Confirmation of quantitative trait loci for resistance to multiple-HG types of soybean cyst nematode (<Emphasis Type="Italic">Heterodera glycines</Emphasis> Ichinohe)

Genetic analysis of resistance of plant introduction (PI) 438489B to soybean cyst nematode (SCN) have shown that this PI is highly resistant to many SCN HG types. However, validation of the previously detected quantitative trait loci (QTL) has not been done. In this study, 250 F_2:3 progeny of a Magellan (susceptible) × PI 438489B (resistant) cross were used for primary genetic mapping to detect putative QTL for resistance to five SCN HG types. QTL confirmation study was subsequently conducted using F_6:7 recombinant inbred lines (RILs) derived from the same cross. Simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers were employed for molecular genotyping. Interval mapping (IM), permutation tests, cofactor selection, and composite interval mapping (CIM) were performed to identify and map QTL. Results showed that five QTL intervals were associated with resistance to either multiple- or single-HG types of SCN. Among these, two major QTL for resistance to multiple-SCN HG types were mapped to chromosomes (Chr.) 8 and 18, consistent with the known rhg1 and Rhg4 locations. The other QTL were mapped to Chr. 4. The results of our study confirmed earlier reported SCN resistance QTL in this PI. Moreover, SSR and SNP molecular markers tightly linked to these QTL can be useful for the near-isogenic lines (NILs) development aiming to fine-mapping of these QTL regions and map-based cloning of SCN resistance candidate genes.     

Improving controlled pollination methodology for breeding <Emphasis Type="Italic">Acacia mangium</Emphasis> Willd.

Acacia mangium is a major plantation species for the pulp and paper industry in south-east Asia and there are a number of active breeding programs. The species is predominantly outcrossing, but with a demonstrated capacity to set selfed seed where outcross pollen is limited, with consequent inbreeding depression in the progeny. Current controlled pollination methods therefore include a time-consuming emasculation step. We used microsatellite genotyping of seedlings to determine the consequences of outcross pollination with and without emasculation. Only 1 of 3 mother trees set a small amount (5%) of selfed seed. Using whole inflorescences from the male parent as the pollen applicator rather than sieved pollen reduced outcross contamination rates from 19.1 to 8.7% and substantially increased worker productivity. Application of sugar solution to the female flowers immediately prior to pollination increased yield of sound seeds per spike. Additional improvements to the pollination protocols are discussed.     

Spatial prediction of saline and sodic soils in rice‒shrimp farming land by using integrated artificial neural network/regression model and kriging

In the context of widespread saline and sodic soil, mapping and monitoring spatial distribution of soil salinity and sodicity are important for utilization and management in agriculture lands. In this study, two-stage assessment was proposed to predict spatial distribution of saline and sodic soils. First, artificial neural network (ANN) and multiple linear regressions (MLR) model were used to predict sodium adsorption ratio (SAR) and exchangeable sodium percentage (ESP) based on soil electrical conductivity (EC) and pH. Then, the Kriging interpolation method combined with overlay mapping technique was used to perform saline spatial predictions in the study area. The model accuracy level is evaluated based on coefficient of determination (R²) and root mean square error (RMSE). In the first stage, the values of R² and RMSE of SAR and ESP were 0.94, 0.17 and 0.94, 0.24 for ANN, and 0.35, 0.52 and 0.34, 0.76 for MLR, respectively. Similarly, in the second stage, the RMSE of ANN-Kriging were much closer to 0 and relatively lower than MLR-Kriging and Kriging. The results show that ANN-Kriging can be used to improve the accuracy of mapping and monitoring spatial distribution of saline and sodic soil in areas that develop the rice-shrimp cultivation model.     

CD205-positive,Sepharose-induced peritoneal exudate cells: a new resource for DC research in the chicken

Veterinary Research Communications - Dendritic cells (DC) are important antigen-presenting cells and are among the least characterized immune cells in the chicken. In order to obtain chicken DC,...     

Susceptibility of freshwater rearing Asian seabass (Lates calcarifer) to pathogenic Streptococcus iniae

Asian seabass (Lates calcarifer) has been recognized as an economically important aquaculture species which can be adapted to and cultivated in wide range of salinities. The number of freshwater intensive seabass farms in Thailand is increasing annually. Here, we first describe the susceptibility of Asian seabass, which were cultured in freshwater, to Streptococcus inae (SI) and their pathological changes. Three isolates of putative SI were identified using a combination of standard biochemical assays and species‐specific PCR prior subjected to in vivo challenge. Accumulated mortalities of the fish which received 10⁷ CFU fish^?1 of either SI1J, SI SGSA or SI2J were 90%, 90% and 100% at 7 days‐post infection (dpi), respectively, and mortalities increased sharply between 3 and 5 dpi. Clinical signs such as erratic swimming and opaque eyes were identified from a few infected fish, while most died rapidly without any abnormal signs. Histopathological manifestations were observed in the multiple organs (kidney, liver and brain). Haemorrhage, hyperhemia, cellular degeneration and inflammatory cells infiltration were commonly found within the internal organs. Notably, the formation of numerous encyst‐like lesion aggregated by eosinophilic cells, resembling macrophages, were typically found in the brain of the infected fish. Summarily, this study first revealed that freshwater reared Asian seabass is highly susceptible to SI infection and haemorrhagic septicaemia was a major pathological change that could be found in the infected fish.