Molecular epidemiology of pathogens Flashcards

1
Q

What is epidemiology?

A

→A resolved measure (diversity) of differences (variables)

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2
Q

What does molecular epidemiology determine?

A

→Disease distribution in time and place

→Disease transmission

→Disease manifestation

→Disease progression

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3
Q

How many targets do functional characteristics have?

A

→single

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4
Q

How many targets do genomic characteristics have?

A

→multiple

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5
Q

What are the types of diversities?

A

→Single Weighting

→Additive Weighting

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6
Q

What are single weighting diversity?

A

→Biochemical test
→Presence of O157 antigen
→Presence of Verotoxin

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7
Q

What are the different types of multiple weighting genomic factors?

A

→factoral- Presence or absence of a gene/base/s change
in genome/gene relative to location in the genome

→functional- Type of substitution (synonymous/non synonymous )

→temporal- Mutation rate (time since the last alteration)

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8
Q

What type of dendogram shows pattern relatedness?

A

→Spoligotyping

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9
Q

What does variable number tandem repeats result in?

A

→Result is a profile of the number of specific repeats at multiple genomic loci

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10
Q

Examples of corruptive mutations

A

→Deletions or Insertions (disrupting coding frame)
→Creation of STOP codons (truncation)
→Corruption of STOP codons (elongation)

→Corruption of CONTROL sequences (eg. promoters)

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11
Q

What is antigenic drift?

A

→the same antigen changing its sequence base by base

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12
Q

What does accurate predictions in molecular epidemiology assume?

A

→constant molecular clock

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13
Q

What does a high division rate result in?

A

→higher mutation rate

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14
Q

What are factors affecting molecular clock?

A
→Bacterial replication rate
→proof reading fidelity
→pressure from the host 
→Degree of redundancy in the genome
→Transmission rate
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15
Q

Why is proof reading fidelity important to calculate molecular clock?

A

→Some species (eg HIV) have low fidelity promoting high mutation rate

→Gives idea on how much weighting is placed on a variant

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16
Q

Why is pressure from the host or environment important to calculate molecular clock?

A

→High selection pressure removes ‘weak’ mutants and emphasises clusters

→Loss of selection pressure allows deletions

17
Q

Why is the degree of redundancy in the genome important for molecular clock?

A

→multiple copies of a single gene in the genome allow for mutations in one copy without compromising overall functionality

→Movement or recombination within genome may not effect phenotype

18
Q

Which genes change the most?

A

→Hyper-variable genes

19
Q

What genes are more likely to be associated with phenotype and virulence?

A

→conserved genes

20
Q

What is antigenic shift?

A

→a sudden replacement of an antigen by recombination with another viral type that has evolved separately

21
Q

What is molecular restriction typing?

A

→can monitor effectiveness of control measures

22
Q

What does choosing the most appropriate system require?

A

→Knowing the most appropriate variable/s

→Quantitating variations and deriving diversity

→Generating identities or clusters

→Applying related data