pathogenesis of bacterial infection Flashcards

1
Q

normal flora ( microbiomes as good bugs commensals and microbiota ) are in or on our body and they —— diseases as most of them are —–
- may cause infection if:
1. —- from usual location
2. —– breached
3. host is —-

A
  • don’t cause diseases
  • non-pathogenic
  • escape
  • barrier
  • immunospression
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2
Q

—– bacteria has increased ability to invade or damage the host
—- able to cause a disease bc of their presence within the host
these bacteria can live along normal flora without causing any disease in host aka —-
the genetic/biochemical/structural features of pathogens that enable it or enhances the ability to produce disease is known as —-

A
  • virulent bacteria
  • primary pathogens
  • colonised
  • virulent factors
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3
Q

1.opportunitic bacteria have —- intrinsic virulence which usually don’t cause infections in non immunocompromised patients
2. they may cause serious infections in situations as :

A
  • low
  • immunocompromised and forge in body
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4
Q

1.why does infection occur ( steps )
2. how pathogens are transmitted

A

-the organism is virulent –> the size of the inoculum —-> the portal of entry —> survival in the host —> the state of the host
- get in –> attach to cells —> invade immune system —> cause damage to host cells —> get out and spread further

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5
Q

the 5 types of entry :
1. —– as salmonella in food poisoning
2. ——– as tucerculosrosis
3. ——— staphylococcus aurous
4. —— chalamydia
5. —— group b strepcoccous

A
  • ingestion
  • inhalation of droplets of aerosols
  • penetration/inoculation
  • sexual
  • vertical
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6
Q

—- of the bacteria to host cell is required to establish a stable population of bacteria within the host and prevents bacterial clearance from mechanical host defences

A
  • adhesion
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7
Q

adhesion occurs through —– mediated process called —- by which they are small bacterial protein ligands which recognise specific receptors on host cells

A
  • receptor / ligand
  • adhesins
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8
Q

—– formation protectrs the bacteria and makes eradication difficult with our the removal of prosthesis

A
  • biofilm
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9
Q

to facilitate invasions pathogens can employ biochemical virulence factors called —– these can be:

A
  • invasins
    1. proteins
    2. damaged host cells and facilitate spread and invasion
    3. hylauronidase , kinase , and collagenase
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10
Q

-the presence of bacteria in the host induces — responses to attempt bacterial eradication
-to ensure ongoing survival bacteria have developed numerous mechanisms to prevent immune mediated clearance which are:

A
  • immune
    1. prevents phagocytosis which is the ingestion go bacteria by phagocyte immune wbc as neutrophils
    2. survival within the phagocytes
    3. immune cell destruction
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11
Q

-inhibition of phagocytosis is done by — which is composed of polysarchide which sits outside the cell membrane
- pathogens associated w meningitis and penunomia as: neisseria meningitides , streptococcus penunomia , hemolphilus influenza )

A
  • capsule
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12
Q

survival within phagocytes:
- they escape the —- aka listeria monocytogene
- prevents —— fusion aka mycobacterium tuberculosis
- survival within —– aka staphylococcus aureus

A
  • phagosome
  • phagosome / lysozyme fusion
  • phagolysosome
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13
Q

some bacteria are able to produce —- that directly target immune cells or prevent their function such as:
1. —- pore forming enzyme which targets phagocytes ( canton - Valentin leucodicin of staphylococcus aureus )
2. —- pore forming enzyme produced by streptococci
3. —- produced by s. aureus , converts fibrongigen to fibrin which promotes clotting , coats bacteria in fibrin which acts as a barrier to immune cells ( can be tested in the lab to help identify S. auerous )

A

-enzymes
- leucocidins
- streptolysins
- coagulase

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14
Q

bacterial enzymes damage — cells as well as being important in —- evasion. this is done by:

A
  • host cells
  • immune
    1. invasins
    2. toxins
    2. superantigens
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15
Q

—- are compounds/chemicals which are toxic to host cells by directly harming host tissue or by interacting with immune cells. the two types are:

A
  • toxins
  • endotoxins and exotoxins
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16
Q

1- is integral part of bacterial cell envelop
2.release from bacterial cell due to cell lysis or turnover
3. LPS is prototypical example of gram — bacteria
4. can indue pro inflammatory cascade leading to septic shock
these are all under —– toxins

A
  • gram -ve
  • endotoxins
17
Q

-are polypeptide molecules produced by living and mostly gram +ve bacteria , secreted and released during cell lysis , bacterial replication m or by certain antibiotic use ( b lactam antibiotic )
- many target specific cells to induce toxic effects and can act locally or distally as: cytotoxins , neurotoxins , enterotoxins

A
  • exotoxins
18
Q

-superantigeen is a type of — which initially was discovered in strain of straph aureus TSST-1
- superantigen can cause —- of immune system mediated via interaction of MHC class II on T cells
- non specific binding at these sites cause polyclonal expansion of T cells leading to a shock syndrome

A
  • exotoxins
  • hyper activation
    ( check slide 39 soooo important !!)
19
Q

dissemination - how pathogens are spread in the body :

A
  1. Spread through tissues or tissue planes
    (contiguous)
  2. Spread through the bloodstream
    (haematogenous)
  3. Spread through the lymphatic system
  4. Carriage within macrophages (e.g. Typhoid)
  5. Ascending/descending spread within a tract
20
Q

how are pathogens transmitted :

A

. Person-to-person by direct contact: skin carriage
2. Respiratory: coughing, sneezing
3. Gastrointestinal: diarrhoea
4. Sexually: genital discharge /ulcer
5. Vertically & Perinatally (from mother to newborn)
6. Transmission from the environment e.g. a
contaminated inanimate object (fomite)

21
Q

host risk factors for infection :
- certain factors will —- the susceptibility of the host in infection
- increases the likelihood of — manifestation of infection
- extremes of —
- diabetes
- Immunosuppression
– Disease induced: cancer / asplenism / HIV/ renal
failure / hepatic failure
– Medications: chemotherapy, steroids, other
immunosuppressive medications
* Major breach in —–
– Recent major surgery
* —— material (portal of entry and biofilm
formation)
– IV lines
– Urinary catheters
– Ventilation
– Prosthetic joints/heart valve
* Anatomical abnormality or malfunction
– Complications post surgery
* Antibiotic therapy
– Clostridium difficile infections post antibiotics

A
  • increase
  • severe
  • age
    -skin/mucosa
    -Prosthetic