Spread of potato leafroll virus is decreased from plants of potato clones in which virus accumulation is restricted

Tubers of eight potato clones infected with potato leafroll luteovirus (PLRV) were planted as ‘infectors’ in a field crop grown, at Invergowrie, of virus-free potato cv. Maris Piper in 1989. The mean PLRV contents of the infector clones, determined by enzyme-linked immunosorbent assay (ELISA) of leaf tissue, ranged from c. 65 to 2400 ng/g leaf. Myzus persicae colonised the crop shortly after shoot emergence in late May and established large populations on all plants, exceeding 2000/plant by 27 June. Aphid infestations were controlled on 30 June by insecticide sprays. Aphid-borne spread of PLRV from plants of the infector clones was assessed in August by ELISA of foliage samples from the neighbouring Maris Piper ‘receptors’. Up to 89% infection occurred in receptor plots containing infector clones with high concentrations of PLRV. Spread was least (as little as 6%) in plots containing infectors in which PLRV concentrations were low. Primary PLRV infection in guard areas of the crop away from infectors was 4%. Some receptor plants became infected where no leaf contact was established with the infectors, suggesting that some virus spread may have been initiated by aphids walking across the soil.     

Quantitative studies on the uptake and retention of potato leafroll virus by aphids in laboratory and field conditions

Enzyme-linked immunosorbent assay (ELISA) was adapted for the efficient detection and assay of potato leafroll virus (PLRV) in aphids. Best results were obtained when aphids were extracted in 0.05 M phosphate buffer, pH 7.0, and the extracts incubated at 37 °C for 1 h before starting the assay. Using batches of 20 green peach aphids (Myzus persicae), about 0.01 ng PLRV/aphid could be detected. The virus could also be detected in single aphids allowed a 1-day acquisition access period on infected potato leaves. The PLRV content of aphids depended on the age of potato source-plants and the position of source leaves on them. It increased with increase in acquisition access period up to 7 days but differed considerably between individual aphids. A maximum of 7 ng PLRV/aphid was recorded but aphids more usually accumulated about 0.2 ng PLRV per day. When aphids were allowed acquisition access periods of 1–3 days, and then caged singly on Physalis floridana seedlings for 3 days, the PLRV content of each aphid, measured subsequently, was not strongly correlated with the infection of P. floridana. The concentration of PLRV in leaf extracts differed only slightly when potato plants were kept at 15, 20, 25 or 30 °C for 1 or 2 wk, but the virus content of aphids kept on leaves at the different temperatures decreased with increase of temperature. PLRV was transmitted readily to P. floridana at all temperatures, but by a slightly smaller proportion of aphids, and after a longer latent period, at 15 °C than at 30 °C. The PLRV content of M. persicae fed on infected potato leaves decreased with increasing time after transfer to turnip (immune to PLRV). The decrease occurred in two phases, the first rapid and the second very slow. In the first phase the decrease was faster, briefer and greater at 25 and 30 °C than at 15 and 20 °C. No evidence was obtained that PLRV multiplies in M. persicae. These results are compatible with a model in which much of the PLRV in aphids during the second phase is in the haemocoele, and transmission is mainly limited by the rate of passage of virus particles from haemolymph to saliva. The potato aphid, Macrosiphum euphorbiae, transmitted PLRV much less efficiently than M. persicae. Its inefficiency as a vector could not be ascribed to failure to acquire or retain PLRV, or to the degradation of virus particles in the aphid. Probably only few PLRV particles pass from the haemolymph to saliva in this species. The virus content of M. euphorbiae collected from PLRV-infected potato plants in the field increased from early June to early July, and then decreased. PLRV was detected both in spring migrants collected from the plants and in summer migrants caught in yellow water-traps. PLRV was also detected in M. persicae collected from infected plants in July and August, and in trapped summer migrants, but their PLRV content was less than that of M. euphorbiae, and in some instances was too small for unequivocal detection.     

