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PNEUMOCOCCUS

RATHEESH R L
• Medically important species is

pneumococcus pneumonia
MORPHOLOGY
• They are Gram-positive (I mm diameter),
lanceolate shaped cocci arranged in pairs
(diplococci) with one end broad & another
pointed (flame shaped).
• They are capsulated (capsule enclosing each
pair) nun-motile & non-sporing
CULTURAL CHARACTERISTICS
• They are aerobic/ facultative anaerobic and
grow best at 37 degree C at pH 7.6.
• Growth occurs best in atmosphere of 10-20%
of carbon dioxide.
Serum & glucose broth

• After 24 hours, show uniform turbidity.


• Non-capsulated strains
Blood agar medium

• Colonies are raised, circular about 1 mm in


diameter surrounded by zone of alpha-
hemolysis but few strains also show beta-
hemolysis under anaerobic conditions under
refrigeration at 6°C.
PATHOGENLSIS
• The virulence of the organism is due to its capsule which
protects the organism from phagocytes.

• The organism gets attached to nasopharyngeal cells &


subsequently migrates through bronchial mucosa to
peribronchial lymphatics.

• Inflammatory reaction occurs in alveoli with an outpouring


of fibrinous edema fluid into alveoli, followed by red cells &
leucocytes leading to consolidation of portion of lung.
• The usual lesion in adults is segmental or lobar
in distribution (lobar pneumonia) but in
children & aged, there Is patchy involvement
of lung (bronchopneumonia).

• Microorganisms are found throughout the


exudates & bacteraemia is common.
• Pneumococcal meningitis:
Strep. pneumoniae are the second
most important cause of pyogenic meningitis
after N.meningitides.
It is most serious Pneumococcal
infection more common in children with 40-50%
mortality rate
LABORATORY DIAGNOSIS
• Hematological investigation:
1…..TLC: Shows increase in leucocytes
(> 15000/mm3>.
II…..DLC. Shows increase in
polymorphonuclear cells.
• Bacteriological investigation:

– Specimen: sputum, CSF, pleural fluid, peritoneal


fluid, pericardial fluid & pus discharges.
Microscopy
• Gram staining of the above specimen shows
flame shaped diplococci.
• India ink preparation shows capsule as a clear
halo.
Culture
• Specimen is inoculated on BAM & incubated
at 37 C for 24-48 hours in atmosphere of
5-10% CO 2.
• Colonies develop after 24 hours which appear
as flat, umbonate (depressed at centre)
showing alpha hemolysis (greenish
discoloration).
Biochemical tests
• Sugar fermentation test - Positive with acid
production only.
• Bile solubility test - Positive
• Catalase test - Negative
• Oxidase test - Negative
Serological tests
• Co-agglutination test (COA)
• Latex agglutination test (LA).
• Counter current immuno electrophoresis
(CCIE)
Animal pathogenicity test
• Mice are most susceptible to Pneumococcal
infection; therefore, this test provides rapid
diagnosis.
• Sputum from infected patient is emulsified
with saline & one ml of this suspension is
inoculated/injected intraperitoneally into 2
mice (test & control).
• The test mouse dies within 24 hours. The
heart blood and peritoneal fluid of the animal
shows diplococci within capsules under
microscope.
TREATMENT
• Antibiotics:
– Sulphonamides and penicillin are effective
medication

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