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Sylvia S. Mader
Michael Windelspecht
Chapter 20
Viruses, Bacteria, and
Archaea
Lecture Outline
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Outline
Virus
Associated with a number of plant, animal, and human diseases
Can only reproduce using the metabolic machinery of the host
cell
noncellular
May have a DNA or RNA genome.
Invention of the electron microscope allowed these infectious
agents to be first seen
French chemist Louis Pasteur suggested that something
smaller than a bacterium was the cause of rabies
Capsid (protein)
Covering
Envelope (not found in all viruses)
Virus particle
Nucleic acid molecule (DNA or RNA)
Inner core
Various proteins (enzymes)
Viruses
Viruses
Viruses:
10
Viral reproduction does not occur immediately but may occur in the future.
Virus becomes integrated into the host genome and may reenter lytic cycle.
This is known as latency and the latent viral DNA is called a prophage.
Diphtheria is caused by a prophage-carrying bacterium, which produces a
toxin that damages the lining of the upper respiratory tract, restricting
breathing.
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1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
bacterial
DNA
nucleic acid
capsid
12
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
bacterial
DNA
nucleic acid
capsid
2. PENETRATION
Viral DNA enters host.
viral
DNA
13
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
bacterial
DNA
nucleic acid
capsid
2. PENETRATION
Viral DNA enters host.
LYTIC
CYCLE
viral
DNA
3. BIOSYNTHESIS
Viral components are synthesized.
14
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
nucleic acid
bacterial
DNA
capsid
2. PENETRATION
Viral DNA enters host.
LYTIC
CYCLE
4. MATURATION
Assembly of viral components.
viral
DNA
3. BIOSYNTHESIS
Viral components are synthesized.
15
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
nucleic acid
bacterial
DNA
capsid
2. PENETRATION
Viral DNA enters host.
5. RELEASE
New viruses leave host cell.
LYTIC
CYCLE
4. MATURATION
Assembly of viral components.
viral
DNA
3. BIOSYNTHESIS
Viral components are synthesized.
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nucleic acid
bacterial
DNA
capsid
2. PENETRATION
Viral DNA enters host.
5. RELEASE
New viruses leave host cell.
viral
DNA
LYTIC
CYCLE
4. MATURATION
Assembly of viral components.
viral
DNA
3. BIOSYNTHESIS
Viral components are synthesized.
LYSOGENIC
CYCLE
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nucleic acid
bacterial
DNA
capsid
5. RELEASE
New viruses leave host cell.
2. PENETRATION
Viral DNA enters host.
LYTIC
CYCLE
4. MATURATION
Assembly of viral components.
3. BIOSYNTHESIS
Viral components are synthesized.
LYSOGENIC
CYCLE
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nucleic acid
bacterial
DNA
capsid
5. RELEASE
New viruses leave host cell.
2. PENETRATION
Viral DNA enters host.
LYTIC
CYCLE
4. MATURATION
Assembly of viral components.
3. BIOSYNTHESIS
Viral components are synthesized.
LYSOGENIC
CYCLE
prophage
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daughter cells
20
Eye of Science/Science Source
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall
nucleic acid
bacterial
DNA
capsid
2. PENETRATION
Viral DNA enters host.
5. RELEASE
New viruses leave host cell.
LYTIC
CYCLE
viral
DNA
LYSOGENIC
CYCLE
4. MATURATION
Assembly of viral components.
3. BIOSYNTHESIS
Viral components are synthesized.
prophage
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daughter cells
Eye of Science/Science Source
1. Attachment
receptor
nuclear
pore
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1. Attachment
receptor
envelope
spike
capsid
2. Entry
nuclear
pore
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
host DNA
provirus
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
host DNA
provirus
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
host DNA
ribosome
viral
mRNA
provirus
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
host DNA
ribosome
viral
mRNA
4. Biosynthesis
ER
provirus
viral
enzyme
capsid
protein
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1. Attachment
receptor
envelope
spike
2. Entry
capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA
Integration
host DNA
ribosome
viral
mRNA
4. Biosynthesis
ER
provirus
viral
enzyme
capsid
protein
5. Maturation
6. Release
viral RNA
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Flu Virus
A flu virus has an H (hemagglutinin) spike and an N
(neuraminidase) spike
H spike allows the virus to bind to the receptor
16 different types
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capsid
RNA genome
envelope
N (neuraminidase)
spike
H (hemagglutinin)
spike
mutation 1
mutation 2
Human
flu virus
Bird
Flu
virus
combination
In host cell
b. Combination of viral genes occurs in human host
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Emerging Viruses
Emerging viruses are new or previously uncommon
illnesses.
