Journal of Integrative Agriculture 2018, 17(6): 1401–1408 Available online at www.sciencedirect.com
ScienceDirect
RESEARCH ARTICLE
In field control of Botrytis cinerea by synergistic action of a fungicide and organic sanitizer Fatima Ayoub1, Najwa Ben oujji2, Mohamed Ayoub1, Athman Hafidi1, Rachid Salghi1, Shehdeh Jodeh3 1
Laboratory of Applied Chemistry and Environment, National School of Applied Science, Ibn Zohr University, P.O Box 1136, Agadir 80000, Morocco
2
Ecolink International, Zone Industrielle, Ait Melloul, Agadir 80000, Morocco Department of Chemistry, An-Najah National University, P.O. Box 7, Nablus, Palestine
3
Abstract A new Integrated Pest Management program based on the combination of synthetic pesticide with a GRAS (generally recognized as safe)-classified sanitizer for the control of Botrytis cinerea in field conditions was described. The aim behind this research was to determine whether the use of this mixture would enhance the efficiency of pesticides while decreasing the recommended dose. Naturally infected tomato plants, grown in the greenhouse, were treated with two commonly used fungicides SWITCH (Syngenta, Switzerland) and SIGNUM (BASF, Germany) each alone or combined with a commercially available organic sanitizer PERACLEAN®5 (Evonik Industries, Germany). A total of 27 treatments were tested consisting of three concentrations of synthetic fungicide (×1, ×1/2 and ×1/4 of the recommended dose) either applied separately or combined with three concentrations of the tested sanitizer (0.5, 1 and 1.5%). The control efficacy achieved by the fungicides applied alone ranged between 0 and 66.7% while all fungicide-sanitizer mixtures resulted in up to 70% control of grey mould. The treatment that provides the maximum control of B. cinerea was the result mixture of ×1/4 of the recommended concentration of SWITCH (15 g L–1) with 0.5% of PERACLEAN®5. This combination suppressed 85% of grey mold infections while decreasing the usually used amount of this pesticide by 75%, reducing therefore the well known negative impacts of chemical pesticides on environment and consumers health. Keywords: Botrytis cinerea, tomatoes, peroxyacetic acid, PERACLEAN®5, SIGNUM, SWITCH
species of pests, including insects, mites, plant pathogens,
1. Introduction Agricultural crops are exposed to approximately 70 000
and weeds that potentially cause the reduction of world food production by more than 40% if pesticides are not applied (Suprapta 2016). These phytosanitary products play a vital role in the economic production of wide ranges of vegetable, fruit, cereal, forage, fibre and oil crops which now constitute a large part of successful agricultural
Received 22 August, 2017 Accepted 5 January, 2018 Correspondence Fatima Ayoub, E-mail: ayoub.fatima@gmail. com; Rachid Salghi, E-mail:
[email protected] © 2018 CAAS. Publishing services by Elsevier B.V. All rights reserved. doi: 10.1016/S2095-3119(17)61875-6
industry in many countries (Al Hattab and Ghaly 2012). Although tremendous benefits have been derived from the use of pesticides in agriculture, increasing awareness on their negative effects on human health and biodiversity urges to find more eco-friendly and healthier alternatives
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(Andersson et al. 2014; Bernardes et al. 2015). In the last few years, different alternatives to chemical products have been reported in the literature, including: i) biocontrol agents (Heydari and Pessarakli 2010; Liu et al. 2010); ii) biologically active natural products (Ben-Shaloma et al. 2003; Daferera et al. 2003; Nigro et al. 2006; Vitoratos et al. 2013; Amini et al. 2016; Suprapta 2016; Todorović et al. 2016); (iii) GRAS (generally recognized as safe)-classified sanitizers (Venditti et al. 2008; Elbouchtaoui et al. 2015); and iv) Integrated Pest Management (IPM) methods (Romanazzi et al. 2006; Xu et al. 2007; Camili et al. 2010; Soliman et al. 2015). In that regard, we describe in this paper a new IPM method based on combination of an organic sanitizer and fungicide for the control of B. cinerea in tomato fields in the attempt to reduce the negative impacts of chemical pesticides on environment and consumer’s health. IPM is increasingly perceived as a workable solution to chemical pesticides problems. It can be defined as an ecosystem approach to crop production and protection that combines different management strategies and practices to grow healthy crops and minimize the use of pesticides (FAO 2012). Therefore, IPM utilizes the best mix of control tactics for a given pest problem when compared with the crop yield, profit and safety of other alternatives (Ehi-Eromosele et al. 2013). Gray mold caused by Botrytis cinerea (Botrytis cinerea Persoon: Fries (teleomorph Botryotinia fuckeliana) is one