5.2 Microbial adaptations Flashcards

1
Q

Define microbial adaptation

A

ability of microbes to endure the selective pressures of their environment.

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2
Q

Give 3 ways in which microganisms adapt

A

1) replicate at a very fast rate in a very short period of time
2) change genetic makeup very quickly
3) large number of them also allows selective choices of gaining virulence from one and other

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3
Q

label this diagram

A
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4
Q

Describe the 3 types of horizontal transmission by bacteria that allow transfer of genetic information

A

1) Conjugation; bacteria-bacteria transfer
2) Transduction; viral-mediated transfer (of genetic info between bacterium)
3) Transformation; free DNA transfer (involves changing the permeability of the bacterial cell capsule/wall to share free DNA)

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5
Q

What method of gene transfer does this image show and briefy explain it

A

Conjugation

1) bacteria A meets bacteria B and through pili the bacteria connect and create passageway
2) a number of molecular mechanisms in bacteria A produce proteins that allow transfer of material + conversion of genetic info from the circular plasmid into a single length of extracellular DNA
3) this is then replicated and transferred from bacteria A to bacteria B through pili
4) Bacteria B is now in possession of new gene and has proteins which allow it to be expressed

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6
Q

How does a bacteriophage initially enter a cell?

Following this what are the two life cycles the phage can follow?

A

1) virus adheres to bacteria (virus + bacteria = bacteriophage)
2) Bacteriophage specialised to have a capsid head (containing genetic info) and a very strong centre coil
3) via a series of movements and contractions it injects its centre (containg genetic info) through the cell surface
4) This causes the virus RNA/DNA to be injected into the bacteria and incorperated into the host cell
5) It will then either follow the lytic or the lysogenic cycle

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7
Q

Describe the LYTIC cycle of a bacteriophage

A

1) Attachment: the phage attaches to the surface of the host
2) Penetration: the viral DNA enters the host cell + digests host DNA
3) Biosynthesis: phages DNA replicates (capsids and virulence factors) using host machinery to form phage proteins
4) Maturation: many daughter phage particles are assembled
5) Lysis: the host cell is weakened and lyses occurs releasing newly made bacteriophages into circulation

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8
Q

Describe the LYSOGENIC cycle of a bacteriophage

A

1) Attachment: the phage attaches to the surface of the host
2) Penetration: the viral DNA enters the host cell BUT becomes integrated into the host DNA using integrases
3) Replication: It is replicated along with host genome, as the host cell divides as does the newly integrated phage DNA which means it is passed on to host daughter cells
4) Dormancy: this continues and the phage remains dormant within host until environment is suitable OR it acquires the correct proteins to allow it to transition into the lytic phase

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9
Q

What is transduction and what are the 2 types that can occur to transfer genes, compare these

A

When genes from a host cell bacteria are incorporated into the genome of a bacteriophage and then carried to another host cell when the bacteriophage initiates another cycle of infection

1) Generalised transduction: associated with the lysogenic cycle
* the bacteriophages can pick up ANY portion of the host’s genome
2) Specialised transduction:
* the bacteriophages pick up ONLY specific portions of the host’s DNA

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10
Q

What is Transformation and how does it assist bacteria in gene transfer?

Give an example of when this may occur

A

Movement of genetic information from a donor cell to a recipient cell

Done by changing permeability of the outer capsule allowing the bacteria to take up the genetic information

Example: In the gut we have bacteria, some of which will be dying. This creates a slushy solution which causes their membrane to become less rigid allowing genetic information to be taken up by other bacteria into their cell

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11
Q

Why would bacteria produce antibiotics?

A

Remember an antibiotic is a chemical produced by a micro-organism that kills or inhibits the growth of other micro-organims

Hence bacteria will produce antibiotics to to target processes essential to other bacteria in order to compete with them in the environment

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12
Q

Copare antibiotic resistance to antimicrobial resistance

A

Antibiotic resistance: refers specifically to the resistance to antibiotics that occurs in common bacteria that cause infections

Antimicrobial resistance: is a broader term, that also includes resistance to other drugs that treat infections caused by other microbes (bacteria, parasites, viruses and fungi)

Remember all antibiotics are antimicrobials but not all antimicrobials are antibiotics

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13
Q

Name the 3 ways bacteria can become antibiotic resistant

A

1) Enzymatic Degradation:

  • an existing cellular enzyme is modified to react with the antibiotic in such a way that it no longer affects the microorganism
  • eg. B-lactamase inhibits Penicillin binding

2) Efflux pump:

  • these are naturally found within the bacteria and help them to pump out metabolites.
  • If bacteria can identify the specific genetic information encoding specific antibiotics, they can be recognised and pumped out

3) Target resistance: changes in cell wall shape

  • genes expressed by bacteria may encode proteins that either give protection of the target site or modifications in the target site
  • results in decreased affinity for the antibiotic molecule
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14
Q

Briefly describe the WHO’s 5 step action plan to target antibiotic resistance

A

1) Improve awareness and understanding of antimicrobial resistance
2) strengthen knowledge through surveillance and research
3) reduce the incidence of infection
4) optimize the use of antimicrobial agents
5) Investing in innovation, supply and access to tackle AMR

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15
Q

Name three ways bacteria can become resistant to antibiotics on a molecular level

A

1) Develop point mutations in one of the target genes
2) Acquire plasmids or transposons through macro-evolutionary changes
3) Acquir DNA from an exogenous source (i.e Neisseria can acquire DNA from the environment)

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16
Q

Define Cross-resistance, when does it occur?

A

When a single resistance mechanism confers resistance to an entire class of antibiotics.

It can also occur across different classes of agents as a result of either overlapping drug targets or if there is a drug efflux pump with a broad range of activity

17
Q

Define co-resistance

A

Refers to resistance to more than one class of antibiotics in the same bacterial strain

18
Q

Define co-selection

A

The selection of multiple antibiotic resistance genes when one of these genes is selected (since all the antibiotic-resistant mechanisms are linked together on a plasmid)

19
Q

Name four methods that antimicrobial resistant genes use to become widely spread

A

1) Clonal spread of the resistant strain; under selective pressure of antibiotics a strain carrying antimicrobial resistance genes may be selected and transferred within a population
2) Plasmid transfer: can be transferred among different bacterial strains or species by conjugation or transduction
3) Free DNA: naturally transformable species can acquire native DNA from the environment and integrate this genetic info into the chromosome
4) Bacteriophage transduction

20
Q

List 3 key protective features of the respiratory tract against microbes

A

1) IgA within mucous membranes that line the trachea, bronchi and bronchioles
2) mucociliary escalator: microbes trapped in the mucous are beaten up to the pharynx to prevent them from entering the body
3) Alveolar macrophages enter alveoli from blood capillaries to fight microbes