Wissadula Proliferation in Jamaica II. Psyllid transmission and antibiotic therapy

Field symptoms of Wissadula proliferation (WP) in Jamaica were reproduced on W. periplocifolia (L.) C. Presl. ex Thwaites test plants, using field-collected or laboratory reared and infected Paracarsidara concolor Crawford. This psyllid naturally is associated with W. periplocifolia in the field. Diseased plants contained phloem-restricted prokaryotes, most of which resembled the phloem-restricted rickettsialike organisms (RLO) known to be associated with a small group of plant diseases. They were bound by a “cell wall” composed of a double unit membrane separated by an electron-lucent layer. A small proportion of the prokaryotes, which were bound by only one recognizable unit membrane and were ill-defined at the periphery, were difficult to distinguish from mycoplasmalike organisms (MLO). Penicillin, applied as a soil drench of 200—400 %mUg/ml caused remission of symptoms of the psyllid-infected test plants 6—17 days after first effective application, with the concomitant disappearance of all of the structures in the resulting new growth. Since MLO are not known to be penicillin-sensitive, it is proposed that the “MLO” were in fact, poorly preserved RLO and it is suggested that RLO may be the aetiological agent of WP. Achromycin also caused symptom remission in WP at a soil drench of 100—400 %mUg/ml, but was generally slightly slower-acting than penicillin, eliciting a response in 12—23 days. Both antibiotics could produce lengthy remissions; neither seemed curative since two penicillin- and two achromycin-treated plants redeveloped symptoms after cessation of treatment. WP was not transmitted by two cicadellids, Protalebra maculata Baker and Scaphytopius fuliginosus Osborn. P. concolor did not transmit disease to test plants of Abutilon hulseanum (Torr. & A. Gray) Torr, ex. Chapm. which was affected by a proliferation disease (Abutilon proliferation), symptomatologically similar to, and which occurred in the same locations, as WP. WP and AP thus may be aetiologically distinct. The putative RLO aetiology of WP provides evidence against Wissadula being an alternate host of the MLO-associated coconut lethal yellowing (CLY) disease in Jamaica, a fact reinforced by negative psyllid transmission tests to CLY-susceptible palms. The results for WP are discussed in relation to other diseases possibly caused by phloem-restricted RLO.     

Attachment of the Flavescence doree pathogen (MLO) to leafhopper vectors and other insects

Flavescence doree (FD) is an important yellows disease of grapevine, caused by mycoplasma-like-organism (MLO) and is transmitted in the field by the leafhopper Scaphoideus titanus Ball. It can be transmitted in the laboratory between Vicia faba test plants by the leafhopper, Euscelidius variegatus Kbm. A technique to identify a specific attachment system between the MLO and the leafhopper vectors was developed. In this method, called “Double Dot”, extracts of macerated healthy whole insects or organs applied to a support membrane or cryosections of healthy whole leafhoppers, are incubated with a MLO-enriched extract from FD-infected V. faba or FD-infected E. variegatus. Attached MLO cells were identified by immunolabelling using FD-MLO specific monoclonal antibodies. Attachment of MLO cells was obtained on extracts of healthy S. titanus and E. variegatus and on tissues such as salivary glands, hemolymph and alimentary tract. On cryosections, MLO attachment was obtained on acini IV and V of the salivary glands and on some acini III, on the ventriculus of the alimentary tract, and on the abdomen fat bodies. “Double dot” experiments were done using other insect species, and MLO cells attachment was obtained on most MLO-vector insects but also on insects from a few non-vector species.     

Etiology and Transmission of Sesame Phyllody in Iran

Phyllody is a destructive disease of sesame (Sesamum indicum L.) in Iran. The major symptoms of the disease are floral virescence, phyllody and proliferation. Other symptoms which sometimes accompany the disease are yellowing, cracking of seed capsules, germination of seeds in the capsules and formation of dark exudates on the foliage. Light microscopy of hand-cut sections of sesame and colza (Brassica napus L. cv. Oro) stems treated with Dienes' stain showed blue areas in the phloem region of phyllody infected plants. Mycoplasma-like bodies were found in the sieve cells of infected sesame stems when thin sections were examined m an electron microscope. Sesame phyllody was successfully transmitted from sesame to sesame by grafting. Among various leafhoppers collected in sesame fields only Neoaliturus haematoceps transmitted the disease. This is the first report on the identification of a Mycoplasma-like organism (MLO) as the cause of sesame phyllody and N. haematoceps as an MLO vector in Iran. In host range studies using the leafhopper vector, only B. napus cv. Oro, Lepidium sativum, Catharanthus roseus, Lactuca sp. and Portulaca oleracea, but not 17 other species, developed symptoms. The species of vector and host range of MLO indicate that sesame phyllody in Iran is different from that reported in India and Upper Volta.     

