Difference between revisions of "Trypanosomosis"

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Also Known As '''''Nagana''''''''''Typanosomiasis''''''''''Chagas' Disease''''''''''Sleeping sickness'''''—'''''Parrot Sickness
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Also Known As: '''''Nagana — Trypanosomiasis — Chagas' Disease — Sleeping Sickness — Parrot Sickness  Dourine'''''
  
 
==Introduction==
 
==Introduction==
[[File:Trypanosoma brucei.gif|thumb|300px|right|Schematic diagram of Trypanosoma brucei]]
+
[[File:Trypanosoma.jpg|thumb|200px|right|''T.cruzi''. Wikimedia Commons]]
 
Trypanosomosis is a disease caused by '''[[Protozoa | protozoan]]''' pathogens of the genus [[Trypanosoma]]. They are '''obligate parasites''' and can infect mammals, birds, reptiles, amphibians and fish.
 
Trypanosomosis is a disease caused by '''[[Protozoa | protozoan]]''' pathogens of the genus [[Trypanosoma]]. They are '''obligate parasites''' and can infect mammals, birds, reptiles, amphibians and fish.
  
 
Trypanosomes are divided into two categories depending upon their lifecycle:
 
Trypanosomes are divided into two categories depending upon their lifecycle:
'''Stercorarian trypanosomes''' develop within an '''insect'' vector and are transmitted to mammals in the faeces of the vector.  
+
'''Stercorarian trypanosomes''' develop within an '''insect''' vector and are transmitted to mammals in the faeces of the vector.  
  
'''Salivarian''' trypanosomes develop within '''[[Glossinidae | tsetse flies]]''' and mammals are infected through their bites.
+
'''Salivarian''' trypanosomes develop within '''[[Glossinidae |tsetse flies]]''' and mammals are infected through their bites.
 
   
 
   
 +
For more information about the various species see [[Trypanosoma]] page.
 +
 
Trypanosomosis causes a '''wasting disease''' in cattle and '''sleeping sickness''' in humans.
 
Trypanosomosis causes a '''wasting disease''' in cattle and '''sleeping sickness''' in humans.
  
'''''T. cruzi''''' is the most important species in veterinary medicine.
+
'''''T. cruzi''''' is the cause of Chagas disease in humans but can also  affect dogs, cats and pigs. ''T. vivax'' and ''T. congolense'' are the main pathogens of cattle. In horses, ''T. equiperdum'' is the cause of '''Dourine'''.
  
Trypanosomosis is '''notifiable''' to the World Organisation for Animal Health [http://www.oie.int/ (OIE)]
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Trypanosomosis is '''notifiable''' to the World Organisation for Animal Health [http://www.oie.int/ (OIE)].
  
 
==Signalment==
 
==Signalment==
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'''Calves''' less than a year old are more resistant than adults, but lambs and kids appear more susceptible to ''T. congolense'' infections.  
 
'''Calves''' less than a year old are more resistant than adults, but lambs and kids appear more susceptible to ''T. congolense'' infections.  
 
Cattle 6-9yrs old appear most susceptible to trypanosomosis.
 
Cattle 6-9yrs old appear most susceptible to trypanosomosis.
 
==Causative Organisms==
 
===Salivarian Species===
 
''T. brucei'' affects '''all domestic mammals''', including small and farm species, and humans. It also causes a specific [[Protozoal Skin Infections - Donkey|skin disease in donkeys]].
 
 
''T. vivax'' infects ruminants, horses and camels causing significant disease.
 
 
''T. equiperdum'' causes '''venereal''' equine disease '''dourine'''. It is the only trypanosome that does not immediately require an insect vector for transmission, being spread through coitus.
 
 
''T. simiae'' causes fatal pyrexia in '''pigs''' while ''T. congolense'' is milder in the same species.
 
 
''T. congolense'' can also affect '''dogs and cats''' causing acute fever, anaemia and neurological signs.
 
 
''T. evansi'' also affects all domestic mammals.
 
 
===Stercorarian Species===
 
'''''T. cruzi''''' occurs in '''South America''' where it is transmitted by a triatomid (kissing)  bug and infects armadillos, possums and humans. It is known as '''''Chagas’ Disease'''''.
 
