Fluazifop-butyl causes membrane peroxidation in the herbicide-susceptible broad leaf weed bristly starbur (Acanthospermum hispidum)

In order to clarify the action mechanism of fluazifop-butyl, an aryloxyphenoxypropionate (AOPP) herbicide in bristly starbur (Acanthospermum hispidum DC.), a unique fluazifop-butyl-susceptible broad-leaved weed, ethylene evolution and membrane lipid peroxidation in the plant seedlings were investigated. Foliar application of fluazifop-P-butyl induced ethylene evolution only from bristly starbur, but not from oat (Avena sativa L.), another fluazifop-butyl-susceptible species, and two tolerant species, pea (Pisum sativum L.) and hairy beggarticks (Bidens pilosa L.). The other AOPP herbicides, quizalofop-ethyl and fenoxaprop-ethyl, and a cyclohexanedione (CHD) herbicide, sethoxydim, did not enhance ethylene production from bristly starbur. This fluazifop-butyl-induced ethylene production in bristly starbur was completely suppressed by aminoethoxyvinylglycine (AVG), a 1-aminocyclopropane-1-carboxylic acid (ACC) synthase inhibitor, but not by p-chlorophenoxyisobutyric acid (PCIB), an anti-auxin compound, suggesting this evolved ethylene was not auxin-induced. Phytotoxic action by fluazifop-P-butyl (5 μM) in bristly starbur was reduced markedly by two lipid-soluble antioxidants, vitamin E, and ethoxyquin. The ethylene production from the plant was also inhibited by these two antioxidants. Content of malondialdehyde, an indicator of lipid peroxidation, increased only by fluazifop-P-butyl in bristly starbur seedlings but not in oat, and this increase was inhibited by ethoxyquin. These results strongly suggest that the primary site of action for fluazifop-butyl in bristly starbur is on the membranes and active oxygen species and/or free radicals are involved in peroxidation. Ethylene evolution is probably induced by these reactive oxygen species.     

Nitrogen metabolism disorder in watermelon leaf caused by fusaric acid

The effect of fusaric acid (FA) on the activity of leaf nitrogen (N) metabolism enzymes in watermelon seedlings supplied with different N forms was studied. The results showed that FA inhibited nitrogen uptake and caused decreased leaf amide and protein but increased the content of ammonium and amino acids. When treated with FA the activities of enzymes in the pathway for the synthesis of amino acid in leaves (GS, GOGAT, and GDH) were decreased by 15–23%, 13–40%, and 71–86%, respectively. The activity of asparagine synthetase was decreased by 34–57%. The proteinase activity was initially increased by 37–125% at 12 h after treatment of FA but then subsequently decreased. The activity of glutamate-pyruvate aminotransferase was increased by 280–400%, though the activity of glutamate-oxaloacetate aminotransferase was decreased by 30–63%. It was suggested that FA inhibited the uptake of ammonium in seedlings and suppressed the activities of amino acid and amide synthases, while stimulating proteinase activity.A new pathogenic mechanism of watermelon infection by Fusarium spp. was found as FA caused the complete disorder and collapse of the host plant's nitrogen metabolism. This work provides a new insight into the progression of watermelon wilting caused by Fusarium oxysporum f.sp. niveum.     

Effects of light conditions on prodigiosin stability in the biocontrol bacterium Serratia marcescens strain B2

Serratia marcescens strain B2 is a potential biocontrol agent that produces the antibiotic pigment prodigiosin. When this strain was incubated under white or blue light conditions (<100µmol m^–2s^–1), prodigiosin concentration in bacterial cells decreased, but growth did not. However, red and far-red light had no effect on prodigiosin concentration in bacterial cells. Purified prodigiosin was degraded under white or blue light conditions but was not degraded under red and far-red light. Because white and blue light appeared to affect the stability of prodigiosin itself, light conditions may affect the suppressive effects of the biocontrol agent S. marcescens strain B2.     

Isophorone‐induced light‐independent lipid peroxidation and loss of cell membrane integrity

Isophorone (3,5,5‐trimethylcyclohex‐2‐en‐1‐one) is a plant‐derived volatile compound with strong phytotoxic activity. Here, we aimed to elucidate the mechanism of action of isophorone, and to this end, the effects of isophorone on shoot fresh weight, chlorophyll content, electrolyte leakage, and lipid peroxidation of Lactuca sativa L. and photosynthetic electron transport activity in chloroplast isolated from Spinacia oleracea L. were investigated. Isophorone induced light‐independent decreases in shoot fresh weight and light‐dependent chlorosis. In addition, increased electrolyte leakage and lipid peroxidation occurred under light conditions. However, the inhibitory activity on photosynthetic electron transport was unexpectedly low, and electrolyte leakage and lipid peroxidation were induced even under dark conditions. These results suggest that the inhibition of photosynthetic electron transport is not the main mechanism of action of isophorone and that the phytotoxic effects are mainly due to light‐independent oxidative damage and subsequent loss of cell membrane integrity.     

