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Chapter 6 Topics Structure Classification Multiplication
Cultivation and replication Nonviral infectious agents Treatment
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Structure Size and morphology Capsid Envelope Complex Nucleic acid
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The size of viruses compared to yeast, bacteria, and the molecular protein hemoglobin.
Fig. 6.1 Size comparison of viruses with a eucaryotic cell and bacteria.
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Negative staining, positive staining, and shadow casting are methods of viewing viruses.
Fig. 6.2 Methods of viewing viruses
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There are two major structures of viruses called the naked nucleocapsid virus and the enveloped virus. Fig. 6.4 Generalized structure of viruses
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Capsid Protective outer shell that surrounds viral nucleic acid
Capsid spikes Composed of capsomer subunits Two types of capsids Helical Icosahedral
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Helical capsid Naked helical virus Enveloped helical virus
Ex. Tobacco mosaic virus Nucleocapsid is rigid and tightly wound into a cylinder-shaped package Enveloped helical virus Ex. Influenza, measles, rabies Nucleocapsid is more flexible
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Helical capsids have rod-shaped capsomers that form hollow discs that resemble a bracelet.
Fig. 6.5 Assembly of helical nucleocapsids
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Comparison between a naked helical plant virus and an enveloped helical human virus.
Fig. 6.6 Typical variation of viruses with helical Nucleocapsids.
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Icosahedron capsid Three-dimensional, 20-sided with 12 evenly spaced corners Variation in capsomer number Polio virus 32 capsomers Adenovirus 240 capsomers
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The structure and formation of an adenovirus.
Fig. 6.7 The structure and formation of an icosahedral virus.
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Icosahedral viruses can be naked or enveloped.
Fig. 6.8 Two types of icosahedral viruses
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Envelope Lipid and proteins Envelope spikes
During release of animal viruses, a part of the host membrane is taken Enable pleomorphic shape of the virus Spherical filamentous
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Function of the capsid/envelope
Protect nucleic acid from the host’s acid- and protein-digesting enzymes Assist in binding and penetrating host cell Stimulate the host’s immune system
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Complex viruses Structure is more intricate than helical and icosahedral viruses Pox virus Several layers of lipoproteins Course surface fibrils Bacteriophage Polyhedral head Helical tail Fibers for attachment
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` Fig Detailed structure of complex viruses
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Comparison of the morphology (helical, icosahedral, complex) of a naked virus, enveloped virus and a complex virus. Fig. 6.9 Morphology of viruses
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Nucleic acid Viruses contain either DNA or RNA
Possess only the genes to invade and regulate the metabolic activity of host cells Ex. Hepatitis B (4 genes) and herpesviruses (100 genes) No viral metabolic genes, as the virus uses the host’s metabolic resources
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Examples of medically important DNA viruses.
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Examples of medically important RNA viruses.
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Classification Structure Chemical composition Genetic makeup
Host relationship Type of disease
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Three orders of viruses have been developed for classification.
Table 6.4 Examples from the three orders of viruses.
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Classification of important human viruses.
Table 6.5 Important human virus families, genera, common names, and types of viruses.
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Multiplication Adsorption Penetration Uncoating Synthesis Assembly
Release
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Adsorption to the host cell of a enveloped spike virus and naked capsid spike virus.
Fig The mode by which animal viruses adsorb to the host cell membrane
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Penetration of animal viruses occur by endocytosis or fusion between the viral envelope and the the host cell membrane. Fig Two principal means by which animal viruses penetrate.
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Uncoating and synthesis of viruses rely on the host’s metabolic systems.
Fig General feature in the multiplication cycle of an enveloped animal virus.
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A mature virus can obtain an envelope by budding off the host cell.
Fig Maturation and release of enveloped viruses
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Cytopathic effects Damage to the host cell due to a viral infection
Inclusion bodies Syncytia Chronic latent state Transformation
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Examples of syncytia and inclusion bodies.
Fig Cytopathic changes in cells and cell cultures infected by viruses
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Bacteriophage Bacterial virus
Multiplication is similar to animal viruses except for the penetration (inject DNA), release (lyses) and prophage (lysogeny) stages
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T-even bacteriophage penetrate the host cell by specifically binding and injecting their DNA into the host cell. Fig Penetration of a bacterial cell by a T-even bacteriophage.
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After viral multiplication inside the host cell, viral enzymes will weaken the host cell membrane, rupture the cell (lyses), and release numerous virions. Fig A weakened bacterial cell, crowed with viruses.
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Lysogeny is when the bacteriophage can insert its DNA into the bacterial host genome.
Fig The lysogenic state in bacteria
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Comparison of bacteriophage and animal virus multiplication.
Table 6.7 Comparison of bacteriophage and animal virus multiplication.
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Cultivation and Replication
In vivo methods Laboratory animals Embryonic bird tissues In vitro methods Cell or tissue culture
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The early developing bird embryo contains a protective case, providing an ideal environment for viral propagation. Fig Cultivating animal viruses in a developing bird embryo
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A monolayer of monkey kidney cells is a cell culture enabling the propagating viruses.
Fig Appearance of normal and infected cell cultures
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Noncellular Infectious Agents
Prions Satellite viruses Viroids
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Prions Protein particle with no nucleic acid, no envelope, no capsid
Diseases Creutzfeldt-Jakob “mad cow disease”
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Satellite viruses Dependent on other viruses for replication
Ex. Delta agent, which is only expressed in the presence of hepatitis B virus
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Viroids Plant pathogens 1/10th the size of normal viruses
Tomatoes, potatoes, cucumbers. 1/10th the size of normal viruses Naked strands of RNA, no capsid
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