A Technique for the Prevention of Greenhouse Whitefly (Trialeurodes vaporariorum) Using the Entomopathogenic Fungus Beauveria bassiana M130
A Technique for the Prevention of Greenhouse Whitefly (Trialeurodes vaporariorum) Using the Entomopathogenic Fungus Beauveria bassiana M130
Journal of Microbiology and Biotechnology. 2014. Jan, 24(1): 1-7
Copyright © 2014, The Korean Society For Microbiology And Biotechnology
  • Received : June 13, 2013
  • Accepted : September 03, 2013
  • Published : January 28, 2014
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About the Authors
Chang-Su Kim
Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea
Jung-Bok Lee
Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea
Beam-Soo Kim
Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea
Young-Ho Nam
Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea
Kee-Sun Shin
Biological Resource Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 305-600, Republic of Korea
Jin-Won Kim
Yecheon Agriculture Technology Center, Yecheon 757-802, Republic of Korea
Jang-Eok Kim
School of Applied Biosciences, Kyungpook National University, Daegu 702-701, Republic of Korea
Gi-Seok Kwon
Department of Bioresource Sciences, Andong National University, Andong 760-749, Republic of Korea

The possibility of using hyphomycete fungi as suitable biocontrol agents against greenhouse whitefly has led to the isolation of various insect pathogenic fungi. Among them is Beauveria bassiana , one of the most studied entomopathogenic fungi. The objective of this study was to use B. bassiana M130 as an insecticidal agent against the greenhouse whitefly. M130 isolated from infected insects is known to be a biocontrol agent against greenhouse whitefly. Phylogenetic classification of M130 was determined according to its morphological features and 18S rRNA sequence analysis. M130 was identified as B. bassiana M130 and showed chitinase (342.28 units/ml) and protease (461.70 units/ml) activities, which were involved in the invasion of the host through the outer cuticle layer, thus killing them. The insecticidal activity was 55.2% in petri-dish test, 84.6% in pot test, and 45.3% in field test. The results of this study indicate that B. bassiana has potential as a biological agent for the control of greenhouse whitefly to replace chemical pesticides.
The interdependence of global markets for agricultural products is necessary for the development of agricultural practices while, simultaneously, it can mitigate negative side effects on the environment. As a result, agricultural products are safer for human consumption; however, loss of agricultural products has increased because of insects, plant diseases, and weeds. This potential loss of production is up to 40% [25] despite a marked increase in pesticide use; thus, crop losses have remained relatively constant [18] .
On this account, insect pest control has relied mostly on chemical insecticides since the late 1940s. Chemical controls have not only improved agricultural productivity, but can also lead to efficient cultivation. Thanks to such controls, the productivity of crops worldwide has been improved. There are also, however, serious side effects such as groundwater and soil pollution, and ecocide. To solve these problems, many advanced countries have instituted the use of biological control agents. Biological control is a method of controlling pests using other living organisms and the extraction of natural products. It relies on predation, parasitism, or other mechanisms, and there are many types. Recently, some commercial bioinsecticides have been developed and registered to control diamondback moth, beet armyworm, oriental tobacco budworm, greenhouse whitefly, and root knot nematodes [15] .
Entomopathogenic fungi have been recognized as important natural enemies of insect pests and can be used as effective biological control agents against agricultural pests. Entomopathogenic fungi are usually identified based on fungal growth observed on insect cadavers. Most research on entomopathogenic fungi, however, has been aimed at their development as biological control agents of insects, mites, and ticks, despite their great potential for use in conservation and classical biocontrol strategies. This is normally achieved through a strategy in which pest control relies on the action of the released agent but not on successive generations of the fungus. Under this paradigm, over 170 products have been developed based on at least 12 species of fungi [8] . Despite the fact that there are an estimated 700 species of entomopathogenic fungi in approximately 90 genera [21] , most commercially produced fungi are species of Beauveria , Metarhizium , Lecanicillium , and Isaria that are relatively easy to mass produce [28] . Among these, Beauveria bassiana is a fungus with a broad natural distribution. Its potential to control more than 70 insect pests has been responsible for a substantial increase in the large-scale production of the fungus for applications in the field [26] . Beauveria bassiana infects the host insect by penetrating the cuticle. The fungal conidium attaches to the cuticle and then germinates. Germinating conidia produce extracellular enzymes such as lipases, chitinases, and proteases to initiate cuticle invasion. Once inside the host, the fungus develops as a yeast-like form, producing metabolites that inhibit the insect’s immune system, modify the insect’s behavior, or act as post-mortem antibiotics against competing microorganisms [11 , 29] . After death, the fungus reverts to a filamentous form and typically digests the remaining internal organs, leaving only the chitin and protein exoskeleton [6 , 13] . Moreover, this fungus appears to be harmless to most non-target organisms.
