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United States Department of Agriculture

Agricultural Research Service


Location: Imported Fire Ant and Household Insects Research

2010 Annual Report

1a. Objectives (from AD-416)
Objective 1: Develop functional genomic resources and employ these resources to examine the genetic basis of biological traits that can potentially be used for biologically based control, including implications for the geographic origins of infestations. Objective 2: Expand current biocontrol efforts by discovering and developing new parasites and pathogens; improving mass culture and field release systems; and defining host specificity of natural enemies. Objective 3: Characterize semiochemicals through investigation of pheromone biosynthesis and release; use these findings to develop novel biologically-based control and surveillance methods, including the detection and treatment of incipient or low level populations. Objective 4: Develop integrated pest management plans that utilize available control methods, perform comprehensive risk assessment, and that can be adapted to specific stakeholder needs, including local eradication.

1b. Approach (from AD-416)
1. Normalized cDNA libraries will be sequenced using 454-pyrosequencing technology. Resulting sequences assembled and automatically and manually annotated for key words, gene function, and Gene Ontology terms. The 454 data will be used to search for potential microbes infecting fire ants and determine their nature, distribution, relationship, and effects of these microbes in fire ants. SNPs within the data will be identified and applied to high-resolution identification of the source population of introduced S. invicta. Microarrays will be constructed and used to identify differentially expressed genes from parasite-infected and -uninfected fire ants and identify genes co-expressed with the social form-specific gene Gp-9 allelic variants. 2. Microsporidia: After approval, V. invictae will be released in the U.S. following the procedures for K. solenopsae introductions. Phorid Flies: Additional decapitating phorid flies will be released using procedures based on our previous successful releases in the U.S. The impact of phorid flies will be assessed by multiple methods, e.g. monitoring the establishment, expansion, distribution and parasitism rates of phorid fly species across the fire ant range. Viruses: Baculovirus expression methodology will be emulated in order to express Solenopsis invicta viruses (SINV-1, -2 or -3) for study and development as a microbial pesticide. With purified preparations of SINV, a number of basic studies will be conducted, including lethal dose evaluations against different stages of ants, transmission studies within and between colonies, field-testing, and formulation development. Other potential biocontrol agents will be investigated as time and importance dictate. 3. The function of the fire ant PBAN/pyrokinin family of neuropeptides will be investigated by: a) in vivo injection into female and male sexuals and immatures and observed for phenotypic changes; b) manipulation of hormone/receptor capabilities through the use of agonists, hyper-agonists, and antagonists of the neuropeptide hormones; and c) use of RNAi gene knockout methods – followed by monitoring for phenotypic and/or behavioral changes. Monitoring and surveillance methods will be developed for fire ants, using known attractants. A variety of existing fire ant bioassays will be adapted and applied to non-fire ant invasive pest ant species to generate the tools to create better baits and effective monitoring systems, e.g. attractants and repellents. 4. Potential geographic range expansion of tramp ant species will be modeled using CLIMEX a program that can be used to predict where a pest ant of interest can survive. Phagostimulants will be studied to improve the acceptability of baits for non-Solenopsis pest ants by adapting methods used for fire ants. Standard laboratory colony tests will be used to assess bait formulation effects on brood volume, adult populations, and queen survivorship. A combination of monitoring tools, baits, and biologically based-control methods will be applied to selected invasive ant species as these new tools become available.

3. Progress Report
The little decapitating fly, Pseudacteon cultellatus, was approved for field release as a self-sustaining biocontrol agent of imported Solenopsis fire ants. A colony of these flies was transferred to the USDA-APHIS mass rearing facility (operated by the Division of Plant Industries, Florida Department of Agriculture, Gainesville, FL) along with the necessary training and support. Unit personnel also began field releases of P. cultellatus on fire ant populations with multiple-queen colonies around Gainesville and Miami, Florida. Multiple-queen populations produce smaller workers and are thus ideally suited as hosts for these very small parasites. First-generation field-reared flies have already been recovered. Fire ant decapitating flies that develop in fire ants infected with the fire ant pathogen Kneallhazia (=Thelohania) solenopsae, can acquire the pathogen. Infected fly tissue could be deleterious to the flies, which are biocontrol agents of fire ants, or infected flies may be capable of vectoring the pathogen to other fire ants. Thus far, there is no evidence of infection in fly tissue, but research is continuing. Kneallhazia solenopsae infection was confirmed in the tropical fire ant, Solenopsis geminata, indicating this pathogen has a broader host range than previously reported. Using samples of the tropical fire ant provided by cooperators from the University of Texas and universities in northern and central Mexico, two distinct molecular variants of K. solenopsae were discovered. Analyses are also being conducted on K. solenopsae infecting the black imported fire ant from different locations in Argentina. Solenopsis invicta virus 3 is associated with significant fire ant colony mortality. The virus genome was cloned and inserted into an expression vector in an attempt to grow the virus in culture. This is a crucial requirement for industry adoption of the virus as a natural pesticide. Interest in the technology was expressed from the Center for Innovative Food Technology, Ohio. An assessment of genetic variation at a diverse set of molecular markers in 2,144 colonies from 75 geographic sites worldwide revealed that at least nine separate introductions of S. invicta have occurred into newly invaded areas and that the main southern USA population likely is the immediate source of all but one of these introductions. The sole exception involves a putative serial invasion event from the southern USA to California to southern Taiwan. RNA interference of the expression of a specific target gene was shown to have deleterious effects on fire ant larvae. This result follows a great deal of basic research that now shows potential for the development of a novel biologically-based fire ant control method. A patent application is being prepared for submission. A laboratory bioassay was developed to evaluate the efficacy of ant baits on the Caribbean crazy ant, Paratrechina pubens, which will facilitate the development of more effective control strategies for this invasive species.

