Academic literature on the topic 'Phytophthora cinnamomi diseases control'
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Journal articles on the topic "Phytophthora cinnamomi diseases control"
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Sumida, Ciro Hideki, Lucas Henrique Fantin, Karla Braga, Marcelo Giovanetti Canteri, and Martin Homechin. "Control of root rot (Phytophthora cinnamomi) in avocado (Persea Americana) with bioagents." Summa Phytopathologica 46, no. 3 (September 2020): 205–11. http://dx.doi.org/10.1590/0100-5405/192195.
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ABSTRACT Despite the favorable edaphoclimatic conditions for avocado production in Brazil, diseases such as root rot caused by the pathogen Phytophthora cinnamomi compromise the crop. With the aim of managing root rot in avocado, the present study aimed to evaluate chemical and biological control with isolates of Trichoderma spp. and Pseudomonas fluorescens. Thus, three assays were conducted to assess: (i) mycelial inhibition of P. cinnamomi by isolates of Trichoderma spp. and P. fluorescens from different crop systems; (ii) effect of autoclaved and non-autoclaved metabolites of P. fluorescens, and (iii) chemical or biological treatment of avocado seedlings on the control of root rot under field conditions. The isolates of Trichoderma spp. from maize cultivation soil and the commercial products formulated with Trichoderma presented greater antagonism (p <0.05) to the pathogen P. cinnamomi in the in vitro tests. Similarly, non-autoclaved metabolites of P. fluorescens presented antagonistic potential to control P. cinnamomi. Under field conditions, the fungicide metalaxyl and the bioagents showed effectiveness in controlling P. cinnamomi, as well as greater root length and mass. Results demonstrated potential for the biological control of avocado root rot with Trichoderma spp. and P. fluorescens.
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Alvarado, Laureano, Sebastián Saa, Italo F. Cuneo, Romina Pedreschi, Javiera Morales, Alejandra Larach, Wilson Barros, Jeannette Guajardo, and Ximena Besoain. "A Comparison of Immediate and Short-Term Defensive Responses to Phytophthora Species Infection in Both Susceptible and Resistant Walnut Rootstocks." Plant Disease 104, no. 3 (March 2020): 921–29. http://dx.doi.org/10.1094/pdis-03-19-0455-re.
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Clonal rootstocks are one alternative used by the walnut industry to control damage caused by Phytophthora species, traditionally using plants grafted on susceptible Juglans regia rootstock. Vlach, VX211, and RX1 are clonal rootstocks with a degree of resistance to Phytophthora species. The resistance to pathogens in these rootstocks depends on the resistance mechanisms activated by the presence of the pathogen and subsequent development of responses in the host. In this work, we analyzed how plants of J. regia, Vlach, VX211, and RX1 responded to inoculation with Phytophthora cinnamomi or Phytophthora citrophthora isolates obtained from diseased English walnut plants from Chilean orchards. After inoculation, plants of Vlach, VX211, and RX1 showed canopy and root damage indexes that did not differ from noninoculated control plants. In contrast, plants of J. regia, which is susceptible to P. cinnamomi and P. citrophthora, died after inoculation. Vlach, VX211, and RX1 plants inoculated with P. cinnamomi or P. citrophthora showed greater root weight and volume and greater root growth rates than their respective controls. These results suggest that short-term carbohydrate dynamics may be related to the defense mechanisms of plants; they are immediately activated after inoculation through the production of phenolic compounds, which support the further growth and development of roots in walnut clonal rootstocks. To our knowledge, this is the first study that comprehensively characterizes vegetative and radicular growth and the dynamics of sugars and phenols in response to infection with P. cinnamomi or P. citrophthora in walnut rootstocks.
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Casonato, S. G., M. A. Manning, P. A. Rheinlander, and R. A. Fullerton. "Control of Phytophthora cinnamomi in Erica sessiliflora and Erica davisii." New Zealand Plant Protection 61 (August 1, 2008): 86–90. http://dx.doi.org/10.30843/nzpp.2008.61.6823.
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A field trial was conducted to test the efficacy of two fungicides (metalaxyl and phosphorous acid) and supplementary organic matter for the control of Phytophthora cinnamomi root rot in Erica sessiliflora and E davisii Five treatments were applied (1) untreated control (2) metalaxyl (3) phosphorous acid (4) metalaxyl plus phosphorous acid and (5) organic soil amendment Plants were assessed for plant health as an indication of possible P cinnamomi infection Phosphorous acid applied alone or in combination with metalaxyl resulted in a significant reduction in the number of diseased or dead E sessiliflora plants compared with the untreated control plants (P0011 and P0004 respectively) The mean health index of phosphorous acid treated E davisii plants was not different (P>005) to control plants Results suggest that this species of Erica has some tolerance to P cinnamomi Metalaxyl applications alone or organic matter treatments did not reduce disease relative to controls in either species
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Lawrence, Scott A., Hannah F. Robinson, Daniel P. Furkert, Margaret A. Brimble, and Monica L. Gerth. "Screening a Natural Product-Inspired Library for Anti-Phytophthora Activities." Molecules 26, no. 7 (March 24, 2021): 1819. http://dx.doi.org/10.3390/molecules26071819.
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Phytophthora is a genus of microorganisms that cause devastating dieback and root-rot diseases in thousands of plant hosts worldwide. The economic impact of Phytophthora diseases on crops and native ecosystems is estimated to be billions of dollars per annum. These invasive pathogens are extremely difficult to control using existing chemical means, and the effectiveness of the few treatments available is being jeopardized by increasing rates of resistance. There is an urgent need to identify new chemical treatments that are effective against Phytophthora diseases. Natural products have long been regarded as “Nature’s medicine chest”, providing invaluable leads for developing front-line drugs and agrochemical agents. Here, we have screened a natural product-inspired library of 328 chemicals against two key Phytophthora species: Phytophthora cinnamomi and Phytophthora agathidicida. The library was initially screened for inhibition of zoospore germination. From these screens, we identified twenty-one hits that inhibited germination of one or both species. These hits were further tested in mycelial growth inhibition studies to determine their half-maximal inhibitory concentrations (IC50s). Four compounds had IC50 values of approximately 10 µM or less, and our best hit had IC50s of approximately 3 µM against both Phytophthora species tested. Overall, these hits may serve as promising leads for the development of new anti-Phytophthora agrochemicals
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Zinati, Gladis M. "Compost in the 20th Century: A Tool to Control Plant Diseases in Nursery and Vegetable Crops." HortTechnology 15, no. 1 (January 2005): 61–66. http://dx.doi.org/10.21273/horttech.15.1.0061.
