RESUMEN
In England, Cryphonectria parasitica was detected for the first time in 2011 in a nursery and in 2016 in the wider environment. Surveys between 2017 and 2020 identified the disease at different sites in Berkshire, Buckinghamshire, Cornwall, Derbyshire, Devon, Dorset, London, West Sussex, and the island of Jersey, while the present study comprises the results of the 2020-2023 survey with findings in Derbyshire, Devon, Kent, Nottinghamshire, Herefordshire, Leicestershire, London, West Sussex, and the islands of Jersey and Guernsey. A total of 226 suspected samples were collected from 72 surveyed sites, as far north as Edinburgh and as far west as Plymouth (both of which were negative), and 112 samples tested positive by real-time PCR and isolation from 35 sites. The 112 isolates were tested for the vegetative compatibility group (VCG), mating type, and Cryphonectria hypovirus 1 (CHV1). Twelve VCGs were identified, with two of them (EU-5 and EU-22) being the first records in the UK. Both mating types were present (37% MAT-1 and 63% MAT-2), but only one mating type was present per site and VCG, and perithecia were never observed. Cryphonectria hypovirus 1 (CHV1), consistently subtype-I haplotype E-5, was detected in three isolates at a low concentration (5.9, 21.1, and 33.0 ng/µL) from locations in London, Nottinghamshire, and Devon.
RESUMEN
Biological control of Cryphonectria parasitica fungus, causal agent of chestnut blight, by virus infection (hypovirulence) has been shown to be an effective control strategy against chestnut blight in Europe and some parts of North America. The most studied mycovirus is the Cryphonectria hypovirus 1 (CHV-1) type species of the Hypoviridae family. To efficiently provide biocontrol, the virus must be able to induce hypovirulence in its fungal host in chestnut trees. Here, two different CHV-1 subtype I virus strains (E-5 and L-18), gained by transmissions, were tested for their hypovirulence induction, biocontrol potential, and transmission between vegetatively compatible (VCG) and incompatible fungal isolate groups in sweet chestnut seedlings and branches. Both strains of CHV-1 showed great biocontrol potential and could protect trees by efficiently transmitting CHV-1 by hyphal anastomosis between fungal isolates of the same VCG and converting virulent to hypovirulent cankers. The hypovirulent effect was positively correlated with the virus concentration, tested by four different reverse-transcription PCRs, two end-point and two real-time methods, one of which represents a newly developed real-time PCR for the detection and quantification of CHV-1.
Asunto(s)
Ascomicetos , Virus Fúngicos , Virus ARN , Virus Fúngicos/genética , Enfermedades de las Plantas , Virus ARN/genéticaRESUMEN
Plant performance in any one generation is affected not only by the prevailing environmental conditions, but also by the conditions experienced by the parental generation of those plants. These maternal effects have been recorded in a many plant species, but the influence of external biotic (as opposed to abiotic) factors on shaping maternal effects have been rarely examined. Furthermore, almost all previous studies have taken place over one plant generation, rather than across multiple generations. Here, we studied the influence of insect herbivory and arbuscular mycorrhizal (AM) fungal colonisation on the shaping of maternal effects in the annual forb Senecio vulgaris. We grew plants with and without aphids (Myzus persicae) and AM fungi (hereafter termed 'induction events') over four successive generations, wherein seeds from plants in any one treatment were used to grow plants of the same treatment in the next generation, all in identical environmental conditions. We found strong evidence of maternal effects in the second plant generation, i.e., after one induction event. These plants took longer to germinate, flowered in a shorter time, produced lighter seeds and were shorter and of lower biomass than their parents. Aphid attack tended to enhance these effects, whereas AM fungi had little influence. However, thereafter there was a gradual recovery in these parameters, so that plants experiencing three inductions showed similar life history parameters to those in the original generation. We conclude that experiments investigating maternal effects need to be performed over multiple plant generations and that biotic factors such as insects and mycorrhizas must also be taken into account, along with abiotic factors, such as nutrient and water availability.