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African dry and starchy (DS) orange-fleshed sweetpotato [Ipomoea batatas (L.) Lam] (OFSP) cultivars, distinct from American moist or medium dry and sweet OFSP, have potential to fight vitamin A deficiency (VAD) in the world. This study assessed the genotype X environment (G X E) interactions in multienvironment trials (METs), the genetic correlations for total root yield (TYLD), biomass (BIOM), harvest index (HI), root dry matter (RDM), root starch (RST), root sucrose (RSU), root β-carotene, (RBC), root Fe (RFE), root Zn (RZN), root Ca (RCA), and root Mg (RMG) and the potential contributions of the cultivars to fight VAD and mineral deficiencies. Nine DS OFSP cultivars, (Ejumula, Zambezi, Carrot_C, Kakamega, KMI61, Abuket_1, SPK004/6/6, SPK004/6 and Naspot_5/50) and a medium dry and sweet OFSP cultivar (Resisto) were tested in METs in Uganda. The components were smaller than σ2G components for HI, RDM, RST, RSU, and RBC, making it possible to ably select for the traits in the early stages. The σ2GXE components were larger than σ2G components for TYLD and mineral traits. Thus, like yield, breeding for mineral traits in sweetpotato is complex, requiring prior data on the causes of the G X E interactions. Medium to high positive correlations among mineral traits favor parallel selection, and it merits further study to efficiently improve the mineral trait complex by an index. Clearly, a 50- to 100-g ration of all the cultivars, except Naspot_5/50, can provide 100% recommended dietary allowance of vitamin A for a 5- to 8-yr-old child. [ABSTRACT FROM AUTHOR]

The present study evaluated selected East African (EA) sweetpotato varieties for storage root dry matter and nutrient content and obtained information on the potential contributions of the varieties to alleviate vitamin A and mineral deficiencies. Roots obtained from 89 farmer (white- and orange-fleshed) varieties and one introduced variety ('Resisto') were analyzed for storage root quality using near-infrared reflectance spectroscopy technology. Location differences were only significant for starch content. The σG² variance was significant (P < 0.01) for all the traits except sucrose content. Overall, the farmer varieties had higher dry matter, higher starch, and lower sucrose contents than the control clone, 'Resisto'. It is these qualities that make sweetpotato attractive as a starchy staple in EA. A low population's mean β-carotene content (19.0 ppm) was observed. However, deep orange-fleshed farmer varieties, 'Carrot_C', 'Ejumula', 'Carrot Dar', 'Mayai', and 'Zambezi', had β-carotene content that can meet 350% or greater of recommended daily allowance (RDA) with 250-g serving to a 5- to 8-year-old child. More but light orange-fleshed farmer varieties 'K-118', 'K-134', 'K-46', 'KMI61', 'MLE162 Nakahi', 'PAL161', 'Sowola6', 'Sponge', 'SRT34 Abuket2', 'SRT35 Anyumel', 'SRT52', and 'Sudan' can provide 50% to 90% RDA of pro-vitamin A for the child. The root minerals' content was generally low except for magnesium whose content can meet 50% or greater RDA in many farmer varieties. However, in areas with high sweetpotato consumption, varieties 'Carrot_C', 'Carrot Dar', 'KRE nylon', 'MLE163 Kyebandula', and 'SRT49 Sanyuzameza' can make good intakes of iron, zinc, calcium, and magnesium. In conclusion, some EA farmer varieties can contribute greatly to alleviation of vitamin A deficiency and substantial mineral intakes. [ABSTRACT FROM AUTHOR]

The most important potato viruses in Uganda are Potato virus Y (PVY), Potato leafroll virus (PLRV), Potato virus X (PVX), Potato virus S (PVS), Potato virus A (PVA) and Potato virus M (PVM). Utilization of R genes in breeding for resistance to viruses has not been explored in Uganda due to limited information on the prevalence of R genes in the available genotypes. This study aimed at identifying potato genotypes with R genes for resistance to potato viruses important in Uganda. The study screened 71 potato accessions from the National Potato Breeding Programme at Kachwekano Zonal Agricultural Research and Development Institute for the presence of resistance genes to viruses using diagnostic molecular markers. The results indicated that 21 out of 71 genotypes had resistance markers, of which nine genotypes, NKRN59.58, Derby, Markies, Sifra, 395017.229, Nakpot 5, 20108.5, Royal and 393220.54, had Ryadg gene for PVY resistance and two genotypes, Kimuri and 319919.3, had Rysto gene for resistance to PVY and PVA. Nine genotypes, 395011.2, Markies, Nakpot 5, 20108.5, Sifra, 20157.6, Royal, 2015.8 and Ambition, had the Nbtbr gene for resistance to PVX. In addition, 14 genotypes, 395011.2, Markies, Nakpot 5, Sarpouna, 393220.54, 391046.14, Sarpomira, 395077.12, Sifra, 20157.6, Royal, Ambition, Kimuri and Caruso, had the Nsadg gene conferring resistance to PVS. Four genotypes, Markies, Sifra, Nakpot 5 and Royal, had the Ryadg, Nbtbr and Nsadg genes for combined resistance to PVY, PVX and PVS. The resistant genotypes could be used as parents to introgress resistance genes into susceptible cultivars. [ABSTRACT FROM AUTHOR]