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The discovery of disease suppression in certain bark composts increased the interest in using compost as growing substrate to control root rot diseases caused by Phytophthora cinnamomi. Disease suppression mechanisms include antibiosis, competition, hyperparasitism, and induced systemic resistance. Although abiotic factors may influence disease suppression, the latter is often based on microbial interactions—the two common mechanisms being general for pythium (Pythium spp.) and phytophthora root rot (Phytophthora spp.) and specific for rhizoctonia (Rhizoctonia solani). The discovery of disease suppression agents in compost led to the development of biocontrol agent-fortified compost during the last decade of the 20th century. The suggested recommendations for future research and extension outreach may include 1) development of methods to manage bacterial and viral diseases through the use of compost; 2) exploration of the potential effects of fortified compost on insect pests suppression; 3) improvement of inoculation methods of composts with biocontrol agents to produce consistent levels of disease suppression at the commercial scale; 4) development of effective fortified compost teas for suppressing foliar diseases; 5) education of compost producers on methods of production of fortified compost that suppress specific diseases; and 6) education of end-users on uses of fortified compost and its by-products.
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Moon, Jae-Hyun, Sang-Jae Won, Chaw Ei Htwe Maung, Jae-Hyeok Choi, Su-In Choi, Henry B. Ajuna, and Young Sang Ahn. "Bacillus velezensis CE 100 Inhibits Root Rot Diseases (Phytophthora spp.) and Promotes Growth of Japanese Cypress (Chamaecyparis obtusa Endlicher) Seedlings." Microorganisms 9, no. 4 (April 13, 2021): 821. http://dx.doi.org/10.3390/microorganisms9040821.
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Root rot diseases, caused by phytopathogenic oomycetes, Phytophthora spp. cause devastating losses involving forest seedlings, such as Japanese cypress (Chamaecyparis obtusa Endlicher) in Korea. Plant growth-promoting rhizobacteria (PGPR) are a promising strategy to control root rot diseases and promote growth in seedlings. In this study, the potential of Bacillus velezensis CE 100 in controlling Phytophthora root rot diseases and promoting the growth of C. obtusa seedlings was investigated. B. velezensis CE 100 produced β-1,3-glucanase and protease enzymes, which degrade the β-glucan and protein components of phytopathogenic oomycetes cell-wall, causing mycelial growth inhibition of P. boehmeriae, P. cinnamomi, P. drechsleri and P. erythoroseptica by 54.6%, 62.6%, 74.3%, and 73.7%, respectively. The inhibited phytopathogens showed abnormal growth characterized by swelling and deformation of hyphae. B. velezensis CE 100 increased the survival rate of C. obtusa seedlings 2.0-fold and 1.7-fold compared to control, and fertilizer treatment, respectively. Moreover, B. velezensis CE 100 produced indole-3-acetic acid (IAA) up to 183.7 mg/L, resulting in a significant increase in the growth of C. obtusa seedlings compared to control, or chemical fertilizer treatment, respectively. Therefore, this study demonstrates that B. velezensis CE 100 could simultaneously control Phytophthora root rot diseases and enhance growth of C. obtusa seedlings.
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Jung, T., and G. Dobler. "First Report of Littleleaf Disease Caused by Phytophthora cinnamomi on Pinus occidentalis in the Dominican Republic." Plant Disease 86, no. 11 (November 2002): 1275. http://dx.doi.org/10.1094/pdis.2002.86.11.1275c.
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Pinus occidentalis Sw. is an endemic species of the Caribbean island of Hispaniola (Dominican Republic and Haiti). It shows an extreme ecological plasticity and grows on a wide range of soil types from 0 to 3,175 m in elevation with annual mean temperatures ranging from 6 to 25°C and annual precipitation of 800 to 2,300 mm. P. occidentalis is a major component of forests above 800 m in elevation and forms pure climax forests above 2,000 m (4). For more than 10 years, stands of P. occidentalis in the Sierra (Cordillera Central) growing on a wide range of site conditions have suffered from a serious widespread disease. Symptoms include yellowing and dwarfing of needles, a progressive defoliation and dieback of the crown, and finally, death of weakened trees often caused by attacks by secondary bark beetles. Mature stands are mainly affected, but the disease is also present in plantations and natural regeneration that is older than 10 years. Disease spread is rapid, and occurs mainly along roads and from diseased trees downslope following the path of water runoff. Initially, Leptographium serpens was isolated from necrotic roots and was thought to be the causal agent (1). However, the symptoms of the disease more closely resemble those of littleleaf disease of P. echinata and P. taeda in the southeastern United States, which is caused by the aggressive fine-root pathogen Phytophthora cinnamomi Rands (3). Moreover, spread and dynamics of the disease are similar to the diebacks of Chamaecyparis lawsoniana in Oregon and Eucalyptus spp. in western Australia, which are caused by the introduced soilborne pathogens Phytophthora lateralis and Phytophthora cinnamomi, respectively. Soil samples containing the rhizosphere and fine roots of diseased P. occidentalis trees were collected in February 2002 at five sites near Celestina and Los Montones (Dominican Republic) and transported to the Bavarian State Institute of Forestry. The pathogen was baited from the soil by floating 3- to 7-dayold leaves of Quercus robur seedlings over flooded soil and placing the leaves on selective PARPNH agar (2). Phytophthora cinnamomi was isolated from the soil of all five sites. Crossing with A1 and A2 tester strains of Phytophthora cinnamomi confirmed that all isolates belong to the A2 mating type. In cross sections of necrotic fine roots, characteristic structures of Phytophthora cinnamomi such as nonseptate hyphae and chlamydospores could be observed. Our results indicate that the disease of P. occidentalis is caused by the introduced pathogen Phytophthora cinnamomi. Because of the ecological and economical importance of P. occidentalis, the disease poses a major threat to forestry in the Dominican Republic. Future research should include the mapping of the disease, pathogenicity tests on P. occidentalis and alternative pine species, in particular P. caribaea, screening for resistance in the field, and testing of systemic fungicides such as potassium phosphonate, which is known to be effective against Phytophthora cinnamomi. References: (1) G. Dobler. Manejo y Tablas de Rendimiento de Pinus occidentalis. Plan Sierra, San José de las Matas, Dominican Republic, 1999. (2) T. Jung et al. Plant Pathol. 49:706, 2000. (3) S. W. Oak and F. H. Tainter. How to identify and control littleleaf disease. Protection Rep. R8-PR12, USDA Forest Service Southern Region, Atlanta, Georgia, 1988. (4) L. Sprich. Allg. Forst. Jagdztg. 168:67, 1997.
