Interaction of Cucumber mosaic virus and Bean yellow mosaic virus in co-infected plants of bean and broad bean

After evaluation of the responses of bean and broad bean common cultivars against an isolate of Cucumber mosaic virus (CMV-K) and Bean yellow mosaic virus (BYMV-K), interaction of isolates was statistically studied on co-infected plants of bean cv. Bountiful and broad bean cv. Lahijan at two trials. Based on viral relative concentration determined by quantitative enzyme-linked immunosorbent assay, BYMV interacts synergistically with CMV in bean at 14 days post inoculation, while in co-infection with BYMV, CMV interacts antagonistically in both host plants at least in one of the two trials. This suggests that CMV/BYMV interaction is dependent on host species and developmental stage of plant. Co-infection like single infection with CMV in bean plants led to significantly decrease in plants’ height and fresh weight than BYMV singly infected and healthy plants, while viral infection of broad bean plants did not significantly affect growth parameters. Decline effect of viral infection (especially co-infection) on chlorophyll and carotenoids value of bean plants was greater than those of broad bean. Viral infection (singly or doubly) caused irregular changes in nutrient elements values of both hosts compared with healthy ones.     

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.     

Necrosis in field beans (Vicia faba) induced by interactions between bean leaf roll, pea early-browning and pea enation mosaic viruses

Mixed infections with two or three viruses - bean leaf roll (BLRV), pea early-browning (PEBV) and pea enation mosaic (PEMV) - were detected in plants showing leaf curling, stunting and necrosis in a crop of field beans grown for seed in 1980. In glasshouse tests, field bean plants infected with any one of these viruses showed no necrosis, and plants infected with PEBV and PEMV together showed symptoms of PEMV only. However, mixed infection with BLRV and PEMV almost invariably induced severe stunting and leaf necrosis, and infection with BLRV and PEBV often induced both leaf and stem necrosis and sometimes caused early death. Thus it seems that the necrotic symptoms seen in the field were induced by interactions between BLRV and the other viruses. No transmission of PEBV was detected through seed harvested from the crop, but up to 5% transmission was detected through seed from experimentally-infected plants. The infected seedlings were symptomless.     

Host range and overwintering sources of bean leaf roll and pea enation mosaic viruses in England

Bean leaf roll virus (BLRV) and pea enation mosaic virus (PEMV) were each transmitted by Acyrthosiphon pisum (Harris) to fifteen of thirty species of legumes in the glasshouse; eleven species were susceptible to both viruses. The only biennial or perennial species infected by BLRV were hop trefoil (Medicago lupulina L.), lucerne (M. sativa L.) and red clover (Trifolium pratense L.), but naturally infected sainfoin (Onobrychis viciifolia Scop.) and white clover (T. repens L.) were found. The only perennial species infected with PEMV in the glasshouse was kidney vetch (Anthyllis vulneraria L.). Eggs of A. pisum, which seems to be the main vector of BLRV and PEMV in England, were found in winter on several species of cultivated perennial legumes, most on lucerne, fewest on white clover. In spring, more viviparae of A. pisum were found on lucerne than on other perennial legumes, and many on lucerne, but few on red or white clover, were infective with BLRV. Lucerne is probably the main overwintering source of BLRV in areas where lucerne is common, but elsewhere red and white clovers are probably as important. No aphid collected from perennial legumes between 1965 and 1968 was infective with PEMV, but this virus can overwinter in common vetch (Vicia sativa L.). Lucerne infected with BLRV was usually symptomless or showed only transient mild yellowing of young leaves. Lucerne plants showing vein-yellowing, similar to that previously reported as a symptom of BLRV, were possibly infected with an aberrant strain of BLRV but more probably with BLRV and another aphid-transmitted agent. Inoculations from lucerne with vein-yellowing symptoms sometimes caused vein-yellowing, and sometimes typical BLRV-symptoms, in crimson clover (Trifolium incarnatum L.).     

