Bacterial Genetics: Phenotypic and Genotypic Variability

 
Bacterial genetics II
 
Dr. Ali Abdulwahid
 
Phenotypic and genotypic
Variability of Bacteria
 
O
v
e
r
v
i
e
w
 
1.
Phenotypic variation :
phenotype : The physical expression of various characters by bacterial
cells in a given environment.
These properties are determined by its genome and by environment.
It is 
reversible
, 
temporary
 and 
not inheritable
Example
 : production of the enzyme beta-galactosidase by the
bacterium 
E. coli 
when it is grown in a medium containing lactose.
When grown in a medium containing glucose only, the enzyme is not
synthesized.
 
 
 
2.
Genotypic variation :
Genotype : It is the hereditary constitution of the cell that is
transmitted to its progeny
Its heritable, stable and does not affected by environment
Genotypic variability may occur due to different mechanisms include :
1.
mutations
2.
Intercellular transfer of genomic material
 
 
 
1. Mutation
It is random, undirected, heritable variation caused by an alteration in the
nucleotide sequences at some points of the DNA of the cell due to 
addition
,
deletion 
or 
substitution
 of one or more bases.
During DNA replication, some ‘errors’ may occur  during copying the  progeny
strands
For instance, instead of thymine bonding to adenine, it binds to guanine
Different mutations in the a particular gene may produce different effect in the
cell
 
Types of Mutation
 
Mutations can be divided conveniently into:
A.
Spontaneous mutation: 
occur spontaneously in nature in the
absence of any mutation-causing agents.
 
B. 
Induced mutation: 
enhanced by exposure of cells to several agent
(mutagens) include :
1.
Physical agents: 
(i) UV rays; (ii) lionizing radiation, e.g. X-rays
2. Chemical agents: 
 Alkylating agents, Acridine dyes and Nitrous acid.
 
 
 Point mutations:
affect just one point (base pair) in a gene.
Leads to change to or substitution of a different base pair.
Alternatively, can result in the deletion or addition of a base pair.
 It is in general, reversible and is of two classes:
1.
Base pair substitution
2.
Frameshift mutations (insertion or deletion):
 
 
1.
Base pair substitution
:
Depending on the placement of the substituted base,
 
can be divided into :
silent mutation 
, cause no change in the amino acid of the protein
missense mutation , 
lead to the insertion of the wrong amino acid
nonsense mutation
 , lead to generate a stop codon and prematurely
terminating the protein synthesis (the polypeptide)
 
Silent mutation
 
M
i
s
s
e
n
s
e
 
m
u
t
a
t
i
o
n
 
N
o
n
s
e
n
s
e
 
m
u
t
a
t
i
o
n
2.
Frameshift mutations (insertion or deletion): 
If the number of bases inserted or deleted is not a multiple of three, there
will be shift in the reading frame (codons sequence), forming newest of
triplet codon.
the new codons will specify the incorrect amino acids, or leading to
premature termination for the translation process (truncated protein)
F
r
a
m
e
s
h
i
f
t
 
m
u
t
a
t
i
o
n
s
 
2- Intercellular transfer of genomic material
 
 
Horizontal gene transfer :
DNA can be transferred from one organism to another, and that DNA can be stably
incorporated in the recipient cell, 
permanently changing 
its genetic composition.
This Process is so called 
horizontal 
gene transfer to differentiate it from the inheritance of
parental genes, a process called 
vertical 
inheritance.
Three broad mechanisms mediate efficient movement of DNA between bacterial
cells :
Conjugation
T
ransduction
transformation
.
 
Conjugation
 
 
A process in which one cell, 
the donor or male cell
, makes contact
with another, the recipient or female cell
DNA is transferred directly from the donor into the recipient
Certain types of plasmids, known as 
transfer factors or sex factors
,
carry the genetic information necessary for conjugation to occur.
These are also called 
self-transmissible plasmids
, and they  can
mobilize other plasmids or portions of the chromosome for
transfer.
Only cells that contain such a plasmid can act as donors; those
lacking a sex factor act as recipients.
Such Plasmid  codes for specialized fimbria (sex pilus) which
projects from the surface of the cell.
The tip of the pilus attaches to the surface of a recipient cell and
holds the two cells together so that DNA can then pass into the
recipient cell.
 
A male and a female cell joined by a pilus (sex pilus).
 
