Effect of temperature on head blight of wheat caused by Fusarium culmorum and F. graminearum

The effect of small temperature differentials (16 vs. 20°C) on the pathogenicity of deoxynivalenol producing single isolates of Fusarium culmorum and F. graminearum and on the fusarium head blight (FHB) response of eight wheat cultivars was examined. Fusarium culmorum inoculation caused greater visual disease symptoms at 20°C than at 16°C, both overall and on an individual cultivar basis (overall AUDPC = 13·5 and 9·6, respectively) ( P  < 0·05). In contrast, F. graminearum inoculation caused greater overall visual disease symptoms at 16°C than at 20°C, both overall and at the individual cultivar level (overall AUDPC = 12·8 and 10·9, respectively) ( P  < 0·05). Results showed both F. culmorum and F. graminearum inoculations caused a greater loss in yield at 20°C (54·3 and 46·9% relative 1000-grain weight, respectively) compared with 16°C (73·3 and 66·9% relative 1000-grain weight, respectively) ( P  < 0·05). Fusarium culmorum -inoculated heads contained similar amounts of fungal DNA at both 16 and 20°C (1·9 and 1·7 ng mg⁻¹ of plant material, respectively) (not significant), while for F. graminearum inoculation, plants contained higher amounts of fungal DNA at 20°C (2·0 and 1·0 ng mg⁻¹ of plant material, respectively) ( P  < 0·05). Overall, there was a significant negative correlation between AUDPC and percentage relative 1000-grain weight at both 16 and 20°C ( r  =−0·693 and −0·794, respectively, P  < 0·01).     

Leaf scald (Xanthomonas albilineans) incidence and its effect on yield in seven sugarcane cultivars in Guadeloupe

Seven 5—month-old sugarcane cultivars difTering in resistance to leaf scald disease were inoculated by the decapitation technique with Xanthomonas albilineans. The effects of disease progress and incidence on yields were studied for the plant (first harvest) and two ratoon crops (second and third harvest). The percentage of diseased stalks and disease severity at first harvest 5 months after inoculation were 0·7 and 0·4, respectively, for the most resistant cultivar and 71·0% and 63·3, respectively, for the most susceptible cultivar. They decreased in all cultivars in both ratoon crops, but were still important in one cultivar (B69379). Significant ( P = 0·05) yield reductions of 12% and 21% occurred in two of the seven cultivars (B69566 and B69379, respectively). The number of symptomatic sugarcane stalks in the first ratoon crop (second harvest) was lower than the number of stalks colonized by the pathogen. Symptoms and yield losses of cultivars R570 and B69566 varied with the crop. Yield losses occurred in cultivar R570 only in the plant crop when this cultivar displayed numerous symptoms. Cultivar B69566 appeared to recover from the disease to a certain extent from the plant to the second ratoon crop (third harvest), as did the resistant cultivars in the first ratoon crop. In contrast, severe leaf scald symptoms were observed in the case of cultivar B69379 regardless of the crop, and significant yield losses occurred in the two ratoon crops. These results support the recommendation that cultivar B69379 should not be replanted in Guadeloupe.     

Stilbene glucoside levels and the resistance of Sitka spruce (Picea sitchensis) tissues to colonization by root- and butt-rotting fungi

The relationship between constitutive stilbene glucoside (astringin and isorhapontin) levels in Sitka spruce (Picea sitchensis) bark and resistance of these tissues to colonization by the root- and butt-rot fungi Heterobasidion annosum and Phaeolus schweinitzii was determined in vitro in excised bark tissues. Two experimental systems were developed. In one, 15-mm-diameter bark discs taken from mature forest trees were challenged with mycelial cultures of the fungi; in the other, 70- or 100-mm lengths of stem, up to c. 30 mm diameter, were similarly challenged at the lower cut end. The extent of fungal colonization or necrosis in the challenged tissues was determined. The results indicated that both systems were capable of detecting differences in bark susceptibility to colonization between individual trees. No consistent correlation between stilbene levels and resistance to colonization by either fungus was found.     

