Influence of curettage on Esca-diseased Vitis vinifera L. cv. Sauvignon blanc plants on the quality of musts and wines
Abstract
Aim: A study on Sauvignon blanc (SB) cultivar in France showed that curettage had an effect on the resilience of GTD grapevines. No experiments, however, have been conducted on its effects on wine quality, particularly on white Sauvignon blanc cultivar wines.
Methods and results: Grapevines from Sauvignon blanc cultivar that had expressed Esca-foliar symptoms were used for the study, with some of them having been curetted in 2014. Subsequently, bunches from Control (asymptomatic), Curetted and Esca-symptomatic vines were harvested in 2017 and 2018 in order to produce white wine. Technical and chemical results on both must and wine showed that wines from curetted plants were similar to those from asymptomatic vines. There were differences, however, for Esca-diseased vines, where the alcoholic fermentation of musts was faster than for the other modalities. Olfactometry results showed that, for the one-year-old 2017 vintage wines, no differences were detected, although they were for the 2018 vintage.
Conclusion: The results of the chemical analyses and wine tasting showed that the wines from curetted and asymptomatic grapevines were similar, and that their quality was the same.
Significance of the study: The quality of wines from curetted vines compared to asymptomatic ones was confirmed and validated through chemical and sensory analyses of the must and the one-year-old wines.
Introduction
Esca of grapevine (Vitis vinifera L.) is one of the most harmful and difficult Grapevine Trunk Diseases (GTDs) to control in many vineyards worldwide, including in Europe (e.g., France, Italy, Portugal and Spain) (Scheck et al., 1998; Mugnai et al., 1999; Armengol et al., 2001; Rumbos and Rumbou, 2001; Bruez et al., 2013; Edwards and Pascoe, 2004; Gimenez-Jaime et al., 2006). Worldwide increases in GTD incidence have been recorded ever since the banning in 2001 of sodium arsenite (the only chemical solution to control GTD diseases) (Carter, 1991; Graniti et al., 2000; Surico et al., 2000; Úrbez-Torres et al., 2006; Úrbez-Torres et al., 2008; Úrbez-Torres et al., 2009; Sosnowski et al., 2007; Bertsch et al., 2012). Increased GTD proliferation affects berry quality, leading to harvest loss (Calzarano et al., 2004) and plant death (Larignon et al., 2009).
Esca, known since Greek antiquity, comes in two forms: chronic and apoplectic. The chronic form corresponds to symptoms in the trunk, and to the presence of external secondary symptoms on leaves, shoots and sometimes berries (Mugnai et al., 1999). Inside the trunk, the most common symptom is white-rot (Esca proper) that becomes spongy, with thick black or dark brown lines often separating the rot tissue from the necrotic wood. Esca-foliar symptoms can also appear, with interveinal islands of chlorotic and yellowish tissues that can become necrotic (leaf-tiger-stripe symptoms), but these do not systematically appear on the same plant every year (Larignon and Dubos, 1997). Berries can also present other symptoms, as observed in California and Southern Italy, especially in white grape cultivars (Mugnai et al., 1999). The plants can suddenly die within a few days, which correspond to the apoplexy form (Mugnai et al., 1999).
In an attempt to fight Esca, due to the ban on sodium arsenite in 2003, various international teams have been trying to (I) investigate the complex development of GTDs, in order to identify the factors responsible for decay, and (II) establish control methods compatible with sustainable vineyard management. Currently, no chemical or biocontrol products prove as effective as sodium arsenite. Consequently, various practices such as double pruning (Weber et al., 2007) and curettage are now being revived. Curettage is an old viticultural technique, reintroduced into France by Ravaz in 1909. Removing the white-rot, currently done by means of a chain saw, prevents the development of fungi involved in the GTDs, particularly F. mediterranea, by stopping the non-necrotic tissue from becoming necrotic. Necrotic tissue blocks normal sap flow and increases pathogenic fungi colonisation. Cholet et al. (2019) showed the impact of curettage on grapevine physiology and its ability to enhance plant resilience. The present study was designed to determine whether curettage also affects the quality of musts and one-year-old wines.
In a previous study, it was demonstrated that Esca had an impact on the aromatic composition of red wine (Lorrain et al., 2012), indicating that this disease affected the phenolic composition of grapes and decreased the organoleptic quality of these red wines. Calzarano et al. (2001) observed that the rate of sugar and assimilable nitrogen differed between musts from diseased or healthy vines. Another study showed that the grapevines affected by Esca produced methyl salicylate (induced by a host defence mechanism against fungi attack) and modified bunch composition (Poitou et al., 2018). Methyl salicylate is a good volatile indicator of a vineyard's infection state, being a volatile organic compound (VOC) synthesised from salicylic acid (SA), and a secondary plant metabolite associated with induced resistance plant defence (Tiedemann et al., 1988; Tang et al., 2015). Poitou (2016), also showed a strong correlation between the percentage of Esca-bunches used to make the wine and the quantity of methyl salicylate (MeSA) detected in it.
Dry, white Sauvignon blanc wines have characteristic aromas, usually described as green pepper, box tree, broom, grapefruit, passion fruit, and smoke. The major part of this broad range of nuances is released by yeast during the vinification stage from the non-volatile precursor aromas present in grape. Thus, grape maturation conditions and harvest date can impact wine quality. The main contributors to this grape variety's aromatic nuances are considered to be volatile thiols, such as 4-methyl-4-sulfanylpentan-2-one, 3-sulfanylhexyl acetate (4MSP, 3SHA, reminiscent of box tree and broom), or 3-sulfanylhexan-1-ol (3SH, with a grapefruit flavour) identified by Darriet et al. (1995) and Tominaga et al. (1998) respectively. 3SH and 4MSP are initially found as odourless precursors in grape and juice, subsequently becoming volatile thiols during the enzymatic reactions generated during alcoholic fermentation (Dixon et al., 2010; Kobayashi et al., 2011). In the case of Sauvignon blanc wines, the specific precursors are identified as S-conjugate forms (Tominaga et al., 1998; Peyrot des Gachons et al., 2002; Fedrizzi et al., 2009; Murat et al., 2001a).
