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A researcher microinjects (a small needle is inserted into the nucleus and the sample dispensed) increasing amounts of vRNA into the nuclei of cells. Would you expect any of the microinjected cells to produce virus? If so, would all cells or only those receiving a certain amount of vRNA produce progeny virus? Explain. Would a provirus form in any of the microinjected cells? Explain.

Short Answer

Expert verified
In cells that receive adequate amounts of vRNA, it is possible for them to produce virus particles since vRNA serves as the blueprint for virus replication. Only those cells receiving an appropriate amount of vRNA would be able to produce progeny virus. The formation of a provirus would depend on the type of virus the vRNA belongs to. If the vRNA was from a retrovirus, provirus formation is possible upon reverse transcription and integration into the host genome. However, if it were not from a retrovirus, then provirus formation is unlikely.

Step by step solution

01

Understand vRNA and virus production

Viral RNA (vRNA) carries the genetic information for virus replication. When vRNA enters a host cell's nucleus and is successfully transcribed and translated, it can lead to the production of viral proteins and the assembly of new virus particles. #Step 2: Determine the production of virus in microinjected cells
02

Determine the production of virus in microinjected cells

In cells that receive an adequate amount of vRNA, it is possible for the cell to produce virus particles since vRNA serves as the blueprint for virus replication. However, if the amount of vRNA injected is insufficient, the necessary viral proteins might not be produced or unable to assemble into progeny virus particles. #Step 3: Role of vRNA amount in producing progeny virus
03

Role of vRNA amount in producing progeny virus

The probability of successful virus production would depend on the amount of vRNA microinjected into the cell nucleus. Cells receiving higher amounts of vRNA are more likely to produce progeny virus as compared to cells with lower amounts. This suggests that only those cells receiving an appropriate amount of vRNA would be able to produce progeny virus. #Step 4: Understanding provirus formation
04

Understanding provirus formation

A provirus is formed when a virus integrates its genetic material into the host cell's genome. This typically occurs in the case of retroviruses, which consist of RNA genomes that are reverse transcribed into DNA and inserted into the host's DNA. The viral DNA in this integrated state is called a provirus. #Step 5: Determine the possibility of provirus formation in microinjected cells
05

Determine the possibility of provirus formation in microinjected cells

Given that the exercise mentioned "vRNA" and not a specific type of virus, we cannot assume that the vRNA belongs to a retrovirus class. Therefore, we cannot definitively conclude whether a provirus would form in the microinjected cells or not. If the vRNA was from a retrovirus, then the formation of a provirus would be possible upon reverse transcription and integration into the host genome. However, if it were not from a retrovirus, then provirus formation is unlikely.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Virus Production
When discussing virus production, it's essential to understand the role of viral RNA (vRNA). vRNA is like the blueprint for the creation of new virus particles. This genetic code is responsible for directing the host cell machinery to produce viral proteins.
Once these proteins are assembled correctly, they form new viruses that can infect additional cells.
In the context of vRNA microinjection, when adequate amounts of vRNA are delivered into a cell's nucleus, virus production becomes possible.
  • vRNA enters the nucleus and is transcribed and translated into viral proteins.
  • The proteins then come together to form new virus particles.
  • If insufficient vRNA is present, there's a reduced chance for virus production, as not all necessary proteins can be synthesized.
This process highlights that virus production heavily depends on the amount of vRNA present. Too little, and the cell may struggle to produce new viruses.
Provirus Formation
Provirus formation is a specialized process that occurs when viral genetic material integrates with the host cell's DNA. This often happens with viruses from the retrovirus family. Retroviruses contain RNA that, once inside the host, is reverse transcribed into DNA. This DNA is then integrated into the host's genome, becoming a provirus.
  • The virus stays hidden within the host DNA, effectively becoming a part of it.
  • As a provirus, it can remain dormant or become active, producing new viruses at later stages.
Not all viruses form proviruses. The possibility of a provirus forming in a microinjected cell depends on whether the vRNA belongs to a retrovirus. Without this detail, it's challenging to predict provirus formation definitively. If vRNA is from a retrovirus, then the integration into the host DNA is possible, leading to provirus formation. Otherwise, a provirus is unlikely to form.
vRNA Amount
The amount of vRNA microinjected into cells is critical for determining whether virus production or provirus formation can occur. The success of these processes heavily rests on whether cells receive adequate amounts of vRNA.
  • Higher amounts of vRNA increase the likelihood of virus production by providing enough genetic material to generate necessary viral proteins.
  • Conversely, low vRNA amounts may not suffice to kickstart the production of new viral particles, preventing virus assembly.
As with potential provirus formation, the type of virus is crucial. Sufficient vRNA from a retrovirus increases the chances of provirus formation due to integration processes. Thus, in microinjection studies, gauging the amount of injected vRNA becomes pivotal for predicting the occurrence of virus production and provirus formation.

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Most popular questions from this chapter

The predominant cell type infected by HIV is CD4 \(^{+}\) cells. The most important of these are the T-helper cells. (Review the immunogenetics chapter for a description of \(\mathrm{T}_{\mathrm{H}}\) -cells.) As the disease progresses through latency into AIDS-related complex and finally ful1-blown AIDS, the absolute number of CD4 \(^{+}\) cells (i.e., \(\mathrm{T}_{\mathrm{H}^{-}}\) cells \()\) decreases. The rate of \(\mathrm{T}_{\mathrm{H}}\) -cell deletion increases as the patient enters \(\mathrm{ARC}\). As the number of \(\mathrm{T}_{\mathrm{H}}\) -cells decreases, the ratio of \(\mathrm{CD} 4^{+}\) to \(\mathrm{CD} 8^{+}\) cells inverts, going from about \(2: 1\) to less than \(1: 2 .\) Why is the \(\mathrm{T}_{\mathrm{H}^{-}}\) cell such a devastating target?

The great majority of viral diseases/illnesses manifest their symptoms within days or weeks after infection. The specific immune system responds within about two weeks, usually eradicating the virus within a couple of weeks. HIV's latency period measures in years. The infection also elicits an immune response that would be expected to overcome the virus. Yet the virus often is not eradicated. Suggest how the virus might with stand the initial immune response and why it has such a long latent period.

Describe the retrovirus life cycle, starting with the free virus.

Retroviruses are also divided into three official taxonomic groups, assignments into which are purely functional. Name the three taxonomic divisions and the characteristics of each. To which group or groups do the human pathogens belong?

As a member of the lentiviruses, HIV-1 encodes more gene products than a simple oncovirus. What are these additional gene products, and what functions do they serve?

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