Many farmers in West and Central Africa (WCA) prefer tall (>3 m) grain sorghum [Sorghum bicolor (L.) Moench] for various reasons. This study seeks to determine (i) what yield superiority newly bred, tall, photoperiod‐sensitive guinea‐race sorghum hybrids can provide relative to an adapted landrace variety across a wide range of productivity conditions, and (ii) the risk of these hybrids failing to provide yield superiority for individual farmers. Seven hybrids, one local check, and eight pure‐line progenies were evaluated in 37 farmer‐managed, on‐farm yield trials across three Malian zones and 3 yr. Environments were classified into four productivity groups (low [0.78–1.10 Mg ha−1], mid‐low [1.10–1.50 Mg ha−1], mid‐high [1.50–2.00 Mg ha−1] and high [2.00–2.65 Mg ha−1]) based on their trial mean grain yield. Mean yields of the seven tall hybrids were 3 to 17% (ranging from 0.06 to 0.28 Mg ha−1) higher than that of the local check across all environments and were highest (14–47%) averaged across the seven trials with the lowest mean yields. The individual overall highest‐yielding hybrid showed superiorities over the local check in the low, mid‐low, mid‐high, and high productivity levels of 0.43 (47%), 0.14 (10%), 0.47 (27%), and 0.34 (14%) Mg ha−1, respectively. The tall hybrids rarely had yields significantly inferior to the local check. Farmers’ preference for, and the possible benefits of, taller plant types may lead farmers to grow tall hybrids, particularly under the typical low‐productivity production conditions of WCA.
Potato virus Y (PVY) and Phytophthora infestans (Mont.) de Bary that causes potato late blight (LB), pose serious constraints to cultivated potatoes due to significant yield reduction, and phenotyping for resistance remains challenging. Breeding operations for vegetatively propagated crops can lead to genotype mislabeling that, in turn, reduces genetic gains. Low-density and low-cost molecular marker assessment for phenotype prediction and quality control is a viable option for breeding programs. Here, we report on the development of kompetitive allele specific PCR (KASP) markers for LB and PVY resistance, and for routine quality control assessment of different breeding populations. Two KASP markers for LB resistance and two for PVY Ryadg were validated with an estimated assay power that ranged between 0.65 and 0.88. The developed QC KASP markers demonstrated the capability of discriminating tetraploid calls in breeding materials, including full-sibs and half-sibs. Routine implementation of the developed markers in a breeding program would assist with better allocation of resources and enable precise characterization of breeding material, thereby leading to increased genetic gains.
S orghum bicolor (L.) Moench is a major staple cereal crop in the Sahelian and savannah zones of West Africa (WA), where it constitutes the main cereal in the diet of millions, mostly living in rural areas. Yields on farmers' fields average only 100 g m −2 (1 t ha −1 ) (FAOSTAT, 2018), despite the development of new varieties (Yapi et al., 2000;Atokple, 2003). In recent years, farmers in the savannah zones of WA have replaced sorghum with early-maturing maize (Zea mays L.) varieties, especially in cotton (Gossypium hirsutum L.)-producing systems, where fertilizer is easily available (Staatz et al., 2011;Theriault et al., 2018). However, area under sorghum has been increasing in these countries (FAOSTAT, 2018), because sorghum is the cereal crop that can be grown successfully without the use of mineral fertilizer. Thus, new sorghum varieties can provide advantages to farmers, especially if they are well adapted to low soil fertility, especially low-P (LP) conditions. This is particularly important
Key message Major A 1 cytoplasm fertility restoration loci, Rf 2 and Rf 5 , were found in the West African sorghum. A potential causative mutation for Rf 2 was identified. KASP markers were validated on independent material. AbstractTo accelerate the identification and development of hybrid parental lines in West African (WA) sorghum, this study aimed to understand the genetics underlying the fertility restoration (Rf) in WA A1 cytoplasmic male sterility system and to develop markers for a routine use in WA breeding programs. We genotyped by sequencing three F2 populations to map the Rf quantitative trait loci (QTL), validated the molecular KASP markers developed from those QTL in two F2:3 populations, and assessed the most promising markers on a set of 95 R- and B-lines from WA breeding programs. Seven QTL were found across the three F2 populations. On chromosome SBI-05, we found a major fertility restorer locus (Rf5) for two populations with the same male parent, explaining 19 and 14% of the phenotypic variation in either population. Minor QTL were detected in these two populations on chromosomes SBI-02, SBI-03, SBI-04 and SBI-10. In the third population, we identified one major fertility restorer locus on chromosome SBI-02, Rf2, explaining 31% of the phenotypic variation. Pentatricopeptide repeat genes in the Rf2 QTL region were sequenced, and we detected in Sobic.002G057050 a missense mutation in the first exon, explaining 81% of the phenotypic variation in a F2:3 population and clearly separating B- from R-lines. The KASP marker developed from this mutation stands as a promising tool for routine use in WA breeding programs.Electronic supplementary materialThe online version of this article (10.1007/s00122-018-3161-z) contains supplementary material, which is available to authorized users.