Pathogenicity of four blue-stain fungi associated with aggressive and nonaggressive bark beetles

ABSTRACT The pathogenicity of two isolates of each of four bark beetle-associated blue-stain fungi was evaluated after mass inoculation of about 40-year-old Norway spruce trees (Picea abies). Trees were inoculated with a different isolate of each fungus in 1995 and 1996 at a density of 400 inoculations per m(2) in a 1.2-m-wide band on the lower bole (about 270 inoculations per tree). Trees were felled 15 weeks after inoculation. In 1995, Ceratocystis polonica was the only fungus that had stained the sapwood (56.3% of cross-sectional sapwood area). It induced five times longer phloem necroses, 21 times more dead cambium, and 11 times more dead phloem than any other fungus. In 1996, C. polonica induced less extensive host symptoms and an unidentified Ambrosiella sp. induced comparable symptoms to C. polonica in the phloem and cambium. No trees showed any foliar symptoms 15 weeks after inoculation, but six out of eight trees inoculated with C. polonica in 1995 had only 0 to 25% functional sapwood and probably would have died if felling had been delayed. This study confirms that C. polonica, an associate of the aggressive bark beetle Ips typographus, is pathogenic to Norway spruce. The pathogenicity of the Ambrosiella sp., which is associated with a nonaggressive bark beetle, seems moderate and varies between isolates. The two remaining fungi included in this study (Ophiostoma piceae and a dark fungus with sterile mycelium), which are associated with nonaggressive bark beetles, were nonpathogenic in both experiments. These results are consistent with the hypothesis that aggressive bark beetle species vector virulent fungi that may help them kill trees, but the results also show that some nonaggressive bark beetles may vector phytopathogenic fungi.     

苹果树腐烂病的发病过程和药剂防治研究

本文分两部分。第一部分概述了陕西风县秦岭高地苹果树腐烂病的发生发展过程,指出腐烂病菌主要是先在树皮的落皮层内潜伏侵染,进而侵害健组织。第二部分为防治试验。根据腐烂病的发生发展过程,于6月下旬和11月中旬对主干和大枝下部涂40%福美砷可湿性粉剂50倍悬浮液二次,获得了施药部位新病减少90%,“病疤重犯”减少80%的防治效果。与在辽宁兴城的试验,防效近似。     

Assessing the virulence of four bark beetle-associated bluestain fungi using Norway spruce seedlings

The virulence of two isolates of each of four different bark beetle-associated bluestain fungi was evaluated by wound-inoculating 2- and 4-year-old Norway spruce seedlings. One isolate of Ceratocystis polonica killed 40% of the 2-year-old plants and 20% of the 4-year-old plants, whereas the other fungi ( Ophiostoma piceae , Ophiostoma sp., an unidentified fungus with dark sterile mycelium) and the control treatments (inoculation with sterile agar and unwounded plants) did not kill any plants during the 11-week incubation period. Only C. polonica and the Ophiostoma sp. caused any bluestain of the sapwood. The two C. polonica isolates caused significantly deeper bluestain penetration into the sapwood and longer necrotic lesions on the sapwood surface than all other isolates. The symptoms caused by the other fungi were similar to those on the sterile inoculated control plants. The virulence of the fungal isolates tested in this study agrees largely with results from a previous mass inoculation study using the same isolates inoculated into 40-year-old Norway spruce trees. Thus, inoculation of seedlings seems to be a reliable, inexpensive and convenient bioassay for determining the virulence of bark beetle-associated bluestain fungi.     

