Saturday, June 5, 2021

Chapter 20 Viruses And Prokaryotes Test Answers


  • Most viruses comman-deer the cellular machinery for macromolecular synthesis during the late phase of infection, directing it to synthesize large amounts of a small number of viral mRNAs and proteins instead of the thousands of normal cellular...
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  • Such virus-infected cells have been used extensively in studies on synthesis of cell-surface glycoproteins. Similarly, much information about the mechanism of DNA replication has come from studies with bacterial cells and animal cells infected with...
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  • Viral Capsids Are Regular Arrays of One or a Few Types of Protein The nucleic acid of a virion is enclosed within a protein coat, or capsid , composed of multiple copies of one protein or a few different proteins, each of which is encoded by a single viral gene. Because of this structure, a virus is able to encode all the information for making a relatively large capsid in a small number of genes. This efficient use of genetic information is important, since only a limited amount of RNA or DNA , and therefore a limited number of genes, can fit into a virion capsid. A capsid plus the enclosed nucleic acid is called a nucleocapsid.
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  • Nature has found two basic ways of arranging the multiple capsid protein subunits and the viral genome into a nucleocapsid. Tobacco mosaic virus TMV is a classic example of the helical nucleocapsid. In TMV the protein subunits form broken disklike structures, like lock washers, which form the helical shell of a long rodlike virus when stacked together Figure a. Figure Two basic geometric shapes of viruses. The electron micrograph to the right is of tobacco more The other major structural class of viruses, called icosahedral or quasi-spherical viruses, is based on the icosahedron, a solid object built of 20 identical faces, each of which is an equilateral triangle.
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  • The atomic structures of a number of icosahedral viruses have been determined by x-ray crystallography Figure a. The first three such viruses to be analyzed — tomato bushy stunt virus , poliovirus, and rhinovirus the common cold virus — exhibit a remarkably similar design, in terms of the rules of icosahedral symmetry as well as in the details of their surface proteins. Interaction of these clefts with cell-surface receptors attaches the virus to a host cell, the first step in viral infection Figure b.
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  • Neutralizing antibodies specific for a particular virus also interact with these clefts, thereby inhibiting attachment of the virus to the host cell. Figure Structure of picornaviruses. These icosahedral viruses include poliovirus and the rhinoviruses, which cause the common cold. This model more In some viruses, the symmetrically arranged nucleocapsid is covered by an external membrane , or envelope, which consists mainly of a phospholipid bilayer but also contains one or two types of virus -encoded glycoproteins Figure The phospholipids in the viral envelope are similar to those in the plasma membrane of an infected host cell. The viral envelope is, in fact, derived by budding from that membrane, but contains mainly viral glycoproteins. Figure Electron micrograph of a negatively stained influenza virus virion. The virion is surrounded by a phospholipid bilayer; the large spikes protruding outward from the membrane are composed of trimers of hemagglutinin protein and tetramers of neuraminidase more The components of simple viruses such as TMV, which consists of a single RNA molecule and one protein species, undergo self-assembly if they are mixed in solution.
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  • More complex viruses containing a dozen or more protein species do not spontaneously assemble in vitro. The multiple components of such viruses assemble within infected cells in stages, first into subviral particles and then into completed virions. The genomes of these complex viruses encode proteins that assist in the assembly of the virion , but the assembly proteins are not themselves components of the completed virion. Most Viral Host Ranges Are Narrow The fact that the host range — the group of cell types that a virus can infect — is generally restricted serves as a basis for classifying viruses. A virus that infects only bacteria is called a bacteriophage , or simply a phage. Viruses that infect animal or plant cells are referred to generally as animal viruses or plant viruses. A few viruses can grow in both plants and the insects that feed on them. The highly mobile insects serve as vectors for transferring such viruses between susceptible plant hosts.
