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1.
Michelle T. Hulin Andrea Vadillo Dieguez Francesca Cossu Samantha Lynn Karen Russell Helen C. Neale Robert W. Jackson Dawn L. Arnold John W. Mansfield Richard J. Harrison 《Plant pathology》2022,71(4):949-965
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. 相似文献
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Fusarium oxysporum f. sp. pisi (Fop) is an important pathogen of field pea (Pisum sativum) worldwide. The constant evolution of the pathogen drives the necessity to broaden the genetic basis of resistance to Fop. To achieve this, it is important to have a large germplasm collection available and an accurate and efficient method for disease assessment. Here, a detailed evaluation method coupling disease incidence, disease rating over time and its related area under the disease progression curve (AUDPC) was established and used to screen a Pisum spp. germplasm collection against one isolate of Fop race 2. A large variation in the disease response of specific pea accessions ranging from highly resistant to susceptible was observed within the collection, indicating the quantitative expression of the resistance. The repetition of the inoculation experiments on a subset of 19 accessions, including two susceptible accessions, indicated that the scoring method was robust and reproducible and confirmed the highly resistant phenotypes of 11 accessions. To initiate the characterization of resistance mechanisms within these accessions, the external and internal stem symptoms were compared between these selected pea accessions, together with the extent of fungal colonization within plants. All these tests indicated that, in all resistant accessions, the resistance mechanisms efficiently stopped pathogen progression at the crown. Incorporation of these sources of resistance to breeding programmes will contribute to improved Fop resistance in pea cultivars. 相似文献
4.
Beers EH Van Steenwyk RA Shearer PW Coates WW Grant JA 《Pest management science》2011,67(11):1386-1395
BACKGROUND: The spotted wing drosophila, Drosophila suzukii Matsumura (Diptera: Drosophilidae), is a newly introduced pest of sweet cherry on the west coast of North America which produces about 97% of the value of the US sweet cherry crop. D. suzukii initially caused considerable economic loss to cherry growers, who were unaware of this new pest. Little control information was available at the time of initial infestation. Pest control studies were initiated to examine the materials, timings and application methods to control D. suzukii in three major cherry‐producing states (California, Oregon and Washington). RESULTS: Three classes of registered insecticides, organophosphates, pyrethroids and spinosyns, have demonstrated good topical or residual activity against D. suzukii. Neonicotinoids and the systemic organophosphate dimethoate appear to be able to kill eggs or larvae in fruit. Preliminary timing studies indicate that at least two preharvest insecticide sprays are required to obtain control of D. suzukii in California cherry orchards. Aerially applied malathion ULV (ultra‐low volume) appears to be a viable control tactic for this pest. CONCLUSION: The results presented here form the basis for developing D. suzukii management programs in the western United States. Additional studies are needed to refine management practices for the different growing regions and conventional versus organic production requirements. Cherry growers will likely need to apply broad‐spectrum insecticides in a prophylactic manner until treatment thresholds and monitoring methods have been developed and validated. Copyright © 2011 Society of Chemical Industry 相似文献
5.
