Suitability and use of two molecular markers to track race-specific resistance striga gesnerioides in cowpea (Vigna unguiculata (L.) Walp.)

The obligate root parasitic weed Striga gesnerioides poses a severe constraint to cowpea productivity in the dry savannahs of West and Central Africa, where cowpea is a major crop. At least seven races of S.gesnerioides have been identified within the cowpea-growing regions of West and Central Africa, based onhost differential response and genetic diversity analysis. Molecular markers linked to resistance to  different races of S. gesneriodes have been identified. It was desirable to demonstrate the applicability and efficiency for use in marker-assisted selection (MAS) to fast-track the development of cowpea for resistance to S. gesnerioides. The objective of the study was to determine the suitability of two molecular markers in tracking race-specific S. gesnerioides resistance in cowpea (SG3), the predominant race found in Nigeria. F2 mapping populations and recombinant inbred lines (RILs) derived from the cross involving IT97K-499-35 and a susceptible local landrace (Borno Brown), and another resistant parent B301 with the same susceptible land race (Borno Brown) were assayed using two linked markers. Genetic analysis showed that resistance to S. gesnerioides in cowpea is qualitatively inherited with single dominant gene action. Two SCAR markers, 61RM2 and C42-2B were validated in the same F2 populations and subsequent recombinant inbred lines (RILs). The two markers were able to discriminate between resistance and susceptibility and the genotypic score was quite similar to the phenotypic score with the markers score showing greater efficiency in selection than phenotypic score. The 61RM2 had two bands in resistant cultivars and amplified a ~450 bp fragment with marker efficiency of 98% while C42-2B amplified a single ~250 bp fragment with marker efficiency of 96% in resistant cultivars and absent in susceptible cultivars. The genetic distance between 61RM2 and phenotypic score was 3.5 cM while that of C42-2B and phenotypic score was 8.5 cM. The two marker data set were significantly correlated with the phenotypic data (r=0.95). Based on the tight linkage with the resistant locus, 61RM2 was found to be a utility marker to initiate MAS in cowpea breeding for resistance to S. gesnerioides.Key words: Cowpea, Striga, molecular marker, genetic distance, race-specific, obligate parasitic weed, Vigna unguiculata

Differential Brain Development with Low and High IQ in Attention-Deficit/Hyperactivity Disorder

Attention-Deficit/Hyperactivity Disorder (ADHD) and intelligence (IQ) are both heritable phenotypes. Overlapping genetic effects have been suggested to influence both, with neuroimaging work suggesting similar overlap in terms of morphometric properties of the brain. Together, this evidence suggests that the brain changes characteristic of ADHD may vary as a function of IQ. This study investigated this hypothesis in a sample of 108 children with ADHD and 106 typically developing controls, who participated in a cross-sectional anatomical MRI study. A subgroup of 64 children also participated in a diffusion tensor imaging scan. Brain volumes, local cortical thickness and average cerebral white matter microstructure were analyzed in relation to diagnostic group and IQ. Dimensional analyses investigated possible group differences in the relationship between anatomical measures and IQ. Second, the groups were split into above and below median IQ subgroups to investigate possible differences in the trajectories of cortical development. Dimensionally, cerebral gray matter volume and cerebral white matter microstructure were positively associated with IQ for controls, but not for ADHD. In the analyses of the below and above median IQ subgroups, we found no differences from controls in cerebral gray matter volume in ADHD with below-median IQ, but a delay of cortical development in a number of regions, including prefrontal areas. Conversely, in ADHD with above-median IQ, there were significant reductions from controls in cerebral gray matter volume, but no local differences in the trajectories of cortical development

Gender differences in the use of cardiovascular interventions in HIV-positive persons; the D:A:D Study

Peer reviewe

Biophysical interactions in tropical agroforestry systems

sequential systems, simultaneous systems Abstract. The rate and extent to which biophysical resources are captured and utilized by the components of an agroforestry system are determined by the nature and intensity of interac-tions between the components. The net effect of these interactions is often determined by the influence of the tree component on the other component(s) and/or on the overall system, and is expressed in terms of such quantifiable responses as soil fertility changes, microclimate modification, resource (water, nutrients, and light) availability and utilization, pest and disease incidence, and allelopathy. The paper reviews such manifestations of biophysical interactions in major simultaneous (e.g., hedgerow intercropping and trees on croplands) and sequential (e.g., planted tree fallows) agroforestry systems. In hedgerow intercropping (HI), the hedge/crop interactions are dominated by soil fertility improvement and competition for growth resources. Higher crop yields in HI than in sole cropping are noted mostly in inherently fertile soils in humid and subhumid tropics, and are caused by large fertility improvement relative to the effects of competition. But, yield increases are rare in semiarid tropics and infertile acid soils because fertility improvement does not offse

Safety and immunogenicity of the two-dose heterologous Ad26.ZEBOV and MVA-BN-Filo Ebola vaccine regimen in children in Sierra Leone: a randomised, double-blind, controlled trial

10.1016/S1473-3099(21)00128-6The Lancet Infectious Diseases221110-12

Safety and long-term immunogenicity of the two-dose heterologous Ad26.ZEBOV and MVA-BN-Filo Ebola vaccine regimen in adults in Sierra Leone: a combined open-label, non-randomised stage 1, and a randomised, double-blind, controlled stage 2 trial

10.1016/S1473-3099(21)00125-0The Lancet Infectious Diseases22197-10