White wines, especially Sauvignon blanc, can be affected by the oxidative evolution of their aromas and a loss of sensory quality. Generally, the floral and fruity aromas disappear in favour of new aromas reminiscent of cooked vegetables and honey. In the present study, we focused on methional, phenylacetaldehyde and o-aminoacetophenone components. These aldehyde components developed “honey-like” and “boiled-potato” off-flavours (Silva Ferreira et al., 2002; Bueno et al., 2010).
Grape maturity level can significantly affect the contents of specific varietal aromatic compounds. It has been shown, for example, that the alkyl-methoxypyrazine content of grapes, particularly 2-methoxy-3-isobutylpyrazine (MIBP), was directly linked to ripening conditions (Guillaumie and Ilg, 2013). The MIBP produces a vegetal, bell pepper flavour and aroma. It is a volatile component contributing to flavour at a very low concentration (1 to 30 ng/L) (Ebeler and Thorngate, 2009). The concentration of this wine component depends on its concentration in berries (Roujou de Boubée et al., 2000; Ryona et al., 2008). Other volatile components are impacted by the level of berry maturation. The family of lactones proves a good marker of maturity level (Allamy et al., 2017). The lactone smell is described, for example, as “coconut-like” (gamma-octalactone) and “peach-like and milky” (gamma-decalactone) (Câmara et al., 2006). Although it has little impact on white wines (Cooke and Capone, 2009; Pérez-Olivero and Pérez-Pont, 2014), the content of these compounds in Esca-diseased wines has never been studied.
As the aim of this work is to show the chemical quality of must and one-year-old-wine of curetted plants, it was important to determine whether the curettage had an impact on (I) the production of methyl salicylate as a host defence mechanism, and (II) the volatile components characterising Sauvignon blanc wine.
Materials and methods
1. Experimental vineyard
The sampling site was a commercial vineyard located at Beguey (near Bordeaux, in Gironde, France). To study the effects of curettage on Esca-diseased grapevines, a vine plot of Sauvignon blanc was selected in this vineyard, which was planted in 1994. This cultivar was selected for its high susceptibility to GTDS. Vines were omega-grafted onto the 101-14 rootstock (row distance x vine distances = 1.8 x 1 m). This conventional vineyard was trained in simple ‘Espalier’ trellis and a double Guyot pruning regime, with two cordons per plant.
2. Design and Esca symptom assessment
Vine stocks expressing Esca-foliar symptoms were mapped from 2014 to June 2018. Leaf GTD symptoms were assessed according to a gradual scale previously used in a similar study (Lecomte et al., 2018). Symptoms (chronic form) were categorised according to their severity into two groups: (I) E1/E2 corresponding to light leaf symptoms, mostly discolorations, on one or two cordons; and (II) E3/E4 corresponding to severe symptoms, with many drying zones and some wilts on one or both arms. Apoplectic vines were not used in this study.
The plot was divided into two equal parts. The first plot represented the asymptomatic vines that had not expressed Esca-foliar symptoms. The second plot represented the symptomatic plants that had expressed Esca-foliar symptoms, whether curetted or not in 2014. (Cholet et al., 2019)
Thus, four experimental categories of vine were studied from 2014 to 2018:
1) Apparently healthy and asymptomatic vine stocks from 2014 to 2018 (hereafter referred to as “Control”)
2) Vines curetted in 2014 showing low foliar symptoms before curettage (hereafter referred to as “Curetted E1/E2”)
3) Vines curetted in 2014 showing strong Esca-foliar symptoms before curettage (hereafter referred to as “Curetted E3/E4”)
4) Esca-foliar symptomatic vines from 2014 to 2018 (hereafter referred to as “Esca”)
3. Small-scale winemaking
The day of harvest, bunches of grapes (Vitis vinifera L. cv. Sauvignon blanc) were collected from the vineyard in the morning. 8 kg of harvested grapes per vine category (asymptomatic vines, E1/E2 Curetted, E3/E4 Curetted and symptomatic vines) were rapidly returned to the laboratory and stocked overnight at 4° C. Each replicate was prepared in the same way. Before being pressurised, each category’s batch of bunches was separated into two replicates. Microvinifications were conducted in duplicate. 50 mg/L of sulphur dioxide (SO2) was added, and the juice clarified overnight at 4 °C with pectolytic enzymes (10 mg/L, LAFAZYM® CL Laffort oenologie). Must turbidity was adjusted to 180 - 200 NTU, and Yeast Available Nitrogen (YAN) was amended to 220 mg/L with Thiazote (0.1 mg/µL). The must was then inoculated with X5 yeast strain (ZYMAFLORE® X5–Laffort, final concentration of 20 mg/mL). Fermentation was carried out on 3.5 L glass fermenters at 20 °C, under nitrogen flux protection, with temperature and density being monitored daily in each tank. At the end of the fermentation, 50 mg/L of SO2 was added and the wines stored at 4 °C before clarification.
Before addition of aqueous bisulphite solution, a 50 mL sample of must was frozen for the chemical must analyses.
4. Chemical analyses
For musts, classical oenological analyses were carried out: total acidity, assimilable nitrogen, acid malic concentration and reducing sugar indexes were determined following the OIV method. The pH was measured by infra-red, using Foss WineScanTM Foss, Nanterre, France).