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  • An example is potato yellow dwarf virus, which can grow in leafhoppers insects that feed on potato plant leaves as well as in potato plants. Wide host ranges are characteristic of some strictly animal viruses, such as vesicular stomatitis virus, which grows in insects and in many different types of mammalian cells. Most animal viruses, however, do not cross phyla, and some e. The host-cell range of some animal viruses is further restricted to a limited number of cell types because only these cells have appropriate surface receptors to which the virions can attach. Viruses Can Be Cloned and Counted in Plaque Assays The number of infectious viral particles in a sample can be quantified by a plaque assay. This assay is performed by culturing a dilute sample of viral particles on a plate covered with host cells and then counting the number of local lesions, called plaques, that develop Figure A plaque develops on the plate wherever a single virion initially infects a single cell.
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  • The virus replicates in this initial host cell and then lyses the cell, releasing many progeny virions that infect the neighboring cells on the plate. After a few such cycles of infection, enough cells are lysed to produce a visible plaque in the layer of remaining uninfected cells. Figure Plaque assay for determining number of infectious particles in a viral suspension. Since all the progeny virions in a plaque are derived from a single parental virus , they constitute a virus clone. This type of plaque assay is in standard use for bacterial and animal viruses.
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  • Plant viruses can be assayed similarly by counting local lesions on plant leaves inoculated with viruses. Analysis of viral mutants, which are commonly isolated by plaque assays, has contributed extensively to current understanding of molecular cellular processes. Viral Growth Cycles Are Classified as Lytic or Lysogenic The surface of viruses includes many copies of one type of protein that binds, or adsorbs, specifically to multiple copies of a receptor protein on a host cell. This interaction determines the host range of a virus and begins the infection process Figure The entering genetic material may still be accompanied by inner viral proteins, although in the case of many bacteriophages, all capsid proteins remain outside an infected cell. The genome of most DNA-containing viruses that infect eukaryotic cells is transported with some associated proteins into the cell nucleus , where the cellular DNA is, of course, also found. The viral mRNA that is produced then is translated into viral proteins by host-cell ribosomes, tRNA, and translation factors.
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  • Figure Electron micrograph of a T4 bacteriophage adsorbed onto an E. Once viral surface proteins interact with receptors on the host cell, the viral DNA is injected into the cell. Levine, , Viruses, Scientific American Library, p. Most viral protein products fall into one of three categories: special enzymes needed for viral replication; inhibitory factors that stop host-cell DNA , RNA , and protein synthesis; and structural proteins used in the construction of new virions.
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  • These last proteins generally are made in much larger amounts than the other two types. After the synthesis of hundreds to thousands of new virions has been completed, most infected bacterial cells and some infected plant and animal cells rupture, or lyse, releasing all the virions at once. In many plant and animal viral infections, however, no discrete lytic event occurs; rather, the dead host cell releases the virions as it gradually disintegrates. These events — adsorption, penetration, replication, and release — describe the lytic cycle of viral replication. The outcome is the production of a new round of viral particles and death of the cell. Figure illustrates the lytic cycle for T4 bacteriophage.
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  • Adsorption and release of enveloped animal viruses are somewhat more complicated processes. Figure The steps in the lytic replication cycle of a nonenveloped virus are illustrated for E. During adsorption step 1 , viral coat proteins at the tip of the tail in T4 interact with specific more We illustrate the lytic cycle of enveloped viruses with the rabies virus , whose nucleocapsid consists of a single-stranded RNA genome surrounded by multiple copies of nucleocapsid protein Figure , upper left.
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  • Within the nucleocapsid of rabies virions are viral enzymes for synthesizing viral mRNA and replicating the viral genome. The envelope around the nucleocapsid is a phospholipid bilayer containing multiple copies of a viral transmembrane glycoprotein. The internal domain interacts with the viral matrix protein, which functions as a bridge between the transmembrane glycoprotein and nucleocapsid protein. Figure outlines the events involved in adsorption of a rabies virion , assembly of progeny nucleocapsids, and release of progeny virions by budding from the host-cell plasma membrane.
