Viruses ot Tc&gM€s I Explaim txhy viru*es are rc*t *lasslfled into amy klragd*rn, I Describa *hanacteristics cf a representative virus. T Explain tlre life cycle of a reBresentative virus. Mu.ry diseases that plague members from each kingdom are caused by bacteria or viruses. You might think, because of this, that bacteria and viruses are roughly similar kinds of micro-organisms. Yet bacteria are classified as living organisms, while viruses are not. What are viruses? You know that scientists consider cells to be the basic units of life. Viruses have no cellular structure. By this definition, therefore, viruses are not organisms and they are not classified in any kingdom of living things. Viruses have no cytoplasm, organelles, or cell membranes. They do not carry out respiration or many other common life processes. Viruses consist of Iittle more than strands of DNA or RNA surrounded by a protective protein coat called a capsid shown in Figure 4.19. In effect, viruses are mobile genes that parasitize cells. The capsid protects the virus from attack by the host cell enzymes, and it helps the virus attach itself to specific receptors on the host cell. Classitying Viruses Since viruses were first identified in 1935, scientists have described more than 160 maior groups. Members of different groups differ in their size and shape as shown in Figure 4,20. The shape is determined by the type and arrangement of proteins in the capsid, Polyhedral viruses such as the polio virus resemble small crystals and may have as many as 20 sides. The HIV virus that causes AIDS, has a spherical shape. The tobacco mosaic virus has a cylindrical shape. The T4 virus infects bacteria. It has a polyhedral head attached to a protein tail and several tail fibres, Some groups of viruses are able to replicate only in a particular species, while others may be found, for example, in both animals and plants, or in both plants and fungi. Viruses are also grouped by the types of diseases they cause, Viruses that infect humans are currently classified into 21 groups. These groups differ in their genomes (set of genes) and their method of replication, o o !n,' ' ; Figure 4.19 HIV viruses budding from the surface of a host T-lymphocyte white blood cell. The viruses are acquiring their protein coat from the host cell's membrane. 122 r MHR. Unit 2 Biodiversity v\ a a'' Figure 4.2o Virus particles have a variety of shapes. The viruses shown here, include (A) the polio virus, (B) the HIV virus, (C) the tobacco mosaic virus, and (D) the T4 virus. Viral Reproduction One characteristic viruses do share with living things is the ability to multiply. However, a virus cannot do this on its own. It depends entirely on the metabolism of a eukaryotic or prokaryotic cell to replicate its DNA or RNA and to make protein coats for each newly formed virus particle. Before a virus can enter any cell, it must attach to a specific receptor site on the cell membrane of the host cell, The proteins on the surface of the virus act as keys that fit exactly into a matching shape on the host cell membrane. For example, a protein in the tail fibres of the T4 virus shown in Figure 4.20 recognizes and attaches the T4 to the specific host ceII. In other viruses, the attachment protein is in the capsid or in the envelope. This attachment sequence, where the virus recognizes and attaches to the host cell, is like two jigsaw pieces fitting together. Because each virus has a specifically shaped attachment protein, the virus can only attach to a few specific types of cells. The T4 virus mentioned above, for example, can only VITUS infect certain bacterial cells. It cannot attach to a plant or animal cell. Some viruses are even specialized to the type of cells within an organism. The polio virus, for example, infects human nerve and intestinal cells. This specificity is very important for controlling the spread of viral diseases. Therefore, each virus can only enter particular cells with specific receptor sites. Outside of their host ceII, viruses are completely inert. Viruses can enter cells in two different ways. In the first, once attached to the host celi, the virus can inject its nucleic acid into the ceII. Figure 4.21 shows the steps to this cycle of viral replication, called the lytic cycle. The lytic cycle is typical of bacteriophages - viruses that attack bacterial cells. A typical lytic cycle takes about 30 min, and may produce up to 200 new viruses. If a virus is contained in an envelope, it may enter in a second way. After the virus attaches, the membrane of the host cell surrounds the virus. This creates a vacuole inside in the host cell's cytoplasm that contains the virus. When the virus breaks out of the vacuole, it releases its nucleic acid into the cell. bacterial DNA nucleic acid @ Attachment bacterial host cell Figure 4.21 The lytic cycle occurs when