Infection of potato plants with potato leafroll virus changes attraction and feeding behaviour of Myzus persicae

Potato leafroll virus (PLRV; genus Polerovirus, family Luteoviridae) is a persistently transmitted circulative virus that depends on aphids for spreading. The primary vector of PLRV is the aphid Myzus persicae (Sulzer) (Homoptera: Aphididae). Solanum tuberosum L. potato cv. Kardal (Solanaceae) has a certain degree of resistance to M. persicae: young leaves seem to be resistant, whereas senescent leaves are susceptible. In this study, we investigated whether PLRV‐infection of potato plants affected aphid behaviour. We found that M. persicae's ability to differentiate headspace volatiles emitted from PLRV‐infected and non‐infected potato plants depends on the age of the leaf. In young apical leaves, no difference in aphid attraction was found between PLRV‐infected and non‐infected leaves. In fact, hardly any aphids were attracted. On the contrary, in mature leaves, headspace volatiles from virus infected leaves attracted the aphids. We also studied the effect of PLRV‐infection on probing and feeding behaviour (plant penetration) of M. persicae using the electrical penetration graph technique (DC system). Several differences were observed between plant penetration in PLRV‐infected and non‐infected plants, but only after infected plants showed visual symptoms of PLRV infection. The effects of PLRV‐infection in plants on the behaviour of M. persicae, the vector of the virus, and the implications of these effects on the transmission of the virus are thoroughly discussed.     

Restricted distribution of potato leafroll virus antigen in resistant potato genotypes and its effect on transmission of the virus by aphids

Enzyme-linked immunosorbent assay was used to measure the concentration of potato leafroll virus (PLRV) antigen in different parts of field-grown secondarily infected plants of three potato genotypes known to differ in resistance to infection. The antigen concentration in leaves of cv. Maris Piper (susceptible) was 10–30 times greater than that in cv. Pentland Crown or G 7445(1), a breeder's line (both resistant). Differences between genotypes in antigen concentration were smaller in petioles and tubers (5–10-fold) and in above-ground stems (about 4-fold), and were least in below-ground stems, stolons and roots (about 2-fold). PLRV antigen, detected by fluorescent antibody staining of tissue sections, was confined to phloem companion cells. In Pentland Crown, the decrease in PLRV antigen concentration in leaf mid-veins and petioles, relative to that in Maris Piper, was proportional to the decrease in number of PLRV-containing companion cells; this decrease was greater in the external phloem than in the internal phloem. The spread of PLRV infection within the phloem system seems to be impaired in the resistant genotypes. Green peach aphids (Myzuspersicae) acquired < 2800 pg PLRV/aphid when fed for 4 days on infected field-grown Maris Piper plants and < 58% of such aphids transmitted the virus to Physalis floridana test plants. In contrast, aphids fed on infected Pentland Crown plants acquired <120 pg PLRV/aphid and <3% transmitted the virus to P. floridana. The ease with which M. persicae acquired and transmitted PLRV from field-grown Maris Piper plants decreased greatly after the end of June without a proportionate drop in PLRV concentration. Spread of PLRV in potato crops should be substantially decreased by growing cultivars in which the virus multiplies to only a limited extent.     

The effects of temperature on the availability and acquisition of potato leafroll luteovirus by Myzus persicae

The concentration of potato leafroll luteovirus (PLRV) did not differ in potato plants with secondary infections grown at 15°C or 27°C. Detached leaves of plants grown at 15°C or 27°C were used as sources of PLRV for peach-potato aphids (Myzus persicae Sulz.) both at 15°C and 27°C. At comparable temperature during virus acquisition, aphids which fed on leaves of plants kept previously at 15°C contained more viral antigen detected by ELISA than aphids which fed on leaves of plants grown at 27°C. The aphids which acquired PLRV at 27°C contained evidently more viral antigen than those which acquired PLRV at 15°C. The greatest amount of PLRV was found in the aphids which acquired the virus at 27°C from the leaves of plants kept at 15°C. The ability of M. persicae to transmit PLRV to Physalis ftoridana Rydb. generally decreased with decrease in the amount of PLRV in vectors.     