A similar acute disease is thought to be caused by ''T. cruzi'' in dogs in the USA.
 
 
''T. melophagum'' and ''T. Theileri'' are '''non-pathogenic''' species present in the '''UK''' infecting cattle, buffalo and antelope. Stress and concurrent disease are thought to be contributors to the development of clinical disease from ''T. theileri''.
 
  
 
==Transmission==
 
==Transmission==
 +
[[File:Tsetse fly.jpeg|thumb|200px|right|Tsetse fly]]
 
Trypanosomosis is spread by '''[[Glossinidae|Tsetse flies]]''' and other insect vectors.
 
Trypanosomosis is spread by '''[[Glossinidae|Tsetse flies]]''' and other insect vectors.
 +
[[File:Triatoma infestans.jpg|thumb|200px|right|Triatomid - "kissing bug". (WHO - Wikimedia Commons)]]
 +
[[Tabanidae | Horse flies]]  and [[Stomoxys calcitrans |stable flies]] can also act as mechanical vectors for some [[Trypanosoma | ''trypanosoma'']] species, but the parasites cannot undergo lifecycle development within these hosts.
  
[[Tabanidae | Horse flies]]  and [[Stomoxys calcitrans | stable flies]] can also act as mechanical vectors for some [[Trypanosoma | ''trypanosoma'']] species, but the parasites can not undergo lifecycle development within these hosts.
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''T. vivax'' and ''T. evansi'' are reported to achieve transplacental transmission. <ref>Ikede, B. O., Loso, G. J.(1972). '''Hereditary transmission of Trypanosoma vivax'''. Brit Vet J, 128:i-ii</ref>
 
 
''T. vivax'' and ''T. evansi'' are reported to achieve Transplacental transmission. <ref>Ikede, B. O., Loso, G. J.(1972). '''Hereditary transmission of Trypanpsoma vivax'''. Brit Vet J, 128:i-ii</ref>
 
  
 
==Distribution==
 
==Distribution==
 
Worldwide
 
Worldwide
  
''T. brucei'', ''T. uniforme'', ''T. congolense'' and ''T. simiae'' are found only in the tsetse fly belt of Africa due to the restricted spread of their vector.
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''T. brucei'', ''T. uniforme'', ''T. congolense'' and ''T. simiae'' are found only in the tsetse fly belt of Africa due to the restricted spread of their vector. ''T. vivax'' is more widespread occurring in Sub-saharan Africa as well as South America.
  
 
==Clinical Signs==
 
==Clinical Signs==
Clinical disease varies widely with death occurring from 1 week to months after infection. ''T. vivax'' is known for its rapid mortality while ''T. brucei'' and ''T. congolense'' hosts often survive for prolonged periods. Infection of large numbers of insect vectors is common in these circumstances.
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Clinical disease varies widely with death occurring from 1 week to months after infection.  
 +
''T. vivax'' is known for its rapid mortality while ''T. brucei'' and ''T. congolense'' hosts often survive for prolonged periods. Infection of large numbers of insect vectors is common in these circumstances.
 +
 
 
Significant losses may also be caused by increased susceptibility and prevalence of other concurrent diseases where trypanosomosis is present.  
 
Significant losses may also be caused by increased susceptibility and prevalence of other concurrent diseases where trypanosomosis is present.  
Multisystemic signs can be seen in any species so diagnosis from clinical examination is often impossible as no pathognomic signs are evident.
+
 
 +
Multisystemic signs can be seen in any species so diagnosis from clinical examination is often impossible as no pathognomonic signs are evident.
  
 
===Ruminants===
 
===Ruminants===
Enlarged '''[[Lymph Nodes - Anatomy & Physiology|lymph nodes]]''' and '''[[Spleen - Anatomy & Physiology|spleen]]'''.  
+
Enlarged '''[[Lymph Nodes - Anatomy & Physiology|lymph nodes]]''' and '''[[Spleen - Anatomy & Physiology|spleen]]''' are the most common sign. Later in the disease course the lymph nodes and spleen shrink due to '''lymphoid exhaustion'''.  
Later in the disease course the [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] and [[Spleen - Anatomy & Physiology|spleen]] shrink due to '''lymphoid exhaustion'''.  
 
