Effect of irradiance upon the population of Pseudomonas coronafaciens in leaves and symptom expression of halo blight of rye.

The toxin-induced chlorosis caused by Pseudomonas coronafaciens is influenced by irradiance. Three levels of irradiance caused differences in symptom expression but did not affect the rate of increase or final population of viable cells of P. coronafaciens in rye leaves. Distinct and faint halo blight symptoms appeared in 3--4 days in full light (1425 microW cm-2), and 58% shade (598 microW cm-2) respectively. No symptoms or only faint symptoms appeared after 7 days at 86% shade (202 microW cm-2). When plants kept in 58 and 86% shade were moved to full light 5 days after inoculation, lesion size and chlorosis increased rapidly during the next 2 days. On the 7th day after inoculation, the size of lesions from the 58 and 86% shade treatments exceeded those in full light by 2.5 and 5 times, respectively. A chlorosis index based on lesion size and chlorophyll loss within lesions also reflected this trend although chlorophyll loss was greater in lesions in full light for 7 days. Conditions of low irradiance such as that caused by overcast weather and (or) a dense leaf canopy followed by bright sunshine can cause greater losses from halo blight than a continuous period of high irradiance. Sympton expression may be masked by low irradiance but increase of inoculum is not impaired. Although increased light enhances chlorosis, toxin diffusion or production may be reduced.     

The effect of carbendazim-generating fungicides with and without a mineral oil additive on tomato stem lesions caused by carbendazim-sensitive and tolerant strains of Botrytis cinerea

Isolates of Botrytis cinerea were obtained from tomatoes in several localities in the West Scotland. Some isolates grew on agar containing 100 mg/1 benomyl (carbendazim-tolerant), while others did not (carbendazim-sensitive). Pot-grown tomato plants treated with benomyl and other carbendazim-generating fungicides, applied either as sprays or soil drenches, were inoculated on the leaf scars with some of these isolates. On treated plants the carbendazim-tolerant isolates formed lesions which were about as large as those on untreated plants. Sensitive isolates formed much smaller lesions on treated plants. There was evidence that the increase in lesion size during the period 7–14 days after inoculation with a carbendazim-sensitive isolate was less on plants sprayed with benomyl or carbendazim with added mineral oil (2% Actipron) than on plants to which the fungicides alone had been applied. No such effect was recorded with thio-phanate-methyl. There was also an indication that the addition of Actipron to a benomyl spray improved the effect of the fungicide against two tolerant isolates, though there was no effect on the relative increase in lesion size during the second week after inoculation. In two tests the addition of 2% and 4% Actipron to benomyl soil drenches did not improve the level of leaf scar lesion control.     

Effects of Chicken-excrement Amendments on Meloidogyne arenaria

The effects of chicken litter on Meloidogyne arenaria in tomato plants cv. Rutgers were determined in the greenhouse. Tomato seedlings were transplanted into a sandy soil amended with five rates of chicken litter and inoculated with 2,000 M. arenaria eggs. After 10 days, total numbers of nematodes in the roots decreased with increasing rates of chicken litter. After 46 days, egg numbers also decreased with increasing litter rates. In another experiment, soil was amended with two litter types, N-P-K fertilizer, and the two primary constituents of chicken litter (manure and pine-shaving bedding). After 10 days, numbers of nematodes in roots were smaller in chicken-excrement treatments as compared to nonexcrement treatments. At 46 days, there were fewer nematode eggs in chicken-excrement treatments compared to nonexcrement treatments. Egg numbers also were smaller for fertilizer and pine-shaving amendments as compared to nonamended controls. Chicken litter and manure amendments suppressed plant growth by 10 days after inoculation but enhanced root weights at 46 days after inoculation. Amendment of soil with chicken litter suppressed M. arenaria and may provide practical control of root-knot nematodes as part of an integrated management system.     