4. Accomplishments

Review Publications
Allen, H.R., Valles, S.M., Miller, D.M. 2010. Characterization of Solenopsis invicta (Hymenoptora: Formicidae) populations in Virginia: Social form genotyping and pathogen/parasitoid detection. Florida Entomologist. 93(1): 80-88.

Choi, M.Y., Jurenka, R.A. 2010. Site-directed mutagenesis and PBAN activation of the Helicoverpa zea PBAN-receptor. Federation of European Biochemical Societies Letters. 584:1212-1216.

Shoemaker, D.D., Ascunce, M.S. 2010. A new method for distinguishing colony social forms of the fire ant Solenopsis invicta. Journal of Insect Science. 10(73):1-11.

Ross, K.G., Gotzek, D., Ascunce, M.S., Shoemaker, D.D. 2009. Species delimitation: A case study in a problematic ant taxon. 59(2):162-184.

Vander Meer, R.K., Preston, C.A., Choi, M.Y. 2010. Isolation of a pyrazine alarm pheromone component from the fire ant, Solenopsis invicta. Journal of Chemical Ecology. 36:163-170.

Hokit, G., Ascunce, M.S., Ernst, J., Branch, L., Clark, A. 2009. Landscape Characteristics influence spatial genetic variation of the Florida scrub lizard (Sceloporus woodi). Conservation Genetics. 11(1):149-159.

Valles, S.M., Strong, C.A., Hunter, W.B., Dang, P.M., Pereira, R.M., Oi, D.H., Williams, D.F. 2008. Expressed sequence tags from the red imported fire ant, Solenopsis invicta: Annotation and utilization for discovery of viruses. Journal of Invertebrate Pathology. 99(1):74-81.

Vander Meer, R.K., Preston, C.A., Hefetz, A. 2008. Queen regulates biogenic amine level and nestmate recognition in fire ant, Solenopsis invicta, workers. Naturwissenschaften. 95(12):1155-1158.

Patrock, R.J., Folgarait, P.J., Gilbert, L.E., Porter, S.D. 2009. Distributional patterns of Pseudacteon associated with the Solenopsis saevissima complex in South America. Journal of Insect Science. 9:60, 17 pp.

Valles, S.M., Hashimoto, Y. 2008. Characterization of structural proteins of Solenopsis invicta virus 1. Virus Research. 136(1):189-191.

Hashimoto, Y., Valles, S.M. 2008. Infection characteristics of Solenopsis invicta virus-2 in the red imported fire ant, Solenopsis invicta. Journal of Invertebrate Pathology. 99(2):136-140.

Valles, S.M., Oi, D.H., Porter, S.D. 2009. Kneallhazia (=Thelohania) Solenopsae infection rate of Pseudacteon Curvatus flies determined by multiplex PCR. Florida Entomologist. 92(2):344-349.

Porter, S.D. 2010. Distribution of the Formosa strain of the fire ant decapitating fly Pseudacteon curvatus (Diptera: Phoridae) three and a half years after releases in North Florida. Florida Entomologist. 93(1):107-112.

Oi, D.H., Valles, S.M., Briano, J. 2010. Laboratory host specificicty testing of the fire ant microsporidian pathogen Vairimorpha invictae (Microsporidia: Burenellidae). Biological Control. 53:331-336.

Caldera, E.J., Ross, K.G., Deheer, C.J., Shoemaker, D.D. 2008. Putative Native Source of the Invasive Fire Ant Solenopsis invicta in the U.S.A. Biological Invasions. 10(8):1457-1479.

Yang, C., Shoemaker, D.D., Wu, J., Lin, Y., Lin, C., Wu, W., Shih, C. 2009. Successful establishment of the invasive fire ant Solenopsis invicta in Taiwan: Insights into interactions of alternative social forms. Diversity and Distributions. 15(4):709-719.

Valles, S.M., Varone, L., Ramirez, L., Briano, J. 2009. Multiplex detection of Solenopsis invicta viruses -1, -2, and -3. Journal of Virological Methods. 162:276-279.

Kafle, L., Wu, W., Vander Meer, R.K., Shih, C. 2009. Effect of surfaces on the foraging efficiency of Solenopsis invicta (Hymenoptera: Formicidae). Formosan Entomologist. 29:51-58.

Choi, M.Y., Vander Meer, R.K., Valles, S.M. 2010. Molecular diversity of PBAN family peptides from fire ants. Archives of Insect Biochemistry and Physiology. 74(2):67-80.

Valles, S.M., Allen, C., Varone, L., Briano, J. 2010. Complete genome sequence of an Argentinean isolate of Solenopsis invicta virus 3. Virus Genes. 40:293-297.

Lalzar, I., Simon, T., Vander Meer, R.K., Hefetz, A. 2010. Alteration of cuticular hydrocarbon composition affects heterospecific nestmate recognition in the carpenter ant Camponotus fellah. Chemoecology. 20:19-24.

Allen, C., Briano, J.A., Varone, L., Oi, D.H., Valles, S.M. 2010. Exploitation of a high genomic mutation rate in Solenopsis invicta virus 1 to infer demographic information about its host, Solenopsis invicta. Journal of Invertebrate Pathology. 105(1):105-111.

Last Modified: 10/18/2017
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