Unit 4: Viral Virulence Flashcards
what is pathogenicity?
the ability to cause disease or not
what is virulence?
the capacity of a pathogen to cause disease (symptoms within the host)
is a measure of pathogenicity
what are some host factors for virulence?
- productivity
- age
- gender
- nutritional status
- species/ breed resistance
- immunity
- geographical location
- physiological stress
what are some environmental factors for virulence?
- climate
- exposure to insect vectors
- pasture/ feed quality
- stocking density
- management and policies
why are comparative assays used to assess viral virulence?
to determine if what is seen is due to differences in v.virulence factors/ genetic modifications rather than host differences or the experimental protocol
what is used to quantify virulence?
LD50 - the dose of virus which kills 50% of the animals
how would you assess viral induced damage?
- pathological lesions
- reduction in circulating CD4+ lymphocytes
- levels of liver enzymes
what are the 4 classes of determinants of virulence?
- affect the ability of the virus to replicate
- affect host defence mechanisms
- affect tropism, body spread and transmissibility
- encode directly toxic products
give an example of a virus whose virulence determinant affects the virus’ ability to replicate (class 1) and how this is achieved
alpha-herpesvirus
- encodes TK genes - associated with nucleoside salvage pathway
- TK mutation = effects growth in neurons = decrease in neurovirulence
- expressed abundantly in early infection (rapid proliferation)
give an example of a virus whose virulence determinant affects host defence mechanisms (class 2) and how this is achieved
orf
- production of virokines = mimic cytokines etc = homology to IL-10 = immunosuppression
- production of viroceptors = homologs of host cell receptors
give an example of a virus whose virulence determinant affects tropism, body spread and transmissibility (class 3) and how this is achieved
newcastle disease virus (paramyxoviridae)
- virulence determined by cleavage of precursor F0 into F1/F2 and recognition of monobasic or multi-basic cleavage sites
- viscerotropic velogenic = 100% mortality (multi-basic + F117 intracellularly), mesogenic = intermediate virulence, lentogenic = low virulence (monobasic + F117 intracellularly)
give an example of a virus whose virulence determinant encodes directly toxic products (class 4) and how this is achieved
rarely seen, but rotaviruses
- NSP4 = enterotoxin = inhibits Na+-glucose lumenal co-transporter
- increase intracellular Ca by phospholipase C-dependent calcium signalling pathway induction
what are the 4 modes of molecular variation?
- point mutation
- recombination
- reassortment
- selection
what are some features of DNA viral replication?
- not as error prone
- hijack host DNA polymerases
- less diversity, evolve slower
what are some features of RNA viral replication?
- error prone
- use of RDRP, lack proofreading + 3’-5’ exonuclease domain
- error rate of 1 in 104 - 105 per nucleotide
- coronavirus = virally encoded proofreading repair ability = 15-fold accuracy increase
what general assumption could be made about the size of the genome and the mutation rate?
the larger the genome, the lesser the mutation rate
what is a quasispecies?
highly dynamic, non-identical but related viral species. High variation seen in a species of virus due to high mutation rate
what is the error threshold?
the point at which accumulated mutations reduce fitness
what does LI50 help define?
the mutation frequency at which 50% of the viral genomes are lethally mutated
what are the implications of quasispecies?
- unique challenges to the host
- at any given time, viral population reservoir of both genotypic and phenotypic variants
- variant differences in virulence, immune evasion, antiviral resistance and tissue tropism
- variant replication favoured with certain selective pressures
give an example of a virus which shows intra-host tropism as an adaptation
HCV (hep C)
- found in many tissues and fluids eg liver, brain, semen…
- tissue-specific mutations in HCV IRES = alter translation efficiency
- variants adapt for certain cell/tissue
describe the haemagglutination (HA) test
viruses receptor binding to sialic acid on RBCs
round button of RBCs = neg (no virus)
‘shield’/ lining of RBCs = pos (virus)
describe the haemagglutination inhibition (HAI) test
virus mixed + inoculated with virus-specific antibody before RBCs added, antibody sticks + masks virus receptors
round button of RBCs = no HA = pos
‘shield’/lining of RBCs = HA = neg
what are some common methods used to quantitate the number of infectious viral particles?
- end point dilution assay
- plaque assay
what does a plaque assay determine?
the number of plaques formed relative to dilution of virus to determine the number of infectious units per ml of sample
pfu/ml
what does an end point dilution assay determine?
the end point at which 50% of cultures are infected
TCID50/ml