Difference between revisions of "Mycobacteria spp."

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===Overview===
 
===Overview===
  
 +
*Mycobacterial infections are caused by bacteria belonging to the family Mycobacteriaceae, order Actinomycetales
 
*Includes obligate pathogens, opportunistic pathogens and saprophytes
 
*Includes obligate pathogens, opportunistic pathogens and saprophytes
 
*Cause chronic, progressive, granulomatous infections
 
*Cause chronic, progressive, granulomatous infections
 
*Cause tuberculosis, Johne's disease and feline leprosy
 
*Cause tuberculosis, Johne's disease and feline leprosy
 +
*''M. bovis'', ''M. tuberculosis'' and ''M. avium'' cause [[Respiratory Bacterial Infections - Pathology#Tuberculosis|tuberculosis of cattle]], [[Respiratory Bacterial Infections - Pathology#Tuberculosis in pigs|tuberculosis of pigs]] and [[Respiratory Bacterial Infections - Pathology#Tuberculosis in dogs|tuberculosis of dogs]] respectively
 
*Environmental species found in soil, vegetation and water
 
*Environmental species found in soil, vegetation and water
  
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===Characteristics===
 
===Characteristics===
  
*Aerobic acid-fast rods
+
*Aerobic, weakly Gram-positive acid-fast rods
 
*Non-motile, non-spore forming
 
*Non-motile, non-spore forming
 
*Cell walls contain mycolic acid
 
*Cell walls contain mycolic acid
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*Slow-growing colonies
 
*Slow-growing colonies
 
*Resistant to disinfectants and environmental conditions; susceptible to pasteurisation
 
*Resistant to disinfectants and environmental conditions; susceptible to pasteurisation
 +
*Mycobacteria stain with carbol dyes and resist subsequent decolorization with inorganic acids; this characteristic which is due to the spatial arrangement of mycolic acids within the cell wall makes them acid fast
  
  
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*Pathogenesis and pathogenicity
 
*Pathogenesis and pathogenicity
 +
**The ability of mycobacteria to survive and multiply within macrophages determines whether disease will occur within the host
 
**Survival and multiplication in macrophages at primary site of infection due to prevention of phagosome-lysosome fusion
 
**Survival and multiplication in macrophages at primary site of infection due to prevention of phagosome-lysosome fusion
 +
**Mycobacteria utilize several virulence factors including cord factor or trehalose dimycolate, surface glycolipid, sulfatides, lipoarabinomannan, heteropolysaccharide, heat shock protein, complement, and tubuloprotein 
 +
**The types of immune responses that are critical in responding to mycobacterial infection are cell-mediated immunity and the delayed hypersensitivity response
 +
**Pathogenicity of mycobacteria depends on their ability to escape phagocytic killing
 +
**Mostly imparted by the cell wall consitiutents
 +
***Cord factor (trehalose dimycolate) – surface glycolipid responsible for serpentine growth in vitro
 +
***Suphatides – surface glycolipid containing sulphur which prevents fusion of phagosome with lysosome. cAMP secreted by the bacteria may also facilitate this. Also something about the cholesterol content of the phagosome….. nature article
 +
***LAM – heteropolysaccharide which inhibits macrophage activation by IFNγ and induces macrophages to secrete TNFα -induces fever, etc and IL-10 which suppresses mycobacteria-induced T cell proliferation
 +
***The wax of the cell wall, peptidoglycans and other glycolipids are responsible for the adjuvant activity – attracts APCs
 +
***Tubuloprotein – important Ag, purified tubuloprotein is the basis of the tuberculin test
 +
 
**Mycobacteria are released from macrophages and also migrate within macrophages around the body
 
**Mycobacteria are released from macrophages and also migrate within macrophages around the body
 
**Waxy cell wall contributes to the host immune response to the mycobacteria and the development of lesions
 
**Waxy cell wall contributes to the host immune response to the mycobacteria and the development of lesions
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*''M. bovis'' and ''M. tuberculosis'' and ''M. avium'' in [[Respiratory Bacterial Infections - Pathology#Tuberculosis|tuberculosis of cattle]] and [[Respiratory Bacterial Infections - Pathology#Tuberculosis in pigs|tuberculosis of pigs]] and [[Respiratory Bacterial Infections - Pathology#Tuberculosis in dogs|tuberculosis of dogs]]
 
  
===Overview===
 
  
*Mycobacterial infections are caused by bacteria belonging to the family Mycobacteriaceae, order Actinomycetales. 
 