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  • Budding virions are clearly visible in electron micrographs, as illustrated by Figure Figure The steps in the lytic replication cycle of an enveloped virus are illustrated for rabies virus, which has a single-stranded RNA genome. The structural components of this virus are depicted at the top. Note that the nucleocapsid of this virus is helical more
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  • A modified centrifugation method recently applied to Cryptosporidium is the use of a blood cell separator Borchardt and Spencer, Water is continuously centrifuged through the device at about 1,x gravity, and Cryptosporidium oocysts and other particles are deposited in a separation channel. The deposited Cryptosporidium oocysts and other particles are then recovered from the separation channel and collected for microscopic examination.
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  • Viruses also can be recovered and concentrated by centrifugation, but because of their small size this requires ultracentrifugation Sobsoy, Typical ultracentrifugation conditions for viruses are RCFs of 50, to ,x gravity for periods of several hours. Ultracentrifugation is not widely used to concentrate and purify viruses from water because of the high cost and lack of portability of ultracentrifuges and the tendency for low levels of viruses to be recovered with poor and variable efficiency.
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  • Using simple centrifugation methods, other particles in the same size and density range of the target microbes also are recovered and concentrated. This lead of other nontarget particles often greatly exceeds the concentration of target microbes, and these excess nontarget particles can 'interfere with further separation, concentration, assay, and characterization of the target microbes. Filtration Microbes can be recovered and concentrated from water by a variety of filtration methods Brock, The most widely used filtration method for recovering bacteria is membrane filtration using microporous membranes typically composed of cellulose esters.
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  • This method is the basis of the widely used membrane filtration methods for detecting indicator bacteria, including total and fetal coliforms, enterococci, and Clostridium perfringens Eaton et al. These methods and modifications of them are also widely used for initial concentration and recovery of bacterial pathogens in water, including Salmonella, Shigella, and Campylobacter. The cells recovered on a membrane filter can be directly cultured on differential and selective broth liquid or agar solid media in order to detect and assay the recovered bacteria by enrichment or presence-absence or by the development of bacterial colonies. The enriched bacteria or bacterial colonies are further characterized to confirm their identity.
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  • Alternative filtration methods have been used to recover and detect bacteria and parasites, including microporous filters composed of nylon, Page Share Cite Suggested Citation:"9 Methods to Identify and Detect Microbial Contaminants in Drinking Water. Identifying Future Drinking Water Contaminants. Track-etched polycarbonate and other membrane filters have been used to concentrate and recover bacteria and parasites for direct microscopic detection. These microscopic methods often employ immunofluorescence assays to facilitate identification, assays for determination of cellular activity as a measure of viability e.
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  • Another filtration method used for recovery and concentration of bacteria as well as viruses, parasites, and other microbes is ultrafiltration. As the name implies, ultrafilters have much smaller pore sizes that are expressed as the molecular weight of the smallest retained particles or molecules molecular weight cutoff or MWCO. Typically, this is in the range of several thousand to , MWCO. Ultrafiltration is often done using tangential flow systems in which the water is made to flow parallel to the membrane surface. This is done in order to keep the microbes and other particles suspended in the retained water retentate and prevent them from accumulating at the filter surface where they would cause clogging and reduce hydraulic flux. Tangential flow ultrafiltration systems include stirred cells, hollow fibers, spinning cartridges, and stacked sheets.
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  • Because of the small size of viruses, they are recoverable from water by pore size exclusion filtration only with ultrafilters or even smaller pore size filters nanofilters and reverse osmosis filters. Ultrafiltration has been used for virus concentration from water for decades, although the high costs of ultrafiltration hardware and the ultrafilters themselves have limited the use of these methods Sobsey, Recently economical, disposable hollow fibers have been used to concentrate viruses as well as bacteria and the parasite Cryptosporidium parvum from raw source water and finished drinking water Juliano and Sobsey, Size exclusion filtration is widely used to concentrate parasites from water, with most of the historical and current focus on Giardia and Cryptosporidium. The filters initially and still widely used are yarn-wound, inch-long, cartridge filters composed of polypropylene or other media, and having nominal pore sizes of one to several micrometers in diameter EPA, A disadvantage of these filters is the need to remove them from the filter housing and manually cut them apart in order to recover the parasites and other retained particles by physically washing them from the filter medium using an aqueous detergent solution.
