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Biology

Sylvia S. Mader
Michael Windelspecht

Chapter 20
Viruses, Bacteria, and
Archaea
Lecture Outline
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Outline

20.1 Viruses, Viroids, and Prions


20.2 The Prokaryotes
20.3 The Bacteria
20.4 The Archaea

20.1 Viruses, Viroids, and Prions

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

Pasteur used the word virus, Latin for poison.

Viral Diseases in Humans

Viruses, Viroids, and Prions


Viral Structure and Classification:
Each type has at least two parts (capsid and core)
Viruses are characterized by
Size and shape
10400 nm in diameter

Type of nucleic acid core


Single stranded or double stranded? DNA or RNA?

Capsid or no capsid (outer layer composed of protein


subunits):
Some are enveloped by membrane
Others naked
5

Viruses, Viroids, and Prions


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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, Viroids, and Prions

Viruses:

Are obligate intracellular parasites


Cannot reproduce outside a living cell
Are either active or inactive, instead of living or non-living

Can be cultured only inside living cells


Chicken egg
Tissue culture
Three hypotheses about viral origin and evolution
Proteins and nucleic acids, organic molecules in viruses, evolved and
viruses may have arisen from these two basic polymers when cells did.
Viruses may have been derived from pieces of cell genomes.
Viruses may have evolved backwards from living cells.
Viruses degenerated from living cells.

Viruses, Viroids, and Prions


Reproduction of Viruses:
1. Attachment: Virus gains entry into specific host cell based on
host-specific match between virus surface molecules and host
cell receptors.
2. Penetration: Host cell engulfs virus or virus injects its genome
into the cytoplasm.
3. Biosynthesis: New viral components are synthesized using
host cells machinery and energy.
4. Maturation: Viral components are assembled into new viruses.
5. Release: New viruses exit host cell through lysis or budding in
order to infect new host cells.

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Viruses, Viroids, and Prions


Bacteriophages Viruses that infect bacterial cells
There are two types of bacteriophage life cycles.
The lytic cycle
Viral reproduction occurs
The host cell undergoes lysis
Hundreds of virus particles are released

The lysogenic cycle

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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Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall

bacterial
DNA

nucleic acid

capsid

12

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall

bacterial
DNA

nucleic acid

capsid

2. PENETRATION
Viral DNA enters host.

viral
DNA

13

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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.

16

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
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.

viral
DNA

LYTIC
CYCLE

4. MATURATION
Assembly of viral components.

INTEGRATION Viral DNA is integrated


into bacterial DNA and then is passed
on when bacteria reproduce.

viral
DNA

3. BIOSYNTHESIS
Viral components are synthesized.

LYSOGENIC
CYCLE

17

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall

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.

INTEGRATION Viral DNA is integrated


into bacterial DNA and then is passed
on when bacteria reproduce.
viral
DNA
viral
DNA

3. BIOSYNTHESIS
Viral components are synthesized.

LYSOGENIC
CYCLE

18

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
1. ATTACHMENT
Capsid combines with receptor.
bacterial
cell wall

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.

INTEGRATION Viral DNA is integrated


into bacterial DNA and then is passed
on when bacteria reproduce.
viral
DNA
viral
DNA

3. BIOSYNTHESIS
Viral components are synthesized.

LYSOGENIC
CYCLE
prophage

19
daughter cells

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

20
Eye of Science/Science Source

Lytic and Lysogenic Cycles in Prokaryotes


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

INTEGRATION Viral DNA is integrated


into bacterial DNA and then is passed
on when bacteria reproduce.
viral
DNA

viral
DNA

LYSOGENIC
CYCLE
4. MATURATION
Assembly of viral components.

3. BIOSYNTHESIS
Viral components are synthesized.
prophage

21
daughter cells
Eye of Science/Science Source

Viruses, Viroids, and Prions


Reproduction of Animal Viruses:
Animal virus enters the host cell
Uncoating releases viral DNA or RNA
Budding:
Viral particles released in a bud
Acquires a membranous envelope

Retroviruses (HIV, the virus that causes AIDS)


Contain reverse transcriptase
Carries out RNA cDNA reverse transcription
cDNA becomes integrated into host DNA
Replicated as host DNA replicates
HIV may remain latent for years
Viral DNA is transcribed; new viruses are produced
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Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor

nuclear
pore

23

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike
capsid

2. Entry
nuclear
pore

24

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike

2. Entry

capsid

nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase

25

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike

2. Entry

capsid

nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA

26

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike

2. Entry

capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA

Integration

27

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike

2. Entry

capsid

nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA

Integration

host DNA

provirus

28

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

1. Attachment
receptor
envelope
spike

2. Entry

capsid
nuclear
pore
3. Reverse transcription
viral RNA
reverse transcriptase
cDNA

Integration

host DNA

provirus

29

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

30

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

31

Reproduction of the Retrovirus HIV


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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

N spike attacks host plasma membranes


Allows mature viruses to exit the cell
9 different types

Each type of spike can occur in different varieties.