Vector and Host-Plant Relationships of the Leafhopper-Borne Maize Yellow Stripe Virus

Maize yellow stripe virus (MYSV), associated with tenuivirus-like filaments, is transmitted in a persistent manner by the leafhopper Cicadulina chinai. In this vector, MYSV acquisition and inoculation threshold times were 30 min each, latent period ranged from 4.5 to 8 days depending on temperature (14-25 °C), and retention periods were as long as 27 days. Up to 26 % of C, chinai collected from maize fields in Giza, Egypt, during September and October 1985 were naturally infective with MYSV. Two symptom-types (fine and coarse stripe) appeared on experimentally infected plants, usually on separate leaves of the same plant. However, these two symptom-types could not be isolated on separate plants through transmission by single C. chinai leafhoppers. MYSV was transmitted by nymphs and adults of C. chinai from maize to maize, wheat and barley, and from wheat to maize plants. Up to 6 % of the wheat plants examined in Naga Hamadi (Southern Egypt) in February 1986, were naturally infected. It is suggested that wheat, barley and possibly graminaceous weeds may serve as winter hosts or reservoirs for MYSV and its leafhopper vector in Egypt.     

Epidemiological studies on the stunt disease of highbush blueberry

Population levels of Scaphytopius spp., possible sharpnosed leafhopper vectors of blueberry stunt disease (BBSD), were monitored during 1989,1990 and 1991, using yellow sticky traps and a D-Vac power aspirator. Scaphytopius magdalensis (Prov.), S. frontalis (Van D.) and 5. acutus (Say) had two population peaks, one after the petal fall stage and a larger second peak in late Summer to early Autumn. Healthy cv. Bluecrop highbush blueberry (Vaccinium corymbosum L.) plants were placed under stunt-diseased bushes in the field for 2-wk periods during 1989 and 1990. These plants and some of the leafhoppers trapped during 1990 and 1991 were tested for mycoplasma-like organism (MLO) infection with a DNA probe that detected BBSD-associated MLO. The percentage of plants and the number of Scaphytopius spp. that were MLO-positive tended to follow the same bimodal distribution found in the population studies. BBSD transmission tests were performed with Scaphytopius spp. collected from the field. Stunt-related MLO transmission was achieved with S. magdalensis, S. acutus and 5. frontalis.     

Use of Polyclonal Antibodies to Identify Mycoplasma-like organisms (MLOs) From the Sudan and from Thailand

Rabbit polyclonal antibodies prepared against faba bean phyllody MLO from the Sudan reacted with its homologous antigen and with extracts of Catharanthus roseus experimentally infected with the same or a related MLO from Crotalaria saltiana showing symptoms of phyllody disease, as well as with extracts of naturally MLO-infected C. saltiana growing in the field in the Sudan. The antibodies also reacted positively with extracts of C. roseus experimentally infected with Crotalaria juncea phyllody MLO and soybean phyllody MLO from Thailand. Polyclonal antibodies prepared against an MLO associated with witches' broom disease in C. juncea reacted positively in ELISA tests with homologous antigen extracts from naturally infected C. juncea as well as with extracts from experimentally infected C. roseus and with extracts prepared from Sesamum indicum plants with phyllody symptoms growing in Thailand. There was no reaction between these antibodies and extracts from C. roseus plants infected with the MLOs associated with C. juncea phyllody or with soybean phyllody. No cross reactions were observed among the antigens and antibodies of the two MLO groups by immunoflorescence, ELISA or western blotting. However, the molecular weight of the principal protein antigen, determined by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting was the same for both types of MLO. Serologically-similar MLOs thus occur in the Sudan and in Thailand, where they are associated with phyllody symptoms in C. saltiana and faba bean and with C. juncea and soybean, respectively. A second, serologically distinct MLO group was also found infecting C. juncea and S. indicum in Thailand but MLOs from this group have not yet been identified in crops from the Sudan.     

