Difference between revisions of "Tuberculosis - Cattle"

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If the mycobacteria disseminated from the primary complex then lymph nodes in other regions will also be affected and there will be multiple small foci of infection on other organs.  
 
If the mycobacteria disseminated from the primary complex then lymph nodes in other regions will also be affected and there will be multiple small foci of infection on other organs.  
 
+
 +
 
==Treatment==
 
==Treatment==
 
Treatment is not usually an option due to the chronic nature of the disease, zoonotic potential and test and slaughter policy.  
 
Treatment is not usually an option due to the chronic nature of the disease, zoonotic potential and test and slaughter policy.  
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The mycobacterium reside within macrophages in the lungs where they multiply and result in characteristic [[Lungs Inflammatory - Pathology#Granulomatous pneumonia|granulomatous inflammation]] The regional lymph nodes and also affected  
 
The mycobacterium reside within macrophages in the lungs where they multiply and result in characteristic [[Lungs Inflammatory - Pathology#Granulomatous pneumonia|granulomatous inflammation]] The regional lymph nodes and also affected  
  
**90% of cases exhibit the pulmonary form
+
Microscopically:
**Grossly:
+
Epithelioid cells, with large vesicular nuclei and pale cytoplasm and giant cells, formed by the fusion of macrophages, are found at the centre of tubercles. Surrounding this there is a narrow layer of lymphocytes, mononuclear cells and plasma cells, more advanced cases show peripheral fibroplasia and central necrosis.
***Ulcers in [[Trachea Inflammatory - Pathology|trachea]] and [[Bronchi and Bronchioles Inflammatory - Pathology#Infectious causes of bronchitis or bronchiolitis|bronchi]] due to coughed up bacteria
 
***Spreads into [[Pleural Cavity & Membranes Inflammatory - Pathology|pleura]]
 
**Microscopically:
 
***Epitheliod and giant cells at centre of tubercles
 
****Macrophages with ingested bacteria, forming epithelioid cells - large vesicular nuclei, abundant pale cytoplasm
 
****Giant cells, formed by fusion of macrophages, with multiple nuclei
 
***Narrow layer of lymphocytes, mononuclear cells and plasma cells at the periphery of the tubercle
 
***With time, peripheral fibroplasia and central necrosis develop
 
*If the infection is not contained in the primary complex described above, the mycobacteria can disseminate via lymphatics to other organs and lymph nodes
 
*This can allow the development of '''miliary tuberculosis''', i.e. numerous small foci of infection in many organs/ tissues
 
  
  
*some tubercle bacilli enter the lymph and travel to the bronchial or mediastinal nodes
+
phagocytosed by alveolar macrophages
*inhaled bacilli reach the alveoli, set up a focus of inflammation
 
*phagocytosed by alveolar macrophages
 
 
*two processes may develop if the animal has not encountered the organism before:
 
*two processes may develop if the animal has not encountered the organism before:
 
:- the organism may grow in the phagocytes as intracellular parasites
 
:- the organism may grow in the phagocytes as intracellular parasites
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::- ultimately, macrophages are killed and infection spreads
 
::- ultimately, macrophages are killed and infection spreads
 
:- the organism may be broken down and some antigens taken up by the immune system
 
:- the organism may be broken down and some antigens taken up by the immune system
::- cell mediated immune system produces cytotoxic T-lymphocytes
+
cell mediated immune system produces cytotoxic T-lymphocytes which attack and destroy infected cells, leading to a type IV hypesensitivity reaction.
::- T-lymphocytes can attack and destroy cells harbouring bacilli
 
::- leads to type IV (delayedd type) hypesensitivity
 
::- 'caseous' or cheesy type of necrosis
 
 
 
=====Tuberculosis pleurisy=====
 
caseous lymph node ruptures results from extensive tissue necrosis
 
if located in lung alveoli, the follicle may rupture into a bronchus, causing spread of the disease to all the other lobules served by that bronchus
 
the necrosis may erode the wall of a large pulmonary vessel resulting in fatal haemoptysis.
 
 
 
  
 
[[Category:Cattle]][[Category:To_Do_- lizzyk]]
 
[[Category:Cattle]][[Category:To_Do_- lizzyk]]
 
[[Category:Respiratory_Bacterial_Infections]]
 
[[Category:Respiratory_Bacterial_Infections]]
 
[[Category:zoonoses]]
 
[[Category:zoonoses]]

Revision as of 21:11, 2 August 2010

Tuberculosis caused by M. bovis (Image sourced from Bristol Biomed Image Archive with permission)


Description

Tuberculosis in cattle is caused by Mycobacterium bovis. It is a chronic disease characterised by nodular lesions in any organ, although the respiratory system is most commonly affected. The nodules often become nectroic with a caseous centre. The primary lesions may disseminate to involve other body systems.

