scholarly journals Shallot Basal Bulb Rot Management through Integration of Trichoderma asperellum, Composted Plant Residues and Natural Mulch

2020 ◽  
Vol 14 (3) ◽  
pp. 1779-1788
Author(s):  
Nurmasita Ismail ◽  
Ade Rosmana ◽  
Sylvia Sjam ◽  
Ratnawati Ratnawati

Basal bulb rot (BBR) of shallot caused by Fusarium oxysporum f. sp. cepae is one of the highly deleterious diseases on shallot, Allium cepa L. var ascalonicum Backer. in Indonesia. This study aimed to assess the potency of organic mulch, composted plant residues, and endophytic Trichoderma asperellum to control this disease. Treatment with mulch alone, mulch plus compost, mulch plus T. asperellum, and combination of all the three provided the decrease of BBR incidence by 15%, 20%, 29%, and 39% and the increase of shallot productivity by 22%, 66%, 84%, and 125%, respectively. Observation of another treatment impact on the fungal occurrence at harvest time indicated that their population in soil increased by 671%, 771%, 257%, and 814% and the fungal colonization in root tissues mounted by 31%, 77%, 77%, and 74%, respectively. The introduced Trichoderma was found predominantly, especially in leaf tissues of inoculated shallot. These data showed that all the treatments were able to control BBR disease. However, the most effective was the mulch in combination with compost and T. asperellum. Therefore, large-scale disease control could take advantage of this integration.

Agronomy ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 650 ◽  
Author(s):  
Ade Rosmana ◽  
Muhammad Taufik ◽  
Asman Asman ◽  
Nurul Jihad Jayanti ◽  
Andi Akbar Hakkar

Trichoderma asperellum, composted plant residues, and its combination can control vascular-streak dieback (VSD) disease caused by fungus Ceratobasidium theobromae in laboratory conditions. In this trial, we evaluated these treatments in two years through the application of foliar spraying and stem infusion for T. asperellum alone, through soil amendment for compost alone, and T. asperellum plus this organic fertilizer in the field on susceptible cacao clone. The disease is characterized by full-leaf chlorosis and necrosis that can develop rapidly to the entire branch, with around 70% incidence in seven months, and we detected the pathogen in branches showing light symptoms. All treatments except for T. asperellum plus composted plant residues three and seven months post application did not have any impact on the reduction of VSD incidence in the first year. In the second year, we observed a significant reduction of the disease by both T. asperellum in combination with compost and compost alone in a time span of three to seven months, and with T. asperellum spraying and infusion in a time span of five to seven months. By comparing to the control, the efficacy of these treatments in controlling the VSD disease seven months post-first application in the last year was 44.4%, 23.5%, 23.1%, and 15.1%, respectively. Detection of trees inoculated with T. asperellum indicated that this fungus was present in root and branch tissues except for treatment through infusions, while in the uninoculated trees, Trichoderma was not present or was present at a very low level. These data showed that combination of T. asperellum and composted plant residues applied through soil amendment was able to control VSD disease effectively and could potentially be used at large scale to control this disease and other diseases infesting aerial parts of cacao, and to improve soil fertility.


BMC Biology ◽  
2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Elise J. Gay ◽  
Jessica L. Soyer ◽  
Nicolas Lapalu ◽  
Juliette Linglin ◽  
Isabelle Fudal ◽  
...  

Abstract Background The fungus Leptosphaeria maculans has an exceptionally long and complex relationship with its host plant, Brassica napus, during which it switches between different lifestyles, including asymptomatic, biotrophic, necrotrophic, and saprotrophic stages. The fungus is also exemplary of “two-speed” genome organisms in the genome of which gene-rich and repeat-rich regions alternate. Except for a few stages of plant infection under controlled conditions, nothing is known about the genes mobilized by the fungus throughout its life cycle, which may last several years in the field. Results We performed RNA-seq on samples corresponding to all stages of the interaction of L. maculans with its host plant, either alive or dead (stem residues after harvest) in controlled conditions or in field experiments under natural inoculum pressure, over periods of time ranging from a few days to months or years. A total of 102 biological samples corresponding to 37 sets of conditions were analyzed. We show here that about 9% of the genes of this fungus are highly expressed during its interactions with its host plant. These genes are distributed into eight well-defined expression clusters, corresponding to specific infection lifestyles or to tissue-specific genes. All expression clusters are enriched in effector genes, and one cluster is specific to the saprophytic lifestyle on plant residues. One cluster, including genes known to be involved in the first phase of asymptomatic fungal growth in leaves, is re-used at each asymptomatic growth stage, regardless of the type of organ infected. The expression of the genes of this cluster is repeatedly turned on and off during infection. Whatever their expression profile, the genes of these clusters are enriched in heterochromatin regions associated with H3K9me3 or H3K27me3 repressive marks. These findings provide support for the hypothesis that part of the fungal genes involved in niche adaptation is located in heterochromatic regions of the genome, conferring an extreme plasticity of expression. Conclusion This work opens up new avenues for plant disease control, by identifying stage-specific effectors that could be used as targets for the identification of novel durable disease resistance genes, or for the in-depth analysis of chromatin remodeling during plant infection, which could be manipulated to interfere with the global expression of effector genes at crucial stages of plant infection.


