Reduction of Feeding by the Variegated Grasshopper, Zonocerus variegatus , Following Infection by the Fungal Pathogen, Metarhizium flavoviride

The effect of infection by the fungal entomopathogen , Metarhizium flavoviride, on feeding by the tropical grasshopper pest , Zonocerus variegatus, was investigated in field - cage studies . A significant reduction in feeding , as indicated by faecal production , was recorded 2 - 3 days after inoculation for a range of spore doses (104 , 105 and 5 105 spores per insect) . This was before any mortality was recorded due to infection . All infected individuals died by day 7 . At this time , faecal production of the treated grasshoppers was equivalent to less than 2 days faecal production by grasshoppers untreated with spores . This reduction in feeding (69 , 71 and 74% total reduction by day 7 in the 104 , 105 and 5 105 doses respectively in comparison to controls) is a substantial contribution to the overall effects of the slow acting pathogen . Furthermore , the rapid reduction in feeding indicated that this effect was not simply due to invasion of the host tissues by the pathogen or production of secondary metabolites . The possibility that reduction in feeding is associated with a behavioural response in which there is a trade - off between host defence and feeding during early stages of infection is discussed     

Effects of Temperature, Humidity and Inoculation Method on Susceptibility of Schistocerca gregaria to Metarhizium flavoviride

The effects of temperature on conidial germination and susceptibility of adults of the desert locust , Schistocerca gregaria, to four isolates of Metarhizium flavoviride were determined . In addition , the effects of inoculation method (topical or spray) , spore carrier (oil or water) and ambient relative humidity (RH) on susceptibility of the locust to the most thermotolerant isolate (Mf324) were investigated . There were differences among the isolates in the effects of temperature on germination of conidia after a 24 - h incubation period . Over 90% of conidia of all isolates germinated after 24 h at 30 o C . In contrast , at 40 o C , none of the isolates germinated for up to 72 h . However , there were differences in germination between the isolates at 35 o C . Locust mortality and disease progression were significantly affected by temperature . At both 25 and 30 o C , all isolates induced 98 - 100% mortality within 8 days; however , there were differences between isolates at 35 o C . None of the isolates caused significant mortality at 40 o C . Humidity and inoculation method had no influence on levels of mortaility in fungus treated locusts . In contrast , carrier type significantly affected cumulative mortality . Topical oil treatment resulted in higher overall mycosis than the three other treatments . Control mortality on the other hand was strongly affected by inoculation method and to a lesser extent by humidity and carrier . In these conditions , application of oil by spray was generally toxic at all humidities whereas topical application of water was most toxic at near saturation . The results of these laboratory studies demonstrate the importance of strain selection , formulation and application method in the development of a microbial control agent against the desert locust . Low RH should not impede use of this fungus under dry conditions .     

Field Treatment of Desert Locust ( Schistocerca gregaria Forskal) Hoppers in Mauritania Using an Oil Formulation of the Entomopathogenic Fungus Metarhizium flavoviride

A field trial was conducted to test the efficacy of an oil formulation of the entomopathogenic fungus , Metarhizium flavoviride Gams & Rozsypal (Deuteromycotina: Hyphomycetes) , as a control agent for the desert locust , Schistocerca gregaria Forskal (Orthoptera: Acrididae) , in Mauritania . The treatment was applied to hopper bands in the field . In caged samples of the treated insects , 99% mortality was observed in 15 days . On average during application only 51% of the hoppers received spray droplets directly , the additional mortality being due to pick - up of spores from the spray residue . This mortality was assessed by exposing insects to a treated plot at intervals , and monitoring disease levels during subsequent incubation in cages . The spray residue remained highly infective for a period of 6 days after application . The number of nymphs in the hopper bands was estimated using a computer - based photographic image - processing technique . Unfortunately , most of the hopper bands dispersed into small groups , but a population reduction could be demonstrated for one hopper band . Maximal daily mortality in the field was observed 10 - 11 days after application , compared with 6 - 10 days in cages .     

