Relevance of the project

Bacteria play a fundamental role in human life and they are still the preferred models to study the molecular dynamics of organisms. One example are probiotics because of their vital importance in industry and food manufacturing. Infection by phages represents a relevant and expensive problem in these areas. For this reason we decided to construct a system to contend with bacteriophage infection at a population level.

Given this global protection vision emerges the idea of dividing our project in two subsystems: delivery and defense. Their coupled expression leads to a cascade dependent on the presence of an infectious phage. This property gives an extra versatility to the project because the defense subsystem turns on faster enough to hold back the infection and then lasts enough to give "immunity" to the population. Therefore, it is feasible to achieve a faster and wider protection response by amplifying the infection signal delivered by the phage in order to increase the number of "immune" bacteria at every lytic cycle.

Portability

The project is designed in such a way that contributes with molecular biology as well as with industry. To achieve this, the defense system should be portable enough to be used as a tool for protecting profitable bacteria. Portability means that the device should work in a wide range of bacterial species. The system activation depends only on the presence of the replication machinery of the infectious phage. Hence, if the identity of the protected bacteria doesn´t matter, there is the possibility to modify the multi-promoter so it can be triggered against specific phages. On the other hand, phage P4 seems to be able to infect a wide range of bacteria, which could contribute to the portability of the system.

Standarization and delivery

Standardization of biobricks has become an alternative in the development of easier and more profitable tools for genetic engineering. In this context, our project takes advantage of the phages property for infecting and transducing genetic material into bacteria. We will modify P4 bacteriophage in such a way that facilitates gene cloning into phage’s genome for its subsequent transduction into bacteria harboring the P2 genes for completing lytic cycle of the carrier phage and its exponential release.

Logic of the project subsystems

The first level of the expression cascade consists on the delivery (Phage Delivery) of the kamikaze system that will be instantly activated when a lytic phage is detected inside the cell (Defense system: Phage sabotage). While formation of infectious viral particles is being held back, a diffusing signal will alarm neighboring cells of the presence of infection. (Gossip). The reaction of alarmed cells consists on triggering a device which activates a delay for invading phage multiplication in case of turning on the kamikaze system (Paranoia).

• • • Aqui estaria bien poner una animaci[on o imagen con los elementos logicos del sistema, o los pasos, como modificar p4, produccion, entrega, deteccion d fagos, respuesta anti fago,....
      
      

Logic design of the project subsystems

The first level of the expression cascade consists on the delivery (Phage Delivey) of the protection system that will be immediately activated when a phage is detected (Defense system: Phage sabotage). At the same time formation of infectious viral particles is hold back, a diffusing signal warns the neighboring cells of the presence of infection (Defense system: Gossip). The reaction of alarmed cells consists on turning on a device, which allows a delay in case of turning on the defense system (Paranoia).

• • • En esta parte podemos justificar el sistema o almenos detallar las partes que usaremos. puede ser igual en una aimacion

Project subsystems

a) Delivery

Main objective

The main goal of the delivery device is the construction of a new iGEM vector capable of being used in a system for transduction of biobricks and synthetic devices in several bacterial hosts.

We propose a complete, standardized and controllable system for production of phage vectors for delivery of over 25 kb of synthetic constructs to a wide range of bacterial hosts. The relationships between bacteria and phages is quite rich and dynamic, so hacking this system for our control will be an interesting challenge!

The system starts with a modified bacteriophage P4 genome. This viral vector will be modified to be compatible with iGEM standards for biobrick assembly. The second part of the system involves controlled production of the modified P4 phages under our control.

As can be imagined, this promises to be a powerful tool in Synthetic Biology with a great potential for expansions and applications. We like the analogy of this modified P4 as an USB *** memory device, where you can store information or a complete program and just "plug" it into another machine that will handle such information.

Background

P2-P4 bacteriophages

Bacteriophage P2 and P4 are double stranded DNA enterobacteria viruses. Phage P4 is a satellite phage because it is dependent on the machinery of P2. Sometimes, it is called a "parasite phage", since it takes over the elements of P2 and leaves its "host phage" practically neutralized. There are several interesting features of the P4 genome, including transactivation zones (the genes that respond to the presence of P2 along with P4 and vice versa) that function in domination of the late P2 genes. Important elements of this kind are gene P4 delta and P2 ogr, which work synergistically together in activating P2 genes. Given these interesting properties, P4 has been exhaustively studied.

P4 genome structure

We can divide P4 genome into two main regions: the essential and non-essential region. The essential region contains operons intended for replication and hijacking of P2, and the non-essential region contains accessory genes for special situations as lambda infections, as well as the integrase and attachment site. Removing the latter two would result in a permanent plasmid-state P4 with a unique multicopy replication system.

P4 sid mutation

As P4 thoroughly depends on P2 for capsid, tail and lysis functions, the difference in size between both genomes (+- 33kb for P2 whereas +-11kb for P4) came to attention. P4 protein sid is able to scaffold a smaller capsid with the same structural proteins as P2. A sid mutant was found that made P4 pack its genome inside bigger-sized capsids, which can hold up to 1, 2 or 3 copies of its genome. The extra genome copies could be “something else”; this means P4 can transport over 20 kbs of extra foreign DNA attached to its genome.

Cos sites

Another important point is that the signal for encapsidation is located in the “cos” sites. It means that you only need this region (about 20 pb, but you increase the efficency of transduction with a region of more than 100 pb) to encapsidate a double DNA strand disregarding the sequence in between the cos sites.