Biocontrol strain of Bacillus subtilis AF 1 rapidly induces lipoxygenase in groundnut (Arachis hypogaea L.) compared to crown rot pathogen Aspergillus niger

Metabolic products of polyunsaturated fatty acids have been variously implicated in control of microbial pathogens. Induced resistance has been shown as one of the mechanisms of biological control by plant growth promoting rhizobacteria (PGPR). This paper reports a significant lipoxygenase (LOX) activity in groundnut seedlings with production of 13-hydroperoxyoctadecadienoic acid (13-HPODE) and 13-hydroperoxyoctadecatrienoic acid (13-HPOTrE) as major products with linoleic acid (LA) and -linolenic acid (ALA), respectively. Both the hydroperoxides are inhibitory to the growth of Aspergillus niger as measured in micro titer plates. Ours is the first report on induction of LOX activities in groundnut on treatment with a PGPR strain Bacillus subtilis AF 1, and with crown-rot pathogen, A. niger. Treatment with B. subtilis AF 1 enhanced LOX levels in groundnut similarly but earlier to A. niger – treatment. This induction of LOX during activation of growth and pathogen infection was discussed in light of the reported involvement of LOX both in growth and development as well as in plant-pathogen interaction, particularly induced disease resistance.     

Introduction

The effect of soil water potential on wheat seedlings infected withPuccinia recondita was studied. The seedlings were grown in soil of which the initial water potential was –200 Jkg^–1, –500 Jkg^–1, or –800 Jkg^–1. Uredospore production per seedling was retarded when the soil water potential was low, and soil water potential decreased more rapidly near the roots of diseased seedlings than it did near the roots of uninoculated seedlings.samenvatting Tarwekiemplanten werden geplaatst in plastic kolommen (een plant per kolom) gevuld met grond van bekende waterpotentiaal. Bij een deel der planten werd het eerste blad geïnoculeerd met bruine roest. De spruit boven het eerste blad werd regelmatig weggeknipt. Periodiek werden bepaald (veelal middels destructieve bemonstering) vers en droog gewicht van het eerste blad, roestsporenproduktie, en waterpotentiaal van de grond op drie niveau's in de kolommen. Voor de resultaten zie Fig. 1 t/m 4. Twee weken na inoculatie gaan zieke planten geleidelijk meer water verdampen dan onbehandelde planten (Fig. 1). Vers gewichten van zieke bladeren waren kleiner dan die van onbehandelde planten (Fig. 2). Het watergehalte van zieke bladeren werd lager dan dat van onbehandelde bladeren (Fig. 3). De uredosporenproduktie was bij hogere grondwaterpotentiaal groter dan bij lagere potentiaal (Fig. 4).     

Phytotoxic activity of middle-chain fatty acids I: effects on cell constituents

Phytotoxic activity of several middle-chain fatty acids, especially pelargonic acid (C9 acid) was investigated. C9–C11 acids caused strong non-selective damage to plants such as crabgrass, cucumber, velvetleaf, and tobacco, while C6 and C14 fatty acids had almost no activity. Middle-chain fatty acids caused a strong and rapid electrolyte leakage. They reached highest conductivity in 3 h in the case of cucumber cotyledons. Middle-chain fatty acids caused a decrease of the amount of polar lipids, particularly MGDG and PG, and chlorophylls. They also caused an increase of free fatty acids in 24 h after treatment. These results suggested that middle-chain fatty acids caused severe damage to cell membranes and thylakoid membranes of treated leaves. C6 volatile compounds such as cis-3-hexenal, trans-2-hexenal, and cis-3-hexenol were generated in less than 1 h after spraying pelargonic acid to tobacco leaves. The application of pelargonic acid was thought to be the trigger for linolenic acid degradation in the thylakoid membranes.     