The transmission of potato virus Y by aphids of different vectoring abilities

Adult apterae of Myzus persicae and Macrosiphum euphorbiae that did not transmit potato virus Y^N (PVY^N) in a first test were as likely to transmit the virus in a subsequent test as those that did transmit on the first occasion. Only 16% of M. persicae that were allowed a single acquisition probe into a leaf infected with both PVY^O and PVY^N transmitted both strains, 37% transmitted either PVY^O or PVY^N and 47% did not transmit. There was no difference in the duration of probes that did or did not result in virus transmission. Statistical models were fitted to data on the frequency of transmission of PVY^O, PVY^N or both PVY^O and PVY^N by M. persicae and by aphids of poorer vector species, M. euphorbiae and Rhopalosiphum padi. Transmission of the two viruses ocurred independently of each other and consequently transmission of both was rare with M. euphorbiae and R. padi. Mineral oil applied to leaves infected with both strains diminished the frequency of transmission by M. persicae. Fitted models suggested that the aphids that probed through the oil droplets on leaves treated 30 min previously did not transmit virus, and that 24 h later, when the droplets had spread, aphids probing through them could transmit but with a decreased ability.     

Effects of pesticide treatments on the yield of swedes

The effects of insecticide and fungicide applications to swedes (Brassica napus var. napobrassica) were examined at 15 sites in England from 1974 to 1978. Several different pesticide combinations were applied including carbofuran granules at drilling (63 mg a. i./m of row), demeton-S-methyl sprays (0·24 kg a. i./ha) and fluotrimazole sprays (0·18 kg a. i./ha). The best treatments, which varied in different years, gave significantly higher yields than no treatment in 12 out of a total of 15 trials, with varying levels of damage attributable to cabbage root fly (Delia brassicae), aphids (Myzus persicae) and powdery mildew (Erysiphe cruciferarum) in each of the 4 years. In 10 of 12 trials, plots receiving a complete insecticide and fungicide programme yielded on average 40% (range 21–61%) more than untreated plots, mainly through control of root fly and aphids in 1975 and of aphids and mildew in 1976. Aphid damage to swedes was exceptionally severe in both years. Granular formulations of aldicarb, carbofuran, chlorfenvinphos or fonofos used alone to prevent cabbage root fly damage gave significant yield benefits in only 8 of the 15 trials, with least effect in 1977 and 1978 when growing conditions for swedes were good and damage relatively light.     

Transgenic Bt potato and conventional insecticides for Colorado potato beetle management: comparative efficacy and non-target impacts

Field studies were conducted in 1992 and 1993 in Hermiston, Oregon, to evaluate the efficacy of transgenic Bt potato (Newleaf^®, which expresses the insecticidal protein Cry3Aa) and conventional insecticide spray programs against the important potato pest, Leptinotarsa decemlineata (Say), Colorado potato beetle (CPB), and their relative impact on non-target arthropods in potato ecosystems. Results from the two years of field trials demonstrated that Newleaf potato plants were highly effective in suppressing populations of CPB, and provided better CPB control than weekly sprays of a microbial Bt-based formulation containing Cry3Aa, bi-weekly applications of permethrin, or early- and mid-season applications of systemic insecticides (phorate and disulfoton). When compared with conventional potato plants not treated with any insecticides, the effective control of CPB by Newleaf potato plants or weekly sprays of a Bt-based formulation did not significantly impact the abundance of beneficial predators or secondary potato pests. In contrast to Newleaf potato plants or microbial Bt formulations, however, bi-weekly applications of permethrin significantly reduced the abundance of several major generalist predators such as spiders (Araneae), big-eyed bugs (Geocorus sp.), damsel bugs (Nabid sp.), and minute pirate bugs (Orius sp.), and resulted in significant increases in the abundance of green peach aphid (GPA), Myzus persicae (Sulzer) – vector of viral diseases, on the treated potato plots. While systemic insecticides appeared to have reduced the abundance of some plant sap-feeding insects such as GPA, lygus bugs, and leafhoppers, early and mid-season applications of these insecticides had no significant impact on populations of the major beneficial predators. Thus, transgenic Bt potato, Bt-based microbial formulations and systemic insecticides appeared to be compatible with the development of integrated pest management (IPM) against other potato pests such as GPA because these CPB control measures have little impact on major natural enemies. In contrast, the broad-spectrum pyrethroid insecticide (permethrin) is less compatible with IPM programs against GPA and the potato leafroll viral disease.     