P4 Modifications

The key steps in modifing P4 genome are:

• Standardize P4 by removing forbidden restriction sites (EcoRI, XbaI, SpeI, PstI).
• Add preffix and suffix at the ends so you can clone biobricks in it like any other standard plasmid.
• Remove the integrase from the genome so P4 will be maintained as a plasmid in the bacterial host.
• Remove P4 non-essential region. Coupled with the usage of P4sid1 variant, this raises cloning capacity inside the genome up to 25 kb.
• Add an antibiotic resistance.
• Add transcriptional terminators surrounding the cloning region.
• Add annealing sequences for universal primers.

P4sid1 standardized production

We thought of a way to overproduce our viral particles without being forced to infect with P2 or getting P2 particles as a byproduct. The solution planned was to construct an E. coli strain containing all the useful genes for P4 in P2 (capsid, tail and lysis operons). In addition to these genes, the helper cell would also contain the main P2 transactivators (cox and ogr) under a lac operator. This way, after we transform the helper cell with our desired P4 plasmid, we would decide when to promote stock production by lysis of the helper bacteria by adding IPTG. Then we have our biobrick assembled inside ready-to-use phages that can deliver their genome to wildtype bacteria.

We have also biobricked the cos sites of P4. This biobrick should be cloned in any vector with your construction. If you transform the P4 producing strain with this vector and then infect with P4, you will have as a result some P4 phages and some of your vectors with the P4 cos sites inside a capsid. It means you can encapsidate up to 33 kb with this system. Until your production is pure, you can add a marker in the plasmid (e.g. an antibiotic resistance or color) so after infection you select the colonies with the desired plasmid.

System delivery: benefits and perspectives

One of the main motivations for the construction of this delivery system using P4 as the vector is to achieve insertion of devices into cells by transduction as an alternative way from traditional transformation. This extends the panorama of synthetic biology to the whole P4 host range, which involves especies of genera such as Rhizobium, Klebsiella, and Serratia besides Enterobacteria like E. coli. The delivery of parts into wildtype bacteria could be a pool for innovative applications and properties, such as the following:

1) A defense system against another phages for E. Coli delivered by P4 phage.

The idea we love is hacking one system that is harmful (if you are a bacterium) and using it for your own protection against similar systems.

2) Refined phage therapy.

In addition to bacterial protection, we propose the use of this system to protect humans. This could be done using phage therapy to transduce DNA into pathogenic bacteria. It would be an advantage in cases where extra control is needed, as in degrading toxins before killing the pathogen and so avoiding further immune response. Another benefit would be response specificity in hacking pathogen-specific regulators while the system is bypassed in non-hazardous strains.

As a first step in this area, we have adapted the kamikaze system to detect pathogenicity instead of phages. The target pathogen is EHEC and EPEC (Enterohemorragic and Enteropathogenic Escherichia coli). P4 will introduce a specific binding site for a pathogenicity-specific regulator LER, which in turn will activate the kamikaze system at the moment LER activates pathogenic [http://en.wikipedia.org/wiki/Locus_of_Enterocyte_Effacement effacement].

3) Phage mediated switching

Another usage could be to "train" the bacterial population by P4 infection so that it is sensitive to a future stimulus, like indirect activation of medicine producing devices inside bacteria through phage contact. For instance, imagine you load a device of interest in the P4 genome and you transduce native E. coli with it. Now this E. coli will turn the device on in response to a new stimulus, say a body substance like a hormone.

Model Validation

We expect the Burst-Size to be significantly reduced. An optimal result would be a Burst-Size of 0; we see in our results that this is not the case. The BSD has mean ___ and variance___. We can calculate the likelihood of the model (BSD) given the observed burst size for both the wild type and modified E.Coli. The CA and the ODE’s generate growth curves that can be compared with those obtained experimentally.

b) Defense

Main objective

An important artefact concerning with the defense system is the use of toxins as the main element in the disruption of phage’s assembly and scattering. Even though the contention of the infection implies that some bacteria will die, the use of a RNAse and a DNAse induces a delay of the phages production by beating host machinery. This in turn, avoids the possibility of the phage to getting resistance against toxins.

Phage detection

When phage T7 or T3 transduce their DNA into the host cell, the phage's polymerase will be able to bind the multi-promoter of the system, which will activate two subsequent actions: production of toxins to inhibit further phage propagation, and a neighborhood alarm. The first thing translated is GFP.

The part contents, in order of appearance, are as follows:

Translation process sabotage

One of the elements transcribed by T7 RNA polymerase at early stages of T7 cycle in our transformed bacteria is the suicide system which consists of a polycistronic mRNA that codes among other proteins, the rRNAse domain of colicin E3, this toxin cleaves 16s rRNAs in active ribosomes from E. Coli, which causes inactivation of the ribosome and a subsequent decay in the overall bacterial translation, this response of our system affect T7 Cycle by reducing the number of bacteriophage proteins and then lowering the number of T7 phages at the end of the cycle.

Gossip and Paranoia

luxI is another product from the suicide system, infected cells produce it in order to warn surrounding cells of phages' presence through AHL. When a neighboring cell has been reached by AHL it turns on an antisenseRNA against a T7 messenger to interrupt its life cycle if it becomes infected, this delay in the life cycle of T7 gives more time to colicins to act upon the translation machinery reducing active ribosomes to zero before the assembly of any T7 particle.

Model

In order to simulate the spatial dynamics of the Defence System we designed and implemented a Cellular Automata (CA). Using the CA we can approach several problems at the same time: E. Coli movement and duplication, AHL and phage diffusion and the infection process. Parameters for the bacteria in the CA are random variables so we sample the distributions created by the Stochastic Kinetic Simulations:

Finally we constructed the multi-scale model by sampling the distributions obtained with the Stochastic Kinetic Simulations and used those values as parameters for the cells in the CA.