1.1 - Intro to Infection Flashcards

1
Q

What is an infection

A

the invasion of a host’s body tissues by disease-causing agents, followed by multiplication of these agents and the subsequent reaction of these agents with the host’s defences
Disease caused by
- Microbial multiplication
- Toxins (in some cases)
- Host response

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2
Q

What are the 5 generic stages for how a microorganism could cause an infection within a human

A

exposure
- How the microbe comes into contact with the host
- This can be vertical or horizontal transmission (on sep card)
adherence
- The binding of a pathogen to a host cell
- This is done using an adhesion protein (ligand) on bacterial cell wall or viral capsule surface
- This then binds to a receptor on the host cell
invasion
- The mechanism of this is unique to the pathogen
multiplication
- In bacteria, this is done by binary fission (replication of main strand → replication of plasmids → move to opposite poles of the cell → division)
- In viruses, host cell’s multiplication machinery are taken over → produce further viruses → released from the cell to infect further cells
dissemination
- Involves spreading of the bacteria / viral load from one part of the body to another
- Ie through blood and lymphatics

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3
Q

Vertical and horizontal transmission

A

vertical
- Transmission of infection from mother → fetus/baby during pregnancy or childbirth
- Transmission may occur during pregnancy across the placenta
- May occur if baby comes into contact during delivery in the birth canal
- Could also occur postnatally via mother’s breast milk

horizontal
any form of transmission that is not from parent to child. Subdivided into three main categories:
☞ CONTACT: involving direct contact between source and host. Can be direct (physical contact between infected + susceptible persons. Most STIs are this way) and indirect (susceptible patient comes into contact with a vector or contaminated surface)
☞ INHALATION: involves entry of microorgansims through resp tract. Aerosols + droplet spread (more detail on separate card)
☞ INGESTION: involves entry of microorganisms through digestive system. Eg faeco-oral ingestion where food/water is contaminated by faeces

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4
Q

What is the difference between direct + indirect contact (transmission)

A

direct is where there is direct contact between source and host. Most STIs are spread this way
indirect is where susceptible patient comes into contact with a vector or contaminated surface/object. Must be an act of making physical contact with an object that an infected person has contaminated.

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5
Q

Difference between droplet and aerosol spread

A

droplets are larger particles. Coughed out etc. Short range (so don’t stay in air very long)
aerosols are much smaller particles. Remain suspended in air (and can drift) for a much longer period of time.

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6
Q

What are commensals

A
  • Types of microbes that reside on surface of the body or the mucosal surfaces
  • Normally harmless or even beneficial
  • Transfer to other sites can be harmful and cause disease
  • Ie bowel perforation can lead to periotonitis (commensals that populate large bowel can escape into the usually sterile peritoneal cavity)
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7
Q

What is virulence definition

A

The ability of a micro-organism to infect a host (at all steps of the process)

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8
Q

What are virulence factors

A
  • chemicals that enhance the survival of the microorganisms and their reproduction inside the host
  • These include toxins and haemolysins (proteins + lipids that cause lysis of erythrocytes by destroying their cell membrane) etc
  • Toxins are subdivided into endotoxins + exotoxins (sep card)
  • The virulence facts cause damage or harm to the patient, and cause the signs + symptoms of disease
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9
Q

Exotoxins + endotoxins

dont need to know??

A

endotoxins
- consist of the lipopolysaccharide part of the cell wall of gram negative bacteria
- Cause an inflammatory response
- If the response is severe and unregulated the patient may become septic/ develop other systemic symptoms
- Not immunogenic, so don’t produce an aquired immune response
exotoxins
- toxins that are secreted by bacteria
- can destroy body cells + affect normal cellular metabolism

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10
Q

what factors determines the severity of disease

A

pathogen
- virulence factors
- size
- antimicrobial resistance (doesn’t make pathogen more virulent, but infective process will carry on until there is an effective antibiotic used)

patient
- site of infection (ie the heart is more serious than skin infection)
- co-morbidities (is patient immunosuppressed etc?)

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11
Q

Infection history and clinical examination

A

history
- potential exposures including travel, contact with infected person, contact with animals
- relative time from exposure to presentation (suggests incubation time)
- vaccination history
- symptoms of the presenting complaint (ie severity, duration, rash, muscular problems, vomiting etc)
examination
- organ dysfunctions
- rashes

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12
Q

investigations for determining cause of infection

A
  • full blood count
  • C-reactive protein (acute phase protein that is a sign of systemic inflammation, produced by liver)
  • LFTs (liver function tests)
  • Urea + electrolytes (can suggest kidney issues)
  • Imaging (x-ray, ultrasound and MRI)
  • Blood cultures (to grow bacteria if it is present)
  • Antigen detection (of micro-organism)
  • Antibody detection (understand the patient’s response)
  • Amplification of nucleic acids by PCR (to detect specific viruses or bacteria)
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13
Q

Specific vs supportive investigations

A

specific identifies causative organism ie bacteriology and virology
supportive helping to confirm diagnosis ie imaging and blood tests

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14
Q

Virology and bacteriology

A

virology
- Antigen detection (the virus)
- Antibody detection (the patient’s response)
- Detecting viral nucleic acid (RNA or DNA)
- Elisa testing can be used (on another slide)
bacteriology
- Growing the causative organism using the specimen
- Culturing using agar (nutrient source for bacteria)
- Using microscopy to try to identify

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15
Q

Basic principles of ELISA testing

A
  • Enzyme-lined immunosorbent assay
  • Bottom of tube coated with antibodies against the virus
  • Tissue sample added – binds to antibodies
  • Another antibody added that is complimentary, with an enzyme attached
  • Substrate added that changes colour in the presence of the enzyme
  • Washed between each stage to ensure no false positives
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