Bacterial Strategies For Host Colonisation Flashcards

1
Q

Sites of vulnerability/ routes of entry

A

Respiratory tract
Intestinal tract
Urogenital tract
Conjunctiva

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2
Q

Physical removal strategies

A

Coughing/sneezing
Vomiting and diarrhoea
Urination
Tear production

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3
Q

Attributes invoked in effective host colonisation

A

Adhere to host cells + Resist physical removal
Invade host cells
Compete for iron + other nutrients
Evade the immune system

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4
Q

What are virulence factors

A

Virulence factors are molecular or cellular components produced by pathogens, such as bacteria, viruses, fungi, or parasites, that contribute to their ability to cause disease in a host organism. These factors can be categorized into different types based on their functions, such as:

Adhesion factors: These are proteins or other molecules on the surface of a pathogen that allow it to attach to host cells, tissues or extracellular matrix. Examples include fimbriae, pili, adhesins, and capsules.

Invasion factors: These are factors that allow pathogens to enter and survive within host cells. Examples include bacterial toxins, enzymes, and proteins that alter host cell membrane permeability.

Toxins: These are molecules produced by pathogens that damage host cells or tissues, and contribute to the symptoms of disease. Examples include exotoxins, endotoxins, and cytotoxins.

Immune evasion factors: These are molecules that help pathogens avoid detection and destruction by the host immune system. Examples include bacterial capsules and surface proteins that mimic host molecules.

Nutrient acquisition factors: These are molecules that allow pathogens to obtain nutrients from the host, such as iron or other essential nutrients. Examples include siderophores and proteases.

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5
Q

Pili function

A

Promote attachment + resistance to physical removal

  • Pili are generally found in gram-negative bacteria
  • Made up of protein called pilin
  • Pili bind to sugar receptors in surface of eukaryotes
  • Can colonise gut + urinary tract
  • can be considered an adhesion
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6
Q

How do gram positive cells typically adhere to host cells and resist removal

A

They have proteins (adhesins) on their cell wall that binds to specific receptors on epithelial cells

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7
Q

How does Streptococcus pyogenes ( a gram positive bacteria ) bind to host cell

A
  • causes throat infection
    Protein F on bacteria binds to fibronectin on epithelial cells
  • Fibronectin is part of the host cells cytoskeleton
  • Lipid teichoic acid also binds to fibronectin
  • M protein also functions as adhesin
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8
Q

How does flagella/motility of Helicobacter pylori (a gram - bacteria) help colonisation at mucosal surfaces

A

-causes gut infections
-associated with stomach ulcers and cancers
-colonises the gut
- flagella allow it to love against the peristaltic action of the gut
- urease is produced in the bacterias cytosol and it produces ammonia from urea
The ammonia that’s produced is passed into the periplasmic space of the bacteria - this buffers the bacteria against the low ph of the gut

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9
Q

What are invasins

A

Molecules that activate the host cells cytoskeleton and promote cell entry by phagocytosis
In doing this they facilitate the growth and spread of the pathogen

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10
Q

Why do bacteria want to be in host cell

A

Host cell provides bacteria with ready supply of nutrients
Protects the bacteria from complement, antibodies and other body defence mechanisms

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11
Q

What are bacterial secretion systems

A

Bacterial secretion systems are specialized molecular machines that enable bacteria to transport proteins and other molecules across their cell membranes. These systems are critical for bacterial survival, as they allow bacteria to interact with their environment, acquire nutrients, and establish infections.

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12
Q

Explain the differences between the 6 different type of systems

A

Type I: This system involves the one-step secretion of proteins directly from the cytoplasm of the bacterial cell to the extracellular space.

Type II: This system involves a two-step process, with proteins first being translocated across the inner membrane and then across the outer membrane via a protein complex called the “secretin”.

Type III: This system involves the direct injection of proteins into host cells by pathogenic bacteria. This allows the bacteria to manipulate host cell functions and establish infection.