For wine: reducing sugar indexes, total acidity, malic acid alcohol (% vol.) and pH were measured by infra-red, using Foss WineScanTM (Foss, Nanterre, France).
5. Volatile compounds analyses
5.1. Quantification in wines of volatile thiols, lactones and oxidative compounds
Volatile thiols (3SH, 3SHA, and 4MSP), lactones (massoia lactone, γ-octanolactone, γ-nonalactone, γ-decalactone, and δ-decalactone), and oxidative compounds (methional, phenylacetaldehyde, and o-aminoacetophenone were quantified in wines by gas chromatography-tandem mass spectrometry (GC-MS/MS) adapted from (Thibon et al., 2015). In brief, a 20 mL wine sample was spiked with an internal standard mix (50 µl) containing 6-sulfanylhexanol (6SH, 500 µg/L, EtOH), 4-methoxy-2-methyl-2-sulfanylbutan (MMSB, 500 µg/L), ethyl maltol (EM, 1 mg/L, EtOH), and 3-octanol (1 mg/L, EtOH). The sample was percolated through a conditioned SPE column (HR-X, 500 mg 6 mL, Macherey Nagel, France). After the adsorption step, the SPE columns were rinsed twice with 2 mL of hydro-alcoholic solution (10 %) and the aromas were eluted with 3 mL of pentane/dichloromethane (50/50; v/v), followed by 3 mL of dichloromethane/methanol (95/5; v/v). The organic phases obtained were blended, dried over anhydrous sodium sulfate, and concentrated to 150 µL under a nitrogen stream.
5.2. Quantification of IBMP, IPMP, SBMP, 1,4-cineole, 1,8-cineol and methyl salicylate
The method for detecting pyrazine, 1,4-cineole and 1,8-cineole and methyl salicylate (MeSA) was detected according to Poitou (2016). Sample preparation involved 2.5 mL of grape juice or wine diluted in 7.5 mL of deionized water in a brown 20 mL SPME vial, along with 4 g of sodium chloride (NaCl) and internal standard mix (2H3-IBMP and 3-octanol at 10 µg/L and 100 mg/L in ethanol respectively). The analyses were performed on a Carbowax 20 M capillary column (BP20, 50 m, 0.25 mm internal diameter, 0.2 μm film thickness, Scientific Glass Engineering). Helium 6.0 (Messer France) was used as a carrier gas at a flow rate of 0.9 mL/min. The temperature settings were as follows: 45 °C held for 5 min, then a 3 °C/min increase to 140 °C, followed by 30 °C min increase to 240 °C at which it was held for 10 min. The injector port was set at 240 °C. Data processing was carried out using MSD Chemstation software (5973n Data Analysis, Agilent Technologies©).
Selected ions for internal standards were m/z 83, 59 (3-octanol), quantitated ions were m/z 83. Methyl salicylate was detected using m/z 152, 120, 92, and quantitated using m/z 152. Ethyl salicylate was detected using m/z 166, 120, 92, and quantitated using m/z 120.
6. Sensory analyses
The sensory analyses of wines from the 2017 and 2018 vintages were carried out three months after the wines were bottled. The wines were evaluated by twenty judges, from the Oenology research unit, ISVV, Bordeaux University. They were all selected on the basis of their interest and availability, as well as their experience in white wine sensory analysis. Each of them came with a trainee. The candidates were screened for their sensitivity to descriptors conventionally used to describe Sauvignon blanc wines (good or bad example of Sauvignon wine, oxidation reminiscence or green aroma) in triangular tests in order to select those with good abilities to discriminate between samples. For this, we used spiked wines with increasing concentrations of a 3SH-4MSP mix, methional or IBMP. Next, two training sessions were set up, using linear-structured scales of 10 cm to indicate the intensity of the descriptive terms, in which “0” meant “low intensity” and “10” meant “high intensity”.
All analyses were performed in a specific room at 20 °C with isolated booths. Six different triangle tests were first done using FIZZ software (Biosysteme©, France) in order to determine any significant overall difference between the control wine sample and wines from symptomatic and curetted plants. 20 mL samples were randomly presented in dark ISO-approved wine glasses labelled with three-digit random codes to panelists. Four different 20 mL-wine samples were presented per session, in the same conditions as for the triangular tests. Panellists were asked to describe the aromatic profile of each wine. After smelling and tasting, the panellists marked the intensity of each attribute on a scale of 0 to 5. The attributes were chosen from a list traditionally used for white wine sensory description. The panellists rinsed their mouths with water and paused for 30 s between samples. After checking that the factor panellists was not significant (homogeneity of the panel), one-way analysis of variance (ANOVA) was performed to test for the effects on each sensory attribute.
7. Statistical analyses
All measurements were performed in duplicate. Results are expressed as mean standard deviation. All the statistical analyses were carried out using the R statistical software, version 3.1.1. To compare different samples, an analysis of variance (Levene test) and a Kruskal-Wallis or ANOVA tests were performed using the Rcommander package.
Results and discussion
1. Must quality
The results of the must and wine analyses showed that there were no significant differences between the Curetted and Control experimental categories of vine (Table 1). In 2017 and 2018, the quantity of assimilable nitrogen was lower in musts from Control (47 g/L in 2017; 151 g/L in 2018) than in Curetted, with the highest quantity in the musts from Esca (89 g/L in 2017; 169 g/L in 2018). Titratable acidity in 2017 was very similar for all vine categories, except for Curetted E1/E2. In 2018, acidity was higher in wines from Esca wines, and lower in those from Curetted and Control. These results correlated with the malic acid analysis, with wines from Esca having the highest quantities. The quantity of sugar differed for the four types of wine for both years, and was highest for wines from Control (217.2 g/L in 2017; 211.5 g/L in 2018). All pH values ranged from 2.95 to 3.06.
