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Revision as of 18:32, 4 October 2023

shRNA(cyp51)-1

In order to kill B. cinerea, the pathogen of grey mold and control the disease in tomato, we designed two pieces of shRNAs targeting the Bccyp51 gene of the pathogen, which is essential for maintaining its cell membrane, based on RNAi technology. shRNA can be actively absorbed by B. cinerea, then enter into its cells to be processed into siRNA, and further specifically target mRNA to achieve degradation. Or, entering plant cells, the related proteins in the cell will process and deliver shRNAs to B. cinerea, which can also achieve the effect of silencing mRNA, reducing the level of its specific protein, and finally forming the inhibition of the pathogen.

Essential information

Sequencing

Sequence and Features

Biology

- Ergosterol (ERG) is a C28 sterol that is particularly present in fungal cell membranes and plays a crucial role in the structure and function of fungal cell membranes. Ergosterol is responsible for maintaining membrane fluidity, regulating membrane permeability, affecting membrane-related enzyme activity, and influencing fungal cell growth. Silencing Bccyp51, a key gene in the ergosterol biosynthesis pathway, can destroy the cell membrane of B. cinerea and produce killing effect on it. By silencing the important chitin synthase gene Bccyp51, the formation of the cell membrane of B. cinerea could be affected, thus killing pathogenic fungi.

Design of shRNA

After confirming the selection of targets Bccyp51, we searched the cDNA library of B. cinerea according to the sequences or primes provided in the literature, and found the homologous cDNA sequence of B. cinerea. Then, the sequence was input into the National Center for Biotechnology Information (NCBI) website for analysis and prediction, and the CDS sequence of the target gene was input into the total nucleic acid database BLAST to query the homologous similarity of neighboring species. siRNA sequences were designed in non-conserved regions to ensure species-specific and biosafety of our shRNAs.

Next, we used a professional siRNA designed website ( https://www.genscript.com/tools/sirna-target-finder) to predict the siRNA sequences that would effectively target the mRNA, and then screened out siRNA fragments with high potential activity in a series of predictions based on shRNA design principles. By making structural predictions of the mRNA (http://rna.tbi.univie.ac.at/cgi-bin/RNAWebSuite/RNAfold.cgi), we ensured that the selected siRNA sequences targeted relatively loose positions in the mRNA structure. For biosafety reasons, we BLAST the candidate siRNA fragments into the total mRNA database to ensure that it does not target any genes of common species (such as human, tomato, dog, rice, wheat, etc.), ensuring sequence specificity.

Finally, we assembled the selected siRNA sequence into our shRNA in the sequence of siRNA sense strand - loop - reversed siRNA antisense strand.

Plasmid construction

We have assembled our shRNA in the sequence of siRNA sense strand - loop - reversed siRNA antisense strand, then sequence was assembled in the pET28a (+) plasmid. The recombinant vector was transferred into RNase-deficient E. coli HT115(DE3), and the large-scale fermentation production of shRNA in E. coli could be achieved by induction of IPTG. In our experiment, the results of treatment of different shRNAs at both phenotypic and molecular levels were analyzed to screen out the effective shRNAs.

Usage

The shRNA(cyp51) will be used in crop protection through the way of spraying induced gene silencing (SIGS), which is an emerging, non transgenic RNAi strategy. After screening out an effective shRNA against B. cinerea, the shRNA will be wrapped in KH9-BP100, which belongs to cell-penetrating peptides in a spherical shape and can be used to deliver biological molecules, to forming a CPP-shRNA complex. Then, spraying the complex on the tomato infected by B. cinerea, we hope that it can play a more effective and more steady role in controlling grey mold.

Characterization

shRNA production induced by IPTG

After plasmid extraction, we transformed the constructed shRNA expression vector into E.coli HT115 (DE3) and performed PCR. Our specific primers successfully amplified a 260 bp band from the plasmid, confirming the successful transformation of the plasmid. This indicates that the shRNA expression vector has been successfully introduced into E.coli and can be detected and confirmed by PCR. This is an important milestone that lays the foundation for further experiments.

Compared to the non-induced sample, there is a brighter band between 50-100 bp and 100-150 bp in the induced sample lane. Our shRNA has a size of 69 bp, while the Box-Survival shRNAs, being a concatenation of two shRNAs, have a size of 124 bp. This confirms the successful extraction of our shRNA, and the generated shRNA is of the expected size.

Distribution of disease spots

We designed shRNA to target and silence genes necessary for the survival of B. cinerea and virulence genes of infected tomatoes. Therefore, we wanted to test whether spraying shRNA can really reduce the attack of B. cinerea on tomato fruits. We used a black marker to draw a circle with a diameter of about 3 mm on the surface of the tomato fruit, and poked five small holes within the circle with a sterilized thin needle.

For the naked shRNA treatment, we added 10 μL solution containing 10 μg shRNA in and around the circle of the fruit surface. After the liquid dried, we drilled holes on the edge of the B. cinerea plate with a 10 μL transparent suction head, and then covered the surface of the fruit in the dotted line area with the mycelium side of the cake. In the control group, we selected non-specific shRNA GFP. The treated tomato fruits were placed in a humid environment at 21 ℃. After three days, ImageJ software was used to conduct a quantitative analysis of the lesion area, which was determined by the area covered by mycelia. Error bars represent standard deviations (SD) obtained from 11-15 biological replicates, the data are F-tested and T-tested, the level of significant difference is passed by a single-tail test, and shown above the bar chart (ns P > 0.05；* P  < 0.05；** P  < 0.01；*** P  < 0.001). For the treatment coated with transmembrane peptide (CPP), the treatment was consistent with the naked shRNA treatment, except that the solution of dripping per sample was changed to 12 μL containing 10 μg shRNA and 8.2 μL 1mg/mL CPP (Figure 5).

At the phenotypic level, the shRNA(cyp51)-1 treatment was effective in reducing the relative plaque area by 16.8% compared with the control group. However, there was no significant difference between the experimental group and the control group, indicating that naked shRNA(cyp51)-1 was not effective.

Detection of inhibition effect by qRT-PCR

On the third day of the experiment, after sampling the lesions of tomato fruits, the sample RNA was extracted, reverse-transcribed, and qRT-PCR was performed to detect the inhibition effect of shRNA on mycelium target mRNA in infected fruits (Figure 6).

From the results of molecular experiments, the silencing rates of the experiment that spraying the naked shRNA(CHSIIIa)-2 is 22.7%, after binding with CPP, the silencing rates could reach 21.0%. There was no significant difference before and after combining with CPP.

References