The Potential of Transgenic Mice Models for Virus Research

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SUMMARY

The discussion centers on the design of transgenic mice models for studying poliovirus infection. Participants debate two options: one involving a mouse expressing a human receptor gene for viral docking and internalization, and another that includes a gene for viral protein expression at puberty. The consensus is that expressing the human receptor is essential for infection, while the addition of viral protein may complicate the study of immune response. The goal is to create a model that allows for effective infection by the poliovirus.

PREREQUISITES
  • Understanding of transgenic mouse models
  • Knowledge of poliovirus biology
  • Familiarity with gene expression mechanisms
  • Basic concepts of viral infection and immune response
NEXT STEPS
  • Research techniques for creating transgenic mice using CRISPR-Cas9
  • Study the role of MHC class II in viral peptide presentation
  • Explore methods for assessing viral infection in animal models
  • Investigate the implications of viral protein expression on immune response
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Researchers in virology, genetic engineering, and immunology, particularly those focused on developing animal models for viral infection studies.

TytoAlba95
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Homework Statement
While attempting to create a model of poliomyelitis in mice, it was found that the mice cannot be infected with the said virus. Since human beings are susceptible to this viral infection, which kind of transgenic mice should be generated to have a transgenic mouse model that can be infected with polio virus. Select the right approach from below:
Relevant Equations
a. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus.
b. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus along with a gene designed to express surface protein of this virus at puberty.

Ans:a
I think the answer should be (b) and not (a) because to study the mice model, there should be a gene designed to express the protein of this virus on the cell surface (but I don't know the what it has got to do with puberty ).
 
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Not sure what the problem is, a. and b. differ only by that puberty part - so why would you choose b over a?
 
Borek said:
Not sure what the problem is, a. and b. differ only by that puberty part - so why would you choose b over a?

Option b. is slightly different from a. , (b) talks about incorporating a gene (MHC class II,I guess) that will express the viral peptide after internalization and processing of the virus particle.

I don't understand what puberty has to do with this. May be the puberty part rules out option (b).
 
Perhaps you misquoted the question then, I fail to see a single letter by which these things differ:

a. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus

b. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus
 
Borek said:
Perhaps you misquoted the question then, I fail to see a single letter by which these things differ:
I don't know why it is not displaying correctly to you.
I quoted the following two options:

a. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus.
b. A mouse expressing human receptor gene which makes cell surface protein for docking and internalization of polio virus along with a gene designed to express surface protein of this virus at puberty.
 
The key part to the question is this:
SanjuktaGhosh said:
which kind of transgenic mice should be generated to have a transgenic mouse model that can be infected (my emphasis) with polio virus.
If you’re trying to build an animal model of infection, do you want the mouse to express the viral protein?
 
TeethWhitener said:
If you’re trying to build an animal model of infection, do you want the mouse to express the viral protein?

Yes, I would like the viral protein to be expressed to study how the animal's immunity handle's the infection(which I believe would be the aim of building the model).
 
Here’s how I’m reading the question: you want to build a mouse model that can be infected with the poliovirus. It’s clear that you will want to express the human receptor protein on the mouse cells’ surface, so that when the virus is introduced, it will be able to dock with and infect the model organism’s cells. If the mouse is also expressing viral surface protein, what advantage does that give you for reaching your goal? I’m assuming you aren’t interested in immune response yet, you’re just interested in seeing if the cell can be infected with the virus. Having a viral protein that’s expressed both by the virus and by the model organism is only going to confuse things.
 
TeethWhitener said:
Here’s how I’m reading the question: you want to build a mouse model that can be infected with the poliovirus. It’s clear that you will want to express the human receptor protein on the mouse cells’ surface, so that when the virus is introduced, it will be able to dock with and infect the model organism’s cells. If the mouse is also expressing viral surface protein, what advantage does that give you for reaching your goal? I’m assuming you aren’t interested in immune response yet, you’re just interested in seeing if the cell can be infected with the virus. Having a viral protein that’s expressed both by the virus and by the model organism is only going to confuse things.

I see your point. Thank you.
 

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