1. 
Plasmid transfer
 
Bacterial Populations can be divided into two types of cells.
1.
F+ : 
the donor cell, contains an 
Fertility plasmid or F plasmid  
and is
designated 
F+
.
2.
F – :
 
the recipient cell, does not contain this plasmid and is called 
F
.
DNA is transferred only in one direction, from F+ to F–
F Factor or F plasmid
 
(Fertility Factor)
Is a transfer factor that contains the genetic information necessary for
the synthesis of the sex pilus  
(Conjugation tube)
, and for self-
transfer.
 
Mechanism of DNA transfer during conjugation.
 
 
A.
Connection between two bacterial cells by
means of sex pili..
B.
Formation of a specific conjugal bridge
between donor cell  and receptor cell.
C.
An endonuclease cleaves one strand of the
circular DNA double helix at a specific point .
The single strand with the “leader region”
enters the recipient cell.
D.
The double-stranded structure of both the
transferred single strand and the remaining
DNA strand is restored by means of
complementary DNA synthesis.
The recipient cell, now plasmid-positive, is called
a 
transconjugant cell.
 
2. Chromosomal transfer
 
The F factor in some cases can be integrated into the
host chromosome in a very small proportion of F+
cells, creating : 
high frequency recombination (Hfr)
donor cells
 In which, the entire chromosome behaves like an F+
plasmid
chromosomal genes (fragments) can be transferred
(from the site of insertion)  in a direction determined
by the orientation of insertion in the normal sex
factor manner to a recipient cell at a relatively high
frequency
 
M
e
d
i
c
a
l
l
y
 
I
m
p
o
r
t
a
n
t
 
F
a
c
t
o
r
s
 
T
r
a
n
s
f
e
r
r
e
d
 
b
y
 
C
o
n
j
u
g
a
t
i
o
n
 
 
1.
Colicinogenic (Col) Factor
Several strains of coliform bacteria produce colicins— antibiotic-like substances which are
specifically and selectively lethal to other enterobacteria.
Colicin production is determined by a plasmid called the Col factor, which resembles the F
factor in promoting conjugation, leading to self-transfer and, at times, transfer of
chromosomal segments.
2. Resistance Factors or R Plasmids
Resistance factors (R factors) 
are plasmids that have significant medical importance as it
leads to the spread of multiple drug resistance among bacteria.
This R plasmid consists of two components: 
RTF+r determinants
.
Resistance transfer factor (RTF): 
The transfer factor that
 
is responsible for conjugal transfer.
Resistance determinant (r): 
code for resistance against various drugs.
The whole plasmid 
(RTF+r determinants) 
is known as the 
R factor
An 
R factor 
can have 
several r determinants
, and resistance to as many as eight or more
drugs can be transferred simultaneously.
 
Transduction
 
 
The transfer of a portion of the DNA from one bacterium to
another by a bacteriophage
Bacteriophages are viruses that parasitise bacteria and
consist of a nucleic acid core and a protein coat.
Bacteriophages exhibit two types of life cycle.
(1) Virulent or lytic cycle;
(2) Temperate or nonlytic cycle:
Virulent or lytic cycle:
virus attached to the bacterial surface, inject its DNA inside
the bacterial cell , its DNA then controls the bacterial cell
activity to synthesis phage particles
large numbers of progeny phages are built up inside the host
bacterium, which ruptures to release them.
 
 
During the assembly of bacteriophage progeny
inside infected bacteria, 
‘packaging errors
’ may
occur occasionally.
 A phage particle may have at its core a segment of
the host DNA besides its own nucleic acid.
When this particle infects another bacterium, DNA
transfer is effected and the recipient cell acquires
new characteristic coded by the donor DNA.
 Bacterial genes have been transduced by the phage
into the second cell
 
T
e
m
p
e
r
a
t
e
 
o
r
 
n
o
n
l
y
t
i
c
 
c
y
c
l
e
 
In the temperate or nonlytic cycle, the host bacterium is unharmed.
The phage DNA becomes integrated with the bacterial chromosome as 
prophage
,
and is replicated stably as part of the host cell chromosome and is transferred to
the daughter cells.
This process is called lysogeny and bacteria harboring prophages are called
lysogenic bacteria
.
the prophage behaves as an additional segment of the bacterial chromosome,
coding for new characteristic
 
Medical Importance of transduction
 
 
1. 
Toxigenicity in diphtheria bacilli:
Diphtheria bacilli 
acquire toxigenicity (and therefore virulence) by lysogenization with the phage beta.
Elimination of the phage from a toxigenic strain renders it nontoxigenic.
2. 
Production of staphylococci, streptococci and clostridia toxins:
It is probable that the production of many toxins by 
staphylococci, streptococci 
and 
clostridia 
is also
dependent upon lysogenic conversion by specific bacteriophages.
 