Suspensions of conidia are spread by spray applications for the control of insect pests and require improved dispersion. To improve dispersion, hydrophobic conidia are often formulated in oil or added to spray mixes containing wetting agents as adjuvants. Since spore persistence of fungi on the foliar surface is affected by solar radiation, considerable effort has focused on the protection of these entomopathogens by incorporating solar blockers and sunscreens [14] .
Meanwhile, the greenhouse whitefly ( Trialeurodes vaporariorum ) has been focused on as a major harmful insect in many countries [2 , 4] . Adults and immature flies are phloem feeders and reduce productivity of agricultural products. Furthermore, they produce large amounts of honeydew on the leaf and this honeydew reduces leaf photosynthesis [3] . Crops in the families Cruciferae, Leguminosae, Malvaceae, and Solanaceae are mainly targeted [2] . Tomato, cucumber, and tobacco, which are cultivated widely in Korea, are also seriously affected by the greenhouse whitefly. These insects have been controlled primarily using various chemical insecticides [12 , 20] . However, the greenhouse whitefly continues to constitute a major problem on crops because insecticide-resistant populations have developed [5 , 20] .
Thus, the objective of this study was to effectively control the greenhouse whitefly using entomopathogenic fungi. To achieve this goal, a strain with a high pathogenicity was isolated from infected insects. The phylogenetic relationships of selected entomopathogenic fungi were analyzed. Additionally, proteolytic enzyme and chitinase enzyme activities, which are involved in insect pathogenicity, were measured. Finally, a bioassay was conducted in order to investigate the potential of the control agent.
Materials and Methods
- Microorganism
Beauveria bassiana M130 was isolated from an infected insect. It was stocked at -80℃ in 30% glycerol containing sterile 0.1% Tween 80 and mineral oil. The fungal strain was cultured on potato dextrose agar (PDA; Difco, USA) at 28℃ for 8 days and stored at 4℃ until use.
- Identification of Beauveria bassiana M130
For identifying its phylogenetic classification, the morphological features of M130 were determined through the use of a light microscope (Olympus CX21, Japan), scanning electron microscope (Hitachi S-2500, Japan), and 18S rRNA sequencing.
- Chitinase Activity
Chitinase activity was determined by a modified dinitrosalicylic acid (DNS) method [17] . This method is based on the concentration of N -acetyl glucosamine (NAG) that is released as a result of enzymatic action [16 , 27] . The 2.5 ml reaction mixture contained 0.5 ml of 1% colloidal chitin in 1 ml of phosphate buffer (0.1M,pH7.0), and 1 ml of crude enzyme. The mixture was vortexed well and incubated in a water bath at 40℃ for 30 min. About 1 ml of the reaction was arrested by the addition of 3 ml of DNS reagent, followed by heating at 100℃ for 5 min. The colored solution was centrifuged at 10,000 rpm for 5 min and the absorption of the appropriately diluted test sample was measured at 545 nm using a UV Spectronic Genesys 5 (Milton Roy, USA) along with substrate and enzyme blanks. One unit of enzyme activity was defined as the amount of enzyme that catalyzed the release of 1 μM of N -acetyl-D-glucosamine per hour [9 , 24] .
- Protease Activity
A 0.6% (w/v) casein solution (prepared by mixing 6 mg/ml casein i n 1/15 p otassium p hosp hate b uffer a nd a djusting to pH 7.0 with 1 N NaOH; 3 ml) was incubated with 1 ml of enzyme at 30℃ for 10 min. It was then added to 0.4 M trichloroacetic acid (TCA) solution, which was incubated at 30℃ for 30 min. Afterwards, the product was centrifuged for 5 min at 10,000 rpm. To 0.5 ml of sup ernatant was added 1 .25 ml of 0 .4M Na 2 CO 3 and 0.25 ml of 2 N Folin. The final product was measured at 660 nm [1 , 9] . One unit of protease was defined as the amount of enzyme that released 1 μM of tyrosine per hour.