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  • Parasite cysts and oocysts in the recovered solution of several liters volume are further concentrated and recovered by centrifugation to sediment them. Because these depth filters have only nominal pore size ratings and the cartridges are typically pressure held in their plastic housings by flexible O-ring or gasket seals, Cryptosporidium oocysts have penetrated or bypassed the filters, resulting in appreciable losses.
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  • Furthermore, recoveries from the filters are highly variable, resulting in large coefficients of variation. These other particles can interfere with subsequent purification and microscopic examination of the parasite cysts and oocysts. Other filters having absolute pore size ratings smaller than the size of the target cysts, oocysts, and spores are alternatives for concentrating parasites from water. These filters are preferred because they are expected to achieve absolute retention of the protozoan cysts, oocysts and spores and because their physical characteristics facilitate easier and more efficient recovery of the retained microorganisms by simpler elution methods than cutting apart and macerating the filter material.
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  • Formats for these filters include flat track-etched polycarbonate disks, cellulose acetate membranes that are dissolved in acetone to recover Cryptosporidium oocysts , pleated capsule filters 1 um pore size polyether-sulphone filters in a polycarbonate housing , and ultrafilters spinning cartridge and hollow fiber units. Such filters, as well as the smaller water sample volumes, are now recommended by the EPA, and some of them are specified in the recently developed Method EPA, Another type of filter being used to concentrate Cryptosporidium from water is a compressible "sponge" filter. This filter is compressed into a water pipe to achieve a small pore size, and water is allowed to flow through the compressed filter for a period of time. The filter is recovered from the pipe, and the parasite cysts and oocysts are readily washed off of the now decompressed sponge-like filter medium for further processing and analysis. The most widely used methods for initial concentration and recovery of viruses from water employ microporous filters that retain viruses primarily by adsorption to the filter medium Sobsey, ; Sobsey, ;.
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  • De Leon and Sobsey, These filters retain viruses by both electrostatic and hydrophobic interactions between the surfaces of viruses and the filter media. Formats used for virus adsorbent filters include membranes, disks, and pleated cartridges. The media used initially as virus adsorbent filters were negatively charged cellulose esters, fiberglass, and other materials. Relatively large volumes of conditioned water are passed through the filter, and viruses adsorb to the filter medium surfaces. Subsequently, filters that are electropositive near neutral pH and adsorb viruses directly without acidifying or adding cations salts to the water were developed for virus concentration De Leon and Sobsey, Electropositive filter media are composed of charge-modified fiberglass sold commercially as disks or pleated cartridges, fiberglass filter disks that are coated with precipitated aluminum or iron salts, or positively charged, natural quartz fiberglass that one packs into a column to make an adsorbent filter.
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  • The current EPA-approved ICR method to detect culturable enteric viruses in drinking water supplies specifies use of commercially available, electropositive filter EPA, Viruses adsorbed to both electronegative or electropositive filters are subsequently eluted and recovered by passing a relatively small volume of aqueous elution medium through the filter. Viruses in the resulting filter eluates are assayed directly or after further steps of concentration, purification, and extraction.
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  • Which of the following statements about drug resistance is false? A it may be carried on a plasmid B it may be transferred from one bacterium to another during conjugation C it may be due to enzymes that degrade some antibiotics D it is found only in gram-negative bacteria E it may be due to increased uptake of a drug Definition D. It is found only in gram-negative bacteria. Term Which of the following does not constitute an advantage of using two antibiotics together? A it can prevent drug resistance B It lessens the toxicity of individual drugs C two are always twice as effective as one D it allows treatment to be provided prior to diagnosis E all of the above are advantages Definition C. Two are always twice as effective as one Term The structure of the influenza drug Tamiflu and Salic acid, the substrate for influenza virus's neuramidase, are shown in figure What is the method of action of Tamiflu?
