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Viruses and Bacteria

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Lack most of structures found in bacteria ... Are little more than aggregates of nucleic acid and protein 'genes' in protein ... Figure 18.02x1 Adenovirus ... – PowerPoint PPT presentation

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Title: Viruses and Bacteria


1
Viruses and Bacteria
2
Size comparisons
3
Viruses
  • Much smaller and simpler in organization than
    bacteria
  • Lack most of structures found in bacteria
  • Lack most of metabolic machinery, so must hijack
    another cell to reproduce
  • Are little more than aggregates of nucleic acid
    and protein genes in protein coats

4
History of discovery of viruses
  • 1883 Mayer tobacco mosaic disease, spread by
    spraying sap from infected plant onto healthy
    plant was it a tiny bacteria?
  • 1893 Ivanowsky filtered sap from tobacco
    mosaic disease, still caused disease
  • 1897 Beijerinck found that infectious agent in
    filtered sap could reproduce sprayed plants
    with filtered sap, when developed disease, used
    their sap to infect more plants ability to
    infect was UNDILUTED over several generations, so
    had to be reproducing

5
  • Found that tobacco mosaic disease could only
    reproduce within the infected host could not be
    cultivated in culture
  • Not inactivated by alcohol (which kills bacteria)
  • 1935 Stanley crystallized the infectious
    particle Tobacco Mosaic Virus (TMV)
  • no cells aggregate into crystals, so what ARE
    viruses?????
  • Infectious particles consisting of a nucleic acid
    inside of a protein coat, and occasionally in
    some cases, a membraneous envelope.

6
Viral Genomes
  • May be double-stranded DNA, single-stranded DNA,
    double-stranded RNA, or single-stranded RNA
  • Called a DNA-like or RNA-like virus depending on
    the nucleic acid found
  • Organized as a single linear or circular model of
    nucleic acid

7
Capsids and Envelopes
  • Capsid protein shell that encloses the nucleic
    acid built from large numbers of protein
    subunits called capsomeres (but the number of
    proteins of different kinds in one virus is
    small)
  • Shapes helical, polyhedral, very complex
  • Some have accessory structures that aid in host
    infection.
  • Ex. viral envelopes cloak viral capsid,
    derived from hosts membrane, have
    glycoproteins that can act as anchoring
    spikes
  • Ex. Head and tail, act as hypodermic syringe

8
Figure 18.2 Viral structure
9
Virus Replication
  • Viruses are obligate intracellular parasites
    must have a host cell
  • Viruses lack the enzymes for metabolism and have
    not ribosomes, so cant make own proteins
  • Each type of virus can only infect and parasitize
    within a HOST RANGE this specificity depends on
    the lock-and-key fit between proteins on the
    outside of the virus and specific receptor
    molecules on cell surface. Some ranges are
    specific, some are broad.

10
Figure 18.3 A simplified viral reproductive cycle
11
Viral reproductive cycle
  • Virus uses hosts nucleotides and enzymes to
    replicate itself.
  • At the same time, other host resources are used
    to make new capsid proteins by transcription and
    translation.
  • The new viral genomes and capsids are assembled
    into new virus particles when the number exceeds
    the cells surface area limitations, the cell
    bursts open and new viruses are released to
    infect other cells exponential increase

12
5 basic steps of virus replication
  • 1. Attachment
  • 2. Penetration
  • 3. Replication and Synthesis
  • 4. Assembly
  • 5. Release

13
Speed of takeover
  • Lytic vs. Lysogenic cycles
  • In the lytic cycle, the virus takes over the host
    cell immediately and reproduces quickly the
    host cell can lyse within a few minutes (Ex.
    Cold virus)
  • Viruses that reproduce by lytic cycles are called
    virulent viruses
  • In the lysogenic cycle, the virus hides in the
    original host cells DNA until optimal conditions
    for viral survival are present (provirus) then,
    because the host cell has reproduced, the virus
    will reproduce and emerge from MULTIPLE cells at
    once, causing much more severe cellular damage
    (Ex. AIDS, ebola)
  • Viruses that reproduce by both lytic and
    lysogenic cycles are called temperate viruses

14
Figure 18.02x2 Phages
15
Figure 18.4 The lytic cycle of phage T4
16
Figure 18.02x1 Adenovirus
17
Figure 18.5 The lysogenic and lytic reproductive
cycles of phage ?, a temperate phage
18
So why arent all cells wiped out?
  • Natural Selection favors mutations with receptor
    sites that viruses cannot attach to.
  • Cellular enzymes of cell may break down virus
    before it can replicate and take over
    (restriction nucleases act as DNA/RNA scissors
    for foreign DNA).
  • BUT, natural selection also favors viral mutants
    that are resistant to destruction, so virus-host
    relationship is in constant evolutionary flux.