The serological relationships and some other properties of isolates of broad bean wilt virus from faba bean and pea in China

An isolate (N15) of broad bean wilt virus (BB W V) from faba bean in China was compared with some other isolates and strains including the nasturtium ringspot strain (NRSV, BBWV serotype I), parsley virus 3 (PV3, serotype I) and BBWV isolate PV131 (serotype II). In host range studies, N15 infected 12 of 14 species, including soybean and spinach. It was purified from Chenopodium quinoa and pea by a method that yielded up to 8mg/100g tissue. By the same method, NRSV yielded up to 4mg/100 g. Purified preparations of N15 and NRSV contained isometric particles c. 26 nm in diameter which sedimented as three components, N15 at 62, 93 and 117 S, and NRSV at 60, 91 and 116 S. In immunodiffusion tests using antisera to N15 and NRSV, N15 was distinguishable from NRSV but indistinguishable from PV131. In ISEM tests, many more particles of N15 and NRSV were trapped by homologous than by heterologous antiserum; in decoration tests, much antibody attached to homologous particles but none to heterologous particles. In DAS ELISA using N15 antiserum, N15 and six other Chinese faba bean or pea isolates, and a Chinese spinach isolate, were readily detected and were indistinguishable from each other and from PV131; unlike NRSV and PV3, none of the Chinese isolates, nor PV131, was detected using NRSV antiserum. These results indicate that the Chinese isolates belong to BBWV serotype II group.     

Reinigung und serologischer Nachweis des Erbsenenationenmosaik-Virus (pea enation mosaic virus)

Trotzdem von einer zunehmenden Bedeutung der Schneeschimmelkrankheit, hervorgerufen durch den Pilz Microdochium nivale, berichtet wird, liegen nur wenige Information über die Physiologie der Schadwirkung dieses Pilzes, insbesondere bei Blattbefall vor. Daher werden in dieser Arbeit die Einflüsse einer Inokulation mit M. nivale auf die Stickstoffaufnahme, ‐Verteilung sowie die source‐sink‐Beziehungen der Wirtspflanze untersucht. Die Weizenpflanzen wuchsen in Glaskabinen oder im Rhizotron unter Semifreilandbedingungen bzw. in Klimakammern. Durch Gabe von ¹⁵NH₄ ¹⁵NO₃ (2, 5 at‐% ¹⁵N exc.) zur Inokulation des Saatgutes, der Ähren oder verschieden inserierten Blättern wurden die Wirkungen der Krankheit auf den Stickstoffhaushalt des Weizens untersucht. Wenn keine zusätzliche Beeinflussung durch andere, biotische oder abiotische Streßfaktoren erfolgte, waren weder die Stickstoffaufnahme durch die Wurzeln, der Transport in die Körner, der Einbau in diese noch die Remobilisierung und Retranslokation zuvor gespeicherter N‐Verbindungen durch die Inokulation gehemmt. In einigen Versuchen war der Stickstoffhaushalt sogar stimuliert; die Stickstoffaufnahme, der Transport und Einbau in die Körner waren in den befallenen Pflanzen bis zur Reife höher als in den gesunden Pflanzen. Die Folgen dieser Wirkungen für den Kohlen‐hydrathaushalt und die Beteiligung von Phytohormonen an diesen Veränderungen werden diskutiert.     

Transmission characteristics and some other properties of bean yellow vein-banding virus, and its association with pea enation

Bean yellow vein-banding virus (BYVBV) has been found occasionally in mixed infection with pea enation mosaic virus (PEMV) in spring-sown field beans (Vicia faba minor) in southern England. Glasshouse tests confirmed that, like PEMV, BYVBV is transmissible by manual inoculation and by aphids in the persistent manner. However, BYVBV can be transmitted by aphids only from plants that are also infected with a helper virus, usually PEMV. Thus after separation from PEMV by passage through Phaseolus vulgaris it was no longer aphid-transmissible. It became aphid-transmissible again only after re-mixing in plants with PEMV or with a substitute helper, bean leaf roll virus (BLRV). It was not transmitted by aphids that fed sequentially on plants singly infected with PEMV and BYVBV. Thus the interaction between BYVBV and PEMV (or BLRV) that enables BYVBV to be transmitted by aphids seems to occur only in doubly infected plants. However, it was not transmitted by aphids from plants doubly infected with BYVBV and broad bean wilt virus (BBWV). BYVBV and PEMV were transmitted more readily by Acyrthosiphon pisum than by Myzus persicae; neither virus was transmitted by Aphis fabae. Phenol extracts of BYVBV-infected leaves were more infective than phosphate buffer or bentonite-clarified extracts and were sometimes infective when diluted to 1/1000. The infectivity of BYVBV in phosphate buffer extracts of leaves singly infected with BYVBV, unlike that in extracts of leaves doubly infected with BYVBV and PEMV (or BLRV), was destroyed by treatment with organic solvents. BYVBV infected 11 of 28 plant species that were inoculated with phenol extracts; seven of the infected species were legumes. No transmission of BYVBV was detected through seed harvested from infected field bean plants. Isometric particles c. 30 nm in diameter were seen in extracts of plants doubly infected with BYVBV and PEMV but not in extracts of plants infected with BYVBV alone. Leaves of plants infected with BYVBV, alone or with PEMV, contained membrane-bound structures c. 50–90 nm in diameter associated with the tonoplast in cell vacuoles. These structures were not found in healthy leaves. BYVBV has several properties in common with other known aphid-borne viruses that are helper-dependent and transmitted in a persistent manner. Possibly, as suggested for some of them, aphid transmission of BYVBV depends on the coating of its nucleic acid with helper virus coat protein.     

