Effects of temperature,free moisture duration and inoculum concentration on infection of sweet cherry by<Emphasis Type="Italic">Pseudomonas syringae</Emphasis> pv.<Emphasis Type="Italic">syringae</Emphasis>

The effects of temperature, free moisture duration and inoculum concentration on infection caused byPseudomonas syringae pv.syringae (Pss), on sweet cherry (Prunus avium) were investigated. Epiphytic populations ofPss are an important source of inoculum for bacterial canker and it has been demonstrated that a cyclic pattern exists during the year, from undetectable during the warm and dry periods to large populations following cool and wet periods. The effects of temperature and inoculum concentration on the infection caused byPss on immature fruits and 1-yr-old twigs were significant (P<0.001). Fruit and twig infection increased linearly in proportion to the logarithm ofPss when bacterial concentrations were higher than 10³ cfu ml⁻¹ and temperatures were between 5 and 20°C. Regardless of the inoculum concentration and the free moisture duration, fruit and twig infection was either absent or low at 5°C but it increased linearly as temperature increased from 5 to 20°C. Growth ratein vitro was very slow (0.03–0.04 cfu h⁻¹) at 5°C and fast (0.21–0.23 cfu h⁻¹) at 20°C. Therefore, it is possible that multiplication of the epiphytic populations may be significantly reduced in the field with air temperatures below 5°C. A significant (P<0.001) effect of free moisture was obtained only when a low inoculum concentration (10³ cfu ml⁻¹) was used, and a significant linear response between free moisture and disease incidence was obtained only at 10°C. An apparent threshold population ofPss higher than 10³ cfu ml⁻¹ was needed to infect immature fruits and 1-yr-old twigs of sweet cherry. http://www.phytoparasitica.org posting July 10, 2002.     

<Emphasis Type="Italic">Colletotrichum acutatum</Emphasis> occurs asymptomatically on sweet cherry leaves

Leaves of sweet cherry, exposed to either paraquat or freezing to quickly senesce the leaf tissue, were incubated in about 100% RH at 25°C for 6 d. Sporulating colonies of Colletotrichum acutatum, the cause of anthracnose, developed on up to 100% of the paraquat-treated and frozen leaves, and on none of the untreated controls. Number of leaves and leaf area containing C. acutatum on naturally infected leaves increased over time from May to September. Mean incidence of C. acutatum on leaf blades on fruit spurs and vegetative shoots from eight orchard/year samplings were 41 and 33%, respectively. Secondary conidiation (formation of short hyphae and new conidia) from conidia applied to detached leaves took place 6 h after inoculation, but only up to 3% of the conidia formed new conidia. It may be concluded that asymptomatic sweet cherry leaves frequently host C. acutatum and may be a potential inoculum source for cherry fruit.     

Identifying resistance in wild and ornamental cherry towards bacterial canker caused by Pseudomonas syringae

Bacterial canker is a major disease of stone fruits and is a critical limiting factor to sweet cherry (Prunus avium) production worldwide. One important strategy for disease control is the development of resistant varieties. Partial varietal resistance in sweet cherry is discernible using shoot or whole tree inoculations; however, these quantitative differences in resistance are not evident in detached leaf assays. To identify novel sources of resistance to canker, we used a rapid leaf pathogenicity test to screen a range of wild cherry, ornamental Prunus species and sweet cherry × ornamental cherry hybrids with the canker pathogens, Pseudomonas syringae pvs syringae, morsprunorum races 1 and 2, and avii. Several Prunus accessions exhibited limited symptom development following inoculation with each of the pathogens, and this resistance extended to 16 P. syringae strains pathogenic on sweet cherry and plum. Resistance was associated with reduced bacterial multiplication after inoculation, a phenotype similar to that of commercial sweet cherry towards nonhost strains of P. syringae. Progeny resulting from a cross of a resistant ornamental species Prunus incisa with susceptible sweet cherry (P. avium) exhibited resistance indicating it is an inherited trait. Identification of accessions with resistance to the major bacterial canker pathogens is the first step towards characterizing the underlying genetic mechanisms of resistance and introducing these traits into commercial germplasm.     

