Seasonal variation in lucerne foliar diseases and cultivar reaction to leaf spot pathogens in the field in southern Queensland

1993 ◽  
Vol 33 (3) ◽  
pp. 343 ◽  
Author(s):  
MJ Inch ◽  
JAG Irwin ◽  
RA Bray

Detailed assessments were made of leaf and stem disease incidence and severity on 16 lucerne cultivars and lines over 10 months in the field near Gatton, Queensland (27�34'S., 152�17'E.). The 4 major pathogens encountered were Leptosphaerulina trifolii, Uromyces striatus, Pseudopeziza medicaginis, and Cercospora medicaginis. The diseases caused by these pathogens showed a seasonality in occurrence. Both U. striatus and P. medicaginis were more severe on older shoots, whereas L. trifolii caused highest disease levels on shoots sampled 2 weeks after cutting. The relative rankings of the lucerne entries changed across pathogens, but breeding line MSA showed the best resistance to rust, L. trifolii, and P. medicaginis. This work has indicated that there is genetic variability in disease reaction to foliar pathogens which could be exploited in the development of cultivars for subtropical Queensland.

Author(s):  
Sabiya Bashir ◽  
Mohammad Najeeb Mughal ◽  
Zahida Rashid ◽  
Shabeena Majid ◽  
Sabeena Naseer ◽  
...  

Sixty-three genotypes of  french bean was screened against leaf spot (Alternaria  alternata) in sick plots at Research Farm of Dryland Agriculture Research Srinagar, Rangreth during  Kharif  2018 and 2019. The highest mean disease incidence ranged from 0.00 to 85.00 per cent  with  the mean disease intensity ranged from 0.00 to 53.26 per cent .One genotype namely  ‘Local Pulwama’ was highly susceptible in their disease reaction. Among the screened germplasm, ‘Highly Resistant’ genotypes was SKU-R-601, SKUA-R-105, SKU-R-927, DARS-25, DARS-66, DARS-R-615,  while as ‘Susceptible’ genotypes was  DARS-8, DARS-12,  DARS-11, SKUAST-R-155, SKU-R-928, DARS-7, DARS-R-4, Bhaderwah (L),  Local  Kupwara black and Raj Jawala. Local Pulwama was found to be a highly susceptible (HS) genotype.  Twenty nine genotypes namely., DARS-16, DARS-9, DARS-54, DARS-39, VL-125, DARS-63, ENTO-504, SKUAST-204,SKU-R-925, DARS-60, DARS-109, DARS-43, DARS-44, SKU-R-23, DARS-4, DARS-74, SKU-R-105, DARS-40, DARS-23, DARS-18, SKU-R-71, WB-341, SKU-R-605, Uri local, Shopian (L), SKU-R-23, DARS-71, SSGB-729, DARS-R-19 showed resistant reaction to disease. The selection for resistance was based on the reaction of varieties on leaves.


2004 ◽  
Vol 84 (1) ◽  
pp. 311-317 ◽  
Author(s):  
H. Wang ◽  
S. F. Hwang ◽  
K. F. Chang ◽  
B. D. Gossen ◽  
G. D. Turnbull ◽  
...  

The disease reaction of alfalfa (Medicago sativa) cultivars to spring black stem was evaluated in field trials and greenhouse experiments. In field trials, differences in cultivar reaction to leaf spot (predominantly spring black stem) were observed in 9 of 16 station years. The reaction of certain cultivars was consistent across most trials, but other cultivars were quite variable. Under controlled conditions, one isolate each of Phoma sclerotioides and P. exigua produced symptoms on alfalfa leaves that were similar to those caused by P. medicaginis. These results indicate that P. medicaginis is not the only pathogen responsible for symptoms of spring black stem on alfalfa in the prairie region. In a detached-leaf study, one isolate each of P. medicaginis, P. sclerotioides and P. exigua produced leaf lesions on all 18 alfalfa cultivars assessed. Disease incidence in Absolute, Algonquin, Pickseed 3006 and Anik (M. sativa subsp. falcata) was lower than in 630 and AC Blue J. Inoculation of eight selected cultivars using a range of spore concentrations under controlled conditions showed a similar pattern; all three isolates produced leaf lesions on all eight cultivars. Ino culation with conidial suspensions of P. medicaginis resulted in a lower disease incidence on Absolute than on Beaver. Key words: Medicago sativa, Medicago sativa subsp. falcata, Phoma medicaginis, P. sclerotioides, P. exigua, detached leaves.