Apple mosaic virus isolated from hop plants in Japan

A strain of apple mosaic virus was isolated from hop plants in Japan. The virus was purified from young hop plants and back-inoculated to virus-free hop plants obtained by meristem tip culture. Inoculated plants developed chlorotic spots, ringspots and a band pattern accompanied by necrosis in the inoculated and systemically infected leaves. Shoot tips of infected plants sometimes became necrotic and these symptoms resembled those of a ring- and band-pattern mosaiclike disease prevalent in hop gardens in Japan. Since apple mosaic virus was recovered from infected plants, it is likely that the virus was the causal agent of this disease. Agar gel double diffusion tests and ELISA showed the hop virus to be serologically closely related to apple mosaic virus (ApMV), and distantly related to prunus necrotic ringspot virus (PNRSV). The virus had a narrow host range, and infected only cucumber of 18 species of Cucurbitaceae, Chenopodiaceae, Leguminosae or Solanaceae inoculated. It produced chlorotic spots on the inoculated cotyledons of cucumber, but no systemic infection. By contrast, ApMV from apple and PNRSV from peach had wide host ranges and infected cucumber plants systemically.     

Risk assessment for non-crop hosts of pea enation mosaic virus and the aphid vector Acyrthosiphon pisum

1. Viral insect-borne plant pathogens have devastating impacts in agroecosystems. Vector-borne pathogens are often transmitted by generalist insects that move between non-crop and crop hosts. Insect vectors can have wide diet breadths, but it is often unknown which hosts serve as pathogen reservoirs and which non-crop host harbours the highest density of vectors.
2. In the Pacific Northwest USA, the pea aphid (Acyrthosiphon pisum) is a key virus vector in pulse crops. Despite pea aphid having a large number of potential non-crop plant hosts occuring in the region, no reservoir has yet been identified for the economically-costly pathogen Pea Enation Mosaic Virus (PEMV).
3. We addressed these issues by linking field surveys of an aphid vector and plant virus with statistical models to develop risk assessments for common non-crop legumes; in 2018, we completed a 65-site survey where aphids were surveyed in weedy legumes within and outside dry pea fields.
4. We quantified the abundance of pea aphids on 17 hosts, and plant tissue was tested for PEMV. Relatively high densities of A. pisum were found in habitats dominated by hairy vetch (Vicia villosa), which was the only legume other than cultivated dry pea where PEMV was detected.
5. Our results indicate that V. villosa is a key alternative host for PEMV, and that pest management practices in this region should consider the distribution and abundance of this weedy host in viral disease mitigation efforts for pulses.

     

The effect of oil on the transmission of pea enation mosaic virus during short inoculation probes

The transmission efficiency of pea enation mosaic virus by Acyrthosiphon pisum (Harris) in short inoculation periods to pea plants sprayed with oil prior to the test, was compared with that to plants which were not coated with an oil film. The transmission of virus to the former group was lower (approximately 11%). However, this difference was not significant. The probing behaviour measured by parameters such as test-probe frequency prior to phloemseeking probes, duration of the probes and the cumulative duration of the short inoculation periods, did not differ for aphids probing on plants with and without oil film. The results suggest that the mechanism of pea enation mosaic virus transmission in short inoculation access periods differs from that of the non-persistent viruses.