Current situation of sharka disease in Ankara,Turkey

Sharka disease has a limited distribution in Turkey and does not present a problem for stone fruit production. However, sharka is the most common virus disease of apricots, plums and peaches in Ankara, although it is not a common disease in other cities in Turkey. In different parts of Ankara, 212 private gardens in 21 locations were surveyed forPlum pox virus (PPV) incidence. All together 935 trees of apricot, plum, peach, sweet cherry and sour cherry were sampled and tested for the presence ofPPV by double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA).PPV was identified in numerous trees,viz. 286 apricots, 172 plums and 65 peaches. Strain differentiation ofPPV was accomplished using double-antibody sandwich indirect enzyme-linked immunosorbent assay (DASI-ELISA). These assays confirmed the presence of isolates belonging toPPV-M, PPV-D and mixed infections ofPPV-M+D. This is the first report of the presence ofPPV-D and mixed infections ofPPV-M+D in Turkey. http://www.phytoparasitica.org posting July 14, 2004.     

Incidence and genetic diversity of Peach latent mosaic viroid and Hop stunt viroid in stone fruits in Serbia

Tissue-imprint hybridization (TIH) assay was validated for large-scale detection of Peach latent mosaic viroid (PLMVd) and Hop stunt viroid (HSVd). All 72 collected leaves (100%) from 2 PLMVd- and 2 HSVd-infected trees were positive in TIH, regardless of the geographic orientation of the scaffold, level of the canopy and position of the leaf in the shoot. In a large-scale survey in Serbia, we tested by TIH 871 trees of stone fruits, representing 602 cultivars from fruit collections in Belgrade, Čačak and Novi Sad. PLMVd was detected in 185 (50%) peach trees or 95 (54%) cultivars and HSVd in 2 apricot trees and cultivars (2%). The occurrence of HSVd is a new report for Serbia. No viroid infection was found in European plums, sweet cherries, sour cherries and wild Prunus spp. PLMVd-infected peach cultivars originated from the world’s main breeding centres of this crop. Western European and Asian cultivars were the most infected (58%) followed by those originating from North America (50%). Nine PLMVd and two HSVd isolates were sequenced and analyzed. All showed PMLVd sequences clustered together in the previously reported phylogenetic group III. Both HSVd isolates were found to be derived from recombinant events, but that of the cv. Saturn represented a putative new phylogenetic group of HSVd.     

<Emphasis Type="Italic">Helicobasidium mompa</Emphasis> isolates from sweet potato in continuous monoculture fields

 Isolates of the violet root rot fungus Helicobasidium mompa were collected from herbaceous and tree plants. Their host preference was studied by inoculation experiments using carrots, sweet potatoes, and apple stocks. It was found that sweet potato isolates from Kyushu produced infection cushions on carrots and sweet potatoes but not on apple stocks. Other isolates did not show host preference. Sweet potato isolates were also characterized by ready hyphal mass (sclerotium) production. They were thought to have adapted to the habitat with high disturbance by annual tillage. Received: July 15, 2002 / Accepted: September 26, 2002     

Characterization of the pathogenicity of strains of Pseudomonas syringae towards cherry and plum

Bacterial canker is a major disease of Prunus avium (cherry), Prunus domestica (plum) and other stone fruits. It is caused by pathovars within the Pseudomonas syringae species complex including P. syringae pv. morsprunorum (Psm) race 1 (R1), Psm race 2 (R2) and P. syringae pv. syringae (Pss). Psm R1 and Psm R2 were originally designated as the same pathovar; however, phylogenetic analysis revealed them to be distantly related, falling into phylogroups 3 and 1, respectively. This study characterized the pathogenicity of 18 newly genome‐sequenced P. syringae strains on cherry and plum, in the field and laboratory. The field experiment confirmed that the cherry cultivar Merton Glory exhibited a broad resistance to all clades. Psm R1 contained strains with differential specificity on cherry and plum. The ability of tractable laboratory‐based assays to reproduce assessments on whole trees was examined. Good correlations were achieved with assays using cut shoots or leaves, although only the cut shoot assay was able to reliably discriminate cultivar differences seen in the field. Measuring bacterial multiplication in detached leaves differentiated pathogens from nonpathogens and was therefore suitable for routine testing. In cherry leaves, symptom appearance discriminated Psm races from nonpathogens, which triggered a hypersensitive reaction. Pathogenic strains of Pss rapidly induced disease lesions in all tissues and exhibited a more necrotrophic lifestyle than hemibiotrophic Psm. This in‐depth study of pathogenic interactions, identification of host resistance and optimization of laboratory assays provides a framework for future genetic dissection of host–pathogen interactions in the canker disease.     