Effects of Leaf Age, Inoculum Dose and Freezing on Development of Chocolate Spot (Botrytis fabae) Lesions on Field Bean (Vicia faba) Leaves

Botrytis fabae spore suspensions containing c. 1, 10, 10², 10³, 10⁴, 10⁵, or 10⁶ spores/ml were used to inoculate 5, 17 or 30-day-old field bean leaves. The percentages of the leaf areas covered by, chocolate spot lesions and the percentages of the leaf areas bearing conidiophores were assessed 1, 6, 12, 14, and 19 days after inoculation. The percentage of the area covered by lesions and the percentage of the area bearing conidiophores (logit-transformed) increased linearly with increasing spore concentration (log₁₀-transformed). The proportions of leaf areas covered by lesions and bearing conidiophores were both greater on 17 and 30-day-old leaves than on 5-day-old leaves. The rate of lesion growth increased with both increasing inoculum dose and increasing leaf age. Generally there was no interaction between the effects of leaf age and the effects of inoculum dose on either lesion growth or sporulation. Two days after inoculation with suspensions of either 10⁴ or 10⁶ spores/ml, 7-day-old leaves grown at 15°C were transferred to –16°C or 2.5°C or kept at 15°C for 4 days. Two days later more spores had been produced on leaves which had been frozen (–16°C) than on, leaves kept at 2.5°C.     

Systemic Acquired Resistance to Virus Infections and Ethylene Biosynthesis in Asparagus Bean

Systemic acquired resistance (SAR) was induced in asparagus bean following inoculation with tobacco necrosis virus (TNV) or tobacco rattle virus (TRV), viruses that produce a hypersensitive reaction in this plant. SAR was expressed against challenge by TNV as reduction in lesion size, but not as inhibition of viral antigen accumulation. Systemic stimulation of ethylene-forming enzyme (EFA) activity, in the absence of any ethylene increase or 1-aminocyclopropane-1-carboxylic acid (ACC) accumulation, was associated with SAR. Formation of local necrotic lesions was necessary for both induction of SAR and stimulation of EFA, because early removal of inducer leaves prevented both events. SAR was expressed at rather constant level between 7 and 12 days after inducing infection. EFA stimulation declined with time and was no longer detected 7 days after inducing infection. SAR was not expressed against cucumber mosaic virus, that infect asparagus bean systemically. Prior inoculation with TNV or TRV was ineffective to reduce CMV antigen content or to minimize the pathogenic effect of this virus in systemically infected leaves.     

Induction of Growth Increase and Systemic Resistance to Exserohilum turcicum in Maize by Foliar Spray of Phosphates

A single foliar spray of 0.1 M solution of phosphate salts on the upper side of maize (cv. ‘jubilee') leaves 1, 2 and 3 at the 5–6 fully–expanded leaf-stage, 2-4 h before inoculation induced systemic resistance to northern leaf blight caused by Exserohilum turcicum. Nine days after challenge, protection was demonstrated by 91% reduction in the size and 69% in the number of E. turcicum lesions developing on leaves 4, 5, 6 and 7. Appropriate mixing of phosphate solution with KOH revealed that the level of protection was not necessarily dependent on the pH of the solution. The size and number of lesions decreased to 62% and 56%, respectively, 12 days after challenge. There was no damage or chlorotic stipling on the induced leaves (1, 2, and 3) as a result of the phosphate spray. There were no significant differences in the reduction in the number or size of the lesions obtained when the foliar spray was applied 2-4 h or 1, 3, 6, 8, or 10 days before inoculation. One foliar spray ofK₂HPO₄ on leaves 1, 2 and 3 in these intervals before inoculation, remarkably stimulated growth of inoculated plants, which was expressed by several parameters. The possible dual use of phosphate salts as foliar fertilizers and as resistance-inducing agents is discussed     

