Effects of sucrose sprays and darkness on aphid colonization of sugar beet and on aphid transmission of yellowing viruses

In the glasshouse, adult, apterous Myzus persicae (Sulz.) and Aphis fabae Scop, settled better and deposited more larvae on sucrose-sprayed sugar-beet plants than on water-sprayed plants. M. persicae settled badly and deposited few larvae on plants that were kept in the dark before or after infestation. The effects of darkness on aphids were reduced by spraying the host plants with 10% solutions of sucrose before infestation. Viruliferous M. persicae transmitted beet yellows virus (BYV) and beet mild yellowing virus (BMYV) less efficiently to dark-treated plants than to those grown in normal daylight. Spraying sugar beet with sucrose before inoculation with viruliferous M. persicae increased the proportion of successful BYV transmissions but only when the plants were dark-treated. The effects of sucrose and darkness on settling and larviposition of aphids and on virus transmission may be related to changes in the concentration of carbohydrates, particularly sugars, in the leaves.     

The use of monoclonal antibodies to detect beet mild yellowing virus and beet western yellows virus in aphids

Information on infectivity of the aphids which invade sugar beet root crops each Spring is required for forecasting incidence and providing advice on control of virus yellows. Monoclonal antibodies, produced in the USA to barley yellow dwarf virus (BYDV) and in Canada to beet western yellows virus (BWYV), were used to distinguish between sugar-beet-infecting strains of the luteovirus beet mild yellowing virus (BMYV), and the non-beet-infecting strains of the closely-related BWYV in plant and aphid tissue. Totals of 773 immigrant winged Myzuspersicae and 124 Macrosiphum euphorbiae were caught in water traps in a crop of sugar beet between 25 April and 5 August 1990. Using the monoclonal antibodies and an amplified ELISA, 67%M. persicae and 19%M. euphorbiae were shown to contain BWYV; 8%M. persicae and 7%M. euphorbiae contained BMYV. In studies with live winged aphids collected from the same sugar beet field during May, 25 of 60 M. persicae and two of 13 M. euphorbiae transmitted BWYV to the indicator host plant Montia perfoliata; two M. persicae and two M. euphorbiae transmitted BMYV. In another study three of 65 M. persicae and one of three M. euphorbiae in which only BWYV was detected, transmitted this virus to sugar beet.     

Inherited resistance of sugar beet to aphid colonization

Results of glasshouse experiments have confirmed that inbred lines of sugar beet differ in each of three types of resistance to Myzus persicae Sulz. and Aphis fabae Scop., namely: resistance to settling, resistance to multiplication, and tolerance. Resistance to multiplication was not invariably associated with resistance to settling, although plants of some lines showed both forms of resistance. Plants that were resistant to settling of alatae were not always resistant to apterae of the same species, and there was not a close relationship between resistance to M. persicae and to A. fabae. The mechanisms involved in resistance to aphids in sugar beet are not understood. Progenies of plants, selected for resistance to aphids from inbred lines, were often more resistant than progenies of unselected plants. Inheritance of each type of resistance is probably polygenic. The potential value of the different kinds of resistance, in reducing direct feeding damage and controlling the spread of virus yellows in the field, is discussed. The ultimate breeding objective is to produce commercial varieties in which appropriate kinds of resistance to aphids are combined with resistance to virus yellows. The use of such varieties would reduce the need to control aphids in the field by applications of chemicals.     

Studies on beet western yellows virus in oilseed rape (Brassica napus ssp. oleifera) and sugar beet (Beta vulgaris)