Vector activity of three aphid species (Hemiptera: Aphididae) modulated by host plant selection behaviour on potato (Solanales: Solanaceae)

Viral diseases non-persistently transmitted by aphids are of great economic importance in several annual crops. Transmission efficiency of these non-persistent phytoviruses is dependant on vector efficiency (i.e. vector intrinsic ability to transmit the virus) but also on the vector activity that implies the early steps of aphid host plant selection process (i.e. brief intracellular stylet punctures after landing) and to their interplant movement ability. In Europe, Macrosiphum euphorbiae (Thomas 1878) is considered as one of the most serious virus vectors on potato (Solanum tuberosum L. 1753). Nevertheless, several alate aphid species that do not colonise potato plants are trapped in potato crops. Therefore, we investigated, through laboratory experiments, vector activity of one potato colonising aphid, M. euphorbiae, and two non-colonising potato aphids, the bird cherry-oat aphid Rhopalosiphum padi (L. 1758) and the pea aphid Acyrthosiphon pisum (Harris 1776). A settling experiment was used to evaluate dispersal activity, and the electrical penetration graph (EPG) technique was used to investigate probing activity on potato plants. Results showed that M. euphorbiae exhibited a better vector activity than other two aphid species in terms of landing and probing. By contrast, interplant movements were only recorded on non-colonising aphids, suggesting a better vector activity than M. euphorbiae in terms of locomotive behaviour. These data confirm the involvement of A. pisum and R. padi in the spread of non-persistent viruses.     

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.     

Comparative analysis of Solanum stoloniferum responses to probing by the green peach aphid Myzus persicae and the potato aphid Macrosiphum euphorbiae

Abstract Plants protect themselves against aphid attacks by species‐specific defense mechanisms. Previously, we have shown that Solanum stoloniferum Schlechtd has resistance factors to Myzus persicae Sulzer (Homoptera: Aphididae) at the epidermal/mesophyll level that are not effective against Macrosiphum euphorbiae Thomas (Homoptera: Aphididae). Here, we compare the nymphal mortality, the pre‐reproductive development time, and the probing behavior of M. persicae and M. euphorbiae on S. stoloniferum and Solanum tuberosum L. Furthermore, we analyze the changes in gene expression in S. stoloniferum 96 hours post infestation by either aphid species. Although the M. euphorbiae probing behavior shows that aphids encounter more probing constrains on phloem activities–longer probing and salivation time– on S. stoloniferum than on S. tuberosum, the aphids succeeded in reaching a sustained ingestion of phloem sap on both plants. Probing by M. persicae on S. stoloniferum plants resulted in limited feeding only. Survival of M. euphorbiae and M. persicae was affected on young leaves, but not on senescent leaves of S. stoloniferum. Infestation by M. euphorbiae changed the expression of more genes than M. persicae did. At the systemic level both aphids elicited a weak response. Infestation of S. stoloniferum plants with a large number of M. persicae induced morphological changes in the leaves, leading to the development of pustules that were caused by disrupted vascular parenchyma and surrounding tissue. In contrast, an infestation by M. euphorbiae had no morphological effects. Both plant species can be regarded as good host for M. euphorbiae, whereas only S. tuberosum is a good host for M. persicae and S. stoloniferum is not. Infestation of S. stoloniferum by M. persicae or M. euphorbiae changed the expression of a set of plant genes specific for each of the aphids as well as a set of common genes.     

