Viruses

1. Helical e.g tobacco mosaic
2. Icosahedral e.g. adenovirus
3. Enveloped e.g. influenza
4. Complex e.g. T4 bacteriophage

1. Types
   1. RNA
   2. DNA
   3. ss
      1. Linear
      2. Circular
   4. ds
   5. Single
   6. Multiple
2. Function
   1. Synthesis of viral components and viral enzymes for replication and assembly of a virion.

Anotações:

• Capsid + viral nucleic acid = nucleocapsid

1. Protects, attaches and introduces viral genome into host cells
2. Protein Subunits - capsomeres
3. Nucleocapsid

   Anotações:

   • capsid + nucleic acid (genome)

1. Lipid bilayer
   1. Phospholipids
   2. Glycoproteins
2. Derived from host cell membranes by budding
   1. Virus incorporates its own proteins - appearing as glycoprotein spikes
3. in most animal viruses
4. Presence?
   1. Yes - enveloped virus
   2. No - naked virus

1. Lytic
   1. Lyse the host bacterium
   2. E.g. T4 Bacteriophage (ds DNA)
      1. Lytic life cycle
         1. 1. Attachment
            1. attachment sites on tail fibres recognise and adsorb to complementary receptor sites on bacterial surface
            2. Viral specificity: specific strains of bacteriophages can only adsorb to specific strains of host bacteria
               1. most adsorb to cell wall (but some attach to flagella/pili)
         2. 2. Penetration
            1. Phage TAIL releases lysozyme
               1. digests bacterial cell wall, allowing release of molecules
                  1. molecules trigger a change in shape of phage base plate
                     1. initiating contraction of tail sheath
                        1. which drives hollow core tube through cell wall
            2. tip of core reaches plasma membrane --> phage DNA injected into bacterial cell
               1. empty capsid remains outside cell
         3. 3. Replication

            Anotações:

            • Early replication: Phage genes expressed Enzymes produced to hydrolyse bacterium’s DNA to nucleotides. Phage takes complete control of host cell macromolecular synthesising machinery to replicate its own genome. Early proteins digest host cell genome. Late replication: Uses bacteria’s metabolic machinery + resources to express phage enzymes and phage components (late proteins)
            1. Eclipse period
               1. Period when complete, infective virions are not yet present in host cell
               2. only separate components e.g. DNA, protein present
            2. Phage enzymes take over host cell's macromolecular synthesising machinery
               1. Host cell DNA degraded into nucleotides
                  1. Nucleotides from host cell's degraded DNA used to synthesise many copies of phage DNA
               2. viral DNA escapes degradation due to DNA methylation
               3. early proteins
            3. Phage DNA immediately transcribed
               1. synthesise mRNA using host RNA polymerase
            4. Biosynthesis of viral proteins
               1. uses bacterium's metabolic machinery
                  1. synthesise phage enzymes and phage structural components
               2. late proteins
         4. 4. Maturation
            1. Phage DNA + capsid assemble into DNA-filled head
            2. Head, tail, tail fibres assembled independently, joined in specific sequence
               1. tail fibres to tail, then head to tail
         5. 5. Release
            1. phage lysozyme breaks down bacterial cell wall
            2. host cell plasma membrane lyses
               1. newly formed mature phage virions released, ready to infect other cells and repeat cycle
2. Temperate
   1. Incorporates its DNA into the host bacterium's DNA and becomes a prophage
   2. E.g. Lambda bacteriophage (ds DNA)
      1. Lysogenic life cycle
         1. 3. Replication
            1. linear phage DNA circularises
               1. inserted into host cell genome by integrase
                  1. integrase binds at attachment site sequences of viral DNA and host cell DNA, forming lambda integrase protein complex
                     1. catalysis of double strand breakage and rejoining
                        1. integrase dissociates --> phage DNA integrated into bacterial chromosome
                  2. integrated DNA = prophage
                     1. prophage gene expression repressed by phage repressor proteins
                        1. genes directing synthesis and release of new virions are not transcribed
                           1. phage DNA not synthesised
                     2. prophage DNA replicates along with bacterial chromosome
                        1. prophage remains latent in all progeny cells
         2. 4. Spontaneous induction
            1. cellular proteases activated
            2. Repressor proteins destroyed
               1. prophage no longer repressed
            3. prophage excised, enters lytic cycle
         3. 5. Maturation - same as lytic
         4. 1. Attachment - same as Lytic
         5. 2. Penetration - same as lytic
         6. 6. Release - same as lytic
   3. Host cells immune to re-infection by same phage
   4. capable of specialised transduction

      Anotações:

      • phage packages adjacent bacterial DNA together with its own viral DNA in same capsid, transferred to new bacterial cell along with prophage when virion infects a new cell.

1. Influenza (ss RNA)
   1. Structure
      1. Genome
         1. 8 different segments of ss RNA associated with nucleoproteins
            1. 3 RNA segments code for 3 different polymerases
               1. 3 polymerases form RNA-dependent RNA polymerase enzyme complex

                  Anotações:

                  • or RNA replicase
                  1. Function: replication and transcription of viral genome
            2. Other 5 segments
               1. haemmagglutinin
                  1. impt for recognition and attachment to host cell
               2. neuraminidase
                  1. impt for leaving host cell
               3. nucleoprotein, matrix protein M1, non-structural proteins
         2. negative strand genome
            1. sequence of viral genome is complementary to sequence of viral mRNA
      2. Capsid - Present
      3. Envelope
         1. Embedded with haemagglutinin (glycoprotein) and neuraminidase (enzyme)
            1. diff types of h and n give rise to diff strains of influenza
   2. Replication cycle
      1. 1. Attachment
         1. Protruding glycoproteins bind specific receptor molecules on host cell
            1. Humans - haemagglutinin on influenza binds sialic acid receptor on host cell membrane
      2. 2. Penetration and uncoating
         1. Virus enters by endocytosis
            1. Host plasma membrane invaginates and pinches off
               1. Virus placed in endocytic vesicle/endosome
                  1. Vesicle fuses with lysosome --> pH of environment lowered --> viral envelope stimulated to fuse with lipid bilayer of vesicle membrane
            2. Nucleocapsid released into cytoplasm
               1. Capsid degraded by cellular enzymes
                  1. Helical nucleoprotein enters nucleus of cell
      3. 3. Replication
         1. Viral genome used as template to synthesise viral mRNA (+ strand RNA)
            1. catalysed by viral RNA-dependent RNA polymerase
            2. mRNA acts as template for synthesis of new viral RNA genome
               1. mRNA strands exit nucleus to cytosol and rER
                  1. translated into viral structural components e.g. glycoproteins and capsid proteins
      4. 4. Maturation
         1. Viral glycoproteins transported out of ER, incorporated into plasma membrane
            1. Associate with capsid proteins
         2. viral genome associates with all other proteins to form helical nucleoprotein
            1. interaction with capsid proteins--> budding initiated
      5. 5. Release by budding
         1. Evagination - each new virus buds from cell
            1. host cell may/may not lyse
         2. new viruses acquire host membrane with viral glycoproteins embedded
         3. neuraminidase facilitates release
            1. Cleaves sialic acid and progeny virions from cell surface
2. HIV - Retrovirus (ss RNA)
   1. Structure
      1. Genome
         1. 2 copies of ss RNA
            1. tightly bound to nucleocapsid proteins (nucleoprotein in HIV)
         2. both positive strands
            1. genome has same sequence as viral mRNA
         3. 3 major genes 5'-gag-pol-env-3'
            1. gag: structural proteins
               1. capsid
               2. matrix
               3. nucleocapsid protein
            2. pol: viral enzymes
               1. integrase
               2. reverse transcriptase
               3. HIV protease
            3. env: glycoproteins
               1. gp120
               2. gp41
      2. Capsid
         1. conical-shaped
         2. contains reverse transcriptase, integrase and protease
      3. Envelope
         1. embedded with gp120 and gp41
            1. Have specific conformation allowing virus to bind certain receptors on T4 helper cells
   2. Replication cycle
      1. 2. Penetration and uncoating
         1. gp41 helps fuse viral envelope with host cell membrane
            1. Capsid released into cell, leaving envelope behind
         2. Capsid + nucleocapsid protein degraded
            1. viral enzymes and RNA released into host cell cytoplasm
      2. 3. Replication
         1. Step 1
            1. Viral reverse transcriptase catalyses conversion of viral RNA into DNA
            2. First, DNA strand complementary to viral RNA strand is synthesised
               1. RNA-DNA hybrid formed
         2. Step 2
            1. Viral DNA enters host cell nucleus --> integrated into host's genetic material
               1. becomes provirus
               2. may remain latent for years afterwards
            2. catalysed by integrase
            3. Activation of host cell --> viral DNA transcribed into viral RNA
               1. serves as mRNA
         3. Step 3
            1. mRNA exits nucleus into cytoplasm
               1. translated into viral polyproteins
            2. gp120 & gp41 made in ER
               1. transported by vesicles to plasma membrane
      3. 4. Maturation
         1. Polyproteins and HIV RNA genome assemble at inner surface of host cell's plasma membrane
      4. 1. Attachment
         1. virus must contact cell with CD4 protein on surface
            1. T lymphocytes/T- helper cells
            2. macrophages
         2. gp120 binds complementary CD4 receptors on cells, with the help of co-receptor
      5. 5. Release
         1. virus buds off/evaginates
         2. Viral envelope derived from host cell membrane
         3. HIV protease cleaves polyproteins into functional proteins
            1. structural proteins
            2. viral enzymes
         4. mature virions

1. accumulation of mutations in genes encoding surface glycoproteins
   1. Influenza: Haemagglutinin and neuraminidase
   2. surface antigens/glycoproteins have different conformations
2. Results from
   1. RNA-dependent RNA polymerase: lack of proof-reading ability
   2. Virus: Fast/high rate of replication
   3. Virus is ss RNA, no backup for replication

Anotações:

• When a bird strain and a human strain of the same virus infect a single cell of an intermediate host e.g. a pig, genetic reassortment can occur.  When new viruses are assembled in the host cell, they can have new combinations of RNA segments. Sometimes genetic reassortment produces viruses with new antigens. Host becomes susceptible to the virus if the host does not have antibodies that recognises these modified antigens once infected.

1. Results from
   1. 2 ot more different strains of a virus/different viruses combine to form a new subtype
      1. having a mixture of surface antigens of the original types.
   2. segmented RNA genome allows for reassortment

      Anotações:

      • the segments of genes that code for haemagglutinin and neuraminidase, 
2. sudden and major change in the surface antigens of a virus
   1. genetic reassortment, conferring phenotypic change

      Anotações:

      • http://www.virology.ws/2009/06/29/reassortment-of-the-influenza-virus-genome/
      1. host cell forms new viruses combining surface antigens of the two different strains that infect the same cell
         1. may further evolve to spread from person to person
3. enables strains to jump from species to species
4. mostly influenza

1. antigens are on virus particles
2. antibodies and other receptors are in our immune systems
3. immune receptors are virus-specific --> recognise and bind to antigens on viruses
   1. body produces more after an infection --> re-infection prevented --> acquired immunity
      1. antigens constantly mutate to produce new forms --> no longer specific to receptors --> no longer bind --> evade immunity