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  • A inhibits cell wall synthesis B inhibits plasma membrane synthesis C inhibits synthesis of neuramidase D competitive inhibition E prevents synthesis of virus spikes Definition D. Competitive inhibition Term The antibiotic chloramphenicol Binds to the 50s subunit of the ribosome as shown in figure Definition A. Prevent attachment of tRNA Term.
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  • Section Stimulates the body's own immune response against invading microbes. Upgrade to remove. Start studying Holt McDougal Biology. Chapter Viruses and Prokaryotes. Learn vocabulary, terms, and Key concepts: acquired immune a blood protein produced in response to and counteracting a specific antigen. Image: Antibody. Characteristics of prokaryotic cells. As mentioned in the previous page, prokaryotes include the kingdoms of Monera simple bacteria and Archaea. Ch Protists and Fungi. Ch Plant. Viruses and Bacteria - nlsd.
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  • Viruses Biology Quiz - Quizizz. How do viral, prokaryotic, and eukaryotic genomes differ. Archaea, Bacteria, and Viruses. Is a Virus a Prokaryote or a Eukaryote? Are viruses prokaryotic - Answers. Holt Biology Answer Key Chapter 2 - hrtechstartups. Biology Student Edition Chapter 20, Viruses. Prokaryotes, Eukaryotes, Viruses Tutorial. Studying Viruses And Prokaryotes Answers. Holt Biology Answer Key Chapter 3 - pompahydrauliczna. Introduction to Prokaryotes, Eukaryotes. Holt McDougal Biology. Chapter Viruses and Prokaryotes - Quizlet. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Connect to Your World Bacteria are everywhere, including in and on your own bodysuch as the bacteria that live in our digestive tracts. You may use this website for access to PPT's, guided notes, and make up assignments. Any disease-causing agent is called a pathogen.
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  • Prokaryotes are single-celled organisms that lack a a. The structure labeled C in Figure is a. Unit 6: Chapter 18 Viruses and Prokaryotes - Mrs. Answer Key. Cop y right. While viruses have key traits similar to living cells, they also have are always fatal, because the body has no immune response against a protein. Viruses, bacteria, viroids, and prions can all cause infection. Eukaryotic cells - prokaryotic cells — viruses — viroids - prion.
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  • Name Key. Date In your textbook, read about the diversity of prokaryotes. Respond to each statement. The Viruses Prokaryotes chapter of this Holt McDougal Biology Companion Course helps students learn the essential lessons associated with viruses and prokaryotes. Rather than enjoying a good book with a cup of tea in the afternoon, instead they juggled with some infectious bugs inside their desktop computer. This answer key mcdougal viruses and prokaryotes, as one of the most effective sellers here will definitely be in the course of the best options to review. The free Kindle books here can be borrowed for 14 days and then will be automatically returned to the owner at that time. Answer Key Mcdougal Viruses. Some of the worksheets displayed are Holt algebra 2 chapter 5 project answers, Holt civics in practice chapter 1 section 2 pdf, Interactive reader and study guide holt mcdougal united, Name class date chapter 3 main idea activities 3, Section quizzes and chapter tests, Unit 2 answer key, Academic Holt mcdougal biology study guide a answer.
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  • You have remained in right site to begin getting this info. Viruses that infect bacteria are called bacteriophages. They enter living cells and, once inside, use the machinery of the infected cell to produce more viruses. Viral Infections Viruses have two methods of infection once insideViruses And Prokaryotes Answer Key actionbioscience promoting bioscience literacy. Yeah, even many books are offered, this book can steal the reader heart in view of that much. Skills Worksheet Active Reading.
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