Table 1. Values for assimilable nitrogen, sugars, total acidity, malic acid and pH of musts from 2017 and 2018 harvests.
|
2017 |
2018 |
||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
Assimilable nitrogen |
Sugars |
Total acidity |
Malic Acid |
pH |
Assimilable nitrogen |
Sugars |
Total acidity |
Malic Acid |
pH |
Control |
47 |
217 |
5.4 |
5.1 |
3 |
151 |
212 |
5 |
4.8 |
3.1 |
Curetted E1/E2 |
72 |
215 |
4.6 |
4.5 |
3.1 |
176 |
199 |
5.7 |
5.5 |
2.96 |
Curetted E3/E4 |
87 |
209 |
5.4 |
5 |
2.96 |
173 |
201 |
6.1 |
5.4 |
3 |
Esca |
89 |
208 |
5.4 |
5.1 |
2.95 |
169 |
187 |
6.6 |
6 |
2.98 |
Data are means to duplicate determination. In units of volume (mg/L) for assimilable nitrogen, (g/L) for sugars, (g/L) for total acidity equivalent sulfuric acid, (g/L) for malic acid and pH.
No differences were observed between the musts from Curetted and Control vine categories for the 2017 and 2018 vintages. Even though Cholet et al. (2019) showed that the vigour and bunch quantity differed for the control and curetted vines, must quality remained the same. In our study, the resulting recovery in wine quality confirmed that curettage allowed Esca grapevine to re-establish wine quality.
The results of the 2018 vintage, in comparison to 2017 vintage, showed a lower quantity of sugars and the highest total acidity, particularly as regards acid rates, which indicated that Esca-grapevines bunches were harvested too early (before maturity).
The results of Lorrain et al. (2012) for red musts, and of Calzarano et al. (2004) for white musts, showed differences between berry quality of symptomatic and asymptomatic vines.
The curetted grapes recuperated the same quality as the grapes from Control category.
2. Alcoholic fermentation kinetics
The alcoholic fermentation kinetics (Figure 1) showed that, whatever the year of study, values for the fermentation of Esca-grape wine were lower than for that of Control. In 2018, alcoholic fermentation time was the same, but in 2017 alcoholic fermentation was faster for the Esca-grape wines than for Control. The quantity of sugars in must was highest in wines from Control, which could explain why alcoholic fermentation was longer. In 2018, however, sugar levels were still high in the control wines, but the kinetics remained the same for all vine categories.
Figure 1. Alcoholic fermentation kinetic of Sauvignon blanc wines from Control (blue), Curetted E1/E2 (green), Curetted E3/E4 (purple) and Esca (red) vines from the 2017 and 2018 vintages.
3. Plant resilience and defence
The results for the curetted and control grapevines showed that, four years after curettage, 58 % were asymptomatic, 33 % showed typical Esca-foliar symptoms, and 9 % were dead. For the uncuretted Esca-foliar vines, only 15 % were asymptomatic, 46 % expressed Esca-foliar symptoms, and 39 % were dead (Cholet et al., 2019).
In addition, the quantification of methyl salicylate (MeSA) showed that the Esca-foliar symptomatic vines produced more methyl salicylate than the asymptomatic and curetted vines (Figure 2). The lowest quantity could not be identified in the wine tasting, even if the quantity for Esca wines was 4 times greater (2 µg/L) than for the other wines (less than 0.5 µg/L).
Figure 2. Methyl salicylate (MeSA) concentration (µg/L) in the vines opened 3 months after the end of alcoholic fermentation of Control, Curetted E1/E2, Curetted E3/E4 and Esca vines from the 2017 and 2018 vintages.
Poitou (2016) found that red wines from Esca-infected grapes had a concentration of 1.48 µg/L methyl salicylate, whereas the control only had 0.37 µg/L. Even though there were sufficient quantities of methyl salicylate for sensory detection, that could pose a problem in the future if berries from another cultivar or grapevines have a high quantity of it. The quantity of methyl salicylate in wines from curetted plants could prove a strong indicator of Esca-disease vine resilience, indicating that those grapevines can synthetise fewer plant defence components.
4. Chemical analyses of the wines
The results showed that the quantity of thiols varied depending on the vintage (Table 2). Due to the low quantity of must per vine category (Control, Curetted E1/E2; or Curetted E3/E4, Esca), the volatile component analyses were performed once without replicates for the 2017 or 2018 vintages. 4MSP was more abundant in 2017 than 2018. For both vintages, 4MSP content was higher in wines produced from Curetted E1/E2 and lower in Esca (2017: 122.1 ng/L E1/E2, 57.8 ng/L Esca; 2018: 22.1 ng/L E1/E2, 4.8 ng/L Esca). Control and Curetted E3/E4 produced wines with intermediate level in 4MSP. Curettage (E1/E2) revealed similar values to those of Control.
Table 2. Analyses of volatile components in the 2017 and 2018 vintages.
