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A Vannini - One of the best experts on this subject based on the ideXlab platform.
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in a...
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in agroforestry systems.
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occurrence of Phytophthora cinnamomi in cork oak forests in italy
Forest Pathology, 2013Co-Authors: Bruno Scanu, A M Vettraino, A Vannini, Benedetto Teodoro Linaldeddu, A Franceschini, N AnselmiAbstract:Summary An increasing decline and mortality of cork oak trees have been recently observed in central Italy and Sardinia Island. Following surveys conducted in three declining cork oak forests, a Phytophthora species was consistently isolated from soil samples collected from trees displaying different level of decline. Based on morphological features, growth rates at different temperatures and analysis of DNA sequences of the ITS region, all isolates were identified as Phytophthora cinnamomi Rands. This pathogen caused large brownish lesions on inoculated freshly cut branches of cork oak. It was re-isolated from all infected tissues. These findings represent the first report of P. cinnamomi on cork oak trees in Italy.
Carmen Moralesrodriguez - One of the best experts on this subject based on the ideXlab platform.
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in a...
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in agroforestry systems.
A M Vettraino - One of the best experts on this subject based on the ideXlab platform.
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in a...
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efficacy of biofumigation with brassica carinata commercial pellets biofence to control vegetative and reproductive structures of Phytophthora cinnamomi
Plant Disease, 2016Co-Authors: Carmen Moralesrodriguez, A M Vettraino, A VanniniAbstract:The efficacy of biofumigation with Brassica carinata pellets (BioFence) to control vegetative and reproductive structures of Phytophthora cinnamomi was investigated in vitro at different doses and temperatures. Biofumigation was effective in inhibiting mycelial growth (culture diameter) and chlamydospore and zoospore germination, and was lethal at 24 mg of pellet per plate (approximately 0.4 mg/liter). The 50% effective concentration values showed that efficacy of B. carinata pellets in inhibiting or killing the vegetative and reproductive structures of P. cinnamomi was maximum at 15°C and decreased as temperature rose to 25°C. However, the fungicide effect was independent of the temperature. In vivo biofumigation of Quercus cerris seedlings with BioFence confirmed efficacy by reducing the inoculum density (CFU/g) of P. cinnamomi, thus protecting the host from root infection. The use of BioFence provides an alternative to synthetic pesticides to control P. cinnamomi within disease management programs in agroforestry systems.
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occurrence of Phytophthora cinnamomi in cork oak forests in italy
Forest Pathology, 2013Co-Authors: Bruno Scanu, A M Vettraino, A Vannini, Benedetto Teodoro Linaldeddu, A Franceschini, N AnselmiAbstract:Summary An increasing decline and mortality of cork oak trees have been recently observed in central Italy and Sardinia Island. Following surveys conducted in three declining cork oak forests, a Phytophthora species was consistently isolated from soil samples collected from trees displaying different level of decline. Based on morphological features, growth rates at different temperatures and analysis of DNA sequences of the ITS region, all isolates were identified as Phytophthora cinnamomi Rands. This pathogen caused large brownish lesions on inoculated freshly cut branches of cork oak. It was re-isolated from all infected tissues. These findings represent the first report of P. cinnamomi on cork oak trees in Italy.
Mark P Dobrowolski - One of the best experts on this subject based on the ideXlab platform.
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selection for decreased sensitivity to phosphite in Phytophthora cinnamomi with prolonged use of fungicide
Plant Pathology, 2008Co-Authors: Mark P Dobrowolski, B.l. Shearer, I J Colquhoun, P A Obrien, G E St J HardyAbstract:To test the hypothesis that resistance in Phytophthora cinnamomi to control by the fungicide phosphite (phosphonate) would arise in sites with prolonged use of phosphite, 30 P. cinnamomi isolates were collected from a range of sites with different phosphite-use histories, including phosphite-treated and untreated avocado orchards, and phosphite-treated and untreated native vegetation sites. The colonizing ability of these isolates was tested by different inoculation methods against a range of host tissues, treated and untreated with phosphite, including mycelial stem inoculation on clonally propagated Leucadendron sp., mycelial root inoculation of lupin seedlings and zoospore inoculation of Eucalyptus sieberi cotyledons. Isolates from avocado orchards with a long history of phosphite use were, on average, more extensive colonizers of the phosphite-treated Leucadendron sp., lupin seedling roots and Eucalyptus sieberi cotyledons. These isolates did not colonize untreated plant tissue (Leucadendron sp.) more extensively than isolates from sites with no history of phosphite use and no isolates were resistant to control by phosphite. Analysis of all isolates with microsatellite markers revealed the majority were from a single clonal lineage. Selection for decreased sensitivity to phosphite in planta has taken place within asexual clonal lineages of P. cinnamomi in sites with prolonged use of phosphite.
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three clonal lineages of Phytophthora cinnamomi in australia revealed by microsatellites
Phytopathology, 2003Co-Authors: Mark P Dobrowolski, B.l. Shearer, I C Tommerup, P A ObrienAbstract:ABSTRACT The genetic structure of populations of Phytophthora cinnamomi, a pathogen of an enormous variety of woody plants, was investigated using microsatellites. Three intensively sampled disease sites in southwest Australia were analyzed along with a large culture collection of Austra-lian isolates and some isolates from elsewhere in the world. The mutation in the four microsatellite loci analyzed revealed spatial patterns at the disease sites that correlated with the age of the infestation. Only three clonal lineages were identified in Australian populations and these same clonal lineages were present in worldwide populations, where it is suggested that a limited number of clonal lineages have spread in most regions. No evidence for sexual reproduction between these clonal lineages in Australia has been found even though the pathogen has the opportunity. Instead, mitotic recombination is frequent within the clonal lineages. The implications of this are discussed.
