Figure 1.
Snail organs transfected with the jPEI/fluorescent siRNA nanoparticles visualized by light and fluorescence microscopy.
Panels A and C: Images of hepatopancreas and ovotestis regions of juvenile snails that were soaked either in jPEI/Alexa 555 siRNA for either 24 or 72 hrs viewed without fluorescence (10× magnification). Panels B and D: Images of the hepatopancreas and ovotestis tissues shown in panels A and C, subjected to fluorescence microscopy as described in Materials and Methods. Note the intense flourescence (red stain) in the hepatopancreas compared to the ovotestis, indicating preferential uptake of the jPEI/fluorecent siRNA nanoparticles into this tissue.
Figure 2.
Snail organs transfected with or without the fluorecent siRNA visualized by either light or fluorescence microscopy.
Panels A and C: Images of snail hepatopancreas and ovotestis tissues of juvenile snails that were either soaked in fluorescent siRNA (A) for 72 hrs or left untreated (C) viewed without fluorescence (10× magnification). Panels B and D: The same images of hepatopancreas and ovotestis regions shown in panels A and C, subjected to fluorescence microscopy as described in Materials and Methods. Note the very weak flourescence (red stain) in the hepatopancreas (B) indicating less uptake of the fluorescent siRNA into this tissue occurs without PEI (10× magnification).
Figure 3.
Analysis of Cath B gene expression by real time qPCR.
(A) Relative expression of Cathepsin B gene in CathB1 siRNA/jPEI, CathB2siRNA/jet PEI, ‘mock’ CathB siRNA, CathB1siRNA, and PEI treated snails versus untreated snails. Treatments were done at room temperature for 72 hrs. (B) Relative expression of Cathepsin B gene in CathB dsRNA/PEI, Myo dsRNA/PEI, CathB dsRNA, and PEI treated versus untreated juvenile snails. Treatments were done at room temperature for 72 hrs.
Figure 4.
Analysis of Prx expression by real time qPCR and ELISA.
(A) Relative expression of peroxiredoxin gene in Prx dsRNA/PEI, Myo dsRNA/PEI, Prx dsRNA alone and PEI treated snails versus untreated snails. Treatments were done at room temperature for 72 hrs. (B) Prx protein suppression analyzed by ELISA as described in Materials and Methods with recombinant B. glabrata Prx antibody. Each bar represents the geometric mean end point titre ± standard error (SE) of each experimental group as indicated on the y-axis.
Figure 5.
Time course for optimum gene knockdown after soaking snails in either dsRNA/PEI or siRNA/PEI nanoparticles.
(A) Relative expression of Cathepsin B gene in juvenile snails soaked for between 1 and 4 days in CathB dsRNA/PEI. (B) Relative expression of peroxiredoxin gene in snails soaked for between 1 and 4 days in Prx dsRNA/PEI. (C) Relative expression of Cathepsin B gene in snails soaked for 1 to 4 days in CathB1-siRNA/PEI. Note in all time course studies that the optimum knockdown of transcripts occurs at day 3 of incubating in either dsRNA/PEI or siRNA/PEI complexes.
Figure 6.
Survival of juvenile snails treated with PEI.
Percentage survival of juvenile snails (n = 117) soaked in PEI compared to untreated control snails (n = 29).