lecture 8 - introduction to microobiology Flashcards

1
Q

WTF is microbiology

A

Any “living” thing you can see down a microscope

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2
Q

Categorising cells

A
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3
Q

examples

A
  • Initial binding of Haemophilus influenzae type b to the human nasopharynx is facilitated by Hib pili, filaments expressed on the bacterial surface.
  • Mutant strains ofS. pneumoniaethat have lost the ability to form a capsule are readily taken up by white blood cells and do not causedisease
  • Mutated forms of C. jejuni do not cause disease as can’t move to infect cells.
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4
Q

staining

A
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5
Q

gram positive cocci

A
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6
Q

gram positive bacilli

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7
Q

gram negative bacilli

A
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8
Q

Microscopic Fungi

A
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9
Q

What other things can we use for diagnosis?

A
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10
Q

Variables in bacterial growth

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11
Q

bacterial growth curve

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12
Q

Which bacterial structures can be used as antibiotic targets?

A
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13
Q

targets vs resistance

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14
Q

What fungal structures can we target with antifungals?

A
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15
Q
A
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16
Q

Antimicrobial Resistance

17
Q

antibiotics

18
Q

Action of Penicillin

A
  • The bacterial cell wall consists of strands of repeating N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM) subunits.
  • The NAM subunits have short peptide chains attached to them. (The proximal alanine is usually L-ala and the distal two are usually D-ala.)
  • The PBP binds the peptide side chains and forms the cross-link with the expulsion of one D-Alanine from one peptide side chain.
  • The PBP dissociates from the wall once the cross-link has been formed.
  • Penicillin is added to the system. It enters the active site of the PBP and reacts with the serine group that is important in its enzymatic activity.
  • The beta-lactam ring of penicillin (represented here as the top of the “P”) is irreversibly opened during the reaction with the PBP.
  • Penicillin remains covalently linked to the PBP and permanently blocks the active site.
19
Q

Methicillin-Resistant Staphylococcus aureus (MRSA)

A

MRSA strains contain Staphylococcal cassette chromosome mec (SCCmec).
This is a mobile genetic element which contains the mecA gene.
The gene mecA encodes for PBP2a – an altered PBP with low affinity for penicillin drugs.

20
Q

β-lactamase producing Pseudomonas aeruginosa

A

Enzymes to degrade the β-lactam ring (β-lactamases) can be encoded on transmissible genetic elements (plasmids, integrons, transposons etc.) or the chromosome

21
Q

There are many ways to be resistant

23
Q

kosh postulates

A

If only it was that simple.

Famous exceptions;
Viruses
Prions
H. pylori
Biofilms and synergistic pathogens
Many more

24
Q

Where are microorganisms found in the normal healthy body?

25
How do we find organisms?
Majority of microbiome research is bacteria only Only bacteria have 16S rRNA (and 16S rRNA gene) Research starting to also include; Fungi (nuclear ribosomal internal transcribed spacer (ITS) region) Viruses (shotgun metagenomics and others)
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Development of microbiome begins at birth…
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but changes over time
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The microbiome is temporally dynamic
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Microbiome varies across body sites
Densely populated: Mouth, Large intestine, Upper respiratory tract Moderately populated: Skin, Stomach Fewer microbes: Lower respiratory tract, Bladder Sterile sites: Blood, Tissues, Joint fluids, CSF
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The microbiome is highly personal
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and influenced by many factors*
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Dysbiosis – a disbalance in the community
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How is normal flora important?
Protection from pathogen colonisation Nutritional capability e.g. provision of vitamins and amino acids Development of immune function If disrupted, can lead to overgrowth of a pathogen
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