2014 ◽  
Vol 65 (12) ◽  
pp. 1249 ◽  
Author(s):  
M. J. Barbetti ◽  
M. P. You

Foliar pathogens result in significant losses in herbage and seed yields and regeneration capacity in annual clover pastures, the last leading to their rapid deterioration and lack of persistence. The most important pathogens include Kabatiella caulivora (clover scorch), Cercospora zebrina (cercospora), Uromyces trifolii-repentis (rust), Erysiphe trifoliorum (powdery mildew), and Leptosphaerulina trifolii (pepper spot). Several other foliar pathogens on annual clovers, in particular Phoma medicaginis (black stem and leaf spot), one or more Stemphylium spp. (stemphylium leaf spot), Pseudopeziza trifolii (common leaf spot), Stagonospora spp. (stagonospora leaf spot), Colletotrichum trifolii (anthracnose) and Sclerotinia trifoliorum (sclerotinia), occur widely and together contribute to reduce productivity in some localities. Severe attack by the most important pathogens (e.g. K. caulivora, U. trifolii-repentis, E. trifoliorum) not only greatly reduces winter–spring pasture production but frequently also coincides with the critical feed shortage across autumn–winter, leading to significantly decreased autumn–winter biomass production in regenerating stands. Approaches to disease control include a range of management strategies. Wider utilisation of cultural and fungicidal control strategies offers producers greater management flexibility, particularly in conjunction with deployment of cultivars with useful resistance. Host resistance offers the greatest potential for delivering the most cost-effective and long-term control. Many of these foliar pathogens co-occur, magnifying losses; this highlights the need for individual host genotypes with resistance to multiple pathogens and unique geographic locations such as Sardinia offer enormous scope to select such clovers. Future research opportunities and critical priorities to improve management of foliar pathogens in annual clover pastures across southern Australia include the need to: (i) define pathogen strain–race structures, particularly for K. caulivora and U. trifolii-repentis, and determine associated host resistances against specific strains–races to allow strategic deployment of host resistances; (ii) define relative resistances to major fungal foliar pathogens of all parental and near-release breeding genotypes and all commercial cultivars across important annual clover species; (iii) identify new sources of host resistance, particularly genotypes with cross-resistance to multiple pathogens, for breeders to utilise; (iv) identify and demonstrate the benefits to farmers of effective cultural (e.g. grazing, removal of infested residues) and fungicidal control options that allow greater management flexibility to reduce the impact of fungal foliar diseases; and (v) determine current incidences and impacts (losses and economic importance) of major fungal foliar diseases in the different agro-climatic regions across southern Australia. Failure to address these critical issues leaves livestock industries carrying the risks from release of new varieties of unknown susceptibilities to one or more of the major foliar diseases, and the risks from continued use of older varieties exposed to new pathogen races; with few if any flexible management options during periods of critical feed shortage; and without the basic information on current disease impacts that is needed to make sensible management and funding decisions.


Author(s):  
Rocío Rodríguez ◽  
Pedro L. Meléndez

Two foliar diseases of beans, Phaseolus vulgaris L., namely angular leaf spot and ascochyta leaf spot, caused by Isariopsis griseola and Ascochyta phaseolorum, respectively, were effectively controlled with chemicals. Biweekly applications of mancozeb and chlorothalonil (1.12, 2.48 and 4.48 kg/ ha) effectively protected the foliage of bean cultivars Bonita and Naranjito against attacks by both pathogens. Cultivar Bonita responded better to treatments than cv. Naranjito in terms of yield. Some dosages of mancozeb and chlorothalonil increased yield of cv. Bonita affected by angular leaf spot. Yield increases in plots treated with benomyl increased only when the highest rate of this chemical was used. Even at the lowest dosages, the three chemicals tested increased yield in cv. Bonita affected by the ascochyta leaf spot disease.


Plant Disease ◽  
1997 ◽  
Vol 81 (8) ◽  
pp. 892-896 ◽  
Author(s):  
E. L. Little ◽  
S. T. Koike ◽  
R. L. Gilbertson

Pseudomonas syringae pv. apii, causal agent of bacterial leaf spot (BLS) of celery, was first identified in California in 1989. By 1991, BLS was apparent in all celery-growing areas of the state. Greenhouse-produced transplants were affected most severely, and disease incidence approached 100% in some greenhouses. In this study, sources of inoculum and factors contributing to disease development were investigated in three Salinas Valley greenhouse operations during the 1991, 1992, and 1993 celery transplant seasons (January to August). Epiphytic P. syringae pv. apii was not detected on celery transplants until April or May of each year. Increased epiphytic populations preceded BLS outbreaks, and high-pressure, overhead irrigation favored bacterial infiltration and disease development. In seed-wash assays, P. syringae pv. apii was recovered from 5 of 24 commercial celery seed lots. In field tests, epiphytic P. syringae pv. apii was found on umbels of inoculated celery plants, and seeds from these plants were heavily contaminated with P. syringae pv. apii. Contaminated seed produced seedlings with large epiphytic P. syringae pv. apii populations. Hot-water treatment (50°C for 25 min) eliminated >99.9% of seed contamination. Based on these results, disease management techniques are proposed.