A greenhouse assay to screen sunflower for resistance to Alternaria helianthi

A greenhouse assay to screen sunflower for resistance to Alternaria helianthi is described. A comparison of conditions led to the following standard conditions being recommended. The first or second pair of leaves of seedling plants at the V8 growth stage are inoculated using inoculum grown on sunflower leaf extract agar for 5–10 days at an inoculum density of 1–2 spores cm² of leaf tissue. A 48 h dew period should be applied to plants covered by a plastic tent. A dew period temperature of 26/26°C night/day and a post-dew period temperature relative to that experienced under local growing conditions should be applied. Lesions are measured 7 days after inoculation, and mean lesion size per plant is calculated. Mean lesion size of lines being tested is expressed as a proportion of the mean lesion size of a susceptible standard included in each screening experiment.     

Duration of effects of benomyl on growth and wilt (Verticillium dahliae) development in the strawberry, cv. Cambridge Vigour, in relation to time of inoculation

Single doses of benomyl, 0–4 g/plant in 1972 or 0–04 g in 1973, were applied in 100 ml water to the surface of the soil in 12-5 cm pots containing Cambridge Vigour strawberry plants, either before inoculation with Verticillium dahliae or at various times up to 56 days afterwards. Pre-inoculation treatments were terminated by washing the potting medium from the roots at the time of inoculation and their effects on pathogenesis and growth were relatively small. Post-inoculation treatments with benomyl prevented or suspended pathogenesis for at least as long as fungistatic activity could be detected in petiole segments by bioassay; this was for more than 150 days after the larger dose, 50–60 days after the smaller dose applied 7–28 days after inoculation and 30 days when applied 56 days after inoculation. There were no consistent differences in the uptake and persistence of benomyl in inoculated and non-inoculated plants. Early post-inoculation treatment caused some retardation of plant growth, but benomyl-treated inoculated plants were generally comparable in size with similarly treated non-inoculated ones, and much larger than untreated inoculated plants. Increasing the dose of benomyl applied to the soil apparently had little influence on the intensity of its effects but greatly increased their duration, probably because of the low solubility of the systemic chemical.     

Cyanobacterial inoculation and nitrogen fertilization in rice

During three rice-growing seasons in Uruguay, field experiments were conducted to study the contribution of cyanobacterial inoculation and chemical N fertilization to rice production. Neither grain yield nor fertilizer recovery by the plant were affected by inoculation with native cyanobacterial isolates. A low fertilizer use efficiency (around 20%) was observed when labelled (NH₄)₂SO₄ was applied at sowing. Recovery of applied ¹⁵N by the soil–plant system was 50%. Inoculation did not modify ¹⁵N uptake by the plant when the fertilizer was three-split applied either. The total N-fertilizer recovery was higher when the fertilizer was split than when applied in a single dose. Plant N-fertilizer uptake was higher when the fertilizer was applied at tillering. Uptake of ¹⁵N from cyanobacteria by rice was studied in a greenhouse pots experiment without chemical nitrogen addition. Recovery of ¹⁵N from labelled cyanobacteria by rice in greenhouse growth conditions was similar to that of partial recovery of (NH₄)₂SO₄ applied at sowing in the field. Cyanobacterial N mineralization under controlled conditions was fast as cyanobacterial N was detected in plants after 25 days. Moreover 40 days after inoculation non-planted and inoculated soil had more inorganic N than the non-inoculated one.     

Resistance reactions of Cucumis melo to inoculation with Pseudoperonospora cubensis

Reactions of several cultivars and breeding lines of melons to artificial inoculation at the seedling stage with a local isolate of Pseudoperonospora cubensis were compared under growth chamber and field conditions. Four different reactions were distinguishable: highly susceptible, susceptible, partially resistant and resistant. The differences in the reactions were more clear-cut under growth chamber conditions. Selection for resistance could be carried out at the seedling stage using sporangia production and lesion size, shape, colour and number as criteria. Under growth chamber conditions, plants of resistant lines had minimal sporangia production and circular or angular lesions 1–2 cm in diameter which became necrotic within 5 days after inoculation.     

