Among the most economically important fruit crops in South and North Kyrgyzstan affected by scab disease are apples ( Malus domestica). Natural isolates of Venturia inaequalis were isolated from diseased parts of apple trees, selected from different regions, through sedimentation of air microflora on the crowns of fruit trees. Two biocontrol agents as Trichoderma viride and Streptomyces sр. were tested for apple scab control in vitro and field conditions. Two applications of Trichoderma viride within 35 days completely stopped the scab disease in seedling leaves. Within 40 days, the seedlings were recovered; the new leaves have blossomed on branches. The Streptomyces sp. antagonists were inferior in effectiveness compared to Trichoderma viride; nevertheless, they prevented progression of the disease in the leaves. Seedlings grew new shoots and leaves around 50 days after the second treatment. Orchard experiment results provide great hope that a biological product based on Trichoderma viride could work as an effective agent to suppress the development of the pathogen in the early spring, when leaves start to show scab disease symptoms.
Among the economically most important fruit crops in South and North Kyrgyzstan affected by scab disease are apples (Malus domestica). In 2015, 16,189 hectares of gardens in Kyrgyzstan were surveyed, of which 4643 hectares were infected by scab disease. During the most intensive development period, this disease affected 5% - 55% of trees and 1% - 56% of their fruits; 1267 hectares of garden were treated by chemical fungicides [
Venturia inaequalis (Cooke Wint) is the causal agent, affecting the leaves and fruit tissue of trees. The pathogen was placed into the genus Venturia by Winter in 1880. These historical accounts and the genus’ taxonomy have been reviewed by MacHardy [
In the presence of moisture, the pathogen ascospores germinated on the leaves, breaking the thin surface epithelium of young leaves. Upon contact with a cuticle, the germ tube is differentiated into an appressorium and produces adhesive mucilaginous substances, assumed to be used to facilitate attachment to the host surface [
Then, an intermittent cycle of secondary infections can begin, through newly developing conidiophores. As a rule, after secondary and third infections, scab disease reaches maximum intensity. Further development of the disease depends on atmospheric humidity. Summer drought suppresses the development of scab disease; conidiophores quickly lose their ability to germinate and infect the leaves. Full development of the parasitic phase scab pathogen ends with the cessation of growth of the apple trees, when the leaves are falling and the fungus again enters a saprophytic way of life. Weather conditions-temperature and humidity in particular-are important for the development of apple scab disease, especially in the first half of the growing season [
Once an infection is established, curative preparations are required to stop further development of the mycelium. In organic apple-growing, scab disease control is focused on the protective use of sulphur, lime sulphur and copper. Additional sprays of lime sulphur during the germination period of the scab fungus are applied during severe infection periods. These specific applications are difficult to schedule, as the time period for the application is often short and in most cases these sprays have to be performed during rainfall and at night [
Pseudomonas syringae (isolate 508) prevented spore germination and effectively suppressed scab disease to a level comparable to that provided by the fungicide, captan. This isolate provided greater suppression of apple scab disease than did other pathogenic isolates of P. syringae, isolated from various crops [
Objectives of our study were 1) to study the biology and spread of V. inaequalis on apple trees, 2) to select possible antagonists to suppress sporulation of the pathogen, 3) to test selected antagonists under field conditions.
The diseased organs (leaves, shoots, buds and fruits) of different varieties of apple (Malus domestica M.) were selected in the orchards and fruit farms of the Chui and Issyk-Kul provinces (
Time of sampling | Sampling place | Species of plants | Plant organs |
---|---|---|---|
The end of April and May, 2014 and 2015 | Botanical garden named after Gareev, the city of Bishkek | Different varieties of apples | Young buds; leaves with symptoms |
The end of May, 2014 and 2015 | Orchards of Issyk-Kul province | Different varieties of apples | Young buds; leaves with symptoms |
September-October, 2015 | Orchards of Issyk-Kul and Chy provinces | Young nursery stock of apple varieties | Affected shoots and leaves |
pathogen (Venturia inaequalis (Cooke) Wint).
