Pathogens And Hosts Flashcards

1
Q

What is the difference between a pathogen and a commensal?

A

A pathogen is an organism which can cause disease whereas a commensal is an organism which is part of the normal flora.

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2
Q

What is Koch’s postulates on a pathogen causing the disease?

A

The organism must be found in all cases of the disease.
It must be able to be cultured outside the body for several generations.
It should reproduce the disease on inoculation.

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3
Q

What is pathogenicity and what are two requirements for it?

A

The capacity of a microorganism to cause an infection.
Infectivity is the ability to become established in the host.
Virulence is the ability to cause harmful effects once established.

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4
Q

Name four virulence factors

A

Genetically determined microbial components
Invasiveness
Toxin production
Evasion of immune system

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5
Q

What are the three types of toxins and what do they do?

A

Exotoxins are released extracellularly by the organism.
Enterotoxins are exotoxins which act on the GI tract.
Endotoxins are structurally a part of the gram negative wall.

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6
Q

Give an example of an exotoxin

A

Clostridium tetani (gram positive) infects dirty wounds and produces toxins that bind to nerve synapses and inhibit the release of inhibitory neurotransmitters so death is caused by respiratory paralysis. Treated by debridement, antitoxins and antibiotics.

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7
Q

Give an example of an enterotoxin

A

Vibrio cholerae colonises the small intestine and the toxins increase cAMP which inhibits the uptake of sodium and chlorine ions and secretes more chlorine and carbonate ions so there is a massive outflow of water. Death is caused by dehydration.

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8
Q

What are superantigens and what do they do?

A

They are certain exotoxins of strep pyogenes and staph aureus. They’re able to stimulate division of T cells in the absence of the specific antigen. The overwhelming cytokine production causes toxic shock.

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9
Q

What is the structure of endotoxins and what do they do?

A

They’re made up of a polysaccharide antigen, oligosaccharide core and a Lipid A which is what causes the damage.
They induce a severe uncontrolled host response.

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10
Q

What are three virus pathogenic mechanisms?

A

Cell destruction after virus infection such as HIV killing T4 helper cells.
Virus induced changes to cellular gene expression such as cellular transformation by rumour viruses.
Immunopathogenic disease such as influenza A virus.

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11
Q

Name four types of viruses in terms of time periods.

A

Acute infections start and finish early such as influenza.
Latent infections are acute early then lie dormant before getting a secondary infection such as herpes.
Chronic infections are acute early then are always present at low levels such as Hepatitis B.
Tumour virus infections have a small response early but will have a large latent response.

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12
Q

What is viraemia and how does it differ from acute infection?

A

It means the virus is in the bloodstream whereas acute infection is localised to a specific site of the body.

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13
Q

What are antigenic shift and drift?

A

Shift is abrupt major changes in virus antigenic structures. Non human hosts can help generate new virus types through antigenic shift.
Drift is minor changes in the genes of flu viruses that occur over time to generate antigenic variants.

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14
Q

Name some enteroviruses and what they cause

A

Poliovirus causes poliomyelitis.
Coxsackie B viruses causes myocarditis and pancreatitis.
Many enteroviruses cause aseptic meningitis and respiratory infections.

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15
Q

How does the latent infection of herpes work?

A

There is a primary infection of the epithelium then the virus migrates to the ganglia where it lies latent in the nucleus and doesn’t replicate. A stimuli reactivates the virus and it migrates back to epithelial cells to replicate.

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16
Q

Name two viruses and the cancers they cause

A

Papillomaviruses cause cervical cancer.

Retroviruses cause lymphomas and leukaemias.

17
Q

What does human T-lymphotropic Virus-1 (HTLV-1) do and cause?

A

It transmits from mother to child and infects T cells. It modifies the host cell gene expression using a transactivsting protein. Directly produces tumours in variety of diseases of leukaemia.

18
Q

What are five host defence mechanisms?

A
Innate immunity 
Phagocytic mechanisms
Acquired immunity 
Antibody and complement system 
Cell mediated immunity
19
Q

What mechanisms and structures does innate immunity involve?

A

Skin, gastric acid, muco-ciliary escalator etc.
Phagocytic cells ingest foreign bodies.
Polymorphs are acute.
Macrophages are chronic.
Fixed macrophages are found in the liver, spleen and lymph nodes.
Free macrophages are in the tissue.

20
Q

What are the three types of polymorphs?

A

Neutrophils
Basophils
Eosinophils

21
Q

How does phagocytosis work?

A

Organism is held in phagosome and fuses with a lysosome to make phagolysosome and then it is killed intracellularly.

22
Q

What organisms are resistant to phagocytosis?

A

Capsulate bacteria such as streptococci pneumoniae are resistant.
Mycobacterium tuberculosis are resident to intracellular killing.

23
Q

What do the spleen, liver and lymph nodes do?

A

The spleen clears blood.
The liver clears entero-hepatic circulation.
The regional lymph nodes drain peripheral sites.

24
Q

What is opsonisation and what is it important for?

A

The pathogen is coated with antibody or complement so the efficiency of phagocytosis is improved. This is important for capsulate bacteria.

25
Q

What is acquired immunity?

A

It is a specific response to an antigen so antibodies and T cells are produced. It creates immunological memory.

26
Q

What are immunoglobulins and what are the five classes?

A
They are proteins with antibody activity. 
Immunoglobulins-Ig
Primary response-IgM
Secondary response-IgG
Mucosal immunity-IgA
Allergy and Helminth infection-IgE
27
Q

What is the difference between monoclonal and polyclonal antibodies?

A

Monoclonal antibodies from one close of plasma cells has a specificity for one epitope.
Polyclonal antibodies have multiple epitope specificity.

28
Q

What is the complement process?

A

It is a complex cascade of approximately 20 proteins. A combination of antibody (IgG or IgM) and it’s antigen can trigger the process. It is a fixed response.

29
Q

What do antibodies do?

A
Neutralise bacterial toxins. 
Neutralise viruses in viraemic stage. 
Prevents adherence of microorganisms. 
Opsonises capsulate organisms. 
Useful means of diagnosis-serology.
30
Q

What can complement do?

A

It can opsonise.
Can lyse gram negative organisms.
Cascades byproducts are chemotactic (attract polymorphs)

31
Q

How does cell mediated immunity work?

A

Macrophages present antigens and stimulate the T cells. Cytokines are produced and control response.

32
Q

What are the two kinds of T cell and what do they do?

A

CD4 helper cells include Th1 which activate macrophages to ingest and kill pathogens and Th2 which control B cell antibody response.
CD8 suppressor and cytotoxic cells kill infected host cells or foreign cells.

33
Q

Why is cell mediated immunity important?

A

It combats intra cellular infection from viruses and certain bacteria and fungi.
Important for fighting mycobacterium tuberculosis which resists intracellular killing.
It kills most viral and fungal infections.
Lymphocytosis-increases the number of lymphocytes.