Lytic viral lifecycles involve using the host's machinery to mass produce further copies of the virus.

Lysogenic lifecycles can become lytic under the right circumstances. The key difference is the time period and method of infection. In the lysogenic cycle, viral DNA is incorporated into the host genome and remains dormant, rather than becoming active immediately to generate more virions. After a period of time the viral DNA will be synthesized in large quantities, transitioning into the lytic cycle, and eventually lysing the cell.

Latent is a term used to refer to the period when a virus lays dormant within a host. Invasive is not a term commonly used to refer to a viral lifestyle. 

The lytic life cycle is the most basic life cycle for a virus. The virus injects its nucleic acid into the host, synthesizes the parts needed for new viruses using the host cell's ribosomes, assembles the viruses, and then breaks out of the host cell (lysis).

At no point in the lytic life cycle will a virus integrates its genome into the host's chromosomes. This technique is employed by viruses with a lysogenic life cycle.

Virulent viruses are those that reproduce only by the lytic cycle. It takes a bacteriophage only ~30 minutes to complete a lytic cycle. Prophages are latent forms of lysogenic bacteriophages that are incorporated into the host genome. Prophages can remain inactive within the genome through may cell divisions. Temperate viruses are those that may display lysogeny. Once a phage injects its nucleic acid into the host cell, the lytic cycle consists of two stages. In the early stage, transcription of viral genes that code for shutting down host transcription. In the late stage, viral genes are transcribed which code for capsid proteins and proteins that lyse the host cell to release the new viruses. 

There are two types of viral life cycles. First, a virus enters the host cell, replicates, lyses the cell, and infects another host cell. This life cycle is called the lytic cycle and results in immediate infection, symptoms, and immune response (such as inflammation). Second, a virus can enter the host cell, incorporate itself into the host cell’s genome, and stay latent for years. This life cycle is called the lysogenic cycle and it can take years for symptoms to appear. Symptoms occur when the inactive virus is activated due to some environmental cue. The virus gets activated, replicates, lyses the cell, and causes infection.

A typical virus life cycle includes the attachment of virus to host cell, entry, replication or latency (depending on the type of life cycle), and exit. If the virus immediately replicates and lyses the cell, it undergoes a lytic cycle. If the virus incorporates itself into the host cell’s genome and becomes latent, then it undergoes lysogenic cycle. Note that a virus in lysogenic cycle never exits the cell; to exit the cell, the virus must become reactivated by environmental cues. Once activated, the virus enters the lytic cycle and causes the eventual lysis of the cell. Therefore, the only common theme between lytic and lysogenic cycles is the mode of entry.

Lysogenic cycle of a virus involves the incorporation of the viral genome into the host cell’s genome. Upon incorporation, the virus becomes a provirus and remains latent until activated. The only remnant of the virus found in provirus is its genome, or its nucleic acid content. Note that viruses can have DNA or RNA. If it has RNA, virus uses an enzyme called reverse transcriptase to convert the RNA to DNA. The DNA can now incorporate itself into the host cell’s genome (host cell genome is made up of DNA only).

One of the key characteristics of a provirus is that it does not cause any symptoms such as fever, headaches, etc. It can only cause infection and symptoms after reactivation, which can occur due to environmental cues.

Cell rupture, or cell lysis, is caused by viruses in lytic cycle. In a lytic cycle, the virus replicates and exits the host cell, causes an infection, and elicits an immune response.

The question states that the virus is known to cause a deadly disease. It also states that the rat did not develop any symptoms for the entire observatory period (2 weeks). One possible explanation for this result is that the virus enters the cell and becomes latent. It incorporates itself into the host cell's genome and causes disease once re-activated. This reactivation can occur years after the primary infection; therefore, a patient infected with this virus can have no symptoms for years. Recall that a virus that enters the cell and becomes latent is undergoing the lysogenic cycle; therefore, this virus must be undergoing this life cycle.

The question states that the rat is immunosuppressed. This means that the rat does not have the ability to activate the immune system (B cells, T cells, macrophages, etc.) to fight infections. Also, remember that even a completely immuno-competent rat will not produce an immune response to this virus. This is because the immune system does not recognize a latent virus in the lysogenic cycle and cannot, therefore, produce an immune response.

The correct answer is that cells must be actively replicating. Retroviral gene integration into host genomes can only occur when the host is actively replicating. Pantropic retroviruses are able to infect many different cell types from many species. Additionally, the presence of a lipopolysaccharide layer indicates that the target cell is a bacterium. Bacteriophages, not retroviruses, infect bacteria. 

Temperate phages a so named because after infecting a bacterial cell, they can enter either the lysogenic or lytic cycle. Other phages cannot enter the lysogenic cycle and will always enter the lytic one. Since they have the choice to either hide out in the cell unnoticed or immediately replicate and lyse the cell lysogenic phages are refereed to as temperate.

During assembly, newly synthesized viral proteins and the replicated viral genomes associate with one another to form new virions. The build up of new virions causes rupture and release. Replication describes the production of viral mRNAs which are translated using host machinery. Penetration describes the entry of the original virus into the cell.