Pathogenicity and aggressiveness in populations of <Emphasis Type="Italic">Pseudomonas syringae</Emphasis> from Belgian fruit orchards

The pathogenicity of 99 Belgian Pseudomonas syringae strains representative of the genetic diversity encountered in Belgian fruit orchards was evaluated by using 17 pathogenicity tests conducted on pear, cherry, plum, lilac, sugar beet and wheat. The P. syringae pv. morsprunorum strains were pathogenic to stone fruit species but the race 1 strains possessing the cfl gene involved in coronatine production were pathogenic in more tests than those lacking the gene. Also, sweet cherry twigs were a better material to detect pathogenic strains of race 1 and sour cherry twigs of race 2, which accorded with race 2 presence in sour cherry orchards in Belgium. Three groups were defined in the pv. syringae based on pathogenicity. One group pathogenic in 71.1% of the tests and to lilac included toxic lipodesipeptide-producing (TLP+) strains. The second group pathogenic in 26.8% of the tests and non-pathogenic to lilac included TLP+ strains. The thirth group pathogenic in 9.1% of the tests and almost specifically pathogenic to pear included TLP− strains. The three groups were genetically heterogeneous. Although strain-host relationships were noted within the pv. syringae, aptata and atrofaciens when considering the strain origins, such relationships were not found in the pathogenicity tests, suggesting that pathogenicity tests could probably not reproduce all the aspects of the host-pathogen interactions. None of the pathogenicity tests was able to provide all the information provided by the complete study. A test on pear buds indicated that strains different from the pv. syringae were pathogenic to pear.     

Genetic diversity and pathogenicity of Monilinia polystroma – the new pathogen of cherries

Brown rot caused by fungi belonging to the genus Monilinia is one of the major limiting factors of sour and sweet cherry production. Up to now, three species, M. fructigena, M. laxa and M. fructicola, have been identified as causal agents of brown rot on cherries worldwide. From 2010 to 2013, during the monitoring of cherry orchards in different areas of Poland, a fourth species, M. polystroma, was isolated from brown rot symptoms on sour and sweet cherry fruits. To the best of the authors’ knowledge, this is the first time M. polystroma has been reported as the causal agent of brown rot on cherries. The genetic diversity of M. polystroma isolates from cherries and other hosts was analysed using PCR MP, ISSR and RAPD techniques and showed its clear distinctness from other Monilinia spp. tested. The cluster analysis of fingerprinting data revealed a high similarity of M. polystroma isolates from Poland and their close relationship with the reference strain from Japan, indicating that this species is a recently introduced pathogen. The highest genetic distance between the examined isolates and the highest number of different genotypes was observed in an ISSR assay. Detailed genetic diversity characteristics revealed that M. polystroma isolates from cherries did not create a distinct group but were intermingled with M. polystroma isolates from other hosts. The results of the pathogenicity test conducted on different fruit species indicated a lack of host specificity for M. polystroma isolates.     

Frequency of brown rot fungi on blossoms and fruit in stone fruit orchards in Greece

Brown rot is a devastating disease of stone fruits caused by Monilinia spp. This study was conducted to investigate the disease aetiology on blossoms and fruit in peach, apricot, sweet cherry and plum orchards, in Greece. In total, 1433 isolates obtained from orchards located in the main stone fruit production regions of Greece were identified to species based on the presence/size of a cyt b intron. Monilinia laxa and M. fructicola were detected at frequencies of 59 and 41%, respectively, while M. fructigena was absent. Monilinia fructicola was more common on fruit whereas M. laxa occurred in similar frequency on blossoms and fruit. Monilinia laxa was replaced by M. fructicola in fruit infections of peach in both regions investigated and in fruit infections of plum in the Imathia region. Assessments of aggressiveness of 30 isolates of both species on the petals and fruits of the hosts showed that M. fructicola isolates were more aggressive. This suggests that the predominance of M. laxa on the blossoms cannot be explained by higher aggressiveness. Measurements of the effect of temperature on mycelial growth showed that M. laxa isolates had a higher growth rate than M. fructicola at the lowest temperature tested of 5°C, whereas M. fructicola isolates showed higher growth rates at higher temperatures. The observed high frequency of M. fructicola in Greece represents a major threat for stone fruit production. Furthermore, the information obtained about delineation of species and plant organ preference could be useful for the implementation of disease management strategies.     