Oilseed rape (Brassica napus L. ssp. oleifera) was studied as a potential overwintering host for the sugar-beet yellowing viruses, beet yellows virus (BYV) and beet mild yellowing virus (BMYV), and their principal vector, Myzus persicae. In spring 1982, plants infected with a virus which reacted positively in enzyme-linked immunosorbent assay (ELISA) with BMYV antibody globulin were found in oilseed-rape crops; none of the plants contained virus which reacted with BYV antibody globulin. This virus was subsequently identified as beet western yellows virus (BWYV). No leaf symptoms could be consistently associated with infection of oilseed rape, but the virus was reliably detected by sampling any leaf on an infected oilseed-rape plant. Some isolates from oilseed rape did infect sugar beet in glasshouse tests, but the proportions of inoculated plants which became infected were low. Apparently there is therefore little danger of much direct transmission of BWYV by M. persicae from oilseed rape to sugar beet in spring. BWYV was introduced to and spread within oilseed-rape crops in autumn by M. persicae, and autumn-sown oilseed rape proved to be a potentially important overwintering host for M. persicae. In a survey of 80 autumn-sown crops of oilseed rape in East Anglia, northern England and Scotland in spring 1983, 78 were shown to be extensively infected with BWYV. Experimental plots of oilseed rape with 100% BWYV-infection yielded approximately 13.4% less oil than plots with 18% virus infection, the result of a decrease in both seed yield and oil content.     

Factors affecting the relative abundance of two coexisting aphid species on sugar beet

1 The two most common species of aphid colonizing sugar beet Beta vulgaris L. are Myzus persicae (Sulzer) (Hemiptera: Aphididae) and Aphis fabae Scopoli (Hemiptera: Aphididae). 2 M. persicae colonizes sugar beet earlier than A. fabae but the population of the former also declines earlier. Despite similar numbers of each species migrating at the time of colonization, M. persicae is usually less abundant on the crop than A. fabae, suggesting differences between the species in their selection of, and performance on, sugar beet. 3 The intrinsic rate of increase of both species declines as sugar beet matures, however, at any given plant age the intrinsic rate of increase of A. fabae is one and a half times greater than that of M. persicae. This results in more rapid population growth and a later decline of the population. 4 Intraspecific competition appears to result in M. persicae becoming very restless, but there is no evidence for interspecific competition between the two species on this host. 5 A population growth model which takes account of the decline in host quality of sugar beet shows that the M. persicae population peaks 30 days before that of A. fabae, and, excluding differences in emigration rate, the maximum A. fabae population is 14 times greater than the maximum M. persicae population. These results are compared to field data.     

Aphids from mangold clamps and their importance as vectors of beet viruses

Mangold clamps are over-wintering sources of the aphid-transmitted beet mosaic, beet yellows and beet mild yellowing viruses, and of several species of aphid, three of the most common in clamps being Myzus persicae, Rhopalosiphoninus staphyleae tulipaellus and R. latysiphon. This study attempted to assess the relative importance of the different species in spreading viruses from clamps. Compared with M. persicae, R. s. tulipaellus and R. latysiphon are seldom trapped in flight, except near large infestations. Alatae of M. persicae and R. s. tulipaellus become common in clamps in April, but few fly below 15d? C., a temperature seldom reached in eastern England in early spring. Flight muscle autolysis, which occurs later in R. s. tulipaellus and R. latysiphon than in some aphid species, also probably prevents many alatae in clamps from flying. We confirmed the importance of clamps as sources of beet viruses, the percentage of infected plants decreasing with increasing distance from infested clamps. M. persicae is shown to be a better vector of beet viruses than the other clamp aphids, and is probably responsible for most virus spread from clamps. R. s. tulipaellus did not transmit beet mosaic virus, but it is a fairly efficient vector of beet yellows and beet mild yellowing viruses, and, although we did not find this species on sugar beet in the field, it probably spreads these viruses from clamps. R. latysiphon did not transmit any of the viruses, and the role of Macrosiphum euphorbiae, Aulacorthum solani and Myxus ascalonicus is probably small.     