Results described here span a total of three field seasons and quantitatively depict the effects of an economically important fungal pathogen (Blumeriella jaapii) on tart cherry (Prunus cerasus 'Montmorency') leaf physiology. For the first time, leaf photosynthesis, stomatal conductance (g(s)), maximum ribulose-1,5-bisphosphate carboxylation rate (V(cmax)), and maximum electron transport (J(max)) were measured as functions of visible cherry leaf spot disease (CLS) severity. Defined as the proportion of chlorotic and necrotic tissue per leaf, CLS severity was estimated from leaves of mature 'Montmorency' trees in 2007, 2008, and 2009. Briefly, as visible disease severity increased, all of the leaf-level physiological parameters decreased significantly (P < 0.01) and disproportionately. Thus, the effects of visible symptoms on leaf photosynthetic metabolic function encroached upon asymptomatic tissue as well. Impairment of photosynthetic metabolism in 'Montmorency' tart cherry leaves due to CLS appears to be mediated through disproportionately large perturbations in g(s), V(cmax), and J(max). These findings offer a new perspective on the amount of damage that this serious disease can inflict. 相似文献
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The interactions of four pathotypes of Diplocarpon rosae with 34 species and hybrids of Rosa were compared in an ongoing search for criteria of potential relevance to rose breeding. There were greater similarities in the resistance‐susceptibility interactions of these roses to the pathotypes DA1, CW1 and ZM1, than to a fourth pathotype, DA2. Among the species roses, only those of the section Cinnamomeae were susceptible to DA2 and this susceptibility was transmitted in several cases to hybrid progeny. CW1 had the greatest pathogenicity of the four pathotypes. In a cross between R. rugosa cv. Scabrosa, which was resistant and R. rugosa f. alba, which was susceptible to all pathotypes, the progeny were tested for resistance to pathotypes DA1, CW1 and ZM1. Each of the 20 progeny was susceptible to all three pathotypes. This shows that, unlike the well characterized Rdr1 gene for resistance to D. rosae, the resistance of R. rugosa cv. Scabrosa is not determined by a dominant major gene. The diploid hybrid, R. rugosa cv. Martin Frobisher × cv. Mistress Quickly, was resistant to all four pathotypes, but an induced tetraploid of this hybrid was susceptible to all pathotypes. The relevance of these findings to the breeding of roses for resistance to black spot disease is discussed. 相似文献
7.
A. T. Katsiani V. I. Maliogka G. D. Amoutzias K. E. Efthimiou N. I. Katis 《Plant pathology》2015,64(4):817-824
Little cherry virus 1 (LChV‐1), a member of the recently proposed genus Velarivirus, is a sweet cherry pathogen that has been recently reported to infect other Prunus species and is associated with various plant disorders. In this work the incidence of the virus on its putative hosts and possible mechanisms driving its evolution were investigated. Due to problems encountered with LChV‐1 detection, a new nested RT‐PCR assay was developed and applied. The virus was found to be prevalent in cherry plantations in Greece and only occasionally detected in other Prunus species. Sequences corresponding to the partial RNA‐dependent RNA polymerase (RdRp), heat‐shock protein homologue (HSP70h) and coat protein (CP) genes were determined from Greek LChV‐1 isolates originating from different hosts; these were analysed, along with published homologous genomic regions from other isolates. Phylogenetic analysis of the three genes revealed the segregation of four evolutionary distinct groups showing no host or geography‐based clustering. Mean genetic distances among the four groups were high with the CP region showing the highest divergence, although intragroup variability levels were low. Nevertheless, estimations of the mean ratio of nonsynonymous substitutions per synonymous site to synonymous substitutions per synonymous site (dN/dS) for the partial RdRp, HSP70h and CP indicated that these genomic regions are under negative selection pressure. Interestingly, a recombination event was identified at the 3′ end of RdRp on a Greek virus isolate, thus highlighting the role of this mechanism in the evolutionary history of LChV‐1. 相似文献
8.
Plum pox potyvirus on sour cherry in Moldova 总被引：1，自引：0，他引：1
Plum pox potyvirus (PPV) was identified in six cultivars of sour cherry in the collection orchard of the Moldavian Horticultural Research Institute. Study of biological properties of the sour cherry isolate in herbaceous indicators showed its similarity or identity with the PPV isolate of Van Oosten and a significant difference from isolates widespread in Moldova. A purified viral preparation was used to develop antiserum with a working titre of 1:1024. Comparative serological examination of the sour cherry and conventional plum PPV isolates using ELISA, ISEM and SDS-PAGE of the protein capsid could not differentiate these isolates. The sour cherry isolate was transferred to plum resulting in weak but distinctive PPV symptoms in susceptible cv. Sopernitsa. 相似文献
9.
