Diseases + populations Flashcards

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1
Q

Describe the relevance of molecular biology to studies in wild animal health/wild animal biology

A

Detection of pathogens

Microsatellites for looking at relatedness

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2
Q

Understand the difference between DNA, RNA and protein and their roles in the cell.

A

DNA is transcribed into mRNA which is translated into a protein for cellular processes

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3
Q

Describe the principles behind PCR and microsatellites, and how these can be applied to studies in WAB.

A

Polymerase chain reaction (PCR) is a technology used for quick and easy amplifying DNA sequences, which is based on the principle of enzymatic replication of the nucleic acids
A microsatellite is a strand of repetitive DNA in which certain DNA motifs are repeated and they are used as genetic markers to follow the inheritance of genes in families

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4
Q

Design oligonucleotide primers that will work in PCR if given a DNA sequence.

A

Your primers should have a nucleotide content of approximately 50% G:C and 50% A:T base pairs, they should have a minimum length of 17 bp. Second primer needs to be the matching sequence and reversed, because extension is at the 3’ end.

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5
Q

Understand the mechanisms of the host immune response to different pathogen groups and some of the immune evasion strategies employed by some pathogens.

A

Innate response – produces interferon for defence and makes cells more resistant to infection
Adaptive response – B cells produce virus-neutralising antibody, CD8 and killer T cells destruct infected cells
Evasion strategies - e.g. mimicking host cells, hiding within host cells

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6
Q

Describe the different types of immunoassays that can be used for diagnostic purposes.

A

ELISA – using antibody and protein to have an antigen bind if it is present
Immunofluorescence – using a sample and introducing antibodies so that if they bind we know antigens are present

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7
Q

Appreciate how the formulation and delivery of vaccines can influence protective immunity and give some reasons for vaccine failure.

A

Passive immunisation lasts approx. 3 months vs active which lasts longer
It may be a different strain of antigen that the host is exposed to, incorrect storage and administration will also reduce effectiveness

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8
Q

Discuss the evolutionary and ecological drivers for development of the immune system in different species.

A

The host may be too young/old, be immunocompromised, or be genetically pre-programmed with a poor response
Environment may not be suitable for the reproduction of some pathogens

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9
Q

Understanding infectious disease - transmission dynamics

A

Depends on birth, immigration, death, and emigration and also on the level of immunity

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10
Q

Introduction to compartment models

A

Susceptibility, exposure, number of infectious individuals, and those that are removed (immune/dead)

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11
Q

Disease modelling: understanding the importance of demographics

A

Allows for the prediction of an epidemic’s properties, e.g. how the populations within compartments changes over time

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12
Q

What is R0

A

The average number of secondary cases generated from a primary case introduced into a susceptible population

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13
Q

Understanding the importance of critical community size

A

The minimum size of a closed population which a pathogen can persist indefinitely. When the CCS falls below this, the low density of hosts causes extinction of the pathogen.

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14
Q

Impact on wild populations; edge factors

A

Structures of populations change at boundaries, and fragmentation causes an increased exposure to a range of pathogens

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15
Q

Impact on vegetation dynamics

A

Vaccinations developed can increase populations of host, which can impact the landscape, e.g. grazers

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16
Q

Impact on livestock and livelihoods

A

Outbreaks, e.g. foot and mouth disease, can require culling which loses money for farmers

17
Q

Impact on human health

A

Zoonoses are causing more outbreaks due to spill over and increased contact with infected wildlife

18
Q

Approaches to wildlife disease management

A

Direct efforts within target population
Direct efforts to blocking transmission between reservoir and target
Reduce infection prevalence in the reservoir population

19
Q

Age-linked serology to understand the temporal relationships

A

Look for mutations and genetic based changes to look at relationships between cases and the direction of spread

20
Q

Intervention studies: eg vaccination campaigns, culling hosts to remove a population from the epidemiological equation

A

Monitoring population dynamics to see if the intervention has positive effects

21
Q

describe the underlying factors behind disease spread in natural populations

A

Transmission rate, virulence, birth and death rate

22
Q

describe the components required to design and implement models

A

Infected (infectious and latent) and non-infected (susceptible an immune)

23
Q

discuss the advantages and limitations of computer-based modelling in wildlife medicine

A

Can give some predictions which can be used for interventions and control or adapting these methods, but relying on assumptions means they may not be accurate

24
Q

provide definitions of veterinary epidemiology

A

The study of disease, productivity and welfare in animal populations

25
Q

provide examples of multi-factorial webs of causation

A

Age, health status, genetics, environment etc. > infection > tissue invasion and reaction > disease

26
Q

define components of epidemiological triad

A

Agent, environment, host

27
Q

describe different temporal patterns of disease occurrence

A

Continuously increasing rate, fluctuating rate etc.

28
Q

describe the difference between counts, proportions, rates and ratios

A

ratios – relative size of two quantities expressed by dividing a numerator by a denominator
counts – number of individuals infected, diseased, or dead
proportions – a ratio whose numerator is included in the denominator
rates – a ratio representing the magnitude of change in occurrence of an event

29
Q

define prevalence, cumulative incidence and incidence density

A

prevalence – total number of individuals who have a disease at a particular time divided by the population at risk
cumulative incidence – proportion of disease-free individuals developing a disease over a specified time
incidence density – instantaneous potential for change in disease status per unit of time, relative to the size of disease free population at time

30
Q

discuss the differences between non-observational and observational studies

A

non-observational – recording the outcome of a planned intervention
observational – recording what happened

31
Q

describe the design and discuss the advantages/disadvantages of intervention studies, clinical trials

A

Often randomised control trials with comparisons between a placebo group and those receiving the intervention
Control over confounding variables, control over selection bias, assessed intervention effectiveness
Expensive, may need a large sample size, may need a large follow-up, only possible if there’s a suitable intervention

32
Q

describe the design and discuss the advantages/disadvantages of cross-sectional, case-control and cohort studies

A

cross-sectional – data on a factor and outcomes at the same time, inexpensive and easy but information on changes over time is limited
case-control – 2 or more groups e.g. exposed and not exposed and checked later to see if they have the disease, good for rare outcomes but not for rare exposures
cohort studies – disease and non-diseased group comparison looking retrospectively at whether they were exposed to a factor, good for rare exposures but not for rare diseases

33
Q

define measures of strength of association – relative risk, odds ratio

A

relative risk – probability of getting disease if exposed / probability if not exposed, OR probability of outcome if on drug / probability if not on drug
odds ratio – odds that the diseased were exposed / odds the controls were exposed

34
Q

describe measures of potential impact – attributable risk, attributable fraction

A

attributable risk – disease in exposed / disease in not exposed
attributable fraction – AR / risk of disease in exposed group

35
Q

to identify in an example, define and differentiate the terms related to sampling methodology

A

probability based: convenience and haphazard sampling – biased samples and errors in conclusions
non-probability based: simple random and systematic sampling – equal likelihood of selection but each have their downfalls e.g. is it truly random?

36
Q

to give advantages/disadvantages of each sampling method

A

convenience – easy and quick but biased to what’s available
judgement sample – what you think is representative but it’s biased
simple random – easy but the individuals may not all be easily available
systematic – high validity but is it true randomness (takes away equal opportunity of being chosen)

37
Q

Describe contemporary issues in major diseases affecting wild artiodactyls and in the context of livestock

A

There is often an association between wild artiodactyls and livestock, especially when vector borne

38
Q

Critically evaluate the importance of disease in the conservation of wild artiodactyls

A

Artiodactyl loss will continue as each population shrinks and fragments