Assessment of the inheritance of resistance and tolerance in cherry (Prunus sp.) to Blumeriella jaapii,the causal agent of cherry leaf spot

Cherry leaf spot (CLS), caused by Blumeriella jaapii, is a serious fungal disease of sour cherry (Prunus cerasus). Cultivar Montmorency, the major cultivar grown in the United States, is highly susceptible to CLS. As many as 10 fungicide sprays can be required each growing season to combat this disease; therefore, developing CLS‐resistant cultivars is a top breeding priority. Germplasm previously reported to be resistant or tolerant to CLS was acquired and incorporated into the sour cherry breeding programme at Michigan State University (MSU) and included three cherry species: sour cherry, sweet cherry (P. avium), and the wild species P. canescens. This study aimed to: (i) compare the CLS disease progression profile of the susceptible cultivar Montmorency with those of the resistant and tolerant germplasm; and (ii) gain an understanding of the inheritance of these resistance and tolerance traits by evaluating the host response of progeny individuals belonging to families derived from this germplasm. Significant differences were observed between the susceptible Montmorency and the tolerant and resistant accessions in their response to CLS and its progression during the growing season. Evaluation of the CLS host responses of progeny individuals derived from this germplasm supported a dominant two‐gene model for P. canescens‐derived resistance and a recessive gene model for sweet cherry‐derived tolerance. These insights into disease progression and trait inheritance improve the efficiency and potential success of breeding sour cherry cultivars with durable resistance to CLS.     

A greenhouse screening technique to assess rust resistance in sorghum∗

Abstract

Studies were conducted to determine the influence of plant growth stage, inoculum density, temperature, and relative humidity (RH) on development of rust (Puccinia pupurea) in sorghum (Sorghum bicolor). Rust development was maximum (>80% severity), when plants of a susceptible sorghum genotype (IS 18420) were inoculated at the four‐ to five‐leaf stage with an inoculum concentration of 4 × 10⁶ urediniospores per ml and incubated at 20–25°C under high RH (>90%) for 24 h. Disease severity (percentage leaf area covered with rust pustules) scores were taken 2 weeks after inoculation. Using this technique, 29 sorghum genotypes were screened for rust resistance in a greenhouse. This technique proved effective In discerning resistant and susceptible genotypes, and IS 3979, ICSH 110, ICSH 86647 and ICSH 871035 were identified resistant (<20% rust severity) compared with a susceptible control IS 18420 (90% rust severity). This technique is simple and rapid, and can be used effectively and economically to screen, on a large scale, germplasm lines and breeding populations in the greenhouse.     

Mechanical transmission of <Emphasis Type="Italic">Potato spindle tuber viroid</Emphasis> between plants of <Emphasis Type="Italic">Brugmansia suaveoles,Solanum jasminoides</Emphasis> and potatoes and tomatoes

Potato spindle tuber viroid (PSTVd) has been recently found in many solanaceous ornamental plant species. This study reports on the effectiveness of mechanical transmission between Brugmansia suaveolens, Solanum jasminoides, potato and tomato. Inoculation with ‘infected’ plant sap diluted in water, rubbing with contaminated finger tips and cutting with contaminated razor blades all resulted in transmission of PSTVd. Temperature, plant species and source of inoculum were found to be critical factors. An average temperature of 15°C only resulted in a few infections, whereas transmission at 20 and 25°C was more successful. Tomatoes were more susceptible to PSTVd than B. suaveolens, S. jasminoides and potatoes. Furthermore, S. jasminoides was a better source of inoculum than B. suaveolens. No transmission was obtained after repeated addition of inocula to tomato roots. These results indicate that PSTVd can be transmitted between plant species in practice by crop handling.     

Mycoherbicides and other biocontrol agents for Senecio spp

Classical biocontrol of Senecio jacobaea (ragwort) has generally utilised herbivorous insects, although the nisi Puccinia expansa has also been considered. Although this rust is specific and damaging in the glasshouse. It has not been used in the field. Research into the ecophysiology of Senecio vulgaris (groundsel) infected by the rust Puccinia lagenophorae has revealed the extent to which the effects of infection are dependent on environmental factors. The damage caused by rust is enhanced under mild drought conditions, during periods of frost in winter and by competition between groundsel and neighbouring plants, bui is reduced by nutrient deficiency. Rust injury is also greatly increased by secondary infection of pustules by necrotrophic fungi. Such secondary infection can be achieved artificially with a range of opportunistic necrolrophs and can selectively kill groundsel: the effective inoculum dose of both fungi is significantly reduced. Attempts to apply our understanding of rust-necrotroph injury to ragwort have been partially successful but we have not succeeded in causing significant mortality of this host. This paper discusses these, and other weed—pathogen—environment interactions, and their possible application to biocontrol.     