Type IV: This system can transport a wide variety of substrates, including proteins, DNA, and even entire bacterial cells. It is involved in processes such as conjugation, the transfer of genetic material between bacteria.

Type V: This system involves the secretion of proteins across both the inner and outer bacterial membranes via a β-barrel pore-forming protein.

Type VI: This system involves a needle-like apparatus that can inject proteins directly into other bacterial cells, promoting competition between bacteria.

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13
Q

What type of bacterial secretion system is most common in gram negative bacteria

A

Type 3

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14
Q

How do type 3 secretion all system work

A

The central component of the T3SS is a needle-like structure that extends from the bacterial surface and penetrates the host cell membrane.

To deliver proteins into host cells, the T3SS first recognizes a target cell and forms a close association with its surface. The needle then makes contact with the host cell membrane and creates a pore through which the proteins can pass. The proteins are then translocated across the pore and into the host cell, where they can interact with host cell components and manipulate cell functions.

The specific proteins injected by the T3SS vary depending on the bacterial species and the host cell type being infected. Some T3SS effectors can disrupt host cell signaling pathways, inhibit host immune responses, or promote bacterial survival and replication within the host.

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15
Q

What are the specific proteins injected by secretion systems called

A

Effector molecules

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16
Q

How can effector molecules interfere with cytoskeleton of host cell

A

They interfere with the polymerisation of actin
And can encourage epithelial cells to become phagocytic
This leads to cell to cell spread

17
Q

Examples of bacteria that use secretion systems

A

Escherichia coli, Shigella dysenteriae

18
Q

How can extra cellular proteases help with invasion if host tissue

A

They can disrupt things like collagen and cause tissue damage

19
Q

What protease can break down collagen

A

Metalloprotease

20
Q

How is iron carried in the host

A

Because it’s insoluble it’s carried in complexes with glycoproteins
Transferrin-serum
Haemoglobin-rbc
Lactoferrin-tears, sweat, saliva, mucus

21
Q

How to bacteria steal iron

A

They produce siderophores in cytoplasm then release them

Siderophores have very high affinity for iron

When siderophores come into contact with lactoferrin or transferrin they will steal this iron and bring it back to bacterial cell

Siderophores can’t steal iron from haemoglobin

22
Q

How do bacteria steal iron from haemoglobin

A

By producing haemolysins (enzymes)
That break down haemoglobin

23
Q

How do Staphylococcus aureus avoid being destroyed via phagocytosis

A

Gram positive bacteria
Found on skin/nasal passages
S.aureus makes an enzyme called Coagulase

Coagulase interferes with normal blood clotting process

Fibrinogen turning to fibrin is what causes clotting

Coagulase activates blood clotting pathway (activated fibrinogen to turn into fibrin)

Fibrin that’s made will coat the bacteria which will allow it to evade phagocytosis

Coagulase activity is almost always associated with pathogenic strains and not non pathogenic strains of S.aureus

24
Q

What is lysozyme

A

Lysozyme is an enzyme that breaks down bacterial cell walls by hydrolyzing the bonds between the sugars that make up the peptidoglycan layer of the cell wall.
It is found in a variety of bodily fluids, such as tears, saliva, and mucus

25
Q

How to bacteria (especially gram positive) defend against lysozymes

A

They change the chemistry of peptidoglycan
If you knock the acetyl group of the peptidoglycan residue (deacetylation)
Lysozymes can no longer break the bonds between these residues

26
Q

How do bacteria avoid the function of antibodies

A

Prevent opsonisation by altering their epitopes
Lipopolysaccharides are epitopes (on gram - bacteria) and they are very variable
Bacteria can easily vary the sugar molecules to stop recognition by antibodies

Gram + bacteria bind antibodies but do so in the wrong orientation
Certain bacteria such as S.aureus have a protein A
Protein A bind to the wrong side of the antibody (the heavy chain)
Meaning the antibodies won’t work