The ability to stay-green (SG) in later stages of the crop cycle is a valuable trait for plants cultivated in standard or stressful environments. Few QTLs studies for SG have been conducted in temperate maize, apart from some experiments carried out with Chinese lines. The aim of our study was to identify QTLs related to SG in temperate maize using PHG39, an important SG line in private breeding. We developed two large F 2 mapping populations by crossing PHG39 to the no stay-green (NSG) lines B73 (Corn Belt Dent) and EA1070 (European Flint). Samples of individuals of the extreme tails (high and low) of the populations for visual score were genotyped. We found an association between markers and SG in three regions at bins 1.
Cytoplasmic male sterility (CMS) in potato is a common reproductive issue in late blight breeding programs since resistant sources usually have a wild cytoplasmic background (W or D). Nevertheless, in each breeding cycle male fertile lines have been observed within D- and T-type cytoplasms, indicating the presence of a fertility restorer (Rf) mechanism. Identifying sources of Rf and complete male sterility to implement a CMS–Rf system in potato is important since hybrid breeding is a feasible breeding strategy for potato. The objective of this study was to identify male fertile breeding lines and potential Rf candidate lines in the CIP late blight breeding pipeline. We characterized male fertility/sterility-related traits on 142 breeding lines of known cytoplasmic type. We found that pollen viability is not a reliable estimate of male sterility in diverse backgrounds. Breeding lines of the T-type cytoplasmic group had higher levels of male fertility than breeding lines of the D-type cytoplasmic group. With the help of pedigree records, reproductive traits evaluations and test crosses with female clones of diverse background, we identified four male parental lines segregating for Rf and three female parental lines that generated 100% male sterile progeny. These identified lines and generated test cross progenies will be valuable to develop validation populations for mitochondrial or nuclear markers for the CMS trait and for dihaploid generation of Rf+ lines that can be later employed in diploid hybrid breeding.
Sweet potato virus disease (SPVD) is a global constraint to sweetpotato (Ipomoea batatas) production, especially under intensive cultivation in the humid tropics such as East Africa. The objectives of this study were to develop a precision SPVD phenotyping protocol, to find new SPVD-resistant genotypes, and to standardize the first stages of screening for SPVD resistance. The first part of the protocol was based on ELISA results for sweet potato chlorotic stunt virus (SPCSV) and sweet potato virus C (SPVC) with adjustments to a negative control (uninfected clone ‘Tanzania’) and was performed on a pre-breeding population (VZ08) comprising 455 clones and 27 check clones graft-inoculated under screenhouse conditions. The second part included field studies with 52 selected clones for SPCSV resistance from VZ08 and eight checks. In screenhouse conditions, the resistant and susceptible check clones performed as expected, 63 clones from VZ08 exhibited lower relative absorbance values for SPCSV and SPVC than inoculated check Tanzania. Field experiments confirmed SPVD resistance of several clones selected by relative absorbance values (nine resistant clones in two locations, i.e. 17.3% of the screenhouse selection), supporting the reliability of our method for SPVD-resistance selection. Two clones were promising, exhibiting high storage root yields of 28.7–34.9 t ha−1 and SPVD resistance, based on the proposed selection procedure. This modified serological analysis for SPVD-resistance phenotyping might lead to more efficient development of resistant varieties by reducing costs and time at early stages, and provide solid data for marker assisted selection with a quantitative tool for classifying resistance.
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