Examples are AIDS, West Nile encephalitis, hantavirus
pulmonary syndrome (HPS), severe acute respiratory
syndrome (SARS), Ebola, hemorrhagic fever, and avian
influenza
Several types of events can cause emergence of viruses
A virus may extend its range.
Example: West Nile was transported to US and took hold in birds and mosquitoes
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Viroids
Naked strands of RNA
Many crop diseases
Prions
Protein molecules with contagious tertiary structure
TSEs are neurodegenerative diseases which destroy nerve tissue in the brain
They are untreatable and fatal
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Pasteurs Experiment
Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
FIRST EXPERIMENT
SECOND EXPERIMENT
boiling to
sterilize
broth
CONCLUSION:
Hypothesis B is supported because relative concentrations of bacteria in
the air explain the results.
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The Prokaryotes
Prokaryote Structure
Lack a membrane-bounded nucleus (DNA in
nucleoid region)
Outer cell wall
Some move by means of flagella
Lack membranous organelles
May have accessory rings of DNA (plasmids)
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Prokaryote Structure
Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Prokaryotic cell
Cell envelope
Glycocalyx
Cell wall
Plasma membrane
Cytoplasm
Nucleoid
Ribosomes
Thylakoids (cyanobacteria)
Appendages
Flagella
Conjugation pilus
Fimbriae
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a.
capsule
gel-like coating outside the cell wall
made up of a polysaccharide layer
called glycocalyx.
plasma membrane
sheet that surrounds the
cytoplasm and regulates
entrance and exit of molecules
fimbriae
hairlike bristles that allow
adhesion to surfaces
b.
plasma
membrane
cell wall
structure that provides
support and shapes the cell
cell wall
capsule
hook
nucleoid
location of the
bacterial chromosome
conjugation pilus
elongated, hollow appendage
used to transfer DNA to other cells
flagellum
rotating filament that propels the cell
ribosome
site of protein
synthesis
filament
basal body
cytoplasm
semifluid solution surrounded by the plasma
membrane; contains nucleoid and ribosomes
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The Prokaryotes
Reproduction in Prokaryotes
Asexual
Prokaryotes reproduce asexually by means of binary
fission.
Generation time is as short as 12 minutes
Mutations are generated rapidly and passed on to offspring
more quickly than eukaryotes.
Prokaryotes are haploid
Mutations are immediately subjected to natural selection.
Binary Fission
Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
cytoplasm
cell wall
nucleoid
0.5 m
CNRI/SPL/Science Source
44
The Prokaryotes
Methods of genetic recombination in the prokaryotes:
Conjugation
Conjugation pilus forms between two cells
Donor cell passes DNA to recipient cell through the pilus
Transformation
Occurs when bacterium picks up free pieces of DNA from other
prokaryotes
Becomes incorporated into genome
Transduction
Occurs when bacteriophages carry portions of bacterial DNA
from one cell to another
Serve as vectors
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The Bacteria
Structure of cell wall also of diagnostic use
Bacteria can be further classified in terms
of their three basic shapes:
Spiral (spirilli),
Rod (bacilli), and
Round (cocci)
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Diversity of Bacteria
49
The Bacteria
Bacterial Metabolism:
Oxygen requirements:
Obligate aerobes unable to grow in the absence
of free oxygen
Obligate anaerobes unable to grow in the
presence of free oxygen
Examples: Botulism, gas gangrene, and tetanus
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The Bacteria
Autotrophic Bacteria:
Photoautotrophs
Use solar energy to reduce carbon dioxide to organic compounds
Photosynthetic
Anoxygenic Green sulfur and some purple bacteria living in oxygen-poor
conditions
Oxygenic
Chemoautotrophs
Oxidize inorganic compounds to obtain energy
Energy is used to reduce CO2 to an organic compound
Chemosynthetic
Live in environments such as deep sea vents 2.5 km below sea level
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The Bacteria
Heterotrophic Bacteria
Mutualism
Both species benefit from association.
Mutualistic bacteria live in human intestines and release vitamins K and B 12 which help produce blood
components.
Parasitism
Parasite benefits at host expense; disease-causing bacteria are called pathogens
Many form endospores
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Nodules of a Legume
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endospore
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The Bacteria
Antibiotic compounds fall into two classes.
Compounds that inhibit protein biosynthesis
Erythromycin
Tetracycline
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The Bacteria
Cyanobacteria
Formerly called the blue-green algae (Cyanophyta)
Cyanobacteria are Gram-negative bacteria that are
photosynthetic.
Believed to be responsible for introducing oxygen into the
primitive atmosphere
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The Archaea
Many live in harsh conditions:
Anaerobic marshes
Methanogens
Produce methane from hydrogen gas and carbon dioxide
Salty lakes
Halophiles
Require high salt concentrations for growth
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