Leishmania braziliensis: development of primary and satellite lesions in the experimentally infected owl monkey, Aotus trivirgatus

Twelve male and 8 female feral owl monkeys, Aotus trivirgatus, were inoculated intradermally at the dorsal base of the tail with 2 X 10(7) promastigotes (strains WR 128 or WR 539) or 5 X 10(5) amastigotes (strain WR 128) of Leishmania braziliensis panamensis, and the progression and regression of subsequent lesions were examined for up to 13 or 54 weeks after inoculation. Three of these monkeys had been infected previously with L. donovani, had been treated with meglumine antimoniate, and had recovered clinically from visceral leishmaniasis. All monkeys developed a cutaneous nodule at the inoculation site, but the size of the nodule varied (maximum 78 to 326 mm2 between 4 and 16 weeks after inoculation.) The initial nodule became ulcerated after 4 to 8 weeks in 17 of the 20 monkeys, and the ulcers persisted for 4 to 16 weeks until covered by a crust. Primary lesions disappeared by 17 to 52 weeks after inoculation, but satellite lesions, of similar morphology to the primary lesions but smaller, developed after 4 to 21 weeks in 14 of the monkeys. The primary nodule was excised in 4 monkeys at 6 weeks and did not recur nor did satellite lesions subsequently develop. The satellite lesions (median total number of 4, range 1 to 25) were adjacent to or at a maximum distance of 6 cm from the primary lesion, varied in size from 3 to 117 mm2, and persisted for 10 to 37 weeks. At 6 and 8 weeks after inoculation, tissue from the cutaneous leishmanial lesions from five monkeys was excised and examined. The granulomatous leishmanial lesions, located primarily in the dermis and subcutis, consisted of macrophages containing parasites, lymphocytes, plasma cells, and occasionally eosinophils. Satellite lesions at 14 weeks after inoculation were similar grossly and microscopically to the initial nodule. No significant differences were observed between promastigote or amastigote derived infections, between the two strains of L. b. panamensis, or between the course of infection based on the sex, age, karyotype, or country of origin of the owl monkeys. Cutaneous lesions developed when 5 X 10(5) amastigotes of L. b. panamensis (strain WR 128) were inoculated intradermally into the dorsal base of the tail, the upper eyelid, and the thorax of three monkeys. Leishmanial nodules which developed on the thorax regressed rapidly (after 2 to 5 weeks) whereas those on the upper eyelid and at the dorsal base of the tail persisted for 5 to 45 weeks after inoculation.(ABSTRACT TRUNCATED AT 400 WORDS)     

Reaction of sunflower varieties to Sclerotinia sclerotiorum under various inoculation methods,time of field evaluation and phylogenic stages of host

Sunflower cultivation is affected seriously by Sclerotinia sclerotiorum (Lib.) de Bary in Iran, particularly north-western areas. Because of economic and environmental harms by chemical control, it is necessary to develop cultivars with adequate genetic resistance for reduction of yield losses. The purpose of this study was to find an effective method of inoculation with S. sclerotiorum under field evaluations. Three stem-inoculation techniques including: 1 – mycelium plug, 2 – oxalic acid solution (OAS) and 3 – infested wheat seeds with Sclerotinia mycelium were employed under field conditions. Four genotypes including Ghalami (local variety in market), Confeta, Allstar and Master were used in this study. The lesion length, lesion width and lesion as up and down leading on the stem from inoculation site were measured after 3, 7, 10 and 14 days of inoculation. The analysis of variance showed significant difference between all employed techniques and incubation days after inoculation. Mycelial plug (MP) inoculation technique produced significantly more developed lesions on the treated stems. In spite of this effect, Master variety demonstrated reasonable resistance reaction against the disease. The progress of disease in wounded treatments was also faster than the non-wounded ones. And, the shortest time to obtain significant differences between varieties was 10?days after inoculation. By comparison of results of lesion length at flowering and seed-filling stages, the more obvious effectiveness of the disease was observed at the second stage. Finally, there were negative correlations between mean temperature and mean lesion length in all three inoculation methods.     

