Vector Incrimination Flashcards
What needs to be assessed to determine whether a disease is vector borne?
- Confirmation of pathogen in patient
- Who is infected
- When infected
- Disease correspond with reports/observations of increase in arthropod activity
- ?Perturbation of environment
- Evidence of bites
What needs to be assessed when determining a vector?
- Vectors present
- Population studies
- Identify vectors (morphological and molecular)
- Vector proportions in population (and time of year)
Collection methods for ectoparasites
- Anaesthesia
- Brushing
- Tick dragging
Examples of ectoparasites
Ticks, fleas, mites, lice
Trapping methods
- Light traps
- Resting boxes
- Tsetse traps
What are the steps towards vector incrimination?
1) Demonstration of feeding or other infective contact with the host under natural conditions
e. g. Distinguish between zoophilic and anthropophilic -HLC vs Light traps or blood meal analysis
2) A convincing biological association in time and space of the suspected arthropod species and occurrence of clinical or subclinical infection of the host
3) Repeated demonstrations that the arthropod, under natural conditions, harbours the infectious agent in the infective stage
4) Transmission of the agent under controlled conditions
Describe the steps to experimental transmission
1) naturally or experimentally infected animal fed on by arthropods
2) arthropods are then allowed to feed on uninfected animals after extrinsic incubation period
- problems of false positives and negatives with this approach
What are the key factors affecting vector effectiveness or capacity?
1) pathogen receptivity in the vector
2) host specificity (contact with host)
3) longevity ( does the vector live long enough to allow the extrinsic incubation period)
4) frequency of biting
5) mobility
6) numbers
7) physiological and behavioural plasticity
8) susceptibility to control measures
Give an example of vector incrimination
CL in peru -7spp of sandfly -5 anthropophilic -3 confirmed vectors They collected insects then dissected and collected parasites from gut then fed uninfected sand flies on infected hamsters molecular characterisation