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Chapter 13

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Viruses, Viroids, and Prions

General Characteristics of Viruses

Viruses are unique infectious agents that differ fundamentally from bacteria and other microorganisms. They are considered obligatory intracellular parasites, meaning they require living host cells to multiply. Viruses contain either DNA or RNA as their genetic material, but never both, and are surrounded by a protein coat called a capsid. Unlike cells, viruses lack ribosomes and an ATP-generating mechanism, relying entirely on the host cell's machinery for replication.

  • Obligatory intracellular parasites: Cannot reproduce outside a living host cell.

  • Genetic material: DNA or RNA, single- or double-stranded, linear, circular, or segmented.

  • Capsid: Protein coat made of capsomeres.

  • No ribosomes or ATP-generating mechanisms.

Feature

Bacteria

Viruses

Intracellular Parasite

No

Yes

Plasma Membrane

Yes

No

Binary Fission

Yes

No

DNA and RNA

Yes

No (one or the other)

ATP-Generating Metabolism

Yes

No

Ribosomes

Yes

No

Sensitivity to Antibiotics

Yes

No

Sensitivity to Interferon

No

Yes

Host Range: The spectrum of host cells a virus can infect is determined by specific attachment sites and cellular factors. Most viruses infect only specific types of cells in one host species.

  • Bacteriophages: Infect bacteria; receptor sites may be on cell wall, fimbriae, or flagella.

  • Animal viruses: Receptor sites are typically on the plasma membrane.

Influenza: Crossing over and antigenic shift in pigs

Example: Influenza viruses can undergo antigenic shift when genes from human and avian flu viruses mix in pigs, potentially creating new pandemic strains.

Viral Structure

Viruses exhibit diverse structures, but all share certain fundamental components. The complete, fully developed infectious particle is called a virion.

  • Nucleic Acid: DNA or RNA, single- or double-stranded, linear, circular, or segmented.

  • Capsid: Protein coat composed of capsomeres.

  • Envelope: Lipid, protein, and carbohydrate coating present in some viruses, often derived from the host cell membrane.

  • Spikes: Projections from the outer surface, used for attachment.

Morphology of a nonenveloped polyhedral virus Morphology of an enveloped helical virus Morphology of a helical virus Morphology of complex viruses (bacteriophage and orthopoxvirus)

General Morphology

  • Helical viruses: Hollow, cylindrical capsid (e.g., rabies, Ebola).

  • Polyhedral viruses: Many-sided, usually icosahedral (e.g., adenoviruses, poliovirus).

  • Enveloped viruses: Roughly spherical, with a lipid envelope.

  • Complex viruses: Complicated structures (e.g., bacteriophages).

Isolation, Cultivation, and Identification of Viruses

Viruses must be grown in living cells. Bacteriophages are typically cultured in bacteria, while animal viruses can be grown in animals, embryonated eggs, or cell cultures.

Growing Bacteriophages

  • Grown in bacteria; form plaques (clearings) on a lawn of bacteria on agar.

  • Each plaque corresponds to a single virus and can be quantified as plaque-forming units (PFU).

Viral plaques formed by bacteriophages

Growing Animal Viruses

  • In living animals: Mice, rabbits, guinea pigs.

  • In embryonated eggs: Virus injected into egg; used for vaccine production.

Inoculation of an embryonated egg

  • In cell cultures: Primary cell lines, diploid cell lines (from human embryos), and continuous cell lines (from cancerous cells, e.g., HeLa cells).

Cell culture process for growing animal viruses

Cytopathic effect (CPE): Visible changes or deterioration of monolayer cells due to viral infection.

Cytopathic effect of viruses in cell culture

Viral Identification

  • Cytopathic effects in cell culture.

  • Serological tests: Rapid antigen tests, ELISA (antibody-based detection).

  • Nucleic acid tests: PCR for viral genome detection.

Viral Multiplication

Viruses multiply by invading host cells and taking over their metabolic machinery. A single virion can produce thousands of progeny in a host cell. The process can be described by a one-step growth curve.