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Shearer, BL, and M. Dillon. "Impact and Disease Centre Characteristics of Phytophthora cinnamomi Infestations of Banksia Woodlands on the Swan Coastal Plain, Western Australia." Australian Journal of Botany 44, no. 1 (1996): 79. http://dx.doi.org/10.1071/bt9960079.
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Phytophthora cinnamomi Rands was isolated from either dead plants or soil at 46 disease centres in Banksia woodland at national parks and reserves on the Swan Coastal Plain. Phytophthora cryptogea Pethybridge & Lafferty was also isolated from roots of dead Acacia pulchella R.Br. in one disease centre infected with P. cinnamomi. Dead plants were infected with Armillaria luteobubalina Watling & Kile in four disease centres on the Spearwood Dune System, and these centres were excluded from further analysis. Phytophthora cinnamomi diseased areas ranged from 0.01 to 30 ha in size (mean 1.6 ± s.e. 0.7 ha). The total area infested for the 46 disease centres was 71.5 ha. Impact of P. cinnamomi was high in 17% of disease centres and low in 11% of disease centres. Age of plant death was a mixture of old and recent in 85% of disease centres. Mainly old deaths occurred in only 4% of disease centres. The proportion of species dying in infested areas varied between 10-64% (mean 28 ± s.e. 2%) and was positively correlated with impact type. It was found that infestation decreased species number; on average, there were seven fewer species in infested compared to non-infested areas. Four plant species associated with moist sandy sites tended to occur more frequently in centres of high impact than by chance alone. Occurrence of P. cinnamomi was related to soil association with soils of 60% of the disease centres belonging to the Bassendean or Southern River associations of the Bassendean Dune System. Sixteen percent of disease centres occurred in the Cannington, Guildford and Serpentine River associations of the Pinjarra Plain. No disease centres of P. cinnamomi were found on soils of the Speanvood and Quindalup Dune Systems. A water table was found within 3 m of the soil surface in 48% of the centres. Disturbance was associated with all disease centres. Firebreaks were associated with 72% of disease centres. Banksia woodland remnants on the Bassendean Dune System and the Pinjarra Plain are highly vulnerable to infection by P. cinnamomi and their conservation requires control of existing infestatinns and protection from introduction af the pathogen.
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Matei, Petruta, Jesús Martín-Gil, Beatrice Michaela Iacomi, Eduardo Pérez-Lebeña, María Barrio-Arredondo, and Pablo Martín-Ramos. "Silver Nanoparticles and Polyphenol Inclusion Compounds Composites for Phytophthora cinnamomi Mycelial Growth Inhibition." Antibiotics 7, no. 3 (August 16, 2018): 76. http://dx.doi.org/10.3390/antibiotics7030076.
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Phytophthora cinnamomi, responsible for “root rot” or “dieback” plant disease, causes a significant amount of economic and environmental impact. In this work, the fungicide action of nanocomposites based on silver nanoparticles and polyphenol inclusion compounds, which feature enhanced bioavailability and water solubility, was assayed for the control of this soil-borne water mold. Inclusion compounds were prepared by an aqueous two-phase system separation method through extraction, either in an hydroalcoholic solution with chitosan oligomers (COS) or in a choline chloride:urea:glycerol deep eutectic solvent (DES). The new inclusion compounds were synthesized from stevioside and various polyphenols (gallic acid, silymarin, ferulic acid and curcumin), in a [6:1] ratio in the COS medium and in a [3:1] ratio in the DES medium, respectively. Their in vitro response against Phytophthora cinnamomi isolate MYC43 (at concentrations of 125, 250 and 500 µg·mL−1) was tested, which found a significant mycelial growth inhibition, particularly high for the composites prepared using DES. Therefore, these nanocomposites hold promise as an alternative to fosetyl-Al and metalaxyl conventional systemic fungicides.
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Thinggaard, K., and B. Toppe. "First Report of Phytophthora cinnamomi Root Rot, Stem, and Leaf Blight on Ivy." Plant Disease 81, no. 8 (August 1997): 960. http://dx.doi.org/10.1094/pdis.1997.81.8.960c.