Effect of phenology on susceptibility of Norway spruce (Picea abies) to fungal pathogens

Ceratocystis polonica and Heterobasidion parviporum are important fungal pathogens in Norway spruce (Picea abies). Tree susceptibility to these pathogens with respect to phenology was studied using artificial fungal inoculations at six stages of bud development, and assessed by measuring phloem necroses in the stems of 2‐ and 8‐year‐old trees. Tree capacity for resistance was assessed by measuring phloem nonstructural carbohydrates at each stage. Phloem necroses were significantly larger in trees with fungal versus control inoculations and increased significantly over time. Changes in nonstructural carbohydrates occurred in the trees; a significant decline in starch and a slight but significant increase in total sugars occurred over time. These results suggest that susceptibility to fungal pathogens and carbohydrate levels in the stems of the trees were related to fine‐scale changes in bud development. A trade‐off may occur between allocation of starch (the major fraction of the stem carbohydrate pool) to bud development/shoot growth versus defence of the stem. Previous tests of plant defence hypotheses have focused on herbivory on plants growing under different environmental conditions, but the role of phenology and the effect of pathogens are also important to consider in understanding plant resource allocation patterns.     

Role of the Helix aspersa snail as a vector of Phytophthora citrophthora causing branch cankers on clementine trees in Spain

This study investigated the suspected role of invertebrate vectors in the transmission of phytophthora branch canker, a severe disease of clementine cultivars in Spain, caused by Phytophthora citrophthora . Ants ( Lasius grandis ) and snails ( Helix aspersa and Rumina decollata ) were collected in spring and autumn 2005 from 15 commercial citrus fields which were severely affected by the disease. Isolations made from L. grandis and R. decollata bodies did not yield positive results. However, P. citrophthora was isolated from 5·0% of bodies of H. aspersa and 4·8% of samples of their faeces. In one assay, after snails were allowed to feed for 5 h on citrus branches which had been artificially infected with P. citrophthora , the pathogen was isolated from 79% of their faeces. In another experiment, snails were infested by placing them in contact with a substrate colonized by P. citrophthora and then transferred to the base of potted 4-year-old trees of cvs Clemenules, Fortune and Nova in the glasshouse. One day after their release, infested snails were widely distributed throughout the tree canopies and 10 days later bark discoloration and gum exudations were observed on the trees. Phytophthora citrophthora was readily isolated from tissues showing symptoms.     

Dieback symptoms on olive trees caused by the fungus Eutypa lata1

The fungus Eutypa lata was isolated from olive trees for the first time in 1988 from two young 3-year-old trees. It was evident that the infection was initiated from the graft union. The trees were also infected by Armillaria mellea. In a second case in 1991, extensive cankers were observed along the branches which often were girdled and died. The infected area extended from the bark into the sapwood and even into the heartwood. Cultures made on potatodextrose agar from the margin of necrotic and healthy tissues resulted in typical colonies of the fungus E. lata, as well as of Verticillium dahliae. The colonies of E. lata produced the characteristic pycnidia of the anamorph Libertella blepharis 3–4 weeks later. Pathogenicity tests made on olive, apricot, almond and walnut trees resulted in the death of the inoculated twigs or in canker formation and extensive brown discoloration of the wood.     

Virulence of the invasive ash pathogen Hymenoscyphus fraxineus in old and recently established populations

Following its introduction from Asia in the 1990s, the ascomycete Hymenoscyphus fraxineus has caused a severe dieback of Fraxinus excelsior in Europe. In this study, the virulence of 200 H. fraxineus isolates were assessed and compared. These isolates equally represented (i) two geographically distant populations with a different disease history (Switzerland, recently established populations at the epidemic front versus Lithuania, old established populations), and (ii) isolates from two different types of host tissue (necrotic bark lesions as dead‐end tissue versus fallen leaf petioles as primary host tissue). Inoculations conducted on 3‐year‐old F. excelsior seedlings showed that the vast majority of the isolates (98%) were able to induce necrotic bark lesions after 10 months. Although a high variation in virulence was observed among isolates, no significant differences were detected between the older and the epidemic‐front populations. Decline in virulence of populations of invasive organisms is generally assumed with increasing age of epidemics. However, this does not appear to hold true for H. fraxineus. Either the Lithuanian population is still too young (15 to 20 years old) to show a decline in virulence, or the size of the host population may still not be critical for pathogen survival. Given that bark lesions represent an epidemiological dead end and do not benefit the survival of H. fraxineus, a trend towards reduced ‘bark virulence’ of isolates originating from leaf petioles compared to isolates from the bark lesions was expected. However, such a trend was observed neither in old, nor in recently established populations.     

