The present project will determine the genomic basis for evolved resistance to Beauvaria bassiana in the genetic model insect, Drosophila melanogaster. Entomopathogenic fungi, such as B. bassiana, are used in biological control of mosquito vectors of dengue fever and malaria, and of other insect pests, such as bedbugs and those that affect food security. However, mechanisms of insect resistance to fungal entomopathogens are poorly understood. Understanding resistance has additional implications for human health because of strong homology between insect and mammalian innate immune systems. An evolve and resequence approach will be applied to determine the genetic basis for evolved resistance to fungal infection in Drosophila. D. melanogaster will be artificially selected for increased resistance to B. bassiana in very large, replicated experimental populations. The pre-selection source population will be derived from a cosmopolitan sample of D. melanogaster representing common natural variation worldwide. Whole-genome sequence data will be collected from selected and control populations at multiple intermediate generations throughout the selection regime, allowing observation of the temporal trajectory of adaptive alleles. It is expected that the response to selection will primarily derive from standing genetic variation, so these allele frequency dynamics will illustrate the poorly understood soft sweep mode of adaptation in natural populations. This study will determine mechanistic factors that shape antifungal defense, including elucidation of the basis for a striking sexual dimorphism in resistance, and will serve as a general model of adaptive evolution.

Public Health Relevance

The present proposal will determine the genomic basis for the evolution of resistance to fungal infection in a genetic model insect, Drosophila melanogaster. Understanding the genomic basis for evolved resistance to infection has implications for human health, both due to homology of the insect and mammalian innate immune systems, and because pathogens are used in biological control of insect vectors of human disease and pests that threaten food systems. The fungus to be used in the present experiment, Beauveria bassiana, has potential use in biological control of malaria-transmitting mosquitos, but the mechanisms of mosquito resistance to the fungus are poorly understood.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM109700-02
Application #
8804186
Study Section
Special Emphasis Panel (ZRG1-F08-A (20))
Program Officer
Reddy, Michael K
Project Start
2014-02-01
Project End
2016-01-31
Budget Start
2015-02-01
Budget End
2016-01-31
Support Year
2
Fiscal Year
2015
Total Cost
$56,042
Indirect Cost
Name
Cornell University
Department
Zoology
Type
Schools of Earth Sciences/Natur
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Shahrestani, Parvin; Chambers, Moria; Vandenberg, John et al. (2018) Sexual dimorphism in Drosophila melanogaster survival of Beauveria bassiana infection depends on core immune signaling. Sci Rep 8:12501