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Phytophthora cinnamomi was isolated from varieties of Hedera helix pot plants in 1989 in two Danish greenhouse nurseries. The symptoms were brown, rotten roots and stems, and brown areas developing from the base of the leaves. The fungus was isolated directly from roots, stems, leaves, and soil, and by baiting the nutrient solutions of the watering systems with needles of Cedrus deodara. The fungus was isolated on Phytophthora selective agar medium containing hymexazol and identified with the keys of Kröber (1) and Stamps et al. (2). The fungus was characterized by coralloid hyphal swellings, chlamydospores, lack of oogonia in single culture, and production of numerous, ovoid sporangia with a nonpapillate, wide pore. The sporangia produced many zoospores after 2 days flooding with autoclaved pond water on V8 juice agar, followed by internal proliferation. The fungus was also isolated in Norway in 1993 from ivy pot plants. The fungus was widespread in Danish and Norwegian pot plant nurseries in 1997 and caused losses in most varieties, especially at temperatures above 23°C. Effective fungicides are not available for use in Denmark and the disease is easily spread with cuttings, and through the watering system with recirculation of the nutrient solution. A Danish isolate of P. cinnamomi originating from roots of H. helix was used in a pathogenicity test. Five-week-old cuttings were inoculated by adding zoospores (5 per ml) to the recirculating nutrient solution. Control plants were on a separate bench with nutrient solution without the fungus. After 1 week, symptoms of root rot were observed, and 2 weeks after inoculation, 75% of plants expressed severe symptoms on roots, stems, and leaves. P. cinnamomi was reisolated from roots, stems, and leaves of diseased plants, but was not isolated from the control plants. The reisolate was morphologically identical to the original isolate. This is the first report of P. cinnamomi from ivy in Europe. References: (1) H. Kröber. Mitt. Biol. Bundesanst. Land Forstwirtsch. Berlin-Dahlem 225:73, 1985. (2) D. J. Stamps et al. 1990. Mycol. Pap. No. 162. CAB Int. Mycol. Inst., Kew, England.
Dissertations / Theses on the topic "Phytophthora cinnamomi diseases control"
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Finlay, Annabelle Ruth. "Microbial suppression of Phytophthora cinnamomi." Thesis, Queen's University Belfast, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317116.
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King, Michaela. "The phosphite responsive transcriptome of Phytophthora cinnamomi /." King, Michaela (2007) The phosphite responsive transcriptome of phytophthora cinnamomi. PhD thesis, Murdoch University, 2007. http://researchrepository.murdoch.edu.au/132/.
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Phosphite has been used to effectively control the soil borne plant pathogen Phytophthora cinnamomi in many horticultural crops, forest trees and natural ecosystems. However, the molecular mechanisms behind phosphite action on this pathogen are poorly understood.
Several studies have shown that phosphite inhibits growth and zoospore production of P. cinnamomi and in addition induces significant physiological and metabolic changes in the mycelium. As an approach to understanding the mechanisms and relevance of these changes in the pathogen, the effect of phosphite on gene expression was investigated using microarray analysis. To construct the microarray, RNA was extracted from phosphite-treated (40 ug/ml) mycelium of P. cinnamomi isolate MP 80. The chosen phosphite concentration inhibited the mycelial growth by 70% but provided sufficient mycelium for RNA extractions after 4 days growth at 25C.
The mRNA was reverse transcribed into cDNA and cloned into lambda to construct a library consisting of 2 million pfu of which 80 % were recombinant phage. The inserts were sequenced for a random selection of clones from the library. The nucleotide sequences generated revealed a range of different P. cinnamomi genes being expressed and demonstrated that the cDNA library provided a good representation of the transcripts expressed in P. cinnamomi. The types of genes found to be expressed in the mycelium of P. cinnamomi included genes encoding GTP binding proteins involved in vesicle transport, structural proteins involved in maintaining cell membrane integrity,elicitors, phosphatases and ribosomal proteins.
Over nine thousand cDNA transcripts were randomly selected from the cDNA library and prepared by PCR amplification and purification for microarray construction. Custom made cDNA arrays containing 9216 cDNA transcripts were constructed and probed with RNA from untreated mycelium and mycelium grown in medium with 40 ug/ml phosphite.
Two genes, EF-1 alpha and cinnamomin gene, identified by qRT-PCR as being constitutively expressed were also positioned on the arrays as positive controls. In the process of identifying constitutively expressed genes, qRT PCR revealed that phosphite down-regulated a gene encoding ubiquitin-conjugating enzyme, a component of the ubiquitin/proteasome pathway involved in the removal of abnormal and short lived-regulatory proteins and rate limiting enzymes.
From the arrays a further seventy-two transcripts with altered patterns in gene expression (fold change > 2) were identified. The majority of the cDNA transcripts spotted on the array were down-regulated with changes in gene expression ranging from 2- to 3.5-fold. Thirty-two cDNA transcripts were up-regulated with changes in gene expression ranging from 2- to 16-fold. Characterisation by sequencing revealed that the most highly induced transcripts coded for ADP-ribosylation factors, an ABC cassette transporter and a glycosyl transferase. A transcript encoding a vitamin B6 biosynthesis protein was also identified as up-regulated by 2.9-fold. In contrast, the down-regulated transcripts coded for cellulose synthase I, annexin, glutamine synthetase, metallothionein and an alternative oxidase. The results are discussed in terms of possible roles and mechanism(s) of phosphite action within the mycelium of P.cinnamomi.
This work is the first comprehensive screen for phosphite regulated-gene expression in P. cinnamomi and represents a significant step towards an understanding of the mode of action of phosphite on this organism. This thesis provides valuable information on the molecular interaction between phosphite and P. cinnamomi, which in future studies may stimulate the discovery of novel methods and cellular targets for the control of plant pathogenic Oomycetes.
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McCarren, Kathryn. "Saprophytic ability and the contribution of chlamydospores and oospores to the survival of Phytophthora cinnamomi." McCarren, Kathryn (2006) Saprophytic ability and the contribution of chlamydospores and oospores to the survival of Phytophthora cinnamomi. PhD thesis, Murdoch University, 2006. http://researchrepository.murdoch.edu.au/190/.
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Phytophthora cinnamomi has been recognised as a key threatening process to Australia's biodiversity by the Commonwealth's Environment Protection and Biodiversity Conservation Act 1999. Despite over 80 years of extensive research, its exact mode of survival is still poorly understood. It is widely accepted that thin- and thick-walled chlamydospores are the main survival propagules while oospores are assumed to play no role in the survival of the pathogen in the Australian environment, yet evidence is limited. The saprophytic ability of the pathogen is still unresolved despite the important role this could play in the ability of the pathogen to survive in the absence of susceptible hosts. This thesis aimed to investigate chlamydospores, oospores and the saprophytic ability of P. cinnamomi to determine their contribution to survival.
