Grapevine red blotch-associated virus (GRBaV) is the causal agent of red blotch, a recently recognized viral disease of grapevines. We showed that GRBaV can infect rootstocks following agroinoculation, including 3309C that is asymptomatic while infected. This makes clear the potential for rootstocks to be involved in virus dissemination. Efforts to develop a serological detection assay for GRBaV have been challenging, suggesting a need to investigate the expression mechanism of the coat protein gene to facilitate developing approaches to produce antibodies that will recognize virions in infected grapevine tissue. The spatial distribution of GRBaV was mapped in selected vineyards in California and New York, and preliminary work designed to identify insect vectors has provided candidate leads among a few hemipteran insects. Survey efforts of alternative hosts revealed that free-living grapevines in riparian areas in close spatial proximity to diseased vineyards in California can be infected by GRBaV. Research progress was extended to stakeholders through presentations at grower’s conventions.
Grapevine red blotch-associated virus (GRBaV) is the latest virus to be identified in grapevines. Since discovery in 2011, its widespread presence has been confirmed in several states and in different white and red wine grape varieties. At this stage very little is known about the effect of the red blotch virus on both grape development and composition at harvest as well as the long term effect on wine composition and quality. Several varieties should be studied to determine if the effects of the virus are variety specific. Preliminary data from the currently funded AVF investigation into the impact of GRBaV on grape and wine composition and quality show significant differences in basic chemical data for red blotch positive and negative grapes sampled at harvest. Berry samples were taken from vines at harvest from multiple sites investigated (three Chardonnay sites in Sonoma County, two Cabernet Sauvignon sites and one Merlot site in Napa County). A decrease in Brix was mostly obtained at harvest for grapes from red blotch infected grapevines irrespective of cultivar or clone compared to healthy grapevines. This decrease was up to 6%in Chardonnay grapes and respectively a maximum of 20 and 16%in Cabernet Sauvignon and Merlot grapes. Differences in pH were minor with TA values mostly higher in grapes from red blotch diseased grapevines.
The first year’s data indicate that red blotch disease resulted in a decrease in total phenols and tannins in Chardonnay grapes of up to 25%. Phenolic results for the different Cabernet Sauvignon and Merlot sites were more variable. There was only a clear decrease in tannin concentration for one of the Cabernet Sauvignon sites (18%). However, the total anthocyanin concentration was 20 to 38%lower in all red blotch infected red grapes. This indicates variability in response to red blotch infection within a variety. Future analyses to determine the individual phenolic profiles and tannin compositions of red blotch infected and non-infected grapes may shed more light on these findings. Wines could only be made from one of the Chardonnay sites in addition to the two Cabernet Sauvignon sites described due to the fact that we were unable to obtain enough GRBaV negative grapevines for winemaking. All analyses will be repeated on the completed wines to coincide with descriptive sensory analysis. Final results will enable us to relate grape and wine composition as well as potentially find a correlation between differences in mouthfeel properties of the wines and changes in phenol and tannin compositions due to red blotch disease. At least one more year’s data is needed to confirm results and determine the potential impact of seasonal variability on the expression of GRBaV. It is important to determine the impact of GRBaV on grape and wine composition so that recommendations can be made to the industry regarding the future of infected vines.
Grapevine red blotch-associated virus (GRBaV) is associated with red blotch, a newlyrecognized emerging viral disease. We showed that GRBaV is the causal agent of the disease and microshoot tip culture can eliminate the virus from infected vines. Two distinct groups of GRBaV isolates exist in infected vines and currently available diagnostic tools are robust for a reliable detection of all isolates. Efforts to develop a serological detection assay for GRBaV are under way. Monitoring incidence of GRBaV in vineyards over time did not provide compelling evidence of spread. Research progress was extended to stakeholders through 15 presentations at conventions, field days and IPM conferences.
The mission of this research is to increase the economic sustainability of grape production by providing decision support tools to aid in management of grape powdery mildew. In this project we propose to test the utility of a quantitative Loop mediated isothermal AMPlification assay (qLAMP) and handheld device for detection and quantification of airborne inoculum; thereby extending our esearch on the use of inoculum detection as a decision support tool for managing grape powdery mildew. The specific objectives are:
- Test implementation of a grower preformed quantitative LAMP assay.
- Examine the effectiveness of adjusting fungicide interval based inoculum density.
- Assessment of quantitative LAMP (qLAMP) for estimating amount of fruit infection
Results: Due to reduced funding, Objective 1 had to be reduced and Objective 3 eliminated in the second year of this 3 year project. The extensive cooperation of several participating growers who shuttled samples from the upper Willamette Valley to Corvallis, allowed for us to complete Objective 2 using lab processed samples only.
