Difference between revisions of "Team:NTNU Trondheim/Description"

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               Bacteriophages have the potential to solve one of the greatest medical threats of our time: antibiotic resistant bacteria. They are capable of killing select bacteria, while leaving other bacteria, as well as animal and plant cells, unharmed. For this reason they are not harmful to humans and animals. Moreover they are easily available as they exist more or less everywhere, and are plentiful in both soil and aquatic environments. For engineering purposes some advantages are that they have intrinsic evolutionary capabilities, as well as being easily manipulated and grown in large numbers. This is something we will try to take advantage of in our project.  
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               Bacteriophages have the potential to solve one of the greatest medical threats of our time: antibiotic resistant bacteria. They are capable of killing select bacteria, while leaving other bacteria, as well as animal and plant cells, unharmed. For this reason they are not harmful to humans and animals. As with antibiotics, bacteria are able to develop resistance against phages, but this process is much slower for phages, and it's much easier to develop new effective phages than to make new antibiotics. Moreover bacteriophages are easily available as they exist more or less everywhere, and are plentiful in both soil and aquatic environments. For engineering purposes some advantages are that they have intrinsic evolutionary capabilities, as well as being easily manipulated and grown in large numbers. This is something we will try to take advantage of in our project.  
  
 
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Revision as of 11:37, 27 July 2017

Why phages?

Bacteriophages have the potential to solve one of the greatest medical threats of our time: antibiotic resistant bacteria. They are capable of killing select bacteria, while leaving other bacteria, as well as animal and plant cells, unharmed. For this reason they are not harmful to humans and animals. As with antibiotics, bacteria are able to develop resistance against phages, but this process is much slower for phages, and it's much easier to develop new effective phages than to make new antibiotics. Moreover bacteriophages are easily available as they exist more or less everywhere, and are plentiful in both soil and aquatic environments. For engineering purposes some advantages are that they have intrinsic evolutionary capabilities, as well as being easily manipulated and grown in large numbers. This is something we will try to take advantage of in our project.

There are many potential applications of bacteriophages. In the area of medicine, phage therapy is the most obvious use of phages, but they might also be used for sanitazion purposes. Bacteria also play a major role in areas such as agriculture, both in terms of livestock feed and plant health, aquaculture, food processing, especially of cheese and dairy products, as well as wine production and brewing. Bacteriphages could potentially be used to counter unwanted bacterial growth in all these areas. Precision control of microbial growth might also be a possible future application.

Why not yet?

Phage therapy does however have several issues to be ironed out before becoming a mainstream medical treatment. One major stumbling block for phage therapy is the high host specificity of phages. Many phages can only infect certain strains of a bacterial species. This creates the need for either large libraries of potential phages, or a quick method of developing a phage capable of fighting a given bacterial infection. In order to solve this problem, our project attempts the latter method.

Our project

For our project, we aim to develop a method of evolving phages capable of infecting a target bacteria strain. We plan to first harvest a catalogue of phages and identify their host bacteria. Phages are plentiful in nature, and by taking different water and soil samples, we will collect a variety of phages capable of infecting different bacteria. By genetically modifying host bacteria, we will accelerate the natural mutation rate of our respective phages. We plan to set up a controlled environment that favorizes phages capable of also infecting the target bacteria. We believe this method will be capable of quickly producing tailored phages, keeping us one step ahead of the resistant bacteria.