First report of Rhizomonas sp. causing corky root of lettuce in Europe

Typical symptoms of corky root were observed on iceberg lettuce (Lactuca sativa L.) in the Netherlands and England, on prickly lettuce (Lactuca serriola L.) in Spain, and on sowthistle (Sonchus oleraceus L.) in Greece. Slow-growing bacteria with similar colonies as strains ofRhizomonas suberifaciens or otherRhizomonas species were isolated from soil surrounding plants with corky root symptoms using lettuce seedlings as bait. Crude lysate from all strains was tested for DNA homology with DNA fromR. suberifaciens strain CA1 (R. sub. CA1) andRhizomonas sp. strain WI4 (R. sp. WI4). Strains that had homology values higher than that ofR. sp. WI4 orR. sub. CA1 were tested for pathogenicity on 1-wk-old lettuce seedlings, cv. Salinas, Two strains from the Netherlands induced typical symptoms of corky root on lettuce. These strains tested negative with monoclonal antibody MAb-Rs1 specific forRhizomonas suberifaciens in an enzyme-linked immunosorbent assay (ELISA). They had low DNA homology withR. sub. CA1 (4–9%) and low to moderate DNA homology withR. sp. WI4 (4–17%). Some nonpathogenic strains had moderate to high levels of DNA homology withR. sub. CA1 orR. sp. WI4 (19–84%). All strains had fatty acid profiles similar to those ofRhizomonas species. This is the first report ofRhizomonas sp. causing corky root of lettuce in Europe.     

活性氧及膜脂过氧化与棉花对枯萎病抗性的关系

 萎病菌侵染后,抗病品种棉苗及经氟乐灵诱发处理产生对枯萎病诱导抗性的棉苗茎与根组织中,膜脂过氧化产物丙二醛(MDA)含量上升,膜系统中不饱和脂肪酸含量下降,表明有膜脂过氧化的发生,超氧阴离子(O₂^·)的产生速率、H₂O₂的积累水平及脂氧合酶(LOX)活性也明显增加,但超氧化物歧化酶(SOD)及过氧化氢酶(CAT)活性无显著差异。与此相反,感病品种棉苗受侵后MDA含量、O₂^·产生速率、H₂O₂的积累及LOX酶活性增加幅度较小,SOD及CAT酶活性则明显上升,膜系统中不饱和脂肪酸含量仅有小幅度下降。氟乐灵播前土壤处理可诱发棉苗对枯萎病的诱导抗性,同时也增加了LOX酶活性及活性氧(O₂^·、H₂O₂)的积累。这些结果说明,枯萎病菌侵染后棉苗体内活性氧的积累、LOX酶活性的上升以及由此引起的膜脂过氧化,可能在棉苗对枯萎病的抗性中起作用。     

Influence of soil type and pH on the colonisation of sugar beet seedlings by antagonistic Pseudomonas and Bacillus strains,and on their control of Pythium damping-off

In five different soils originating from Scotland (Craibstone and Cruden Bay), Germany (Magdeburg and Uelzen) and Greece (Tymbaki), Pseudomonas fluorescens B5 reached higher population sizes (4.7–5.7logCFU/plant) on 12-day-old sugar beet seedlings than Bacillus subtilis MBI 600 (4.1–4.8logCFU/plant). Total population size per plant was not affected by soil type. In all five soils, the antagonists reached highest population densities in the hypocotyl and the upper 2cm root section (P. fluorescensB5: 5.2–6.8log₁₀CFU/g plant fresh weight, Bacillus subtilisMBI 600: 5.2–6.1log₁₀CFU/g plant fresh weight) and declined to 0–3log₁₀CFU below 4cm root depth. Colonisation by P. fluorescens B5 down the root was slightly increased in the soils from Craibstone, Magdeburg, and Uelzen compared to the sandy clay loam from Tymbaki. In lux-marked P. fluorescens B5, population density was positively correlated with light emission in all soils; the light emission indicated physiological activity of the strains. However, P. fluorescens B5 reduced Pythium damping-off (measurement after 14 days plant growth) only in three of the five soils (Craibstone, Cruden Bay and Magdeburg). Co-inoculation of B. subtilis MBI 600 increased downward colonisation of the root by P. fluorescens B5, but not the total population ofP. fluorescens B5 per plant. Bacillus subtilisMBI 600 did not reduce Pythium damping-off in any of the soils nor did it influence the efficiency of co-inoculated P. fluorescens B5; its population consisted mainly of physiologically inactive spores. In Craibstone soil, pH did not affect population density, distribution along the root or biocontrol activity against P. ultimum of P. fluorescens B5 or B. subtilis MBI 600.     