of the most economically important diseases and the most redoubtable threat of commercially produced tomatoes (McDougall 2016). This fungus can affect yield in different ways. The pathogen may cause blight on leaf or petal tissues, crown rot, stem cankers, cutting rot, and dampingoff (Li et al. 2014). The fungus produces germ tubes from conidia that can infect through natural openings or wounds. It is a cool-season disease and infection is favored under wet conditions with temperatures below 22°C. In addition to actively causing disease during the growing season, the fungus is also able to cause latent infections leading to disease after harvest, either during storage or transit, in the store, or after purchase by the consumer (Li et al. 2014). In the absence of resistant tomato varieties to this pathogen, the control of this disease is still based upon multiple applications of fungicides, mainly benzimidazoles and dicarboximides, which can leads to the development of pathogen resistance, chemical residues in fruits, phytotoxicity to other organisms or serious environmental and public health problems as described above. In a previous work (Ayoub et al. 2017), we have described a new treatment approach based on the combination of a commercially available peroxyacetic acid mixture (PERACLEAN®5) with two commonly used fungicides (each alone) to control grey mold. The in vitro tests described in Ayoub et al. (2017) allowed us to suppress the pathogen
while minimizing the amounts of applied fungicides by more than 95%. In this paper, the in field trials of this new developed approach is presented. This new practice presents several advantages over the conventional methods to control B. cinerea: i) It will minimize the 100% effective concentration of the two products, enhance fungicidal action and consequently reduce the well known negative impacts of pesticide; ii) lengthen the period of effectiveness; iii) peroxyacetic acid being rapidly active will speed up the biocide action against the pathogen; iv) being highly acid, Peroxyacetic acid will induce the acidification of the fungicide, necessary before application on field, so no additional acidifying product is needed; v) the use of this mixture will delay the selection of resistant strains; and vi) it’s a cost effective way to limit the grey mold incidence. To the best of our knowledge, this new practice was not previously described elsewhere.
2. Materials and methods 2.1. Chemical products A commercially available 5% peracetic acid (PAA) solution PERACLEAN®5 was kindly provided by Green Solutions Company, Morocco. It’s a fungicidal, bactericidal and yeast-active disinfectant with a broad spectrum of action, consisting of 5% of peroxyacetic acid, 26.4% of hydrogen peroxide and 6.8% of acetic acid. Two commonly used fungicides to control grey mold disease caused by B. cinerea were selected so as to study their antifungal efficacy, separately and in combination with PERACLEAN®5: (1) SIGNUM® WG by BASF, Germany; active ingredients: 26.7% (w/w) boscalid and 6.7% (w/w) pyraclostrobin; chemical groups: pyridinecarboximide and methoxy-carbamate, respectively and (2) SWITCH® 62.5 WG by Syngenta Crop Protection Pty Ltd., Switzerland; active ingredients: 375 g kg–1 cyprodinil and 250 g kg–1 fludioxonil; chemical groups: anilinopyramidine and phenylpyrrole, respectively.
2.2. Antifungal activities The antifungal activities of the above cited chemicals were tested in field against growth of B. cinerea on stems, leaf and fruits. PERACLEAN®5, SWITCH and SIGNUM were tested either separately or as combinations as described in Table 1. The choice of the concentrations was made according to the manufacturers recommended field doses for both fungicides: The highest concentrations of SWITCH and SIGNUM reported in Table 1 (60 and 125 g L –1, respectively) represent the advised concentrations used by the Moroccan farmer for the control of B. cinerea in tomato
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Table 1 Tested treatments Treatment T1 T2 T3 T4 T5 T6 T7 T8 T9 T10 T11 T12 T13 T14 T15 T16 T17 T18 T19 T20 T21 T22 T23 T24 T25 T26 T27
Chemicals concentration SWITCH SIGNUM PERACLEAN®5 (%) (g L–1) (g L–1) 0.5 0 0 1 0 0 1.5 0 0 0 0 125 0 0 62.50 0 0 31.25 0 60 0 0 30 0 0 15 0 0.5 0 125 1 0 125 1.5 0 125 0.5 0 62.50 1 0 62.50 1.5 0 62.50 0.5 0 31.25 1 0 31.25 1.5 0 31.25 0.5 60 0 1 60 0 1.5 60 0 0.5 30 0 1 30 0 1.5 30 0 0.5 15 0 1 15 0 1.5 15 0
fields. Since our goal is to decrease the used concentrations of pesticide, 50 and 25% of these concentrations were tested either alone or combined with the organic sanitizer (PERACLEAN®5) to test their efficiency. All the solutions were prepared immediately before their application in the greenhouse where a randomized complete block design was adopted.