Use of Polyclonal Antibodies to Identify Mycoplasma-like organisms (MLOs) From the Sudan and from Thailand

Rabbit polyclonal antibodies prepared against faba bean phyllody MLO from the Sudan reacted with its homologous antigen and with extracts of Catharanthus roseus experimentally infected with the same or a related MLO from Crotalaria saltiana showing symptoms of phyllody disease, as well as with extracts of naturally MLO-infected C. saltiana growing in the field in the Sudan. The antibodies also reacted positively with extracts of C. roseus experimentally infected with Crotalaria juncea phyllody MLO and soybean phyllody MLO from Thailand. Polyclonal antibodies prepared against an MLO associated with witches' broom disease in C. juncea reacted positively in ELISA tests with homologous antigen extracts from naturally infected C. juncea as well as with extracts from experimentally infected C. roseus and with extracts prepared from Sesamum indicum plants with phyllody symptoms growing in Thailand. There was no reaction between these antibodies and extracts from C. roseus plants infected with the MLOs associated with C. juncea phyllody or with soybean phyllody. No cross reactions were observed among the antigens and antibodies of the two MLO groups by immunoflorescence, ELISA or western blotting. However, the molecular weight of the principal protein antigen, determined by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting was the same for both types of MLO. Serologically-similar MLOs thus occur in the Sudan and in Thailand, where they are associated with phyllody symptoms in C. saltiana and faba bean and with C. juncea and soybean, respectively. A second, serologically distinct MLO group was also found infecting C. juncea and S. indicum in Thailand but MLOs from this group have not yet been identified in crops from the Sudan.     

Multiplication of the agent of X-disease in a non-vector leafhopper Macrostelesfascifrons

The relative titre of the causal agent of X-disease of stone fruits in the non-vector leafhopper Macrosteles fascifrons was tested by injecting dilutions of M. fascifrons extracts into non-infective Colladonus montanus leafhopper vectors. The recipient C. montanus were fed on celery test plants which were then observed for X-disease symptoms. M. fascifrons were assayed at various intervals for up to 37 days after they were fed on X-diseased celery or injected with infectious extracts of the X-agent. Infectivity was detected in M. fascifrons only after 25 or 37 days in separate trials. Whole body extracts but not extracts from detached heads of M. fascifrons that had fed on X-diseased celery were infectious, whereas extracts prepared from the heads of M. fascifrons previously injected with X-agent extracts were infectious. This infectivity was retained for up to four serial passages in M. fascifrons. Electron microscopy of M. fascifrons that had been injected with extracts of the X-disease agent revealed mycoplasma-like organisms (MLO) only intercellularly and appressed to various organs in the haemocoele. No MLO were observed in uninjected M. fascifrons or those injected with extracts from non-infectious C. montanus. These results suggest that, despite multiplication of the X-agent in vivo. barriers in the gut and salivary glands prevent its transmission to plants by M. fascifrons.     

Transmission of Spiroplasma citri by the aster leafhopper Macrosteles fascifrons (Homoptera: Cicadellidae)

The aster leafhopper (Macrosteles fascifrons), injected with an isolate of Spiroplasma citri obtained from brittle root-diseased horseradish (Armoracia rusticana), transmitted the spiroplasma to horseradish and China aster (Callistephus chinensis.) After feeding on plants infected with S. citri, M. fascifrons transmitted the spiroplasma from aster to aster and horseradish, from yellow rocket (Barbarea vulgaris) to aster, and from turnip (Brassica rapa) to turnip. Symptoms in infected horseradish were chlorosis and stunting of newly formed leaves, discoloration of root phloem, and reduced plant growth typical of brittle root disease. Chlorosis, stunting, and asymmetry of young leaves occurred in affected aster and turnip. Flowers of infected aster were small and pale in colour and occasionally showed other symptoms including asymmetry, petal distortion, or light green petals. Spiroplasmas were isolated from all plants showing symptoms. Transmission rates by M. fascifrons which acquired S. citri by feeding on infected plants were very low, but injected leafhoppers transmitted more frequently. This is the first report of the transmission of S. citri from diseased to healthy plants by M. fascifrons.     