Phytophthora cinnamomi did not show saprophytic ability in non-sterile soils. The production of thick-walled chlamydospores and selfed oospores of P. cinnamomi in vitro was documented. Thick-walled chlamydospores were sporadically formed under sterile and non-sterile conditions in vitro but exact conditions for stimulating their formation could not be determined. The formation of thick-walled chlamydospores emerging from mycelium of similar wall thickness was observed, challenging the current knowledge of chlamydospore formation.
Selfed oospores were abundant in vitro on modified Ribeiro's minimal medium in one isolate. Three other isolates tested also produced oospores but not in large numbers. Although the selfed oospores did not germinate on a range of media, at least 16 % were found to be viable using Thiozolyl Blue Tetrazolium Bromide staining and staining of the nuclei with 4', 6-diamidino-2-phenylindole.2HCl (DAPI). This indicated the potential of selfed oospores as survival structures and their ability to exist dormantly.
The ability of phosphite to kill chlamydospores and selfed oospores was studied in vitro. Results challenged the efficacy of this chemical and revealed the necessity for further study of its effect on survival propagules of P. cinnamomi in the natural environment. Phosphite was shown to induce dormancy in thin-walled chlamydospores if present during their formation in vitro. Interestingly, dormancy was only induced by phosphite in isolates previously reported as sensitive to phosphite and not those reported as tolerant.
Chlamydospores were produced uniformly across the radius of the colony on control modified Ribeiro's minimal medium but on medium containing phosphite (40 or 100 mcg ml-1), chlamydospore production was initially inhibited before being stimulated during the log phase of growth. This corresponded to a point in the colony morphology where mycelial density changed from tightly packed mycelium to sparse on medium containing phosphite. This change in morphology did not occur when the pathogen was grown on liquid media refreshed every four days, and chlamydospores were evenly distributed across the radius of these colonies. This trend was not observed in selfed oospores produced in the presence of phosphite. Selfed oospore production was found to be inhibited by phosphite at the same concentrations that stimulated chlamydospore production.
Isolates of P. cinnamomi were transformed using a protoplast/ polyethylene glycol method to contain the Green Fluorescent Protein and geneticin resistance genes to aid in future studies on survival properties of the organism. Although time constraints meant the stability of the transgene could not be determined, it was effective in differentiating propagules of the transformed P. cinnamomi from spores of other microrganisms in a non-sterile environment. Two different sized chlamydospores (approximately 30 mcg diameter and < 20 mcg diameter) were observed in preliminary trials of transformed P. cinnamomi inoculated lupin roots floated in non-sterile soil extracts and these were easily distinguished from microbial propagules of other species. The growth and pathogenicity was reduced in two putative transformants and their ability to fluoresce declined over ten subcultures but they still remained resistant to geneticin.
This study has improved our knowledge on the survival abilities of P. cinnamomi in vitro and has provided a useful tool for studying these abilities under more natural glasshouse conditions. Important implications of phosphite as a control have been raised.
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Pilbeam, Ros. "Effects of phosphite on disease development and histological responses in Eucalyptus marginata infected with Phytophthora cinnamomi." Murdoch University, 2003. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20040820.140206.
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Phosphite is currently used for the management of Phytophthora cinnamomi in native plant communities. A greater understanding of how phosphite affects the host-pathogen interaction is required in order to determine the most effective treatment. This thesis aimed to investigate the effects of applied phosphite concentration on phytotoxicity, in planta concentration of phosphite, disease development and anatomical responses of Eucalyptus marginata.
Spraying the foliage to run-off with 7.5 and 10 g phosphite/L led to the development of severe leaf necrosis within 7 days, with greater than 60% of the leaf area damaged. Moderate phytotoxicity was observed after treatment with 5 g phosphite/L. In planta concentration of phosphite in stems, lignotubers and roots did not differ significantly between applied concentrations of phosphite.
Stem tissue contained the largest concentration of phosphite at one week after spraying, with approximately 210 and 420 µg phosphite/g dry weight detected after treatment with 5 and 10 g phosphite/L, respectively. In a subsequent field trial, the applied concentration of phosphite was found to affect the duration of effectiveness of phosphite in protecting E. marginata seedlings from stem colonisation by P. cinnamomi. Plants were wound-inoculated with P. cinnamomi at 6-monthly intervals after spraying with phosphite. The 2.5 and 5 g phosphite/L treatments were effective against colonisation by P. cinnamomi when inoculated 0 and 6 months after spraying, but only the 5 g phosphite/L treatment inhibited P. cinnamomi within 12 months of spraying. Phosphite had no effect on colonisation by P. cinnamomi when plants were inoculated at 17 months after spraying. The in planta concentration of phosphite detected in the leaves, stems and roots of plants treated with 5 g phosphite/L did not differ significantly between the time of harvest or tissue type at 0.2 and 6 months after spraying. P. cinnamomi remained viable in plants treated with phosphite.Treatment with 2.5 and 5 g phosphite/L when P. cinnamomi was well established in the stems was ineffective at preventing the death of E. marginata.
Between 45 and 89% of plants were girdled on the day of spraying. Spraying plants with 2.5 and 5 g phosphite/L when conditions were less favourable for the pathogen reduced the mortality of E. marginata for up to 10 months.
E. marginata seedlings responded to damage by P. cinnamomi with the production of kino veins and woundwood. Bark lesions were in the process of being sloughed off by 7 months after inoculation in plants that remained alive. In plants of a resistant (RR) clonal line and susceptible (SS) clonal line, phosphite treatment inhibited lesion extension in stems, but lesions did not indicate the amount of stem colonised by P. cinnamomi. The pathogen was isolated from up to 17 cm beyond the lesion front in the RR clonal line. Treatments that reduced the mortality of E. marginata were 5 g phosphite/L in the RR clonal line (RR/5) and 10 g phosphite/L in the SS clonal line (SS/10).
