S10: E-Coli & influenza Flashcards

1
Q

Describe the biology of E. coli including the identification and serology

A

Escherichia coli is a gram-negative bacillus bacterium
Normal microbiota of large bowels & protects us from salmonella
Lactose-fermenting – can use MacConkey agar where the bacteria will grow into pink/red colonies (pH become acidic from breakdown of lactose into lactic acid)
Contain O, H, K & F antigens -> encode a specific structure of the bacteria

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2
Q

Describe E. coli as a cause of diarrhoea including its pathogenesis & role of toxins

A

6 strains of diarrhoeagenic E. Coli

  • enterotoxigenic E. Coli (ETEC) = ‘travellers diarrhoea’ through production of 2 toxins
  • enteropathogenic E. Coli (EPEC) = creates a translocation tube to access & anchor into the enterocyte
  • shiga toxin-producing E. Coli (STEC) = shiga toxin inhibits protein synthesis within the cell & this causes cell death
  • enteroaggregative E. Coli (EAEC)
  • enteroinvasive E. Coli (EIEC)
  • diffusely adherent E. Coli (DAEC)
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3
Q

Describe E. coli as a cause of urinary tract infections with virulence factors

A

Uropathogenic E. Coli (UPEC)

  • adhesins: type 1 fimbriae
  • toxins: lipopolysaccharide, a-haemolysin
  • iron acquisition: bacteria produce their own iron-complexing proteins (siderophores) to acquire iron
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4
Q

Describe E. coli as a cause of blood stream infections and sepsis

A

E. Coli bacteria = commonest cause of bacterial bloodstream infections
Causal factors: 50% UTIs, 21% have urinary catheters, 16% hepatobiliary infections & 7% GI infections

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5
Q

Describe the management of E. coli infections

A

Diarrhoea: prevention is key – avoid food & drinks that could be contaminated with bacteria; treatment – most will recover within a few days, lots of fluids & avoid antibiotics
UTIs: trimethoprim or nitrofurantoin

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6
Q

Describe the structure of the influenza virus

A

Genetic material: negative segmented sense RNA (8 genes), encoding 11 proteins including 3 RNA polymerases (high error rates)
Two surface antigens
-haemagglutinin – 18 types – binds to cells of the infected person
-neuraminidase – 11 types – releases the virus from the host cell surface

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7
Q

Describe the replication of the influenza virus

A

Negative segmented sense RNA -> positive segmented sense RNA -> multiple negative segmented sense RNA
Negative segmented sense RNA -> mRNAs -> viral proteins
Negative segmented sense RNA and viral proteins are assembled into nucleocapsids

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8
Q

Describe the three different types of influenza virus

A

1) influenza A = affects many animals, undergoes antigenic drift & shift and is responsible for pandemics
2) influenza B = only affects humans and undergoes antigenic drift – it mainly affects older adults
3) influenza C = affects humans & pigs and undergoes antigenic drift and produces mild disease

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9
Q

Describe how influenza virus is spread

A

1) Small particle aerosols which remain suspended in air for many hours
2) Larger particles/droplets infect individuals in direct contact
3) Viral particles land on surfaces – infect others through indirect contact

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10
Q

Explain how the influenza virus gains entry to the human host

A

1) Attachment of viral hemagglutinin (HA) to NANA residues on receptor (sialic acid–containing glycoproteins/glycolipids)
2) Invagination of the membrane
3) Entry occurs via receptor-mediated endocytosis

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11
Q

List the clinical symptoms of influenza virus infection

A
Headache
High fever
Sore throat
Runny nose
Muscle aches & pains
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12
Q

List the complications of influenza virus infection

A

Viral pneumonia
Secondary (bacterial) pneumonia
CNS syndromes
Reye syndrome

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13
Q

Describe how you would diagnose flu in a clinical setting

A

Usually diagnosis from symptoms & clinical assessment

Can do a sample from a nasopharyngeal swab eg. antigen detection or nucleic acid detection

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14
Q

Outline the treatments for influenza

A

1) Antivirals (rimantadine) – inhibit viral uncoating after uptake = influenza A
2) Neuraminidase inhibitors – inhibit viral release from the infected cell & cause aggregation of viral particles = influenza A & B
3) Prevention = vaccines
- formalin-inactivated vaccine by injection = influenza A & B
- live, attenuated, cold-adapted vaccine by nasal spray (CHILDREN) = influenza A & B

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15
Q

What is antigenic drift?

A
Minor changes (natural mutations) in the genes of flu viruses that occur gradually over time – cause seasonal epidemics 
Refers to minor antigenic changes in H & N proteins that occur each year
Does not involve a change in viral subtype
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16
Q

What is antigenic shift?

A

Major changes in the genes of flue viruses that occur suddenly when two or more different strains combine – results in a new subtype & cause widespread epidemics/pandemics
Refers to major changes in H and N proteins
Does involve a change in the viral subtype resulting in different H and N proteins

17
Q

What are the consequences of antigenic shift? Define epidemic and pandemic

A

Leads to a new subtype of influenza virus
Immune systems of many individuals have no defence against this new subtype
Epidemic = widespread occurrence of an infectious disease in a community at a particular time
Pandemic = epidemic over a very large area; affecting a large proportion of a population; often the world