Préparation des Antigenes des Mycoplasmes (MLO) Pathogènes de la Flavescence Dorée, à Partir de Tissus Végétaux

Antigen preparation from plant tissues of pathogenic mycoplasms (MLO) causing flavescence doree disease Extraction and purification of plant yellow's pathogen mycoplasms (MLO) from plant tissues is a difficult problem. It concerns indeed non cultivable, heterogeneous and fragile organisms which are localized in the fibrous and resistant phloem tissue. In a work directed by an infectivity test by leafhopper injection, our laboratory investigated the best host plant and the best extraction method for this type of pathogen. Broad bean, Vicia faba gave better extracts than Vitis vinifera. Stems are better than petioles or lamina. The best results were obtained with the top region of the stem, at the level where symptoms are apparent on young plants. The most efficient mincing method is achieved with razorblades moved alternatively by the rapid vertical movement of an electric knife. The extraction medium already published (Caudwell and Kuszala 1986) has to be modified for plants by various additional components, histidine buffer, antioxidizers (glutathion 0.2 mg per ml) and polymers 0.5 to 1 p 100 PVP or Polyclar, 1–2 p 100 PEG). 1 g of plant infected tissue is minced in 4 ml of medium. The extracts are filtered through a 100 mesh nylon cloth. After this stage the purification method goes parallel to that used for leafhopper extracts (Caudwell and Kuszala 1986). It is possible to obtain 4 × 10⁶ infectious units from 1 g of broad bean stem (for calculation, see C 1986). It is possible to obtain 4 × 10⁶ infectious units from 1 g of broad bean stem (for calculation, see Caudwell 1977). The possibility to extract MLO, either from infectious leafhoppers or from diseased plants enabled cross immunological assays involving antigens from one host and antibodies directed towards the other host antigens. The first step was the successful ISEM visualization of ttie MLOs (Caudwell et al. 1982), the second is the immunoenzymatic MLO-detection (Boudon et al. 1986).     

Rearing and transmission techniques for Haplaxius sp. (Horn: Cixiidae), a suspected vector of lethal yellowing disease of coconuts

Adult Haplaxius sp., identified from Jamaica as H. crudus or H. cocois, are common on coconut foliage in both Jamaica and Florida and are suspected vectors of lethal yellowing disease in both regions. Nymphs, which are subterranean, were mass-reared on roots of the grasses Stenotaphrum secundatum, Axenopus compressus and Cynodon spp. Transmission of the disease was tested by feeding the nymphs on roots of diseased palms, rearing them on grasses and transferring the emergent adults to foliage of test palms for infection feeds. No transmission was proven.     

Corn Stunt Spiroplasma in Dicotyledonous Plants

Corn stunt spiroplasma (CSS) was transmitted by the leafhopper vector Euscelidius variegatus (Kirschbaum) and produced symptoms on four dicotyledonous plant species, Sinapis alba L. (mustard), Pisum sativitm L. (pea), Raphanus sativus L. (radish) and Spinacia oleracea L. (spinach). The vectors became infective by microinjection with a broth culture of CSS. This insect also acquired CSS from infected mustard plants and transmitted it to healthy ones.     

Spiroplasmas are the causal agents of citrus little-leaf disease

A spiroplasma isolated from citrus with little-leaf disease was grown in a cell-free medium and injected into leafhoppers (Euscelis plebejus) Injected leafhoppers, but not those fed on infected plants, transmitted the spiroplasma to white clover (Trifolium repens cv. S100) and sweet orange (Citrus sinensis cv. Valencia). Infected clover plants were severely stunted; infected sweet orange plants showed typical symptoms of citrus little-leaf disease. The spiroplasma was detected in clover and sweet orange plants by electron microscopy; the helical morphology of the organisms was most easily recognizable in sections 150–200 nm thick. The organism was re-isolated in cell-free media both from infected plants and from injected E. plebejus. The original isolate and those re-isolated from experimentally infected clover and sweet orange appeared by morphological, cultural, biochemical and serological criteria to be identical to each other and to the R8-A2 (type) and C-189 strains of Spiroplasma citri. Serological tests and electrophoretic analysis of protein preparations indicated no relationship to Acholeplasma laidlawii, although this organism survived for at least 10 wk after injection into E. plebejus. Our results show that the causal agent of little-leaf disease is related to S. citri.     

