Notes on Viruses in IB Biology (HL)
Virus Structure (HL)
Structural Features of Viruses
- Definition: Viruses are non-cellular infectious particles that are not classified as organisms because they lack characteristics of life.
- Non-living: They do not possess cellular structures and cannot metabolize.
- Classification: Viruses do not fit into the three-domain classification system of life. - Size:
- Much smaller than prokaryotic cells, with diameters ranging from 20 nm to 300 nm.
- Can only be visualized using an electron microscope.
Common Structural Features of All Viruses
- Small Size: Generally consist of few molecules, hence do not form large structures.
- Fixed Size: Viruses do not grow in size.
- Nucleic Acid Core:
- Composed of either DNA or RNA.
- Nucleic acids can be single-stranded or double-stranded.
- Genetic material can exist in linear or circular forms. - Protein Coat (Capsid):
- Protects the viral nucleic acid.
- Composed of protein subunits; contains attachment proteins on the surface that facilitate binding and entry into host cells. - Absence of Cellular Structures:
- Lack cytoplasm and have very few, or no, enzymatic functions. - Lipid Envelope:
- Some viruses possess an additional lipid layer formed from the host cell membrane.
- Involves membrane-phospholipids that assist with cell recognition. - Parasitic Nature:
- Viruses can only reproduce by infecting living host cells, utilizing the host's cellular machinery (like ribosomes) to synthesize new virus particles.
- They do not respire and derive energy needed for replication from the host cell.
General Virus Structure Diagram
- (Insert diagram illustrating typical virus structure)
Structural Diversity of Viruses
- Variety in Structure and Shape: Although they are simple, viruses exhibit a wide diversity in structure and shape.
- Genetic material may be RNA or DNA (double or single stranded).
- Enveloped versus non-enveloped forms.
- Shapes include threadlike, polyhedral, and spherical forms. - Specificity in Infection: Different viruses target specific types of host cells, dictated by their attachment proteins.
- Example: HIV infects white blood cells while Hepatitis viruses target liver cells.
Examples of Diverse Virus Structures
- Bacteriophage Lambda:
- A bacterial virus infecting E. coli.
- Contains double-stranded DNA within a capsid head.
- Utilizes a tail and fibrils for attachment and DNA injection into the host cell.
- Tail structure helps penetrate the bacterial cell wall. - Coronaviruses:
- Cause respiratory diseases in mammals and birds.
- Transmitted via respiratory fluids.
- Structure includes single-stranded RNA, spherical shape, and an envelope.
- Examples: SARS-CoV-2, MERS, SARS. - HIV (Human Immunodeficiency Virus):
- Transmitted through intimate contact or exchange of body fluids (e.g., sexual intercourse, blood donation).
- Structure includes:
- Two RNA strands.
- Proteins (e.g., reverse transcriptase is an enzyme that converts viral RNA into DNA).
- A protein capsid.
- Viral envelope consisting of a lipid bilayer and glycoproteins for attachment.
Virus Structure Diagrams
- (Insert diagrams illustrating Bacteriophage Lambda, Coronaviruses, and HIV)
Replication in Viruses (HL)
The Lytic Cycle
- Non-living Nature: Viruses do not replicate through cell division but instead through host infection.
- Parasitic Reproduction: All viruses must infect living host cells to reproduce.
Steps of Viral Replication
- Attachment: Virus attaches to specific receptor sites on the host cell membrane using its attachment proteins.
- Injection: Virus injects its nucleic acid into the cytoplasm of the host cell.
- Utilization of Host Machinery: The virus commandeers the host's cellular machinery for protein synthesis, leading to the production of new viral proteins. This is referred to as biosynthesis.
- Assembly: New virus particles are assembled from the synthesized proteins and nucleic acids, maturing into virions.
- Release: The host cell undergoes lysis, releasing the newly formed virions into the environment to infect other cells.
Lytic Cycle Diagram
- (Insert diagram depicting the lytic cycle)
The Lysogenic Cycle
- Distinction from Lytic Cycle: Unlike the lytic pathway, new virus particles are not immediately released following infection.
- Viral nucleic acid integrates with host DNA, remaining dormant.
- This latency allows the host cell to continue normal functions including division, producing daughter cells that also contain viral DNA. - Latency: Occurs until a trigger (e.g., environmental factors like UV exposure or chemicals) prompts the viral DNA to become active and enter the lytic pathway.
Steps of the Lysogenic Cycle
- Integration: Viral nucleic acid combines with the host cell's DNA.
- Repressor Gene: A viral gene codes for a repressor protein that inhibits transcription of the viral genome.
- Activation: External triggers can activate the virus, prompting a shift to the lytic cycle.
Lysogenic Cycle Diagram
- (Insert diagram illustrating the lysogenic cycle)
Origin & Evolution of Viruses (HL)
Origin of Viruses
- Timeline: Viruses are believed to have existed for approximately 3.5 billion years, evolving alongside other species through a process called coevolution.
- Human Genome Evidence: Around 8% of the human genome consists of endogenous retroviruses (ERVs), remnants from ancient viral infections.
- Debate in Origin Theories: Due to the absence of fossil evidence, the exact origin of viruses remains debated, and three prominent theories have emerged:
- Escape Theory: Proposes that viruses originated from genetic elements (DNA/RNA) that gained the ability to move between cells and acquired an outer boundary, forming a virus.
- Regressive/Reduction Theory: Suggests that viruses are remnants of once-living cellular organisms that became parasitic, shedding unnecessary cellular structures over time.
- Virus-First Theory: Posits that viruses predated cellular life, implying that simpler organisms (viruses) evolved before more complex ones.
Theories of Virus Origin Diagram
- (Insert diagram summarizing virus origin theories)
Common Features of Viruses
- Convergent Evolution: Shared characteristics among viruses indicate potential convergent evolution. Common features include:
- Capsid protein outer shell with no cytoplasm.
- Genetic material (DNA or RNA) that utilizes a common genetic code.
- Parasitic nature requiring a host cell for replication.
Evolution in Viruses
Viral Evolution Characteristics
- Rapid Evolution: Some viruses undergo rapid evolutionary changes due to high mutation rates largely attributable to their RNA genetic material, along with large population sizes and short generation times.
- Examples: The evolution of influenza and HIV demonstrates this rapid change.
Mechanisms of Genetic Change
- Antigenic Drift:
- Refers to minor, gradual changes in the viral genome leading to variations in surface proteins.
- Over time, the immune system may no longer recognize the virus (notable in HIV). - Antigenic Shift:
- Involves significant, rapid changes due to genetic material recombination when multiple virus types infect the same cell.
- Results in new viruses that the host immune system fails to recognize (prominent in influenza).
Implications for Vaccine Development
- Vaccination Adjustments: For viruses with antigenic drift, vaccines are updated regularly to maintain effectiveness.
- Adjustments are successful in response to small changes in the virus. - Challenges:
- For rapidly evolving viruses like HIV, creating successful vaccines is challenging due to high mutation rates.
- Antigenic shift complicates vaccine development because changes are often unpredictable. - Adjunct Strategies: Isolating infected individuals may be necessary to curtail the spread of fast-evolving viruses.
Summary on HIV Vaccine Development
- Although HIV mutates quickly, no effective vaccine has been achieved due to this rapid evolving nature.
- Strategies for dealing with viruses that undergo antigenic shift may include isolating infected individuals to manage spread effectively.
Concluding Notes
- Understanding viral structure, replication, and evolution is crucial for developing effective treatments and preventive measures against viral diseases. Health initiatives and resources should target the dynamic nature of viral pathogens.