*Mycobacterium sp. are aerobic, weakly gram-positive, non-spore forming,  non-motile bacilli with wide variations in host affinity. 
 
*Mycobacteria stain with carbol dyes and resist subsequent decolorization with inorganic acids.  This characteristic which is due to the spatial arrangement of mycolic acids within the cell wall makes them acid fast.
 
  
*The ability of mycobacteria to survive and multiply within macrophages determines whether disease will occur within the host. 
 
*Mycobacteria sp. utilize several virulence factors including cord factor or trehalose dimycolate, surface glycolipid, sulfatides, lipoarabinomannan, heteropolysaccharide, heat shock protein, complement, and tubuloprotein. 
 
*The types of immune responses that are critical in responding to mycobacterial infection are cell-mediated immunity and the delayed hypersensitivity response.
 
*Pathogenicity of mycobacteria depends on their ability to escape phagocytic killing.
 
**Mostly imparted by the cell wall consitiutents…
 
***Cord factor (trehalose dimycolate) – surface glycolipid responsible for serpentine growth in vitro
 
***Suphatides – surface glycolipid containing sulphur which prevents fusion of phagosome with lysosome. cAMP secreted by the bacteria may also facilitate this. Also something about the cholesterol content of the phagosome….. nature article
 
***LAM – heteropolysaccharide which inhibits macrophage activation by IFNγ and induces macrophages to secrete TNFα -induces fever, etc and IL-10 which suppresses mycobacteria-induced T cell proliferation.
 
***The wax of the cell wall, peptidoglycans and other glycolipids are responsible for the adjuvant activity – attracts APCs.
 
***Tubuloprotein – important Ag, purified tubuloprotein is the basis of the tuberculin test.
 
  
 
==Four major disease groups are recognised:==
 
==Four major disease groups are recognised:==

Revision as of 19:10, 29 December 2008


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BACTERIA



Overview

  • Mycobacterial infections are caused by bacteria belonging to the family Mycobacteriaceae, order Actinomycetales
  • Includes obligate pathogens, opportunistic pathogens and saprophytes
  • Cause chronic, progressive, granulomatous infections
  • Cause tuberculosis, Johne's disease and feline leprosy
  • M. bovis, M. tuberculosis and M. avium cause tuberculosis of cattle, tuberculosis of pigs and tuberculosis of dogs respectively
  • Environmental species found in soil, vegetation and water


Characteristics

  • Aerobic, weakly Gram-positive acid-fast rods
  • Non-motile, non-spore forming
  • Cell walls contain mycolic acid
  • Require egg-based media for growth
  • Slow-growing colonies
  • Resistant to disinfectants and environmental conditions; susceptible to pasteurisation
  • Mycobacteria stain with carbol dyes and resist subsequent decolorization with inorganic acids; this characteristic which is due to the spatial arrangement of mycolic acids within the cell wall makes them acid fast


Identification

  • Identified by Ziehl-Neelson staining
  • Differentiated by culture, biochemical tests, chromatography and molecular techniques
  • Pathogenic species require at least three weeks for growth on egg-based media