Mycoplasma-like bodies inSolanum laciniatum plants infected with potato witches’ broom disease

Mycoplasma-like organisms (MLO) spread from the infectious grafts intoSolanum laciniatum Ait. stock plants relatively slowly. MLO were present in all sprouts ofS. laciniatum four weeks after grafting, but the infected plants remained under glasshouse conditions mostly symptomless and flowered normally and formed fruits like healthy plants. The growth of plants with infectious tomato grafts was identical with the controls but that of plants with infectious tobacco (Nicotiana glauca Grah.) grafts was expressively stimulated. The first flower symptoms appeared onS. laciniatum plants with tomato grafts after five and half months and on.S. laciniatum plants with tobacco grafts after seven months of graft symbiosis. Electron micrographs of ultrathin sections showed the presence of MLO in sieve tubes of potiols and midribs of the infected but symptomless plants. In the phloem parenchyma cells of the witches’ broom diseased plants, highly ordered crystals were occasionally found lying in a microbody surrounded by a membrane. The possible reasons of the disease latency are discussed.     

Comparative transmission of bean leaf roll and pea enation mosaic viruses by aphids

Acyrthosiphon pisum was a more efficient vector than Myzus persicae of bean leaf roll virus (BLRV), but the two species transmitted pea enation mosaic virus (PEMV) equally well and much more often than Megoura viciae. M. viciae did not transmit BLRV, and Aphis fabae did not transmit BLRV or PEMV. BLRV and PEMV were transmitted more often by nymphs of A. pisum than by adult apterae or alatae that fed on infected plants only as adults, but both viruses were readily transmitted by adults that had developed on infected plants. The shortest time in which nymphs acquired BLRV was 2 h, and 50 % transmitted after an acquisition period of 4 days. Some nymphs acquired PEMV in 30 min and 50% in 8 h. The shortest time for inoculation of BLRV by adults was 15 min, but some transmitted PEMV in probes lasting less than 1 min. The median latent periods of BLRV and PEMV in aphids fed for 12 h on infected plants were, respectively, 105 and 44 h. Clones of A. pisum differed in their ability to transmit BLRV and PEMV, and efficiency in transmitting the two viruses seemed to be unrelated. Some aphids that fed successively on plants infected with each virus transmitted both viruses, and infectivity with one virus did not seem to affect transmission of the other.     

Contribution to the problem of mycoplasma-like organism transmigration in plants

Anatomical-histological investigations of slide series revealed that the secondary vascular formations appearing scattered in callus tissue culture derived from a stem piece containing mycoplasma-like organisms (MLO) (potato witches’ broom agent) have no connection with the vascular tissues of the original stem piece. 77% of reconstituted tobacco plants (Nicotiana glauca Grah.) from these callus cultures were infected with MLO. When diseasedNicotiana glauca scions are grafted on healthy tomato plants as stocks, MLO transmigration into the stocks is realized in all cases ten days after grafting; at that time, the scions and stocks are united only by a zone of a few layers of parenchymatous cells without any indication of vascular tissue union between the two components. In both cases, the MLO transmigration could not be realized by passage through sieve pores in sieve tubes. Our results bring indirect evidence of MLO transmigration through parenchymatous cells and thus support the hypothesis of MLO passage through the plasmodesmata.     

Evidence that maize wallaby ear disease is caused by an insect toxin

Colonies of the leafhopper Cicadulina bimaculata were established from single male and female insects raised from surface sterilised eggs and shown to be free of leafhopper A virus (LAV). Insects from these colonies were as capable of inducing maize wallaby ear disease (MWED) in maize seedlings as those with LAV indicating that the virus is not involved in the etiology of MWED. Maize seedlings colonised by C. bimaculata in glasshouse trials developed initial MWED symptoms within 6–8 days of infestation. The symptoms intensified thereafter and many plants died after more than 16 days' exposure, even after the insects were killed with insecticide. However, when freed from the insects before symptoms became very severe, plants recovered and assumed normal growth. These observations support the view that MWED is caused by an insect toxin.     