A sample consisted of different plant parts selected from one tree. Each sample contained at least five copies of plant parts with disease symptoms (the affected leaves, ovary, young shoots, the slices of damaged tissue branches and trunks), which were placed in a safe package with a label with the name of the culture, varieties, age, place, time of collection and an indication of the type of lesion.
Samples were placed in a 150 ml container with a lid, before a 30 ml phosphate buffer or phosphate-buffered saline was added. The container was placed on a rotary shaker and then incubated at 200 rev/min from 1.0 to 1.5 hours. For samples with symptoms, the appropriate amount of macerate was selected for qualifying analysis. For asymptomatic samples, a suspension concentrated by centrifugation was used. The sample was also frozen at −18˚C. Macerate was carefully poured directly into a 50 ml centrifuge tube, leaving the pulp in a container or pre-filtered through filter paper, then centrifuged for 10 minutes at 8000 g and for 15 minutes at an acceleration of 7000 g, at a temperature below 10˚C. The supernatant was discarded without damaging the sediment. The pellet was resuspended in 1 ml of phosphate buffer and transferred to a sterile microtube.
The following culture media were used for the primary isolation of scab pathogens:
1) Potato agar (g/distilled water): potatoes―200 g; Agar―15 g; water―1 L; pH―6.2;
2) Apple agar: chopped apple fruit weight―200 g; Agar―15.0; water―1 L; pH―6.5;
3) Czapek’s medium; pH―6.2;
4) Wort agar: wort―50 ml; agar―20 g; water―1.0 L; pH―6.5.
A special technique was used to determine the morphological features of Venturia inaequalis proposed by [
Biocontrol antagonistic microorganisms (Streptomyces and Trichoderma) from our laboratory collection were used in this study.
N.S. Egorov’s [
Also, the agar blocks method was used. Biocontrol antagonistic microorganisms (Streptomyces and Trichoderma) were plated onto the surface of the agar medium, formed during the growth of a continuous lawn in a Petri dish. Cultures are incubated at a suitable temperature for four to five days. Then, a sterile cork drill (6 - 8 mm diameter) was cut from the layer agar blocks and transferred to the surface of the agar medium, inoculated only that the test organism (Venturia inaequalis). Agar blocks were placed in increasing (lawn) up at an equal distance from each other and from the edge of the cup, connected tightly to the agar plate.
The potential of candidate antagonists to suppress the conidia production of Venturia inaequalis on infected leaves was tested on the local “Aychurok” variety of apple seedlings, highly susceptible to scab disease. Seedlings were sprayed with conidial suspensions of Venturia inaequalis (1 × 105 ml−1) until runoff and placed in a moist chamber consisting of a plastic tray enclosed by a transparent plastic top. After two days of incubation at 15˚C with diffuse light, the tops were removed from the trays and seedlings were further incubated for five days at 85% RH, 15˚C and with 16 hrs light per day. Thereafter, V. inaequalis-inocu- lated seedlings were sprayed with antagonist suspensions (containing 1 × 106 spores or cells ml−1) or water (containing 0.01% Tween 80) as control. Two seedlings were used for each replicate of each treatment. Touching of leaves of neighbouring plants or the polyethylene was avoided. Seedlings were grown for nine to 12 days at 15˚C, with 16 hrs light per day at 138 µE・s−1・m−2. From both seedlings of each replicate, the youngest five true leaves were carefully removed and put into Duran bottles (100 ml) containing 35 ml of tap water with 0.01% Tween 80. Bottles were shaken with a flask shaker and the concentration of conidia of V. inaequalis was determined for each suspension with the aid of a haemocytometer [
Two rows of three-year-old apple trees of the Aychurok variety were used to test the antagonists in the Plant Research field at the Agriculture Faculty, KTU Manas, and Bishkek. For each experiment, two to four trees in two replicates were used. Within each replicate, two treatments were carried out.
