Dog and Cat CVRS Nematodes + Linguatula

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34 Terms

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Dog and Cat CVRS Nematodes Summary

(lungworms and heart worms)

Metastrongyles (Lungworm)

  • mollusc intermediate host

  • not zoonotic

  1. Angio-strongylus vasorum→ Dog lungworm

    • french heartworm/lungworm

  2. Os-ler-us osleri

    • atypical (no intermediate host), dog,

  3. Ae-leuro-strongylus ab-stru-sus→ Cat lungworm

Filaroidea (Heartworm)

  1. Dirofilaria immi-tis- Dog and cat

    • indirect lifecycle

    • zoonotic mosquito intermediate host

    • no eggs → microfilaria (preL1)

    • imported in UK

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Penta-sto-mid parasite

  • infects adult nasal cavity and frontal sinuses of canids

  • closely resembles arthropod (+ worm)

  • zoonotic

Lingua-tula serrata

  • have nymphs and adults

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Angio-strongylus vasorum appearance

  • Slender, <2.5cm

  • Separate males/females

    • Females like Haemonchus contortus (ruminant GI nematode) → red barber’s pole (uterus + intestine)

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Angio-strongylus vasorum hosts

  • Final host: canid (dogs + foxes)

    • Young dogs more prone

    • Foxes wild reservoir

      • US- sporadic fox and coyote

  • Intermediate host: mollusc

  • (rat version is zoonotic)

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Angio-strongylus vasorum target organs

  • French lungworm → pulmonary arteries

  • French heartworm → RHS heart

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Angiostrongylus vasorum prepatent period

6-10 weeks

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Angio-strongylus vasorum life cycle [7]

  1. Mollusc eats L1 from canid faeces

  2. L1 → L3 in mollusc

  3. Dog eats mollusc or slime trail with infective L3

  4. L3 travels to gut mesenteric lymph nodes → mature to L4

  5. L4 lymph nodes → pulmonary artery/ right ventricle migration → mature to L5

  6. L5 lay eggs → hatch to L1 in lung capillaries

  7. L1 coughed up and swallowed → egestion in faeces

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Angiostrongylus vasorum disease symptoms

  • Can be subclinical

    • esp. foxes → natural host with resistance

  • 3 clinical syndromes in dogs:

    1. Cardiorespiratory

      • Blockage of blood vessels by worms

      • Inflammation of lungs by L1 breaking into alveoli

    2. Coagulopathy

      • Reduced platelet numbers and clotting factors

      • Bleeding into skin, eyes, body cavity, lungs

    3. Neurological

      • Result of coagulopathy → bleed into brain

      • Rarely larvae in brain

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Angiostrongylus diagnosis

  • Clinical signs (if not subclinical) → e.g. subconjunctival haemorrhage due to coagulopathy

  • Chest radiograph → enlarged RHS heart

  • L1 detected faeces and sputum

  • Blood tests

    • Lateral flow → subclinical infection

    • Coagulation test

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Angiostrongylus vasorum treatment

  • Anthelmintics

  • Supportive care

    • Blood transfusion + oxygen

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Angiostrongylus vasorum epidemiology

  • Worldwide emerging disease

  • Hotspots (endemic foci) → prophylactic treatment

    • SE England

    • S Wales

  • Prevalent in W Europe

  • Sporadic cases

    • Canada

    • North America

    • South America

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Oslerus osleri hosts

  • Special metastrongyle → NO INTERMEDIATE HOST → direct lifecycle

  • Canid host

  • Associated with breeding kennels and racing greyhounds

  • L1 infective stage

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Oslerus osleri organs

Adult worms form tracheal nodules

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Oslerus osleri life cycle [4]

  1. L1 (infective) transmitted in saliva from bitch to puppies when grooming

  2. L1 → L2 in gut

  3. L2 migrates gut → lungs

  4. Matures into adult in lungs and trachea

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Oslerus osleri disease symptoms

Usually asymptomatic but may have chronic dry debilitating cough

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Ae-luro-strongylus ab-stru-sus hosts

  • 1cm adult worm

  • not very common

  • Intermediate: mollusc → rodent host

    • rodent eats mollusc

  • Final: cat

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Ae-luro-strongylus ab-stru-sus target organ

