Due to our work in the lab, we had one person who was in charge for the safety precaution. Our “safety authorized person” organized a training for all team members including fire drill and evacuation, how to behave in case of an accident and how to render first aid. This safety training was also about good laboratory practice – correct waste disposal and clean and decent laboratory work. To fulfill a good laboratory practice, everyone had to wear lab coats, safety glasses and gloves. In addition to this lab safety training, we further had a safety seminar where all people who worked at the institute participated. There we got used to all institute related safety questions. Both safety seminars took place before starting with the lab work. Every lab work was carried out within the biosafety guidelines established by the Technical University of Graz. Due to our project, we took part at a skype conference about safety organized by the University of Uppsala. Five teams from all over Europe participated at the conference .  The discussion was about general safety in lab as well as the potential risk of the designed constructs and what might happen if they are released. One of the questions was if we could anticipate how our GEM (Genetically Engineered Machine) would behave if released. We came to the conclusion, that there are no major security vulnerabilities, since we planned our construct according to the iGEM safety guidelines. Aside from the safety precautions for the construct, we only used lab strains with deficiencies such as BL21, XL1-blue, TOP10 or DH5a. Lab strain deficiencies are a selection disadvantage, like lower fitness or lower survivability. On the other hand, the DNA is beneficial for more fit bacteria if transferred. However, we took arrangements to prevent the uncontrolled release, especially the working steps of our student team members have been carefully examined. Here we took special attention that all the work was performed regarding the lab safety regulations. If you are interested in more details, you can check out the video here.

For our project we used E. coli BL21, XL1-blue and TOP10 strains. These common lab strains provide no risk for the general public. The antibiotic resistances we used were spectinomycin, kanamycin and chloramphenicol. These are common markers that have been used for many years in molecular biology practice regarded as safe. Their use in medicine is not relevant anymore since they have been substituted by more efficient and safe antibiotics with less side effects. Horizontal gene transfer, HGT, could lead to some problems, but that concerns all iGEM teams and synthetic biology projects and is not unique to our work. In our case, we used fluorescence proteins and we cannot imagine a scenario in which fluorescence proteins help bacteria to survive or provide a selective advantage. Therefore, HGT is not a high risk.

Since we are dealing with a new application, we cannot accurately determine what our project will evolve to in the future. Connecting bacteria to computer is a completely new way of data exchange, but due to long expression times of fluorescent proteins, it is very unlikely that this interaction might be used for risky actions. There might be many applications but we cannot imagine a hazardous one. The potential for the misuse of the biobrick database is an inherent problem not only for iGEM, also to all the DIY biology, biohacker movement. To conclude, all team members and all the people who supported us could not imagine a negative and unsafe usage of our project for the future. We are all glad that our project was performed safe.