Medical Microbiology: Pathogenesis of Parasitic Infections Flashcards

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1
Q

What is Leishmaniasis?

A
  • A parasitic disease caused by Leishmania parasites
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2
Q

What are the different types of Leishmaniasis?

A
  • Visceral leishmaniasis
    • Asia: Leishmania donovani
    • Middle East/Africa/Asia: L. infantum variants
    • Latin America: L. chagasi
  • ​Cutaneous Leishmaniasis
    • ​Old world disease: Mediterranean/Middle East - L. Infantum/L. major/L. tropica
    • New world disease: Central and South America - L. braziliensis/amazonensis/mexicana
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3
Q

Describe the life cycle of Leishmania

A
  • Sand fly bites you and transfers promastigote into the body
  • Promastigotes invades macrophages
  • Inside macrophage promastigotes form nests of amastigotes
  • This causes macrophage to burst resulting in release of amastigotes which go on to infect other cells
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4
Q

What is the vector for leishmaniasis?

A
  • Lutzomyia/Phlebotomus
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5
Q

What causes diffuse cutaneous leishmaniasis?

A
  • Occurs as a result of someone not being able to produce an adequate immune response to the parasite
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6
Q

Describe the pathogenesis of cutaneous leishmaniasis

A
  • Acute lesions
    • Due to tissue damage caused by inflammatory response to presence of parasites in macrophages
    • Parasite killed by Th1 pro-inflammatory responses and macrophages
  • Latency
    • Regulatory immune response which causes parasites to remain dormant long-term
    • Characterized by balance of Th1 and anti-inflammatory responses
  • Relapse (rare)
    • Alteration in immune response e.g. change in Th1 vs immune regulation due to HIV infection
    • Mucocutaneous disease associated with strong but inadequate inflammatory response to parasites that have metastasized to mucosa
    • Diffuse cutaneous leishmaniasis associated with uncontrolled parasite replication
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7
Q

What are the 3 main species of Helminths that can cause Schistosomiasis?

A
  • Schistosoma mansoni
  • Schistosoma haematobium
  • Schistosoma japonicum
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8
Q

Decribe the life cycle of Schistosoma

A
  • People exposed to infective stage in contaminated water
  • Get infected with cercariae which migrate through the body
  • Cercariae fbecome adults in mesenteric system
  • Female and male mate and female releases eggs into mucosal epithelium
  • Eggs get excreted either through faeces or urine
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9
Q

What is cercarial dermatitis?

A
  • Allergic type reaction caused by exposure to cercariae from animal or bird schistosomes
  • Requires pre-sensitization
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10
Q

What is a key feature of the immune response to Schistosomiasis?

A
  • Granuloma formation - Eggs from female become organized in granulomas
  • Repeated insults and tissue repair leads to fibrosis and organ damage
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11
Q

What is Hepato-intestinal schistosomiasis?

A
  • Schistosomiasis infection caused by S.mansoni and S. japonicum
  • Pathology caused by immune response to eggs - eggs are pushed through intestinal wall and mucosa and are then excreted
  • This causes hepatosplenomegaly
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12
Q

What diseases/conditions can urinary schistosomiasis cause?

A
  • Haematuria - blood in the urine
  • Can also lead to bladder cancer due to inflammation of bladder wall caused by eggs
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13
Q

What is onchocerciasis?

A
  • Major blinding disease caused by filarial parasite (Onchocerca volvulus)
  • Transmitted by blackflies
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14
Q

Describe the life cycle of Onchocerca volvulus

A
  • Blackfly bites you and transmits infectious larvae
  • Larvae migrates under the skin and develops into adults
  • Male and female adult mate and female releases 1000s of larvae called microfilariae
  • Microfilariae get taken up by blackfly and develop in blackfly until they can be trasnmitted themselves
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15
Q

What is the vector of Onchocerca volvulus?

A
  • Simulium
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16
Q

Describe the pathology of Onchocerciasis

A
  • Repeated episodes of inflammation due to presence of microfilariae leads to permanent damage and scarring in skin and eyes
17
Q

What diseases/conditions are caused by Onchocerciasis?