Data were analysed following the GLIM program of the Royal Society of London [
The scab pathogen infection cycle begins in spring, when appropriate temperature and humidity promote the release of ascospores. These spores are released into the air, on the ground and onto the surface of the sensitive tree, where they germinate and form a germ tube that can directly penetrate the waxy cuticle of the plant. Natural isolates of Venturia inaequalis were isolated by sedimentation of air microflora on the crown of fruit trees in April.
The cultural and physiological characteristics of the selected natural isolates were studied on the Czapek’s agar, the apple agar and wort agar mediums and incubated at a temperature of 18˚C - 28˚C. A rapid growth of pathogen colonies on the first day was observed in apple agar. Young colonies were fluffy, light brown in colour, growing on the radial radiant. With maturation, the colony colour changed to milky brown and the texture also changed; it became more homogeneous and dense. The microscopy has shown that the colonies growing on apple fruits are thin, with a pale yellow septate mycelium and oval/round conidia, transparent and pale yellow in colour. The conidiophores had interwoven to form clusters. This is the pathogen’s asexual reproduction stage, i.e., conidia generation continues throughout the summer, until the fall of the tree leaves and fruits at the beginning of winter. This cycle is called a secondary infection (
On the second day after planting on the Czapek’s medium, isolates of Venturia inaequalis began to grow at high speed. Young colonies were dense, with a cotton-like texture and white in colour, while mature colonies became a darker colour and smoother. Microscopy of the colonies growing on the Czapek’s
medium for three days identified longitudinally extending colourless conidiophores; conidia were dark in colour and oblong-circular in shape (
Venturia inaequalis isolates formed soft, fluffy and thick white colonies on the wort medium. However, compared with the growth on the Czapek’s and apple fruit mediums, the wort medium pathogen showed weak growth, although the growth did not stop. Under the microscope, multicellular, thin and colourless mycelium was observed (
To study the phenotypic characteristics of Venturia inaequalis isolates disaccharides as carbon sources, glucose, cellulose, mannitol and sorbitol were used. Natural isolates of Venturia inaequalis were able to utilize the glucose and cellulose, changing the colour of the liquid medium (with indicator) to red and the mannitol and sorbitol to yellow.
For the development of environmentally friendly local control measures against scab pathogen of fruit trees, the biotests were conducted using soil actinomycetes and Trichoderma virida against Venturia inaequalis. The following actinomycetes strains were used as antagonists: Streptomyces sр. С1-4; Streptomyces sр. Pr-3; Streptomyces sр. KK-4; Streptomyces sр. K-4; Streptomyces sр. K-7; Streptomyces sр. SK-3.3, Streptomyces sр. PАТ-3. Antagonist activity is measured by size of the lysis zones of the test object in mm (
As the results have shown, the antagonistic activity of Streptomyces strains against Venturia inaequalis was different. The C1-4 strain showed a strong antifungal effect against the phytopathogens; a lysis zone was 10.0 mm after 96 hours.
The Streptomyces strains, such as PAT-3 and Pr-3, inhibited the growth of the pathogen culture, using its colonies as a source of nutrients. Other strains, such as Streptomyces KK-4, K-4 and SK-3.3 were not active against Venturia inaequalis (
Two strains (Streptomyces sp. C1-4 and Streptomyces sp. PAT-3) with strong antagonistic and hyper-parasitic effects were selected for the experiment in a liquid medium. A liquid culture of these antagonists was cultivated with Venturia inaequalis for 48 hours.
