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Viruses are typically described as obligate intracellular parasites , acellular infectious agents that require the presence of a host cell in order to multiply. Viruses that have been found to infect all types of cells — humans, animals, plants, bacteria, yeast, archaea, protozoa…some scientists even claim they have found a virus that infects other viruses!

But that is not going to happen without some cellular help. Viruses can be extremely simple in design, consisting of nucleic acid surrounded by a protein coat known as a capsid. The capsid is composed of smaller protein components referred to as capsomers. Viruses can also possess additional components, with the most common being an additional membranous layer that surrounds the nucleocapsid, called an envelope. The envelope is actually acquired from the nuclear or plasma membrane of the infected host cell, and then modified with viral proteins called peplomers.

Some viruses contain viral enzymes that are necessary for infection of a host cell and coded for within the viral genome. A complete virus, with all the components needed for host cell infection, is referred to as a virion. While cells contain double-stranded DNA for their genome, viruses are not limited to this form. Some viruses even start with one form of nucleic acid in the nucleocapsid and then convert it to a different form during replication.

Viral nucleocapsids come in two basic shapes, although the overall appearance of a virus can be altered by the presence of an envelope, if present. Helical viruses have an elongated tube-like structure, with the capsomers arranged helically around the coiled genome. Icosahedral viruses have a spherical shape, with icosahedral symmetry consisting of 20 triangular faces.

The simplest icosahedral capsid has 3 capsomers per triangular face, resulting in 60 capsomers for the entire virus. Some viruses do not neatly fit into either of the two previous categories because they are so unusual in design or components, so there is a third category known as complex viruses. Examples include the poxvirus with a brick-shaped exterior and a complicated internal structure, as well as bacteriophage with tail fibers attached to an icosahedral head.

While the replication cycle of viruses can vary from virus to virus, there is a general pattern that can be described, consisting of five steps:. Outside of their host cell, viruses are inert or metabolically inactive.

Therefore, the encounter of a virion to an appropriate host cell is a random event. The attachment itself is highly specific, between molecules on the outside of the virus and receptors on the host cell surface. This accounts for the specificity of viruses to only infect particular cell types or particular hosts. Many unenveloped or naked viruses inject their nucleic acid into the host cell, leaving an empty capsid on the outside.

This process is termed penetration and is common with bacteriophage, the viruses that infect bacteria. With the eukaryotic viruses, it is more likely for the entire capsid to gain entrance into the cell, with the capsid being removed in the cytoplasm.

An unenveloped eukaryotic virus often gains entry via endocytosis , where the host cell is compelled to engulf the capsid resulting in an endocytic vesicle. An enveloped eukaryotic virus gains entrance for its nucleocapsid when the viral envelope fuses with the host cell membrane, pushing the nucleocapsid past the cell membrane.

If the entire nucleocapsid is brought into the cell then there is an uncoating process to strip away the capsid and release the viral genome. Viral specific enzymes, such as RNA-dependent RNA polymerases, might be necessary for the replication process to proceed. Protein production is tightly controlled, to insure that components are made at the right time in viral development. The complexity of viral assembly depends upon the virus being made.

The simplest virus has a capsid composed of 3 different types of proteins, which self-assembles with little difficulty. You can follow the question or vote as helpful, but you cannot reply to this thread. I have the same question Report abuse. Details required :. Cancel Submit. Previous Next. SpiritX Volunteer Moderator. Hi, Some programs, particularly system maker's included programs, do not identify themselves by name in the StartUp tab.

If you Right Click on any of the existing Column Names at the top of the columns in the StartUp tab there are other column display choices. Select "Command Line" and you can see what program is opening. You can use AutoRuns again and check the command line and the file name with those programs running in Task Manager's - StartUp tab - Command line column. How satisfied are you with this reply?

Thanks for your feedback, it helps us improve the site. In reply to SpiritX's post on January 8, Brilliant SpiritX! Thank you!!! Once I enabled the show "Command line" column in the Task Manager Setup tab—something I did not know could be done—I found that "Program" is an application that does not exist on my system.

The command line points to "LAN Messenger," lmc. Now I remember I was looking for a network messenger, back before Christmas, that I could install so that I could easily communicate with other users on my local network.

I downloaded LAN Messenger, installed it, didn't like it it did not seem to play well with Windows 8 , and uninstalled it. Normand's Advice. In reply to One4Peace's post on January 8, I had the same issue here I fix it. Stefan Babos.

This process can also be referred to as maturation. Virion release: There are two methods of viral release: lysis or budding. Lysis results in the death of an infected host cell, these types of viruses are referred to as cytolytic.

An example is variola major also known as smallpox. Enveloped viruses, such as influenza A virus, are typically released from the host cell by budding.

It is this process that results in the acquisition of the viral phospholipid envelope. These types of virus do not usually kill the infected cell and are termed cytopathic viruses. Residual viral proteins that remain within the cytoplasm of the host cell can be processed and presented at the cell surface on MHC class-I molecules, where they are recognised by T cells.

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