Here you can read detailed descriptions of the experiments we've done. To read about how we structured and planned our work, see the Design. You can get straight to a section by following these links:

 

---

Plasmid Construction

Introduction

In order to let the P. aeruginosa inject the antigens into the antigen presenting cells (APCs), we first need to add the DNA sequences of antigens into the T3SS plasmid. The plasmid we use is Escherichia-Pseudomonas shuttle expression plasmid pExoS54F (shows in Figure 1), which encodes the promoter of T3SS effector ExoS with N-terminal ExoS1–54 signal sequence, followed by a FLAG-tag and a multiple cloning site (MCS). The pExoS54F plasmid contains two promoter region which can be activated simultaneously by ExsA's binding to their common promoter region. PexoS is the promoter region which originally belongs to the toxin gene ExoS and the wild type P. aeruginosa inject the toxin ExoS into the host cells through the T3SS. The ExoS gene of the P. aeruginosa strain we use has been knocked out so we utilize its promoter and its N-terminal ExoS1–54 signal sequence which act as a T3SS secretion signal to let the T3SS secret proteins of interest. SpcS is a kind of T3SS chaperone and helps the proteins of interest to enter the T3SS secretion channel.

The proteins encoded by the pExoS54F plasmid are actually not all the proteins that function in the process of T3SS protein delivery. There are approximately 40 proteins that regulate the secretion of T3SS effector proteins and many of them are encoded in the P. aeruginosa genome. The protein ExsE, ExsC, ExsD and ExsA are four cytoplasmic proteins (shows in the Figure 2) that control the coupling of transcription and secretion. ExsA is a DNA-binding protein required for transcriptional activation of the entire T3SS. The second regulatory protein, ExsD, functions as anti-activator by directly binding to ExsA. ExsC functions as an anti-anti-activator by directly binding to and inhibiting ExsD. ExsE functions as a direct inhibitor of ExsC and provide an initiating signal for the whole process. Figure 2 shows the situation when the T3SS secretion is inhibited because the direct activator ExsA is inhibited by the binding ExsD.

Overview

1.Sequence Synthesis
2.Plasmid Restricted Digestion
3.Ligation & Transformation

Results

1.Sequence Synthesis

As we successfully filtered many antigens which may active the immune system and guide the T cells to target to the tumor cells, we choose 4 of them and two positive controls: NY-ESO-A and NY-ESO-B. NY-ESO is widely known as a germ cell protein that is often expressed by tumor cells but not normal somatic cells. The frequent finding of humoral and cellular immune responses against this antigen in cancer patients with NY-ESO-expressing tumors makes it one of the most immunogenic human tumor antigens ever known. Table 1 shows the sequences of these antigens.

Part name	Antigen	Sequence
BBa_K2730001	NY-ESO-A	atgtcgttgttgatgctgatcacccagtgcccgttgtga
BBa_K2730002	NY-ESO-B	atgcagttgtcgttgttgatgctgatcacctga
BBa_K2730003	0201	atgttgcacttgtagggctcgtagccgccggcgtga
BBa_K2730004	0301A	atgcacttgtagggctcgtagccgccggcgcggtga
BBa_K2730005	0301B	atggcgatctcgacccgggacccgttgtcgaagtga
BBa_K2730006	0301C	atgaagttgttgaagcggcaggcggaaggcaagtga

Because the antigen sequences are quite short, we cannot choose the common way of synthesizing double strands. So we synthesize the 5’-3’ single strands and the 3’-5’ single strands with restriction site on both sides, then take the method of annealing (see in the protocol) to pair two single strands into a double strand (Figure 3). Table 2 shows all the single strands we synthesized.

2.Plasmid Restriction Digestion

We use the restriction endonuclease Xbal I and Sal I to digest the pExoS54F plasmid (see in the protocol). Also the antigen sequences we synthesized have the restriction site of Xbal I and Sal I. we set the single digestion control and the plasmid control to figure out whether the plasmid is digested completely. The DNA gel electrophoresis results (Figure 4) show that the digestion is complete.

3. Ligation & Transformation

We ligase the digestion product and double-stranded fragments using T4 DNA ligase and conduct the chemical transformation (see in the protocol). We conduct the colony PCR to test whether the colonies contain the right plasmids (see in the protocol). The DNA gel electrophoresis results (Figure 5) show that some of the colonies contain the right plasmids we want.

 

---

Electroporation of P. aeruginosa

To deliver antigens into cells T3SS system, plasmids containing antigen sequences should be transfered to Pseudomonas aeruginosa. We choose Pseudomonas aeruginosa strain PAK-JΔ9 which is an attenuated strain, for it has many advantages varies from efficiency and safety.

The transform technique we use is electroporation, the most efficient bacterial transformation method available, which orders of magnitude more efficient and versatile than chemical methods. Electroporation uses accurately pulsed electric currents to induce transient gaps in the phospholipid bilayer of cells, and extracellular genetic material passes through these transient gaps. Genetic material is assimilated by the target cells’ DNA.