In transduction, the phage acts only as a vehicle carrying bacterial genes from one cell to
another but in lysogenic conversion the phage DNA itself is the new genetic element.
 
Transformation
 
Is the uptake of exogenous DNA by living bacteria from surrounding environment
Bacterial cells that have such ability called 
competent cells
Competence can be naturally developed or induced artificially.
Natural competence is unusual among bacteria, and some of these strains are
require  the presence of 
competence factors
, produced only at a specific point in
the growth cycle
competence factors 
(an activating protein) is released by competent cell to
induce competence in non- competent cells 
(may involve 
proteins that are involved in
the assembly of 
type IV pili
 as well as DNA 
translocase
 complex at the cytoplasmic membrane)
.
Naturally competent bacteria are found in very few genera include 
Bacillus
subtilis, Haemophilus influenzae, Neisseria gonorrhoeae, Neisseria meningitidis,
and 
Streptococcus pneumoniae.
 
The main steps of bacterial
transformation are:
 
Transforming DNA
+
Competent cells
 
 
Binding
 
 
Resistance to exogenous Dnase
 
 
Fragmentation and uptake
 
 
Integration
 
 
Expression
 
Adapted from : http//www.lamission.edu>lifesciences> chapter 8: microbial genetics
 
Reference
 
Jawetz, M. & Adelberg’s. 2019. Medical Microbiology , Twenty-Sixth Edition. The
McGraw-Hill Companies, Inc. USA
Kumar, S. 2012. Textbook of microbiology.  
Jaypee Brother Medical Publishers (P)
Ltd
. New Delhi, India.
Kayser, F.H., Bienz, K.A., Eckrt, J. and R. M. Zinkernagel. 2005. Medical
Microbiology. 
Georg
 
Thieme Verlag
. Stuttgart, Germany.
Passarge, E. 2001. Color atlas of genetics. 
Georg
 
Thieme Verlag
. Stuttgart,
Germany.
http//www.lamission.edu/lifesciences/chapter 8: Microbial genetics
 
THANK YOU
 
Slide Note
Embed
Share

Phenotypic and genotypic variations in bacteria are crucial for their adaptation and survival. Phenotype reflects the physical expression influenced by both the genome and the environment, while genotype represents the hereditary constitution passed to offspring. Mutations are a primary source of genotypic variability, leading to different effects in cells. Mutations can be spontaneous or induced by various agents, such as UV rays or chemicals. Different types of mutations, like point mutations and frameshift mutations, can alter the genetic code, affecting protein synthesis. Understanding these genetic variations is essential for studying bacterial evolution and behavior.

  • Bacterial Genetics
  • Phenotypic Variability
  • Genotypic Variation
  • Mutations
  • Adaptation

Uploaded on Oct 10, 2024 | 0 Views


Download Presentation

Please find below an Image/Link to download the presentation.

The content on the website is provided AS IS for your information and personal use only. It may not be sold, licensed, or shared on other websites without obtaining consent from the author. Download presentation by click this link. If you encounter any issues during the download, it is possible that the publisher has removed the file from their server.

E N D

Presentation Transcript


  1. Bacterial genetics II Dr. Ali Abdulwahid

  2. Phenotypic and genotypic Variability of Bacteria

  3. Overview Overview 1.Phenotypic variation : phenotype : The physical expression of various characters by bacterial cells in a given environment. These properties are determined by its genome and by environment. It is reversible, temporary and not inheritable Example : production of the enzyme beta-galactosidase by the bacterium E. coli when it is grown in a medium containing lactose. When grown in a medium containing glucose only, the enzyme is not synthesized.

