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Sand Fly Phlebotomus papatasi Embryo Microinjection for CRISPR/Cas9 Mutagenesis
Published on: November 17, 2020
CRISPR/Cas9 Mutagenesis in Phlebotomus papatasi: the Immune Deficiency Pathway Impacts Vector Competence for
Isabelle Louradour1, Kashinath Ghosh1, Ehud Inbar1
1Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Abstract:
Sand flies are the natural vectors for the Leishmania species that produce a spectrum of diseases in their mammalian hosts, including humans. Studies of sand fly/Leishmania interactions have been limited by the absence of genome editing techniques applicable to these insects. In this report, we adapted CRISPR (clustered regularly interspaced palindromic repeat)/Cas9 (CRISPR-associated protein 9) technology to the Phlebotomus papatasi sand fly, a natural vector for Leishmania major, targeting the sand fly immune deficiency (IMD) pathway in order to decipher its contribution to vector competence. We established a protocol for transformation in P. papatasi and were able to generate transmissible null mutant alleles for Relish (Rel), the only transcription factor of the IMD pathway. While the maintenance of a homozygous mutant stock was severely compromised, we were able to establish in an early generation their greater susceptibility to infection with L. major Flies carrying different heterozygous mutant alleles variably displayed a more permissive phenotype, presenting higher loads of parasites or greater numbers of infective-stage promastigotes. Together, our data show (i) the successful adaptation of the CRISPR/Cas9 technology to sand flies and (ii) the impact of the sand fly immune response on vector competence for Leishmania parasites.IMPORTANCE Sand flies are the natural vectors of Leishmania parasites. Studies of sand fly/Leishmania interactions have been limited by the lack of successful genomic manipulation of these insects. This paper shows the first example of successful targeted mutagenesis in sand flies via adaptation of the CRISPR/Cas9 editing technique. We generated transmissible null mutant alleles of relish, a gene known to be essential for the control of immune response in other insects. In addition to the expected higher level of susceptibility to bacteria, the mutant flies presented higher loads of parasites when infected with L. major, showing that the sand fly immune response impacts its vector competence for this pathogen.
Insights
We successfully adapted CRISPR/Cas9 gene editing in Phlebotomus papatasi sand flies to study their immune response. This research reveals the sand fly
Area of Science:
- Vector biology
- Genetics
- Immunology
Background:
- Sand flies transmit Leishmania parasites, causing disease in humans.
- Understanding sand fly-Leishmania interactions is crucial for disease control.
- Genome editing tools were previously unavailable for sand flies, limiting research.
Purpose of the Study:
- To adapt CRISPR/Cas9 gene editing technology for use in Phlebotomus papatasi.
- To investigate the role of the immune deficiency (IMD) pathway in sand fly vector competence.
- To generate null mutant alleles of the Relish (Rel) gene.
Main Methods:
- CRISPR/Cas9 technology was adapted for P. papatasi transformation.
- Targeted mutagenesis of the Relish (Rel) gene within the IMD pathway was performed.
- Homozygous and heterozygous mutant P. papatasi lines were generated and analyzed for Leishmania major infection.
Main Results:
- Successful generation of transmissible null mutant alleles for Relish (Rel).
- Homozygous mutant sand flies showed significantly increased susceptibility to Leishmania major infection.
- Heterozygous mutant flies exhibited a more permissive phenotype with higher parasite loads.
Conclusions:
- CRISPR/Cas9 technology is successfully adapted for targeted mutagenesis in sand flies.
- The sand fly's immune response, specifically the IMD pathway, significantly impacts its vector competence for Leishmania parasites.
- This work provides a foundation for further genetic studies of sand fly-pathogen interactions.
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