Plant Disease ◽  
2011 ◽  
Vol 95 (3) ◽  
pp. 263-268 ◽  
Author(s):  
S. K. Gremillion ◽  
A. K. Culbreath ◽  
D. W. Gorbet ◽  
B. G. Mullinix ◽  
R. N. Pittman ◽  
...  

Field experiments were conducted in 2002 to 2006 to characterize yield potential and disease resistance in the Bolivian landrace peanut (Arachis hypogaea) cv. Bayo Grande, and breeding lines developed from crosses of Bayo Grande and U.S. cv. Florida MDR-98. Diseases of interest included early leaf spot, caused by the fungus Cercospora arachidicola, and late leaf spot, caused by the fungus Cercosporidium personatum. Bayo Grande, MDR-98, and three breeding lines, along with U.S. cvs. C-99R and Georgia Green, were included in split-plot field experiments in six locations across the United States and Bolivia. Whole-plot treatments consisted of two tebuconazole applications and a nontreated control. Genotypes were the subplot treatments. Area under the disease progress curve (AUDPC) for percent defoliation due to leaf spot was lower for Bayo Grande and all breeding lines than for Georgia Green at all U.S. locations across years. AUDPC for disease incidence from one U.S. location indicated similar results. Severity of leaf spot epidemics and relative effects of the genotypes were less consistent in the Bolivian experiments. In Bolivia, there were no indications of greater levels of disease resistance in any of the breeding lines than in Bayo Grande. In the United States, yields of Bayo Grande and the breeding lines were greater than those of the other genotypes in 1 of 2 years. In Bolivia, low disease intensity resulted in the highest yields in Georgia Green, while high disease intensity resulted in comparable yields among the breeding lines, MDR-98, and C-99R. Leaf spot suppression by tebuconazole was greater in Bolivia than in the United States. This result indicates a possible higher level of fungicide resistance in the U.S. population of leaf spot pathogens. Overall, data from this study suggest that Bayo Grande and the breeding lines may be desirable germplasm for U.S. and Bolivian breeding programs or production.


Plant Disease ◽  
2014 ◽  
Vol 98 (10) ◽  
pp. 1434-1434
Author(s):  
J.-H. Kwon ◽  
D.-W. Kang ◽  
M.-G. Cheon ◽  
J. Kim