  4. 2.Genotypic variation : Genotype : It is the hereditary constitution of the cell that is transmitted to its progeny Its heritable, stable and does not affected by environment Genotypic variability may occur due to different mechanisms include : 1.mutations 2.Intercellular transfer of genomic material

  5. 1. Mutation It is random, undirected, heritable variation caused by an alteration in the nucleotide sequences at some points of the DNA of the cell due to addition, deletion or substitution of one or more bases. During DNA replication, some errors may occur during copying the progeny strands For instance, instead of thymine bonding to adenine, it binds to guanine Different mutations in the a particular gene may produce different effect in the cell

  6. Types of Mutation Mutations can be divided conveniently into: A. Spontaneous mutation: occur spontaneously in nature in the absence of any mutation-causing agents. B. Induced mutation: enhanced by exposure of cells to several agent (mutagens) include : 1. Physical agents: (i) UV rays; (ii) lionizing radiation, e.g. X-rays 2. Chemical agents: Alkylating agents, Acridine dyes and Nitrous acid.

  7. Point mutations: affect just one point (base pair) in a gene. Leads to change to or substitution of a different base pair. Alternatively, can result in the deletion or addition of a base pair. It is in general, reversible and is of two classes: 1. Base pair substitution 2. Frameshift mutations (insertion or deletion):

  8. 1. Base pair substitution: Depending on the placement of the substituted base, can be divided into : silent mutation , cause no change in the amino acid of the protein missense mutation , lead to the insertion of the wrong amino acid nonsense mutation , lead to generate a stop codon and prematurely terminating the protein synthesis (the polypeptide) Silent mutation Nonsense mutation Missense mutation DNA Protein DNA Protein

  9. 2. Frameshift mutations (insertion or deletion): If the number of bases inserted or deleted is not a multiple of three, there will be shift in the reading frame (codons sequence), forming newest of triplet codon. the new codons will specify the incorrect amino acids, or leading to premature termination for the translation process (truncated protein) Frameshift mutations INSERTION DELETION

  10. 2- Intercellular transfer of genomic material Horizontal gene transfer : DNA can be transferred from one organism to another, and that DNA can be stably incorporated in the recipient cell, permanently changing its genetic composition. This Process is so called horizontal gene transfer to differentiate it from the inheritance of parental genes, a process called vertical inheritance. Three broad mechanisms mediate efficient movement of DNA between bacterial cells : Conjugation Transduction transformation.

  11. Conjugation A process in which one cell, the donor or male cell, makes contact with another, the recipient or female cell DNA is transferred directly from the donor into the recipient Certain types of plasmids, known as transfer factors or sex factors, carry the genetic information necessary for conjugation to occur. These are also called self-transmissible plasmids, and they can mobilize other plasmids or portions of the chromosome for transfer. Only cells that contain such a plasmid can act as donors; those lacking a sex factor act as recipients. Such Plasmid codes for specialized fimbria (sex pilus) which projects from the surface of the cell. The tip of the pilus attaches to the surface of a recipient cell and holds the two cells together so that DNA can then pass into the recipient cell. A male and a female cell joined by a pilus (sex pilus).

  12. 1. Plasmid transfer Bacterial Populations can be divided into two types of cells. 1. F+ : the donor cell, contains an Fertility plasmid or F plasmid and is designated F+. 2. F : the recipient cell, does not contain this plasmid and is called F . DNA is transferred only in one direction, from F+ to F F Factor or F plasmid (Fertility Factor) Is a transfer factor that contains the genetic information necessary for the synthesis of the sex pilus (Conjugation tube), and for self- transfer.

  13. Mechanism of DNA transfer during conjugation. A. Connection between two bacterial cells by means of sex pili.. Formation of a specific conjugal bridge between donor cell and receptor cell. An endonuclease cleaves one strand of the circular DNA double helix at a specific point . The single strand with the leader region enters the recipient cell. The double-stranded structure of both the transferred single strand and the remaining DNA strand is restored by means of complementary DNA synthesis. The recipient cell, now plasmid-positive, is called a transconjugant cell. B. C. D.