Our immune system only recognizes H spikes and N spikes it has
been exposed to.
Currently the H7N9 and H5N1 subtypes of flu virus are of great
concern because they can potentially become pandemics (global
outbreaks).

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Spikes of Bird Flu Virus


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capsid
RNA genome
envelope
N (neuraminidase)
spike
H (hemagglutinin)
spike

mutation 1

mutation 2

a. Viral genetic mutations occur in a bird host

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

A genetic mutation may occur.


Example: Influenza strains H5N1, H1N1, and H7N9 were created through mutation
of flu viruses which only infected animals
It is necessary to obtain flu vaccine each year due to the rapidly mutating flu virus

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Viruses, Viroids, and Prions


Viruses are best known for causing infectious diseases in
plants and animals.
Herpes, HIV, cancer
Viruses lack metabolism; thus, antibiotics have no effect

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

Some human and other animal diseases: Mad cow disease


Some practices, including eating brains of cattle, transmitted the cattle
disease (BSE or bovine spongiform encephalopathy) to humans.

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20.2 The Prokaryotes


Include bacteria and archaea, which are fully
functioning cells
Means before a nucleus
Microscopic
Range in size from 110 m in length and 0.71.5 m in
width

Abundant in air, water, and soil and on most objects


Louis Pasteur showed that a previously sterilized
broth cannot become cloudy with growth unless it is
exposed directly to the air.
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Pasteurs Experiment
Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

HYPOTHESIS A: Bacteria arise spontaneously in a broth.


HYPOTHESIS B: Bacteria in the air contaminate a broth.

FIRST EXPERIMENT

SECOND EXPERIMENT

flask is open to air


flasks outside building
opened briefly
boiling to
sterilize
broth

89% show growth

boiling to
sterilize
broth

air here is pure

air enters here


flasks inside building
opened briefly
boiling to
sterilize
broth

bacteria collect here


32% show growth

CONCLUSION:
Hypothesis B is supported because relative concentrations of bacteria in
the air explain the results.

100% have no growth


CONCLUSION:
Hypothesis B is supported because when air reaching the broth contains
no bacteria, the flask remains free of growth.

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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)

40

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

41

Features of Prokaryotic Cells


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

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.

Some bacteria form resistant endospores under


unfavorable conditions.
43

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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20.3 The Bacteria


Bacteria are the more common type of
prokaryote.
Over 9,000 different bacteria have been named.

Most bacterial cells are protected by a cell wall.


Contains peptidoglycan

Bacteria are commonly differentiated using the Gram


stain procedure.
When washed after staining:
Gram-positive bacteria retain dye and appear purple
Gram-negative bacteria do not retain dye and appear pink
Gram-negative bacteria have a second plasma membrane which blocks antibiotic
drugs, making infections difficult to treat

The difference is dependent on the construction of the cell wall.

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47

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

Facultative anaerobes able to grow in either the


presence or absence of free oxygen

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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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52

The Bacteria

Heterotrophic Bacteria

Most prokaryotes are chemoheterotrophs that take in organic nutrients.


Aerobic saprotrophs decompose most large organic molecules to smaller molecules.
Essential components of a healthy ecosystem

May be free-living or symbiotic (two different species live together in an


intimate way)
Commensalism
One population modifies the environment in such a way that a second population benefits.
Obligate anaerobes live in our intestine because bacterium E. coli uses up oxygen.

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

53

Nodules of a Legume

54

The Endospore of Clostridium tetani


Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

endospore

Alfred Pasieka/SPL/Science Source

55

Bacterial Diseases in Humans

56

The Bacteria
Antibiotic compounds fall into two classes.
Compounds that inhibit protein biosynthesis
Erythromycin
Tetracycline

Compounds that inhibit cell wall biosynthesis

These affect bacterial but not animal cells


Penicillin
Ampicillin
Fluroquinolone

Bacterial resistance to antibiotics is increasing.


Genes conferring resistance can be transferred among bacteria by
transformation, conjugation, or transduction.
Now 90% of Staphlococcus aureus are resistant to penicillin and
increasingly to methicillin (MRSA).
MRSA is common in hospitals and nursing facilities.

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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

Lack visible means of locomotion


Can live in extreme environments
In association with fungi, form lichens
They possess heterocysts, cells without nuclei, where nitrogen fixation
occurs.
Cyanobacterial blooms result from pollution in lakes and ponds.

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Diversity Among the


Cyanobacteria

59

20.4 The Archaea


Archaea were formerly considered bacteria
Carl Woese and George Fox discovered that the
base sequence of their rRNA differs from
bacteria.
Other differences:
Archaea do not have peptidoglycan in their cell walls
like the bacteria.
Archaea are biochemically more like eukarya than
bacteria.

Archaea are now thought to be more closely


related to eukarya than to bacteria.
60

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

Hot sulfur springs


Thermoacidophiles
Reduce sulfides and survive best at temperatures above 80C
Plasma membranes contain unusual lipids that confer tolerance
of high temperatures.
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Extreme Habitats: Salt Lakes

62

Extreme Habitats: Hot Springs

63

Extreme Habitats: Swamps

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