Vavilov wheat accessions provide useful sources of resistance to tan spot (syn. yellow spot) of wheat 
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下载免费PDF全文 E. G. Dinglasan I. D. Godwin H. T. T. Phan K.‐C. Tan G. J. Platz L. T. Hickey 《Plant pathology》2018,67(5):1076-1087
Host genetic resistance is the most effective and sustainable means of managing tan spot or yellow spot of wheat. The disease is becoming increasingly problematic due to the adoption of minimum tillage practices, evolution of effector‐mediated pathogenicity, and widespread cultivation of susceptible cultivars from a narrow genetic base. This highlights the importance of broadening the diversity of resistance factors in modern breeding germplasm. This study explored 300 genetically diverse wheat accessions, originally sourced from the N. I. Vavilov Institute of Plant Genetic Resources (VIR), St Petersburg, Russia. The collection was screened for resistance to tan spot at seedling and adult stage under controlled conditions, and in the field across 2 years. The phenotypic datasets, coupled with ToxA bioassay screening, identified a number of accessions with useful sources of resistance. Seedling disease response corresponded well with ToxA sensitivity (r = 0.49, P < 0.000), but not adult responses (r = ?0.02 to ?0.19, P < 0.002), and overall reactions to ToxA appeared to show poor correspondence with disease response at the adult stage. ToxA‐insensitive accessions were generally found resistant across different growth stages (all‐stage resistance, ASR) in all experiments (seedling and adult stage under controlled conditions and field). ToxA‐sensitive accessions that were susceptible at seedling stage, but resistant at both adult‐plant stages, were deemed to carry adult‐plant resistance (APR). This study provides detailed information on the degree of tan spot resistance in the Vavilov wheat collection and discusses strategies to harness these sources to boost the diversity of resistance factors in modern wheat breeding germplasm. 相似文献
10.
棉花抗黄萎病品种选育方法探讨 总被引：11，自引：0，他引：11
在棉花抗病育种中,通过病圃或重病地选择抗病单株是常规的选育方法,但其在抗黄萎病育种中的效果并不理想。如何提高抗黄萎病育种效率,促进育种进程是目前急需解决的问题之一。为此,19982002年我们在北京人工病圃,对不同抗病杂交组合和选育方法的选育效果进行了研究。结果表明,在双亲本均为抗(耐)品种的杂交后代群体中,以9月中旬是抗病还是感病并没有多少关联,对黄萎病抗性的选育应选群体抗病性强的株系或组合,以其丰产性为主要选育目标;只有抗与抗(或高耐)的组合中才能选出黄萎病抗性更高的株系;在抗(耐)品种中,后期无论是抗或感的单株其后代的抗病性差异不明显 相似文献
11.
Selection pressure effects on the proportion and movement of resistance alleles introgressed from wheat in Aegilops cylindrica 下载免费PDF全文
下载免费PDF全文 In winter wheat in the USA, Aegilops cylindrica is one of the most troublesome weeds, while the pathogen Oculimacula spp. causes foot rot disease. Imazamox‐resistant (IR) and foot rot‐resistant (FR) wheat cultivars represent effective tools to control the weed and prevent disease infection. However, resistance allele (RA) movement between wheat and A. cylindrica facilitates the introgression process under herbicide and disease selection pressure. Field experiments using IR and FR A. cylindrica plants intermixed with susceptible plants were conducted to measure the proportion of the RAs in the progeny and RA movement with and without herbicide and disease selection. Yield components of A. cylindrica plants were determined across treatments. The herbicide RA proportion in the progeny was greater when plants were treated with the herbicide imazamox in both years. Disease RA proportion was greater with disease occurrence only in one year. Herbicide RA movement from resistant to susceptible plants was greater with herbicide than without it only in one year. Plants carrying the RAs had greater total spikelet weight and 1000‐spikelet weight compared with susceptible plants with or without selection. However, susceptible plants produced more spikelets than the resistant ones in the absence of selection. If plants within an A. cylindrica population acquire the herbicide RA, its proportion will increase each generation under selection. These findings contribute to the understanding of crop allele introgression into related species and the evolution of increased weediness, with weed management implications. 相似文献
12.