  
'''Haemolytic anaemia''' is a cardinal feature.
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'''Haemolytic anaemia''' is a cardinal feature. Chronic infection causes '''[[:Category:Heart Failure|heart failure]]''' and associated signs and death.
  
Chronic infection causes '''heart failure''' and associated signs and death.
+
Plasma cell hypertrophy and '''hypergammaglobulinaemia''' are evident on haematology and biochemistry.
  
Plasma cell hypertrophy and hypergammaglobulinaemia are evident on haematology and biochemistry.
+
Emaciation, '''abortion''', premature births and infertility are features, and '''orchitis''' in males reduces fertility.
  
Emaciation
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===Horses===
 +
'''Oedema''' of the '''limbs''' and '''genitalia''' is very common.
  
Abortion, premature births and infertility are features, and orchitis in males reduces fertility also.
+
'''Dourine''' – genital and abdominal '''oedema''', paraphimosis, '''urticarial plaques''' known as “silver dollar spots” and neurological signs may all be present. The disease is usually mild and recurrent but can be fatal.
 
 
===Horses===
 
'''Oedema''' of the '''limbs''' and '''genitalia'''.
 
'''Dourine''' – genital and abdominal oedema, paraphimosis, urticarial plaques known as “silver dollar spots” and neurological signs. Disease is usually mild and recurrent but can be fatal.
 
  
 
===Donkeys===
 
===Donkeys===
[[Protozoal Skin Infections - Donkey|Skin infections]]
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See [[Protozoal Skin Infections - Donkey|donkey skin infections]] page for details.
  
 
===Dogs and Cats===
 
===Dogs and Cats===
'''Pyrexia''', myocarditis, '''myositis''', corneal opacity and '''neurological signs'''.
+
'''Pyrexia''', myocarditis, '''myositis''', corneal opacity and occasionally '''neurological signs''' may all be present.
  
 
==Diagnosis==
 
==Diagnosis==
 
 
[[File:Trypanosomes blood.gif|thumb|200px|right|Trypanosomes in blood]]
 
[[File:Trypanosomes blood.gif|thumb|200px|right|Trypanosomes in blood]]
Microscopic identification on trypanosome parasites in the host blood on a '''smear''' with Giemsa staining.
+
Microscopic identification on trypanosome parasites in the host blood on a '''smear''' with Giemsa staining is commonly performed. Where low levels of parasitaemia are present, filtration or haemolysis of a whole blood sample may be required and motile trypanosomes may be demonstrable in a haematocrit tube at the '''plasma: buffy coat''' interface.
 
 
Where low levels of parasitaemia are present, filtration or haemolysis of a whole blood sample may be required and motile trypanosomes may be demonstrable in a haematocrit tube at the '''plasma: buffy coat''' interface.
 
  
 
On '''post-mortem''' examination, carcasses are often pale and oedematous due to anaemia and emaciation. Degenerative lesions can be found on the heart, liver, lymph nodes, testes, brain, conjunctiva, cornea, spleen, kidney and endocrine organs.
 
On '''post-mortem''' examination, carcasses are often pale and oedematous due to anaemia and emaciation. Degenerative lesions can be found on the heart, liver, lymph nodes, testes, brain, conjunctiva, cornea, spleen, kidney and endocrine organs.
  
 
Many other seroimmunological techniques are also available variably in laboratories.
 
Many other seroimmunological techniques are also available variably in laboratories.
 +
 
==Treatment==
 
==Treatment==
A variety of drugs can be used to treat trypanosomosis including '''diminazene''', '''homidium''', '''isometadium''', '''suramin'' and '''melarsomine'''.
+
A variety of drugs can be used to treat trypanosomosis including '''diminazene, homidium, isometadium, suramin''' and '''melarsomine'''.
Diminazene acetrate is most commonly used and is frequently curative. It however causes frequent local reactions in horses so should be given in multiple deep muscular sites and massaged well. The drug is also contraindicated in dogs and camels due to vascular damage. Diminazene also has a prophylactic effect for up to 3 months.
+
 
 +
'''Diminazene aceturate''' is most commonly used and is frequently '''curative'''. It however causes frequent local reactions in horses so should be given in multiple deep muscular sites and massaged well. The drug is also ''contraindicated in dogs and camels'' due to vascular damage. Diminazene also has a prophylactic effect for up to 3 months.
 +
 
  
Resistance is increasing in Africa to trypanosomicidal drugs so multiple treatments may be required in some areas.  
+
'''Resistance''' is increasing in Africa to trypanosomicidal drugs so multiple treatments may be required in some areas.
  
