The Potential of Transgenic Mice Models for Virus Research

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Discussion Overview

The discussion centers around the use of transgenic mice models for studying poliovirus infection. Participants explore the implications of different genetic modifications in mice, particularly regarding the expression of viral proteins and human receptor genes, and how these modifications relate to the goal of creating an effective model for infection.

Discussion Character

  • Debate/contested
  • Technical explanation
  • Exploratory

Main Points Raised

  • Some participants argue that a gene should be designed to express the viral protein on the cell surface for effective study, while others question the relevance of this expression to the goal of infection.
  • There is confusion regarding the differences between two options presented for the transgenic mice model, with some asserting that the only difference is the mention of puberty in one option.
  • One participant emphasizes the importance of expressing the human receptor protein on the mouse cells to facilitate viral docking and infection, suggesting that expressing viral proteins may complicate the study.
  • Another participant expresses uncertainty about the necessity of expressing viral proteins in the context of studying infection, indicating a focus on whether the model can be infected rather than on immune response.

Areas of Agreement / Disagreement

Participants do not reach a consensus on whether expressing viral proteins is beneficial for the model aimed at studying poliovirus infection. Multiple competing views remain regarding the necessity and implications of such expressions.

Contextual Notes

Participants highlight potential misunderstandings regarding the question's wording and the implications of genetic modifications, indicating that assumptions about the role of puberty and protein expression are not fully resolved.

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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