- Optimization of Culture Temperature
Spore suspension (1.0×10 6 conidium/ml) was inoculated into a 250 ml Erlenmeyer flask containing 50 ml of potato dextrose broth (PDB; Difco, USA), and the flasks were incubated at 23℃, 25℃, 28℃, and 33℃ at 130 rpm. The dry cell weight (DCW) of mycelia was measured at 48 h intervals on a regular basis for 8 days .
- Preparation of Beauveria bassiana M130 Conidia
An inoculum of conidia for liquid culture was obtained from a 14-day sporulated culture on a PDA plate at 28 ± 1℃. After 14 days of incubation at 28℃, sterile 0.1% (v/v) Tween 80 was poured onto the culture on the surface of the PDA and the conidia were collected by scraping the culture with a glass hockey stick and suspension-filtering using glass wool. The number of conidia in the spore suspension was counted using a hemocytometer (Superior, Germany). The filtrate was thoroughly vortexed and diluted to achieve a suspension of 1.0 × 10 6 conidia/ml.
- Incubation of Greenhouse Whitefly
Greenhouse whiteflies were bred on potted pepper at 28 ± 1℃ in a 16L/8D (L: light; D: darkness) photoperiod. All insects were grown on pepper leaves until use. All potted plants were covered with an insect rearing cage to prevent escape.
- Greenhouse Whitefly Pot Test
Tomato pots were prepared in an environment with a relative humidity of 85% and temperature of 28℃ or 30℃, and whiteflies were released in each pot. After 3 days, the spore concentration was adjusted to 1.0 × 10 8 conidia/ml to conduct the bioassay on the greenhouse whitefly. Greenhouse whiteflies were sprayed with spore suspension, and after 8 days, mortality rates were identified.
- Greenhouse Whitefly Field Test
The experiment was conducted in greenhouses to identify the greenhouse whitefly control effect of M130. To this end, a spore suspension was sprayed, and after 8 days, the greenhouse whitefly mortality rate was identified.
- Scanning Electron Microscopy
The samples were fixed for 1 h in a solution of glutaraldehyde (2.5% in 0.1 M phosphate buffer, pH 6.8), and then dehydrated in an ethanol gradient (50%, 60%, 70%, 80%, 90%, 95%, and 99.9%). In the next step, ethanol was replaced by CO 2 , followed by “criticalpoint drying”. In a sputter coating process, infected eggs, nymphs, and greenhouse whitefly were covered with a gold layer to increase their electrical conductivity.
Results and Discussion
- Selection of Beauveria bassiana
The fungal growth of five strains was evaluated and the results are shown in Fig. 1 . Results for measurements of enzyme activity are shown in Figs. 2 and 3 . Among the five selected strains, J157 and M130 showed similar fungal growth patterns over 4 days, but afterwards, M130 fungal growth was greater than that of J157.
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Mycelial growth of five strains at 28℃ for 8 days. Vertical lines indicate standard deviations.
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Chitinase activity produced by isolated strains. Vertical lines indicate standard deviations.
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Protease activity produced by isolated strains. Vertical lines indicate standard deviations.
Until day 2, the five strains did not show chitinase activity, but as time elapsed, J157 and M130 showed activity. However, strain J157 showed the maximal enzyme activity (63.74 unit/ml) at 2 days, which gradually decreased. M130 showed the maximal enzyme activity (342.29 unit/ml) at 6 days.
In the case of protease, all strains showed maximum enzyme activity at 2 days, and the activity gradually decreased. However, strain M130 maintained high enzyme activity after 4 days. Based on the above results, B. bassiana M130 was selected for use in this study.
- Identification of Beauveria bassiana M130
The selected strain, M130, was cultured in PDB at 25℃ to determine its phylogenetic classification and investigate its biochemical features. The mycelium color of M130 is white, the conidial shape is cylindrical, the spore size is 2.0-5.0 μm, and the appressorium is almost cylindrical ( Fig. 4 ). These results are similar to those of Stephen and Rehner [23] . The sequences could be identified in NCBI database. A comparative 18S rRNA gene sequence analysis revealed that strain M130 is the most closely related to members of the genus Beauveria . Moreover, in a neighbor-joining phylogenetic tree constructed on the basis of the 18S rRNA gene sequences, strain M130 also fell within the radiation of the cluster comprising the Beauveria species. Strain M130 exhibited 18S rRNA gene sequence similarity values of 100% with B. bassiana IMI 393155. Therefore, strain M130 was identified as B. bassiana M130 ( Fig. 5 ).