Sweetpotato (Ipomoea batatas) is a widely grown food crop, in which the most important diseases are caused by viruses. Genetic variability of three widely distributed sweetpotato viruses was analysed using data from 46 isolates ofSweet potato feathery mottle virus(SPFMV), 16 isolates ofSweet potato mild mottle virus(SPMMV) and 25 isolates ofSweet potato chlorotic stunt virus(SPCSV), of which 19, seven and six isolates, respectively, are newly characterized. Division of SPFMV into four genetic groups (strains) according to phylogenetic analysis of coat protein (CP) encoding sequences revealed that strain EA contained the East African isolates of SPFMV but none from elsewhere. In contrast, strain RC contained ten isolates from Australia, Africa, Asia and North America. Strain O contained six heterogeneous isolates from Africa, Asia and South America. The seven strain C isolates from Australia, Africa, Asia, and North and South America formed a group that was genetically distant from the other SPFMV strains. SPMMV isolates showed a high level of variability with no discrete strain groupings. SPCSV isolates from East Africa were phylogenetically distant to SPCSV isolates from elsewhere. Only from East Africa were adequate data available for different isolates of the three viruses to estimate the genetic variability of their local populations. The implications of the current sequence information and the need for more such information from most sweetpotato-growing regions of the world are discussed in relation to virus diagnostics and breeding for virus resistance. [ABSTRACT FROM AUTHOR]

Spatial and temporal expression patterns of the sbeII and sbeI genes, encoding starch branching enzyme II and I, respectively, in cassava (Manihot esculenta Crantz) were studied at different phenological stages of the crop. A partial cDNA for sbeII in cassava was cloned and used along with a cDNA-specific fragment of sbeI. As the cassava plant aged, the transcriptional activity of the sbeII and sbeI genes in the underground storage roots increased, whereas the activity in other organs remained the same or declined. At 180 days after planting (d.a.p.), levels of sbeII and sbeI transcripts in storage roots were very low, whereas at 360 d.a.p., the levels had increased dramatically. The 360 d.a.p. old storage roots also accumulated gbssII and gbssI transcripts, as well as a longer gbssI transcript, gbssI′. The difference between the gbssI and gbssI′ transcripts was shown to be due to differential splicing, whereby the gbssI′ transcript retained the first three introns. Unexpectedly, expression of sbeII and sbeI in the 360 d.a.p. storage roots exhibited fluctuations during the 24 h cycle, both under the normal light/dark regime and under continuous light or continuous dark conditions. [Copyright &y& Elsevier]

Background:The bipartite single-stranded RNA genome of Sweet potato chlorotic stunt virus (SPCSV, genus Crinivirus; Closteroviridae) encodes a Class 1 RNase III (RNase3), a putative hydrophobic protein (p7) and a 22-kDa protein (p22) from genes located in RNA1. RNase3 and p22 suppress RNA silencing, the basal antiviral defence mechanism in plants. RNase3 is sufficient to render sweetpotato (Ipomoea batatas) virus-susceptible and predisposes it to development of severe diseases following infection with unrelated virus. The incidence, strains and gene content of SPCSV infecting wild plant species have not been studied. Methodology/Principal Findings:Thirty SPCSV isolates were characterized from 10 wild Ipomoea species, Hewittia sublobata or Lepistemon owariensis (family Convolvulaceae) in Uganda and compared with 34 local SPCSV isolates infecting sweetpotatoes. All isolates belonged to the East African (EA) strain of SPCSV and contained RNase3 and p7, but p22 was not detected in six isolates. The three genes showed only limited genetic variability and the proteins were under purifying selection. SPCSV isolates lacking p22 synergized with Sweet potato feathery mottle virus (SPFMV, genus potyvirus; Potyviridae) and caused severe symptoms in co-infected sweetpotato plants. One SPCSV isolate enhanced accumulation of SPFMV, but no severe symptoms developed. A new whitefly-transmitted virus (KML33b) encoding an RNase3 homolog (<56% identity to SPCSV RNase3) able to suppresses sense-mediated RNA silencing was detected in I. sinensis. Conclusions/Significance:SPCSV isolates infecting wild species and sweetpotato in Uganda were genetically undifferentiated, suggesting inter-species transmission of SPCSV. Most isolates in Uganda contained p22, unlike SPCSV isolates characterized from other countries and continents. Enhanced accumulation of SPFMV and increased disease severity were found to be uncoupled phenotypic outcomes of RNase3-mediated viral synergism in sweetpotato. A second virus encoding an RNase3-like RNA silencing suppressor was detected. Overall, results provided many novel and important insights into evolutionary biology of SPCSV. [ABSTRACT FROM AUTHOR]