Effect of treating soybean with 2,6-dichloroisonicotinic acid (INA) and benzothiadiazole (BTH) on seed yields and the level of disease caused by Sclerotinia sclerotiorum in field and greenhouse studies

Field or greenhouse grown soybeans were treated with 2,6-dichloroisonicotinic acid or benzothiadiazole and subsequently assessed for severity of white mold disease caused by Sclerotinia sclerotiorum. Three or four applications of 2,6-dichloroisonicotinic acid to field plots in 1993–1995 reduced severity of white mold after natural infection by 20–70&percnt; compared with water-treated controls in soybean cultivars Elgin 87 and Williams 82, which are considered to be highly susceptible to the disease. The effect was not as large in the cultivars Corsoy 79 and NKS19-90 which are more resistant to white mold. Two or four applications of benzothiadiazole to field plots in 1995 and 1996 reduced white mold severity by 20–60&percnt;, with the greatest reductions again observed in the more susceptible cultivars. Corresponding yields were increased compared with controls, particularly for the susceptible cultivars under conditions of high disease pressure. In greenhouse trials multiple applications of either compound resulted in significantly smaller lesion diameters following subsequent leaf inoculations with the fungus. The compounds did not result in observable phytotoxicity or inhibit growth of Sclerotinia sp. in vitro. We hypothesize that the decrease in disease severity following treatment with INA or BTH is a result of resistance induction.     

Effect of acetochlor treatment on Fusarium wilt and sugar content in melon seedlings

Pretreatment of soil with the herbicide acetochlor at 0.1–1g g^–1 significantly decreased incidence of wilt due toFusarium oxysporum f. sp.melonis in melon seedlings. Glucose, fructose and sucrose increased in leaves of inoculated and uninoculated melon plants following acetochlor treatment. The increase in sugar levels in stems and roots was less pronounced. Light intensity affected sugar content and disease incidence. The percentage of diseased plants was significantly higher in untreated plants grown under 165E m^–2 sec^–1 compared to plants grown under 300E m^–2 sec^–1. Lowering light intensity resulted in reduction of levels of total sugars on the third and sixth day after inoculation. Acetochlor had little or no effect on growth rate or sporulation of the pathogen in culture. The colonization rate of diseased plant stems by the pathogen was similar in herbicide-treated and untreated plants, thus excluding the possibility that disease reduction by the herbicide is related to direct fungitoxicity.Contribution from the Agricultural Research Organization. No. 1560-E, 1995 series.     

Studies on the Inherent Resistance Risk to Fenhexamid in Botrytis cinerea

After chemical mutagenesis with N-methyl-N-nitrosoguanidine (MNNG) two phenotypes that were highly or moderately resistant to fenhexamid, were isolated from a wild-type strain of Botrytis cinerea, at a mutation frequency of 0.9 × 10^–5. Resistance factors, based on EC⁵⁰ values, were 460–570 and 10–15, respectively. The mutation(s) for resistance to fenhexamid did not affect the sensitivity of mutant strains to the benzimidazole benomyl, the phenylpyridinamine fluazinam, the anilinopyrimidine cyprodinil, the guanidine iminoctadine or to the sterol-biosynthesis-inhibiting fungicides fenarimol, fenpropimorph and tridemorph. On the contrary, an increased sensitivity (EC⁵⁰ ratios of 0.2–0.6) of fenhexamid-resistant strains to the phenylpyrrole fludioxonil and the dicarboximide iprodione was observed. Study of fitness parameters of fenhexamid-resistant isolates of both phenotypic classes showed that these mutation(s) had no effect on mycelial growth and sensitivity to high osmolarity, but they did affect one or more of some other characteristics, such as sporulation, conidial germination and sclerotia production. In tests on cucumber seedlings under greenhouse conditions, all highly fenhexamid-resistant isolates tested presented decreased infection ability compared with the wild-type. Preventive applications of a commercial formulation of fenhexamid, Teldor 50 WP, were effective against lesion development on cotyledons by the wild-type, but ineffective, even in high concentrations, against disease caused by the fenhexamid-resistant isolates. The risk of resistance problems arising during commercial use of fenhexamid is discussed.     