19
Table 18.1 Classes of Animal Viruses, Grouped by
Type of Nucleic Acid
20
Animal Viruses
  • Many animal viruses have a membranous envelope
    present.
  • This envelope is a lipid bilayer with
    glycoproteins for attachment.
  • Viral envelope is derived from the host cells
    plasma membrane, so host cell may not be killed.

21
Figure 18.6 The reproductive cycle of an
enveloped virus
22
Nuclear membrane-derived envelopes
  • Herpesviruses genomes of double-stranded DNA
  • Reproduce within the cell nucleus
  • Can become a provirus (like the prophages
    earlier)
  • Infections tend to recur throughout life in times
    of stress as the proviruses exit the cell

23
RNA viruses
  • Found mostly in animals
  • Classified according to the strandedness of their
    RNA and how functions in host
  • single stranded RNA that serves as mRNA
  • single stranded RNA that is mRNA
    template
  • single stranded RNA that is template for
    DNA synthesis

24
Retroviruses
  • Have most complicated reproductive cycles
  • Have reverse transcriptase which transcribes DNA
    from and RNA template (backwards from normal)
  • Newly made DNA integrates as a provirus into a
    chromosome in animal cell nucleus
  • Hosts RNA polymerase transcribes the viral DNA
    into RNA
  • Ex. HIV human immunodeficiency virus

25
Figure 18.7 HIV, a retrovirus
26
Figure 18.7x1 HIV infection
See page 336 for color pictures
27
Viral Infection and symptoms
  • No clear link
  • some viruses damage or kill cells by
    causing lysosomes to release killing enzymes
  • some cause infected cells to produce toxins
    that lead to disease symptoms
  • some have toxic molecular components

28
How much damage?
  • Depends on regeneration ability of tissue
  • Ex. Colds pass b/c respiratory epithelium
    efficiently repairs
  • Ex. Polio attacks nerve cells, so no
    healing
  • Temporary symptoms (fever, aches, inflammaiton)
    are result of bodys own attempt to defend itself
    -- immune response

29
Controlling Viruses
  • Diseases causes by viruses are difficult to treat
  • Drugs are only used to treat SYMPTOMS, not cure
    the disease (just make patient feel better for
    short duration)
  • Only methods have to control are to PREVENT
    illness vaccines and antibody production, use
    of interferon in body

30
Antibodies
  • Are made by hosts immune system after infection
    occurs (if host survives the infection)
  • Help inactivate viruses and destroy harmful
    bacteria
  • Are specific for viruses or bacteria
  • Once an antibody is produced that recognizes a
    specific virus or bacteria, then that strain will
    be ineffective on that individual organism

31
Vaccines
  • Harmless variants or derivatives of pathogenic
    microbes
  • Stimulate the immune system to mount defenses
    against a specific pathogen
  • Developed by Edward Jenner cowpox used to
    develop smallpox vaccination
  • Vaccinated or immunized again disease
  • Ex. MMR, DPT, polio, smallpox, influenze,
    rabies, hepatitis C

32
Figure 18.x1 Smallpox
33
Figure 18.x2 Measles
34
Figure 18.x3 Polio
35
Interferon
  • Chemical in body that is activated when cells are
    attacked
  • Cell under seige produces interferon which binds
    to neighboring cells cell membranes to warn them
    of the dangerous pathogen

36
Why not Antibiotics?
  • These are powerless against viruses
  • Antibiotics kill bacteria by inhibiting enzymes
    or processes specific to the pathogens since
    viruses have no metabolism of their own, the
    antibiotics do not work.
  • Only drugs that have any effect are ones that
    interfere with nucleic acid synthesis AZT (with
    HIV), acyclovir (with herpesvirus)or with
    protein production (protease inhibitors with AIDS)

37
Emerging Viruses
  • AIDS
  • Hantavirus
  • Ebola (hemorrhagic fever)
  • Nipah virus
  • Influenza
  • What contributes?
  • 1. Mutation
  • 2. Spread from one species to another
  • 3. Dissemination from small, isolated population
  • so, 2 and 3 require close contact travel
    allows

38
Plant Viruses
  • Most are RNA viruses
  • Two major routes plant viruses spread
  • 1. horizontal transmission plant is
    infected from an external source
  • 2. vertical transmission plant inherits a
    viral infection from parent plant
  • Once infected, crops must be burned to prevent
    transmission

39
Viroids
  • Viroids tiny molecules of naked circular DNA
    that infect plants
  • -do not encode proteins
  • -can replicate in host plant cells using
    cellular enzymes
  • -disrupt the metabolism of cell and stunt
    growth of whole plant
  • Point is that MOLECULES can be an infectious
    agent.

40
Prions
  • Prions Infectious proteinmisfolded form of a
    protein normally found in brain cells
  • Cause degenerative brain diseases
  • Ex. Scrapie, mad cow disease,
  • Creutzfeldt-Jakob disease
  • When prion gets into a cell containing the normal
    form of the brain cell protein, prion converts
    the normal protein to the prion version

41
Figure 18.10 A hypothesis to explain how prions
propagate
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