Application of Metarhizium flavoviride (Deuteromycotina: Hyphomycetes) Spores Against the Tree Locust, Anacridium melanorhodon (Orthoptera: Acrididae), in Sudan

Spores of the entomopathogenic fungus Metarhizium flavoviride were applied against the tree locust Anacridium melanorhodon melanorhodon in the field for the first time. The treated areas covered a total of 55 ha in the vicinity of Tendelti in the White Nile State of Sudan. At a dose of 100 g of spores/ha applied in 5 l of oil formulation, the application led to a reduction in population densities of 66-76% after 18 days. Correction of the data with the Henderson/ Tilton formula gave an overall control efficiency of 68%.     

Effects of Rehydration on the Conidial Viability of Metarhizium flavoviride Mycopesticide Formulations

The rehydration of dried conidia of Metarhizium flavoviride was investigated in an attempt to increase speed of kill of locusts and grasshoppers by formulations of this fungus. Conidia were dried to 4-5% moisture content with no apparent adverse effects on viability, but rapid rehydration (by putting dried conidia directly in free water) reduced viability. Rehydration in an atmosphere of high humidity allowed dry conidia to absorb sufficient moisture to avoid imbibition damage. Rehydrating and pre-germinating conidia prior to spraying (in an oil-based formulation) on to the desert locust, Schistocerca gregaria, did not decrease the time to death, suggesting that moisture uptake by dry conidia on the desert locust cuticle is easily achieved.     

Selection of a Highly Virulent Fungal Isolate,Metarhizium anisopliae Ma TB 101, for Control of Taro Beetle,Papuana uninodis (Coleoptera: Scarabaeidae)

Fungal isolates (31 Metarhizium anisopliae var. anisopliae , five M. anisopliae var majus , three Beauveria bassiana and four B. brongniartii ) originating from a wide range of geographical locations, insect species and soil types were tested against Papuana uninodis (Coleoptera: Scarabaeidae). In a first test series, spores were applied topically to third-instar larvae and adults. The most effective strain against P. uninodis larvae and adults was Ma TB 101, a M. anisopliae isolate from adult P. woodlarkiana . For adults, strain Ma FI 384, a M. anisopliae from Popillia japonica , was almost equally effective. The 11 most effective isolates (nine M. anisopliae var. anisopliae , one B. brongniartii and one B. bassiana ) with LT values of less than 6 weeks in 50 adults and/or less than 4 weeks in larvae were tested for their efficacy against adults and larvae of P. uninodis by application of spores to soil (107 spores/g). Ma TB 101 was significantly more effective against both adults and larvae (LT ca. 10 days) than all other isolates (LT > 50 50 3 weeks). Two other M. anisopliae strains, Ma F 248 from soil and Ma FI 384 from P.japonica , were more effective than most isolates in adults. The latter three M. anisopliae isolates were tested in a concentration series against third-instar larvae and adults. Mortality was concentration related. Isolates Ma F 248 and Ma FI 384 did not achieve 50% mortality within the test period at concentrations lower than 107 spores/g of soil or feed. For concentrations of Ma TB 101 from 1 107 to 2 105 spores/g the LT ranged from 13 to 30 days in adults and 12 to 24 50 days in third-instar larvae. Accordingly, concentrations causing 50% mortality (LC ) for Ma 50 TB 101 were significantly lower than for the two other M. anisopliae isolates tested.     

Field Trial with the Entomopathogenic Fungus Metarhizium anisopliae var. acridum against Bands of the Grasshopper Rhammatocerus schistocercoides in Brazil

The efficacy of a mycoinsecticide formulated in vegetable oil was tested in Brazil against the grasshopper Rhammatocerus schistocercoides . A set of experiments was conducted in the Chapada dos Parecis region (Mato Grosso state), a permanent zone of outbreaks for this pest. Experiments were performed in zones of natural vegetation, against grasshopper bands in the third nymphal instar. Three nymphal bands were treated with a mycoinsecticide formulation based on conidia of the entomopathogenic fungus Metarhizium anisopliae var. acridum ( =M. flavoviride ), strain CG 423. Three non-treated bands were used as control. The application was made with the aid of a hand-held ULV sprayer adjusted to deliver 2 l of the formulation ha -1 , each containing 1 ×10 13 conidia. Treatments were limited to the surface of the grasshopper bands and their immediate borders (5-10 m). The efficacy of the mycoinsecticide was evaluated through band survival after treatment (grasshopper numbers, surface, density, behaviour and daily movement of the band), allowing the insects to move freely in their natural environment. Insects were regularly surveyed and maintained in the laboratory, allowing estimates of the infection rate. Field and laboratory studies showed a clear effect of the product 10 days after treatment. At 14 days post-spraying, mortality caused by the mycoinsecticide in the field was approximately 88%.     