Polygalacturonase isoenzymes and oxalic acid produced by Sclerotinia sclerotiorum in soybean hypocotyls as elicitors of glyceollin

The polygalacturonases (PG) and oxalic acid produced by Sclerotinia sclerotiorum in infected soybean hypocotyls were investigated as elicitors of the phytoalexin glyceollin I.Purification to homogeneity through isoelectrofocusing and ion-exchange fast protein liquid chromatography revealed three endo-PG isoenzymes (PG-I, PG-II and PG-IV) and one exo-PG (PG-III) in 6-day-old etiolated soybean hypocotyls infected with the B-24 isolate of S. sclerotiorum.PG-I and PG-III, in the range of concentrations tested (0·15–1·2 reducing units ml⁻¹), did not act as elicitors of glyceollin I synthesis. Some elicitor activity was shown by PG-II at 0·6–1·2 reducing units ml⁻¹. PG-IV, at lower doses (0·038–0·30 reducing units ml⁻¹), was even more effective in inducing phytoalexin synthesis. However higher concentrations of PG-IV induced tissue softening and decreased phytoalexin accumulation.PG-II and PG-IV released heat-stable elicitors from purified soybean cell walls supporting the evidence that uronides are intermediate inducers in elicitation by endo-PGs. Oxalic acid was an active elicitor of glyceollin I over the range of concentrations tested (0·31–20 m ) with the maximum at a concentration of 5 m . The inability of oxalic acid to release uronides from purified cell walls makes it unlikely that uronide intermediate elicitors are involved in elicitation by oxalic acid.     

Requirement of Host Signaling Mechanisms for the Action of Ptr ToxA in Wheat

Ptr ToxA, the host-selective toxin produced by Pyrenophora tritici-repentis, is genetically associated with the development of tan spot disease of wheat. The toxin was shown previously to cause a programmed cell death in the host that requires de novo mRNA and protein synthesis. In the present study, inhibitors of plant signaling mechanisms protected wheat leaves from toxin action, as determined by electrolyte leakage bioassays, when applied to leaves with toxin. Okadaic acid, calyculin A and phenylarsine oxide, all inhibitors of protein phosphatase activity, reduced toxin-induced electrolyte leakage by more than 90%. Inorganic calcium channel blockers (LaCl₃ and CoCl₂ reduced toxin-induced electrolyte leakage by 78–95%, depending on inhibitor and time of measurement. By comparison, about 50% protection was achieved by the application of the protein kinase inhibitors staurosporine and K-252A. Nonetheless, the reduction in toxin-induced electrolyte leakage by protein kinase inhibitors was reproduced in multiple trials and was statistically significant. The data indicate that host signaling mechanisms, including calcium fluxes and a protein phosphorylation cascade, are required for the Ptr ToxA-induced cell death in wheat. Our current model holds that the signaling events occur between toxin perception by the cell and the toxin-directed gene expression in the host associated with cell death. As an alternative, the toxin-induced mRNA synthesis required for cell death may be for protein phosphatase and/or protein kinase genes. Additional work is required to resolve these possibilities.     

Possible Root Infection of Cercospora beticola in Sugar Beet

A potential primary infection site of the foliar pathogen Cercospora beticola in sugar beet is described. Sugar beet seedlings of the susceptible cv. Auris were grown in a standard soil for 14 days. A monoconidial culture of a C. beticola isolate was grown to produce conidia. In experiment 1, roots were immersed in a conidial suspension of isolate code IRS 00-4, or in tap water (control), for 2 days. After incubation seedlings were potted in a peat – fine river sand mixture and placed at low relative humidity (RH) (<80%) or high RH (100%). Twelve days after infection, seedlings at high RH showed more disease incidence (90%) than seedlings grown at low RH (disease incidence = 25%), whereas no disease symptoms developed in the control seedlings. Cercospora leaf spots (CLSs) developed on the cotyledons, leaves, petioles and stems of the seedlings. In experiment 2, roots were immersed in a conidial suspension of isolate code IRS 00-2 for 5 h. Thirty-four days after infection at high RH, 100% disease incidence was observed in the treated seedlings and one CLS in the control treatment. First indications of leaf spot development were observed as reddish purple discolouration of individual parenchymatic cells. Because splash dispersal and symptoms due to infested soil were excluded, we showed that it is possible to obtain CLS symptoms in sugar beet seedlings when their roots were immersed in conidial suspensions of C. beticola, thus demonstrating that roots can be a primary infection site.     

