substitution lines, chromosomal location of the resistance genes was determined and further molecular mapping of the resistance genes for race 3 was conducted in 80 RILs of the cross T. turgidum no. 283/Coulter. Plants were inoculated at the two-leaf stage and disease reaction was assessed 8 days after inoculation based on lesion type. Disease reaction of the LDN(DIC) lines and molecular mapping on the T. turgidum no. 283/Coulter population indicated that the gene, designated tsn2, conditioning resistance to race 3 is located on the long arm of chromosome 3B. Genetic analysis of the F(2) generation and of the F(4:5) and F(6:7) families indicated that a single recessive gene controlled resistance to necrosis induced by race 3 in the cross studied.     

A quantitative trait locus on chromosome 5B controls resistance of <Emphasis Type="Italic">Triticum turgidum</Emphasis> (L.) var. <Emphasis Type="Italic">diccocoides</Emphasis> to Stagonospora nodorum blotch

Stagonospora nodorum blotch (SNB) is an important foliar disease of durum wheat (Triticum turgidum var. durum) worldwide. The combined effects of SNB and tan spot, considered as components of the leaf spotting disease complex, result in significant damage to wheat production in the northern Great Plains of North America. The main objective of this study was the genetic analysis of resistance to SNB caused by Phaeosphaeria nodorum in tetraploid wheat, and its association with tan spot caused by Pyrenophora tritici-repentis race 2. The 133 recombinant inbred chromosome lines (RICL) developed from the cross LDN/LDN(Dic-5B) were evaluated for SNB reaction at the seedling stage under greenhouse conditions. Molecular markers were used to map a quantitative trait locus (QTL) on chromosome 5B, explaining 37.6% of the phenotypic variation in SNB reaction. The location of the QTL was 8.8 cM distal to the tsn1 locus coding for resistance to P. tritici-repentis race 2. The presence of genes for resistance to both SNB and tan spot in close proximity in tetraploid wheat and the identification of molecular markers linked to these genes or QTLs will be useful for incorporating resistance to these diseases in wheat breeding programs.     

Flanking SSR markers for alleles involved in the necrosis of hybrids between hexaploid bread wheat and synthetic hexaploid wheat

Hybrid necrosis in wheat (Triticum aestivum L.) is the premature death of leaves or plants caused by the interaction of two dominant complementary genes, Ne1 and Ne2, located on chromosomes 5B and 2B, respectively. We examined allelic interaction effects of necrosis alleles using simple sequence repeat (SSR) markers in F₂ populations derived from crossing the cultivar “Alsen” with a synthetic hexaploid “TA4152-37”. The SSR marker Xbarc7 was linked at a distance of 3 cM to the quantitative trait loci (QTL) located on chromosome 2B, and Xgwm639 was 11 cM from the 5B QTL. A significant additive by additive epistatic interaction was detected between Ne1 and Ne2 QTL, and the results suggest that Alsen possesses a moderate necrosis allele, Ne2^m; whereas, TA4152-37 possesses a moderate necrosis allele, Ne1^m. The Ne2^m allele had a stronger effect than the Ne1^m allele, and a total of 94.6% of phenotypic variance was explained by these genes and their interactions. This demonstrates the strong phenotypic effect due to even moderate necrosis alleles, and emphasizes the need for breeders to accurately predict and identify hybrids that will result in necrosis.     

Effect of temperature on symptom expression and accumulation of tomato spotted wilt virus in different host species

The effect of two temperature regimes (daytime, 29 ± 2°C, night-time, 24 ± 3°C; and daytime, 23 ± 1°C, night-time, 18 ± 2°C) on the symptoms caused by tomato spotted wilt virus (TSWV), and the accumulation of TSWV virions, was compared in Datura stramonium , Nicotiana tabacum cv. White Burley and Physalis ixocarpa . Tobacco plants were more severely affected by TSWV at the high temperature regime, but the incidence (percent of plants with symptoms) was 100% for both regimes. In P. ixocarpa and D. stramonium the higher temperature caused an increase in both incidence and rate of development of symptoms. At high temperature, all three species showed both local and systemic symptoms; however, at low temperature only P. ixocarpa consistently developed systemic symptoms. In general, virus accumulation in the inoculated leaves (presumably the combined effect of virus replication and local movement) of all plants was higher at the lower temperature. Long distance movement in tobacco, leading to virion accumulation in other plant organs, was favoured by high temperature; but there was relatively little effect in P. ixocarpa and D. stramonium .     

Control by ATR-FTIR of surface treatment of cork stoppers and its effect on their mechanical performance

Fourier transform infrared (FTIR) spectroscopy was applied to determine the type of surface treatment and dose used on cork stoppers and to predict the friction between stopper and bottleneck. Agglomerated cork stoppers were finished with two different doses and using two surface treatments: P (paraffin and silicone), 15 and 25?mg/stopper, and S (only silicone), 10 and 15?mg/stopper. FTIR spectra were recorded at five points for each stopper by attenuated total reflectance (ATR). Absorbances at 1,010, 2,916, and 2,963?cm^?1 were obtained in each spectrum. Discriminant analysis techniques allowed the treatment, and dose applied to each stopper to be identified from the absorbance values. 91.2% success rates were obtained from individual values and 96.0% from the mean values of each stopper. Spectrometric data also allowed treatment homogeneity to be determined on the stopper surface, and a multiple regression model was used to predict the friction index (If?=?Fe/Fc) (R ²?=?0.93).