Difference between revisions of "Leishmania"
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− | == | + | <br> |
+ | ==''Leishmania''== | ||
[[Image:Leishmania Life Cycle.jpg|thumb|right|150px|Leishmania Life Cycle - Wikimedia Commons]] | [[Image:Leishmania Life Cycle.jpg|thumb|right|150px|Leishmania Life Cycle - Wikimedia Commons]] | ||
[[Image:Leishmania donovani.jpg|thumb|right|150px|''Leishmania donovani'' in bone marrow cell - Dr. L.L. Moore, Jr.]] | [[Image:Leishmania donovani.jpg|thumb|right|150px|''Leishmania donovani'' in bone marrow cell - Dr. L.L. Moore, Jr.]] | ||
− | [[Image:Leishmania tropica.jpg|right|thumb|150px|''L. tropica'' | + | [[Image:Leishmania tropica.jpg|right|thumb|150px|''L. tropica'' - Yutaka Tsutsumi, M.D., Professor, Department of Pathology, Fujita Health University School of Medicine]] |
− | ''Leishmania spp. | + | *''Leishmania'' spp. are intracellular parasites of [[Macrophage|macrophages]] |
− | + | ||
− | + | *Are closely related to ''Trypanosoma'' spp. | |
− | + | ||
+ | *Cause diseases in humans, dogs and wild animals | ||
+ | |||
+ | *Present in southern Europe, Africa, Asia and south America | ||
+ | |||
+ | *Can cause both cutaneous and visceral diseases | ||
+ | |||
+ | '''Recognition''' | ||
+ | *Ovoid shaped | ||
+ | |||
+ | *Possesses a rod-shaped kinetoplast | ||
+ | |||
+ | *Has a rudimentary flagellum which does not project beyond the cell margin | ||
+ | |||
+ | *After the amastigote has transformed into a promastigote inside the [[Biting Flies#Psychodidae|sand fly]], the kinetoplast is situated in the posterior of the body | ||
− | + | '''Life Cycle''' | |
− | '' | + | *Transmitted by blood sucking [[Psychodidae|sand flies]] |
+ | **''Phlebotomus'' spp. in the Old World | ||
+ | **''Lutzomyia'' spp. in the New World | ||
− | + | *The amastigote (morphological form) is found in vertebrate [[Macrophage|macrophages]] | |
− | The | ||
− | + | *Ingested by [[Psychodidae|sand fly]] during feeding | |
+ | **Transforms in [[Insecta|insect]] gut | ||
− | + | *Multiplies and migrates to [[Insecta|insect]] proboscis | |
+ | **Inoculated during feeding | ||
+ | **Can be transmitted percutaneously if [[Psychodidae|sand fly]] crushed on skin | ||
− | + | *Invades [[Macrophage|macrophages]] and reverts to amastigote | |
− | |||
− | + | *Multiplies by binary fission | |
− | + | '''Pathogenesis''' | |
− | + | *Infection of vertebrate host | |
+ | **Produces foci of proliferating ''Leishmania''-infected [[Macrophage|macrophages]] in skin ('''cutaneous''') or internal organs ('''visceral''') | ||
− | + | *Very long incubation period | |
+ | **Months to years | ||
− | + | *Many infected dogs are asymptomatic | |
− | |||
− | + | *Cutaneous form | |
− | + | **Produces areas of ulceration on pinnae of [[Ear - Anatomy & Physiology|ears]], eyelids or on the [[Lips - Anatomy & Physiology|lips]] | |
− | + | *Visceral form causes chronic wasting condition | |
− | + | **Generalised eczema | |
+ | ***Loss of hair around eyes producing 'spectacle' effect | ||
+ | **Intermittent fever | ||
+ | **Generalised lymphadenopathy | ||
− | + | *Long periods of remission followed by recurrence of clinical signs is not uncommon in infections | |
− | + | *Involved in [[Parasitic skin infections - Pathology#Protozoa|skin infections]] | |
− | | | + | |
− | | | + | '''Epidemiology''' |
− | [[ | + | *Disease dependent on [[Psychodidae|sand fly]] vectors |
− | | | + | **E.g. Common in dogs around the Mediterranean coast, foci around southern Europe and around Madrid |