Quantitative Inoculations of Poplars with Melampsora Larici-populina

Four poplar clones were inoculated with four isolates of Melampsora larici-populina at seven spore concentrations (inoculum densities up to 680 spores cm^–2 using a leaf-disc method. Disease reactions were recorded using a digital camera. The number and size of uredinia were examined using image analysis software and the number of spores produced per leaf disc was counted. The infection efficiency was estimated in a range of 0.008–0.167 and the pustule diameter measured 0.75–0.94 mm. Rust resistance/susceptibility was expressed by the differences in both the number and the size of uredinia. Within a clone/isolate combination, pustule diameter and the number of spores produced per pustule did not differ significantly between different levels of inoculum density. There was a close correlation between the pustule area and spore yield. When Spearman rank correlation was tested between the disease variables, a close correlation was found between pustule number and pustule area per leaf disc (0.98) and between the number of spores produced and the pustule area/number per leaf disc (0.94 and 0.92, respectively). There was significant correlation between the number and the diameter of pustules (0.54, P < 0.001).     

San José Scale in Deciduous Fruit Orchards of Some European Countries (Survey of Scale Insect Infestations in European Orchards No. IV)

Fruit tree branch and bark samples have been collected from several European countries (Czechoslovakia, Greece, Hungary, Poland, Turkey, European part of USSR) from apple, pear, peach, plum, cherry and sour cherry. Twenty-five scale insect species were found in the samples. Distribution maps of Quadra & pidiotus perniciosus on different fruit species are given. No significant changes in the distribution of this species in Central Europe can be observed in the last 30 years. Q. perniciosus is present in higher density on apple wherever it occurs, and is less frequent on pears and plums. It is frequent on peach and sometimes on cherry, but generally at low densities. It is rare on sour cherry.     

Detection ofplum pox virus in ornamentalPrunus cerasifera

Plum pox virus (PPV) is the causal agent of sharka disease. It is a serious threat for temperate fruit, mainly apricots, plums and peaches. In order to study the ability ofPPV to infect wild and ornamentalPrunus species, several wild, native ornamental stone fruits and weeds were analyzed as possible reservoirs ofPPV. Five species of ornamental stone fruits and 24 species of weeds were evaluated between 2000 and 2004. The virus was not found in the weeds but was detected in one species of ornamental stone fruit, purple cherry-plums (Prunus cerasifera Pissardii). ThePPV strain M was identified by DASI-ELISA and confirmed by IC-RT-PCR. Additionally, mealy plum aphid (Hyalopterus pruni) was determined as a vector ofPPV inP. cerasifera. This is the first report on the reservoir potential of ornamental stone fruit trees and weeds forPPV in Turkey. http://www.phytoparasitica.org posting July 19, 2006;     

Fruit spot of sweet lime (<Emphasis Type="Italic">Citrus limetta</Emphasis>) caused by <Emphasis Type="Italic">Septoria</Emphasis> sp. in Peru

In 2002, a severe fruit spot of sweet lime (Citrus limetta) was observed in Piura and Lambayeque provinces in northern Peru. Affected fruits showed large oval and sunken lesions, often surrounded by chlorotic haloes. Septoria sp. was isolated from affected fruits. Sweet lime isolates showed larger pycnidia and pycnidiospores than those of Septoria spp. previously described on citrus. In addition, phylogenetic analysis of the ITS sequences clearly separated the sweet lime isolates from S. citri and S. citricola. Isolates were pathogenic to detached sweet lime fruits and the fungus was isolated from lesions on inoculated fruits.     

Mendelian inheritance of rust resistance to Melampsora larici‐epitea in crosses between Salix sachalinensis and S. viminalis

Two F₁, two F₂ and two backcross (BC) full‐sib families of Salix sachalinensis × S. viminalis were tested for resistance to two pathotypes of Melampsora larici‐epitea in leaf‐disc inoculation experiments. Two single‐pustule isolates, VM and ST, belonging to pathotypes LET1 and LET5, respectively, were used in the tests. Disease was scored based on the number of uredinia, uredinial diameter and inoculum densities. Both F₁ families were completely resistant to both VM and ST. Resistance to VM segregated at a 9:6:1 ratio in the F₂ families and at a 1:2:1 ratio in the BC families, suggesting that two independently segregating genes controlled rust resistance, with resistance dominant over susceptibility. This also indicates incomplete dominance of the resistance alleles over the susceptibility to VM. For ST, the equivalent ratios were 3:1 and 1:1, showing that a single dominant gene was responsible for rust resistance. The broad sense heritabilities were >0·91 for uredinial diameter and 0·1–0·33 for the number of uredinia. There were significant overall correlations between data from inoculations with VM and those from inoculations with ST in the number of uredinia, uredinial diameter and disease scores (Spearman’s rank correlation coefficients = 0·31–0·75).