Local and systemic changes in glucosinolates in Chinese and European cultivars of oilseed rape (Brassica nap us L.) after inoculation with Sclerotinia sclerotiorum (stem rot)

Four Chinese Brassica napus lines, generated through a breeding programme to identify Sclerotinia sclerotiorum tolerant and susceptible lines, and three European varieties were analysed for changes in glucosinolates (qualitative and quantitative), and general host reactions, after localised inoculation with a UK S. sclerotiorum isolate. Plants at the fifth leaf stage were either singly inoculated (third leaf) or were inoculated once (third leaf) and then challenged a second time (seventh leaf) 7 days after the first inoculation. The results showed very distinct reactions in the different lines and cultivars to the fungus, both locally and systemically. Of the European lines B. napus cv. Bienvenu showed good resistance (small lesions and less host damage) both 3 and 7 days post-inoculation. Capricorn was the most susceptible followed by Cobra; the third leaves of these cultivars were showing strong chlorotic and necrotic reactions by day 3 and lesions were well developed. By day 7 the third leaves of Capricorn were completely rotten whilst Cobra still had a little healthy tissue. Inoculation of the four Chinese lines showed that two had moderate resistance (014 and 020 — slightly less resistant than Bienvenu) and two were very susceptible (016 and 024 — similar reactions to Capricorn and Cobra), based on lesion size and host tissue damage. Glucosinolate induction in line 014 was good both locally and systemically, with clear local and systemic induction of indolylglucosinolates and 2-phenylethylglucosinolate both 3 and 7 days post-inoculation. Line 020 did not show no particular increases in glucosinolates after inoculation either locally or systemically. In line 016 there was a small local increase and a large systemic reduction in total glucosinolates. Inoculation of line 024 caused no major local changes in glucosinolates and again a big reduction in glucosinolates systemically. The dual inoculation system, with lines 014 and 016, produced comparable results, with line 014 showing good local and systemic induction of glucosinolates (after the first inoculation) and a further local and systemic induction after the second inoculation. This induction in pre-inoculated line 014 plants was associated with a reduction in lesion size of the second inoculum. Line 016 responded poorly both locally and systemically, and there were no real decrease in the lesion size of the second inoculum. It appears that in line 014 glucosinolate induction may be an important part of resistance, whereas in line 020 there are clearly other non-glucosinolate factors involved. The poor local and systemic induction of glucosinolates in lines 016 and 024, and subsequent susceptibility, implies that glucosinolate induction may be an important marker of resistance to S. sclerotiorum in oilseed rape.     

Effects of Bean Leaf Age on Pathogenicity by Botrytis fabae

Leaves from field bean plants grown out of doors were inoculated with conidia of B. fabae immediately after detaching from stems. The oldest leaves developed more lesions than youngest ones, although they were not chlorotic. On intact plants at high humidities, established lesions on young leaves increased in size at only half the rate of those on old. but still green leaves. Seven days after inoculation a higher proportion of lesions on old leaves bore conidia than those on young leaves, but leaf age had no significant effect on numbers of conidia per mm² of lesion area. Young leaflets from bean plants grown in a controlled environment or in the field challenged with β. cinerea accumulated more phytoalexins than did old ones.     

An Analysis of the Effects of Tobacco Mosaic Virus on Growth and the Changes in the Free Amino Compounds in Young Tomato Plants