In South Korea, the culture, production, and consumption of blueberry (Vaccinium corymbosum) have increased rapidly over the past 10 years. In June and July 2012, blueberry plants with leaf spots (~10% of disease incidence) were sampled from a blueberry orchard in Jinju, South Korea. Leaf symptoms included small (1 to 5 mm in diameter) brown spots that were circular to irregular in shape. The spots expanded and fused into irregularly shaped, large lesions with distinct dark, brownish-red borders. The leaves with severe infection dropped early. A fungus was recovered consistently from sections of surface-disinfested (1% NaOCl) symptomatic leaf tissue after transfer onto water agar and sub-culture on PDA at 25°C. Fungal colonies were dark olive and produced loose, aerial hyphae on the culture surfaces. Conidia, which had 3 to 6 transverse septa, 1 to 2 longitudinal septa, and sometimes also a few oblique septa, were pale brown to golden brown, ellipsoid to ovoid, obclavate to obpyriform, and 16 to 42 × 7 to 16 μm (n = 50). Conidiophores were pale to mid-brown, solitary or fasciculate, and 28 to 116 × 3 to 5 μm (n = 50). The species was placed in the Alternaria alternata group (1). To confirm the identity of the fungus, the complete internal transcribed spacer (ITS) rDNA region of a representative isolate, AAVC-01, was amplified using ITS1 and ITS4 primers (2). The DNA products were cloned into the pGEM-T Easy vector (Promega, Madison, WI) and the resulting pOR13 plasmid was sequenced using universal primers. The resulting 570-bp sequence was deposited in GenBank (Accession No. KJ636460). Comparison of ITS rDNA sequences with other Alternaria spp. using ClustalX showed ≥99% similarity with the sequences of A. alternata causing blight on Jatropha curcas (JQ660842) from Mexico and Cajannus cajan (JQ074093) from India, citrus black rot (AF404664) from South Africa, and other Alternaria species, including A. tenuissima (WAC13639) (3), A. lini (Y17071), and A. longipes (AF267137). Two base substitutions, C to T at positions 345 and 426, were found in the 570-bp amplicon. Phylogenetic analysis revealed that the present Alternaria sp. infecting blueberry grouped separately from A. tenuissima and A. alternata reported from other hosts. A representative isolate of the pathogen was used to inoculate V. corymbosum Northland leaves for pathogenicity testing. A conidial suspension (2 × 104 conidia/ml) from a single spore culture and 0.025% Tween was spot inoculated onto 30 leaves, ranging from recently emerged to oldest, of 2-year-old V. corymbosum Northland plants. Ten leaves were treated with sterilized distilled water and 0.025% Tween as a control. The plants were kept in a moist chamber with >90% relative humidity at 25°C for 48 h and then moved to a greenhouse. After 15 days, leaf spot symptoms similar to those observed in the field developed on the inoculated leaves, whereas the control plants remained asymptomatic. The causal fungus was re-isolated from the lesions of the inoculated plants to fulfill Koch's postulates. To our knowledge, this is the first report of Alternaria sp. on V. corymbosum in South Korea. References: (1) E. G. Simmons. Page 1797 in: Alternaria: An Identification Manual. CBS Fungal Biodiversity Centre, Utrecht, The Netherlands, 2007. (2) T. J. White et al. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990. (3) M. P. You et al. Plant Dis. 98:423, 2014.


2018 ◽  
Vol 10 (10) ◽  
pp. 513
Author(s):  
M. C. Kottayi ◽  
D. D. Saoji ◽  
S. E. Pawar ◽  
A. D. Choudhary

The disease incidence of Cercosporidium personatum in field was analysed in the hybridized population derived from the resistant mutant lines of the cultivar ICGV-87304 and TAG-24 & TG-26. Reciprocal crosses were performed using the same parents. The comparison of disease incidence in hybridized population was made with resistant cultivar Girnar-1. Susceptible parents TAG-24 and TG-26 showed disease incidence of 14.08 and 16.40%, respectively while Girnar-1 and the resistant mutant parents showed percentage infection ranging from 0.06-0.96%. The plants raised from the hybridized population showed the percent infection ranging from 0.01 to 0.02 %.


Plant Disease ◽  
2021 ◽  
Author(s):  
Yanxiang Qi ◽  
Yanping Fu ◽  
Jun Peng ◽  
Fanyun Zeng ◽  
Yanwei Wang ◽  
...  

Banana (Musa acuminate L.) is an important tropical fruit in China. During 2019-2020, a new leaf spot disease was observed on banana (M. acuminate L. AAA Cavendish, cv. Formosana) at two orchards of Chengmai county (19°48ʹ41.79″ N, 109°58ʹ44.95″ E), Hainan province, China. In total, the disease incidence was about 5% of banana trees (6 000 trees). The leaf spots occurred sporadically and were mostly confined to the leaf margin, and the percentage of the leaf area covered by lesions was less than 1%. Symptoms on the leaves were initially reddish brown spots that gradually expanded to ovoid-shaped lesions and eventually become necrotic, dry, and gray with a yellow halo. The conidia obtained from leaf lesions were brown, erect or curved, fusiform or elliptical, 3 to 4 septa with dimensions of 13.75 to 31.39 µm × 5.91 to 13.35 µm (avg. 22.39 × 8.83 µm). The cells of both ends were small and hyaline while the middle cells were larger and darker (Zhang et al. 2010). Morphological characteristics of the conidia matched the description of Curvularia geniculata (Tracy & Earle) Boedijn. To acquire the pathogen, tissue pieces (15 mm2) of symptomatic leaves were surface disinfected in 70% ethanol (10 s) and 0.8% NaClO (2 min), rinsed in sterile water three times, and transferred to potato dextrose agar (PDA) for three days at 28°C. Grayish green fungal colonies appeared, and then turned fluffy with grey and white aerial mycelium with age. Two representative isolates (CATAS-CG01 and CATAS-CG92) of single-spore cultures were selected for molecular identification. Genomic DNA was extracted from the two isolates, the internal transcribed spacer (ITS), large subunit ribosomal DNA (LSU rDNA), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), translation elongation factor 1-alpha (TEF1-α) and RNA polymerase II second largest subunit (RPB2) were amplified and sequenced with universal primers ITS1/ITS4, LROR/LR5, GPD1/GPD2, EF1-983F/EF1-2218R and 5F2/7cR, respectively (Huang et al. 2017; Raza et al. 2019). The sequences were deposited in GenBank (MW186196, MW186197, OK091651, OK721009 and OK491081 for CATAS-CG01; MZ734453, MZ734465, OK091652, OK721100 and OK642748 for CATAS-CG92, respectively). For phylogenetic analysis, MEGA7.0 (Kumar et al. 2016) was used to construct a Maximum Likelihood (ML) tree with 1 000 bootstrap replicates, based on a concatenation alignment of five gene sequences of the two isolates in this study as well as sequences of other Curvularia species obtained from GenBank. The cluster analysis revealed that isolates CATAS-CG01 and CATAS-CG92 were C. geniculata. Pathogenicity assays were conducted on 7-leaf-old banana seedlings. Two leaves from potted plants were stab inoculated by puncturing into 1-mm using a sterilized needle and placing 10 μl conidial suspension (2×106 conidia/ml) on the surface of wounded leaves and equal number of leaves were inoculated with sterile distilled water serving as control (three replicates). Inoculated plants were grown in the greenhouse (12 h/12 h light/dark, 28°C, 90% relative humidity). Necrotic lesions on inoculated leaves appeared seven days after inoculation, whereas control leaves remained healthy. The fungus was recovered from inoculated leaves, and its taxonomy was confirmed morphologically and molecularly, fulfilling Koch’s postulates. C. geniculata has been reported to cause leaf spot on banana in Jamaica (Meredith, 1963). To our knowledge, this is the first report of C. geniculata on banana in China.