2.3. Greenhouse experiments The current study was conducted in a commercial tomato production site located in Ben Guemoud region (Latitude: 30°14´4.3´´ (30.2345°) North; Longitude: 9°34´28.6´´ (9.5746°) West), Souss-Massa, Agadir-Morocco, where a Canarian greenhouse with soil culture system was adopted. Tomato plants var. Pristyla (from Gautier) susceptible to B. cinerea, were planted at the beginning of August in sandy loam soil that had been disinfected with 1,3-dichloropropene+chloropicrine (55.4%+32.7%) (Ajaanid 2016). Plants were spaced 0.4 m apart and 1.25 m between rows. Natural infestation with B. cinerea occurred in the greenhouses during winter seasons, so the tests were conducted during the winter in January 2017.
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Irrigation, fertilization and other agricultural procedures were carried out according to common practices in Moroccan farming. Naturally infected tomato plants were used. Each of the 27 treatments was applied to a separated tomato row containing 10 to 15 tomato plants with one row treated with distilled water to serve as the control. Buffer rows were used between treated lines and during all the treatment process, care was taken to avoid drift to adjacent plots. The treatments were applied on the entire plant using a backpack-type sprayer. The efficiency of the tested treatments was evaluated by the decrease of the infection rate after 24, 48 and 120 h after treatment application. Before treatment, plants infected with B. cinerea, showing brown or spotted plant material with masses of silver-gray spores on the dead or dying tissue, were counted and considered as initial rate of infection with report to the total number of plants in the row. After treatments, the number of healed plant showing dry spot without spore in surface was counted. The infection rate was calculated as follow: X Infection rate (%)= ×100 X0 Where, X0 and X are the number of infected plants before and after treatments, respectively.
2.4. Chemicals interaction trials For simplicity, most interaction experiments are performed under laboratory or greenhouse conditions (in vivo and in vitro) with a single isolate (Gisi 1996). In this work, the results obtained from a greenhouse trial were used to determine the interaction nature between tested chemicals: antagonistic, additive or synergistic interaction. Fungicide and organic sanitizer interactions were assessed with the widely used model Abotts’ formula (Gisi 1996). The model compares expected and observed suppressions where expected suppressions expressed as percent Cexp (%) can be predicted as follows: AB Cexp (%)=A+B– (1) 100 Where, A and B are the inhibitions caused when the fungicide and sanitizer act alone respectively. The ratio of inhibition (RI) was then calculated as follows for each mixture: (2) RI=Observed inhibition/Cexp Interactive effects were evaluated by comparing RI with 1. RI values>1 indicated synergism; RI values=1 indicated additivity; and RI values<1 indicated antagonism (Chesworth et al. 2004).
2.5. Statistical analysis Data were analyzed using MINITAB statistical software
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version 18. Treatment means were separated by Tukey’s test at P≤0.05.
3. Results
concentration of PERACLEAN®5 permits a good control of B. cinerea with a persistent action, it may cause severe damages to the plant by provoking burns on leaves.