Probing by aphids in the leaf tissues of resistant and susceptible sugar beet

The probing of Aphis fabae and Myzus persicae in the leaves of sugar beet with inherited resistance or susceptibility to aphids was studied by microscopic examination of samples of whole leaves, prepared after 48 h exposure to adult aphids at approximately three aphids cm^-2.The density of saliva stylet-sheaths left by the aphids (cm^-2) and the proportion reaching phloem differed between sugar beet stocks and were inversely associated. Differences in resistance between stocks could not, however, be related directly to either. All beet stocks examined were probed freely. Seasonal differences in sugar beet grown in the glasshouse affected the proportion of sheaths reaching the phloem, but the differences between beet stocks were similar at all times.The densities of sheaths left by different clones of M. persicae corresponded with the aphids' response to sugar beet as a host plant. Among aphid clones which readily colonize sugar beet, the densities of stylet sheaths which reached phloem suggested that the adults of both A. fabae and M. persicae gained sufficient access to sieve tubes to satisfy their nutritional needs. The phloem of sugar beet from the glasshouse was always within the estimated maximum depth to which the aphids probe; but, in leaves from the field, it appeared that the phloem might be inaccessible to young M. persicae in the sugar beet crop during late summer.

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Zusammenfassung Das Proben von Aphis fabae und Myzus persicae in Blättern von Zuckerrüben mit erblicher Blattlausresistenz bzw.-anfälligkeit wurde untersucht durch mikroskopische Durchmusterung von Speichelscheiden in Proben von ganzen Blatt. Rübenblätter wurden mit genähert drei adulten Läusen cm^-2 besetzt und nach 48 Stunden quergeschnittene Streifen der Blätter in Alkohol fixiert, gefärbt und mit der Unterseite nach oben auf Objektträgern eingeschlossen.23890 Speichelscheiden wurden registriert. Die Dichte der Scheiden von M. persicae (cm^-2) und der Anteil der das Phloem erreichenden Scheiden (SRP) unterschieden sich signifikant zwischen den Rübenstämmen. Bei A. fabae ergaben sich entsprechende, aber nicht gesicherte Unterschiede. Scheidendichte und Prozentsatz SRP waren gegenläufig, zwei Rübenstämme zeigten eine hohe Scheidendichte, zwei andere hatten weniger Scheiden, aber einen höheren Prozentsatz SRP. Diese Gruppierung der Stämme korrespondierte aber nicht mit ihrer Blattlausresistenz. Aus der Scheidendichte ergab sich, dass M. persicae und A. fabae auf allen geprüften Rübenstämmen, resistenten und anfälligen, unbehindert probten, so dass jede Laus das Phloem durchschnittlich etwa viermal am Tag erreichte. Ein Klon von M. persicae, der sich an Rüben nicht entwickelt, hinterliess weniger Scheiden in den Blättern aller Stämme.Der Anteil von SRP war bei Prüfungen im März grösser als im November. Dieser Unterschied war besonders deutlich bei Scheiden von Larven, die im übrigen zu allen Zeiten das Phloem weniger oft erreichten als ihre Eltern. Messungen des Abstandes von der unteren Blattfläche zum Phloem ergaben, dass das Phloem den Läusen in Gewächshaus-Zuckerrüben immer zugänglich war. M. persicae-Larven konnten jedoch in Blättern von Freilandrüben das Phloem nicht erreichen.

     

Some effects of spraying with thiabendazole on the susceptibility of sugar beet to yellowing viruses and on their vector, Myzus persicae (Sulz.)

In a field experiment fewer sugar-beet plants became infected with aphid-transmitted yellowing viruses in plots that had been sprayed with solutions of thiabendazole lactate than in water-sprayed plots, after exposure to natural infestation with aphids. Subsequent glasshouse tests showed that foliar sprays of o·o1 % thiabendazole lactate in water significantly reduced the proportion of inoculated sugar-beet plants which became infected with beet yellows virus (BYV) or beet mild yellowing virus (BMYV) after inoculation with viruliferous Myzus persicae (Sulz.). This effect on virus transmission was not apparently due to a direct insecticidal action of thiabendazole, because adult aphids usually survived equally well on sprayed and unsprayed plants. Treatment of test plants with thiabendazole did not affect the transmission of beet mosaic virus to them by M. persicae. The fecundity of M. persicae was greatly reduced by transferring them to plants which had been sprayed with thiabendazole or by spraying them with thiabendazole before transfer to unsprayed plants. The fertility of adult Aphis fabae Scop, was also reduced by spraying with thiabendazole. The mechanisms whereby thiabendazole affected fecundity of aphids and transmission of viruses are not understood.     

