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SHIGELLA
DYSENTERIAE
RATHEESH R.L
MORPHOLOGY
 An enterobacteriaceae
 Gram negative bacilli.
 Mostly non-motile
 Non sporing
 Size varies from 2-4um x 0.4 -0.6um
CULTURAL
CHARACTERISTICS
 They are aerobics and facultative
anaerobics
 Growing well in the temperature of 37
degree C and in the pH of 7.4.
NUTRIENT BROTH
 They produce mild turbidity after 24
hours of incubation.
NUTRIENT AGAR OR BLOOD
AGAR MEDIUM
 Circular, smooth grayish or colorless
Colonies will be formed after overnight
incubation.
 Size of the colonies will be 2-3mm
MACCONKEY AGAR MEDIUM
 They produce colorless colonies in the
medium
XLD(xylose lysine deoxycholate)
AGAR MEDIUM
 It is a selective medium and the
colonies formed are red color without
black centers.
DEOXYCHOLATE CITRATE
AGAR MEDIUM
 It is a selective medium for shigella
dysenteriae
 Small colorless colonies will be formed
in this medium.
PATHOGENESIS
 The species of this genus causes a serious
illness known as dysentery/shigellosis, which
is an acute diarrheal disease characterized by
passage of pus, blood or mucous through the
stool.
 Infection mainly occurs because of the
ingestion of contaminated food or water.
 Incubation period is 12-48 hours but may
vary between 1-7 days.
 Through the ingestion the bacilli will
reaches to the large intestine of the
humans.
 The multiplication occurs in the epithelial
cells of the large intestine.
 Then the bacteria spreads to adjacent
cells and to the lamina propria (is a
thin layer of loose connective tissue
which lies beneath the epithelium)
where the colonization occurs.
 After the growth and multiplication, it
starts to produce toxins.
 The lamina propria and sub mucosa
develops an acute inflammatory reaction
with formation of abscess on the
mucosal surface along with capillary
thrombosis by the production of toxins.
 The necrosed epithelium become soft
and sloughed out and causing
superficial ulcers and bleeding.
 The toxin produced by the shigella
bacteria have both enterotoxic effect
and neurotoxic effect.
 Thus their combined action leads to
severe diarrhea,poly neuritis, coma
and meningitis.
LABORATORY DIAGNOSIS
 Hematological investigations
 Bacteriological investigations
◦ Microscopic studies
◦ Culture studies
◦ Biochemical tests
◦ Slide agglutination test
Hematological investigations
 There will not be any significant
changes in the blood values.
Microscopic studies
 Under the microscope the wet
preparation of specimen shows large
number of pus cells with degenerated
nuclei, macrophages and RBC.
CULTURE STUDIES
 Feces or mucous specimens are
selected for the microscopic studies.
 After 12-18 hours of incubation non
lactose fermenting colonies will be
formed in the macconkey medium.
Biochemical tests
 H2S test: negative
 Citrate utilization test: negative
 Iodole test: positive
 M.R test: positive
 Urease test: negative
 Motility test: negative
Slide agglutination test
 It is performed with specific antisera
against the shigella dysenteriae.
 We can isolate the bacilli by adding
the antisera over the specimen.
TREATMENT
 Tetracycline and chloramphenicol is
the drug of choice against the shigella
dysenteriae.
 The treatment should be continued for
5-7 days.
15. shigella

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15. shigella

  • 2.
  • 3. MORPHOLOGY  An enterobacteriaceae  Gram negative bacilli.  Mostly non-motile  Non sporing  Size varies from 2-4um x 0.4 -0.6um
  • 4. CULTURAL CHARACTERISTICS  They are aerobics and facultative anaerobics  Growing well in the temperature of 37 degree C and in the pH of 7.4.
  • 5. NUTRIENT BROTH  They produce mild turbidity after 24 hours of incubation.
  • 6. NUTRIENT AGAR OR BLOOD AGAR MEDIUM  Circular, smooth grayish or colorless Colonies will be formed after overnight incubation.  Size of the colonies will be 2-3mm
  • 7. MACCONKEY AGAR MEDIUM  They produce colorless colonies in the medium
  • 8. XLD(xylose lysine deoxycholate) AGAR MEDIUM  It is a selective medium and the colonies formed are red color without black centers.
  • 9. DEOXYCHOLATE CITRATE AGAR MEDIUM  It is a selective medium for shigella dysenteriae  Small colorless colonies will be formed in this medium.
  • 10. PATHOGENESIS  The species of this genus causes a serious illness known as dysentery/shigellosis, which is an acute diarrheal disease characterized by passage of pus, blood or mucous through the stool.  Infection mainly occurs because of the ingestion of contaminated food or water.
  • 11.  Incubation period is 12-48 hours but may vary between 1-7 days.  Through the ingestion the bacilli will reaches to the large intestine of the humans.  The multiplication occurs in the epithelial cells of the large intestine.
  • 12.  Then the bacteria spreads to adjacent cells and to the lamina propria (is a thin layer of loose connective tissue which lies beneath the epithelium) where the colonization occurs.
  • 13.  After the growth and multiplication, it starts to produce toxins.  The lamina propria and sub mucosa develops an acute inflammatory reaction with formation of abscess on the mucosal surface along with capillary thrombosis by the production of toxins.
  • 14.  The necrosed epithelium become soft and sloughed out and causing superficial ulcers and bleeding.  The toxin produced by the shigella bacteria have both enterotoxic effect and neurotoxic effect.
  • 15.  Thus their combined action leads to severe diarrhea,poly neuritis, coma and meningitis.
  • 16. LABORATORY DIAGNOSIS  Hematological investigations  Bacteriological investigations ◦ Microscopic studies ◦ Culture studies ◦ Biochemical tests ◦ Slide agglutination test
  • 17. Hematological investigations  There will not be any significant changes in the blood values.
  • 18. Microscopic studies  Under the microscope the wet preparation of specimen shows large number of pus cells with degenerated nuclei, macrophages and RBC.
  • 19. CULTURE STUDIES  Feces or mucous specimens are selected for the microscopic studies.  After 12-18 hours of incubation non lactose fermenting colonies will be formed in the macconkey medium.
  • 20. Biochemical tests  H2S test: negative  Citrate utilization test: negative  Iodole test: positive  M.R test: positive  Urease test: negative  Motility test: negative
  • 21. Slide agglutination test  It is performed with specific antisera against the shigella dysenteriae.  We can isolate the bacilli by adding the antisera over the specimen.
  • 22. TREATMENT  Tetracycline and chloramphenicol is the drug of choice against the shigella dysenteriae.  The treatment should be continued for 5-7 days.