The microscopy study of a liquid culture showed a clear picture of the destruction of plant pathogenic conidia and conidiophores, as well as, attached to them, the branched mycelium and spores of antagonists-Streptomyces. The hyper-parasitism mechanism is accurately tracked through these micro-pictures (
Five days after artificial infection of highly susceptible apple seedlings of the local “Aychurok” variety, the first symptoms of the disease emerged on the youngest leaves: oil spots on the leaves’ surfaces. After seven days, necrotic or chlorotic lesions were noted on the edges of the leaves (
The antagonistic strains | Activity, lysis zone, mm | |||
---|---|---|---|---|
24 h | 48 h | 72 h | 96 h | |
Streptomyces sр. C1-4 | 0.3 ± 0.01 | 0.5 ± 0.02 | 0.8 ± 0.02 | 10.0 ± 0.02 |
Streptomyces sр. Pr-3 | 0.1 ± 0.01 | 0.1 ± 0.01 | 0.3 ± 0.01 | Hyper-parasitism |
Streptomyces sр. KK-4 | The force between two cultures is equal | The force between two cultures is equal | The force between two cultures is equal | The force between two cultures is equal |
Streptomyces sр. K-4 | Shows no activity | Shows no activity | Shows no activity | Shows no activity |
Streptomyces sр. K-7 | 0.1 ± 0.01 | 0.3 ± 0.01 | The force between two cultures is equal | The force between two cultures is equal |
Streptomyces sр. SK-3.3 | The force between two cultures is equal | Shows no activity | Shows no activity | Shows no activity |
Streptomyces sр. PAT-3 | Strong activity | 0.2 mm | 0.4 mm | Hyper-parasitism |
Trichoderma virida | Strong activity | Hyper-parasitism | Hyper-parasitism | Hyper-parasitism |
Five leaves from each tree were stripped and placed in 100 ml of sterile water. After shaking for one hour, 1 ml of suspension was planted on the nutrient media. Direct microscopy (1000×) of the diseased leaves and the colonies growing on the medium has found mycelium, conidia and conidiophores of the pathogen (
After the appearance of visible signs of the disease, seven days after infection, the seedlings’ leaves were abundantly treated with antagonist cultures. Ten days after the first treatment with antagonist cultures, five leaves of the apple seedling were removed for microscopy and planting on the relevant mediums. Pathogen colonies on a single leaf were counted and the average number of colonies was calculated (
As
On the leaves of seedlings which had been sprayed with Trichoderma virida suspension (1 × 106 conidia ml−1), conidia production of the pathogen decreased sharply, up to 30% after five days, reducing by up to 80% after 10 days in comparison with control seedlings. After 15 days. a second treatment was carried out. 25 and 35 days after the second treatment the number of pathogen conidia had reduced by up to 90% and 95% respectively (
There has been a pattern of preventing the progression of the disease caused by V. inaequalis. Before the use of antagonists, the diseased seedlings had an average of three to four infected leaves, with either a single necrotic lesion or several lesions scattered over the leaf’s surface. After the first and second treatments with Trichoderma virida, the number of infected leaves had not increased and progression of the disease had completely stopped.
When Streptomyces sp. C1-4 was used in some leaves, there was still some
disease progression. So, while tested Streptomyces sр. C1-4 strains have statistically significantly reduced conidia of V. inaequalis, their efficiency was lower than that of Trichoderma virida. Streptomyces sр. С1 strain has caused a significant reduction of V. inaequalis on leaves, which could be repeated in subsequent independent experiments.
To determine the shelf life of antagonist spores on the leaf surfaces of seedlings after treatment, the treated leaves of seedlings were removed and relocated to the surface of culture media with outer and inner surfaces. The leaves were treated with Streptomyces sp. C1-4 and planted on an ammonium starch medium (for actinomycetes), while the leaves treated with Trichoderma virida were planted on a Czapek’s medium.
The intensity and density of antagonist colonies growing around the leaves in the mediums showed their persistence on leaf surfaces after treatment. The longer they remained on the surface of diseased leaves, the greater their probability of being able to suppress the development of the pathogen.