− | + | ||
+ | *Reservoirs of infection | ||
+ | **E.g. Wild animals such as rodents and stray dogs | ||
+ | |||
+ | *Mechanisms of transmission | ||
+ | **[[Psychodidae|sand fly]] bite | ||
+ | **Rarely through direct contact | ||
+ | |||
+ | *Leishmaniasis in British dogs | ||
+ | **Susceptible to infection if exposed whilst abroad in endemic areas as have no immunity | ||
+ | **No [[Psychodidae|sand flies]] in Britain but dogs have become infected whilst in contact with infected imported animals | ||
+ | |||
+ | '''Diagnosis''' | ||
+ | *Demonstrate ''Leishmania'' organisms | ||
+ | **In skin scraping or smears | ||
+ | **In joint fluid, [[Lymph Nodes - Anatomy & Physiology|lymph node]] or [[Bone Marrow - Anatomy & Physiology|bone marrow]] biopsies | ||
+ | |||
+ | '''Treatment and Control''' | ||
+ | *Chemotherapy | ||
+ | **Prolonged treatment, expensive, suppresses infection | ||
+ | **Does not cure infection | ||
+ | |||
+ | *Prevent [[Psychodidae|sand flies]] biting | ||
+ | **Collars, sprays containing [[Ectoparasiticides|insecticide]] with repellent effect | ||
+ | |||
+ | *Destruction of infected and stray dogs | ||
+ | **[[Psychodidae|Sand flies]] biting infected dogs may spread the disease to other dogs, humans and wildlife | ||
+ | **There is a slight possibility of transmission to humans by direct contact | ||
+ | |||
+ | ==''Trypanosoma''== | ||
+ | [[Image:Trypanosoma.jpg|thumb|right|150px|''Trypanosoma cruzi'' - CDC/Dr. Myron G. Schultz]] | ||
+ | [[Image:T.cruzi in monkey heart.jpg|thumb|right|150px|''T. cruzi'' in monkey heart - Dr. L.L. Moore, Jr.]] | ||
+ | [[Image:T.cruzi Life cycle.jpg|thumb|right|150px|''T. cruzi'' Life Cycle Diagram - Wikimedia Commons]] | ||
+ | [[Image:Triatoma infestans.jpg|thumb|right|150px|''Triatoma infestans'' the Kissing bug - WHO Wikimedia Commons]] | ||
+ | [[Image:Chagas endemic zones 2005.jpg|thumb|right|150px|Chagas endemic zones 2005 - Wikimedia Commons]] | ||
+ | [[Image:Ndama.jpg|thumb|right|150px|N'dama - Trypanotolerant West African Bos taurus - Wikimedia Commons]] | ||
+ | *Protozoal parasites found in the blood and tissues of vertebrates | ||
+ | |||
+ | *Worldwide distribution | ||
+ | |||
+ | *Causes sleeping sickness in humans | ||
+ | |||
+ | *Particularly seen in sub-Saharan Africa | ||
+ | **Affects cattle production | ||
+ | **Causes Nagana (Wasting disease) | ||
+ | |||
+ | *Divided into two groups depending on the mode of development in the insect vector | ||
+ | **'''Salivarian''' | ||
+ | ***Multiply in the foregut and proboscis | ||
+ | ***Transmitted via inoculation during feeding | ||
+ | ***Transmitted by [[Glossinidae|''Tsetse'' flies]] | ||
+ | ***Also known as '''anterior station development''' | ||
+ | **'''Stercorarian''' | ||
+ | ***Multiply in the hindgut | ||
+ | ***Infective form migrates to the [[Rectum - Anatomy & Physiology|rectum]] | ||
+ | ***Transmitted via contamination of wounds with insect faeces | ||
+ | ***Also known as '''posterior station development''' | ||
+ | |||
+ | *All ''Trypansomes'' except for ''T. equiperdum'' have arthropod vectors | ||
+ | **''T. equiperdum'' is a venereally transmitted disease | ||
+ | |||
+ | *'''Non-cyclical''' transmission can also occur | ||
+ | **Mechanical transmission | ||
+ | **Transferred by interrupted feeding from one host to another | ||
+ | **Usually transmitted by [[Biting Flies|biting flies]], e.g. [[Tabanidae|''Tabanidae'']] and [[Stomoxys calcitrans|''Stomoxys'']] | ||
+ | |||
