Project

Mosquito as a natural syringe

Xenosurveillance

•Definition

•Application

•Paper1, 2, 3 showed that

Am J Trop Med Hyg. (2015) Feasibility of Using the
Mosquito Blood Meal for Rapid and Efficient Human and
Animal Virus Surveillance and Discovery.
Yu Yang, et al.

Experiment

↓Anopheles stephensi (primary vector of malaria)

↓Dengue virus serotype 2 (DENV-2)

↓in human red blood cell and serum (Key Biologics, LLC)

↓RNA extracted at 0, 4, 8, 16, 24 hours after blood feeding

↓DENV-2 copy by qRT-PCR

Result

In Anopheles stephensi, which does not allow DENV-2 to replicate, viral RNA titer will reduce gradually but remains detectable for at least

24 hours in the midgut.

Reference

1.Am J Trop Med Hyg. (2017) The Use of Xenosurveillance to Detect Human Bacteria, Parasites, and Viruses in Mosquito Bloodmeals.

2.PLoS Negl Trop Dis. (2015) Xenosurveillance: a novel mosquito-based approach for examining the human-pathogen landscape.

3.Am J Trop Med Hyg. (2015) Feasibility of Using the Mosquito Blood Meal for Rapid and Efficient Human and Animal Virus Surveillance and Discovery.

GFP System

To create a reporter system, we constructed a GFP expression vector. We amplified a constitutive promoter from Drosophila actin 5c gene and an eukaryotic poly A signal by PCR from pAc5.1 vector. The resulting DNA fragments were assembled with a BioBrick existing part of GFP to generate the reporter vector of Ac5- GFP-polyA / pSB1C3 (K2543004).

To test the reporter system, we cultured a mosquito Aedes albopictus C6/36 cell line and transfected cells with the plasmid of Ac5-GFP-polyA. GFP positive cells and intensity were analyzed 2 days after transfection.

EXPERIMENT

↓C6/36 cells (1.8 x 105 cells/well in a 96-well plate)
↓Liposome-mediated transfection and culture for 2 more days
↓Read fluorescence intensity at Ex/Em = 480/520 nm with a microplate reader
↓Observe GFP+ cells under a fluorescence microscope

RESULT

As data shown here, Ac5 is a strong and constitutive promoters which can drive GFP to high expression level in mosquito cells. And we can transfect more than 50% of GFP positive cell with liposome-mediated DNA delivery.

Mosquito Immune Signaling

Mosquito immune defense signaling involves well-studied and well-known Toll and Imd intracellular pathways to trigger antimicrobial peptide (AMP) production. Gram-positive bacteria induce Toll signaling, while Gram-negative bacteria induce Imd signaling. However, some promoters may be activated in a synergistic and cross-talk way. Even though Mosquito-borne viruses are controlled by immune signaling in mosquitoes in a currently unidentified pathway, AMP promoter activities were enhanced in mosquito cells in the presence of the viruses.

Front Cell Infect Microbiol. (2017) Regulation of Antimicrobial Peptides in Aedes aegypti Aag2 Cells.
Rudian Zhang, et al.

EXPERIMENT

↓Aag2 cell line from Aedes aegypti
↓E. coli or Bacillus at OD600 = 0.05 (≅ MOT = 10)
↓RNA extracted 12 hours after bacteria challenge
↓qRT-PCR with specific AMP primers

RESULT

AMP promoters can be activated by challenging with Gram-negative and Gram-positive bacteria. In addition, some are regulated synergistically by cross-talking Toll and Imd pathways.

REFERENCE

1.Trends Parasitol. (2016) Mosquito Defense Strategies against Viral Infection.
2.Front Cell Infect Microbiol. (2017) Regulation of Antimicrobial Peptides in Aedes aegypti Aag2 Cells

AMP System

Aedes aegypti, a yellow fever mosquito, is a major arbovirus vector to transmit several diseases and spread mosquito-borne viruses such as dengue virus, Ziki virus, yellow fever viruses, etc. It can be genetically modified to control viral transmission. The cell line isolated from Aedes are widely used in the research. The full genome sequence and signaling pathways are defined in the literature. Therefore, it a good host for our study. In our project, we successfully cloned 3 AMP (GAM1, CecN, DefA) promoters from gDNA of Aedes aegypty and confirmed the sequencesby sequences by sequencing.

AMP promoters amplified by PCR

To create AMP reporter system, the AMP promoters of Aedes aegypti amplified from PCR were assembled with GFP-polyA /pSB1C3 (BBa_K2543003)

To test the function of the device, C6/36 cells were transfected with the vectors. And the mosquito cells were challenged with bacteria on 2 days after transfection.

EXPERIMENT

↓C6/36 cells were seeded at the density of 1.8 x 105 cell/well in a 96-well plate
↓Cells were transfected with the AMP-GFP-polyA vectors
↓E. coli was added on 2 days post-transfection at MOI=10
↓GFP positive cells and intensity were analyzed by a fluorescence microscope and a microplate reader at Ex/Em = 480/520 nm,respectively

GAM1-GFP-polyA / pSB1C3 challenged with E. coli

GAM1/CecN/DefA-GFP-polyA / pSB1C3 challenged with E. coli

RESULT

We successfully assembled three AMP promoters with GFP and poly A to pSB1C3 vector. The function of the devices were tested by challenging with E. coli. The intensities were 5.31-fold, 3.02-fold and 2.29-fold increase for E. coli-induced GAM1, CecN and DefA promoter activities, respectively. The GFP positive cells after induction were clearly observed under fluorescence microscope.

To test the AMP promoter in response of Gram-negative and Gram-positive bacteria, we challenged GAM1 promoter with E. coli and Bacillus subtilis, respectively.

EXPERIMENT

↓C6/36 cells were seeded at the density of 1.8 x 105 cell/well in a 96-well plate
↓Cells were transfected with the GAM1-GFP-polyA vector
↓E. coli or B. subtilis was added on 2 days post-transfection at MOI=10
↓GFP intensity was measured by a microplate reader at Ex/Em = 480/520 nm.

RESULT

The data represented in C6/36 cells showed that GAM1 promoter was not only activated by Gram-negative E. coli but also induced by Gram-positive B. subtilis. The result further indicated the AMP promoter activity may cross talk between Toll and Imd signaling pathways.

GAM1-GFP-polyA / pSB1C3 challenged with E. coli & B. subtilis

To apply GAM1 promoter as a biosensor, E. coli at various concentrations were added to the mosquito cells transfected with the GAM1-GFP-polyA / pSB1C3

EXPERIMENT

↓C6/36 cells were seeded at the density of 1.8 x 105 cell/well in a 96-well plate
↓Cells were transfected with GAM1-GFP-polyA or Ac5-GFP-polyA vectors
↓E. coli at MOI=2, 4, 8, 16, 32 were added on 2 days post-transfection
↓GFP intensity was measured by a microplate reader at Ex/Em = 480/520 nm.