Failure of British isolates of beet western yellows virus to infect potato

Potato cultivars were tested for susceptibility to two British isolates of beet western yellows virus originally obtained from sugar beet and oil seed rape. Neither isolate was transmitted by Myzus persicae to virus-free potato plants, either by itself or in association with potato leafroll virus.     

Occurrence of beet western yellows virus in sugar beet in Czechoslovakia

The beet western yellows virus (BWYV) was identified in sugar beet plants with leaf yellowing symptoms. When transmitted toSinapis alba L. the virus isolate caused severe symptoms of yellowing and violetting of the interveinal leaf tissue of this plant. By aphidsMyzus persicae (Sulz.) the virus isolate was transmitted toLactuca sativa L.,Raphanus sativus L. var.radicula Pers.,Baphanus sativus L. ssp.sativus L. ap., and toBrassica oleracea L. var.gemmifera DC. InLactuca sativa plants the virus induces a yellowing along with thickenning and brittleness of leaves and with mild dwarfing of the plants. InBaphanus sativus var.radicula andBaphanus sativus ssp.sativus plants it brings about a yellowing of the leaf margins with a change in consistency as was the case in lettuce, and inBrassica oleracea var.gemmifera it causes violet spots on the lower leaf sides. The transmission was proved in repeated experiments by a backtransmission to beet andSinapis alba and further transmission from beet toSinapis alba. The transmission of the virus isolate toVicia faba L.,Datura stramonium L., andPetunia hybrida hort. was unsuccessful. In the course of transmissions the isolate properties did not change. In its host range the virus resembles the Duffus’ strain 3 BWYV, isolated from beet in the U.S.A. This is the first characteristic of an Europian BWYV isolate, as obtained from naturally infected beet plants.     

Interactive effects of zinc and nickel on the glutathione system state in <Emphasis Type="Italic">Mimulus guttatus</Emphasis> plants

To determine whether the enhanced stress tolerance of ZnSO₄ with NiSO₄-treated Mimulus guttatus Fischer ex DC. plants was associated with the glutathione (GR-GSH) system, we investigated the changes in glutathione redox state (reduced (GSH), oxidized (GSSG) forms, total reduced (GSHt) glutathione, and GSH/GSSG ratio) and in the enzymatic activities of glutathione reductase (GR) and peroxidatic glutathione S-transferases (GST). The 6-week-old plants were grown in water culture during 4 weeks on a modified Rorison’s medium with ZnSO₄ (50, 100, and 200 μM) and NiSO₄ (20 and 80 μM) in a condition of separate or simultaneous supply of the components. Dry biomass accumulations of roots and shoots were not influenced by the examined treatments. The positive correlations between the total external concentrations of ZnSO₄ and NiSO₄ and the total Zn and Ni contents in roots and leaves were found. It was determined that the MDA content was higher in the ZnSO₄-treated plants than in the NiSO₄-treated ones. The supplementation of the ZnSO₄-treated plants with varied concentrations of NiSO₄ decreased the Zn-induced increase in the MDA levels. The inverse proportionality between the MDA and pigment levels in leaves was found. The Zn-Ni interactions were shown to induce the decreases in the GR activity, the total peroxidatic GST activity, and the GSH/GSSG ratio in roots. However, in leaves, the GR activity and the GSH/GSSG ratio were significantly increased and the total peroxidatic GST activity was decreased. The supplementation of the ZnSO₄-treated plants with varied concentrations of NiSO₄ restored the Zn-induced reduction in the GSHt levels in roots and decreased the Zn-induced increase in the GSSG levels in leaves, which resulted in more reduced state of the intracellular environment. It was likely to cause a decrease of the MDA level. Thus, our studies on the Zn?Ni interactions identified the antagonizing role of Ni in Zn toxicity by the GR-GSH system.     

