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*If the infection is not contained in the primary complex described above, the mycobacteria can disseminate via lymphatics to other organs and lymph nodes
 
*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
 
*This can allow the development of '''miliary tuberculosis''', i.e. numerous small foci of infection in many organs/ tissues
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*inhalation of ''Mycobacterium bovis'' most common via droplets
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*some tubercle bacilli enter the lymph and travel to the bronchial or mediastinal nodes
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*inhaled bacilli reach the alveoli, set up a focus of inflammation
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*phagocytosed by alveolar macrophages
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*two processes may develop if the animal has not encountered the organism before:
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:- the organism may grow in the phagocytes as intracellular parasites
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::- produces a nodule of parasitised swollen macrophages known as a tuburculous nodule or a tubercle granuloma
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::- ultimately, macrophages are killed and infection spreads
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:- the organism may be broken down and some antigens taken up by the immune system
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::- cell mediated immune system produces cytotoxic T-lymphocytes
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::- T-lymphocytes can attack and destroy cells harbouring bacilli
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::- leads to type IV (delayedd type) hypesensitivity
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::- 'caseous' or cheesy type of necrosis
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::- if bacterium destroyed, further infection/disease is prevented
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====Sequelae====
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*chronicity
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=====Tuberculosis pleurisy=====
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*caseous lymph node ruptures
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*results from extensive tissue necrosis
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:- 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
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:- if the ensuing necrosis erodes the wall of a large pulmonary vessel, this ruptures into the lung and a fatal haemoptysis might follow
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[[Category:Cattle]][[Category:To_Do_-_Clinical]]
 
[[Category:Cattle]][[Category:To_Do_-_Clinical]]
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