Location: Corn Insects and Crop Genetics Research2013 Annual Report
1a. Objectives (from AD-416):
1) Improve knowledge of the ecology, genetics, and behavior of corn pests such as corn borer, corn rootworm, and western bean cutworm in relation to pest abundance and insect resistance to transgenic corn; 2) Determine the nature and degree of potential impacts of transgenic corn (e.g., Bt corn) on non-target organisms; and 3) Develop genetic and molecular methods to investigate corn insect biology and plant-insect interactions.
1b. Approach (from AD-416):
Laboratory trials will examine how resistance alleles from European corn borer (ECB) colonies impact dispersal and survival of neonates after exposure to various Bt toxins. Movement and avoidance behaviors will be evaluated using video-tracking and bioassays with lyophilized leaf tissue incorporated into artificial diet. Results of the laboratory trials will guide selection of appropriate treatments for subsequent semi-field experiments. The marker development and screening strategies used for identifying Bt resistance linkage groups in ECB will be adapted for developing molecular markers associated with behavioral adaptations in ECB. We will characterize gene flow and genetic structuring among ECB populations in Pennsylvania (PA). We will use a panel of 74 SNP markers, previously identified and verified from EST sequences, in population genetics analyses to determine the effects of potential geographic barriers on ECB gene flow separately for the pheromone races, and determine if genetic structuring is associated with host plant association in the E race. The development of laboratory tests to evaluate possible effects of stressors from GE crops involves two phases. The first phase is development of a standardized protocol for testing an orally administered test substance on a specific insect and life stage. The second phase is using these protocols to parallel test (a.k.a. ring test) the selected insect at three or more laboratories. We will take a mass-screening approach to validate EST-derived SNPs for WCR using the Illumina Golden Gate SNP assay platform. We anticipate that about 75% of the 4,111 candidate SNPs we have identified will produce a designable assay, which would translate into nearly 3,100 assays. These candidate SNPs, for which an assay can be designed, will be tested for polymorphism against samples of rotation-resistant WCR populations from Illinois and wild-type populations from Iowa. Information from the Illumina GenCall and GTS Reports software will be used to remove bad SNPs and bad samples. Complementing the genomics and bioinformatics groundwork, we will investigate Bt resistance traits by integrating structural and functional genome information. SNP markers will be used for mapping QTL studies of ECB, and population studies of ECB and WBC. Our experiments will investigate separate native resistance (NR) sources leading to differential feeding or survival of WCR larvae on roots, of WCR adults on silks, and of corn earworm (CEW) larvae on silks. For both lepidopteran and coleopteran pests, we will narrowly define chromosomal segments of the corn genome that harbor NR alleles. We will also create large sets of inbred and hybrid isolines to enable future mechanistic analysis of the effects of the NR alleles on both target and non-target insects.
3. Progress Report:
The Pheromone Gland Fatty-Acyl Reductase (pgfar) molecular assay we developed is substantially more accurate than previous E or Z pheromone-baited traps at identifying E and Z races of European corn borer (ECB) and their hybrids. The new assay revealed that hybridization between races is much more common than previously suspected. The surprisingly high frequency at which ECB races hybridize suggests that if Bacillus Thuringiensis (Bt) resistance develops in E-race populations, it will spread quickly to the Z race and spread into the Corn Belt. The pgfar assay also was used to re-examine a population genetics study with ECB collected from nine locations in Pennsylvania. Improved identification accuracy along with use of a new analytical technique called "Population Graphs" provided the precision necessary to detect population differentiation across space and time within each race. Genetic differences are not related simply to distance from one another, indicating that something else is serving as a barrier to dispersal, possibly topology (e.g., mountains, forests) or patterns of alternative host use. Results confirmed preliminary tests that gene flow is lower between E-race populations than Z-race populations, which could lead to faster development of resistance to transgenic Bt corn in the E race. The genetic basis of larval ECB resistance to feeding on Bt corn that express Cry1F toxin was investigated in two backcross families, and DNA and RNA have been collected from resistant and susceptible progeny for Quantitative Trait Loci (QTL) mapping and gene expression analyses. Western corn rootworm Bacterial Artificial Chromosome (BAC) clones (37) were fully sequenced and submitted to public databases after gene coding regions were identified. Candidate Bt-resistance genes were isolated from western corn rootworm, and identification BACs carrying these genes is ongoing. Genome sequencing of pools of western corn rootworm individuals was completed for a laboratory strain and a field population, and subsequent low coverage genome assembly allowed isolation of full mitochondrial genome sequences, the genome of the Wolbochia endosymbiont and novel transposons not discovered by prior BAC sequencing. DNA was extracted from two Northern corn rootworm F1 crosses that show one year and extended diapause traits, and QTL analysis is ongoing. Confirmation of resistance to transgenic Bt corn in many western corn rootworm populations has emphasized the urgent need for better understanding of this pest's dispersal behavior, which strongly influences rate of resistance development and the rate at which resistance spreads after it develops. Thorough, systematic sampling of adult population numbers were taken in 50 fields across five locations in the species native home range of eastern Colorado and western Kansas. In combination with follow-up analyses of genetic variation at 500 single-nucleotide polymorphisms markers, we will be able to estimate how far typical individuals fly per generation before reproducing. One more year of such sampling will be conducted to allow the necessary analysis of genetic changes over time.
Kuester, A.P., Jones, R.W., Sappington, T.W., Kim, K., Barr, N.B., Roehrdanz, R.L., Senechal, P., Nason, J.D. 2012. Population structure and genetic diversity of the boll weevil, Anthonomus grandis (Coleoptera: Curculionidae), on Gossypium in North America. Annals of the Entomological Society of America. 105(6):902-916.