+ | '''Recognition''' | ||
+ | *Elongated, spindle shaped protozoa | ||
+ | |||
+ | *Between 8 and 39 μm in length | ||
+ | |||
+ | *Flagellate | ||
+ | **Flagellum runs the length of the body attached to the pellicle which forms an undulating membrane | ||
+ | |||
+ | *Kinetoplast present which contains the DNA of the single mitochondrion | ||
+ | |||
+ | '''Life Cycle''' | ||
+ | *Undergo morphological transformations in intermediate host before becoming infective for the next host | ||
+ | |||
+ | *Blood-sucking [[Biting Flies|flies]] ingest trypanosomes whilst taking a blood meal from an infected animal | ||
+ | **Trypanosomes multiply first in the gut of the [[Biting Flies|fly]] | ||
+ | |||
+ | *Salivarian trypanosomes are transmitted by [[Glossinidae|Tsetse flies]] | ||
+ | **Trypanosomes pass forward to the salivary glands where they transform into the infective stage | ||
+ | **Inoculated with saliva when [[Glossinidae|Tsetse fly]] next feeds on a host | ||
+ | |||
+ | *Stercorarian trypanosomes are transmitted by triatomid bugs, [[Tabanidae|tabanids]] and [[Biting Flies#Melophagus spp.|keds]] | ||
+ | **Trypanosomes pass back to the rectum | ||
+ | **Next host is infected when skin wounds are contaminated with infected [[Insecta|insect]] faeces | ||
+ | |||
+ | '''Pathogenesis''' | ||
+ | *Salivarian | ||
+ | **Causes wasting disease in cattle (nagana) | ||
+ | **Sleeping sickness in humans | ||
+ | |||
+ | *Stercorarian | ||
+ | **''T. cruzi'' most important in veterinary medicine | ||
+ | ***Occurs in South America | ||
+ | ***Infects armadillos, possums and humans | ||
+ | ***Causes Chagas' Disease | ||
+ | **Transmitted by a triatomid (kissing) bug | ||
+ | **Chronic infections are often fatal causing heart failure | ||
+ | **Non-pathogenic species are transmitted by [[Tabanidae|tabanids]] and [[Melophagus spp.|keds]] | ||
+ | ***''T. theileria'' and ''T. melophagium'' | ||
+ | |||
+ | *Enlarged [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] and [[Spleen - Anatomy & Physiology|spleen]] | ||
+ | **Causes lymphoid exhaustion | ||
+ | **Associated with plasma cell hypertrophy and hypergammaglobulinaemia | ||
+ | ***Due to an increase in [[Immunoglobulin M - WikiBlood|IgM]] | ||
+ | **With infections of increased duration, the [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] and [[Spleen - Anatomy & Physiology|spleen]] shrink due to exhaustion of their cellular elements | ||
+ | |||
+ | *Anaemia | ||
+ | **Red blood cells are removed from circulation ('''haemolytic''') | ||
+ | **Is a cardinal feature of the disease | ||
+ | |||
+ | *Degeneration and inflammation of multiple organs | ||
+ | **E.g. Skeletal muscle, myocardium and CNS | ||
+ | |||
+ | '''Clinical Signs''' | ||
+ | *In ruminants: | ||
+ | **Anaemia | ||
+ | **Enlargement of the [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] | ||
+ | **Progressive loss of body condition | ||
+ | **Fever and appetite loss occur during parasite peaks | ||
+ | **Chronic disease usually terminates in death of the animal if untreated | ||
+ | **Can cause abortion, infertility and decreased growth in herds | ||
+ | |||
+ | *In horses: | ||
+ | **Acute or chronic infections of ''T. brucei'' | ||
+ | **Oedema of the limbs and genitalia | ||
+ | |||
+ | *In pigs: | ||
+ | **''T. congolense'' infections are mild or chronic | ||
+ | **''T. simiae'' infections are hyperacute usually leading to death from pyrexia in a few days | ||
+ | |||
+ | *In dogs and cats: | ||