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Non-Mendelian inheritance revealed in a genetic analysis of sexual progeny of Phytophthora cinnamomi with microsatellite markers.
Fungal Genetics and Biology, 2002Co-Authors: Mark P Dobrowolski, Harley D. Blakeman, Inez C. Tommerup, Philip A. O’brienAbstract:We report the development of four microsatellite loci into genetic markers for the diploid oomycete plant pathogen Phytophthora cinnamomi and that (AC)n and (AG)n microsatellites are significantly less frequent than in plant and mammal genomes. A minisatellite motif 14 bp long was also discovered. The four microsatellite loci were used to analyze sexual progeny from four separate crosses of P. cinnamomi. A large proportion of non-Mendelian inheritance was observed across all loci in all four crosses, including inheritance of more than two alleles at a locus and noninheritance of alleles from either parent at a locus. The aberrant inheritance is best explained by nondisjunction at meiosis in both the A1 parent and the A2 trisomic parents, resulting in aneuploid progeny. Two loci on the putative trisomic chromosome showed linkage and no loci were linked to mating type. One aneuploid offspring was shown to have lost alleles at two loci following subculture over 4 years, indicating that aneuploid progeny may not be mitotically stable.
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phenotypic variation in a clonal lineage of two Phytophthora cinnamomi populations from western australia
Fungal Biology, 2001Co-Authors: D Huberli, Mark P Dobrowolski, I C Tommerup, M C Calver, G HardyAbstract:Seventy-three isolates of Phytophthora cinnamomi were collected from diseased Eucalyptus marginata (jarrah) and Corymbia calophylla (marri) trees in two forest communities in the southwest of Western Australia. Both populations of P. cinnamomi were examined for phenotypic and genotypic variation. Microsatellite DNA analysis showed that all isolates were of the same clonal lineage. We show, for the first time for P. cinnamomi, that morphological and pathogenic variation between populations of the clonal lineage are very broad and continuous. The phenotypes examined included growth rates and colony morphology on potato dextrose agar at different temperatures, sporangial and gametangial morphology, ability to form lesions in detached jarrah and marri stems, and ability to cause deaths of clonal jarrah plants in a glasshouse trial. Phenotype variation was derived asexually. All phenotypes investigated varied independently from one another. Cluster analysis of 24 morphological and pathogenicity phenotypes identified two main clusters of isolates corresponding to each population. The ability to cause deaths in both populations ranged from killing all plants within 59 d to plants being symptomless 182 d after inoculation.
G Hardy - One of the best experts on this subject based on the ideXlab platform.
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phenotypic variation in a clonal lineage of two Phytophthora cinnamomi populations from western australia
Fungal Biology, 2001Co-Authors: D Huberli, Mark P Dobrowolski, I C Tommerup, M C Calver, G HardyAbstract:Seventy-three isolates of Phytophthora cinnamomi were collected from diseased Eucalyptus marginata (jarrah) and Corymbia calophylla (marri) trees in two forest communities in the southwest of Western Australia. Both populations of P. cinnamomi were examined for phenotypic and genotypic variation. Microsatellite DNA analysis showed that all isolates were of the same clonal lineage. We show, for the first time for P. cinnamomi, that morphological and pathogenic variation between populations of the clonal lineage are very broad and continuous. The phenotypes examined included growth rates and colony morphology on potato dextrose agar at different temperatures, sporangial and gametangial morphology, ability to form lesions in detached jarrah and marri stems, and ability to cause deaths of clonal jarrah plants in a glasshouse trial. Phenotype variation was derived asexually. All phenotypes investigated varied independently from one another. Cluster analysis of 24 morphological and pathogenicity phenotypes identified two main clusters of isolates corresponding to each population. The ability to cause deaths in both populations ranged from killing all plants within 59 d to plants being symptomless 182 d after inoculation.
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influence of low oxygen levels in aeroponics chambers on eucalypt roots infected with Phytophthora cinnamomi
Plant Disease, 1998Co-Authors: Treena I. Burgess, G Hardy, J A Mccomb, I J ColquhounAbstract:Aeroponics root chambers were designed to evaluate the influence of low oxygen on disease development in clones of Eucalyptus marginata susceptible or resistant to infection by Phytophthora cinnamomi. Actively growing 7-month-old clones of E. marginata were transferred into the aeroponics chambers, into which a nutrient solution was delivered in a fine spray, providing optimal conditions for root growth. Prior to inoculation by zoospores of P. cinnamomi under normal oxygen, the roots were exposed to four treatments: (i) normal oxygen, approximately 8 mg of O2 liter-1; (ii) 6 days of hypoxia, 2 mg of O2 liter-1; (iii) anoxic acclimatization 2 days at 2 mg of O2 liter-1, 2 days at 1 mg of O2 liter-1, 2 days at 0.5 mg of O2 liter-1, 2 days at 2 mg of O2 liter-1, and 6 h at <0.05 mg of O2 liter-1; and (iv) 6 h of anoxia, <0.05 mg of O2 liter-1. Root extension during hypoxia was greatly reduced. Lesion development was least for roots exposed to hypoxia and greatest for roots exposed to anoxia for 6 h, suggesting increased resistance of E. marginata to P. cinnamomi following hypoxia.