The highest transformation efficiencies are obtained when cells are harvested in early mid-log growth, so we need to prepare bacteria before operating and make competent cells.

We transform Pseudomonas aeruginosa (see in the Protocol) following the Gene Pulser Xcell^TM Electroporation System Instruction Manual.



1. Electroporation

We use Gene Pulser Xcell™ Electroporation Systems (Bio-Rad) to transform bacteria.
Gene Pulser Xcell conditions: C = 25 μF; PC = 200 ohm; V = 2.5 kV.
After pulsing the competent cells, incubate for 1 hour and plate cells onto LB agar plates with carbenicillin. Incubate for 12 hours at 37°C. Next day, observe the growth of the bacteria.

From figure 1, we can see that there are some colonies on the LB agar plates, however, the majority are lawns. From many times of experiments, we verify this conclusion.

2. Colony PCR

Though there are colonies on the carbenicillin-resistant LB plate, we are not sure that the colonies contain the plasmids we want, because some colonies may be satellite colonies. So, we did colony PCR to test the presence of plasmids. (Results are shown in Figure 2)

From the electrophoresis results of colony PCR, we can see that the bands of our target DNA fragments are in the corresponding position (~200 bp). Therefore, it is indicated that our recombinant plasmids have been successfully transferred into P. aeruginosa.
 

---

Functional Analysis of T3SS

In normal high calcium environment, antigens can’t be synthesized by bacteria.

Secretion of the antigens can be activated in two ways.

One way is to form the host cell contact. When a contact signal has been sensed by the bacteria, a rapid production and specific insertion into the translocon follows and the antigens can successfully be injected into the host cell cytosol, without wasting them into the culture supernatant. This way is called “polar translocation”.

Another way is triggered by low calcium environment, such as in the presence of calcium chelator EGTA. It can trigger the bacteria to release the antigens into the culture medium without the formation of the T3SS translocon. This way works without the presence of host cells and is defined as “non-polar translocation”.

To analyze the antigen secretion ability of the engineered bacteria we constructed, we use both the “non-polar translocation” way and the “polar translocation” way to conduct the experiment. The signature is detected by the FLAG-tag which is carried in plasmids: pExoS54F-NY-ESO-A, pExoS54F-NY-ESO-B, pExoS54F-0201, pExoS54F-0301A, pExoS54F-0301B, pExoS54F-0301C and pExoS54F-mCherry.



1. First, in order to test whether the bacteria can synthesize the antigens we want, EGTA is used to induce Pseudomonas aeruginosa to secrete the antigen polypeptides into the culture solution, and the presence is detected by western bolt (see result 1).

2. In order to test whether bacteria can inject antigens into cells, we perform in vitro infection of HeLa cells, and the presence of FLAG-tag in the cells was detected by western blot (see result 2) and immunofluorescence (see result 3) to confirm the successful injection of antigens.

3. At the same time, in order to prove that the bacteria do not secrete proteins outside the targeted cells while attaching cells and injecting, we detect the culture supernatant of the infected cells by western blot (see result 4).

4. Finally, using the animal model, the T3SS is further verified in vivo by immunohistochemistry (see result 5).




1.Western Bolt (EDTA Induction)

All the secretion of proteins in the P. aeriginosa strain PAK-J△9 are analyzed by western blot.
We use the calcium chelator EGTA to trigger the secretion of proteins. (To see the exact process of the induction, you can go to the Protocol.) Add 100% TCA to culture medium to reach a final concentration of approximately 10% which can precipitate the proteins form culture medium. But the final concentration of TCA used may vary with the molecular weight of the precipitated protein and shouldn’t be too high, otherwise other substances will be precipitated.

First, we test which TCA concentration can better precipitate proteins from culture medium and set the TCA concentration gradient of 10%, 15% to 20%. We randomly select one type of P. aeruginosa which carrying the antigen in theory to conduct the experiment.

The result is analyzed by western blot (Figure 1.1). As is shown in figure, 20% TCA concentration successfully precipitates the proteins. So we decide to use the 20% TCA concentration.

According to the conclusion we made in the first experiment, we conduct EGTA induction experiment to test whether the engineered P. aeruginosa we constructed can produce and secret the antigens.

We set 6 test groups and a control group. Each test group contains engineered P. aeruginosa carrying the plasmid pExoS54F-NY-ESO-A, pExoS54F-NY-ESO-B, pExoS54F-0201, pExoS54F-0301A, pExoS54F-0301B and pExoS54F-0301C. The culture medium of the control group is without the presence of EGTA and the rest of the conditions are consistent with the test groups.

The result is analyzed by western blot (Figure 1.2). Five antigens (NY-ESO-A, NY-ESO-B, 0201, 0301A and 0301C) are successfully secreted by bacteria.