Plant Disease ◽  
2008 ◽  
Vol 92 (2) ◽  
pp. 318-318
Author(s):  
S. Zhao ◽  
G. Xie ◽  
H. Zhao ◽  
H. Li ◽  
C. Li

Snow lotus (Saussurea involucrata Karel. & Kir. ex Sch. Bip.) is an economically important medicinal herb increasingly grown in China in recent years. In June of 2005, a leaf spot disease on commercially grown plants was found in the QiTai Region, south of the Tianshan Mountain area of Xinjiang, China at 2,100 m above sea level. Disease incidence was approximately 60 to 70% of the plants during the 2006 and 2007 growing seasons. Initial symptoms appeared on older leaves as irregularly shaped, minute, dark brown-to-black spots, with yellow borders on the edge of the leaflet blade by July. As the disease progressed, the lesions expanded, causing the leaflets to turn brown, shrivel, and die. A fungus was consistently isolated from the margins of these lesions on potato dextrose agar. Fifty-eight isolates were obtained that produced abundant conidia in the dark. Conidia were usually solitary, rarely in chains of two, ellipsoid to obclavate, with 6 to 11 transverse and one longitudinal or oblique septum. Conidia measured 60 to 80 × 20 to 30 μm, including a filamentous beak (13 to 47 × 3.5 to 6 μm). According to the morphology, and when compared with the standard reference strains, the causal organism of leaf spot of snow lotus was identified as Alternaria carthami (1,4). Pathogenicity of the strains was tested on snow lotus seedlings at the six-leaf stage. The lower leaves of 20 plants were sprayed until runoff with conidial suspensions of 1 × 104 spores mL–1, and five plants sprayed with sterile distilled water served as controls. All plants were covered with a polyethylene bag, incubated at 25°C for 2 days, and subsequently transferred to a growth chamber at 25°C with a 16-h photoperiod. Light brown lesions developed within 10 days on leaflet margins in all inoculated plants. The pathogen was reisolated from inoculated leaves, and isolates were deposited at the Key Oasis Eco-agriculture Laboratory of Xinjiang Production and Construction Group, Xinjiang and the Institute of Biotechnology, Zhejiang University. No reports of a spot disease caused by A. carthami on snow lotus leaves have been found, although this pathogen has been reported on safflower in western Canada (3), Australia (2), India (1), and China (4). To our knowledge, this is the first report of a leaf spot caused by A. carthami on snow lotus in China. References: (1) S. Chowdhury. J. Indian Bot. Soc. 23:59, 1944. (2) J. A. G. Irwin. Aust. J. Exp. Agric. Anim. Husb. 16:921, 1976. (3) G. A. Petrie. Can. Plant Dis. Surv. 54:155, 1974. (4) T. Y. Zhang. J. Yunnan Agric. Univ.17:320, 2002.


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