H. G. Smith

Biological, Serological, and Molecular Variability Suggest Three Distinct Polerovirus Species Infecting Beet or Rape

Yellowing diseases of sugar beet can be caused by a range of strains classified as Beet mild yellowing virus (BMYV) or Beet western yellows virus (BWYV), both belonging to the genus Polerovirus of the family Luteoviridae. Host range, genomic, and serological studies have shown that isolates of these viruses can be grouped into three distinct species. Within these species, the coat protein amino acid sequences are highly conserved (more than 90% homology), whereas the P0 sequences (open reading frame, ORF 0) are variable (about 30% homology). Based on these results, we propose a new classification of BMYV and BWYV into three distinct species. Two of these species are presented for the first time and are not yet recognized by the International Committee on Taxonomy of Viruses. The first species, BMYV, infects sugar beet and Capsella bursa-pastoris. The second species, Brassica yellowing virus, does not infect beet, but infects a large number of plants belonging to the genus Brassica within the family Brassicaceae. The third species, Beet chlorosis virus, infects beet and Chenopodium capitatum, but not Capsella bursa-pastoris.

The effects of drought on sugar beet growth in isolation and in combination with beet yellows virus infection

The effect of drought stress in isolation, or in combination with beet yellows virus infection, on sugar beet growth was studied in the field and glasshouse. Drought reduced total plant weight by 26%, due to 20 and 29% reductions in foliage and storage root yields respectively. Sugar extraction efficiency was depressed by an increase in amino-nitrogen impurities. Drought did not limit water extraction depth, despite decreasing lateral root growth in proportion to total weight. During the field experiments, total crop cover was decreased in all the droughted treatments (halved in some cases) for at least part of the season. Consequently, these treatments intercepted 12% less light, which in combination with a 16% decrease in the dry matter/light conversion coefficient, led to the decrease in growth. The decrease in conversion coefficient was due to temporary closure of the stomata rather than a function of drought-induced damage to the photosynthetic mechanism. The absolute effect of drought remained the same irrespective of whether the plants were infected with beet yellows virus, i.e. there was no interaction between the two stresses. The reasons for this lack of interaction are discussed but it is likely that the stress effects were mediated at different times of the day and season.

In vitro culture of petioles and intact leaves of sugar beet (Beta vulgaris)

Methods are described for obtaining explants which produce adventitious shoots, for subsequent stimulation of rooting and then transplanting using six commercial sugar-beet cultivars. The rate of adventitious shoot regeneration from petioles or intact leaf explants was affected by the source of donor plants, cytokinin type (BAP or Kin) and concentration and cultivar. Increasing the sucrose concentration of the medium from 3% to 5% or 8% had no apparent effect. Adventitious shoots could be produced directly from callus formed on the base of the petioles. In general adventitious shoots were produced on either the concave surface of the petiole or from the callus, occasionally simultaneously on both, and on the convex surface of the petiole in intact leaf explants. The highest rooting rate with 3% sucrose and 1.0 mg l−1 NAA was obtained using half-strength MS medium. There was considerable variation in the propagules from petioles or callus indicating that this system may provide valuable somaclonal variation.

The use of radiation interception and transpiration to predict the yield of healthy, droughted and virus-infected sugar beet

This paper reports an analysis of the yield of sugar beet crops grown under experimental conditions between 1993 and 1995 in the UK. Crops were either healthy (unstressed) or subjected to drought, infection with Beet yellows virus (BYV) or a combination of both. The study investigated whether the large differences in yield between the crops grown in different seasons and subjected to different stresses could be accounted for by simple relationships between total biomass and radiation interception (e s ), transpiration (e w ) or e s and e w adjusted for mean saturation deficit (Ω s and Ω w respectively). Mean values of e s , e w , Ω s and Ω w in healthy crops were 1.42 g/MJ, 0.89 g/kg, 6.76 g/kPa/MJ and 4.29 g/kPa/kg respectively. Variations in the dry matter yield between seasons were best accounted for by Ω u and less well by e u or e s . Ω s accounted for least variation in yield between seasons. None of these relationships remained constant in stressed plants; both drought and BYV-infection decreased e s (and Ω s ) but Ω u was increased by drought and decreased by BYV-infection. However, in common with healthy crops, seasonal variation in yields was best accounted for by Ω w . Mean values of e s , Ω s , e w and Ω w for all healthy, infected and droughted crops accounted for 61, 50, 88 and 97% of the variation in dry matter yield between experiments respectively. Accurate prediction of the yield of stressed plants requires a knowledge of their infection and drought status. If this information is unavailable then the mean value of Ω w for healthy, infected and droughted crops will provide a reasonable prediction of the yield of such crops.

Micropropagation of wild beet (Beta maritima) from inflorescence pieces

In order to investigate the regeneration of wild beet (Beta maritima) from inflorescence pieces, the effects of growth regulator, genotype, explant source and stage of plant development on adventitious shoot formation and rooting in vitro and subsequent transplanting in the glasshouse were tested. Inflorescence tips produced more adventitious shoots than sub-apical segments and the best micropropagation was achieved on a Murashige and Skoog (MS) medium supplemented with 1.0 mg l−1 BAP. Addition of auxin was not beneficial. The induction rate of adventitious shoots was genotype-dependent and influenced by the stage of plant development. Adventitious shoots were produced from the base of the flower buds, i.e. from the receptacle, not from axils or stalks and only a few buds on inflorescence tip explants produced adventitious shoots. Rooting was increased by using a MS medium with 3% sucrose supplemented with 1.0 mg l−1 NAA. There was no variation in leaf morphology of the transplants. This work shows that inflorescence tips can be used successfully as explants for in vitro multiplication of sugar beet and wild beet.