Title: Chapter 13: Virus of Bacteria
1Chapter 13Virus of Bacteria
2Important Point
If you are having trouble understanding lecture
material Try reading your text before
attending lectures. And take the time to read it
well!
3What is a Phage?
- The agents were called filterable viruses Virus
means poison, a term that once had been applied
to all infectious agents. With time, the
adjective filterable was dropped and only the
word virus was retained. - Bacteriophage were originally described as a
macroscopic phenomenon that was slightly
different from the poisoning of a plant or
animal. - Instead, what was observed was the destruction of
a bacterial culture. - People werent all that sure what a bacterium was
so the destruction was seen more as an eating
of the culture (by an otherwise unseen agent)
rather than a poisoning. - The filterable agent in this case was described
as an eater of bacteria, or Phage from Greek
Bacteriophage Bacteria Eater.
4What is a Phage?
- The agents were called filterable viruses Virus
means poison, a term that once had been applied
to all infectious agents. With time, the
adjective filterable was dropped and only the
word virus was retained. - Bacteriophage were originally described as a
macroscopic phenomenon that was slightly
different from the poisoning of a plant or
animal. - Instead, what was observed was the destruction of
a bacterial culture. - People werent all that sure what a bacterium was
so the destruction was seen more as an eating
of the culture (by an otherwise unseen agent)
rather than a poisoning. - The filterable agent in this case was described
as an eater of bacteria, or Phage from Greek
Bacteriophage Bacteria Eater.
The word bacteriophage or phage that infect
bacteria is both singular and plural when
referring to one type of virus. The word phages
is used when different types of phages are being
referenced.
5Virus Architecture
Minimally, a virus is a proteinaceous carrier of
nucleic acid.
Many viruses are more complicated than that, such
as having a lipid envelope surrounding the
protein capsid.
6Terms Describing Virions
- Virion is another name for virus particle.
Virions are infectious meaning that they can
deliver their nucleic acid to the cytoplasm of a
susceptible cell (which for phages would be a
bacterium). - Capsid is the the protein coat that surrounds the
nucleic acid and defines a virus as a virus. - Capsids are made up of individual proteins called
capsomers. - The virion particle consists, minimally, of
protein and nucleic acid which together is called
a Nucleocapsid. - Many particularly animal viruses have lipid
bilayers surrounding the nucleocapsid those
viruses are described as Enveloped. - Non-enveloped viruses are described as Naked.
- In enveloped viruses the envelope makes initial
contact with cells and subsequent interaction
with the cell surface is mediated by envelope
proteins (proteins found in or on the envelope
lipid bilayer).
7Virus Architecture
Note spikes projecting from protein capsid
surrounding nucleic acid.
Note spikes projecting from lipid
envelope-surrounding capsid (which in turn
surrounds the nucleic acid).
8Virion Attachment Organs
- Some virions are isometric they have a fully
symmetrical capsids, almost spherical. - Isometric virions attach to cells via Attachment
Proteins, a.k.a., Spikes which are proteins that
symmetrically project from their virions. - Spikes project from capsids in Naked viruses.
- Spikes project from envelopes in Enveloped
viruses. - Some virions are helical with attachment proteins
at end or ends. - Most phages have tailed virions which sort of
combine the morphology of isometric and helical
virions, with the isometric part called a head
and the helical part called a tail. - Attachment is made at the end of the tail
opposite the head, and often is mediated by thin
feelers called tail fibers.
9Not-Complex Virions
10Complex (Tailed) Phage Virion
Note that this head actually is elongated top to
bottom rather than isometric.
11Virion Size
Big
Small
Medium
Even Smaller
12Viral Genomes
One way to distinguish different types of viruses
(e.g., influenza virus from HIV) is in terms of
the characteristics of their nucleic-acid genomes.
Nucleic-Acid Virus Genome
http//www.virology.net/Big_Virology/BVFamilyGenom
e.html
13Viruses are Not Cells
Smaller
Bigger
14Some Important Phages
Here complex means tailed
Note various genome architectures.
An example of Lysogenic Conversion.
15Lytic Infection Strategy
This is the productive-infection strategy
followed by most phages including all tailed
phages.
Phages that are obligately lytic are called
Virulent (vs. chronic or temperate).
16Chronic Infection Strategy
This is a process called Extrusion.
This is the strategy followed by filamentous
phages.
17Latent Infection Strategy
For phages this is called Lysogeny.
Only Temperate phages are able to display
lysogeny.
For phages this is called Lysogenic Conversion.
18Viral Infection Strategies
19Virulent Phage Life Cycle
20Chronic Phage Life Cycle
21Temperate Phage Life Cycle(s)
22Temperate Phage Life Cycle(s)
This is a process called Induction.
The prophage DNA can remain integrated
indefinitely.
23Adsorption Host Range
- Adsorption describes the virions attachment
process. - The virion contains proteins that recognize
molecules found on the surface of cells (much as
antibodies bind to antigens). - Receptor Molecules (typically proteins) are
molecules that cells make for various reasons
(e.g., transport proteins) which viruses coopt
for adsorption. - Typically the Host Range of a virus is
determined, at least in part, by the ability of
the virus adsorption proteins to bind to host
Receptor Molecules. - Restriction-Modification systems can also limit
phage host range (as well as biochemical
incompatbilities). - Through mutation (and other means) phages can
overcome these host-range barriers, resulting,
typically in a changed host range. - Because of transduction, these changes in host
range can allow gene exchange between even only
distantly related bacteria.
24G. Eliave Institute, Tbilisi, Georgia
25G. Eliave Institute, Tbilisi, Georgia
26G. Eliave Institute, Tbilisi, Georgia
27G. Eliave Institute, Tbilisi, Georgia
28G. Eliave Institute, Tbilisi, Georgia
29G. Eliave Institute, Tbilisi, Georgia
30G. Eliave Institute, Tbilisi, Georgia
31Link to Next Presentation