低温胁迫下戊唑醇和苯醚甲环唑种子包衣对玉米种子出苗和幼苗的影响

为研究低温胁迫下种子包衣对玉米种子出苗和幼苗生长的影响,以适宜温度(25℃/20℃,白天/晚上,下同)处理为对照,对不同剂量包衣的玉米种子进行低温胁迫。研究结果表明,戊唑醇和苯醚甲环唑种子包衣在适宜温度下对玉米种子出苗具有促进作用,能提高玉米幼苗植株的叶绿素含量,对玉米幼苗的株高和鲜重没有抑制作用。但在17℃/6℃、15℃/0℃、10℃/0℃低温胁迫下,戊唑醇和苯醚甲环唑均能抑制种子出苗和幼苗生长,加剧低温胁迫导致的膜脂质过氧化作用和对叶绿体的分解。但用苯醚甲环唑处理玉米种子比用戊唑醇更安全,前者能抑制低温胁迫导致的叶片细胞内电解质外渗,后者却会加剧电解质的外渗。比较玉米幼苗根系的呼吸作用也可以发现,苯醚甲环唑比戊唑醇更有利于玉米幼苗补偿和修复低温胁迫所致的伤害。     

Resistance Reaction of Conifer Species (European Larch, Norway Spruce, Scots Pine) to Infection by Selected Necrotrophic Damping-off Pathogens

Three conifer species (European larch, Norway spruce, Scots pine) were investigated for their resistance to five damping-off pathogens (Rhizoctonia solani, Fusarium solani, F. oxysporum, F. culmorum, F. avenaceum). Inoculation of the primary roots of seedlings with these pathogens caused host cell death which did not prevent the invasive growth of these fungi; seedlings that had formed secondary and tertiary roots could overcome the infection to a significant degree. Infections with R. solani caused significant mortality to all the conifer species. In contrast, the tree species expressed different levels of resistance when challenged with the Fusarium isolates, with Norway spruce being the most resistant compared to uninoculated controls. Some of the Fusarium isolates were more pathogenic to certain hosts than others; F. oxysporum for European larch, F. avenaceum for Scots pine, F. solani for European larch; only F. culmorum was significantly pathogenic to Norway spruce. No significant differences in disease severity were observed at different soil pH (4.3–7.5). Disease progression was delayed at lower (10–15°C) rather than higher temperatures (20–25°C).     

Effects of exogenous methyl jasmonate and light condition on grape berry coloration and endogenous abscisic acid content

Suitable postharvest treatment methods were investigated to improve the color of grape berries. Culture solutions containing jasmonic acid (JA), methyl jasmonate (MeJA), and prohydrojasmon (PDJ) enhanced the skin coloration of grape berries (‘Pione’) harvested at the initial stage of coloration. MeJA vapor treatment under sealed conditions increased anthocyanin accumulation in grape berries (‘AkiQueen’ and ‘Pione’) harvested at the early stage of skin coloration. Furthermore, promoting skin coloration by MeJA vapor treatment was as effective in mature clusters as it was in detached berries. These effects were confirmed in light conditions but not in constant darkness. Our results showed that postharvest MeJA vapor treatment improved skin coloration in grapes. In addition, postharvest treatment with MeJA was found to have no effect on the endogenous abscisic acid content of grape berry skins. Therefore, we suggest that MeJA vapor treatment can be a useful and labor-saving method for the horticultural industry.     

Differences in temperature requirements between Polymyxa sp. of Indian origin and Polymyxa graminis and Polymyxa betae from temperate areas

The temperature requirements of three single cystosorus strains of Polymyxa sp. from India were studied at 15–18, 19–22, 23–26 and 27–30 °C (night-day temperature), and compared with the temperature requirements of three strains of P. graminis from Belgium, Canada and France and two strains of P. betae from Belgium and Turkey. Sorghum was used as the host-plant for the Indian strains; the strains of P. graminis and P. betae from temperate areas were cultivated on barley and sugar beet, respectively. The cystosori germination and the development of plasmodia, zoosporangia and cystosori of Polymyxa sp. from India were optimal at 27–30 °C. Infection progression was slower at 23–26 °C than at 27–30 °C. At 19–22 °C, infection was insignificant. No infection occurred below 19 °C. In contrast, the infection of barley with P. graminis strains from temperate areas was optimal at 15–18 °C, but at 19–22 °C the progression appeared inconsistent and infection stayed low. Above 22 °C, infection was insignificant. P. betae strains showed consistent infection in the range of 15–18 °C to 27–30 °C. Plasmodia formation and cystosori detection of the Belgian strain were slightly advanced at 23–26 °C compared to 19–22 °C but clearly restrained at 27–30 °C. Fungus development of the P. betae strain from Turkey was almost as high at 27–30 °C as at the lower temperatures. These results strengthen the case for distinguishing between Polymyxa sp. from India and P. graminis or P. betae from temperate areas.