|
2017 |
2018 |
||||||
|---|---|---|---|---|---|---|---|---|
Control |
Curetted |
Curetted |
Esca |
Control |
Curetted |
Curetted |
Esca |
|
Volatile thiols (ng/L) |
||||||||
4MSP |
90 |
122 |
56 |
58 |
9 |
22 |
17 |
5 |
3SH |
204 |
209 |
61 |
124 |
41 |
47 |
94 |
183 |
Lactones (µg/L) |
||||||||
γ-octalactone |
0.6 |
0.4 |
0.4 |
0.6 |
0.3 |
0.2 |
0.4 |
0.5 |
γ-nonalactone |
19.7 |
13.4 |
15.5 |
18.0 |
3.6 |
3.0 |
6.0 |
6.3 |
γ-decalactone |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
δ-decalactone |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
"Green" aroma (µg/L) |
||||||||
MIBP |
2.2 |
2.7 |
2.3 |
1.9 |
5.9 |
4.9 |
4.1 |
5.3 |
MIPP |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
MPBs |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
N.D. |
1,4-cineole |
0.2 |
0.2 |
0.2 |
0.2 |
0.04 |
0.05 |
0.09 |
0.06 |
1,8-cineole |
0.3 |
0.5 |
0.3 |
0.3 |
0.09 |
0.07 |
0.09 |
0.08 |
Oxidation (µg/L) |
||||||||
Methional |
0.8 |
0.7 |
1.7 |
2.2 |
0.7 |
1.3 |
3.4 |
0.9 |
Phenylacetaldehyde |
6.6 |
5.0 |
6.7 |
7.0 |
2.9 |
5.2 |
12.5 |
6.2 |
Ortho-amino-acetophenone |
0.2 |
0.3 |
0.2 |
0.3 |
0.6 |
0.6 |
1.1 |
0.8 |
3SH, with grapefruit reminiscence, was the most abundant volatile thiol in both vintages. In 2017, wines from Control and from Curetted E1/E2 plants had the highest 3SH content (204 and 209 ng/L), but differed for the 2018 vintage in which the quantity was most abundant in wines from Esca (183 ng/L). The role of Esca on the 3SH contents released into wines is, highly dependent on the vintage in question (Wu et al., 2019). This could be due to the impact of the climate on the synthesis of 3SH precursors in the berry. Indeed, 2018 had a drier and sunnier summer than 2017, when rainfall was approximately 130 mm in June. Grapes from the 2018 vintage were more acidic and had fewer sugars, meaning that phenological maturity was hard to obtain. It has been empirically observed that the aromatic potential of the berries is affected by a heat episode before harvest. In addition, the pathways of biogenesis of the precursors of 3SH are induced by biotic or abiotic stresses (oxylipin way) (Thibon et al., 2011), which in our study increased in 2018 for Esca.
The results for the volatile thiols showed that wine from Esca was sometimes less typically “Sauvignon blanc” than wine from the other vine categories, whereas Curetted E1/E2 plants had similar results to Control. It should be remembered, however, that the thiol content of wines results from a balance between synthesis and degradation. Thiol release depends not only on precursor content, but also on must composition (including antioxidant compounds, amino acids, phenolic compounds, pH and Nitrogen), the yeast strains used, and the alcoholic fermentation parameters (Murat et al., 2001a; Murat et al., 2001b; Howell et al., 2004; Masneuf-Pomarède et al., 2006). Most of the thiols released were fairly quickly degraded; they were either trapped by phenolic compounds (Nikolantonaki and Waterhouse, 2012), or formed disulphide compounds (Bencomo-Rodriguez and Gambetta, 2011).
In terms of lactones, in our study, only γ-octa- and γ-nonalactone were detected. Quantities of γ-octalactone were less than 0.6 µg/L for all vine groups in both 2017 and 2018, while γ-nonalactone levels were between 2 and 20 µg/L. As for lactones, no differences were found between Control, Curetted and Esca categories. Curettage, however, like Control, did not increase the lactone rate.
Regarding MIBP, the characteristic “green pepper” aroma was detected more in the wine from the 2018 vintage, but there were no differences between the four vine categories (wines from Control, Curetted E1/E2, Curetted E3/E4 and Esca-diseased bunches).
With respect to oxidation compounds, regardless of vintage, the levels detected of methional, phenylacetaldehyde and o-amino-acetophenone were low and below the olfactory detection threshold (8 µg/L), thus having little or no effect on the organoleptic component. These wines, however, should be considered as young wines, since they were analysed six months after vinification had ended. The wines from both vintages showed different rates for the three above-mentioned components. The 2018 vintage wines from Esca and Curetted E3/E4 showed the highest rates of phenylacetaldehyde; meanwhile, 2017 and 2018 vinatage wines from Esca and Curetted E3/E4 showed the highest rates of methional, a phenomenon which can only increase over time. We could, therefore, assume that wines produced from Esca-diseased vines, or curetted ones with strong Esca-foliar symptoms (E3/E4), have a lower potential for being kept than for the control.
5. Sensory analyses
The triangular test (sensory analysis) showed no differences between the different experimental categories of vine for 2017 (Table 3).
Table 3. Results of sensory analysis of 6-month-old wines from Control compared to the other experimental categories of vine (2017 and 2018 vintages).
|
Wines from curetted E1/E2 vines |
Wines from curetted E3/E4 vines |
Wines from Esca vines |
|---|---|---|---|
Control wines (2017 vintage) |
No sensorial differences |
No sensorial differences |
No sensorial differences |
p value > 0.05 |
p value > 0.05 |
p value > 0.05 |
|
Control wines (2018 vintage) |
Sensorial differences |
No sensorial differences |
Sensorial differences |
p value < 0.05 |
p value > 0.05 |
p value < 0.05 |
The wine tasters could not differentiate the flavours of the wines from the Curetted and Control vine categories. For the 2018 vintage, the tasters were also unable to differentiate between the wines from Curetted and Control. While differences were observed between the wines from symptomatic and control vines (p value = 0.018), they were also observed (p value = 0.048) for wines from Curetted E1/E2.
Descriptive wine analyses were possible for the 2018 vintage (Figure 3).
Figure 3. Using Fizz software, sensory profile of 2018 wines containing grapes from Control or Curetted E1/E2 or Curetted E3/E4 or Esca.
Our results showed that in one-year-old wines, tasters were unable to observe any differences between the wines from Curetted and Control. For the wines from Esca-diseased vines, wine oxidation was observed. In the sensory analyses wines from curetted vines showed no differences from those of the control. The quality of Sauvignon blanc wine remained the same, indicating that curettage practices do not have negative impacts on the final product; i.e., the wine.