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Zusammenfassung Die Übertragung nicht-persistenter Viren wird durch eine Behandlung der Pflanzen mit Mineralöl eingeschränkt. Auf die Übertragung persistenter Viren haben Öle keinen Einfluß. Dies ist offensichtlich auf einen anderen Übertragungsmechanismus bei diesen Viren zurückzuführen. Erbsenenationen-Virus — ein persistentes Virus — kann aber auch in kurzfristigen Infektionszeiten auf Pflanzen übertragen werden.In dieser Untersuchung wurde geprüft, ob die Übertragung dieses Virus bei solchen Infektionszeiten von Öl gehemmt werden kann. Es wurde jedoch keine entscheidende Einschränkung der Übertragungsraten gefunden, wenn die Pflanzen mit Öl behandelt worden waren.Auch das Verhalten der Blattläuse auf diesen Pflanzen wurde durch Anwendung verschiedener Parameter analysiert. Verglichen wurden die Häufigkeit der Probestiche, bevor ein Saugstich gemacht wird, die Dauer der Probestiche und die Summe der Dauer kurzfristiger Infektionszeiten auf Pflanzen, die mit Öl behandelt wurden oder nicht. Die Saugstiche wurden nach einer Dauer von 1 min abgebrochen. Jede Blattlaus machte 4 Stiche an ein und derselben Pflanze.Die genannten Parameter zeigen, daß im Verhalten der Blattläuse auf mit Öl bedeckten Planzen keine Änderung eintritt.

     

Lamium mild mosaic virus: a virus distantly related to broad bean wilt

Lamium mild mosaic virus (LMMV) was compared with some strains of broad bean wilt virus (BBWV). It differed somewhat in host range from BBWV; serologically, it was only distantly related to four strains of BBWV, all belonging to serotype I, but no reaction was detected with serotype II. BBWV and LMMV were not serologically related to six comoviruses. Like BBWV, LMMV sedimented in three components and the two viruses were morphologically indistinguishable, but LMMV had more slowly migrating RNAs and coat proteins. No distinctive pathological changes were seen in LMMV infected cells. It is proposed that LMMV be considered a distinct virus from BBWV but included with it in a new group of plant viruses.     

Some properties of turnip yellow mosaic virus isolated from hybrid Brassica Perko PVH in Yugoslavia

Anhand mikroskopischer Untersuchungen und durch Mittelversuche an A. pisum wurden folgende Kenntnisse zur Endosymbiose gewonnen:

• In L₃‐Stadien von A. pisum sind zwischen 55 und 85 potentielle Bakteriocyten vorhanden, von dene ca. 60–80 % besiedelt sind.

• Eine Reduktion des besiedelten Anteils in der F₁‐Generation auf unter 50% läßt eine deutliche Depression in der F₂‐Generation erwarten.

• Das Kriterium Embryonenlänge ist großen Schwankungen unterworfen und eignet sich nur bedingt als Unterscheidungsmerkmal.

• Die von Fröhlich (1990) vorgeschlagene Methodik zum Symbiontizidscreening bei A. pisum mit dem Standard OTC 2000 ppm und der Auszählung der mit TTC angefärbten Bakteriocyten unter dem Mikroskop läßt eine praktikable Testung von Substanzen auf symbiontizide Wirkung bei A. pisum zu. Es wird jedoch als günstiger angesehen, nicht die Larven mit den Pflanzen zu behandeln, wie von Fröhlich (1990) vorgeschlagen, sondern erst nach dem Antrocknen des Spritzbelages Adulte zur Erzeugung von F₁‐Larven anzusetzen.

• Es konnte eindeutig nachgewiesen werden, daß die von den Prüfsubstanzen hervorgerufenen aphiziden Effekte, insbesondere durch Cycloheximid (100/500 ppm) sowie Neemkernextrakt (50%), nicht auf einem symbiontiziden Wirkungsmechanismus beruhen (Ausnahme Oxytetracyclin 2000 ppm als Standard).

     

Some chemical properties of isolated pea nucleoli

Isolated nuclei and nucleoli of ungerminated pea embryos have been analyzed chemically for their content of DNA, RNA, zinc, iron, phosphorus, and protein sulfhydryl groups. The values obtained cannot be considered to represent the whole of the living nucleolar body as an undetermined amount of material is extracted from nucleoli in the course of their isolation. Only negligible amounts of DNA have been found in the isolated nucleoli; most of the DNA released on disruption of nuclei appears in a fraction showing very few structures under the light microscope. RNA is more concentrated in the nucleolus than in the nucleus or cytoplasm, but since nucleolar protein is 6 per cent of nuclear and less than 1 per cent of cytoplasmic protein, the total amount of nucleolar RNA is comparatively small. None of the other components listed occurs in high concentration in either nucleus or nucleolus.     