+ | **''T. brucei'' and ''T. congolese'' | ||
+ | **Acute infections | ||
+ | **Fever, anaemia, myocarditis, corneal opacity | ||
+ | **Occasionally neurological signs present, such as increased aggression, ataxia and convulsions | ||
+ | |||
+ | *In donkeys: | ||
+ | **''T. brucei'' in [[Protozoal Skin Infections - Donkey|skin infections]] | ||
+ | |||
+ | '''Epidemiology''' | ||
+ | *Vector distribution | ||
+ | **[[Glossinidae|Tsetse flies]] found in riverine, savannah and forest habitats | ||
+ | **Up to 20% [[Biting Flies|flies]] infected | ||
+ | **[[Biting Flies|Flies]] infected for life | ||
+ | |||
+ | *Parasite virulence | ||
+ | **Some parasitaemic animals survive for long periods of time | ||
+ | ***E.g. ''T. brucei'' and ''T. congolense'' | ||
+ | ***Increases the opportunity for infection of [[Biting Flies|flies]] | ||
+ | **Some trypanosomes kill their host in 1-2 weeks | ||
+ | ***E.g. ''T. vivax'' | ||
+ | ***Decreases the chances of [[Biting Flies|fly]] infection | ||
+ | **Trypanosomes avoid host immune defences by altering glycoprotein coat (surface antigen) before host [[Immunoglobulins - WikiBlood|antibody]] response | ||
+ | ***'''Antigenic variation''' can occur many times over several months causes relapsing parasitaemia | ||
+ | |||
+ | *Host response | ||
+ | **Trypanotolerant wild animals remain parasitaemic for prolonged periods without showing clinical signs of disease | ||
+ | ***Cause lasting reservoirs of infection | ||
+ | **Most domestic livestock are susceptible to trypanosomosis | ||
+ | **Some local breeds of sheep, goats and cattle are trypanotolerant | ||
+ | ***E.g. ''Bos indicus'' | ||
+ | |||
+ | '''Diagnosis''' | ||
+ | *Demonstrate trypanosomes in blood | ||
+ | **Giemsa stained smears | ||
+ | **Fresh blood films | ||
+ | ***Motile trypanosomes | ||
+ | **Haematocrit tube | ||
+ | ***Motile trypanosomes at the plasma/buffy coat interface | ||
+ | |||
+ | '''Control''' | ||
+ | *[[Glossinidae|Tsetse fly]] control | ||
+ | **Spraying and trapping | ||
+ | |||
+ | *Prophylactic drug treatment | ||
+ | **Change drug group periodically to decrease the chances of resistance occurring | ||
+ | **May lead to protective immunity but livestock will still be susceptible to heterologous challenges | ||
+ | |||
+ | *Barrier fences and buffer zones | ||
+ | **Separate livestock and wild animals | ||
+ | |||
+ | *Trypanotolerant livestock | ||
+ | '''Other trypanosomes''' | ||
+ | *Mechanically transmitted by [[Biting Flies|biting flies]] | ||
+ | **E.g. Surra affecting horses and camels in North Africa, Asia and South America | ||
+ | **''T. equinum'' in South America | ||
+ | **''T. evansi'' in Asia | ||
− | + | *Venereally transmitted | |
+ | **E.g. Dourine | ||
+ | ***Transmitted by ''T. equiperdum'' | ||
+ | ***Causes genital and abdominal oedema, emaciation and CNS signs | ||
+ | ***Affects horses and donkeys in Africa, Asia, Central and South America | ||
− | + | *Non-pathogenic species occur in the UK | |
+ | **In sheep caused by ''T. melophagium'' | ||
+ | **In cattle caused by ''T. theileri'' | ||
− | [[ | + | ==[[Protozoa Flashcards - Wikibugs#Tropical Protozoa|Tropical Protozoa Flashcards]]== |
− | |||
− |
Revision as of 15:24, 29 March 2010
This article has been peer reviewed but is awaiting expert review. If you would like to help with this, please see more information about expert reviewing. |
|
Leishmania
- Leishmania spp. are intracellular parasites of macrophages
- Are closely related to Trypanosoma spp.
