Parasitology: Endoparasites Flashcards

1
Q

Parasite – a definintion

A

An organism that lives for an appreciable part of it’s life on (ectoparasite) or in (endoparasite) another organism (the host), is dependent on the host and benefits from the association at the expense of the host”

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2
Q

Commensalism:

A

Least intimate of relationships where one or both species may benefit
Transport, cleaning, protection e.g. micro-organisms that live on skin,

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3
Q

Mutualism:

A

An association where both partners benefit

Protozoa in hind gut of horses and fore stomach of ruminants

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4
Q

Why study parasitism?

A

Implications to human and animal health and welfare

Many millions of pounds spent annually on prevention and control

Ubiquitous nature of parasites means they will never be eradicated completely
Can only aim to minimise damage caused

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5
Q

Host

A

Definitive host
Intermediate host
Paratenic host

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6
Q

How do parasites affect the host?

A
Compete for nutrients
Depress appetite
Damage skin or internal organs
Diarrhoea
Liver failure
Respiratory problems
Increase chances of secondary infections
Stimulate immune system so that the animal is more susceptible to disease
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7
Q

Pathogenesis

A

Compete for nutrients
Damage gastrointestinal lining

Clinical Signs

Migrate through liver

Weight loss
Weight loss, diarrhoea, blood in feaces

Jaundice

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8
Q

Endoparasite Groups

A

Trematodes
Cestodes
Nematodes
Protozoa

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9
Q

Nematodes

A

Among the most ubiquitous of all animals:
Antarctic, hot springs, soil, fresh and salt water
Where there is a living organism there will be several nematodes to parasitize it!

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10
Q

Cestodes

A

Indirect lifecycle
Hermaphrodites

Reliant on host – no free living stage

No mouth / anus – absorb pre-digested nutrients through tegument

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11
Q

Trematodes

A

Liver and stomach flukes
Indirect lifecycle - snails
Hermaphrodites
Paedogenesis - production of many new individuals from a single larval form

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12
Q

Protozoa

A

Single celled organisms
50,000 known species
Only one fifth (10,000) of these are parasitic
Important groups in terms of animal health:
Eimeriidae (Eimeria spp. and Isospora spp.)
Cryptosporidium
Sarcocystidae (Toxoplasma, Neospora)
Babesiidae (Babesia)

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13
Q

Basic Nematode Lifecycle

A

egg -> L1 (free living) -> L2( free living) -> L3 (free living/ inefective) -> l4 (within host) -> l5 (within host) -> Adult -> repeate

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14
Q

Cestode Lifecycle

A

Adult (within definitive host) -> Gravid proglottids shed -> Embryophore
(in environment) ->Ingested by intermediate host -> Oncosphere
(within intermediate host) -> Breaks through gut wall of intermediate host and travels to site to form a …
-> Metacestode (cyst within intermediate host) -> Remains within intermediate host until it is ingested by definitive host -> repeate

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15
Q

Trematode Lifecycle

A

Eggs-> Passed in faeces onto pasture ->Miracidium -> Miracidium hatches ->Within intermediate host -> Develop to sporocyst, rediae and cercariae -> Leave intermediate host ->Cercariae -> Metacercariae -> Ingested by grazing animals -> repeate

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16
Q

Protozoa Eimeria Lifecycle (example)

A

Unsporolated oocyst
->Nucleus divides - sporocysts
->Sporolated oocyst
(infective)
->Ingested – liberation of sporocysts and sporozoites within them…
->Sporozoites
t ->Penetrate gut wall cells and reproduce asexually…
-> 1st generation merozoites
->Gut cells burst when full of 1st gen merozoites…
-> 2nd generation merozoites
-> Invade more gut cells…-> Gut cells burst when full of 2nd gen merozoites…-> Male / female
->Fuse = oocysts!
-> repeate

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17
Q

Transmission

A
Faeco-oral
Grazing, bedding, coat,
Fungi
Intermediate host
Paratenic hosts
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18
Q

Pre-Patent Period

ppp

A

Time taken from ingestion of eggs/ larvae/ cysts to eggs being present in faeces

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19
Q

Migration in regards to endo parasites

A

Gastro-intestinal parasites may remain entirely within gut during development into adults

Or may migrate
e.g. Hepatotracheal = From gut > liver > heart > lungs > trachea > gut

20
Q

Migration - examples

A

Nematodes - Toxocara canis
Parascaris equoruum
Dictyocaulus viviparous

Cestodes- Within intermediate hosts to form cysts

Trematodes-Fasciola hepatica (within intermediate and definitive
Protozoa- Toxoplasma gondii (within intermediate host)

21
Q

Hypobiosis

A

Some parasite go through a period of arrested development
E.g. Teladorsagia circumcincta infection in sheep
L4 stage larvae burrow into abomasal gut mucosa
Remain dormant for several months
Inhibited development stage with mass emergence = longer PPP
No inhibited stage = shorter PPP
Environmental or external stimulus at free living stage?
Mass emergence
Examples:
Toxocara canis
Cyathostomins
Teladorsagia

22
Q

Effects of Nematodes on hosts

A

Gastrointestinal effects – next slide
Damage to other tissues / organs where reproduce or migrate through
Triggering of immune system – local effects and susceptibility to disease

23
Q

Gastrointestinal effects

A

Parasitic gastroenteritis (PGE)

Damaging gut / inflammation resulting in mal-absorption of nutrients (diarrhoea)
Increasing nutrient demands on host to repair damaged tissue (weight loss)
Placing high immunological demands on host (more susceptible to other diseases)
Blood sucking (anaemia)
Sheer loading of parasite burden (blockages)