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Scanning electronic microscopy of strain M130 (× 200, 72 h). (A) The spores showed ellipsoidal morphology. (B) Isolated Beauveira bassiana M130 in petri dish state.
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Neighbor-joining tree based on 18S rDNA gene sequences, showing phylogenetic relationships between strain M130 and species from Beauveria. Numbers at nodes indicate levels of bootstrap support (%p) based on 1,000 resembled data sets; only values above 70% are given. Bar, 0.1 substitutions per nucleotide position.
- Optimization of Beauveria bassiana M130 Culture Temperature
The mycelial growth of B. bassiana M130 was examined at different temperatures for 8 days and the results are provided in Fig. 6 . The optimal temperature for mycelial growth was 28℃ and mycelial growth of B. bassiana M130 was best at 28℃. Previous studies [7] have shown that the optimal temperature for mycelial growth of B. bassiana is generally around 25-28℃ and the findings of the present study are consistent with these results.
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Effect of temperature on mycelial growth of B. bassiana M130 over 8 days. Vertical lines indicate standard deviations.
Sato et al . [22] implied that the optimal growth temperature of B. bassiana varies depending on the geographic origin of the isolate. B. bassiana isolated from Okinawa, the southernmost island and warmest region of Japan, exhibited the best growth at 30℃, whereas strains isolated in warmer regions tended to have higher optimal temperatures for mycelial growth. In contrast, Fargues et al . [7] observed no evident relationship between relative growth and climatic origin of B. bassiana isolates. B. bassiana M130 was isolated in Yecheon, Gyeongbuk. Yecheon is not a warmer region of Korea. Therefore, the B. bassiana M130 growth pattern was similar to that reported by Fargues et al . [7] .
- Bioassay
Pot test. Pot test results are shown in Fig. 7 . The control value increased with the number of applications of the biological control agent. With three applications, the maximal control value was up to 84.6%. Generally, B. bassiana spores are known to germinate best at 15-30℃ and a relative humidity of 80% [10] . In this study, the temperature was adjusted to 28℃ and the relative humidity to 85%. Proper temperature and relative humidity appear to be factors in the ability of B. bassiana M130 to control populations of greenhouse whitefly. A control value of 84.6% indicates that B. bassiana M130 may possibly be substituted for chemical pesticides.
Field test. The results of the field test as shown in Fig. 8 are consistent with patterns identified in the pot test. The control value increased with increasing number of applications. The maximum control value was up to 45.3%. The lower control value was due to poor conditions for germinating B. bassiana spores.
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Corrected mortalities of greenhouse whiteflies treated with B. bassiana M130 at a concentration of 1 × 108 conidia/ml in pots. The different letters above the error bars indicate the statistically significant differences analyzed by Duncan’s multiple range test (p ≤ 0.05). Vertical lines indicate standard deviations.
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Corrected mortalities of greenhouse whiteflies treated with B. bassiana M130 at a concentration of 1 × 108 conidia/ml in the field. The different letters above the error bars indicate the statistically significant differences analyzed by Duncan’s multiple range test (p ≤ 0.05). Vertical lines indicate standard deviations.
In this study, the highest greenhouse temperature was 28℃. The lowest temperature was 12℃, and the average relative humidity was 60%. We suspect that if the number of applications of the biological control were increased, the control value will increase in the field test.
- Insecticidal Process of Beauveria bassiana M130
In Fig. 9 , images 1, 2, and 3 show M130 conidia attached to the surface of an egg. Thereafter, they formed appressoria and invaded the egg. Images 4-7 show the internal invasion process in nymphs and imagos. These results illustrate the invasion process of general entomopathogenic fungi.
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Scanning electron micrographs of B. bassiana M130 on greenhouse whitefly egg, nymph, and imago. (A) Conidia adhered to the surface of egg (×500, 0 h after inoculation); (B) germinating conidium, with penetration of the germ tube (×1,300, 24 h); (C) growth of the germ tube (×1,200, 48 h); (D and E) extrusion of the mycelium with degradation of the cuticle of the nymph (×400, 72 h and ×500, 96 h); (F and G) conidia adhered to the tegument of greenhouse whitefly and extrusion of the mycelium on segment (×2,000, 24 h and ×1,200, 96 h); and (H) whole body covered in mycelia of Beauveria bassiana M130 (×120, 144 h).
This research was supported by the Bio-industry Technology Development Program, Ministry for Food, Agriculture, Forestry and Fisheries, Republic of Korea. This Study was supported by the BK21 PLUS Program of Ministry of Education.
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