A virus causing a mosaic disease of broad bean and its vector Aphis craccivora in Egypt

A mosaic disease of broad bean (Vicia fabae) was widely spread in fields near Cairo in the season of 1963.The causal virus seemed to infect only the plants belonging to the family Leguminosae. Definite symptoms of systemic mosaic infection were shown by the following species: Egyptian lupin, garden pea, broad bean and fenugreek. It did not infect cow pea, sesban, pigeon pea, French bean, chickpea, tobacco, jimson weed and Lablab.The virus was inactivated in 10 minutes at 60° C, it withstood dilution of 1 : 1000 but not 1 : 10.000 and its infectivity was lost after storing at room temperature for 96 hours.The virus was transmitted by Aphis craccivora Koch, was nonpersistent, and its host range, properties and vector relation suggest that it is a strain of pea mosaic virus.

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Zusammenfassung Während der Vegetationsperiode 1963 war in ägyptischen Puffbohnenfeldern eine Mosaikkrankheit der Puffbohne (Vicia faba) weit verbreitet.Das isolierte Virus scheint auf Leguminosen beschränkt zu sein. Bei systematischen Infektionsversuchen zeigten sich definierte Symptome bei folgenden Arten: Ägyptischen Lupinen (Lupinus termis), Gartenerbsen (Pisum sativum var. alaska), Puffbohnen (Vicia faba) und Bockshorn (Trigonella Foenum-Graecum). Kuhbohnen (Vigna sinensis var. kentucky und V. catjang), Gartenbohnen (Phaseolus vulgaris), Kichererbsen (Cicer arietinum), Taubenerbsen (Cajanus cajan indicum), Sesban (Sesbania aculeata), Lablab (Dolichos lablab), Tabak (Nicotiana tabacum) und Stechapfel (Datura stramonium) wurden nicht befallen.Das Virus wurde bei 60° nach 10 Minuten inaktiviert, es vertrug Verdünnung auf 1 : 1000, aber nicht auf 1 : 10.000, und seine Infektiosität ging durch 96-stündigen Aufenthalt bei Zimmertemperatur verloren.Es wurde von Aphis craccivora übertragen und erwies sich als nonpersistentes Virus. Die Aufnahme-Saugzeit betrug 5 Sekunden oder weniger. Der Infektionserfolg stieg bei Übertragungssaugzeiten von 5 sec bis 5 min., fiel aber bei längeren wieder auf Null. Nach einer Stunde (Hunger) geht das Virus auf dem Vektor völlig verloren. Es ist leicht mechanisch übertragbar.

     

Some hosts and properties of dahlia mosaic virus

Dahlia mosaic virus (DMV) infected twenty-five of the eighty-five plant species from four of eighteen families inoculated, but only dahlias were found naturally infected. DMV infected fourteen members of the Solanaceae, Amaranthaceae and Chenopodiaceae, and eleven of twenty-nine Compositae. Verbesina encelioides was the best plant for diagnosis, assay and source of virus. Systemically infected hosts contained ovoid intracellular inclusions 2–5–10 μm in diameter which were shown by electron microscopy to consist of a finely granular, vacuolated matrix containing numerous virus particles. V. encelioides sap was sometimes infective after dilution to 1/2000 but not 1/3000, after heating for 10 min to 75 °C but not 80 °C, and after 4 days at 18 °C or 32 days at 2 °C. Sap from infected dahlia, Zinnia elegans or Ageratum houstonianum rapidly became non-infective, but extracts made with 0·05 M sodium thioglycollate or 0·03 M sodium diethyldithiocarbamate remained infective for 24–48 h at 18 °C. Some purified preparations remained infective for up to 3 years at 2 °C. DMV was best purified from V. encelioides by one or more cycles of differential centrifugation, followed by density-gradient centrifugation and further concentration. Composition, molarity, and pH of the extracting buffer had little effect on yield of virus. Best yields were obtained from extracts stored with 8-5% (v/v) n-butanol at 2 °C for 10–14 days. Purified preparations were infective at dilutions up to 1/5000, had ultraviolet absorption spectra typical of a nucleoprotein (Å 260/280 = 1·47), probably contained DNA, and had a single sedimenting component having isometric particles c. 50 nm in diameter with a sedimentation coefficient of 254 S. The cryptogram of DMV is (D)/*:*/(16):S/S:S/Ap. DMV is serologically closely related to cauliflower mosaic virus, but the viruses are distinct pathogens. The two viruses have similar properties, size, shape and other characteristics, and together with at least three others form a small but apparently homogeneous group of aphid-borne viruses.