Characterization of the pathogenicity of strains of Pseudomonas syringae towards cherry and plum 下载免费PDF全文
下载免费PDF全文 M. T. Hulin J. W. Mansfield P. Brain X. Xu R. W. Jackson R. J. Harrison 《Plant pathology》2018,67(5):1177-1193
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. 相似文献
13.
Helen M. Booker Pathmanathan Umaharan 《European journal of plant pathology / European Foundation for Plant Pathology》2007,118(4):401-410
Twelve selected cowpea cultivars were screened for resistance to Cercospora leaf spot (CLS) disease caused by Pseudocercospora cruenta and Cercospora apii s. lat. under artificial epiphytotic conditions in a replicated field trial, with the objective of developing a quantitative measure
of disease resistance. CLS incidence, leaf spotting score, lesion density, lesion size, proportion of nodes infected, diseased
leaf area, conidia number mg−1 and fascicle density were assessed in 12 cowpea genotypes at crop maturity. Proportion of nodes infected and leaf spotting
score were best able to quantitatively differentiate between the levels of resistance, and allow the exploitation of quantitative
resistance to the disease. Both lesion density and lesion size were important in determining the final leaf spotting score
but the former was epidemiologically more important than the latter, indicated by its correlation to most of the CLS symptom
measures. There was differential resistance to the P. cruenta and C. apii s. lat. among the cowpea varieties screened. Among the cowpea lines screened, resistance to P. cruenta was more common than resistance to C. apii s. lat. Nevertheless, P. cruenta was considered the more aggressive and epidemiologically more important than C. apii s. lat. on the varieties tested evidenced by the strong correlation of P. cruenta incidence with acropetal spread of CLS, intensity of leaf spotting, conidia number mg−1 and fascicle density. The highly susceptible varieties namely VRB7, Los Banos Bush Sitao no.1 and CB27 were susceptible to
both Cercospora pathogens. The cowpea variety VRB-10 was completely resistant to both pathogens and is a useful source of
resistance in CLS breeding programmes. 相似文献
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Joana G. Vicente Steven J. Roberts 《European journal of plant pathology / European Foundation for Plant Pathology》2007,117(4):383-392
Bacterial canker is one of the most important diseases of cherry (Prunus avium). This disease can be caused by two pathovars of Pseudomonas syringae: pv. morsprunorum and pv. syringae. Repetitive DNA polymerase chain reaction-based fingerprinting (rep-PCR) was investigated as a method to distinguish pathovars,
races and isolates of P. syringae from sweet and wild cherry. After amplification of total genomic DNA from 87 isolates using the REP (repetitive extragenic
palindromic), ERIC (enterobacterial repetitive intergenic consensus) and BOX primers, followed by agarose gel electrophoresis,
groups of isolates showed specific patterns of PCR products. Pseudomonas syringae pv. syringae isolates were highly variable. The differences amongst the fingerprints of P. syringae pv. morsprunorum race 1 isolates were small. The patterns of P. syringae pv. morsprunorum race 2 isolates were also very uniform, with one exception, and distinct from the race 1 isolates. rep-PCR is a rapid and
simple method to identify isolates of the two races of P. syringae pv. morsprunorum; this method can also assist in the identification of P. syringae pv. syringae isolates, although it cannot replace inoculation on susceptible hosts such as cherry and lilac. 相似文献
16.
