Virus representation

A2.3 — Viruses

Theme A: Form and Function · Higher Level Only

6
HL Understandings
A2.3.1 HL Only

Common Structural Features of Viruses

Key UnderstandingViruses share common structural features, reflecting their nature as obligate intracellular parasites.

Viruses are incredibly small, non-cellular infectious agents. Since they lack cytoplasm, ribosomes, and other metabolic machinery, they must infect a host cell to replicate.

Exam Tip: Viruses are considered non-living because they cannot carry out life processes (like metabolism and reproduction) independently outside of a host cell.
A2.3.2 HL Only

Diversity of Viral Structure

Key UnderstandingDespite shared features, viruses exhibit immense diversity in structure.
Bacteriophage structure diagram

Viruses vary significantly in their structural details:

Genome Diversity

  • Can be DNA or RNA.
  • Can be single-stranded or double-stranded.
  • Can be linear or circular.

Morphological Diversity

  • Shapes: Helical (e.g., TMV), Icosahedral (e.g., Adenovirus), or Complex (e.g., Bacteriophage).
  • Envelopes: Some viruses have a lipid envelope derived from the host cell membrane; others are "naked" (unenveloped).
A2.3.3 HL Only

The Lytic Cycle

Key UnderstandingThe lytic cycle involves the rapid replication of the virus and the destruction of the host cell.

In the lytic cycle, the virus takes over the host's cellular machinery to produce new viral particles, ultimately lysing (bursting) the cell.

1. Attachment: Virus binds to specific receptors on the host cell.
2. Penetration: Viral genetic material enters the host cell.
3. Replication & Synthesis: Host machinery copies viral genome and synthesizes viral proteins.
4. Assembly: New viral particles are assembled.
5. Lysis: The host cell bursts, releasing newly formed virions to infect other cells.
A2.3.4 HL Only

The Lysogenic Cycle & Comparative Analysis

Key UnderstandingThe lysogenic cycle allows viral genomes to integrate and persist within the host cell without immediate destruction.

Some viruses (like temperate phages) can enter a dormant state, where their genetic material integrates into the host cell's genome (forming a provirus or prophage).

1. Integration: Viral DNA integrates into the host chromosome.
2. Replication: As the host cell divides, it replicates the viral DNA along with its own.
3. Latency: The virus remains dormant (latent) for long periods.
4. Induction: An environmental trigger (e.g., UV light, stress) causes the viral DNA to exit the host genome and enter the Lytic Cycle.
Lytic vs Lysogenic Cycle Diagram
Skill: Comparing Lytic and Lysogenic Cycles You should be able to deduce whether a virus is in the lytic or lysogenic cycle based on a diagram or description. Key differentiator: integration into the host genome and cell survival (lysogenic) versus rapid replication and host cell destruction (lytic).
A2.3.5 HL Only

Evolutionary Origins of Viruses

Key UnderstandingThere is evidence for multiple independent origins of viruses from different cellular organisms.

Viruses are highly diverse and do not share a single common ancestor. Instead, it is hypothesized that they have evolved multiple times through convergent evolution.

Application: Horizontal Gene Transfer The lysogenic cycle has profound evolutionary implications. When a prophage excises from a host genome, it can occasionally take a piece of the host DNA with it. When infecting a new cell, it transfers this DNA in a process called transduction, a form of horizontal gene transfer. This drives rapid evolution, such as the spread of antibiotic resistance genes or virulence factors among bacterial populations.
Convergent Evolution: The fact that viruses infecting bacteria, plants, and animals are so distinct suggests that the parasitic "viral lifestyle" evolved independently several times.
A2.3.6 HL Only

Rapid Evolution in Viruses

Key UnderstandingViruses exhibit extremely rapid rates of evolution and adaptation.

Viruses adapt quickly to host defenses (like immune systems or vaccines) and changing environments due to several key factors:

FactorImpact on Evolution
High Mutation Rates Especially in RNA viruses (e.g., HIV, Influenza), replication enzymes (like RNA polymerase or reverse transcriptase) lack proofreading ability, leading to frequent mutations.
Rapid Replication Viruses can produce millions of progeny in a short time. Short generation times mean that mutations accumulate quickly in a population.
Recombination When two different viral strains infect the same cell, their genomes can mix and re-assort, creating entirely new viral strains rapidly (e.g., antigenic shift in influenza).

A2.3 Viruses Complete!

You have successfully reviewed all HL understandings for Biology Theme A2.3.