Intraspecific variation of Myzus persicae on sugar beet (Beta vulgaris)

Differences in inherited resistance among seven sugar-beet stocks had similar effects on Myzus persicae clones representing the range of variation in aphid response to resistant and susceptible sugar beet observed in fifty-eight clones collected between 1969 and 1971. Three sugar-beet stocks were consistently resistant. Statistically significant interactions between beet stocks and aphid clones did not indicate the existence of biotypes with specific abilities to overcome resistance. M. persicae clones differed in their vigour of colonizing sugar beet, irrespective of the differences between beet stocks. The readiness of adult aphids to settle determined the size of aphid population produced and included a component related to the response of the aphid clone to sugar beet as a host, and a component related to the resistance ranking of the beet stock. Breeding sugar beet with resistance to aphids will be simplified, as the results indicate that, at present, differences between aphid biotypes need not be considered a problem.     

The influence of primary infection date and establishment of vector populations on the spread of yellowing viruses in sugar beet

In three field experiments in 1985 and 1986, we studied the effect of the date of primary infection on the spread of beet yellows closterovirus (BYV) and beet mild yellowing luteovirus (BMW) from artificially inoculated sugar beet plants. Laboratory-reared vector aphids, Myzus persicae, were placed on these sources of virus. There was no substantial natural immigration of vectors or viruses. In two experiments, one with BMYV in 1985 and the other in BYV in 1986, populations of vector aphids remained low and there was little virus spread, i.e. c. 50 infected plants from one primarily infected source. The cause of this small amount of spread was the low number of vector aphids. In the third experiment, with BYV in 1986, large populations of M. persicae developed and there was substantial virus spread: c. 2000 infected plants in the plots which were inoculated before canopy closure. In later-inoculated plots in the same experiment, there was much less spread: c. 100 infected plants per virus source plant. Differences between fields in predator impact are implicated as the most probable factor causing differences in vector establishment and virus spread between these three experiments. Virus spread decreased with later inoculation in all three experiments. A mathematical model of virus spread incorporating results from our work has been used to calculate how the initial proportion of infected plants in a crop affects the final virus incidence. This model takes into account the effect of predation on the development of the aphid populations. The processes underlying the spread and its timing are discussed.     

The occurrence of beet mild yellowing virus in Czechoslovakia

The occurrence of beet mild yellowing virus (BMYV) on feeding- and sugar-beet in Czechoslovakia has been proved. The virus was transmitted by aphidMyzus persicae (Sulz.) on indicator plantsSinapis alba L.,Capsella bursa-pastoris Medik, andClaytonia perfoliata Donn and from these plants back to sugar-beet cv. ‘Dobrovická A.’ A weed plantRaphanus raphanistrum L. was identified as a new natural host plant of BMYV. The virus was identified in ten of twelve biologically examined samples of beet with BMYV-like symptoms, which were collected at various places in Czechoslovakia     

Comparison of ethanol production by Zymomonas mobilis from sugar beet substrates

Summary The potential of four sugar beet substrates from the sugar industry [syrup (S), crystallizer effluent 1 (CE1), crystallizer effluent 2 (CE2) and molasses (M)] were compared for ethanol production using an osmotolerant mutant strain of the bacterium Zymomonas mobilis. Sucrose of the substrates was enzymatically hydrolysed to avoid levan formation during fermentation. Nutrient supplementation experiments have shown that reproducible growth and ethanol production could be obtained on the four substrates supplemented only with magnesium sulphate (CE2 and M) or additionally with ammonium sulphate (S and CE1). Thus, addition of costly yeast extract could be avoided. All 20% (w/v) substrates showed nearly complete sugar conversion (>94.9%), good growth (0.16 h^–1) and ethanol production (>40 g 1^–1). However, sorbitol formation reduced the ethanol yield (73–79% of the theoretical value) significantly. Batch kinetic parameters and studies of instantaneous parameters showed that enhanced osmolality of substrates (SZ. mobilis with appropriate supplementation. Offprint requests to: J. Baratti     

The effect of plant age and infection with virus yellows on the survival of Myzus persicae on sugar beet

Survival of Myzus persicae confined in clip-cages on mature leaves of sugar beet declined as the plants aged. Death of aphids was often preceded by the appearance of a black deposit in the aphids' stomachs, which may have been the cause of death. Both the rate of death and the proportion of aphids dying with black deposits was significantly less when plants were infected with beet yellows virus or beet mild yellowing virus, by comparison with healthy plants. The implication of these phenomena on the onset of mature plant resistance is discussed.     