A
  • Onchocercal nodules - only problematic if around joints
  • Skin disease
    • Acute papular onchodermatitis
    • Chronic onchodermatitis
    • Sowda
  • Eye disease
    • Anterior segment (iris)
      • Punctate keratitis
      • Acute iridocyclitis
      • Sclerosing keratitis
    • Posterior segment (retina)
      • Optic neuritis/atrophy
      • Chorioretinopathy
18
Q

What is punctate keratitis?

A
  • Condition caused by death of small groups of cells in the cornea as a result of Microfilariae being killed by immune response
19
Q

What is sclerosing keratitis?

A
  • Condition caused by repeated inflammation of the cornea
  • This results in opacification of the cornea causing blindness
20
Q

Describe the immune response that occurs due to onchocerciasis

A
  • Rapid allergic reactions that kill microfilariae in skin
  • Activation of mast cells which recruit other immune system cells e.g. eosinophils
  • Acute stage
    • Strong TH2 response which produces IL-4 and IL-5
    • IL-4 leads to IgE production and IL-5 leads to recruitment and activation of eosinophils
  • Chronic stage
    • ​Host immune response starts to be regulated and shut down
    • Modified TH2 response - production of IL-10, TReg cells and IgG4 antibodies
21
Q

How do ticks infect their hosts?

A
  • Tick sticks its mouth into skin and releases “cement” which keeps it in the skin
  • Once stuck in skin it feeds off blood
  • Tick also releases toxins into body which produces a block in motor nerve fibres
22
Q

What are some of the diseases transmitted by hard ticks?

A
  • Tick typhus
  • Viral encephalitis
  • Viral fevers
  • Viral haemorrhagic fevers
  • Tick paralysis
23
Q

What are some of the diseases transmitted by soft ticks?

A
  • Q fever
  • Relapsing fever
24
Q

What are some characteristics of head lice?

A
  • Suck blood from scalp and lay eggs on hair
  • Easily spread by close contact, sharing of combs and brushes etc.
25
Q

What are some characteristics of body lice?

A
  • Suck blood from body and lay eggs on clothing
  • Spread via bodily contact, sharing of clothing or bedding
  • Can cause vector diseases such as:
    • Epidemic typhus
    • Trench fever
    • Relapsing fever
26
Q

What are some characteristics of pubic lice?

A
27
Q

Describe the life cycle of the botfly (Dermatobia hominis)

A
  • Mid-flight it grabs a mosquito and lays its eggs on the mosquito
  • Mosquito goes on to bite animal, the change in temperature causes eggs to hatch and larvae to invade the skin
28
Q

What is Myiasis?

A
  • Parasitic infestation of the body of a live animal by Botfly larvae (maggots) which grow inside the host while feeding on its tissue
29
Q

What drugs can be used to treat infections caused by different types of parasites?

A
  • Tinidazole has shorter dose regimens compared to other drugs used to treat protozoa infections - 1g once a day for 3 days
  • Metronidazole has more adverse reaction and has longer dose course - 1 or 2 week course
  • Benznidazole used to treat chagas disease but causes very bad adverse reactions so people can’t complete course
  • Heavy metals used to treat Leishmaniasis
30
Q

How can parasitic infections be controlled?

A
  • Behaviours
    • Education
    • Introducing Hand washing and hygiene behaviours
  • Environmental interventions
    • Spraying of residual insecticides for household vectors
    • Mosquito nets for malaria
    • Improved housing
    • Sewage disposal and potable water
    • Drainage of swamps
  • Poverty reduction
    • Micro-financing
31
Q

Why must treatment of parasitic infections in endemic settings be given periodically over long periods of time?

A
  • Because re-infections are rapid and because the treatment kills larval rather than adult stages
32
Q

Give some examples of treatments of parasitic infections given periodically over a long period of time

A
  • A single dose of albendazole is given to high risk groups such as school children up to every 4 months to control STH infections
  • A single dose of ivermectin is given to endemic communities (mass drug administration) every 6 or 12 months to control onchocerciasis
  • A single dose of praziquantel is given to endemic communities (mass drug administration) every 6 or 12 months to control schistosomiasis