24
Q

Effects of Cestodes on hosts

Definitive Host

A

Nutrient absorption - weight loss
Inflammation to intestinal lining - diarrhoea
Blockage of intestines - colic

25
Q

Intermediate Host

A

Cysts within organs – liver failure, neurological symptoms,

26
Q

Effects of Trematodes on hosts

Definitive Host

A

Larval migration through liver – liver damage, rupture, death
Adults within bile duct – liver failure

27
Q

Effects of Trematodes on hosts

Intermediate Host

A

Snails damaged possibly die as result

28
Q

Effects of Protozoa on hosts

Definitive Host

A

Damage to gastrointestinal cells – diarrhoea, bloody faeces, death

29
Q

Effects of Protozoa on hosts

Intermediate Host

A

Targeting rapidly reproducing cells – abortions, still births,

30
Q

Periparturient Rise

A

Temporary relaxation of female host’s immunity around time of parturition (4 wks before up to 8 wks after)

Decreased immunity to parasites:
Hormonal interactions
Stress
Nutritional stress in late pregnancy and early lactation

31
Q

Zoonotic implications of endo parasites

A

Humans as:
Definitive host – effects as discussed throughout session today
Intermediate host – Cysts (Cestodes)
Accidental host - Visceral larval migrans, cysts,

32
Q

Implications of parasite infections

A
Infected offspring
Colic
Intestinal blockage
Pulmonary damage
Nasal discharge
Coughing
Frothy
Abortions
Gastrointestinal lining damage
Weight loss / stunted growth
Diarrhoea
Death
Organ damage
Liver failure
33
Q

summary of endoparasites

A

Many different types of parasites resulting in many different forms of damage to hosts
Parasites are incredibly adaptable with different strategies to increase spread, infection, development within hosts
Understanding lifecycles is key to successful control strategies

34
Q

Eradication of parasites

A
Eradication???  Unrealistic!
Parasites very adaptable
Eradication prohibitively expensive
Treatment and control
Predominantly chemotherapy
Resistance 
Environmental concerns
Residues
Sustainable alternatives?
35
Q

Chemical treatments

A

Nematodes- Anthelmintics - various- Oral, pour-ons, spot-ons,

Cestodes- Oral praziquantel or double dose pyrantel- Oral

Trematodes-Triclabendazole,
Closantel, Nitroxynil,
Albendazole, Oxyclozanide-Oral

Protozoa- Sulphonamides- Oral
Used in 2 ways:
Against an existing infection

Prophylactically?

36
Q

Anthelmintics for endoparasites

A

Broad Spectrum
Effective against a range of parasite species
E.g. Ivermectin

Narrow spectrum
Effective against a limited range of parasites
E.g. Praziquantel

Benzimadazoles
Levamisoles
Macrocyclic Lactones 
Amino-acetonitrile derivative (AAD)
Spiroindoles
37
Q

Anthelmintic Resistance

A

No chemical treatment is ever 100% effective
Genetically resistant parasites

Excessive, frequent dosing
Under-dosing

38
Q

Avoiding Anthelmintic Resistance

A
Accurately assess weight -correct dose given
Dose for heaviest animal
Ensure full dose is administered
Drenching technique
Rotate chemical groups annually
Some drenches are more effective on empty gut – read the instructions!
Treat at right time of year
Treat all new animals on arrival
Do faecal egg counts
39
Q

Linking lifecycle knowledge to control

A

Knowing when to administer chemicals is essential
Key periods during parasite lifecycles where they are vulnerable
1) Gastrophilus
Which time of year should you treat horses and why?
Which part of the lifecycle are you targeting and where does it live?
2) Dipylidium caninum
What do we need to treat in order to eliminate this parasite in an infected dog and why?

3) Toxocara canis
Which dogs should we treat against this parasite and why?
Which age group of dogs in particular are at risk?
When should anthelmintics be given and why?

40
Q

Reducing incidence of parasitisim

A

No system should rely solely on anthelmintics
An integrated approach to parasite control is better
Breed for resistance
Graze on bioactive forages e.g. chicory, birdsfoot trefoil,
Stocking rates
Rotational grazing
Mixed species grazing, mixed age grazing

Dung lifting / removal / pick up poo
Harrowing
Monitor consumption of potential intermediate hosts
Prevent scavenging
Keep bedding and environment clean, dry, fresh
Treat new arrivals before mixing with other animals

41
Q

Determining parasite infection

A
Faecal examination or egg count
Post-mortem
Antibody tests 
Blood
Saliva
42
Q

Faecal Egg Counts

A

Test for what?
Level of infection
Low, medium or high
What treatment is needed

43
Q

Parasite Control

A

Chemical products
Treat what is present, various periods of activity
Endoparasite products such as anthelmintics used for treatment only
Some ectoparasite products can be active for months and form part of preventive measures but resistance also reported

44
Q

Creating a control plan

A

Need to know:
Which parasites are present, any resistance?
Perform faecal egg counts
Times of year those parasites cause problems
Best time to treat against them or use management to avoid them
e.g. Nematodirus, fluke, midges,
Which management strategies apply
Which chemicals are effective against the parasites that are present

45
Q

Summary of control of endo parasites

A

No chemical parasiticide is 100% effective nor 100% ideal
Where chemicals are used, they must be used correctly!!!
Resistance cannot be prevented but must be minimised / slowed down
Need to understand lifecycle of parasites to know when to treat and what non-chemical measures can be implemented
An integrated approach to control is essential