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<h4>The day long trip was very productive and we must thank the two professors and their faculty members for their enthusiasm and extremely valuable insights they provided to us. We very quickly were able to choose the pathogen we wanted to targets for our vaccination during this meeting. Originally, based on the literature we had a few candidates for our project including: </h4><br> | <h4>The day long trip was very productive and we must thank the two professors and their faculty members for their enthusiasm and extremely valuable insights they provided to us. We very quickly were able to choose the pathogen we wanted to targets for our vaccination during this meeting. Originally, based on the literature we had a few candidates for our project including: </h4><br> | ||
− | <h4> | + | <h4>Both professors were deeply engaged in our discussion and very interested in our ideas. We were received very well and obtained some great insights into future challenges we will face. Professor Gao expressed concern toward the availability of synthesizing antibodies inside the fish gut. Gut is a complicated system where many different types of bacteria coexist, so they cannot be sure if specific antibodies can be expressed and the exact amount will they be expressed in gut. Professor Chen also pointed out that despite the model of iron Qs system can theoretically express target protein, but there are other gene expressions happened in the gut that may disturb the synthesis of antibodies. |
+ | We left our whole day meeting having developed our project design much further than anticipated. A summary is given below:</h4> | ||
+ | <ul> | ||
+ | <li><h4>- We were able to choose the target pathogen for the development of our vaccine based on the availability of genes, the amount of previous research into this particular virus and the historical and economic impact associated with outbreaks of Koi herpes virus diseases (caused by the virus). This target would give us the best chance to have a positive impact on the koi fish industry and would garner interest from the people within it.</h4></li> | ||
+ | <li><h4>- We discussed at length the approaches we would make to develop our vaccine. Plasmid DNA vaccines are tightly regulated and it was recommended that we not pursue this area. Nor was it recommended we use partially attenuated whole virus or virus coats again due to regulations and the fact that we are just a high school. The idea of bacterial vaccines expressing recombinant proteins as antigens was attractive to the professors as they were aware of such research and after learning more about what iGEM was they agreed with us that this seems the most relevant course of action.</h4></li> | ||
+ | <li><h4>- We also got good feedback on the idea of using a lactic acid bacteria as our delivery choice as we were told that many hold generally regarded as safe (GRAS) status and can be easy to work with. </h4></li> | ||
+ | <li><h4>- The questions and problems remained as to how we could protect any antigen we use through the alimentary canal of fish. Bioencapsulation and the use of inducible promoters were discussed as possible solutions. When iron starvation was discussed the professors indicated that they thought it was possible but there will be a lot of metabolite “noise” in the gut environment and the best advice they could give here was that it needed to be tested and see. | ||
+ | </h4></li></ul> | ||
+ | <br/> | ||
<h4></h4><br/> | <h4></h4><br/> | ||
Revision as of 02:07, 22 October 2019
Human Practice
Introduction
Our project’s focus was on the development of engineered bacterial strains which could act as vaccine delivery systems by expressing recombinant genes. Our long term goal would be to have a positive impact of on the aquaculture and fisheries industries, more specifically, the high end and mid level ornamental fish industry which breed varieties of koi fish (Cyprinus rubrofuscus). Our final engineered designs we worked so hard on were designed to be capable of providing these high value fish varieties immunity against the Cyprinid herpes virus-3, which cases the high mortality rate disease Koi herpesvirus disease (KHVD).
As always the design of a genetically engineered system requires many revisions, multiple identification of new problems, and several development of potential solutions all of which needed to be informed by good science and have logical reasoning for pursuing. In this sense, each stage of our project since the early team meetings of our BioBuilder club have been informed by the individuals and organizations we sought out and contacted, in order to ensure we had a safe, consequential, interesting, and scientifically sound project. This section outlines our efforts in that endeavor.
The goals of our integrated Human Practices work can be summarized in the following points:
1. We wanted to first learn what were the issues associated with the koi fish industry and more specifically to see what a potential problems exists that could be solved, or at least improved, with synthetic biology concepts. This was our generating ideas and identifying problems part of the engineering design process.
2. We then wanted advice on the early stages of our genetically engineered systems. Here we sought academic experts that have worked on the health of fish in aquaculture and precisely the health and breeding of Koi. The ideas generated we had at this stage were based on discussion among ourselves and from a review of the associated literature. We were able to discuss in detail our potential solutions with professors and bring back more ideas for the refinement stage of our project design.
3. When we asked Mr. Wang if they vaccinate the fish against any disease, the answer was no. The Koi the school purchased were the cheap ones, so they think the fish food that containing the immune system boost ingredient will be enough for our Koi. The fish themselves are also not vaccinated against anything prior to purchasing. We left this meeting with clearer objective and our project progressed from simply developing a system to help provide a boost to fish health through the production of adjuvants in fish food to one where we wanted to develop a specific vaccine for a specific pathogen that is a common killer I our part of the world (East China). We also had the objective of starting to look for people to learn from that are involved in the high level Koi breeding.