Introduction to Microbial Infections Flashcards

1
Q

What are Koch’s postulates ? List them.

A

Postulates to establish causal relationship between microbe and disease.

  • bacteria must be present in every case of the disease
  • Bacteria must be isolated from host with the disease be grown in pure culture
  • specific disease must be reproduced when a pure culture of the bacteria inoculated into healthy susceptible host
  • bacteria must be recoverable from experimentally infected host
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2
Q

What are the main components of the innate immune system ?

A
  • Normal microbiota
  • Chemical barriers
  • Physical barriers
  • Phagocytic cells
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3
Q

How does the normal microbiota offer protection ?

A

By competing with pathogens for colonisation site. Through:
Antibiotic substances suppressing growth of competing others (e.g. bacteriocins)
Toxic metabolic products to inhibits the others
Alter pH (e.g. lactobacilli)

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4
Q

How can normal microbiota become pathogenic ?

A

Antibiotics given, (e.g. C. Albicans) overgrows and causes thrush

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5
Q

What are possible physical barriers ?

A
  • Skin (secretes sebum and FAs)
  • Mucociliary clearances (mucus traps, cili sweeps)
  • Micturition
  • Peristalisis (and excretion)
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6
Q

What are possible chemical barriers ?

A

-Mucus

-Antimicrobial proteins
Lysozymes (in tears and saliva, good to destroy gram + PGN)
Lactoferrin (in breast milk, binds iron needed for pathogen replication)
Defensins (in Panet cells in base of small intestine. Also produced by epithelial cells and neutrophils)

-Gastric acid (acidic pH 2)

-Plasma proteins
Complement
C-reactive protein (CRP) - acute phase inflammatory protein, increased in infection or inflammation.
Mannose-binding lectin (MBL) - binds to bacteria and goes on to activate complement cascade. Deficiency = higher vulnerability to infection.
Transferrin- binds iron

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7
Q

What are examples of phagocytic cells ? How do they get to the site of infection ?

A

Macrophages, neutrophils, monocytes, dendritic cells, mast cells.

They are recruited by other cells communicating with them.

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8
Q

What are the two ways in which infection can occur ?

A
  1. Invading host tissues

2. Exerting effects from mucosal surfaces

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9
Q

What are the micoorganisms forming part of normal microbiota ?
Capable of causing infection ?

A

Commensals (S. Aureus C. difficil)

Pathogen

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10
Q

What is pathogenicity ? Virulence ?

A

Capacity to cause disease.

Measure of pathogenicity.

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11
Q

What are the main types of pathogen. Give an example for each.

A

Obligate- always associated with disease (e.g. HIV)
Conditional- may cause disease disease if certain conditions (e.g. commensal bacteria such as S. Aureus after antibiotics given)
Opportunistic - usually only infects immunocompromised host (e.g. pneumocystis jiroveci (AIDS-defining condition))

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12
Q

What are the steps of infection ?

A

Recognition –> Attachment and entry (not all pathogens will enter, viruses will) –> Multiplication –> Evasion of host defences –> shedding –> damage (not always)

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13
Q

What are ways in which infections can be established in normally healthy hosts ?

A
  1. Microbes with specific mechanisms to attach and penetrate of host’s body surface
  2. Microbes introduced into host by vector
  3. Microbes introduced via skin wounds or animal bites
  4. Microbes infect when host defences impaired (e.g. chemotherapy)
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14
Q

What is tissue tropism ?

A

Affinity for a specific tissue, defines the cells and tissue on the host which support the growth of particular microbe

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15
Q

What are the factors which influence tissue tropism ?

A
Presence of cell receptors
Transcription factors
Local Temperature
Physical barriers
pH
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16
Q

What is a kind of “picky” pathogen ? How so ?

A
  • Helicobacter pylori, to gastric mucosa (burrows into it gets through to epithelium).
  • Influenza virus, to cilia and microvili on tracheal epithelium
  • Viruses especially picky because need to use host cell machinery for replication
17
Q

What are examples of virulence factors ?

A
  • Capsule
  • Pili formation
  • Toxin secretion (toxigenesis)
  • Antibiotic resistance
  • Fe transport systems
  • Adhesion factors
  • Enzymes (protease, lipases)
18
Q

What are the main differences between endotoxins and exotoxins ?

A

Endo:

  • Low toxicity
  • Part of cell wall of Gram (-) bacteria
  • Lipopolysaccharide
  • Low specificity
  • E.g. E coli, salmonella

Exo:

  • High toxicity
  • Produced by both Gram (+) and (-) bacteria
  • May be produced into toxoids for vaccines
  • E.g tetanus toxin, botulinum toxin
19
Q

Where is the resistance gene located ?

A

On plasmids

20
Q

What are different ways for bacteria to be resistant ?

A

Production of enzymes (e.g beta lacatamases break down beta lactam antiobiotics)

  • Impermeability (cell wall not broken)
  • Efflux mechanisms (pumping antibiotic back out of the cell)
  • Alteration of target site
21
Q

What are examples of drug-resistant pathogens ?

A

Methicillin-resistant staphylococcus aureus (MRSA)
Vancomycin-resistant staphylococcus aureus (VRSA)
Multi-resistant Myobacterium Tuberculosis (MDR TB)
HIV
Malaria

22
Q

What factors does transmission depend on ?

A

Number of micro-organisms shed
Number to micro-organisms required to infect fresh host (efficiency)
Micro-organism stability in the environment outside host

23
Q

Give an example of a spore-forming bacteria.

A

Clostridium difficile

24
Q

What is the difference between vertical and horizontal transmission ?
Give a few examples for each.

A

Vertical: from mother to child (during pregnancy, birth, breast feeding) (through ovum, sperm, breast milk, placenta). E.g. HIV, rubella, Hep B, commensal bacteria

Horizontal: Not from mother to child. Through infected air, water, food, contact, vectors. E.g. polio, influenza, typhoid fever

25
Q

What are possible routes of transmission ?

A
Respiratory 
Faeco-oral
Veneral 
Skin
Perinatal
Semen 
Blood
Breast milk
Saliva
26
Q

What are animal to human transmission called ?

A

Zoonoses/zoonotic diseases

27
Q

How can zoonotic diseases be transmitted ?

A
  • Invertebrate vectors (arthropods-malaria, yellow fever or shellfish- hep A, cholera)
  • Vertebrate vectors (mammals- rabies, leptospirosis, tapeworm)
  • Birds (psitrracosis, salmonella)
28
Q

What are fomite transmissions ?

A

Transmission via inanimate objects

29
Q

What are nosocomial infections ? Give examples of pathgens involved in these.

A

Infections acquired during a hospital stay = HAI.

MRSA, clostridium difficile

30
Q

What are SICPs ?

A

Standard Infection Control Precautions

31
Q

What are examples of SICP rules ?

A

Hand Hygiene
Respiratory/cough hygiene
Personal Protective Equipment

32
Q

What is the chain of infection ? How can we prevent the spread of infection ?

A

Reservoir –> Portal of exit –> Mode of transmission –>Portal of entry –>susceptible host –> Infectious agent –> back to reservoir
Must only break one to stop spread