3.2. Antifungal activity of SWITCH
3.1. Antifungal activity of PERACLEAN 5 ®
The antifungal activity of PERACLEAN ® 5, against B. cinerea, in tomato greenhouse was assessed using three concentrations: 0.5, 1 and 1.5%. The infection rate by grey mould was counted before treatment (0 h), and 24, 48 and 120 h after treatment. The obtained results are presented in Table 2. As reported in Table 2, after 24 h of treatment application, all concentrations of peroxyacetic acid preparation allowed the suppression of the pathogen by 40, 50 and 62.5% using 0.5, 1 and 1.5% of PERACLEAN®5, respectively, which demonstrate that increasing the concentration of PERACLEAN®5 increase to efficiency of the product. After 48 h, the decrease observed in the infection rate has remained constant for the treatments T1 and T3 (0.5 and 1.5% of PERACLEAN®5, respectively) while using treatment T2, new infections with B. cinerea appeared, which may be due to the biodegradation of the product. After 5 days of treatment (120 h), new infections by the fungus were observed in the rows treated with 0.5 and 1% of PERACLEAN®5 while in the row treated with 1.5% the disease incidence remained stable. Even if this Table 2 Disease incidence of Botrytis cinerea after 0, 24, 48 and 120 h of PERACLEAN®5 treatment application Concentration (%) 0.5 1 1.5
0h 100 100 100
Disease incidence (%) 24 h 48 h 120 h 60.0 60.0 80.0 50.0 83.4 100 37.5 37.5 37.5
Three concentrations of SWITCH (37.5% cyprodinil+25% fludioxonil) were tested either alone or combined with 0.5, 1 and 1.5% of PERACLEAN®5 to test their efficiency in the control of B. cinerea. The obtained results are shown in Table 3. In general, all the treatments significantly reduce (P≤0.05) the incidence of fruit and stem infections except 15 g L–1 of SWITCH alone. When the fungicide was used alone, it was observed that increasing the pesticide concentration increases the inhibition of B. cinerea with 62.5% of infection suppressed by the highest concentration: 60 g L–1 of SWITCH. The ×1/2 of this concentration (30 g L–1) only suppresses 25% of the pathogen infection while 15 g L–1 of SWITCH alone doesn’t exhibit any inhibition of the fungus. When combined with PERACLEAN ®5, an increase of the efficiency of the pesticide was observed. The results in Table 3 show that all mixtures of SWITCH with PERACLEAN®5 were more effectives in suppressing B. cinerea than the recommended dose of the fungicide and with a persisting action. The best results were obtained when combining 1/4 of the recommended concentration of SWITCH (15 g L–1) with 0.5% of PERACLEAN®5, a result that may be due to the interactions between the fungicide and the sanitizer which were assessed with the widely used model Abotts’ formula (1925). The obtained results are presented in Table 4. When PERACLEAN ® 5 was combined with the recommended dose of SWITCH (60 g L–1), a slight antagonistic interaction was observed (Table 4). Using 30 g L –1 of the fungicide, a synergistic interaction between the two
Table 3 Disease incidence of Botrytis cinerea on tomatoes plants after 0, 24, 48 and 120 h of treatment with SWITCH alone or mixed with PERACLEAN®5 Concentration of SWITCH (g L–1) 60
30
15
PERACLEAN®5 concentration (%) 0 0.5 1 1.5 0 0.5 1 1.5 0 0.5 1 1.5
0h 100 100 100 100 100 100 100 100 100 100 100 100
Disease incidence (%) 24 h 48 h 37.5 37.5 25.0 25.0 33.4 33.4 16.7 33.3 75.0 75.0 30.0 30.0 27.3 27.3 20.0 20.0 100 100 14.2 14.2 33.3 33.3 37.5 37.5
120 h 37.5 25.0 44.4 33.3 75.0 30.0 27.3 20.0 100 14.2 33.3 37.5
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Table 4 Synergistic interactions between SWITCH and PERACLEAN®5 in the greenhouse conditions SWITCH concentration (g L–1)
PERACLEAN®5 concentration (%)
60
30
15
0.5 1 1.5 0.5 1 1.5 0.5 1 1.5
24 h 0.967 cd 0.819 d 0.969 d 1.272 b 1.163 bc 1.113 bc 2.145 a 1.334 b 1 cd
Ratio of inhibition (RI) 48 h 0.967 cd 0.819 d 0.776 d 1.272 b 1.163 bc 1.113 bc 2.145 a 1.334 b 1 cd
120 h 0.967 cd 0.684 d 0.776 d 1.272 b 1.163 bc 1.113 bc 1.766 a 1.167 b 0.920 cd
Values followed by the same letter in each column are not significantly different from each other according to Tukey’s test at P≤0.05.
products was observed and with 15 g L–1, a synergistic to highly synergistic interaction was expressed. The highly synergistic effect was obtained when combining 15 g L–1 of SWITCH with 0.5% of PERACLEAN®5. The obtained results are in concordance with those reported in Gisi (1996) where the synergistic interactions between biocides always decrease rapidly with increasing control levels of the single component and maybe almost nil at high control levels.
