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Grant: Discovery Grants Program - Individual

Simon Fraser University

$116,000.00

Untangling the complex molecular interplay in vector-pathogen interactions using bioinformatics, gene silencing, and gene editing.

EF 2023-24

Résumé
Insect vectors transmit parasites and pathogens to humans, yet the vast majority of parasites that enter vectors are killed by components of the insects' innate immune system. This response is germ-line encoded and is neither learned nor acquired, unlike the characteristics of vertebrate immunity. Several mechanisms are used by the insects to recognize parasites and pathogens as "non-self". Recognition activates immune pathways (Toll, IMD, RNAi and Jak-STAT) to encapsulate, melanixe, or express potent antimicrobial peptides (AMPs) all of which can kill parasites. Despite the power of innate immunity, many insects still transmit parasites. The relationship between vector and parasite is very specific. Each vector species transmits one, or a very limited number of, parasites or pathogens. If the immune system functions why do vectors not kill all parasites? In Cali Colombia, approximately 30% of field collected Ae. aegypti, the major vector of Dengue and Zika viruses, actually kill the viruses while 70% continue to transmit the viruses to humans. If being refractory to viruses is a benefit, why do all female Ae. aegypti not kill the viruses? Within Ae. aegypti, Dengue viruses exploit existing mosquito proteins to establish, enter cells, and replicate, but in the refractory strains of Ae. aegypti these genes are not expressed. We will determine the role and importance of these genes by knocking down their expression and exposing these mosquitoes to Dengue virus to confirm the role of these genes. We then will use gene editing techniques to render susceptible phenotype-determining genes non-functional to determine their absence on virus development and on general mosquito fitness parameters. The Immune deficiency pathway (IMD) is a highly conserved immune pathway in insects that eliminates infections with Gram-negative bacteria. In the kissing bug, Rhodnius prolixus, however, the IMD pathway was reported to be absent, non-functional, or significantly reduced. The IMD pathway was reported to be absent in highly related insects. Despite these claims, the antimicrobial peptides normally (AMPs) regulated by the IMD pathway are expressed in these insects. We will use a series of bioinformatics and wet bench approaches to determine if the pathway is intact, but hidden in the genome, whether new proteins have replaced "missing: IMD components, or whether these AMPs are controlled by other pathways. Preliminary data indicate that the IMD pathway is present and functional R. prolixus. All of these experiments and approaches are designed to identify the regulation of innate immune responses in insects, how insects respond to parasites and pathogens, what factors determine vector-parasite specificity, and the mechanisms they use to restrict or eliminate parasite development. Ultimately, we may identify essential molecules or pathways that we might exploit to induce incompatibility between vectors and pathogens, and therefore eliminate transmission.
Programme
Discovery Grants Program - Individual
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2019-04259
Name nom
Lowenberger, Carl
Department département
Biological Sciences
Organization id
5
Institution établissement
Simon Fraser University
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2019
Award amount
116000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
6400
Research subject group en
Life sciences research related to human health and disease
Research subject group fr
Life sciences research related to human health and disease
Research subject en
Sciences de la vie liées à la santé publique et aux maladies humaines
Research subject fr
Sciences de la vie liées à la santé publique et aux maladies humaines
Application title
Untangling the complex molecular interplay in vector-pathogen interactions using bioinformatics, gene silencing, and gene editing.
Keyword
CrisprCas; dengue virus development in mosquitoes; Gene knockdown; Genetic manipulation of insects; IMD pathway in Rhodnius prolixus; innate immunity; parasite-host interactions; RNAi; using RNAi and CRISPR-Cas to understand the role of genes
Application summary
Insect vectors transmit parasites and pathogens to humans, yet the vast majority of parasites that enter vectors are killed by components of the insects' innate immune system. This response is germ-line encoded and is neither learned nor acquired, unlike the characteristics of vertebrate immunity. Several mechanisms are used by the insects to recognize parasites and pathogens as "non-self". Recognition activates immune pathways (Toll, IMD, RNAi and Jak-STAT) to encapsulate, melanixe, or express potent antimicrobial peptides (AMPs) all of which can kill parasites. Despite the power of innate immunity, many insects still transmit parasites. The relationship between vector and parasite is very specific. Each vector species transmits one, or a very limited number of, parasites or pathogens. If the immune system functions why do vectors not kill all parasites? In Cali Colombia, approximately 30% of field collected Ae. aegypti, the major vector of Dengue and Zika viruses, actually kill the viruses while 70% continue to transmit the viruses to humans. If being refractory to viruses is a benefit, why do all female Ae. aegypti not kill the viruses? Within Ae. aegypti, Dengue viruses exploit existing mosquito proteins to establish, enter cells, and replicate, but in the refractory strains of Ae. aegypti these genes are not expressed. We will determine the role and importance of these genes by knocking down their expression and exposing these mosquitoes to Dengue virus to confirm the role of these genes. We then will use gene editing techniques to render susceptible phenotype-determining genes non-functional to determine their absence on virus development and on general mosquito fitness parameters. The Immune deficiency pathway (IMD) is a highly conserved immune pathway in insects that eliminates infections with Gram-negative bacteria. In the kissing bug, Rhodnius prolixus, however, the IMD pathway was reported to be absent, non-functional, or significantly reduced. The IMD pathway was reported to be absent in highly related insects. Despite these claims, the antimicrobial peptides normally (AMPs) regulated by the IMD pathway are expressed in these insects. We will use a series of bioinformatics and wet bench approaches to determine if the pathway is intact, but hidden in the genome, whether new proteins have replaced "missing: IMD components, or whether these AMPs are controlled by other pathways. Preliminary data indicate that the IMD pathway is present and functional R. prolixus. All of these experiments and approaches are designed to identify the regulation of innate immune responses in insects, how insects respond to parasites and pathogens, what factors determine vector-parasite specificity, and the mechanisms they use to restrict or eliminate parasite development. Ultimately, we may identify essential molecules or pathways that we might exploit to induce incompatibility between vectors and pathogens, and therefore eliminate transmission.