Conclusions
Curettage is one of the methods currently being used to tackle Esca. Cholet et al. (2019) showed that vines are able to live for several years after curettage and to produce healthy bunches. The take-home message of our study is that musts and wines from curetted plants share similar qualities with those from plant that do not expressed Esca-foliar symptoms. It was only in musts and wines from Esca-diseased vines that the high level of chemical methyl salicylate indicated that the plants were stressed. Lorrain et al. (2012) showed that the red wines produced from grapes from Esca vines differed in chemical composition and aroma flavours compared to wines from asymptomatic vines. The use of curettage to control Esca showed that plant recovered relatively fast because, just two years after curettage, our results showed that the quantity and quality of berries were similar to those of asymptomatic plants. Curettage could thus be a future solution to tackling Esca with the advantages of (I) avoiding having to replace Esca-diseased vines by young plants, and (II) maintaining the bunch quality of aged vines in order to preserve the typicity of Sauvignon blanc.
Acknowledgements
This work was supported by the GTDfree Industrial Chair project, which is funded by JAs Hennessy & Co (Cognac, France) and the French Research Agency (ANR). The authors would also like to thank Chateau Reynon - Denis Dubourdieu Domaines, Denis & Florence Dubourdieu EARL (Beguey, Gironde, France) for allowing them to use the experimental plot.
References
- Allamy, L., Darriet, P., & Pons A., (2017). "Identification and Organoleptic Contribution of (Z)-1,5-Octadien-3-one to the Flavor of Vitis vinifera cv. Merlot and Cabernet Sauvignon Musts." Journal of Agricultural and Food Chemistry, 65(9), 1915-1923. https://doi.org/10.1021/acs.jafc.6b05293
- Armengol, J., Vicent, A., Torne, L., Garcia-Figueres, F., & Garcia-Jimenez, J. (2001). Fungi associated with decline and infections of grapevine wood in various Spanish zones. Plagas, 27, 137-153.
- Bencomo-Rodriguez, J.J., & Gambetta, J.J. (2011). Quantitative determination of varietal disulfides in wine and their behavior during alcoholic fermentation. 9e Symposium international d'œnologie de Bordeaux-Oeno 2011, Bordeaux, France, Dunod.
- Bertsch, C., Ramirez-Suero, M., Magnin-Robert, M., Larignon, P., Chong J., & Abou-Mansour E. (2012). Grapevine trunk diseases: complex and still poorly understood. Plant Pathology, 62(2), 243-265 https://doi.org/101111/j1365-3059201202674x
- Bruez, E., Lecomte, P., Grosman, J., Doublet, B., Bertsch, C., Fontaine, F., Ugaglia, A., Teissedre, P.-L., Da Costa, J.-P., Guerin-Dubrana, L., & Rey, P. (2013). Overview of grapevine trunk diseases in France in the 2000s. Phytopathologia Mediterranea, 52, 262-275. https://doi.org/10.14601/Phytopathol_Mediterr-11578
- Bueno, M., Culleré, L., Cacho, J., & Ferreira, V. (2010). Chemical and sensory characterization of oxidative behavior in different wines. Food Research International, 43(5), 1423-1428. https://doi.org/10.1016/j.foodres.2010.04.003
- Calzarano, F., Cichelli, A., & Odoardi, M. (2001). Preliminary evaluation of variations in composition induced by esca on cv. Trebbiano d’Abruzzo grapes and wines. Phytopathologia Mediterranea, 40, S443-S448. http://digital.casalini.it/10.1400/14663
- Calzarano, F., Di Marco, S., & Cesari, A. (2004). Benefit of fungicide treatment after trunk renewal of vines with different types of Esca necrosis. Phytopathologia Mediterranea, 43, 116-124. https://doi.org/10.14601/Phytopathol_Mediterr-1725
- Câmara, J.S, Alves, M.A., & Marques, J.C. (2006). Changes in volatile composition of Madeira wines during their oxidative ageing. Analytica Chimica Acta, 563, 188-197.
- Carter, M.V. (1991). The status of Eutypa lata as a pathogen. Monograph.Phytopathological Paper No. 32, International Mycological Institute, Egham, UK.
- Cholet, C., Bruez, E., Lecomte, P., Rey, P., Boury, T., Martignon, T., & Geny-Denis, L. (2019). Intérêt du curetage dans la lutte contre l’esca. Phytoma, 728,21-24.
- Cooke, R.C., & Capone, D.L. (2009). Quantification of Several 4-Alkyl Substituted γ-Lactones in Australian Wines. Journal of Agricultural and Food Chemistry, 57(2), 348-352. https://doi.org/10.1021/jf8026974
- Darriet, P., Tominaga, T., Lavigne, V., Boidron, J.N., & Dubourdieu, D. (1995). Identification of a powerful aromatic component of Vitis vinifera L. var. sauvignon wines: 4‐mercapto‐4‐methylpentan-2-one. Flavour Fragrance Journal, 10(6), 385-392.