Uninoculated plants were wounded with liquid nitrogen to determine the microscopic responses to injury in the absence of the pathogen. Wound closure was achieved within 21 days of wounding, with callus formation and vascular cambium regeneration. A wound periderm separated wounded tissue from healthy tissue, adjacent to a lignified boundary zone. Two types of phellem were observed thin-walled phellem (TnP) and thick-walled phellem (TkP). The first-formed TnP layers contained variable-shaped cells, while subsequent layers were more cubical in shape. Multiple TnP layers developed up to 42 days after wounding, with TkP cells sandwiched between the TnP layers. Genotype and phosphite treatment did not affect the wound responses.
Inoculated plants with a restricted lesion extension also formed a wound periderm to separate damaged tissue from healthy tissue. Phosphite treatment stimulated the responses to P. cinnamomi in both clonal lines. Early development of the wound periderm was visible by 6 days after phosphite treatment. It waspreceded by the formation of a ligno-suberised boundary zone in the cambial zone and in phloem parenchyma cells existing prior to injury. Suberin was not detected in the SS/0 treatment. TnP layers completely surrounded lesioned tissue in plants still alive by 24 days after phosphite treatment. Extensive callus production was evident in the SS/10, RR/5 and RR/10 treatments.
Temperature affected the post-inoculation efficacy of phosphite and anatomical responses of E. marginata. At 20°C, lesion extension was restricted in both clonal lines of E. marginata, irrespective of phosphite treatment. Greater than 70% of inoculated plants in all treatments produced a ligno-suberised boundary zone at 20°C and between 30 and 70% formed a wound periderm. At 28°C, lesion extension was reduced in phosphite-treated plants at 7 days after treatment. However, lesions continued to extend up to 5 mm per day in the SS clonal line and very few SS plants formed a wound periderm at the lesion front. This contrasted with the strong responses to abiotic wounding observed in uninoculated SS plants at 28°C. The most extensive responses to P. cinnamomi were detected in the RR/5 treatment at 28°C, with a ligno-suberised boundary zone and differentiated TnP of a wound periderm observed in greater than 70% of plants. This treatment resulted in significantly less girdled plants than all other treatments at 28°C, including the RR/0 treatment. At 23 and 24°C, there was no significant difference in acropetal lesion extension or circumferential lesion spread between clonal lines. The inoculation technique and environmental conditions may have resulted in too high a disease pressure for a full expression of resistance in the RR clonal line.
This thesis demonstrates that phosphite has the potential to enhance the resistance of young E. marginata and enable them to survive infection by P. cinnamomi. However, its effectiveness is dependent upon a number of factors, including host resistance, environmental conditions, the applied phosphite concentration and the timing of application.
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Dunne, Christopher Philip. "Control of Sudden Death in Cultivated Proteas from the Southwest of Western Australia." Murdoch University, 2004. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20041207.140807.
Full textAbstract:
Phytophthora cinnamomi Rands is a common and devastating pathogen of cultivated proteas worldwide. Webb (1997) described a Sudden Death plant disease of proteas in Western Australia (WA) protea plantations. Proteas that suffer the syndrome display symptoms such as stunted growth, wilting, chlorosis and often death. In the current study, a number of protea plantations in the southwest of WA were visited to quantify the extent that P. cinnamomi was attributing to deaths of cultivated proteas. The survey indicated that P. cinnamomi is the major cause of Sudden Death in proteas. A range of other fungi (Fusarium, Botryosphaeria, Pestalotiopsis, Alternaria) and pests (nematodes, mealy bug, scale insects) were also identified to be contributing to protea death and decline in WA plantations. In many cases the factors contributing to protea disease appeared complex, with a range of physical factors or nutritional imbalances commonly associated with these pathogens and pests. As P. cinnamomi was the major cause of death of cultivated proteas the remainder of the experiments described in this dissertation investigated its control in horticultural plantings.
Biofumigation has the potential to become an important technique in an overall integrated management approach to P. cinnamomi. In this thesis, biofumigation refers to the suppression of pathogens and pests by the incorporation of Brassica plants into the soil. Two biofumigants (Brassica juncea (L.) Czern., B. napus L.) were screened for their effect on the in vitro growth of five common Phytophthora species (P. cinnamomi, P. cactorum (Lebert & Colin) Schroeter., P. citricola Sawada, P. cryptogea Pethyb. & Laff. and P. megasperma Drechsler). Growth was determined by the measuring dry weight and radial growth of vegetative hyphae. B. juncea was found to be superior in its suppressive effect compared to B. napus. There was also significant variation in the sensitivity of the Phytophthora species to the suppressive effects of the biofumigants. P. cinnamomi was the most sensitive of the five species investigated. Where the rates of the biofumigant were sufficient to suppress growth of Phytophthora, the suppressive effect was mostly fungicidal.
To determine how B. juncea and B. napus affect the infective ability and survival of P. cinnamomi, their effects on sporangia and chlamydospores production in soil was investigated in vitro. P. cinnamomi colonised Miracloth discs were added to soil amended with the two Brassica species, before being removed every two days over an eight day period for the determination of sporangia production, chlamydospore production and infective ability. Only the soils amended with B. juncea significantly reduced sporangia production in P. cinnamomi. Both Brassica species increased the percentage of aborted or immature sporangia and reduced the infective ability of the pathogen. Neither Brassica species had any effect on zoospore release or chlamydospore production in P. cinnamomi.
Soil cores and soil leachate were collected from biofumigant-amended field soils to determine the inoculum potential and infective ability of the pathogen under glasshouse conditions. Amending the soil with both Brassica species had an immediate suppressive effect on the inoculum potential and infective ability of the P. cinnamomi. However, after this initial suppression there was a gradual increase in the recovery of the pathogen over the monitoring period of four weeks. To determine if the suppression would result in decreased disease incidence in a susceptible host, Lupinus angustifolius L. seeds were planted in the biofumigant amended soil. B. juncea amended soils reduced the disease incidence of P. cinnamomi by 25%. B. napus had no effect on disease incidence in L. angustifolius.