Midatharahally Narasegowda Maruthi Henryk Czosnek Favi Vidavski Shlomo-Yedidia Tarba Judith Milo Shai Leviatov Hagalawadi Mallithimmaiah Venkatesh Attiganal Seetharam Padmaja Rudrappa Subbappa Kulkarni Venkataramappa Muniyappa 《European journal of plant pathology / European Foundation for Plant Pathology》2003,109(1):1-11
The objective of this study was to screen wild and domesticated tomatoes for resistance to Tomato yellow leaf curl virus, Israel (TYLCV-Is) and Tomato leaf curl virus from Bangalore isolate 4, India (ToLCV-[Ban4]) to find sources of resistance to both viruses. A total of 34 tomato genotypes resistant/tolerant to TYLCV-Is were screened for resistance to ToLCV-[Ban4] under glasshouse and field conditions at the University of Agricultural Sciences, Bangalore, India. Resistance was assessed by criteria like disease incidence, symptom severity and squash-blot hybridization. All the tomato genotypes inoculated with ToLCV-[Ban4] by the whitefly vector Bemisia tabaci (Gennadius) produced disease symptoms. In some plants of the lines 902 and 910, however, the virus was not detected by hybridization. The tomato genotypes susceptible to ToLCV-[Ban4] by whitefly-mediated inoculation were also found susceptible to the virus under field conditions. However, there were substantial differences between genotypes in disease incidence, spread, symptom severity and crop yield. Despite early disease incidence, many genotypes produced substantially higher yields than the local hybrid, Avinash-2. Sixteen tomato genotypes from India resistant/tolerant to ToLCV-[Ban4] were also tested for TYLCV-Is resistance at the Hebrew University of Jerusalem, Rehovot, Israel. Accessions of wild species, Lycopersicon hirsutum LA 1777 and PI 390659 were the best sources of resistance to both viruses. Lines 902 and 910, which were, resistant to TYLCV-Is were only tolerant to ToLCV-[Ban4] and accession Lycopersicon peruvianum CMV Sel. INRA, resistant to ToLCV-[Ban4], was only tolerant to TYLCV-Is. Implications of using the resistant lines in breeding programme is discussed. 相似文献
17.
Genetic diversity and pathogenicity of Monilinia polystroma – the new pathogen of cherries 下载免费PDF全文
下载免费PDF全文 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. 相似文献
18.
H. H. Evenhuis 《European journal of plant pathology / European Foundation for Plant Pathology》1955,61(1):56-59
Summary In connection with the investigation of a possible vector of the Eckelrader virus disease of sweet cherry in the Netherlands,
an examination was made of the leaf hopper fauna of cherry.
Five species were found breeding regularly on this hostplant viz.Typhlocyba quercus (F.),Erythroneura alneti (Dhlb.),Erythroneura flammigera (Geoffr.),Empoasca flavescens (F.), andEupteroidea stellulata (Burm.). Some details about their biology are given. Other leafhopper species found on cherry, but which are probably only there
by accident, are mentioned.
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19.
近年来，病毒病在甜樱桃主产区的发生呈上升趋势，制约了甜樱桃产业升级和发展。能够侵染甜樱桃的病毒种类中，樱桃小果病毒1号(little cherry virus 1,LChV-1)导致樱桃果实缩小，彻底丧失经济价值，对甜樱桃产量影响较大。LChV-1通常具有潜伏侵染的特性，在樱桃苗期难以通过症状进行判断。同时，多数品种对LChV-1敏感，因此该病毒的早期检测对甜樱桃的生产尤为重要。传统的病毒检测手段需要专业仪器，不能满足田间快速检测的需求。本研究获取了LChV-1外壳蛋白的多克隆抗体，并研发了一种能够准确检测LChV-1病毒的胶体金免疫层析试纸，确定了胶体金的最佳抗体标记浓度为0.24 mg/mL,检测线最佳重组蛋白浓度为0.25 mg/mL,质检线最佳羊抗兔IgG抗体浓度为0.04 mg/mL。运用该试纸检测只需10～15 min,检测时间短、成本低、结果容易判断，可用于田间快速检测。本研究为樱桃小果病的综合防控提供了有效的监测和检测手段。 相似文献
20.
Jorunn Børve Rolf Tore Djønne Arne Stensvand 《European journal of plant pathology / European Foundation for Plant Pathology》2010,127(3):325-332
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. 相似文献