A higher level of infection is required to establish the alimentary form of the disease and this is reflected by its lower incidence in comparison to the respiratory form.


Inhalation of ruminal gases is the most common route of entry for the mycobacterium organism, and spread of the disease is usually via cow to cow contant. Cattle can also become infected by ingestion of the causative agent, this is thought to be the route of entry when the badger is involved, by infecting grazing land or water troughs. Calves with infected dams can become affected via the milk, and intrauterine infection at coitus has been reported.

Historically bovine TB was a major cuase of human TB, but the introduction of tuberculin testing and slaughter, meat inspection at abatoirs, the pasturisation of milk and the BCG vaccination has dramatically reduced transmission to humans and bovine TB as a cuase of human disease is now very low indeed.

The disease is of serious economic importance to farmers becasue of the stringent control measures which remain in place. These include the slaughter of infected animals and movement restrictions placed on farms with reactors or inconclusive results.

Signalment

The disease usually affects heifers or young stock but cases can occur in cattle of any age. TB is more common in dairy herds.

Incidence of the disease has increased over the past 15 years; it is prevelent in Wales and the south west of England but is re-emerging in other parts of the UK such as the west Midlands and north-west England.

Most warm blooded animals are susceptible to bovine TB and can act as a resevoir for infection. The disease in cattle has been associated with wildlife species in a number of countries; the European badger and red deer in the UK, opossums and ferrets in New zealand, mule deer, white-tailed deer, elk, and bison in North America and water buffalo in Australia.

Diagnosis

The intradermal comparative tuberculin test is widely used in the UK for diagnosis of the disease. Two injections are give subcutaneously in the neck of cattle, one is avian and the second bovine tuberculin purified protein derivative (PPD). The thickness of the skin is recorded at each injection site. The test is read 72 hours later, and the thickness of the skin is remeasured. Interpretation is based on finding a swelling or increase in skin thinkness at the site of the injection. A comparison must be made between the reaction to avian and the bovine tuberculin to account for cross reactivity with related diseases, such as atypical mycobacteriosis, or paratuberculosis- Johne's disease.

A single intradermal test is used in many countries but has the disadvantage of giving reactors to avian tuberculosis and Johne's disease.

Clinical Signs

Location and severity depend on which body systems are affected and the advancement of the disease. Due to the tesing and slaughter policy most cases in the UK are idenified before development of clinical signs.

Respiratory form

  • Chronic cough- soft and productive
  • Tachypnoea
  • Dyspnoea
  • Dull areas on auscultation of the lungs in advanced cases

Alimentary form

  • Few clinical signs
  • Diarrhoea
  • Bloat


Mammary involvement is now rarely seen, the uterine form is also uncommon but may reult in abortion.

Laboratory Tests

An ELISA test has been developed but is not widely used. The gamma interferon test can also be used for diagnosis of the condtion.

Pathology

Findings at post mortem depend on the route of entry of the organism, whether it became generalised or not and the stage of the disease. One or more lymph nodes will display the chacteristic granulomatous tubercules. In the respiratory form the mediastinal and bronchial lymph nodes are affected, with lesions in the lungs.

If the mycobacteria disseminated from the primary complex then lymph nodes in other regions will also be affected and there will be multiple small foci of infection on other organs.


Treatment

Treatment is not usually an option due to the chronic nature of the disease, zoonotic potential and test and slaughter policy.

Control in many countries is centered on tuberculin testing with slaughter of reactors and movement restrictions to the premises. Research work continues into the use of vacination, or a cull strategy for the associated wildlife populations.

Prognosis

Poor.

References

  • Andrews, A.H, Blowey, R.W, Boyd, H and Eddy, R.G. (2004) Bovine Medicine (Second edition), Blackwell Publishing



The mycobacterium reside within macrophages in the lungs where they multiply and result in characteristic granulomatous inflammation The regional lymph nodes and also affected

Microscopically: Epithelioid cells, with large vesicular nuclei and pale cytoplasm and giant cells, formed by the fusion of macrophages, are found at the centre of tubercles. Surrounding this there is a narrow layer of lymphocytes, mononuclear cells and plasma cells, more advanced cases show peripheral fibroplasia and central necrosis.


phagocytosed by alveolar macrophages

  • two processes may develop if the animal has not encountered the organism before:
- the organism may grow in the phagocytes as intracellular parasites
- produces a nodule of parasitised swollen macrophages known as a tuburculous nodule or a tubercle granuloma
- ultimately, macrophages are killed and infection spreads
- the organism may be broken down and some antigens taken up by the immune system

cell mediated immune system produces cytotoxic T-lymphocytes which attack and destroy infected cells, leading to a type IV hypesensitivity reaction.