3.3. Antifungal activity of SIGNUM As for SWITCH, three concentrations of SIGNUM were tested either alone or combined with 0.5, 1 and 1.5% of PERACLEAN®5 to test their efficiency in the control of B. cinerea under the greenhouse conditions. The reported concentrations are the recommended dose of the fungicide (125 g L–1), ×1/2 (62.5 g L–1) and ×1/4 (31.25 g L–1) of this concentration. The obtained results are presented in Table 5. Used alone, the recommended dose of SIGNUM (125 g L–1) resulted in suppression of 66.7% of grey mould infection, while ×1/2 and ×1/4 of this concentration suppressed 59.5 and 54.6%, respectively. When combined with PERACLEAN®5, all mixtures gave better results. The treatment providing the maximum control of B. cinerea was the result mixture of 62.5 g L–1 of SIGNUM with 1.5% of PERACLEAN®5. Even if this combination permits a good control of the fungus, its application maybe limited by the negative impact that a concentration of 1.5% of PERACLEAN®5 may induce to the plant. Therefore, in this study, the recommended mixture will be the combination of 31.25 g L–1 of SIGNUM with 0.5% of PERACLEAN®5, which suppress 66.7% of the disease. This mixture resulted in similar results to these obtained with the recommended concentration of SIGNUM while minimizing the applied amount of pesticide by 75%. In order to better understand the nature of interactions between SIGNUM and PERACLEAN, interactive effects were calculated according to the Abotts’ formula and the
results are presented in Table 6. In general, a slight antagonistic effect was observed between SIGNUM and PERACLEAN®5, which may be due to the chemical composition of both products. This later interpretation is based on the common definition of the synergism where it’s considered as a joint action of mixture components in which the total effect is greater than the sum of the effects of the individual components (Gisi 1996). However, in our case, this definition may be an underestimation of the obtained results since our goal is to enhance the efficiency of the synthetic pesticide while minimizing the applicable amount without taking into consideration the effect of the organic sanitizer.
4. Discussion Peroxyacetic acid (PAA) is a biodegradable product and a highly effective biocide, used in a wide range of applications and demonstrates excellent bactericidal and fungicidal activity against a wide range of microorganisms (Baldry 1983; Ossia-Ongagna and Sabatier 1993; Kitis 2004; Bernet et al. 2005). It had been used for purposes ranging from disinfestations of bulbs to prevention of other horticultural diseases through disinfecting potting soil and cleaning irrigation equipment (Alvaro 2009). There are several registered products on the market, containing peroxyacetic acid, hydrogen peroxide and acetic acid in different proportions as stabilized mixtures. These mixtures are environmentally-friendly products as their manufacture does not involve polluting processes; they have the same function as other chemicals, and after use, there is no toxic residue left in the environment (Carrasco and Urrestarazu 2010). They can be used in the application of green chemistry in agriculture and none of the products formed during the degradation process are harmful. Acetic acid, hydrogen peroxide, water, and oxygen, are biodegradable, not harmful or even secondarily useful (Carrasco and Urrestarazu 2010). Several studies have reported the antifungal activity of these mixtures against Penicillium digitatum
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Table 5 Disease incidence of Botrytis cinerea on tomatoes plants after 0, 24, 48 and 120 h of treatment with SIGNUM alone or mixed with PERACLEAN®5 Concentration of SIGNUM (g L–1) 125
62.5
31.25
PERACLEAN®5 concentration (%) 0 0.5 1 1.5 0 0.5 1 1.5 0 0.5 1 1.5
0h 100 100 100 100 100 100 100 100 100 100 100 100
Disease incidence (%) 24 h 48 h 33.3 33.3 27.3 18.2 30.0 30.0 32.1 32.1 40.5 40.5 50.0 50.0 44.4 44.4 18.2 22.2 45.4 45.4 33.3 33.3 40.0 40.0 42.8 28.6
120 h 33.3 36.4 40.0 32.1 40.5 37.6 44.4 22.2 45.4 33.3 40.0 28.6
Table 6 Synergistic interactions between SIGNUM and PERACLEAN®5 under greenhouse conditions Concentration of SIGNUM (g L–1) 125
62.5
31.25
PERACLEAN®5 concentration (%) 0.5 1 1.5 0.5 1 1.5 0.5 1 1.5
24 h 0.908 a 0.839 ab 0.775 ab 0.660 b 0.696 b 0.964 a 0.916 a 0.776 ab 0.688 ab
Ratio of inhibition (RI) 48 h 1.022 a 0.839 ab 0.775 ab 0.660 b 0.696 b 0.917 a 0.916 a 0.776 b 0.860 ab
120 h 0.795 a 0.719 ab 0.775 ab 0.824 b 0.696 b 0.917 a 0.916 a 0.776 ab 0.860 ab
Values followed by the same letter in each column are not significantly different from each other according to Tukey’s test at P≤0.05.