a virus inserts its nucleic acid into a cell, such as bacterium, and then uses the cell's metabolism to replicate its DNA or RNA and make new viruses. Chapter 4 Patterns of Life . MHR * 123 ln the 1970s, the World Health 0rganization off icially declared that it had rid the world of the smallpox virus. The disease produced by this virus had been a major cause of human deaths throughout history. The extermination of the virus was possible because the virus rnfected only humans and no other species. Viruses and Disease In the lytic cycle of a virus, newly formed viruses burst from the host cell, usually killing it. In multicellular hosts, these new viruses then infect neighbouring cells, thereby causing damage to their host. The amount of damage and its effects on the host vary, Human immunodeficiency virus (HIV) is an example of a type of RNA virus called a retrovirus. Retroviruses contain an enzyme called reverse transcriptase. As you can see in Figure 4.22, this enzyme causes the host cell to copy the viral RNA into DNA. In this form, the viral genome can enter the chromosomes of the host cell and be copied when the cell divides. You wiII learn more about RNA viruses at the end of this section. In other cases, viruses can invade a cell but not kill it. These viruses undergo a different type of replication cycle in which their DNA becomes integrated with the host cell chromosomes. Once inserted into the host chromosomes, the viral DNA is called a provirus. When the host cell divides through the process of mitosis, it replicates the retrovirus P1-.I -,*-* o DNe provirus along with its own DNA. Every descendant of the host cell will carry a copy of the provirus in its chromosomes. This process can continue for years, with no harm to the host. As part of the host chromosomes, the virus cannot be easily detected by medicai tests. At any time, however, the provirus can separate from the host chromosomes and complete the more damaging lytic cycle shown in Figure 4.21. The replication strategies of viruses help explain certain patterns of disease. For example, the herpes simplex virus causes cold sores in people. These sores may appear and disappear on the skin of an infected person throughout her or his lifetime. The sores appear when the viral cycle destroys cells, and they disappear when the virus is in its provirus stage. The exact trigger that causes the switch from one phase to another is not known. Other viruses follow variations of the replication strategies already described. For example, HIV forms a provirus in the host cell chromosomes, but it also produces small numbers of new viruses while the cell continues to function normally. This explains why people may test positive for HIV but remain healthy for many years. Only when the infection spreads to more and more cells do the symptoms of AIDS (Acquired Immune Deficiency Syndrome) eventually appear. The symptoms result from infections by other micro-organisms because the HIV virus has destroyed the body's T-lymphocytes, which help the immune system fight off other diseases. DNA is made from the viral RNA B=-.==. \ _ A ; f,::l:i:i].;;--,) mRNA Retrovirus cycle ,/ @,2gq"f'''*0"n" new virus forming 124 r MHR. Unit 2 Biodiversity Figure 4.22 Reproductive cycle of a retrovirus. Retroviruses contain an enzyme that causes the host cell to copy viral RNA into DNA. This DNA becomes a provirus that continues to produce new viruses without destroying the cell. www. mcgrawhill.callinks/atlbiology To view animations that demonstrate the lytic cycle and the retrovirus reproductive cycle, go to the web site above and click on Electronic Learning Partner. Viruses and Biotechnology Because viruses enter host cells and direct the activity of the host cell's DNA, they can be useful tools for genetic engineers. For example, if researchers want to clone a gene, they first splice the gene into the genome of a virus. The virus then enters a host cell and directs the cell to make multiple copies of the virus. Each new virus in each new cell contains the added gene that the researchers wanted copied. This process is illustrated in Figure 4.23. ln 1997, a Nobel Prize was awarded to American researcher Stanley Prusiner for his discovery of an entirely new type of disease-causing agent called prions. The discovery was remarkable for two reasons. First, prions are proteins that are found normally in the body. Second, they are the only disease-causing agents known not to have RNA or DNA. Diseases result when prions convert from their normal form into harmful particles that have the same chemical composition but a different molecular shape. Prions cause several deadly brai n diseases, i ncl udi n g Creutzfeldt-Jakob disease (CJD) in humans, scrapie in sheep, and Bovine Spongiform Encephalopathy (BSE) or "mad cow disease" in cows. recombinant DNA (DNA that contains