There may be something wrong in our operation with pExoS54F-0301B plasmid, but we don’t have enough time to test. If we have more time, we will do this experiment again using pExoS54F-0201 plasmid as positive control to make sure the whole experiment operation is correct. At the same time, we will do colony PCR to check the pExoS54F-0301B plasmids are still in our engineered P. aeruginosa. If we can’t get successful result, we will repeat experiments from Electroporation of P. aeruginosa.

From another 5 plasmids, we can draw a conclusion that the bacteria can synthesize the antigens we want by the induction of EGTA. 


2.Western Bolt (Lysates of Infected Cells)

We conduct an experiment to analyze whether the host cell contact can trigger the production of the antigens and whether the engineered P. aeruginosa can inject these antigens into host cell cytosol in the level of protein.

We infect the HeLa cells with the engineered P. aeruginosa respectively carrying the plasmid pExoS54F-NY-ESO-A, pExoS54F-NY-ESO-B, pExoS54F-0201, pExoS54F-0301A, pExoS54F-0301B and pExoS54F-0301C, then collect the HeLa cell lysates. We analyze the cell lysates by western blot (Figure 2).

The result shows that all of the six antigens can be detected in the western blot. The engineered P. aerugnosa carrying the plasmid pExoS54F-NY-ESO-A, pExoS54F-NY-ESO-B, pExoS54F-0201, pExoS54F-0301A, pExoS54F-0301B and pExoS54F-0301C can be successfully induced to express and inject the protein into the host cell.


3.Immunofluorescence of Infected Cells

In order to increase the persuasiveness of the experiment, we also used immunofluorescence techniques to prove that bacteria injected antigen into the cells. Immunofluorescence is a technique used for light microscopy with a fluorescence microscope and is used primarily on microbiological samples. This technique uses the specificity of antibodies to their antigen to target fluorescent dyes to specific biomolecule targets within a cell, and therefore allows visualization of the distribution of the target molecule through the sample.

We use anti-FLAG antibody to specificity target Flag-tag, which is supposed to be in the cells. Then we use secondary antibody which carries the fluorophore, recognizes the primary antibody and binds to it. And we also use DAPI to label DNA. (You can see more details in protocol.)

We use an epifluorescence microscope to confirm the presence of intracellular antigens and observe finer structures by using confocal microscope.

We can see several cells are injected antigens by T3SS system. But the efficiency is not high, which is related to the relative amount of cells and bacteria. And what caught our attention is that we can find green antigens in the group of pExoS54F-0301B plasmid, which support this plasmid is worked.

So, we can confirm that, P. aeruginosa can inject antigens into cells in vitro. 

4.Weatern Bolt (Culture Supernatant of Infected Cells)

In order to prove the safety of our system, we conduct an experiment to test whether the culture supernatant of bacterially infected cells contains the antigens.

We collect the culture supernatant of bacterially infected cells and use the TCA-acetone precipitation to precipitate the secreted proteins which may be contained in the culture supernatant. To prove the experimental operation is correct, we set a positive control of cell lysates (These cells are infected by P. aeruginosa carrying pExoS54F-mCherry). Then we analyze the sediment by western blot to figure out the existence of the secreted proteins (Figure 3). As is shown in the figure, all of the culture supernatant of bacterially infected cells do not contain the proteins, which further prove that our system is safe enough.

We can draw a conclusion that our system is safe enough and only inject the antigens into cell cytosol when attaching the cell membrane without wasting the antigens into the culture supernatant.

5.Immunohistochemistry

Finally, using the mouse animal model, the T3SS system was further verified in vivo by immunohistochemistry. We give mice bacteria by oral gavage. After 4 hours, the mice are dissected, frozen sections of the mouse intestine are taken and do immunofluorescence experiment. In this way, we check whether the T3SS system is effective in vivo.

According to the pictures above, comparing to the negative control, two groups with different kind of antigens both have some area with higher green fluorescence. In these areas, we can find blue fluorescence inside and those are the nucleus and the peptides are secreted into the cytoplasm. From the pictures, we can conclude that it is not that efficient for there are only several positive cells in one visual field.

According to the articles before and the experiments done by other institute, the efficient should be higher. For we do not have enough time to revise the experimental conditions, we come up with several possible results for the low efficient. Firstly, about the bacterium, there used to be the bacterium saved in -80℃ which lose the plasmid. Secondly, the concentration of bacterium lavaging to the mice may be a little bit low. Thirdly, we do not add extra termination codon to the antigen so that there are several amino acids behind the antigen which may have the influence to the efficiency. Also, for the background of the negative control is high, there may be something wrong with our sections or antibody.

In all, it is proved that this system works, though the efficiency is low according to our results. With more conditions to be corrected and the experiments to be more precise, the results should be better and it is after all a promising system using in immunotherapy for cancer. And we will continue to work for it.