Results have showed that the conidia of Trichoderma virida were obtained between 10 and 50 days after the second treatment, encouraging intensive growth around the leaves planted on the Czapek’s medium (
Due to this effect, two applications of Trichoderma virida within 35 days completely stopped the disease in seedling leaves. After 40 days, the seedlings had recovered, with new leaves and some damaged leaves which remained on the crown continuing to function normally (
virida; nevertheless, it prevented the progression of the disease on the leaves. Seedlings continued to grow new shoots and leaves 50 days after the second treatment (
In the case of applying a biological product based on Streptomyces sp. C1-4; after the second treatment, Streptomyces sp. C1-4 spores remained on the leaf surfaces of seedlings for between 10 and 25 days. During this period, the spores of the antagonist agent grew slowly, but this encouraged dense actinomycetes growth around the leaves planted on the medium (
Two rows of three-year-old Aychurok apple trees were used to test the antago-
nists in the field. For each experiment, three trees were used (replicates). In the experimental and control plots, the trees were sprayed with a conidia suspension of the pathogen V. inaequalis (1 × 107 conidia / ml) after the complete opening of the leaves and before flowering. After seven days, disease symptoms started to appear on the leaves of the apple trees (
Immediately after the appearance of these symptoms, the diseased leaves of trees in experimental plots were sprayed with a conidia suspension of Trichoderma virida (1 × 107 conidia/ml) and a spore suspension of Streptomyces sp. C1-4 (1 × 108 spor/ml) until runoff at the bottom and upper side of the leaves. Treatment was carried out on a bright day after 17 hours; the air temperature was 18˚C - 20˚C. The disease development was monitored until 40 days after artificial infection was conducted. The damaged leaves and appearance of new leaves with disease symptoms were monitored. The development of the disease on leaves stopped 35 - 37 days after first treatment with the Trichoderma virida antagonist suspension, so that the damaged sections on the leaves did not change size further and the number of new leaves with diseased symptoms did not increase (
Young leaves were quickly exposed to the pathogen, which penetrated their thin cell walls. The matured apple leaves demonstrated ontogenic resistance, because the pathogen growth was suppressed immediately after cuticle penetration and appearance of the disease’s symptoms was delayed [
Biological agents seem to contribute to the strengthening of protective responses and triggered a cascade of antipathogenic mechanisms on the part of the plant body. During the spring, observation of trees treated with Trichoderma viride revealed a sharp decrease in scab disease symptoms. According to Hinze and Kunz [
After seven days, scab symptoms appeared on the leaves of trees in laboratory pots. After 10 days of infection, when the disease’s symptoms had sufficiently developed, apple trees were sprayed with the culture of the antagonists. The climatic conditions were suitable for Trichoderma viride as fungus-antagonist (humidity, 70% - 80%, temperature, 18˚C - 20˚C). When using Trichoderma viride, the disease’s progression stopped for 20 days after the first treatment. Necrotic lesions on leaves decreased; some of them started to show visible recovery and resumption of normal function. Trichoderma conidia remained on the surface of the leaves after a single application for 20 - 25 days. If the weather in spring had been dry, different results would have been obtained. Nevertheless, these results provide great hope that a biological product based on Trichoderma viride could work as an effective agent to suppress the development of the pathogen in the early spring, when leaves start to show scab disease symptoms.
There was no sufficiently favourable condition for the development of the second antagonist agent, Streptomyces, as it prefers dry weather rather than wet.
Efficiency of Streptomyces sp. C1-4 was not high in field conditions, although the disease progressed more slowly than in the controls. Self-sustained survival of spores on the surface of the leaves was short; after 12 days, the spores were not detected. They were been superseded by other microorganisms and by pathogenic fungi in the epiphytic microflora of leaves. However, in dry years, the repeated use of this agent could be used to provide a biocontrol against scab di- sease.
The general conclusion of this study is that Trichoderma viride, used multiple times, could replace copper and other treatments and could be developed as an alternative strategy of treatment in organic orchards.
Doolotkeldieva, T. and Bobusheva, S. (2017) Scab Disease Caused by Venturia inaequalis on Apple Trees in Kyrgyzstan and Biological Agents to Control This Disease. Advances in Microbiology, 7, 450-466. https://doi.org/10.4236/aim.2017.76035