Although the current study had demonstrated that biofumigants could suppress the growth, sporulation and infection of P. cinnamomi, it was unclear if this would equate to a reduction in disease incidence when applied in the field. A field trial was conducted on a protea plantation in the southwest of Western Australia that compared biofumigation with B. juncea to chemical fumigation (metham sodium) and soil solarisation. The three soil treatments were used in an integrated management approach to control P. cinnamomi that included the use of a hardwood compost, mulch and water sterilisation. All treatments were monitored during their application to ensure the treatments were conducted successfully. The three soil treatments significantly reduced the recovery of the pathogen and the infective ability of the pathogen to a soil depth of 20 cm. Metham sodium was the most suppressive soil treatment and soil solarisation was the least suppressive treatment. Only the metham sodium treatment resulted in a significant reduction in the incidence of root rot in Leucadendron salignum P.J. Bergius x laureolum (Lam.) Fourc (c.v. Safari Sunset) over the monitoring period of three years.
Another field trial was conducted on the same protea plantation to compare the effectiveness of B. juncea and B. napus, without the use of other control strategies, to reduce the incidence of P. cinnamomi infection of Leucadendron Safari Sunset. The concentration of isothiocyanates was monitored for seven days after the incorporation of the biofumigants. Although both Brassica species reduced the recovery and infective ability of the pathogen, neither biofumigant reduced the incidence of root rot in Leucadendron Safari Sunset.
In conclusion, P. cinnamomi is the most common and devastating pathogen in WA protea plantations. The current study demonstrated that P. cinnamomi is sensitive to the suppressive nature of biofumigants. Biofumigants can suppress the in vitro growth, sporulation, infective ability of P. cinnamomi and reduce the incidence of the disease caused by the pathogen in the glasshouse. Of the two Brassica species investigated, B. juncea was superior in its ability to control P. cinnamomi compared to B. napus. When applied in the field, biofumigation using B. juncea was found to be more suppressive that soil solarisation, but not as effective as metham sodium.
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Dunne, Christopher P. "Control of sudden death in cultivated proteas from the Southwest of Western Australia /." Access via Murdoch University Digital Theses Project, 2004. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20041207.140807.
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Lucas, Anne. "Water stress and disease development in Eucalyptus marginata (jarrah) infected with Phytophthora cinnamomi." Murdoch University, 2003. http://wwwlib.murdoch.edu.au/adt/browse/view/adt-MU20040820.13290.
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Bekker, Theo Frederik. "Efficacy of water soluble silicon for control of phytophthora cinnamomi root rot of avocado." Diss., Pretoria : [s.n.], 2007. http://upetd.up.ac.za/thesis/available/etd-09172007-084901.
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Aberton, Michael J., and lswan@deakin edu au. "The use of phosphite as a control for Phytophthora cinnamomi in southeastern Victorian vegetation communities." Deakin University. School of Biological and Chemical Sciences, 2005. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20060921.150649.
Full textAbstract:
One of the major aims of the research presented in this thesis was to assist managers of native vegetation communities in southeastern Australia in understanding the dynamics of P. cinnamomi with an important ecological species, Xanthorrhoea australis. It trialed the use of phosphite in large-scale field applications to establish the usefulness of this management option for the first time on Victorian flora.
This thesis describes the process of disease development within mature X. Australia plants. For the first time it was shown that within X. australis plants, secondary disease symptoms are related to the percentage of stem that has been infested by the disease. It was evident that after initial invasion the pathogen moves via root xylem and throughout the plant within vascular to the stem, especially within the desmium. The research shows that the pathogen could not be isolated consistently even though it was considered to be responsible for disease symptoms.
Trials of a control fungicide (Foli-R-fos 200) shows that protection occurs in many susceptible plants when 2 and 6g a.i./L phosphite is applied. Phytotoxicity occurred in native plants at Anglesea and within controlled environment trials when using ≥ 6g a.i./L. It will be shown that 2g a.i./L phosphite controls disease in sprayed plots within heathlands at Anglesea and a recently burnt coastal woodland community at Wilsons Promontory. The proportion of healthy X. australis plants treated with phosphite was significantly higher than the proportion in control plots without phosphite. The research shows that phosphite was recovered from leaves of three species treated with Foli-R-fos 200 in the field. For the first time it has been shown that seed germination was reduced in two species when high concentrations of phosphite were applied. The first documentation of the effect that phosphite has on soil properties showed that nitrogen and oxidised organic carbon were the only parameters to alter significantly.
This thesis provides answers to some important questions, answers that can now be used by managers in formulating better policies and actions at an operational level. There has been a dire need in Victoria to address many issues regarding P. cinnamomi and this thesis provides relevant and informative approaches to disease control, and a better understanding of the disease progress.
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Clayton, Robert Charles. "Integrated control of potato late-blight (Phytophthora infestans)." Thesis, Bangor University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357249.
Full textBooks on the topic "Phytophthora cinnamomi diseases control"
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Shearer, B. L. Jarrah dieback: The dynamics and management of Phytophthora cinnamomi in the jarrah (Eucalyptus marginata) forest of south-western Australia. Como, W.A: Dept. of Conservation and Land Management, 1989.
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Tainter, Frank H. Annotated bibliography of littleleaf and tree decline diseases caused by Phytophthora cinnamomi rands. Clemson, S.C: Clemson University, College of Forest and Recreation Resources, 1987.
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Inglis, Debbie. Late blight of potato and tomato and its control in the home garden. Pullman, Wash: Cooperative Extension, Washington State University, 1996.
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Morgan, Lucy. Gift from the hills: Miss Lucy Morgan's story of her unique Penland School. 2nd ed. Penland, N.C: Penland School of Crafts, 2005.
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Hardy, Giles E. St. J., ed. The potential of the fungicide phosphite to control Phytophthora cinnamomi in native plant communities associated with mining. East Perth, WA: MERIWA, 2000.
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Fernando, W. Gerard Dilantha. Biology, epidemiology, and biological and chemical control of Phytophthora vignae. 1990.
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Tidball, Carolyn Jean. The biology and control of Phytophthora root and stem rot of apple rootstocks from stool beds. 1987.