genes from more than one source) -'&^ ,@ viral DNA recombinant DNA host cell s') I C'r ,J T .:-' I ri1 foreign gene r.t-'= '"Ei: Figure 4.23 Genetic engineers use viruses to introduce new genes into a cell and to clone copies of genes. Viral Replication Viruses are very successful at invading the cells of organisms because they can only reproduce using the metabolism of a host cell. ln this lab you will diagram the steps involved in viral replication in cells. Your teacher will give you 5 photocopies of a drawing showing a bacterial cell. Put one of the following labels on each sheet: Attachment; Penetration; Biosynthesis; Maturation; Release. Using these headings as a guide, on each figure draw the different stages in the process of viral replication, At the bottom of each diagram, summarize each step in words. Analyze How do replication and protein synthesis occur in a cell? ln what way is viral replication different from cell reproduction? Examine your completed diagrams of viral replication. What two processes are directed by viral genes that are activated inside the host cell? Describe the stage that occurs before viruses are released from the cell. To summarize and enhance what you have learned in this lab, write an essay that explains the different ways viruses invade host cells and replicate. Use your library or the lnternet to gather your information. Chapter 4 Patterns of Life . MHR r 125 - The Viral Genome Origin of Viruses The genome of a virus consists of either DNA or RNA. The entire genome may occur as a single nucleic acid molecule or several nucleic acid segments. The DNA or RNA may be single-stranded or double-stranded, and either linear or circular. Because viruses are so small, the size of the genome is limited. For example, the genome includes coded instructions for making only a few different proteins that are needed to make the capsid. In contrast, the human genome codes for over 30 000 different proteins. Most DNA viruses have their genome on a single, linear, doublestranded DNA molecule. Some $oups of these viruses require the presence of helper viruses to reproduce themselves. They are said to be replication defective. RNA viruses comprise Tooh of all viruses. The process of RNA replication frequently involves emors, and as a result these viruses usually have much higher mutation rates than do DNA viruses. Mutations provide new variants of the virus, some of which may be better adapted to invade new hosts. Where do viruses fit into the history of life? Because they cannot replicate without host cells, they must have evolved after the first cells came into existence. They probably originated as fragments of nucleic acid that escaped from their original cell. They survived by becoming parasites of the same or similar types of ceII. Viruses and their hosts evolved together, and each type of virus is probably more closely related to its host cells than to other viruses in different groups. Viruses are much smaller than prokaryotic cells and cannot be seen with a light microscope. They vary in size from about one half to one one-hundredth the size of the smallest bacterium. While bacteria were first observed in the 1670s, viruses were not identified until 1935, after electron microscopes had been invented. I 1. Describe the structure of a virus. Why are viruses considered to be non-living? Measles 9-1 1 days Shingles years Warts months Cold 2-4 days HIV 2-5 years 2. Why must a virus enter a host cell in order to reproduce itself? 3. What are the different ways a virus can reproduce using a host cell? 4. Sketch the lytic and retrovirus reproductive cycles to show the similarities and differences between these two processes. 5. A doctor tells a patient that an antibiotic will not help cure a cold sore. Explain the doctor's reasoning. 6. How is viral replication similar to the making of a product in a factory? How does it differ from the making of a product in a factory? 7. Explain how viruses might be used to copy the gene for producing human insulin. 8. Consider the data table above right, on incubation time of different viral diseases. Use the data to predict which diseases are caused by viruses that undergo the lytic cycle, versus diseases that include a provirus stage. What is a possible public health consequence of the incubation time for diseases caused by proviruses? 126 r MHR.Unit2Biodiversity 9. The following table records the estimated numbers of viruses found in samples taken from a bacterial culture at hourly intervals. Plot the data on a graph and Interpret them to explain what was happening in the bacterial culture. 1 15 2 17 J 49 4 128 5 385 6 386 7 386 a 387 10. lf you were a scientist developing a drug that would block viral replication, which steps would you choose to block? Explain your answer in detail.
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