and B. cinerea (Elbouchtaoui et al. 2015), Monilinia laxa and Rhizopus stolonifer (Mari et al. 2004) and many other pathogens. However, to have a fungicide effect, 1.5 to 2% of a mixture based on 5% of PAA is needed. Even if this concentration may suppress the pathogen, it may cause severe damages when applied to the plant. In addition, the rapid decay of those products limits their application as a biofungicide (Pedersen 2015). To cover these products limitations, we described in this study, a new Integrated Pest Management program (IPM) based on the combination of a commercially available peroxyacetic acid mixture (PERACLEAN®5) with two commonly used fungicides to control grey mold disease in tomato greenhouse. The obtained data showed that treatment with PERACLEAN®5 resulted in interested results in suppression grey mold disease, however, its fast biodegradability limits its use as biocide: When used alone, the PERACLEAN®5 efficiency decreases rapidly with time. After 5 days (120 h) of its application, new infections were observed in the rows treated with 0.5 and 1% of PERACLEAN®5, while in the row treated with 1.5% the infection rate remained stable at 37.5%. Even if this concentration of PERACLEAN®5 permits a good control of B. cinerea with a persistent action, it may
cause severe damages to the plant by provoking burns on leaves. When combined with the fungicides (SWITCH or SIGNUM), the effectiveness period was longer with no loss of activity observed even after 5 days of the application. On the other hand, SWITCH fungicide permits a better control of grey mold disease than SIGNUM followed by PERACLEAN ®5. When combined with the latter, the efficiencies of both fungicides were enhanced. The treatment providing the maximum control of B. cinerea was the result mixture of ×1/4 of the recommended concentration of SWITCH (15 g L –1) with 0.5% of PERACLEAN ®5 followed by ×1/2 of the advised dose of SIGNUM with 1.5% of PERACLEAN®5. These two mixtures suppressed respectively 85 and 78% of gray mould infection. In order to better understand the mode of action of these mixtures, interaction trials were conducted. The results showed that the synergy levels are strongly dependent on the ration of components in the mixture and that minimum amounts of the components give a maximum synergy levels, which is in concordance with the results reported in Gisi (1996) that the synergistic interactions always decrease rapidly with increasing control levels of the single component and maybe almost nil at high control levels. When
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PERACLEAN®5 was combined with the recommended dose of SWITCH (60 g L–1), a slight antagonistic interaction was observed. Using 30 g L–1 of the fungicide, a synergistic interaction between the two products was observed and with 15 g L–1, a synergistic to highly synergistic interaction was expressed. The highly synergistic effect was obtained when combining 15 g L–1 of SWITCH with 0.5% of PERACLEAN®5. Concerning SIGNUM and PERACLEAN mixtures, a slight antagonistic effect was observed between both products. This interpretation of the antagonistic and synergistic interaction between PERACLEAN ®5 and SWITCH or SIGNUM was based upon the common definition of the synergism where it’s considered as a joint action of mixture components in which the total effect is greater than the sum of the effects of the individual components (Gisi 1996). In our study, this definition may be an underestimation of the obtained results since our goal is to enhance the efficiency of the synthetic pesticide while minimizing the applicable amount without taking into consideration the effect of the organic sanitizer. Based on the terminology of Gaddum (1959), where a synergism is declared when the effect of the mixtures exceeds the effect of its more potent component, our results reveal remarkable synergistic effects when combining PERACLEAN®5 with both synthetic fungicides which allowed suppressing grey mould disease with higher efficiency.
5. Conclusion In this work, the efficiency of a fungicide/organic sanitizer mixture to control grey mold disease caused by B. cinerea was described in order to exploit their additive and synergistic interaction, by which the overall activity is increased and the concentration of the pesticide can be reduced without loss of activity. As a conclusion, the combination of an organic peroxyacetic acid preparation (PERACLEAN®5) with two synthetic fungicides (SWITCH or SIGNUM separately) enhances the efficiency of both products while minimizing the amount of pesticides needed to control B. cinerea in the greenhouse conditions. This study allowed us to define the optimum ration of the components (PERACLEAN®5 and SWICH or SIGNUM) in the mixture to achieve the highest control levels of grey mould. This optimum was obtained by mixing 15 g L–1 of SWITCH with 0.5% of PERACLEAN®5. The later combination resulted in suppression of 85% of B. cinerea infections while decreasing the recommended dose of this fungicide by 75% reducing then the well known negative impacts of chemical pesticides on environment and consumer’s health. In SIGNUM case, the recommended mixture will be the combination of 31.25 g L–1 of the fungicide with 0.5% of PERACLEAN®5, which suppress 66.7% of the disease. This mixture resulted in similar results than these
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obtained with the recommended concentration of SIGNUM while minimizing the applicable amount of pesticide by 75%.