 
==Control==
 
==Control==
 +
'''Separation''' of livestock and wild animals is effective but difficult.
  
Separation of livestock and wild animals is effective but difficult.
+
Use of '''trypanotolerant''' livestock breeds is the only option is some areas where economic restraints prevent constant treatment and control.  
  
Use of trypanotolerant livestock breeds is the only option is some areas where economic restraints prevent constant treatment and control.  
+
'''[[Glossinidae |Tsetse fly]] control''' by sprays, traps, dips and release of sterile male flies is effective but expensive and time-consuming.
  
[[Glossinidae | Tsetse fly]] control by sprays, traps, dips and release of sterile male flies is effective but expensive and time consuming.
+
Prophylactic drug therapy is also effective but costly.
 
 
Prophylactic drug therapy with quinapyramine or homidium is effective.  
 
  
 +
{{Learning
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|flashcards = [[Trypanosomosis Flashcards]]
 +
}}
  
 
==References==
 
==References==
 
<references/>
 
<references/>
Animal Health & Production Compendium,'''Trypanosomiasis datasheet''', accessed 05/06/2011 @ http://www.cabi.org/ahpc/
 
  
 
Merck Veterinary Manual, '''Tsetse-transmitted Trypanosomiasis''' accessed online 03/06/2011 @ http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/10413.htm
 
Merck Veterinary Manual, '''Tsetse-transmitted Trypanosomiasis''' accessed online 03/06/2011 @ http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/10413.htm
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 +
{{CABI source
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|datasheet = [http://www.cabi.org/ahpc/Default.aspx?site=160&page=2144&LoadModule=datasheet&CompID=3&dsID=60779  trypanosomosis]
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|date = 5 June 2011
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}}
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<br><br><br>
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{{Nick Lyons
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|date = 15 October 2011}}
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{{OpenPages}}
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[[Category:Cardiovascular Diseases - Cattle]][[Category:Cardiovascular Diseases - Horse]][[Category:Lymphoreticular and Haematopoietic Diseases - Cattle]][[Category:Lymphoreticular and Haematopoietic Diseases - Horse]][[Category:Reproductive Diseases - Horse]][[Category:Reproductive Diseases - Cattle]]
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[[Category:CABI Expert Review Completed]][[Category:CABI AHPC Pages]]
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[[Category:Nick Lyons reviewed]]
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[[Category:Cardiology Section]]

Latest revision as of 17:35, 17 October 2013


Also Known As: Nagana — Trypanosomiasis — Chagas' Disease — Sleeping Sickness — Parrot Sickness — Dourine

Introduction

T.cruzi. Wikimedia Commons

Trypanosomosis is a disease caused by protozoan pathogens of the genus Trypanosoma. They are obligate parasites and can infect mammals, birds, reptiles, amphibians and fish.

Trypanosomes are divided into two categories depending upon their lifecycle: Stercorarian trypanosomes develop within an insect vector and are transmitted to mammals in the faeces of the vector.

Salivarian trypanosomes develop within tsetse flies and mammals are infected through their bites.

For more information about the various species see Trypanosoma page.

Trypanosomosis causes a wasting disease in cattle and sleeping sickness in humans.

T. cruzi is the cause of Chagas disease in humans but can also affect dogs, cats and pigs. T. vivax and T. congolense are the main pathogens of cattle. In horses, T. equiperdum is the cause of Dourine.

Trypanosomosis is notifiable to the World Organisation for Animal Health (OIE).

Signalment

Some breeds appear trypanotolerant and able to resist clinical disease and anaemia, such as African buffalo and N’dama and Keteku cattle.

