Wolbachia pathogen interactions in VBDs Flashcards

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1
Q

What kind of population regulation does wolbachia provide?

A

Population replacement (rather than suppression)

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2
Q

What are ways in which a population could be suppressed?

A

Entomopathogenic fungi, Sterile insects, insecticides.

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3
Q

How do we study endosymbionts and why?

A

Infected cell lines usually to provide an in vitro model as are not usually culturable.

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4
Q

When are gut microbiota acquired?

A

Usually maternally (mother –> progeny) from an early age e.g. larvae or eggs.

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5
Q

What is elizabethkingia? Where is it found? When is it present?

A

A genus of bacteria found in anopheles and aedes in both field caught and lab strains.

Present from L2 to adults.

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6
Q

What is the effect of enterobacter?

A

Thought to reduce vector competence by reducing development of plasmodium ookinetes and sporozoites.

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7
Q

What are the most common microbiota species vs which species are less common but tend to dominate?

A

Flaviobacteria less common but more likely to dominate the microbiome if present whereas Asaia and enterobacter more common but less likely to dominate.

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8
Q

How is it thought (still under debate) that wolbachia stops mosquitos transmitting parasites?

A

Induces ROS production that kills parasites.

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9
Q

Where are asaia bacteria located? Why is this good?

A

Midgut and salivary glands where they colocalise with plasmodium oocysts to have antipathogenic effects.

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10
Q

What is paratransgenesis?

A

Eliminate a pathogen from vector populations through transgenesis of a symbiont of the vector.

GM bacteria and put back into the vector so they can have antipathogenic gene expression that spreads throughout the population.

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11
Q

Where is wigglesworthia found? How is it passed on? What does it allow?

A

Endosymbiont of tsetse in the milk glands (allows transfer to larvae). Allows tsetse to survive on just blood.

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12
Q

How is wigglesworthia antitrypanosomal?

A

Activates pattern recognition receptor PGRP-LB (proteoglycan pattern recognition protein LB) which is antitrypanosomal.

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13
Q

What is sodalis? where is it found? How is it passed on?

A

Endosymbiont of tsetse.
In fat body and haemolymph.
Passed on in milk secretions.
Recombinant sodalis has some experiments done to show it works against some tryps.

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14
Q

Describe the lab experiment working on transgenic R prolixus endosymbionts.

A

Rhodococcus recombined using RNAi interference to inhibit gene expression.

Given back to R prolixus, it outcompetes natural population.

Outcome was an impact on fecundity and lifecycle.

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15
Q

What is the effect of mosquitos ingesting blood containing antibiotics (e.g. penicillin, streptomycin) on malaria transmission?

A

Increases transmission as vectorial capacity is augmented as the microbiome is no longer activating the immune response and being antimalarial

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16
Q

Which families have wolbachia?

A

Arthropods and nematodes.

17
Q

Which is the main species we know not to have wolbachia?

A

A aegypti- doesnt have a natural strain of W.

18
Q

Describe male and female positive and negative pairings that would and would not lead to inheritance.

A

+ve m, -ve f = cytoplasmic incompatibility between sperm and egg = no viable offspring.

All other pairings produce viable offspring but offspring will only inherit W if the mother is infected with W.

19
Q

How does W confer a reproductive advantage?

A

It produces more offspring (2/3) that are infected, meaning that more mating occurs with infected females to increase spread throughout the population.

20
Q

How can wolbachia mosquitos be used to crash populations? Why may this not be the most effective strategy?

A

Lots of W infected males released, which can mate with W uninfected females and cause a crash.

Lab rearing has consequences on mosquito fitness and reproductive success. Also mosquitos are invasive so this strategy can be risky.

21
Q

Describe W virulence in drosohila.

A

If flies had a virulent strain of W, they lived half as long as flies without.

Whereas flies infected with avirulent strains had protection against infect viruses.

22
Q

How can a aegypti be manipulated for dengue control?

A

Put a virulent drosophila W into a cell line which attenuated over time and came out as a less virulent strain that could then be put into aegypti. Salivary spitting showed it completely blocked the transmission of dengue.

23
Q

What are the effects of W in aegypti?

A

No effects on embryo viability and fecundity.

24
Q

What was the result of doubly infecting a aegypti with W strains?

A

Thought would be a good idea if one strain stopped working. Shown NOT to have negative effects on fecundity if doubly infected.

25
Q

What is JEV transmitted by, what is the amplifying host and where is it found? What type of virus is it?

A

Culex tritaeniorhynchus (v hard to rear).
Amplified in pigs.
Africa, Europe and Asia.
Flavivirus.

26
Q

How can wolbachia be used against filarail nematodes?

A

MDA to kill bacteria which kills parasites as they are required for fertility. (In all except loa loa)