References Abbott W S. 1925. A method of computing the effectiveness of an insecticide. Journal of Economic Entomology, 18, 265–267. Ajaanid I. 2016. Les méthodes de culture de la tomate sous abri. [2017-06-17]. http://www.agrimaroc.ma/les-methodesde-la-culture-de-la-tomate-sous-abri/ (in French) Al Hattab M, Ghaly A. 2012. Disposal and treatment methods for pesticide containing wastewaters: Critical review and comparative analysis. Journal of Environmental Protection, 3, 431–453. Alvaro J E, Moreno S, Dianez F, Santos M, Carrasco G, Urrestarazua M. 2009. Effects of peracetic acid disinfectant on the postharvest of some fresh vegetables. Journal of Food Engineering, 95, 11–15 Amini J, Farhang V, Javadi T, Nazemi J. 2016. Antifungal effect of plant essential oils on controlling Phytophthora species. Plant Pathology Journal, 32, 16–24. Andersson H, Tago D, Treich N. 2014. Pesticides and health: A review of evidence on health effects, valuation of risks, and benefit-cost analysis. In: Blomquist G, Bolin K, eds., Preference Measurement in Health in the Series of Advances in Health Economics and Health Services Research. Emerald Group Publishing, UK. p. 62. Ayoub F, Ben oujji N, Chebl, B, Ayoub M, Hafid A, Salghi R, Jode S. 2017. Antifungal effectiveness of fungicide and peroxyacetic acid mixture on the growth of Botrytis cinerea. Microbial Pathogenesis, 105, 74–80. Baldr M G C. 1983. The bactericidal, fungicidal and sporicidal properties of hydrogen peroxide and peracetic acid. Journal of Applied Microbiology, 54, 417–423. Ben-Shaloma N, Ardia R, Pintoa R, Akib C, Fallik E. 2003. Controlling gray mould caused by Botrytis cinerea in cucumber plants by means of chitosan. Crop Protection Journal, 22, 285–290. Bernardes M, Pazin M, Pereira L, Dorta D. 2015. Impact of pesticides on environmental and human health, toxicology studies. In: Andreazza C A, ed., Cells, Drugs and Environment. InTech, Croatia. pp. 195–233. Bernet C, Garcia V, Bimar M C, Colombini N, Denis M A, Elie C, Forissier M F, Pineau L, Prognon P, Rauwel G, Vincent A, Volckmannn C. 2005. Peracetic acid: Activities and uses in health institutions. Coordination Center for the Control of Nosocomial Infections in the South-East InterRegion (C.CLIN South-East). Lyon-Sud Hospital Center 1 M PIERRE-BENITE Cedex Version of 20/01/05. p. 72. (in French) Camili E C, Benato E A, Pascholati S F, Cia P. 2010. Fumigation of ‘itália’ grape with acetic acid for postharvest control of Botrytis cinerea. Revista Brasileira de Fruticultura, 32, 436–443. (in Portuguese) Carrasco G, Urrestarazu M. 2010. Green chemistry in protected
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Fatima Ayoub et al. Journal of Integrative Agriculture 2018, 17(6): 1401–1408
horticulture: The use of peroxyacetic acid as a sustainable strategy. The International Journal of Molecular Sciences, 11, 1999–2009. Chesworth J C, Donkin M E, Brown M T. 2004. The interactive effects of the antifouling herbicides Irgarol 1051 and Diuron on the seagrass Zostera marina (L.). Aquatic Toxicology, 66, 293–305. Daferera D, Ziogas B, Polissiou M. 2003. The effectiveness of plant essential oils on the growth of Botrytis cinerea, Fusarium sp. and Clavibacter michiganensis subsp. michiganensis. Journal of Crop Protection, 22, 39–44. Ehi-Eromosele C O, Nwinyi O C, Ajani O O. 2013. Integrated Pest Management, Weed and Pest Control - Conventional and New Challenges. InTech, Croatia. Elbouchtaoui M C, Chebli B, Errami M, Salghi R, Jodeh S, Warad I, Hamed O, El Yamlahi A. 2015. Efficiency antifungal of perydroxan for Botrytis cinerea and Penicillium digitatum. Journal of Materials and Environmental Science, 6, 1938–1943. (in French) FAO (Food and Agriculture Organization of the United Nations). 