Real-time PCR identification and detection of Fuscoporia torulosa in Quercus ilex

Fuscoporia torulosa is the causal agent of white alveolar wood decay on several species including a large number of forest trees. Early detection of the fungus is essential to identify diseased trees before spread occurs to healthy plants. However, current detection methods based on isolation from infected tissues on semi-selective media are laborious, time consuming and require expertise in identifying the pathogen after isolation. In the present study, a rapid and reliable Scorpion-PCR based molecular method to identify and detect F. torulosa in planta was developed in a highly polymorphic portion of the internal transcribed spacer (ITS) regions. Specificity of primers and probe was assessed by means of both BLAST analyses and by using genomic DNA from 131 F. torulosa isolates and 43 other fungi and oomycetes from different hosts and geographic areas. In Scorpion-PCR the limit of detection was 1 pg of total DNA and a high correlation ( r ² = 0·996) was achieved between target DNA quantity and cycle threshold (Ct). Real-time PCR combined with effective procedures for DNA extraction enabled the detection of F. torulosa from naturally infected tissues of oaks with and without fruit bodies in approximately 6 h. Comparative testing showed that detection of F. torulosa in wood samples is more sensitive and reliable with real-time PCR than with conventional isolation.     

Cocoa production in Ecuador in relation to dry-season escape from pod rot caused by Crinipellis perniciosa and Moniliophthora roreri

Cropping and disease patterns were observed over a period of 4 years in individual cocoa trees at three contrasting sites near Quevedo, Ecuador, with the aim of evaluating the importance of dry season production and the consequent avoidance of pod disease caused by Crinipellis perniciosa and Moniliophthora roreri. Distinction of the diseases on necrotic pods was aided by splitting open pods after removal from the tree. The year was divided into wet season (April to September) and dry season (October to March) harvest periods. The 3-month lag between the actual wet and dry seasons and these harvest periods allowed time for symptom development. Combined disease losses ranged from 19·0% to 62·1 % at the various sites. At all sites and in each year, more ripe healthy pods were harvested in the dry season harvest period than in the wet season harvest period. In general, pod losses caused by C, perniciosa were curtailed more sharply by the dry season than those caused by M. roreri , which at one site caused as much damage in the dry season as in the wet season. The proportion of the annual production falling in the dry season harvest period varied among sites and between years at a given site. A comparison of trees from two progenies growing side by side showed consistent differences in cropping patterns, and identified certain trees that were productive, yielded consistently in the dry season harvest period, and were little affected by M, roreri. Analysis of long-term rainfall data for the Quevedo region indicated that years which lack a normal dry season do occur, but only once every 10 years on average. Further exploitation of disease escape through selection and breeding appears to be both feasible and appropriate.     

Non-Host Volatiles Disrupt the Response of the Stenographer Bark Beetle, Ips sexdentatus (Coleoptera: Scolytidae), to Pheromone-Baited traps and Maritime Pine Logs

Non-host volatiles (NHV) were tested on antennae of Ips sexdentatus with coupled gas chromatographic-electroantennographic detection (GC-EAD). Significant antennal responses were found to aggregation pheromone components, ipsdienol and amitinol, an attraction inhibitor, verbenone, and non-host bark volatiles extracted from Betula pendula, including trans-conophthorin (tC) and alcohols. The tC, a blend of three green leaf alcohols (C6-alcohols), and a blend of two bark alcohols (C8-alcohols) were tested in combination for their ability to disrupt the attraction of the stenographer bark beetle to pheromone-baited traps, unbaited and pheromone-baited maritime pine logs. The strongest disruptive effect resulted from the addition of the tC combined with the blends of NHV alcohols at high release rate, achieving an 83% reduction in trap catches, 89% reduction of attacks on unbaited pine logs, and 60% on baited logs. It is proposed that the two types of NHV have an additive effect, tC playing a major role in pheromone disruption while the alcohols would interrupt host specific signals. The results suggest that I. sexdentatus uses both bark and green leaf volatiles from non-host tree species in the host selection process. These NHV are promising disruptants, which could be used to prevent stenographer bark beetle attacks on log piles or standing trees in forest. A mixture of conifers and broad-leaved species would also disturb olfactory guided host selection supporting the assumption that more diverse forests are less prone to pest insect outbreaks.     