Red varieties of grapevines with leafroll-like symptoms that are not infected with leafroll-associated viruses have been found infected with grapevine red blotch-associated virus (GRBaV), a new virus first identified in 2011 and subsequently shown to be the causal agent of red blotch disease. Diseased vines have been identified in several counties in California and in other states. Effect of GRBaV infection on differences in berry composition over the ripening period have not been documented and foliar symptom development in red and white varieties has also not been characterized. A study was conducted in 2013 to clarify symptom development in foliage, fruit maturity and vine growth in Chardonnay, Cabernet Sauvignon, and Merlot. At each of the three sites, vines selected for the study were determined to be GRBaV positive or negative by qPCR assay as well as negative for all leafroll-associated viruses, vitiviruses and nepoviruses. To determine the effect of crop load on disease expression, crop was reduced at two sites by approximately 35%at the onset of veraison.
Foliar symptom expression in vine canopies increased with time and is greatest in older leaf tissue. The severity of foliar symptoms varied greatly across the three varieties; however, on all evaluation dates, vines positive for GRBaV had significantly greater percentage of symptomatic leaves in the basal and middle regions of canopies. In addition, symptomatic leaves in these regions had larger area (greater symptom severity) with red or chlorotic coloration in red and white varieties, respectively, than younger terminal leaves. At harvest, the severity of interveinal chlorotic blotch symptoms in Chardonnay was greater than the red blotch symptoms in Cabernet Sauvignon or Merlot. In Cabernet Sauvignon and Merlot, initial leaf symptoms in GRBaV positive vines were predominately leaves on which only red veins were present. In Merlot, the development of leaves with red interveinal tissue followed. In Cabernet Sauvignon, blades with only red veins remained the primary leaf symptom. In addition, reducing the crop at veraison in Cabernet Sauvignon may have resulted in an increase in virus symptom expression late in the growing season.
This project has allowed us to associate the presence of GRBaV infection with a consistent delay in fruit maturity. For all three cultivars, fruit maturity was delayed in vines PCR positive for GRBaV. Brix was significantly lower on all sample dates and titratable acidity significantly greater on half the sample dates yet always elevated on other dates. At harvest, juice samples in all varieties had significantly higher malic acid in GRBaV positive vines as compared to GRBaV negative vines. Reducing crop load in GRBaV positive vines in Chardonnay and Cabernet Sauvignon did not significantly improve juice chemistry at harvest when compared to infected vines with full crop loads. Juice from fruit on Cabernet Sauvignon positive vines in which crop was reduced indicated a very slight improvement in ripening parameters although differences were not statistically significant. Red blotch disease did not affect vine yield. Berry weights in vines infected with GRBaV are at least as great as virus negative vines.
The objective of this study was to quantify the amount of N remobilized and/or taken up from the soil or N fertilizer and put into the N reserve pool (within the trunk and root system) of field-grown grapevines. This study also determined the effectiveness of a post-harvest N fertilization application on the dynamics of the reserve N pool. Nitrogen within whole vines was quantified using destructive harvests. Several treatments were imposed to assess their effect on the replenishment of N reserves independent of remobilization. They included: 1.) The application of N during the growing season, 2.) The application of N post-harvest and 3.) Fifty percent of the leaves in the canopy removed after harvest to mimic the effects of mechanically harvesting a vineyard.
Petiole NO3-N at bloom for the non-fertilized treatment averaged less than 100 ppm (dry weight), a value many consider to indicate a N deficiency. The application of a nitrogen fertilizer one month after budbreak (albeit at only ½ the total amount applied) significantly increased NO3-N, NH4-N and total N of the petioles compared to the no N treatment. The NO3-N and NH4– petiole values measured at bloom were in excess of 2500 and 1800 ppm, respectively. These values would be considered excessive by some.
A N budget for vines in the fertilized (‘+N’) and non-fertilized (‘–N’) treatments was determined at fruit maturity and at the end of the season (after leaf fall). While it can be surmised from the previous paragraph that the vines in this vineyard may have been N deficient, vines from the ‘–N’ treatment still accumulated 58.9 g N/vine (78 kg N/ha; 69 lbs N/acre) in the leaves, stems, fruiting canes and clusters at fruit maturity with 82.2 g N/vine (109 kg/ha; 97 lbs N/acre) in the trunk and roots. The amount of N in the leaves, stems, fruiting canes and clusters at fruit maturity for the ‘+N’ treatment was 72.9 g N/vine (96.5 kg/ha; 86 lbs/acre) while that in the trunk and roots was 103 g N/vine (136 kg/ha; 121 lbs/acre). N fertilizer recovery efficiency (REN) can be determined by comparing the uptake of N in plants with that of a non-fertilized treatment. Vines in the ‘+N’ treatment accumulated 35.1 g N/vine more than that of the non-fertilized control at fruit maturity. Since 34 g N/vine was applied to the fertilized vines the REN would be ~100%.
The REN was also calculated for data collected at the end of the season, subsequent to leaf fall. The non-fertilized control would be another ‘–N’ treatment cohort of vines while the fertilized treatment would be the ‘PH +N’ treatment. The amount of N taken up from the soil by the ‘PH +N’ treatment was 7.1 g/vine greater than that of the ‘–N’ treatment. Since the ‘PH +N’ treatment was fertilized with 25.5 g N/vine, the REN would be ~ 28%((7.1/25.5) * 100). Therefore, under the conditions of this study, a fertilizer application one month after budbreak and at berry set was more efficient than the post-harvest application of N.