2020 ◽  
Vol 145 ◽  
pp. 111847 ◽  
Author(s):  
Diogenes dos Santos Dias ◽  
Caio Gomide Otoni ◽  
Robson Rosa da Silva ◽  
Andreia Bagliotti Meneguin ◽  
Luiz Henrique Capparelli Mattoso ◽  
...  

2019 ◽  
Vol 20 (9) ◽  
pp. 2141 ◽  
Author(s):  
Han Yong Park ◽  
Doo Hwan Kim ◽  
Ramesh Kumar Saini ◽  
Judy Gopal ◽  
Young-Soo Keum ◽  
...  

The goal of this study was to establish an efficient protocol for the large-scale propagation of Mertensia maritima (L.) Gray, and evaluate the carotenoid, fatty acid, and tocopherol contents in the leaves of in vitro regenerated shoots. Surface-disinfected node and shoot tip explants were placed on semisolid Murashige and Skoog (MS) medium with 0–16 µM N6-benzyladenine (BA), kinetin, (KN), and thidiazuron (TDZ) alone, or in combination with, 1 or 2 µM α-naphthaleneacetic acid (NAA). Of the three different cytokinins employed, TDZ elicited the best results for axillary shoot proliferation. A maximum frequency of shoot initiation above 84%, with a mean of 8.9 and 4.8 shoots per node and shoot tip, respectively, was achieved on the culture medium supplemented with 4 µM TDZ. A combination of TDZ + NAA significantly increased the percentage of multiple shoot formation and number of shoots per explant. The best shoot induction response occurred on MS medium with 4 µM TDZ and 1 µM NAA. On this medium, the node (93.8%) and shoot tip (95.9%) explants produced an average of 17.7 and 8.6 shoots, respectively. The highest root induction frequency (97.4%) and number of roots per shoot (25.4), as well as the greatest root length (4.2 cm), were obtained on half-strength MS medium supplemented with 4 µM indole-3-butyric acid (IBA). The presence of six carotenoids and α-tocopherol in the leaf tissues of M. maritima was confirmed by HPLC. Gas chromatography-mass spectrometry analysis confirmed the presence of 10 fatty acids, including γ-linolenic acid and stearidonic acid in the leaf tissues of M. maritima. All-E-lutein (18.49 μg g−1 fresh weight, FW), α-tocopherol (3.82 μg g−1 FW) and α-linolenic acid (30.37%) were found to be the significant compounds in M. maritima. For the first time, a successful protocol has been established for the mass propagation of M. maritima with promising prospects for harnessing its bioactive reserves.


Plant Disease ◽  
1998 ◽  
Vol 82 (10) ◽  
pp. 1161-1164 ◽  
Author(s):  
R. G. Pratt ◽  
D. E. Rowe

Previous studies established that excised leaf tissues of alfalfa can be inoculated with Sclerotinia trifoliorum to select for heritable resistance, but the original procedures were not practical for use in large-scale screening programs. In this study, simplified leaf inoculation procedures for more rapid screening for resistance, based on direct application of leaf tissues to colonies of the pathogen on agar media, were evaluated. Cotyledons, unifoliate leaves, and leaflets of trifoliolate leaves of plants 7 to 21 days old from three relatively susceptible cultivars and one resistant germ plasm were applied, with and without wounding, directly to colony margins of S. trifoliorum on cornmeal agar, V8 juice agar, and water agar. Leaves were scored according to the rate and extent of development of necrosis. Significant differences between alfalfa populations were expressed in unifoliate leaves and trifoliolate leaflets but not in cotyledons. Disease severity in the resistant germ plasm (Mississippi Sclerotinia-Resistant [MSR]) was less than in the three cultivars on all agar media. Wounding of leaf tissues increased disease severity and greatly reduced the incidence of symptomless leaves, which are indicated to be escapes, but wounding generally did not prevent expression of resistance in MSR. Results indicate that initial screening for resistance to S. trifoliorum in alfalfa seedlings may be accomplished by applying wounded unifoliate leaves and leaflets of trifoliolate leaves directly to colonies on cornmeal or V8 juice agars.


Genome ◽  
2004 ◽  
Vol 47 (3) ◽  
pp. 579-589 ◽  
Author(s):  
S Hocquigny ◽  
F Pelsy ◽  
V Dumas ◽  
S Kindt ◽  
M-C Heloir ◽  
...  