- Dixon, D.P., Skipsey, M., & Edwards, R. (2010). Roles for glutathione transferases in plant secondary metabolism. Phytochemistry, 71(4), 338-350. https://doi.org/10.1016/j.phytochem.2009.12.012
- Ebeler, S.E., & Thorngate, J.H. (2009). Wine Chemistry and Flavor: Looking into the Crystal Glass. Journal of Agricultural and Food Chemistry, 57(18), 8098-8108. https://doi.org/10.1021/jf9000555
- Edwards, J., & Pascoe, I.G. (2004). Occurrence of Phaeomoniella chlamydospora and Phaeoacremonium aleophilum associated with Petri disease and Esca in Australian grapevines. Australian Plant Pathology, 33, 273-279. https://doi.org/10.1071/AP04016
- Fedrizzi, B., Pardon, K.H., Sefton, M.A., Elsey, G.M., & David Jeffery, W. (2009). First Identification of 4-S-Glutathionyl-4-methylpentan-2-one, a Potential Precursor of 4-Mercapto-4-methylpentan-2-one, in Sauvignon blanc Juice. Journal of Agricultural and Food Chemistry, 57(3), 991-995. https://doi.org/10.1016/j.foodchem
- Gimenez-Jaime, A., Aroca, A., Raposo, R., Garcia-Jimenez, J., & Armengol J. (2006). Occurrence of fungal pathogens associated with grapevine nurseries and the decline of young vines in Spain. Journal of Phytopathology, 154, 598-602. https://doi.org/10.1111/j.1439-0434.2006.01153.x
- Graniti, A., Surico, G., & Mugnai, G. (2000). Esca of grapevine: a disease complex or a complex of diseases? Phytopathologia Mediterranea, 39, 16-20. https://doi.org/10.14601/Phytopathol_Mediterr-1539
- Guillaumie, S., & Ilg, A. (2013). Genetic analysis of the biosynthesis of 2-methoxy-3-isobutylpyrazine, a major grape-derived aroma compound impacting wine quality. Plant Physiology, 162(2), 604-615. https://doi.org/10.2307/41943249
- Howell, K.S., Bartowsky, E.J., Fleet, G.H., & Henschke, P.A. (2004). Microsatellite PCR profiling of Saccharomyces cerevisiae strains during wine fermentation. Letters in Applied Microbiology, 38(4), 315-320. https://doi.org/10.1111/j.1472-765x.2004.01486.x
- Kobayashi, H., Takase, H., Kaneko, K., Tanzawa, F., Takata, R., Suzuki, S., & Konno, T. (2011). Analysis of S-3-(Hexan-1-ol)-Glutathione and S-3-(Hexan-1-ol)-l-Cysteine in Vitis vinifera L. cv. Koshu for Aromatic Wines. American Journal of Viticulture and Enology, 61, 176-185. https://www.ajevonline.org/content/61/2/176
- Larignon, P., & Dubos, B. (1997). Fungi associated with esca disease in grapevine. European Journal of Plant Pathology, 3, 147-157. https://doi.org/10.1023/A:1008638409410
- Larignon, P., Fontaine, F., Farine, S., Clement, C., & Bertsch, C. (2009). Esca and Black Dead Arm: two major actors of grapevine trunk diseases. Compte Rendus Biologies, 332, 765-783. https://doi.org/10.1016/j.crvi.2009.05.005
- Lecomte, P., Diarra, B., Carbonneau, A., Patrice, R. E. Y., & Chevrier, C. (2018). Esca of grapevine and training practices in France: results of a 10-year survey. Phytopathologia Mediterranea, 57(3), 472-487. https://doi.org/10.14601/Phytopathol_Mediterr-22025
- Lorrain, B., Ky, I., Pasquier, G., Jourdes, M., Guérin-Dubrana, L., Geny, L., Rey, P., Doneche, B., & Tesseidre, P.-L. (2012). Effect of Esca disease on the phenolic and sensory attributes of Cabernet Sauvignon grapes, musts and wines. Australian Journal of Grape and Wine Research 18, 64-72.
- Masneuf-Pomarède, I., Mansour, C., Murat, M., Tominaga, T., & Dubourdieu, D. (2006). Influence of fermentation temperature on volatile thiols concentrations in Sauvignon blanc wines. International Journal of Food Microbiology 108(3), 385-390. https://doi.org/10.1016/j.ijfoodmicro.2006.01.001
- Mugnai, L., Graniti, A., & Surico, G. (1999). Esca (Black measles) and brown wood-streaking: Two old and elusive diseases of grapevines. Plant Disease 83, 404-418. https://doi.org/10.1094/PDIS.1999.83.5.404
- Murat, M.L., Masneuf, I., Darriet, P., Lavigne, V., & Dubourdieu, D. (2001a). Effect of Saccharomyces cerevisiae yeast strain on the liberation of volatile thiols in Sauvignon blanc wine. American Journal of Viticulture and Enology 52, 136-139.
- Murat, M.L., Tominaga, T. & Dubourdieu, D. (2001b). Assessing the aromatic potential of Cabernet sauvignon and merlot must used to produce rosé wine by assaying the cysteinylated precursor of 3-mercaptohexan-1-ol. Journal of Agriculture and Food Chemistry 49, 5412-5417. https://doi.org/10.1021/jf0103119
- Nikolantonaki, M., & Waterhouse, A.L. (2012). A method to quantify quinone reaction rates with wine relevant nucleophiles: a key to the understanding of oxidative loss of varietal thiols. Journal of Agricultural and Food Chemistry 60(3), 8484-8490. https://doi.org/10.1021/jf302017j
- Pérez-Olivero, S.J., & Pérez-Pont, ML. (2014). Determination of lactones in wines by headspace solid-phase microextraction and gas chro.matography coupled with mass spectrometry. Journal of analytical methods in chemistry 86, 19-23. https://doi.org/10.1021/jf1034064
- Peyrot des Gachons, C., Tominaga, T., & Dubourdieu, D. (2002). Localization of S-cysteine conju- gates in the berry: effect of skin contact on the aromatic potential of Vitis vinifera L. c.v. Sauvignon blanc must. American Journal of Viticulture and Enology 53, 144-146.
- Poitou, X. (2016). Contribution à la connaissance aromatique des vins rouges : Approche sensorielle et moléculaire des nuances « végétales, vertes » en lien avec leur origine. Thesis, University of Bordeaux.