Effect of undersowing potatoes with grass on potato aphid numbers

The numbers of the potato aphids, Macrosiphum euphorbiae and Myzus persicae, were counted on potatoes undersown and not undersown with perennial ryegrass in field experiments during 1980 and 1981. The numbers of aphids on potatoes undersown with grass were found generally to be smaller than the aphid numbers on potatoes not undersown with grass. Tuber yields were not significantly reduced by the undersowing of potatoes. The agronomic feasibility of undersowing potatoes for aphid control is discussed.     

The induction of top-roll symptoms on potato plants by the aphid Macrosiphum euphorbiae

In the field, caged potato plants of King Edward and Majestic cultivars infested with the potato aphid Macrosiphum euphorbiae developed top-roll symptoms, the proportion of affected plants increasing with the size and persistence of the aphid population. Yield of tubers from plots in which 90% of the plants had top-roll symptoms was 40% less than that from control plots; yield of saleable ware was even less. Foliage produced after the aphids had been killed was symptomless even when it arose from the axil of an affected leaf. Caged field plants treated with phorate granules to prevent aphid attack did not develop top-roll. Prolonged infestation of Pentland Crown, Majestic and King Edward plants by M. euphorbiae in a glasshouse induced rolling of upper leaves similar to top-roll of field plants. Experimental results suggest that rolling was directly attributable to heavy attack by M. euphorbiae, not to an aphid-transmitted pathogen.     

Dynamics of Myzus persicae arrestment by volatiles from Potato leafroll virus‐infected potato plants during disease progression

Green peach aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae), an important pest of potato (Solanum tuberosum L.) (Solanaceae), preferentially settles on Potato leafroll virus (PLRV)‐infected potato plants as compared with non‐infected ones, primarily in response to volatile organic compounds (VOCs) released by the plants. In this study, we examined the dynamics of these effects, measuring arrestment of apterous M. persicae in response to VOC from upper, middle, and lower leaflets of PLRV‐infected potato plants at the same stage in disease progression (4 weeks after inoculation), but inoculated at 1, 3, or 5 weeks after transplanting (WAT). Sham‐inoculated plants were used as controls and VOC were collected and quantified. Aphid arrestment was greater on PLRV‐infected plants inoculated at 1 and 3 WAT as compared with sham‐inoculated plants, but this preference was reversed in plants inoculated at 5 WAT. Relative arrestment of M. persicae by infected plants and VOC release was greater for lower and middle leaflets than for upper leaflets at 1 and 3 WAT compared to sham‐inoculated plants. The reverse was observed in plants inoculated at 5 WAT. Findings indicate that aphid preference is influenced by VOC release from PLRV‐ or sham‐inoculated potato plants and that VOC emissions and aphid preference depend upon the age at inoculation and leaf position within the potato plants. The implications of these dynamics in vector behavior for spread of PLRV in the field in natural and managed systems are discussed.     

Effects of sub-lethal imidacloprid levels on potato leafroll virus transmission by Myzus persicae

The effects of sub-lethal imidacloprid concentrations on acquisition and inoculation of potato leafroll virus (PLRV) by Myzus persicae (Sulzer) (Hemiptera: Aphididae) were investigated. In experiments using two aphid clones to acquire PLRV from infected potatoes, virus transmission declined significantly with increasing concentrations of imidacloprid. The same was true in experiments using imidacloprid-treated Physalis floridana Rydb. as acquisition sources. When viruliferous M. persicae were placed on uninfected, imidacloprid-treated P. floridana, there were significant declines in PLRV transmission. Sub-lethal concentrations of imidacloprid clearly inhibited both acquisition and inoculation of PLRV by M. persicae, either through poisoning, temporary intoxication, and/or antifeedant effects.     