  14. 2. Chromosomal transfer The F factor in some cases can be integrated into the host chromosome in a very small proportion of F+ cells, creating : high frequency recombination (Hfr) donor cells In which, the entire chromosome behaves like an F+ plasmid chromosomal genes (fragments) can be transferred (from the site of insertion) in a direction determined by the orientation of insertion in the normal sex factor manner to a recipient cell at a relatively high frequency

  15. Medically Important Factors Transferred by Conjugation Medically Important Factors Transferred by Conjugation 1. Colicinogenic (Col) Factor Several strains of coliform bacteria produce colicins antibiotic-like substances which are specifically and selectively lethal to other enterobacteria. Colicin production is determined by a plasmid called the Col factor, which resembles the F factor in promoting conjugation, leading to self-transfer and, at times, transfer of chromosomal segments. 2. Resistance Factors or R Plasmids Resistance factors (R factors) are plasmids that have significant medical importance as it leads to the spread of multiple drug resistance among bacteria. This R plasmid consists of two components: RTF+r determinants. Resistance transfer factor (RTF): The transfer factor thatis responsible for conjugal transfer. Resistance determinant (r): code for resistance against various drugs. The whole plasmid (RTF+r determinants) is known as the R factor An R factor can have several r determinants, and resistance to as many as eight or more drugs can be transferred simultaneously.

  16. Transduction The transfer of a portion of the DNA from one bacterium to another by a bacteriophage Bacteriophages are viruses that parasitise bacteria and consist of a nucleic acid core and a protein coat. Bacteriophages exhibit two types of life cycle. (1) Virulent or lytic cycle; (2) Temperate or nonlytic cycle: Virulent or lytic cycle: virus attached to the bacterial surface, inject its DNA inside the bacterial cell , its DNA then controls the bacterial cell activity to synthesis phage particles large numbers of progeny phages are built up inside the host bacterium, which ruptures to release them.

  17. During the assembly of bacteriophage progeny inside infected bacteria, packaging errors may occur occasionally. A phage particle may have at its core a segment of the host DNA besides its own nucleic acid. When this particle infects another bacterium, DNA transfer is effected and the recipient cell acquires new characteristic coded by the donor DNA. Bacterial genes have been transduced by the phage into the second cell

  18. Temperate or nonlytic cycle Temperate or nonlytic cycle In the temperate or nonlytic cycle, the host bacterium is unharmed. The phage DNA becomes integrated with the bacterial chromosome as prophage, and is replicated stably as part of the host cell chromosome and is transferred to the daughter cells. This process is called lysogeny and bacteria harboring prophages are called lysogenic bacteria. the prophage behaves as an additional segment of the bacterial chromosome, coding for new characteristic

  19. Medical Importance of transduction 1. Toxigenicity in diphtheria bacilli: Diphtheria bacilli acquire toxigenicity (and therefore virulence) by lysogenization with the phage beta. Elimination of the phage from a toxigenic strain renders it nontoxigenic. 2. Production of staphylococci, streptococci and clostridia toxins: It is probable that the production of many toxins by staphylococci, streptococci and clostridia is also dependent upon lysogenic conversion by specific bacteriophages. In transduction, the phage acts only as a vehicle carrying bacterial genes from one cell to another but in lysogenic conversion the phage DNA itself is the new genetic element.

  20. Transformation Is the uptake of exogenous DNA by living bacteria from surrounding environment Bacterial cells that have such ability called competent cells Competence can be naturally developed or induced artificially. Natural competence is unusual among bacteria, and some of these strains are require the presence of competence factors, produced only at a specific point in the growth cycle competence factors (an activating protein) is released by competent cell to induce competence in non- competent cells (may involve proteins that are involved in the assembly of type IV pili as well as DNA translocase complex at the cytoplasmic membrane). Naturally competent bacteria are found in very few genera include Bacillus subtilis, Haemophilus influenzae, Neisseria gonorrhoeae, Neisseria meningitidis, and Streptococcus pneumoniae.

  21. The main steps of bacterial transformation are: Transforming DNA + Competent cells Binding Resistance to exogenous Dnase Fragmentation and uptake Integration Adapted from : http//www.lamission.edu>lifesciences> chapter 8: microbial genetics Expression

  22. Reference Jawetz, M. & Adelberg s. 2019. Medical Microbiology , Twenty-Sixth Edition. The McGraw-Hill Companies, Inc. USA Kumar, S. 2012. Textbook of microbiology. Jaypee Brother Medical Publishers (P) Ltd. New Delhi, India. Kayser, F.H., Bienz, K.A., Eckrt, J. and R. M. Zinkernagel. 2005. Medical Microbiology. GeorgThieme Verlag. Stuttgart, Germany. Passarge, E. 2001. Color atlas of genetics. GeorgThieme Verlag. Stuttgart, Germany. http//www.lamission.edu/lifesciences/chapter 8: Microbial genetics

  23. THANK YOU

More Related Content

giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#giItT1WQy@!-/#