Rates of growth and increase ofMyzus persicae on virus-infected potatoes according to type of virus-vector relationship

Growth, reproduction and survival (=performance) of the aphidMyzus persicae Sulzer was measured on virus-free and virus-infected potato plants The principle objective was to evaluate if various viral infections affected aphid performance differently, and if so, whether any order in the performance response of the aphid was discernible according to the type of virus-vector relationship. Three viruses varying in their dependency onM. persicae as a vector were used. Plants infected with potato leafroll virus (PLRV), a circulative virus highly dependent uponM. persicae for dispersal and transmission, were superior hosts as determined by the significantly greater mean relative growth rate (MRGR) and intrinsic rate of increase (r_m) ofM. persicae compared with those of aphids reared on other plants. Plants infected with potato virus Y, a noncirculative virus less dependent uponM. persicae for dispersal than PLRV, were intermediate in their quality based upon intermediate MRGR and r_m values. Plants infected with potato virus X, a nonvectored virus independent ofM. persicae, were least suitable hosts along with the group of virus-free plants according to the lower MRGR and r_m values.     

Forecasting the incidence of virus yellows in sugar beet in England

A new forecasting system for virus yellows incidence in sugar beet in the UK has been devised using multiple regression analyses. The forecast equations include data on (1) the previous year's virus incidence, (2) temperature in January and February and (3) the timing of the spring migration of Mytus persicae. Forecasts using the first two of these variables account for 63% of the variance in virus incidence in the main beet growing area of Eastern England and give growers information in time to decide on whether to apply aphicidal granules at drilling to control the vectors of the disease. Forecasts using all three variables account for 87% of the variance in virus incidence and can forewarn growers and the sugar industry of the likelihood of an epidemic. Forecasts for the northern and western regions of the beet growing area are derived from the forecast for the eastern region.     

Genetic approaches to sustainable pest management in sugar beet (Beta vulgaris)

Sugar beet (Beta vulgaris) is an important arable crop, traditionally used for sugar extraction, but more recently, for biofuel production. A wide range of pests, including beet cyst nematode (Heterodera schachtii), root‐knot nematodes (Meloidogyne spp.), green peach aphids (Myzus persicae) and beet root maggot (Tetanops myopaeformis), infest the roots or leaves of sugar beet, which leads to yield loss directly or through transmission of beet pathogens such as viruses. Conventional pest control approaches based on chemical application have led to high economic costs. Development of pest‐resistant sugar beet varieties could play an important role towards sustainable crop production while minimising environmental impact. Intensive Beta germplasm screening has been fruitful, and genetic lines resistant to nematodes, aphids and root maggot have been identified and integrated into sugar beet breeding programmes. A small number of genes responding to pest attack have been cloned from sugar beet and wild Beta species. This trend will continue towards a detailed understanding of the molecular mechanism of insect–host plant interactions and host resistance. Molecular biotechnological techniques have shown promise in developing transgenic pest resistance varieties at an accelerated speed with high accuracy. The use of transgenic technology is discussed with regard to biodiversity and food safety.     

Decolorization of beet molasses vinasse by Bacillus megaterium ATCC 14581

Beet molasses vinasse is formed in large quantities as a waste product of the distillery industry, where the molasses derived from sugar beet is used as a raw material. This vinasse has a dark color, low pH, and chelating properties. Many microorganisms have the ability to decolorize and biodegrade beet molasses vinasse. In this work, different cultivation parameters (the type of the bacterial culture; static or agitated) and medium components ((NH₄)₂SO₄, KH₂PO₄, yeast extract, glucose, and peptone, and the vinasse concentration) were evaluated utilizing Plackett-Burman design to identify the important factors influencing the vinasse decolorization by Bacillus megaterium ATCC 14581. The significant variables were selected as follows: (NH₄)₂SO₄, KH₂PO₄, glucose, and the concentration of vinasse. These four factors should be chosen as being promising for further optimization studies. The maximum color removal was 38%.