2012. Integrated Pest Management (IPM). http://www.fao. org/agriculture/crops/thematic-sitemap/theme/spi/scpihome/managing-ecosystems/integrated-pest-management/ en/ Gaddum J H. 1959. Pharmacology. 5th ed. Oxford University Press, London. p. 587. Gisi U. 1996. Synergistic interaction of fungicides in mixtures. Phytopathology, 86, 1273–1279. Heydari A, Pessarakli M. 2010. A review on biological control of fungal plant pathogens using microbial antagonists. Journal of Biological Sciences, 10, 273–290. Kitis M. 2004. Disinfection of wastewater with peracetic acid: A review. Environment International, 30, 47–55. Li X P, Fernández-Ortuño D, Chen S N, Grabke A, Luo C X, Bridges W C, Schnabel G. 2014. Location-specific fungicide resistance profiles and evidence for stepwise accumulation of resistance in Botrytis cinerea. Plant Disease Journal, 98, 1066–1074. Liu H M, Guo J H, Cheng Y J, Luo L, Liu P, Wang B Q, Deng B X, Long C A. 2010. Control of gray mold of grape by Hanseniaspora uvarum and its effects on postharvest quality parameters. Annals of Microbiology, 60, 31–35. Mari M, Gregori R, Donati I. 2004. Postharvest control of Monilinia laxa and Rhizopus stolonifer in stone fruit by peracetic acid. Postharvest Biology and Technology, 33, 319–325.
McDougall P. 2016. The Cost of New Agrochemical Product Discovery, Development and Registration. Midlothian: Phillips McDougall. April 2016. CLA/ECPA/CropLife R&D Survey. Nigro F, Schena L, Ligorio A, Pentimone I, Ippolito A, Salerno M G. 2006. Control of table grape storage rots by pre-harvest applications of salts. Postharvest Biology and Technology, 42, 142–149. Ossia-Ongagna Y, Sabatier R. 1993. Comparison of in vitro activity of six disinfectants on bacteria from contamination in hemodialysis water. Journal de Pharmacie de Belgique, 48, 341–351. Pedersen L F, Jokumsen A, Larsen V J, Henriksen N H. 2015. Peracetic acid products expand sanitizing, organic water treatment options. Global Aquaculture Advocate, 66–67. Romanazzi G, Mlikota Gabler F, Smilanick J L. 2006. Preharvest chitosan and postharvest UV-C irradiation treatments suppress gray mold of table grapes. Plant Disease Journal, 90, 445–450. Soliman H M, El-Metwally M A, Elkahky M T, Badawi W E. 2015. Alternatives to chemical control of grey mold disease on cucumber caused by botrytis cinerea Pers. Asian Journal of Plant Pathology, 9, 1–15. Suprapta D. 2016. A review of tropical plants with antifungal activities against plant fungal pathogens. Preprints, doi: 10.20944/preprints201610.0049.v1 Todorović B, Potočnik I, Rekanović E. Stepanović M, Kostić M, Ristić M, Milijašević-Marčić S. 2016. Toxicity of twentytwo plant essential oils against pathogenic bacteria of vegetables and mushrooms. Journal of Environmental Science and Health, 51, 832–839. Venditti T, D’Hallewin G, Dore A, Molinu M G, Fiori P, Angiolino C, Agabbio M. 2008. Acetic acid treatments to keep postharvest quality of “Regina” and “Taloppo” table grapes. Communications in Agricultural and Applied Biological Sciences, 73, 265–271. Vitoratos A, Bilalis D, Karkanis A, Efthimiadou A. 2013. Antifungal activity of plant essential oils against Botrytis cinerea, Penicillium italicum and Penicillium digitatum. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 41, 86–92. Xu W T, Huang K L, Guo F, Qu W, Yang J J, Liang Z H, Luo, Y B. 2007. Postharvest grapefruit seed extract and chitosan treatment of table grapes to control Botrytis cinerea. Postharvest Biology and Technology, 46, 86–94.
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