Tomato plants at the four-leaf stage were inoculated on thefirst leaf with TMV in a growth room and the effects studiedin systemically-mfected leaves with reference to growth, virusmultiplication and changes in water, nitrogen, nitrate and chlorophyllcontents. Parallel changes in the free amino compounds werealso studied in the growth room (incident radiation 152 mwhcm^-2 day^-1) and in two experiments in a glasshouse (352 and226 mwh cm^-2 day^-1) Dry matter accumulation and leaf expansion in leaves 3, 4 and5 were checked by TMV 5–7 days after inoculation but notin leaf 2. In the period 7–25 days after inoculation therelative growth rates of whole plant and leaves 3 and 6 andnet assimilation rate were not affected by TMV. Stem heightand dry weight were not affected by TMV but ‘root’dry weight was reduced from days 5–15. Virus was presentin the stem and in leaves 2 and 6 by days 3, 5 and 15 respectivelyso that infection per se did not always check growth. Chlorophyllcontent of systemically-infected leaves was reduced 10 daysafter inoculation. Total N and ammonia contents were not affectedby TMV but infected leaves contained less nitrate. At the two lower levels of incident radiation the initial effectof TMV was to reduce the content of total free protein aminoacids and amides, which were minimal 5–7 days after inoculation.In the glasshouse experiment a reduction could be measured only1 day after inoculation or before virus was present in the youngerleaves. With high incident radiation there was no initial reductionbut an increase at day 13 when mottling symptoms were visible.Total non-protein amino acids, of which amino butyric acidwas the major constituent, were increased by TMV in all threeexperiments for up to 13 days after inoculation. It is suggested that inoculation of a leaf with TMV temporarilyinterferes with export of photosynthates and import of root-synthesisedamino acids and that the results reported above can be interpretedin this context. Evidence in support of this is adduced froman experiment in which 13 foliar sprays of gibberellic acid(2·5 ppm) were combined with TMV inoculation and thechanges in free amino compounds followed. It is concluded that analyses of the changes in individual freeamino compounds are unlikely to provide useful information concerningthe sources of virus coat protein.     

Inhibition of murine retrovirus-induced neurodegeneration in the spinal cord by explant culture.

The neurovirulent chimeric mouse ecotropic retrovirus FrCasE causes a rapid neurodegenerative disease of the central nervous system (CNS) characterized by the appearance of spongiform lesions in motor areas 10 days after neonatal inoculation. To study the details of the pathogenic process, we examined the ability of an ex vivo spinal cord model to recapitulate disease. Organotypic spinal cord slice cultures were established from IRW mice 7 days after neonatal inoculation. This corresponds to a time when virus expression in the CNS is first detectable but spongiform changes have yet to evolve. Infectivity associated with these cultures peaked at 7 days in vitro and persisted at this level for 6 weeks. FrCasE infection of the spinal cord slices was primarily found associated with microglial cells. Infection of neurons, astrocytes, oligodendroglia, and endothelial cells was not observed; however, significant astrogliosis was found. Despite the presence of extensive microglial infection in close association with spinal motor neurons in organotypic cultures, no virus-specific spongiform degenerative changes were observed. These results suggest that removal of motor neurons from the developing CNS, despite maintaining the local cytoarchitectural relationships, prevents the virus from eliciting its pathological effects. Possible reasons for the interruption of lesion development are discussed.     

Dye-coupling in Tobacco Mesophyll Cells Surrounding Growing Tobacco Mosaic Tobamovirus-induced Local Lesions

Some factors related to cessation of the movement of tobacco mosaic tobamovirus (TMV) in the late phase of a defence response were examined. Mesophyll cells surrounding the local lesions induced by TMV in N. tabacum cv. Xanthi‐nc were micro‐injected with fluorescent dye 2, 3 and 7 days post‐inoculation. At 7 days post‐inoculation, twelve out of 20 injections into cells adjacent to the lesion, showed the expected dye‐coupling (outflow of fluorescent dye from injected cell to adjacent ones via plasmodesmata) whereas 17–20 out of 20 injections were successful in other cases. Callose inhibitor (tunicamycin), dark treatment and incubation of plants with ascorbic acid, which play a role in blocking plasmodesmata or induction of defence responses, did not seem to have an effect on lesion growth. These data imply that defects in the plasmodesmal function, although not total, may account for the formation of late local defence reaction together with other factors that restrict viral spread in the continuous cell‐to‐cell mode in mesophyll tissue.     

