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Viruses: morphology, classification, reproduction & cultivation

The study of viruses encompasses various aspects including their morphology, classification, reproduction/replication, and cultivation.

Viruses: morphology, classification, reproduction & cultivation
Illustration of different kind of viruses

Morphology of Viruses

Morphology of Viruses

Structure:

a) Capsid:

  • The protein coat surrounding the viral genome, composed of protein subunits called capsomeres.

  • The capsid provides protection and aids in the attachment to host cells.

    • Helical: Capsids with a rod-like appearance (e.g., tobacco mosaic virus).

    • Icosahedral: Capsids with a roughly spherical shape (e.g., adenovirus).

    • Complex: Capsids with intricate structures (e.g., bacteriophage).

b) Envelope:

  • Some viruses have an outer lipid membrane derived from the host cell membrane, containing viral glycoproteins (e.g., influenza virus, HIV).

c) Genome:

  • The genetic material of viruses, which can be DNA or RNA, single-stranded or double-stranded, linear or circular.

    • DNA Viruses: Have DNA as their genetic material (e.g., herpesvirus).

    • RNA Viruses: Have RNA as their genetic material (e.g., influenza virus).

Additional Structures:

a) Tegument:

  • A layer of proteins found between the envelope and capsid in some viruses (e.g., herpesviruses).

b) Tail Fibers and Spikes:

  • Structures used for attachment to host cells, commonly found in bacteriophages and some animal viruses.

Classification of Viruses

  • Viruses are classified based on several criteria including the type of nucleic acid, replication strategy, morphology, and host range.

  • The main classification systems include:

Classification of Viruses

Based on Genetic Material:

a) DNA Viruses:

  • Contain DNA as their genetic material.

  • Examples: Adenoviruses, Herpesviruses.

b)RNA Viruses:

  • Contain RNA as their genetic material.

  • Examples: Influenza viruses, Coronaviruses.

Based on Replication Method:

a) Positive-Sense RNA Viruses:

  • RNA serves directly as mRNA.

  • Examples: Poliovirus, Hepatitis C virus.

b) Negative-Sense RNA Viruses:

  • RNA must be transcribed to mRNA.

  • Examples: Rabies virus, Ebola virus.

c) Reverse Transcribing Viruses:

  • RNA viruses that reverse transcribe into DNA.

  • Examples: HIV (retroviruses), Hepatitis B virus (hepadnaviruses).

Based on Morphology:

a) Icosahedral Viruses:

  • Capsid with icosahedral symmetry.

  • Examples: Adenoviruses, Polioviruses.

b) Helical Viruses:

  • Capsid with helical symmetry.

  • Examples: Influenza viruses, Tobacco mosaic virus.

c) Complex Viruses:

  • Combination of icosahedral and helical structures or other complex shapes.

  • Examples: Bacteriophages, Poxviruses.

Based on Host Range:

a) Animal Viruses:

  • Infect animals.

  • Examples: Rabies virus, SARS-CoV-2.

b) Plant Viruses:

  • Infect plants.

  • Examples: Tobacco mosaic virus, Potato virus Y.

c) Bacteriophages:

  • Infect bacteria.

  • Examples: T4 phage, Lambda phage.

Each of these groups can be further divided based on more specific characteristics and genetic differences.

Reproduction/Replication of Viruses

  • The replication cycle of viruses varies between different types, but generally includes the following stages:

Reproduction/Replication of Viruses

1.Attachment:

  • The virus binds to specific receptors on the surface of the host cell.

2.Entry:

  • The viral genome enters the host cell through mechanisms such as fusion with the host membrane, endocytosis, or direct penetration.

3.Uncoating:

  • The viral capsid is removed, releasing the viral genome into the host cell.

4.Replication:

  • DNA Viruses: Replicate in the nucleus using the host's DNA polymerase (e.g., herpesvirus).

  • RNA Viruses: Replicate in the cytoplasm using viral RNA polymerase.

  • Positive-sense RNA Viruses: Can be directly translated into proteins.

  • Negative-sense RNA Viruses: Must be transcribed into positive-sense RNA by RNA-dependent RNA polymerase.

5.Transcription and Translation:

  • Viral mRNA is transcribed (if necessary) and translated into viral proteins using the host's ribosomes.

6. Assembly:

  • New viral particles are assembled from the replicated genome and synthesized proteins.

7. Release:

  • Newly formed viruses are released from the host cell through lysis (breaking open the cell) or budding (enveloped viruses).

Replication Cycles:

Lytic Cycle:

  • Virus replicates rapidly and lyses the host cell to release progeny viruses (e.g., bacteriophage T4).

Lysogenic Cycle:

  • Viral DNA integrates into the host genome and replicates along with it without causing immediate lysis.

  • It can later enter the lytic cycle (e.g., bacteriophage λ).

Cultivation of Viruses

Host Systems:

  • Cell Cultures: Viruses are grown in monolayers of cultured cells. Cell lines can be primary (directly taken from tissues) or continuous (immortalized).

  • Cytopathic Effect (CPE): Observable damage to host cells due to viral infection.

  • Embryonated Eggs: Used for the cultivation of certain viruses (e.g., influenza virus). Different parts of the egg (chorioallantoic membrane, amniotic fluid, yolk sac) are used for different viruses.

  • Laboratory Animals: Some viruses require a whole organism for propagation.

Detection and Quantification:

  • Plaque Assay: Measures the number of virus particles by counting plaques (clear zones) formed on a layer of host cells.

  • Hemagglutination Assay: Measures the ability of viruses to agglutinate red blood cells.

  • ELISA (Enzyme-Linked Immunosorbent Assay): Detects viral antigens or antibodies against viruses.

  • PCR (Polymerase Chain Reaction): Detects and quantifies viral DNA or RNA.

Safety and Ethical Considerations:

  • Proper biosafety protocols must be followed when working with viruses, especially pathogenic ones.

  • Ethical considerations are important when using animals for virus cultivation and research.


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