- Cause diseases in humans, dogs and wild animals
- Present in southern Europe, Africa, Asia and south America
- Can cause both cutaneous and visceral diseases
Recognition
- Ovoid shaped
- Possesses a rod-shaped kinetoplast
- Has a rudimentary flagellum which does not project beyond the cell margin
- After the amastigote has transformed into a promastigote inside the sand fly, the kinetoplast is situated in the posterior of the body
Life Cycle
- Transmitted by blood sucking sand flies
- Phlebotomus spp. in the Old World
- Lutzomyia spp. in the New World
- The amastigote (morphological form) is found in vertebrate macrophages
- Multiplies and migrates to insect proboscis
- Inoculated during feeding
- Can be transmitted percutaneously if sand fly crushed on skin
- Invades macrophages and reverts to amastigote
- Multiplies by binary fission
Pathogenesis
- Infection of vertebrate host
- Produces foci of proliferating Leishmania-infected macrophages in skin (cutaneous) or internal organs (visceral)
- Very long incubation period
- Months to years
- Many infected dogs are asymptomatic
- Visceral form causes chronic wasting condition
- Generalised eczema
- Loss of hair around eyes producing 'spectacle' effect
- Intermittent fever
- Generalised lymphadenopathy
- Generalised eczema
- Long periods of remission followed by recurrence of clinical signs is not uncommon in infections
- Involved in skin infections
Epidemiology
- Disease dependent on sand fly vectors
- E.g. Common in dogs around the Mediterranean coast, foci around southern Europe and around Madrid
- Reservoirs of infection
- E.g. Wild animals such as rodents and stray dogs
- Mechanisms of transmission
- sand fly bite
- Rarely through direct contact
- Leishmaniasis in British dogs
- Susceptible to infection if exposed whilst abroad in endemic areas as have no immunity
- No sand flies in Britain but dogs have become infected whilst in contact with infected imported animals
Diagnosis
- Demonstrate Leishmania organisms
- In skin scraping or smears
- In joint fluid, lymph node or bone marrow biopsies
Treatment and Control
- Chemotherapy
- Prolonged treatment, expensive, suppresses infection
- Does not cure infection
- Prevent sand flies biting
- Collars, sprays containing insecticide with repellent effect
- Destruction of infected and stray dogs
- Sand flies biting infected dogs may spread the disease to other dogs, humans and wildlife
- There is a slight possibility of transmission to humans by direct contact
Trypanosoma
- Protozoal parasites found in the blood and tissues of vertebrates
- Worldwide distribution
- Causes sleeping sickness in humans
- Particularly seen in sub-Saharan Africa
- Affects cattle production
- Causes Nagana (Wasting disease)
- Divided into two groups depending on the mode of development in the insect vector
- Salivarian
- Multiply in the foregut and proboscis
- Transmitted via inoculation during feeding
- Transmitted by Tsetse flies
- Also known as anterior station development
- Stercorarian
- Multiply in the hindgut
- Infective form migrates to the rectum
- Transmitted via contamination of wounds with insect faeces
- Also known as posterior station development
- Salivarian
- All Trypansomes except for T. equiperdum have arthropod vectors
- T. equiperdum is a venereally transmitted disease
- Non-cyclical transmission can also occur
- Mechanical transmission
- Transferred by interrupted feeding from one host to another
- Usually transmitted by biting flies, e.g. Tabanidae and Stomoxys
Recognition
- Elongated, spindle shaped protozoa
- Between 8 and 39 μm in length
- Flagellate
- Flagellum runs the length of the body attached to the pellicle which forms an undulating membrane
- Kinetoplast present which contains the DNA of the single mitochondrion
Life Cycle
- Undergo morphological transformations in intermediate host before becoming infective for the next host
- Blood-sucking flies ingest trypanosomes whilst taking a blood meal from an infected animal
- Trypanosomes multiply first in the gut of the fly
- Salivarian trypanosomes are transmitted by Tsetse flies
- Trypanosomes pass forward to the salivary glands where they transform into the infective stage