Viral one-step growth curve

Multiplication of Bacteriophages

  • Lytic cycle: Phage causes lysis and death of the host cell (e.g., Tequatrovirus/T-even phages).

  • Lysogenic cycle: Phage DNA integrates into host DNA as a prophage, remaining latent (e.g., Lambdavirus/lambda phage).

The lytic cycle of a T-even bacteriophage The lysogenic cycle of Lambdavirus bacteriophage in E. coli

  • Outcomes of lysogeny:

    • Immunity to reinfection by the same phage.

    • Phage conversion (host exhibits new properties, e.g., toxin production).

    • Specialized transduction (specific bacterial genes transferred by phage).

Specialized transduction by bacteriophage

Comparison: Bacteriophage vs. Animal Virus Multiplication

Stage

Bacteriophages

Animal Viruses

Attachment

Tail fibers attach to cell wall proteins

Receptor sites are plasma membrane proteins/glycoproteins

Entry

Viral DNA injected into host cell

Capsid enters by endocytosis or fusion

Uncoating

Not required

Enzymatic removal of capsid proteins

Biosynthesis

In cytoplasm

In nucleus (DNA viruses) or cytoplasm (RNA viruses)

Chronic Infection

Lysogeny

Latency; slow viral infections; cancer

Release

Host cell is lysed

Enveloped viruses bud out; nonenveloped viruses rupture plasma membrane

Comparison table: Bacteriophage and animal viral multiplication

Multiplication of Animal Viruses

  • Attachment: Viruses attach to cell membrane.

  • Entry: By receptor-mediated endocytosis or fusion.

  • Uncoating: Separation of viral nucleic acid from capsid by enzymes.

  • Biosynthesis: Production of nucleic acid and proteins.

  • Maturation: Assembly of viral components.

  • Release: By budding (enveloped viruses) or rupture (nonenveloped viruses).

Entry of viruses into host cells

Biosynthesis of DNA and RNA Viruses

  • DNA viruses: Replicate DNA in nucleus using host enzymes; capsid proteins synthesized in cytoplasm.

  • RNA viruses: Multiply in cytoplasm using RNA-dependent RNA polymerase.

  • Retroviruses: Use reverse transcriptase to produce DNA from RNA genome; DNA integrates into host chromosome as a provirus.

Viruses and Cancer

Some viruses can cause cancer by integrating their genetic material into the host genome, leading to transformation of normal cells into tumor cells.

  • Proto-oncogenes: Genes that regulate normal cell growth; mutations can convert them to oncogenes.

  • Oncogenic viruses: Induce tumors by integrating into host DNA.

  • Oncolytic viruses: Used experimentally to treat cancer by infecting and killing tumor cells.

Latent and Persistent Viral Infections

  • Latent infections: Virus remains dormant in host cell; may reactivate (e.g., herpesviruses, shingles).

  • Persistent infections: Virus is continuously released over a long period; often fatal (e.g., HIV, measles SSPE).

Type

Example Disease

Causative Virus

Latent

Cold sores, Shingles

HHV-1, HHV-2, Varicellovirus

Persistent

HIV/AIDS, Liver cancer, SSPE

HIV, Hepatitis B, Measles virus

Prions

Prions are infectious proteins that cause neurodegenerative diseases. Unlike viruses, prions contain no nucleic acids. Disease results from the conversion of normal cellular prion protein (PrPc) into an abnormal, infectious form (PrPSc), which accumulates in brain cells and forms plaques.

  • Transmission: Inherited, ingestion, transplant, surgical instruments.

  • Diseases: Mad cow disease, Creutzfeldt-Jakob disease, sheep scrapie.

Key difference: Prions are proteins, not viruses, and lack nucleic acids.

Additional info: This summary covers the essential concepts of viral structure, replication, cultivation, identification, and the unique properties of prions, as outlined in Chapter 13 of a standard microbiology textbook. For further study, students should review the mechanisms of viral pathogenesis, immune response, and antiviral strategies.

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