Aetiology and causal agents of mango sudden decline disease in the Sultanate of Oman

Mango sudden decline is a recently introduced, economically serious disease in Oman. Affected mango trees have wilting symptoms that usually begin on one side and later spread to involve the entire tree. Trees exude amber-coloured gum from the bark of their trunks or branches and vascular tissues are discoloured. Having entered Oman in the recent past, survey data is presented that shows the disease to have spread throughout the northern part of the country. Evidence is presented that the vascular wilt pathogen Ceratocystis fimbriata causes mango sudden decline disease in Oman, possibly in concert with Lasiodiplodia theobromae and the recently described Ceratocystis omanensis. Isolates of these fungi from affected trees, cause infection and can be recovered from inoculated seedlings. Bark beetles (Hypocryphalus mangiferae) are shown to carry C. fimbriata and L. theobromae and are presumably responsible for transmitting both pathogens to healthy mango trees. Acting as a wounding agent and vector, the bark beetle is likely to have assisted the rapid spread of the disease across Oman.     

Variability in the reaction of squash (Cucurbita pepo) to inoculation with Sphaerotheca fuliginea and methodology of breeding for resistance

Reaction to inoculation with powdery mildew caused by Sphaerotheca fuliginea was observed on leaf discs and young plants of eleven representatives of seven edible cultivar groups of Cucurbita pepo. Disease intensity (i.e. number of infections per leaf) was highly correlated ( r ²=0·863, P <0·0001) with spore yield per leaf. Spore yield per leaf and frequency of sporulation on leaf disks were moderately ( r ²=0·505), but significantly correlated ( P <0·01), suggesting that frequency of sporulation can be used for initial screening against susceptibility in a breeding programme. Spore yield per leaf and spore yield per artificially inoculated leaf disc were highly correlated ( r ²=0·87, P <0·0001); this suggests that counting of spores on leaf discs, a laborious but accurate procedure, could be used on the remaining plants as a second step in selection for resistance of the variation in the response of edible C. pepo to the pathogen, 85·8% was attributed to differences between the edible groups and only 14·2% to individual cultivars within a group. Cultivars of the cocozelle and vegetable marrow groups were the most susceptible, whereas relatively resistant cultivars were found in the scallop and straightneck groups.     

Importance of Different Pathways for Maize Kernel Infection by Fusarium moniliforme

ABSTRACT The relative importance of several infection pathways (silks, stalks, and seed) leading to kernel infection of maize hybrids by Fusarium moniliforme was investigated in field experiments in 1993 and 1994. Systemic movement of specific fungal strains within plants was detected by using vegetative compatibility as a marker. Transmission of F. moniliforme from inoculated seed to stalks and developing kernels was detected in two of three field experiments; the seed-inoculated strain was detected in kernels on approximately 10% of ears. The percentage of kernels infected with the seed-inoculated strain ranged from 0 to 70%, with a mean of 0 to 2.5% (0 to 8.3% of F. moniliforme-infected kernels). Other pathways to kernel infection were more effective than seed transmission and systemic infection. F. moniliforme strains inoculated into the crowns and stalks of plants were found throughout the stalks and in up to 95% of the kernels in individual plants. Infection through the silks was clearly the most effective pathway to kernel infection. This was the only inoculation method that significantly increased overall incidence of F. moniliforme infection in kernels; the silk-inoculated strain infected up to 100% of the kernels in individual ears, with a treatment mean as high as 83.7% of kernels. When plants were silk-inoculated, the percentage of kernels infected by other F. moniliforme strains from the seed or stalk was reduced, apparently due to competition among strains. This study provides evidence that systemic development of F. moniliforme from maize seed and stalk infections can contribute to kernel infection, but silk infection is a more important pathway for this fungus to reach the kernels.