- Poitou, X., Delière, L., Pons, A., Redon, P., Thibon, C., & Darrie,t P. (2018). Caractérisation de marqueurs volatils associés aux nuances végétales des vins rouges. Etude du lien avec la maturité et le pressurage. Partie 3/3 : Paramètres environnementaux et composante aromatique végétale. Revue des Œnologues et des Techniques Vitivinicoles et Oenologiques 166, 51-53.
- Roujou de Boubée, D., Van Leeuwen, C., & Dubourdieu, D. (2000). Organoleptic Impact of 2-Methoxy-3-isobutylpyrazine on Red Bordeaux and Loire Wines. Effect of Environmental Conditions on Concentrations in Grapes during Ripening. Journal of Agricultural and Food Chemistry 48(10), 4830-4834.
- Rumbos, I., & Rumbou, A. (2001). Fungi associated with Esca and young grapevine decline in Greece. Phytopathologia Mediterranea 40, S330-S335. https://doi.org/10.14601/Phytopathol_Mediterr-1622
- Ryona, I., Pan, B.S., Diego, S., Intrigliolo, S., Lakso, A.N., & Sacks, G.L. (2008). Effects of Cluster Light Exposure on 3-Isobutyl-2-methoxypyrazine Accumulation and Degradation Patterns in Red Wine Grapes (Vitis vinifera L. Cv. Cabernet Franc). Journal of Agricultural and Food Chemistry 56(22), 38-46. https://doi.org/10.1021/jf801877y
- Scheck, H.J., Vasquez, S.J., Gubler, W.D., & Fogle, D. (1998). First report of three Phaeoacremonium spp causing young grapevine decline in California. Plant Disease 82, 590-590. https://doi.org/10.1094/PDIS.1998.82.5.590C
- Silva Ferreira, A.C., Guedes, P., de Pinho, P., & Hogg, T. (2002). Kinetics of Oxidative Degradation of White Wines and How They Are Affected by Selected Technological Parameters. Journal of Agricultural and Food Chemistry 50(21), 5919-5924. https://doi.org/10.1021/jf0115847
- Sosnowski, M.R., Shtienberg, D, Creaser, M.L., Wicks, T.J., Lardner, R., & Scott, ES. (2007). The influence of climate on foliar symptoms of eutypa dieback in grapevines. Phytopathology 97, 1284-1289. https://doi.org/10.1094/PHYTO-97-10-1284
- Surico, G., Marchi, G., Braccini, P., & Mugnai, L. (2000). Epidemiology of Esca in some vineyards in Tuscany (Italy). Phytopathologia Mediterranea 39, 190-205. https://doi.org/10.14601/Phytopathol_Mediterr-1536
- Tang, F., Fu, Y.Y., & Ye, J.R. (2015). The effect of methyl salicylate on the induction of direct and indirect plant defense mechanisms in poplar (Populus × euramericana ‘Nanlin 895’). Journal of Plant Interactions 10(1), 93-100. https://doi.org/10.1080/17429145.2015.1020024
- Thibon, C., Cluzet, S., Merillon, J.M., Darriet, P., & Dubourdieu, D. (2011). 3-Sulfanylhexanol Precursor Biogenesis in Grapevine Cells: The Stimulating Effect of Botrytis cinerea. Journal of Agricultural and Food Chemistry 59(4): 1344-1351. https://doi.org/10.1021/jf103915y
- Thibon, C., Pons, A., Mouakka, N., Redon, P., Méreau, R., & Darriet, P. (2015). Comparison of electron and chemical ionization modes for the quantification of thiols and oxidative compounds in white wines by gas chromatography-tandem mass spectrometry. Journal of Chromatography Analyses 1415, 123-133. https://doi.org/10.1016/j.chroma.2015.08.027
- Tiedemann, S., Brendel, G., & Fehrmann, H. (1988). Investigations on endophytic fungi of grapevine with special emphasis on the vascular system of rootstocks. Journal of Phytopathology 122, 147-165. https://doi.org/10.1128/AEM.07655-11
- Tominaga, T., Furrer, A., Henry, R., & Dubourdieu D. (1998). Identification of new volatile thiols in the aroma of Vitis vinifera L. var. Sauvignon blanc wines. Flavour and Fragrance Journal 13(3), 159-162.
- Úrbez-Torres, J.R., Leavitt, G.M., Voegel, T.M., & Gubler, W.D. (2006). Identification and distribution of Botryosphaeria spp. associated with grapevine cankers in California. Plant Disease 90, 1490-1503. https://doi.org/10.1094/PD-90-1490
- Úrbez-Torres, J.R., Leavitt, G.M., Guerrero, J.C., Guevara, J., & Gubler, W.D. (2008). Identification and pathogenicity of Lasiodiplodia theobromae and Diplodia seriata, the causal agents of bot canker disease of grapevines in Mexico. Plant Disease 92, 519-529. https://doi.org/10.1094/PDIS-92-4-0519
- Úrbez-Torres, J.R., Adams, P., Kamas, J., & Gubler W.D. (2009). Identification, incidence, and pathogenicity of fungal species associated with grapevine dieback in Texas. American Journal of Enology and Viticulture 60, 497-507.
- Weber, E.A., Trouillas, F.P., & Gubler, W.D. (2007). Double pruning of grapevines: A cultural practice to reduce infections by Eutypa lata. American Journal of Enology and Viticulture 58, 61-66.
- Wu, J., Drappier, V., Hilbert, G., Guillaumie, S., Dai, Z., Geny, L., Delrot, S., Darriet, P., Thibon, C., & Pieri, P. (2019). The effects of a moderate grape temperature increase on berry secondary metabolites. OENO One 53(2), 321-333. https://doi.org/10.20870/oeno-one.2019.53.2.2434
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