Wolbachia offer a pesticide-free alternative to curb arbovirus transmission. Current pilot studies release infected mosquitoes to either crash the resident population size or spread mosquitoes with reduced vectorial capacity in the local population. Both efforts rely upon Wolbachia's adaptation to cause cytoplasmic incompatibility (CI) - a sperm modification that causes embryonic arrest in crosses between infected males and uninfected females (unidirectional CI) or between males and females harboring different Wolbachia strains (bidirectional CI). However, infected females with the same strain rescue the sperm modification, giving them a large fitness advantage over uninfected females that in turn enables rapid spread of Wolbachia through host populations. Despite four decades of intense research and current applications to vector control, the underlying genetic basis of CI has not been reported. However, we recently identified two prophage WO gene candidates in the released strain of wMel Wolbachia that natively infects Drosophila melanogaster. These genes are hereafter referred to as cytoplasmic incompatibility factor A (cifA) and cytoplasmic incompatibility factor B (cifB). cifA and cifB exhibit enhanced expression in infected host testes, as expected for genes involved in CI. Expression of cifA and cifB transgenes in uninfected D. melanogaster testes recapitulates induction of CI, while expression in Wolbachia- infected testes enhances the wild type CI. Importantly, wMel-infected females rescue the transgene-associated CI, thereby implicating these candidates as likely CI genes. Phylogenies specify divergent clades of cifA and cifB homologs that covary with bidirectional incompatibility relationships between Wolbachia strains. Additionally, recent genome sequencing and comparisons reveal candidate rescue genes that exhibit parallel phylogenies to those of cifA and cifB and preferential expression in early embryos. As these findings represent a potential breakthrough in the search for CI genes, the central hypothesis of the proposed research is that the candidate modification and rescue genes determine unidirectional and bidirectional CI.
In Aim 1, we will use transgenic expression of genetically divergent cifA and cifB variants to broadly test the essential cif gene regions for inducing CI and whether extant homologs of these genes retain the ability to induce CI.
In Aim 2, we will investigate candidate rescue genes from wMel using transgenic expression in females and crosses with an array of males with CI-inducing Wolbachia or transgene cif homologs.
This aim will also explicitly test the presumption that divergence in modification and rescue genes underlies bidirectional CI. Examinations thus far have yet to yield a comprehensive genetic advance for both sides of CI, and the rising interest in deploying Wolbachia to curb arbovirus transmission necessitates an explanation of Wolbachia's drive system. If successful, this research will pioneer genetic studies of bacteria-induced reproductive parasitism, inform Wolbachia's efficacy and delivery as a tool to control diverse zoonotic diseases, and provide multiple lines of evidence for the discovery of genes that underlie CI.

Public Health Relevance

Wolbachia are obligate intracellular bacteria that are estimated to infect millions of arthropod species worldwide. Despite Wolbachia's extraordinary capacity to modify sexual reproduction and its utility in vector control programs, the genetic basis of their reproductive modifications remains a long-standing enigma. The proposed research will interrogate the first set of Wolbachia candidate genes that cause cytoplasmic incompatibility (CI), and in so doing, will (i) pioneer genetic studies of reproductive parastisim, (ii) inform Wolbachia's efficacy and delivery as a tool to control diverse zoonotic diseases, and (iii) likely provide multiple lines of evidence for the discovery and validation of genes that induce and rescue CI.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI132581-01
Application #
9366789
Study Section
Vector Biology Study Section (VB)
Program Officer
Costero-Saint Denis, Adriana
Project Start
2017-05-24
Project End
2022-04-30
Budget Start
2017-05-24
Budget End
2018-04-30
Support Year
1
Fiscal Year
2017
Total Cost
$381,550
Indirect Cost
$131,550
Name
Vanderbilt University Medical Center
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
965717143
City
Nashville
State
TN
Country
United States
Zip Code
37240
Funkhouser-Jones, Lisa J; van Opstal, Edward J; Sharma, Ananya et al. (2018) The Maternal Effect Gene Wds Controls Wolbachia Titer in Nasonia. Curr Biol 28:1692-1702.e6
Lindsey, Amelia R I; Rice, Danny W; Bordenstein, Sarah R et al. (2018) Evolutionary Genetics of Cytoplasmic Incompatibility Genes cifA and cifB in Prophage WO of Wolbachia. Genome Biol Evol 10:434-451
Shropshire, J Dylan; On, Jungmin; Layton, Emily M et al. (2018) One prophage WO gene rescues cytoplasmic incompatibility in Drosophila melanogaster. Proc Natl Acad Sci U S A 115:4987-4991