6.2.3 Pathogenesis Flashcards

1
Q

What are the stages of viral infection?

A

routes of entry

viral spread/dissemination in the host

virus replication

shedding

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2
Q

What determines the host range of a virus?

A

Tropism (it’s all about receptors)

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3
Q

What are the possible entry portals for viruses? (6)

A

skin

GIT

respiratory system

blood (insect bites, injections etc)

genital

transplacental

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4
Q

What are the innate defences of the skin?

A

keratinised - effective barrier

must be breached by abrasions or bites

macrophages, neutrophils, dendritic cells, natural killer cells

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5
Q

What are the defences of respiratory tract?

A

Mucociliary escalator (in URT and bronchii)

Resident commensal bacteria in URT

sneezing and coughing

innate immunological defences

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6
Q

How can viruses enter the resp tract?

A

aerosolized droplets expelled by an infected individual

spread by coughing or sneezing

contact with saliva from an infected individual

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7
Q

What are the defences of GIT? (5)

A

low pH in stomach denatures protein and kills most microorganisms

bile and proteolytic enzymes in intestines

high pH in duodenum (rapid change)

commensal bacteria (out complete pathogenic bacteria)

mucous and secretory IgA in the intestinal tract

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8
Q

How can viruses enter via blood?

A

via haematophagous (blood biting) insects

via blood products and/or sexual contact

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9
Q

How can viruses enter via genital tract?

A

via infected semen

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10
Q

How can viruses enter transplacentally?

A

viraemic pregnant animals can transmit virus to foetus in utero

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11
Q

What are two types of infections?

A

local

spreading (via blood, lymphatics, CNS, immune cells)

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12
Q

Describe local infections

A

replication in epithelium at initial infection site

cell-to-cell spread, but don’t disseminate to other tissues

usually acute (short incubation period, short duration)

site of shedding = site of entry

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13
Q

Describe systemic infections

A

primary replication at entry site followed by spread to other distant sites

allows entry and exit routes from host to differ

usually longer incubation period and more severe pathology

greater involvement of adaptive immune responses

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14
Q

What is viraemia?

A

haematogenous spread

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15
Q

What is primary viraemia?

A

spread of virus by blood from entry site to other target tissues, e.g. liver, spleen

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16
Q

What is secondary viraemia?

A

may occur following replication in secondary sites

usually allow higher viral titres and further dissemination to other sites

17
Q

How does rabies spread?

A

introduction via bite

primary replication in muscle cells

uses motor neurons to reach CNS

further replication in spinal cord and brain

enters salivary glands for onwards transmission

18
Q

Where does the virus reach the highest titre?

A

in organ tissues from which it is shed

19
Q

How do viruses induce pathology?

A

Direct effects:
-CPE
-cell stimulation
-cell transformation (tumour formation)

Indirect effects
-immune mediated pathology

20
Q

What causes CPE?

A

inhibition of host protein and RNA synthesis (cell can’t repair itself)

lysosomal damage (leakage of enzyme)

cell membrane abnormalities

cell lysis (non-enveloped viruses)

apoptosis

21
Q

what is a negri body?

A

Round or oval inclusion bodies that contain ribonuclear viral proteins
only in rabies

22
Q

What are syncytia?

A

large, multinuclear ‘giant cells’ caused by virus infected cells

23
Q

Describe the mechanism of cell stimulation

A

Poxvirus-infected cells synthesise epidermal growth factor-like protein

stimulates cell cycle of neighbouring cells

makes them ideal infection targets for viral replication (virus can spread to newly dividing cells)

24
Q

What determines disease?

A

host, viral and environmental factors

25
Q

What host factors influence disease outcome?

A

-age
-gender
-nutritional status
-species/breed
-immune status of host
-physiological stress
-co-infections of multiple pathogens

26
Q

What viral properties impact disease?

A

-geographical origin
-transmission route
-infectivity
-immunosuppression

27
Q

What are viral virulence factors?

A

molecules produced by viruses that enable them to invade the host, replicate and disseminate by subverting or eluding host defences

28
Q

What environmental factors can influence disease outcome?

A
  • environment contamination
    -climate conditions
    -quality of nutrition
    -stocking density
    -management practices
    -veterinary policy
29
Q

Describe acute infection

A

virus causes a rapid, self limiting infection

infection cleared by the immune system leading to recovery

30
Q

How can we divide persistent infections?

A

latent

chronic

31
Q

Describe latent infections

A

Virus persists at very low levels following recovery (Quiescent/latent state)

Potential to reactivate (switch from latent to productive infection

32
Q

What is a chronic infection?

A

persistent infection at low levels, following recovery will persist at low lvls

almost eliminated, but then hide in immune-privileged sites (e.g. CNS) and then attack again

don’t cause acute infection, grow slowly in a host until they reach sufficient lvls to cause disease

33
Q

What factors are involved in persistence?

A
  • immune evasion
  • tolerance
  • virus varients with with antigenic variation
    -replication in privilidged sites (to avoid being detected)
    -immune suppression