Screening for Virulent Isolates of Entomopathogenic Fungi Against the Desert Locust, Schistocerca gregaria Forskal

The pathogenicity of 159 isolates of Metarhizium and Beauveria spp. was screened using Schistocerca gregaria adults. The median lethal time MLT , the average survival time and its standard deviation SD were used to describe the rate of kill from the cumulative observed response curve over time, following the application of conidia in bioassays. All screens included a standard strain of Metarhizium sp. from a single spore of IMI 330189ss , which gave an average MLT value of 4.4 days SD 0.4 in 46 assays. Approximately 50 isolates, all belonging to the genus Metarhizium, showed virulence that was comparable with this strain. Two previously unreported preliminary tests were carried out. The first test assessed the response to the standard isolate by an established laboratory stock of desert locusts compared with a recently introduced locust stock from Niger. There were insignificant differences in MLT and LD50 on day 5 between the different locust strains. The second test assessed the effects of inoculation at different times after the final ecdysis. This similarly had little effect, although applications before day 10 appeared to minimize the risk of control mortality. A computer program was developed to store bioassay results in a standardized format and to produce quick estimates of these statistics.     

Long-term Storage of Metarhizium flavoviride Conidia in Oil Formulations for the Control of Locusts and Grasshoppers

Freshly harvested conidia of Metarhizium flavoviride (Gams & Rozsypal) were stored in two vegetable oils, groundnut or soya, or a mineral oil, Edelex. They were diluted with either Shellsol K or deodorized kerosene, and antioxidants were added to half of the vegetable oil formulations. Dried non-indicating silica gel was added to half of the formulations before storage at 8 or 17 C. Undried conidia, those without silica gel, lost viability rapidly, with germination dropping below 40% after 9 and 32 weeks at 17 and 8 C respectively. After 127 weeks (ca. 30 months) in storage, germination remained at over 60 and 80% for the dried formulations at 17 and 8 C respectively (after an unexplained drop in germination after 16-18 months in storage). Comparable figures for 160 weeks (ca. 37 months) were 47 and 68%. These figures represented germination after 24 h of incubation; after 48 h of incubation, germination was 79 and 89% from samples stored for 160 weeks at 17 and 8 C respectively. Representative formulations of the stored conidia were tested in bioassays against the desert locust Schistocerca gregaria (Forskal) up to 30 months into the experiment, and were found to have retained full virulence compared with freshly prepared formulations.     

Generation of Benomyl Resistant Beauveria bassiana Strains and Their Infectivity Against Helicoverpa armigera

Beauveria bassiana transformants were obtained by conventional protoplasting and transformed by eletroporation and polyethylene glycol (PEG) treatment. These displayed mitotic stability in Beauveria bassiana . Strains transformed with pSV50 harbouring the β-tubulin gene of Neurospora crassa grew well on benomyl concentrations of 10 μg ml -1 unlike the recipient strain. The transformants were mitotically stable on either selective or non-selective medium. The efficiency of transformation by linear and circular pSV50 cosmid was 8 and 10 transformants per mug DNA per ml viable protoplast by electroporation, respectively, and 4 and 6 by the protoplast PEG method, respectively. Southern blot and hybridization of undigested fungal DNA of wild type and four transformants, probed with β-tubulin sequence of pSV50, showed hybridization at high M r region of genomic DNA in four transformants, whereas in wild type genomic DNA, no homology of the sequence was observed. Digested genomic DNA, of four transformants gave a complex hybridization pattern. Virulence tests of the transformants showed that there was no significant loss in the pathogenicity toward Helicoverpa armigera third instar larvae. This method of transformation should prove useful with entomopathogenic fungal species in which a genetic transformation system has not yet been established.     

Infection of the Coffee Berry Borer Hypothenemus hampei (Coleoptera: Scolytidae) by Brazilian Isolates of the Entomopathogenic Fungi Beauveria bassiana and Metarhizium anisopliae (Deuteromycotina: Hyphomycetes)

The virulence of four fungal isolates (three Beauveria bassiana and one Metarhizium anisopliae ) against adult female coffee berry borers (CBB) was investigated. The most virulent isolate from initial bioassays, B. bassiana LPP1, with a LT 50 of 3.4 days, was further investigated by application to berries prior to infestation and to berries already infested with CBB. At the highest concentration applied to berries (1 ×10 7 conidia mL -1 ), CBB mortality was 83% (berries inoculated prior to infestation) and 62% (berries inoculated after infestation).     

Storage of Resting Spores of the Gypsy Moth Fungal Pathogen, Entomophaga maimaiga

The fungal pathogen, Entomophaga maimaiga causes epizootics in populations of the important North American forest defoliator gypsy moth ( Lymantria dispar ). Increasing use of this fungus for biological control is dependent on our ability to produce and manipulate the long-lived overwintering resting spores (azygospores). E. maimaiga resting spores undergo obligate dormancy before germination so we investigated conditions required for survival during dormancy as well as the dynamics of subsequent germination. After formation in the field during summer, resting spores were stored under various moisture levels, temperatures, and with and without soil in the laboratory and field. The following spring, for samples maintained in the field, germination was greatest among resting spores stored in plastic bags containing either moistened paper towels or sterile soil. Resting spores did not require light during storage to subsequently germinate. In the laboratory, only resting spores maintained with either sterile or unsterilized soil at 4°C (but not at 20 or -20°C) germinated the following spring, but at a much lower percentage than most field treatments. To further investigate the effects of relative humidity (RH) during storage, field-collected resting spores were placed at a range of humidities at 4°C. After 9.5 months, resting spore germination was highest at 58% RH and no resting spores stored at 88 or 100% RH germinated. To evaluate the dynamics of infections initiated by resting spores after storage, gypsy moth larvae were exposed to soil containing resting spores that had been collected in the field and stored at 4°C for varying lengths of time. No differences in infection occurred among larvae exposed to fall-collected soil samples stored at 4oC over the winter, versus soil samples collected from the same location the following spring. Springcollected resting spores stored at 4°C did not go into secondary dormancy. At the time that cold storage of soil containing resting spores began in spring, infection among exposed larvae was initiated within a few days after bringing the soil to 15°C. This same pattern was also found for spring-collected resting spore-bearing soil that was assayed after cold storage for 2-7 months. However, after 31-32 months in cold storage, infections started 14-18 days after soil was brought to 15°C, indicating a delay in resting spore activity after prolonged cold storage.     

EVect of the Entomopathogenic Nematodes, Steinernema feltiae and S. carpocapsae , on the Potato Cyst Nematode, Globodera rostochiensis , in Pot Trials

Two pot experiments, one in a glasshouse and the other in an outdoor sand plunge, were conducted to examine the influence of the entomopathogenic nematodes, Steinernema feltiae and S. carpocapsae , on the invasion and development of the potato cyst nematode, Globodera rostochiensis . Of a total of eight diVerent treatments with entomopathogenic nematodes in the glasshouse trial, three reduced the invasion of G. rostochiensis and one reduced the numbers of new cysts that were produced compared with controls. In the outdoor experiment, seven of the 12 treatments gave a reduction in invasion but none resulted in changes in the numbers of cysts found at plant senescence. In general, invasion of G. rostochiensis juveniles was reduced more eVectively by S. carpocapsae than by S. feltiae , and was greatest in the outdoor trial where larger inocula of entomopathogenic nematodes were used. Overall, the results indicated that use of S. feltiae and S. carpocapsae is unlikely to provide a viable control strategy for G. rostochiensis .     

Field suppression of the peachtree borer,Synanthedon exitiosa,using Steinernema carpocapsae: Effects of irrigation,a sprayable gel and application method

The peachtree borer, Synanthedon exitiosa, is a major pest of stone fruit trees in North America. In prior studies, the entomopathogenic nematode, Steinernema carpocapsae, caused substantial reductions in S. exitiosa damage when applied by watering can to peach trees that were irrigated regularly. Here we report two additional studies that assessed S. carpocapsae efficacy in suppressing S. exitiosa damage in peach orchards; one study focused on irrigation requirements and the other on application method. In the first experiment we compared S. carpocapsae applied with and without irrigation, and application of a sprayable gel, Barricade®, as a potential replacement for irrigation. In the second experiment, we compared application methods that growers might use including a boom sprayer, handgun, trunk sprayer and watering can (used as a positive control). In both experiments chlorpyrifos was also included as a positive control, and in the application methods experiment an untreated (negative) control was also included. All treatments were applied in the fall of 2012 and 2013 and S. exitiosa infestation was assessed following the spring of 2013 and 2014, respectively. In the first experiment, nematodes applied without irrigation did not prevent high levels of infestation levels (75% of trees were infested) whereas nematodes applied with the sprayable gel suppressed damage at the same level as chlorpyrifos (<20% infestation). Thus, our results indicate that the sprayable gel applied to soil around the tree base can enhance entomopathogenic nematode efficacy, and the gel may be used as a substitute for irrigation when applying S. carpocapsae for S. exitiosa control; this finding may be applicable to similar pests in various cropping systems. This is the first report of direct application of the sprayable gel to soil (previous reports concerned aboveground applications). Also in the first experiment, intermediate levels of damage (31–38% infestation) were observed in plots that received nematodes with irrigation. We suspect that a higher rate of irrigation would have improved efficacy. In the second experiment, the boom sprayer, trunk sprayer and watering can methods of nematode application resulted in S. exitiosa infestations that were similar to the chemical insecticide standard treatment (chlorpyrifos) and below levels in the non-treated control, whereas the handgun treatment was not different from the untreated control or chemical standard.     

Evaluation of Beauveria bassiana and Metarhizium anisopliae for Controlling Chilo partellus (Lepidoptera: Crambidae) in Maize

Maize (variety Katumani) was planted in a greenhouse and plants were infested with 20 Chilo partellus second instar larvae 3 and 4 weeks after plant emergence. One isolate of Beauveria bassiana (BB-01) and four isolates of Metarhizium anisopliae (PPRC-4, PPRC-19, PPRC-61 and EE-01) were sprayed onto the leaf whorl at 2×10⁸ conidia/mL 24 h after infestation. Leaf damage by the larvae was greatly reduced by the treatments. The mean daily temperature and relative humidity in the greenhouse ranged from 10 to 35°C and 30 to 90%, respectively. The growth of infested unsprayed plants was less than that of fungi treated plants. Stem tunneling (1-5%), deadheart (0-33%), number of attacked nodes (0.3-2.5) and holes (0.2-3.3) were also reduced in plants sprayed with conidial suspensions. Isolates PPRC-4, PPRC-19 and PPRC-61 seemed to be the best candidates for further development.     

A Proposed Mode of Action of Oil-Based Formulations of a Microbial Herbicide

Formulation of some microbial herbicides in emulsions of vegetable oil can significantly reduce their dependency on long dew periods to allow infection and control of the host weed. Examination of leaves of Viola arvensis , by a range of microscopy techniques, after spraying with an oilin-water emulsion formulation of the potential microbial herbicide Mycocentrospora acerina , suggests that the effect arises as a result of inversion of water into both oil droplets on the leaf surface and oil that penetrates into the leaf tissue. This oil probably mixes with aqueous components from the leaf tissue and, in doing so, forms an invert emulsion. Wesuggest that this supplies the water required by the fungus to initiate and sustain growth so that infection can result.     

Beauveria bassiana -A Potential Mycopesticide for the Efficient Control of Coffee Berry Borer, Hypothenemus hampei (Ferrari) in India

The Coffee Berry Borer (CBB), Hypothenemus hampei (Ferrari) (Coleoptera: Scolytidae) has been a serious insect pest of coffee cultivars C. robusta and C. catimor in India since 1991, causing 40-80% coffee bean loss. To combat this important pest, an indigenous entomopathogenic fungus Beauveria bassiana (Balsamo) Vuillemin was isolated from dead and moribund coffee berry borers from the wild. The fungus was cultured on yeast extractpeptone supplemented liquid medium. The mycelial mat was harvested from 12-day old cultures and lyophilized. A suspension of the most virulent isolate (Bb2) was prepared in sterile water and used as a mycopesticide. The laboratory studies were conducted on coffee berry borers by applying conidial suspensions at a dosage rate of 1 ×10 6 conidia ml -1 . Pest mortality with the Bb2 isolate increased from 69.3% to 95.3% with an increase in relative humidity (RH) at 25 ±2°C. Field experiments were conducted in a coffee plantation area in the Kodagu district of Karnataka, and the results showed that, under favourable environmental conditions (27- 29°C; 82-91% RH; 10-15 inches rainfall per year), the fungus required only eight days to colonize and kill the target pest. A maximum of 75.6% insect mortality was recorded 24 days after spraying. Large-scale field trials conducted in five plantation plots between September 1995 and September 1998 showed significant insect mortality both in C. robusta and C. catimor cultivars of coffee. The potential use of this indigenous fungal strain of B. bassiana as a mycopesticide for management of CBB in India is discussed.     

Effect of liquid culture media on morphology,growth, propagule production,and pathogenic activity of the Hyphomycete,Metarhizium flavoviride

Two isolates of Metarhizium spp. were studied for propagule production, because of their pathogenic activity towards locusts and grasshoppers (Mf189 = M. flavoviride (or M. anisopliae var. acridum) strain IMI 330189, and Mf324 = M. flavoviride strain ARSEF324). Both isolates were grown in seven different liquid media, which have been developed for mass production of various Hyphomycetes, considered as candidates for microbial control of noxious insects. Shake-flask experiments were carried out at 28 °C in the dark. Production was quantified for 72 h and the effects of the tested media were evaluated on propagule concentration, morphology and pathogenicity. Based on preliminary experiments, all tested media were supplemented with 0.4% Tween 80 to avoid the formation of pellets and to produce unicellular propagules. Submerged propagule yields were higher withMf189 than with Mf324 in all seven media. While high concentrations of propagules (1.4 to 2.4 × 10⁸ propagules ml^-1 for MF189 and1.4 to 8.3 × 10⁷ propagules ml^-1 for Mf324) were produced in four media (Adamek, Catroux, Jackson, and Jenkins–Prior media), production of propagules was lower in the three other media (Goral, Kondryatiev, and Paris media). Both isolates produced oblong blastospore-like propagules, except in Kondryatiev medium in which they provided ovoid propagules. In this case, Mf189 submerged propagules looked like aerial conidia, but scanning observations did not demonstrate a typical conidiogenesis via phialides. In Kondryatiev medium, Mf324 submerged propagules were significantly smaller than aerial conidia. Infection potential of submerged propagules was assayed on Schistocerca gregaria. Second-instar larvae fed for 48 h on fresh wheat previously contaminated by a spraying suspension of each inoculum titrated at 10⁷ propagules ml^-1. All seven media produced submerged propagules that were highly infectious for S. gregaria larvae. Shake flask culture assays permitted us to select three low-costmedia, Adamek, Jenkins–Prior, and Catroux for improving scale-up of liquid fermentation focused on mass-production of Metarhizium propagules for mycoinsecticides devoted to locust control. This revised version was published online in June 2006 with corrections to the Cover Date.     

Laboratory evaluation of the compatibility of a new attractant contaminant device containing Metarhizium anisopliae with Ceratitis capitata sterile males

Laboratory experiments were conducted to evaluate the compatibility of using the entomopathogenic fungus Metarhizium anisopliae, to be dispensed in a new attractant contaminant device (ACD), jointly with sterilized Ceratitis capitata males, as an integrated approach to control this major pest. The exposure of sterile Vienna 8 (V8) strain and wild type (WT) males to the contaminating part (infective dish) of the ACD showed similar susceptibility levels to the fungal strain (LT₅₀ value of 4.52 and 4.72 days, respectively). Sterile V8 males were significantly less attracted to the infective dish (18.4%) than WT males (28.5%).As the success of Sterile Insect Technique (SIT) heavily relies on the mating success of sterile males in the field, mating performance of infected males was assessed. Around 85% of the females were mated, independently of the male strain and treatment (fungus-treated or untreated males) indicating that mating performance was unaffected by the fungus under laboratory conditions. Females showed a greater tendency to remate if previously mated to fungus-treated males, either V8 or WT.Our data suggest that this M. anisopliae based-ACD does not impair the performance of C. capitata sterile males and, therefore, it could be used combined with area wide SIT-based programs, providing that these results are validated in field conditions. The implications of this combined strategy to control C. capitata are discussed.