Calves less than a year old are more resistant than adults, but lambs and kids appear more susceptible to T. congolense infections. Cattle 6-9yrs old appear most susceptible to trypanosomosis.

Transmission

Tsetse fly

Trypanosomosis is spread by Tsetse flies and other insect vectors.

Triatomid - "kissing bug". (WHO - Wikimedia Commons)

Horse flies and stable flies can also act as mechanical vectors for some trypanosoma species, but the parasites cannot undergo lifecycle development within these hosts.

T. vivax and T. evansi are reported to achieve transplacental transmission. [1]

Distribution

Worldwide

T. brucei, T. uniforme, T. congolense and T. simiae are found only in the tsetse fly belt of Africa due to the restricted spread of their vector. T. vivax is more widespread occurring in Sub-saharan Africa as well as South America.

Clinical Signs

Clinical disease varies widely with death occurring from 1 week to months after infection. T. vivax is known for its rapid mortality while T. brucei and T. congolense hosts often survive for prolonged periods. Infection of large numbers of insect vectors is common in these circumstances.

Significant losses may also be caused by increased susceptibility and prevalence of other concurrent diseases where trypanosomosis is present.

Multisystemic signs can be seen in any species so diagnosis from clinical examination is often impossible as no pathognomonic signs are evident.

Ruminants

Enlarged lymph nodes and spleen are the most common sign. Later in the disease course the lymph nodes and spleen shrink due to lymphoid exhaustion.

Haemolytic anaemia is a cardinal feature. Chronic infection causes heart failure and associated signs and death.

Plasma cell hypertrophy and hypergammaglobulinaemia are evident on haematology and biochemistry.

Emaciation, abortion, premature births and infertility are features, and orchitis in males reduces fertility.

Horses

Oedema of the limbs and genitalia is very common.

Dourine – genital and abdominal oedema, paraphimosis, urticarial plaques known as “silver dollar spots” and neurological signs may all be present. The disease is usually mild and recurrent but can be fatal.

Donkeys

See donkey skin infections page for details.

Dogs and Cats

Pyrexia, myocarditis, myositis, corneal opacity and occasionally neurological signs may all be present.

Diagnosis

Trypanosomes in blood

Microscopic identification on trypanosome parasites in the host blood on a smear with Giemsa staining is commonly performed. Where low levels of parasitaemia are present, filtration or haemolysis of a whole blood sample may be required and motile trypanosomes may be demonstrable in a haematocrit tube at the plasma: buffy coat interface.

On post-mortem examination, carcasses are often pale and oedematous due to anaemia and emaciation. Degenerative lesions can be found on the heart, liver, lymph nodes, testes, brain, conjunctiva, cornea, spleen, kidney and endocrine organs.

Many other seroimmunological techniques are also available variably in laboratories.

Treatment

A variety of drugs can be used to treat trypanosomosis including diminazene, homidium, isometadium, suramin and melarsomine.

Diminazene aceturate is most commonly used and is frequently curative. It however causes frequent local reactions in horses so should be given in multiple deep muscular sites and massaged well. The drug is also contraindicated in dogs and camels due to vascular damage. Diminazene also has a prophylactic effect for up to 3 months.


Resistance is increasing in Africa to trypanosomicidal drugs so multiple treatments may be required in some areas.

Control

Separation of livestock and wild animals is effective but difficult.

Use of trypanotolerant livestock breeds is the only option is some areas where economic restraints prevent constant treatment and control.

Tsetse fly control by sprays, traps, dips and release of sterile male flies is effective but expensive and time-consuming.

Prophylactic drug therapy is also effective but costly.


Trypanosomosis Learning Resources
FlashcardsFlashcards logo.png
Flashcards
Test your knowledge using flashcard type questions
Trypanosomosis Flashcards


References

  1. Ikede, B. O., Loso, G. J.(1972). Hereditary transmission of Trypanosoma vivax. Brit Vet J, 128:i-ii

Merck Veterinary Manual, Tsetse-transmitted Trypanosomiasis accessed online 03/06/2011 @ http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/10413.htm


CABIlogo

This article was originally sourced from The Animal Health & Production Compendium (AHPC) published online by CABI during the OVAL Project.

The datasheet was accessed on 5 June 2011.










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