Co‐occurrence of defensive traits in the potato aphid Macrosiphum euphorbiae

1. Insecticide usage selects strongly for resistance in aphid populations, but this could entail fitness costs in other resistance traits. The potato aphid Macrosiphum euphorbiae Thomas exhibits intraspecific variation in susceptibility to parasitism by braconid wasps and provides a suitable species to study the relation between the defensive traits of parasitism and insecticide resistance. 2. Clonal lines (23 in total) of M. euphorbiae were established from aphids collected in 2013 from geographically separate populations in the U.K. Clonal lines belonged to five aphid genotypes, but one genotype predominated (78% of samples), and the facultative endosymbiont Hamiltonella defensa was detected in c. 40% of lines. 3. Total esterase activity in aphid tissues varied significantly between aphid genotypes and collection areas, but there was no clear pattern in relation to H. defensa infection or between collection sites likely to differ in insecticide pressures. 4. Five clonal lines representing low to moderate levels of enzyme activity, which included different aphid genotypes and presence/absence of H. defensa infection, were assayed for their susceptibility to the parasitoid wasp Aphidius ervi Haliday. Aphid mummification varied significantly between aphid genotypes, with low values in one genotype of aphids irrespective of H. defensa presence. 5. The results revealed that aphid lines belonging to the parasitism‐resistant genotype exhibited moderate levels of total esterase activity, indicating a competitve advantage for this genotype of M. euphorbiae when exposed to chemical and biological control factors in agroecosystems.     

Restricted multiplication of potato leafroll virus in resistant potato genotypes

Plants of a range of potato genotypes differing in rating for field resistance to potato leafroll virus (PLRV) were inoculated with the virus by grafting or by aphids (Myzus persicae). Plants of all genotypes tested became infected by each inoculation method and PLRV was detected by ELISA in the upper leaves of all genotypes within 26 days after grafting. Most genotypes with high resistance ratings developed only mild primary and secondary symptoms whereas those with low resistance ratings developed more pronounced symptoms. However, one genotype (G7461(4)) with a high resistance rating was very severely affected. The concentrations attained by PLRV in genotypes with high resistance ratings were only 1–10% of those in genotypes with low resistance ratings. These differences in virus concentration were found in young leaves of plants with primary or secondary infection, whether inoculated by grafting or by aphids and whether grown in the glasshouse or the field. In older leaves, differences in virus concentration between genotypes were at least as pronounced as those in younger leaves. In contrast, PLRV concentration in vascular tissue at the heel end of tubers of plants with primary infection was similar for all the genotypes tested. Although low PLRV concentration was consistently associated with high resistance rating it is not the only form of resistance to PLRV occurring in potato.     

The effect of insecticides and a plant barrier row on aphid populations and the spread of bean yellow mosaic potyvirus and subterranean clover red leaf luteovirus in Vicia faba in South Australia

The effect of the insecticides malathion, demeton-S-methyl and disulfoton, and a barley barrier row on the rate and pattern of spread of bean yellow mosaic potyvirus (BYMV) and subterranean clover red leaf luteovirus (SCRLV) in Vicia faba was investigated in field plots with artificially introduced sources of viruses and vectors. The systemic insecticide treatments reduced aphid populations in the plots and this was associated with reduced spread of SCRLV, but not of BYMV. The barley barrier did not affect aphid populations in plots; however, it reduced the spread of BYMV to rows 1 · 1 m from the source but had only a minor effect on the spread of SCRLV. Apterae rather than alates of Aulacorthum solani were implicated in the spread of SCRLV. Spread of BYMV was attributed mainly to alate migrants of Myzus persicae and Macrosiphum euphorbiae, but other aphid species and morphs which occurred in high populations at the times of most rapid virus spread may also have had an active role as vectors of BYMV.     