Bovine tuberculosis

  • Epidemiology
    • World-wide disease caused by M. bovis
    • Aerosol transmission between cattle kept in close contact
    • Transmission to calves via ingestion od contaminated milk
    • Wildlife reservoirs include badgers and possibly deer in the Europe
  • Pathogenesis and pathogenicity
    • The ability of mycobacteria to survive and multiply within macrophages determines whether disease will occur within the host
    • Survival and multiplication in macrophages at primary site of infection due to prevention of phagosome-lysosome fusion
    • Mycobacteria utilize several virulence factors including cord factor or trehalose dimycolate, surface glycolipid, sulfatides, lipoarabinomannan, heteropolysaccharide, heat shock protein, complement, and tubuloprotein
    • The types of immune responses that are critical in responding to mycobacterial infection are cell-mediated immunity and the delayed hypersensitivity response
    • Pathogenicity of mycobacteria depends on their ability to escape phagocytic killing
    • Mostly imparted by the cell wall consitiutents
      • Cord factor (trehalose dimycolate) – surface glycolipid responsible for serpentine growth in vitro
      • Suphatides – surface glycolipid containing sulphur which prevents fusion of phagosome with lysosome. cAMP secreted by the bacteria may also facilitate this. Also something about the cholesterol content of the phagosome….. nature article
      • LAM – heteropolysaccharide which inhibits macrophage activation by IFNγ and induces macrophages to secrete TNFα -induces fever, etc and IL-10 which suppresses mycobacteria-induced T cell proliferation
      • The wax of the cell wall, peptidoglycans and other glycolipids are responsible for the adjuvant activity – attracts APCs
      • Tubuloprotein – important Ag, purified tubuloprotein is the basis of the tuberculin test
    • Mycobacteria are released from macrophages and also migrate within macrophages around the body
    • Waxy cell wall contributes to the host immune response to the mycobacteria and the development of lesions
    • Cell-mediated immune response with activated macrophages and sensitised T cells
    • Delayed-type hypersensitivity response with granuloma formation
    • Lesions contain macrophages, multinucleate giant cells and later a central area of caseous necrosis, giving a cheesy appearance
  • Clinical signs
    • Initially asymptomatic
    • Loss of condition
    • Cough and intermittent pyrexia with lung pathology
    • Tuberculous mastitis with transmission via milk
  • Diagnosis
    • Tuberculin test - comparative intradermal test
    • Avian and bovine tuberculin (purified protein derivative) is injected intradermally into two different clipped sites on the side of the neck
    • Skin thickness at these sites is compared before and 72 hours after the injection of tuberculin with calipers
    • Increases in skin thickness at the bovine PPD site of more than 4cm greater than the avian PPD site are seen as positive (reactor)
    • Blood tests including the gamma interferon assay are being developed
    • Laboratory examination of lesions, lymph nodes and milk
    • Ziehl-Neelson staining of tissues
    • Isolation requires Lowenstein-Jensen medium
  • Control
    • Eradication programs using a test and slaughter policy
    • Reactors positive to the tuberculin test are slaughtered and restrictions applied to the affected herd


Avian tuberculosis

  • Caused by members of the M avium complex
  • Depression, loss of condition and lameness in affected birds
  • Granulomatous lesions in liver, spleen, bone marrow and intestines
  • Diagnosis by Ziehl-Neelson staining of smears and post-mortem appearance
  • Tuberculin testing of poultry


Feline leprosy

  • Caused by M. lepraemurium
  • Sporadic infections of cats via bites from infected rodents
  • Subcutaneous nodules form usually on the head or limbs and can ulcerate
  • Smears reveal Ziehl-Neelson-positive rods
  • Diagnosis by histopathology
  • Treatment includes excision of lesions


Johne's disease (paratuberculosis)

  • Chronic, contagious enteritis of ruminants
  • Caused by M avium subsp. paratuberculosis
  • Epidemiology
    • Transmitted to young calves by ingestion of mycobacteria in faeces of infected adults
    • Organisms viable in environment for long periods
    • Long incubation period with clinical signs appearing in cattle over 2 years of age
    • Subclinical carriers can occur, shedding organisms in their faeces
  • Pathogenesis and pathogenicity
    • M avium subsp. paratuberculosis is an intracellular pathogen
    • Mycobacteria are ingested by macrophages in the Peyer's patches
    • Survival and replication of mycobacteria in macrophages initiate an immune-mediated granulomatous reaction
    • Lymphocytes and macrophages accumulate in the lamina propria and submucosa, resulting in marked thickening and folding of the intestinal wall
    • Mesenteric lymph nodes are enlarged
    • A protein-losing enteropathy results, along with failure to absorb nutrients and water
  • Clinical signs
    • Diarrhoea, initially intermittent, and weight loss in cattle
    • Weight loss in sheep and goats
    • Rapidly fatal with weight loss and diarrhoea in some deer
  • Diagnosis
    • All diagnostic procedures have faults but include:
    • Microscopy of rectal biopsies
    • Faecal culture
    • Serology of serum including complement fixation tests, agar-gel immunodiffusion test and an ELISA
    • Histopathology of intestines and lymph nodes
    • Isolation and identification of mycobacteria from faeces and tissues
    • Ziehl-Neelson-positive smears
    • Intradermal tuberculin test
    • DNA probes for detection in faeces
  • Control
    • Slaughter of affected animals
    • Detection and slaughter of subclinical shedders using faecal culture, DNA probes and ELISA
    • Good hygiene to protect young calves
    • Separation and isolation of calves from affected dams
    • Inactivated adjuvanted vaccines are available and reduce shedding of mycobacteria but do not eliminate infection




Four major disease groups are recognised: