VII.6
Beauveria bassiana for Mormon Crickets
D. A. Streett and S. A. Woods
Introduction
How Beauveria bassiana
Works
Isolate of B. bassiana
for Mormon Cricket
Laboratory Studies
Field Studies
Conclusions
References
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Introduction
 |
| Figure VII.6-1- The
Mormon cricket is mainly a pest on rangelands but sometimes
moves into planted crops and causes economic damage. (Agricultural
Research Service file photo K4797-1.) |
The first crops planted by the Mormon settlers in Utah were damaged
by the insect now referred to by the common name Mormon cricket
(Cowan 1990). The Mormon cricket, Anabrus simplex Haldeman,
is not a cricket at all but a longhorned grasshopper from the family
Tettigoniidae (fig. VII.6-1). This pest can reach outbreak levels
before Mormon crickets begin migrating into range and cropland.
Mormon crickets can cause significant damage when bands of huge
numbers of insects move onto cropland in the Western United States
(Pfadt 1991, MacVean 1990, Swain 1944). Our studies evaluated the
effectiveness of a fungal pathogen, Beauveria bassiana, to
suppress Mormon cricket populations.
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How
Beauveria bassiana Works
Interest in insect-fungi interactions has centered, for the most
part, on the pathogenic (disease-causing) nature of fungi and their
use as microbial control agents. Unlike other insect pathogens that
must be eaten to infect insects, fungi can infect an insect through
its cuticle (outer skin). The development of fungi pathogenic to
insects typically follows this pattern:
- Attachment of an infectious stage (called a conidium or spore)
to the insect cuticle,
- Germination of the conidium and penetration of the insect cuticle
by a germ tube from the conidium,
- Growth of the fungus inside the insect body (hemocoel) and eventual
death of the insect,
- Penetration of the fungus to the surface of the dead insect
and formation of conidia (plural of conidium) under conditions
of high relative humidity, and
- Dispersal of the conidia to locations where they may encounter
susceptible insects and start the process again.
Among the insect-pathogenic fungi that follow this pattern of development
is Beauveria bassiana. It is commonly known as the white-muscardine
fungus because of the characteristic white covering of conidia (spores)
found on the surface of dead insects. Insect cadavers infected with
the fungus are transformed into white, mummified bodies resembling
in appearance a bonbon candy (muscardin means bonbon in French [Steinhaus
1949]).
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Isolate
of B. bassiana for Mormon Cricket
The B. bassiana strain used in these studies was originally
obtained from Mycotech Corporation in Butte, MT. Mycotech has obtained
Environmental Protection Agency registration of this Beauveria
strain for the suppression of several insect pests, including
grasshoppers and Mormon crickets. Mycotech recently developed a
solid culture system for the production of B. bassiana conidia
(Goettel and Roberts 1992). Mycotech prepared and supplied a B.
bassiana dry conidia powder for the laboratory studies and B.
bassiana formulated in oil (OF) and in an emulsible suspension
(ES) for the 1992 and 1993 Idaho field trials (Onsager et al. 1992,
Kemp and Streett 1993).
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Laboratory
Studies
Conidia were suspended in ES1 and ES2 oil and applied to Mormon
crickets as 0.08 µL (microliter) droplets beneath the pronotum
(on the thorax) at dosages ranging from 0 to 10 6 spores per Mormon
cricket. Mormon crickets were reared individually in plastic cups
and maintained in an incubator at 77 °F (25 °C). Mormon crickets
were fed every 2 days with romaine lettuce, kale, and wheat bran.
Mortality was recorded during feeding, and a damp cotton ball was
added to cups containing cadavers. The cadavers were then stored
at room temperature for 4-6 days to diagnose Beauveria infection
by observing the characteristic white muscardine appearance on the
insect surface.

Figure VII.6-2-Cumulative
mortality among fifth-instar Mormon crickets in a bioassay of Beauveria
bassiana.
The median lethal dose (LD50)
is commonly used to assess the infectivity of a pathogen. The LD50
for the B. bassiana isolate against fifth-instar Mormon crickets
at 12 days was 1,000 conidia (fig. VII.6-2). The two oil formulations
that were compared in laboratory assays showed no consistent differences
in overall mortality or percentage of Mormon crickets with confirmed
infections (table VII.6-1).
Table VII.6-1-Laboratory comparison of ES1 versus ES2 oil
as a carrier for Beauveria bassiana. Cumulative mortality
and incidence of infection for Mormon crickets.
|
|
Mortality
|
Infection
|
|
Dose
|
1 ES1
|
ES2
|
ES1
|
ES2
|
|
|
|
Conidia/ grasshopper
|
----------Percent-----------
|
|
0
|
34
|
46
|
8
|
12
|
|
102
|
50
|
38
|
20
|
18
|
|
103
|
71
|
87
|
42
|
44
|
|
104
|
90
|
98
|
65
|
62
|
|
1ES = emulsifiable suspension.
|
Four replicates of 200 adult Mormon crickets each were treated
with 5 x 105 or 5 x 106
conidia in oil according to the procedures described by Kemp and
Streett, 1993. A check preparation consisting of oil without conidia
and an untreated control were included for each replicate. Each
treatment within a replicate was separated into two groups and reared
either individually in an incubator at 77 °F or transferred to field
enclosures. Four field enclosures 16 ft1
(1.5 m2) for each treatment were
stocked with 25 Mormon crickets. Mormon crickets were fed lettuce
daily. Counts of Mormon crickets were made for each cage, and cadavers
were collected for incubation in cups with a moistened cotton ball
to diagnose Beauveria infection (Kemp and Streett 1993).
Adult Mormon crickets that were inoculated with 5 x 106
conidia per Mormon cricket showed a significant difference in mortality
in laboratory versus field cages (fig. VII.6-3). Adult Mormon crickets
reared in the field enclosures survived more than 3 weeks longer
than Mormon crickets reared in the laboratory. One possible explanation
for these results is that Mormon crickets in the field use a behavioral
thermoregulation to increase body temperature to a point that restricts
fungal development and allows the insect to survive.

Figure VII.6-3-Cumulative
mortality among adult Mormon crickets treated with Beauveria
bassiana in the lab and reared in the lab or in field cages.
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Field
Studies
Field trials against Mormon crickets were conducted near St. Anthony,
ID. Oil (ES1 oil) and clay-oil-water (COW)-100 g clay: 1 liter (L)
oil: 2 L water)-formulations were applied at rates of 4.9 ( 1011
and 4.9 x 1012 conidia/acre (1.2
x 1012 and 1.2 x 1013
conidia per ha) and application volumes of 0.9 and 2.7 qt/acre (2.5
and 7.5 L/ ha). Each replicate consisted of 10 arenas of 14.4 yd2
(12 m2) constructed of aluminum flashing approximately 10-18
inches (25-45 cm) in height. Each arena was stocked with more than
250 Mormon crickets prior to application.
Treatments were replicated four times, and treatments within each
replicate were applied on the same day (weather permitting) in the
sequence outlined by Onsager et al. (1992). An ultralow-volume sprayer
(North American Micron) was used for the applications. After application,
Mormon crickets were collected from each arena for rearing. Approximately
30-50 Mormon crickets per arena were reared individually in the
laboratory; mortality and infection data were recorded as described
earlier. Three field cages (16 ft2 /cage) were each stocked
with 30-50 Mormon crickets from each arena and covered with chicken
wire to keep out birds. Mormon crickets were fed lettuce and sagebrush
daily. Mormon crickets were counted daily, and cadavers were collected
and incubated in cups with a moistened cotton ball to diagnose Beauveria
infection.
Results differed somewhat between the formulations that were used
in the field. The statistical results suggested that the ES1 formulation
produced less mortality but similar rates of infection than the
OF formulations at the 2.7 qt/acre application volume. There were
no differences in overall mortality or infection rates between the
0.9 qt/acre and 2.7 qt/acre application volumes of oil alone formulations.
It should be noted that while the differences in mortality between
formulations at the 2.7 qt/ acre application volume may have been
statistically significant, they were not substantial (80 v. 74
percent at the low conidia concentration).
The application rate of conidia had a more substantial impact on
both the overall mortality and percentage of confirmed infections.
Adjusted for controls, overall mortality averaged 55 percent and
89 percent for the low and high conidia concentrations, respectively.
All comparisons between conidia concentrations were statistically
significant.
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Conclusions
A detailed understanding of the disease dynamics of the B. bassiana
isolate will be necessary before this product can be considered
for use in an integrated pest management program. Gaining this understanding
will entail both laboratory and field studies to evaluate short-term
and longrange impacts of Beauveria on Mormon crickets. The
effects of cannibalism, behavioral fever, and host behavior will
need further evaluation before the potential of B. bassiana as
a microbial control agent against Mormon crickets can be determined.
Formulation of B. bassiana for Mormon cricket control will
also require additional research.
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References
Cited
Cowan, F. T. 1990. The Mormon cricket story. Spec.
Rep. #31. Bozeman, MT: Montana State University and Montana Agricultural
Experiment Station. 42 p.
Goettel, M. S.; Roberts, D. W. 1992. Mass production,
formulation and field application of entomopathogenic fungi. In:
Lomer, C. J.; Prior, C., eds. Biological control of locusts and
grasshoppers. Wallingford, UK: CAB International: 230-238.
MacVean, C. 1990. Mormon crickets: a brighter side.
Rangelands 12: 234-235.
Pfadt, R. E. 1991. Mormon cricket. In: Field guide
to common western grasshoppers. Sta. Bull. 912. Laramie, WY: U.S.
Department of Agriculture, Animal and Plant Health Inspection Service
and Wyoming Agricultural Experiment Station. 4 p.
Steinhaus, E. A. 1949. Principles of insect pathology.
New York: McGraw Hill. 757 p.
Swain, R. B. 1944. Nature and extent of Mormon
cricket damage to crop and range plants. Tech. Bull. 866. Washington,
DC. U.S. Department of Agriculture. 44 p.
References
Cited-Unpublished
Onsager, J. A.; Streett, D. A.; Woods, S. A. 1992.
Grasshopper pathogen evaluation. Cooperative Grasshopper Integrated
Pest Management Project, 1992 annual report. Boise, ID: U.S. Department
of Agriculture, Animal and Plant Health Inspection Service: 179-186.
Kemp, W. P.; Streett, D. A. 1993. Grasshopper pathogen
evaluation. Cooperative Grasshopper Integrated Pest Management Project.
1993 annual report. Boise, ID: U.S. Department of Agriculture, Animal
and Plant Health Inspection Service: 217-224.
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