Vitis vinifera 'Pinot' clones were analysed at 50 microsatellite loci to assess intravarietal genetic diversity. When analysing leaf tissue DNAs, polymorphism mainly resulted from the appearance of a third allele when two were expected for heterozygous loci in a diploid species. The sequencing of the three microsatellite alleles at two loci has confirmed their simultaneous presence in the leaf tissues. A hypothesis explaining the triallelic profiles at a locus is the presence of a periclinal chimera meristem structure, in which genetically different cell layers coexist. The periclinal chimeric state of two Vitis vinifera 'Pinot gris' clones was confirmed by splitting and analysing the genotypes resulting from L1 and L2 cell layers in progeny derived from self-fertilization, in root tissues, and in plants regenerated from somatic embryogenesis. Prevalence of chimerism in polymorphic clones observed in a collection of 145 accessions belonging to 'Pinot gris', 'Pinot noir', Pinot blanc', 'Pinot meunier', and 'Pinot moure' cultivars was demonstrated. The accumulation of somatic mutations and cell layer rearrangements allowed us to deduce the relationships between the various genotypes and to open a way for understanding the diversification process and the phylogeny in the 'Pinot' group.Key words: microsatellite, diversity, somatic mutation, chimerism, Vitis vinifera L., 'Pinot'.


Plant Disease ◽  
2021 ◽  
Author(s):  
jinfeng Zhang ◽  
jianglai Wang ◽  
jinxiu Ma ◽  
Lu Liu ◽  
Tong Shen ◽  
...  

Onion (Allium cepa L.) is one of the most cultivated vegetables throughout the world. With an average annual production quantity of 18 million kg in recent 21 years, China is the world’s biggest onion producer (Hanci F., 2018). Among them, onion is mainly cultivated in the provinces of Gansu, Shandong, Yunnan, Jiangsu, Zhejiang and Henan. A survey in Gansu province in last several years showed that the incidence of onion bulb rot was 30%-80%. In April 2020, bulbs displayed water-soaked, and then rot symptoms observed during storage in Lanzhou City, Gansu Province, China. The initial symptoms of bulb rot disease were yellowish brown, and produced an abundant exudate in the inner bulb scales when cut. Gradually, symptomatic bulbs became soft, watery and decayed. In severe infections, the onions showed total rot of the bulb. Therefore, we sampled some diseased onions and isolated pathogenic bacteria from the junction of lesion along with healthy parts on Luria-Bertani (LB) medium. Three representative single colonies were obtained on LB medium, and the culture characteristics were raised elevation, mucoid texture, round, and smooth with entire margin, the brown at the beginning and turned yellow later, and scanning electron microscopy (SEM) observations showed that these isolates were short rod-shaped (Fig. 1A). The physiological and biochemical determination revealed that the isolates were positive for yellow pigment, v-p test, growth at 37 ℃, nitrate reduced, catalase, glucose, sucrose, D (-)-salicin, starch hydrolysis, motility, pellicle. On the contrary, they were negative for indole production, methyl red, lactose, gelatin liquefaction, glycerol, gram staining (Gavini et al., 1989; Nabrdalik et al., 2018). Based on these morphological, physiological and biochemical characteristics, three isolates were initially identified as Pantoea agglomerans (Guo et al., 2020). A representative isolate L1 was selected to extract DNA, and the conserved sequences of the pathogen gene were sequenced according to 23S ribosomal RNA (23S rRNA), DNA gyrase subunit B (gyrB), elongation factor G (fusA) (She et al., 2021) housekeeping gene. The sequence alignment of the 23S rRNA gene (P. agglomerans, MZ314289, 930bp) showed that the homology between the strain L1 and P. agglomerans (CP016889) with similarity of 99.54%, and based on the sequence alignment of gyrB (P. agglomerans, MZ337547, 1189bp) and fusA (P. agglomerans, MZ350961, 1037bp) genes, the similarity with P. agglomerans (FJ617386 and MG845872) was 100%. A phylogenetic analysis based on the 23S, gyrB, fusA housekeeping gene sequences was performed by using the neighbor-joining methods in MEGA 7.0 under the p-distance (Kumar et al, 2016), which included P. agglomerans strains AR1a, TH81, L15, ASB05, P. eucalypti strain LMG 24197, P. dispersa strains BJQ0007 and DSM 32899, P. ananatis strains LMG 20103 and AJ13355, P. vagans strains C9-1, LMG24199 and PV989. The phylogenetic distribution generated five primary phylogroups, and strain L1 formed a clade with the other four P. agglomerans strains (Fig. 2). Thus, the strain L1 was identified as P. agglomerans. To satisfy Koch's postulates, ten onions were divided into two groups, five in each group, and needle punctured wound on the surface of each onion. In the experimental group, 400 μL bacterial suspensions were injected with sterile syringe, and the other five onions were injected with the same amount of sterile distilled water as the negative conrol. Inoculated onions were incubated in the greenhouse incubator (28 ℃, humidity > 80%). After 4 days of incubation, all onions inoculated with strain L1 appeared water-soaked, rot symptoms, and no symptoms were observed in the negative control (Fig. 1B). Subsequently, pathogens were re-isolated from inoculated bulbs and identified as P. agglomerans according to molecular identification described above. To the best of our knowledge, this is the first report that the bulb rot disease of stored onion caused by P. agglomerans in China.


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