- Inoculated with saliva when Tsetse fly next feeds on a host
- Stercorarian trypanosomes are transmitted by triatomid bugs, tabanids and keds
- Trypanosomes pass back to the rectum
- Next host is infected when skin wounds are contaminated with infected insect faeces
Pathogenesis
- Salivarian
- Causes wasting disease in cattle (nagana)
- Sleeping sickness in humans
- Stercorarian
- T. cruzi most important in veterinary medicine
- Occurs in South America
- Infects armadillos, possums and humans
- Causes Chagas' Disease
- Transmitted by a triatomid (kissing) bug
- Chronic infections are often fatal causing heart failure
- Non-pathogenic species are transmitted by tabanids and keds
- T. theileria and T. melophagium
- T. cruzi most important in veterinary medicine
- Enlarged lymph nodes and spleen
- Causes lymphoid exhaustion
- Associated with plasma cell hypertrophy and hypergammaglobulinaemia
- Due to an increase in IgM
- With infections of increased duration, the lymph nodes and spleen shrink due to exhaustion of their cellular elements
- Anaemia
- Red blood cells are removed from circulation (haemolytic)
- Is a cardinal feature of the disease
- Degeneration and inflammation of multiple organs
- E.g. Skeletal muscle, myocardium and CNS
Clinical Signs
- In ruminants:
- Anaemia
- Enlargement of the lymph nodes
- Progressive loss of body condition
- Fever and appetite loss occur during parasite peaks
- Chronic disease usually terminates in death of the animal if untreated
- Can cause abortion, infertility and decreased growth in herds
- In horses:
- Acute or chronic infections of T. brucei
- Oedema of the limbs and genitalia
- In pigs:
- T. congolense infections are mild or chronic
- T. simiae infections are hyperacute usually leading to death from pyrexia in a few days
- In dogs and cats:
- T. brucei and T. congolese
- Acute infections
- Fever, anaemia, myocarditis, corneal opacity
- Occasionally neurological signs present, such as increased aggression, ataxia and convulsions
- In donkeys:
- T. brucei in skin infections
Epidemiology
- Vector distribution
- Tsetse flies found in riverine, savannah and forest habitats
- Up to 20% flies infected
- Flies infected for life
- Parasite virulence
- Some parasitaemic animals survive for long periods of time
- E.g. T. brucei and T. congolense
- Increases the opportunity for infection of flies
- Some trypanosomes kill their host in 1-2 weeks
- E.g. T. vivax
- Decreases the chances of fly infection
- Trypanosomes avoid host immune defences by altering glycoprotein coat (surface antigen) before host antibody response
- Antigenic variation can occur many times over several months causes relapsing parasitaemia
- Some parasitaemic animals survive for long periods of time
- Host response
- Trypanotolerant wild animals remain parasitaemic for prolonged periods without showing clinical signs of disease
- Cause lasting reservoirs of infection
- Most domestic livestock are susceptible to trypanosomosis
- Some local breeds of sheep, goats and cattle are trypanotolerant
- E.g. Bos indicus
- Trypanotolerant wild animals remain parasitaemic for prolonged periods without showing clinical signs of disease
Diagnosis
- Demonstrate trypanosomes in blood
- Giemsa stained smears
- Fresh blood films
- Motile trypanosomes
- Haematocrit tube
- Motile trypanosomes at the plasma/buffy coat interface
Control
- Tsetse fly control
- Spraying and trapping
- Prophylactic drug treatment
- Change drug group periodically to decrease the chances of resistance occurring
- May lead to protective immunity but livestock will still be susceptible to heterologous challenges
- Barrier fences and buffer zones
- Separate livestock and wild animals
- Trypanotolerant livestock
Other trypanosomes
- Mechanically transmitted by biting flies
- E.g. Surra affecting horses and camels in North Africa, Asia and South America
- T. equinum in South America
- T. evansi in Asia
- Venereally transmitted
- E.g. Dourine
- Transmitted by T. equiperdum
- Causes genital and abdominal oedema, emaciation and CNS signs
- Affects horses and donkeys in Africa, Asia, Central and South America
- E.g. Dourine
- Non-pathogenic species occur in the UK
- In sheep caused by T. melophagium
- In cattle caused by T. theileri