Ecology of the aphid pests of protected pepper crops and their parasitoids

Myzus persicae, Macrosiphum euphorbiae, Aphis gossypii and Aulacorthum solani (Homoptera: Aphididae) are principal pests of protected pepper crops in southeastern Spain. Our goal was to determine the incidence of aphids on pepper crops and the role of vegetation surrounding greenhouses as a source of aphids and their parasitoids. The population dynamics were followed in six commercial greenhouses during 3 years. Another 82 greenhouses and their surrounding vegetation were surveyed occasionally. Myzus persicae had the highest incidence in pepper greenhouses followed by M. euphorbiae and A. solani. Parasitism of all aphid species in greenhouses was low, Aphidius matricariae and Aphidius colemani being the most abundant parasitoids. Myzus persicae and Macrosiphum euphorbiae were the most abundant and polyphagous aphids, being present on 77 and 55% of the plants sampled outside greenhouses, respectively; species of Brassicaceae were the main hosts for both aphids. Aulacorthum solani was only present on Malva parviflora and at low numbers. Outside greenhouses, A. matricariae was the most common parasitoid of M. persicae, followed by Diaeretiella rapae and A. colemani. Aphidius matricariae was the most polyphagous, being present in 10 out of 22 aphid species. Macrosiphum euphorbiae and A. solani were both parasitised by A. ervi and Praon volucre. Aphelinus asychis was found on A. solani. Parasitoids were found in other aphids not attacking pepper. The role of natural vegetation as a reservoir of aphid pests of pepper and of parasitoids is discussed.     

Increased sensitivity of detection of plant viruses obtained by using a fluorogenic substrate in enzyme-linked immunosorbent assay

The fluorogenic substrate 4-methylumbelliferyl phosphate (MUP) of alkaline phosphatase was compared with the chromogenic substrate p-nitrophenyl phosphate (NPP) in tests for plant viruses by enzyme-linked immunosorbent assay (ELISA). In tests on leaf extracts of squash infected with prune dwarf virus, Chenopodium quinoa and apple infected with apple mosaic virus (ApMV), and potato infected with potato leafroll virus (PLRV), MUP increased sensitivity 2–16 times, the smallest and greatest increases being obtained with ApMV (in apple) and PLRV respectively. In similar tests on 21 dormant PLRV-infected potato tubers, sensitivity was increased 2–4 times with 13 tubers, but the two substrates gave the same detection end-points with eight tubers. When individual seeds of potato plants infected with the Andean potato calico strain of tobacco ringspot virus were tested, the virus was detected in virtually all seeds by MUP-ELISA, but detection by NPP-ELISA was inefficient unless absorbance values were measured after overnight incubation at 4 °C, instead of after 2 h at room temperature. In tests on Myzus persicae carrying PLRV and Sitobion avenae carrying barley yellow dwarf virus (BYDV), both viruses were consistently detected in a greater proportion of individual aphids by MUP-ELISA than NPP-ELISA irrespective of whether incubation was for 2 h at room temperature or overnight at 4 °C. The effeciency of detection of virus in single viruliferous aphids by MUP-ELISA was not decreased by grouping with one or four non-viruliferous aphids but was decreased (PLRV) or greatly decreased (BYDV) by grouping with nine. MUP-ELISA and transmission tests to Physalis floridana seedlings (2–3 day inoculation access periods) both detected PLRV in most individual M. persicae, but the results obtained with the two methods did not correlate completely. In similar tests for BYDV in individual S. avenae, virtually all aphids transmitted BYDV to oat seedlings during a 3-day inoculation access period but it was subsequently detected by MUP-ELISA in less than half of them. By contrast, MUP-ELISA detected PLRV in most viruliferous M. persicae even after they had fed for 3 days on Chinese cabbage, a non-host for this virus.