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H, Bohl William, University of Idaho. Cooperative Extension System., Oregon State University. Extension Service., Washington State University Extension, and United States. Dept. of Agriculture., eds. Managing late blight on irrigated potatoes in the Pacific Northwest. [Moscow, Idaho]: University of Idaho Cooperative Extension System, 2003.
Find full textBook chapters on the topic "Phytophthora cinnamomi diseases control"
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Surujdeo-Maharaj, S., T. N. Sreenivasan, L. A. Motilal, and P. Umaharan. "Black Pod and Other Phytophthora Induced Diseases of Cacao: History, Biology, and Control." In Cacao Diseases, 213–66. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-24789-2_7.
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Stouvenakers, Gilles, Peter Dapprich, Sebastien Massart, and M. Haïssam Jijakli. "Plant Pathogens and Control Strategies in Aquaponics." In Aquaponics Food Production Systems, 353–78. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-15943-6_14.
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AbstractAmong the diversity of plant diseases occurring in aquaponics, soil-borne pathogens, such as Fusarium spp., Phytophthora spp. and Pythium spp., are the most problematic due to their preference for humid/aquatic environment conditions. Phytophthora spp. and Pythium spp. which belong to the Oomycetes pseudo-fungi require special attention because of their mobile form of dispersion, the so-called zoospores that can move freely and actively in liquid water. In coupled aquaponics, curative methods are still limited because of the possible toxicity of pesticides and chemical agents for fish and beneficial bacteria (e.g. nitrifying bacteria of the biofilter). Furthermore, the development of biocontrol agents for aquaponic use is still at its beginning. Consequently, ways to control the initial infection and the progression of a disease are mainly based on preventive actions and water physical treatments. However, suppressive action (suppression) could happen in aquaponic environment considering recent papers and the suppressive activity already highlighted in hydroponics. In addition, aquaponic water contains organic matter that could promote establishment and growth of heterotrophic bacteria in the system or even improve plant growth and viability directly. With regards to organic hydroponics (i.e. use of organic fertilisation and organic plant media), these bacteria could act as antagonist agents or as plant defence elicitors to protect plants from diseases. In the future, research on the disease suppressive ability of the aquaponic biotope must be increased, as well as isolation, characterisation and formulation of microbial plant pathogen antagonists. Finally, a good knowledge in the rapid identification of pathogens, combined with control methods and diseases monitoring, as recommended in integrated plant pest management, is the key to an efficient control of plant diseases in aquaponics.
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Ávila Murillo, Mónica Constanza, Erika Andrea Plazas Gonzales, Wilman Antonio Delgado Ávila, and Luis Enrique Cuca Suarez. "Lauráceas como fuente de control de enfermedades de frutas tropicales. Modelo Phytophthora cinnamomi, “tristeza del aguacatero”." In Gulupa (Passiflora edulis), curuba (Passiflora tripartita), aguacate (Persea americana) y tomate de árbol (Solanum betaceum) Innovaciones, 229–49. Centro editorial Facultad de Ciencias, 2019. http://dx.doi.org/10.36385/fcbog-1-13.
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Soytong, Kasem, Somdej Kahonokmedhakul, Jiaojiao Song, and Rujira Tongon. "Chaetomium Application in Agriculture." In Technology in Agriculture [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.99402.
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Chaetomium species for plant disease control are reported to be antagonize many plant pathogens. It is a new broad spectrum biological fungicide from Chaetomium species which firstly discovered and patented No. 6266, International Code: AO 1 N 25/12, and registered as Ketomium® mycofungicide for plant disease control in Thailand, Laos, Vietnam, Cambodia and China. Chaetoimum biofungicide and biostimulants are applied to implement integrated plant disease control. It showed protective and curative effects in controlling plant disease and promoting plant growth. It has been successfully applied to the infested soils with integrated cultural control for the long-term protection against rice blast (Magnaporte oryzae), durian and black Pepper rot (Piper nigram L.) (Phytophthora palmivora), citrus rot (Phytophthora parasitica) and strawberry rot (Fragaria spp.) caused by Phytophthora cactorum, wilt of tomato (Fusarium oxysporum f. sp. lycopersici), basal rot of corn (Sclerotium rolfsii) and anthracnose (Colletotrichum spp.) etc. Further research is reported on the other bioactive compounds from active strains of Chaetomium spp. We have discovered various new compounds from Ch. globosum, Ch. cupreum, Ch. elatum, Ch. cochliodes, Ch. brasiliense, Ch. lucknowense, Ch. longirostre and Ch. siamense. These new compounds are not only inhibiting human pathogens (anti-malaria, anti-tuberculosis, anti-cancer cell lines and anti-C. albicans etc) but also plant pathogens as well. These active natural products from different strains of Chaetomium spp. are further developed to be biodegradable nanoparticles from active metabolites as a new discovery of scientific investigation which used to induce plant immunity, namely microbial degradable nano-elicitors for inducing immunity through phytoalexin production in plants e.g. inducing tomato to produce alpha-tomaline against Fusarium wilt of tomato, capsidiol against chili anthracnose, sakuranitin and oryzalexin B against rice blast, scopletin and anthrocyaidin against Phytophthora or Pythium rot Durian and scoparone against Phytophthora or Pythium rot of citrus. Chaetomium biofungicide can be applied instead of toxic chemical fungicides to control plant diseases.
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Walters, Dale. "Small but Deadly." In Chocolate Crisis, 50–71. University Press of Florida, 2021. http://dx.doi.org/10.5744/florida/9781683401674.003.0005.
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This chapter looks at the first of several major diseases of cacao, black pod, which is responsible for huge losses in cacao production every year. It deals with the pathogens responsible, Phytophthora palmivora and Phytophthora megakarya, looking at their biology, and how understanding their biology and ecology can help in devising methods to control the disease and minimize its impact. The chapter takes us through the history of black pod research and the people involved in trying to understand this devastating disease. The need for vigilance is highlighted, since P. megakarya, which causes large losses in cacao production in West Africa, has not yet spread to other cacao-growing regions of the world.