Effect of abscissic acid on tobacco mosaic virus

Abscisic acid (ABA) did not affect the infectivity of tobacco mosaic virus (TMV) in vitro. The same dilutions of ABA when applied on the leaves of Chenopodium amaranticolor Coste and Reyn. at different intervals before inoculation affected development of local lesions variably at different dilutions. The inhibition of local lesion formation was reduced at other intervals leading to stimulation at thirty minutes and six hours intervals. Post-inoculation treatments with 2 mg/l of ABA gave stimulation of local lesion formation, though other dilutions gave inhibition. Viral concentration was stimulated in the tomato seedlings root dipped in 0.2 mg/l of ABA for 6 hours and inoculated 24 hours after transplantation. Incorporation of different concentrations of ABA into tissue culture medium reduced the growth of the TMV infected tobacco callus tissue and stimulated the infectivity of the tissue grown over it assayed after three weeks.     

Modulation of types I and III procollagen synthesis at various stages of arterial smooth muscle cell growth in vitro

Collagen synthesis was monitored in cultures of rabbit arterial smooth muscle cells (SMC). Both the rate of collagen synthesis per cell and collagen synthesis as a percent of total protein synthesis were measured at specific intervals from 1 to 14 days after inoculation of smooth muscle cells. The proportions of types I and III collagen present in the conditioned incubation medium and in the cell layer were also examined. After inoculation the cells displayed population expansion typical of SMC in which growth slowed but did not cease after the cells attained confluence. Collagen synthesis rates, expressed as [14C]hydroxyproline per cell, were eight-fold higher in preconfluent cells. In these cultures collagen accounted for more than 20% of the newly synthesized, 14C-labeled protein present as trichloroacetic acid (TCA)-insoluble material in 24 h culture media. In post-confluent cultures, this percentage was reduced to about 7% of the total protein synthesized. Synthesis rates of both collagen and non-collagen protein decreased with increasing time after inoculation. However, the rate of decline of collagen synthesis was three times greater than that seen for non-collagen protein. Early cultures synthesized relatively more type I than type III procollagen. The type I to type III ratio was highest at day 3 and declined after that time to day 14. While the synthesis of both types decreased with increasing age, type I declined at a greater rate resulting in a predominance of type III procollagen secretion by older cultures. We conclude that protein synthesis in general and collagen synthesis in particular are quantitatively and qualitatively dependent upon the growth stage of SMC in vitro.     

The Novel Oomycide Oxathiapiprolin Inhibits All Stages in the Asexual Life Cycle of Pseudoperonospora cubensis - Causal Agent of Cucurbit Downy Mildew

Oxathiapiprolin is a new oomycide (piperidinyl thiazole isoxazoline class) discovered by DuPont which controls diseases caused by oomycete plant pathogens. It binds in the oxysterol-binding protein domain of Oomycetes. Growth chambers studies with detached leaves and potted plants showed remarkable activity of oxathiapiprolin against Pseudoperonospora cubensis in cucurbits. The compound affected all stages in the asexual life cycle of the pathogen. It inhibited zoospore release, cystospore germination, lesion formation, lesion expansion, sporangiophore development and sporangial production. When applied to the foliage as a preventive spray no lesions developed due to inhibition of zoospore release and cystospore germination, and when applied curatively, at one or two days after inoculation, small restricted lesions developed but no sporulation occurred. When applied later to mature lesions, sporulation was strongly inhibited. Oxathiapiprolin suppressed sporulation of P. cubensis in naturally-infected leaves. It exhibited trans-laminar activity, translocated acropetaly from older to younger leaves, and moved from the root system to the foliage. Seed coating was highly effective in protecting the developed cucumber plants against downy mildew. UV microscopy observations made with cucumber leaves infected with P. cubensis revealed that inhibition of mycelium growth and sporulation induced by oxathiapiprolin was associated with callose encasement of the haustoria.