Amplification of plasmid DNA to detect plant pathogenic mycoplasmalike organisms

The polymerase chain reaction (PCR) was employed to develop a specific assay for plant pathogenic mycoplasmalike organisms (MLOs). A cloned fragment of a plasmid from a severe strain of western aster yellows (AY)-MLO was sequenced to identify oligonucleotide primers for PCR. Amplified DNA fragments of the predicted size were obtained from DNA extracted from plants and insects infected with pear decline MLO, beet leafhopper-transmitted virescence agent, elm yellows MLO and several AY-MLO strains. No amplification occurred from healthy leafhopper or plant DNA. The PCR-based assay was over 500 times more sensitive than a _tilized_tion-based assay which _tilized a cloned AY plasmid fragment as a probe. With the PCR-based assay, MLOs could be detected using DNA samples of leafhoppers that were only crushed and boiled in buffer. Amplification of the target DNA was confirmed by digestion of the PCR product with Mbo I which yielded predicted sized fragments for all MLO strains except Bradford AY and eastern AY. Sequencing the PCR product from elm yellows and eastern AY-MLOs revealed greater than 90% homology, and the failure to restrict the PCR product with Mbo I was due to a single base change in the restriction endonuclease site. The ability of the assay to detect a wide range of MLOs with minimal sample preparation and high sensitivity will be useful in epidemiological studies of MLO-caused diseases.     

Transmission of a New Mycoplasma-Like Organism (MLO) from Cuscuta odorata (Ruiz et Pav.) to Herbaceous Plants and Attempts to its Elimination in the Vector

A new MLO-type, originating from a holoparasite plant Cuscuta odorata (Ruiz et Pav.) causing stunting and reduction of flower- and leaf size on Catharanthus roseus (L.) G. Don. (HEINTZ 1986) was transmitted to Apium graveolens L., Plantago major L., Bellis perennis L. and Cirsium japonicum hybrid. The observed symptoms on the test plants probably caused by the MLO have not yet been described in the literature. The symptomatology on these herbaceous plants gives further data in order to classify the MLO as a new one which is named Guscuta latent MLO (Cl-MLO). Attempts to transmit the pathogens by the leafboppers Euscelidius variegates (Kirschbaum) and Euscelis lineolatus (Brullé) failed. It also was impossible to elimmate the MLO completely from Cuscuta odorata by heat treatment and antibiotic application. However, we succeeded in eliminating the pathogens from Catharanthus roseus by heat treatment.     

Aphid-injection experiments with carrot mottle virus and its helper virus, carrot red leaf

Carrot mottle virus (CMotV) and its helper virus, carrot red leaf (CRLV), were not transmitted by aphids (Cavariella aegopodii) that had fed through membranes on, or had been injected with, sap from mixedly infected chervil plants or partially purified preparations of CMotV. However, the viruses were transmitted by recipient aphids injected with haemolymph from donor aphids that had fed on mixedly infected plants but not by a second series of recipients injected with haemolymph from the first series. Some of the first series of recipients transmitted both viruses for up to 11 days but others transmitted erratically and many lost ability to transmit after a few days. The results confirm that both viruses are circulative but provide no evidence for multiplication in the vector. Non-viruliferous aphids, or aphids that had acquired CRLV by feeding, did not transmit CMotV when they were injected with haemolymph from aphids that had fed on a source of CMotV alone, confirming that they can only transmit CMotV when they acquire it from a mixedly infected plant. When extracts from donor aphids were treated with ether before injection, recipient aphids transmitted both CRLV and CMotV, although the infectivity of CMotV grown in Nicotiana clevelandii in the absence of CRLV is destroyed by ether treatment. CMotV particles acquired by aphids from mixedly infected plants therefore differed in some way from those in singly infected plants. A plausible explanation of these results, and of the dependence of CMotV on CRLV for aphid transmission, is that doubly infected plants contain some particles that consist of CMotV nucleic acid coated with CRLV protein.