Adults live in cat lung parenchyma and small bronchioles

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Aelurostrongylus abstrusus life cycle [5]

  1. L1 egested in cat faeces

  2. L1 eaten by mollusc

  3. Mollusc eaten by rodent

  4. Rodent eaten by cat

    • Cats unlikely to directly eat mollusc → need rodent intermediate

  5. Adult worm lives in lung parenchyma and small bronchioles

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Aelurostrongylus abstrusus clinical signs

  • Low pathogenicity, usually asymptomatic

    • More clinical effects in immunocompromised cats (e.g. FIV)

  • Chronic mild cough possible

  • Dyspnoea possible in heavy infection

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Diro-filaria immi-tis appearance

  • Long worms, females bigger

    • M 15cm, F 30cm

  • Form mesh → may block blood vessels

  • Female Dirofilaria → release microfilaria (preL1) into blood

    • no eggs

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Dirofilaria immitis hosts

  • Intermediate: mosquito

    • zoonotic (but rare)

  • Final: dog

  • (not natural: cat, ferret, human)

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Dirofilaria microfilaria frequency in dogs

  • Only 60% infected dogs

  • 15% killed by host immunity

  • 25% cannot reproduce

    • sexually immature

    • only 1 worm

    • all worms same sex

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Dirofilaria immitis target organs

  • Dog RHS heart

  • Pulmonary arteries

  • Posterior vena cava

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Dirofilaria immitis life cycle [6]

  1. Female mosquito feeds on host transmitting L3

  2. L3 migrate from blood → subcutaneous tissue to mature

    • 4 month period

  3. Young adult worms (from mosquito bite) migrate from subcutaneous tissueheart and vessels

    • Can survive and build up for years

  4. Worms mate and release microfilariae into blood

    • Microfilariae can survive ~2 years

  5. Female mosquito ingests microfilariae from bloodstream

  6. Microfilariae → L1 → L3 inside mosquito

    • Takes 2 weeks

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Dirofilaria immitis dog clinical signs

  • Clinical signs usually in dogs >2 years old

    • Long prepatent period

    • Worm buildup takes time

  • Adult mesh obstructs blood flow in high numbers → congestive heart failure

    • Exercise intolerance

    • Acute collapse

    • Fatality

    • Abdominal ascites

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Dirofilaria immitis cat clinical signs

  • Not natural host → reduced susceptibility

  • Adults shorter lifespan (<2 years)

    • Fewer adult worms present in heart

  • Transient microfilaraemia

  • Usually respiratory signs

    • Parasites in distal pulmonary arteries → pulmonary pneumonia

  • Larvae in other tissue → eye

    • Potentially fatal (CNS)

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Dirofilaria immitis zoonosis

  • dead end host

    • Microfilaria enter subcutaneous tissue → right ventricle → die

    • Embolise pulmonary vessels

  • Human infection rare

  • small pulmonary infarction (pulmonary vessel embolism) = coin lesion

    • can be mistaken for neoplasia on radiographs due to nodular appearance

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Dirofilaria immitis diagnosis

  • Blood microscopy and serology for microfilaria

    • Only works for 60% dogs

  • Ultrasound → adult worms

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Dirofilaria immi-tis Treatment

  1. Doxy-cycline

    • kills symbiotic intracellular Wol-ba-chia bacteria

    • inhibits embryogenesis and long term survival of parasite in body

  2. Macro-cyc-lic lactones (treatment + prophylaxis)

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Linguatula serrata (pentastomid) hosts

  • NOT A NEMATODE

  • imported to UK

  • Intermediate: herbivores

  • Final: canid (+ human → zoonotic)

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Linguatula serrata target organ

Canid nasal cavity and frontal sinus

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Linguatula serrata life cycle [4]

  1. Raw offal of herbivore host (containing nymphs) eaten by canid

  2. Nymphs migrate up oesophagus → nasopharynx for maturation

  3. Mature adults lay eggs in nasopharynx

  4. Eggs released in nasal secretions (e.g. sneezing) or faeces to infect intermediate hosts

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Linguatula serrata clinical signs

Rhino-sinus-itis (sneezing, nasal discharge etc)

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Linguatula serrata epidemiology

Tropical regions

  • Central Asia

  • N. Africa

  • Middle East

  • E. Europe

Imported into UK