Haemophilus
influenzae
Organism
-
- It is nonmotile.
- Facultative anaerobe (def).
- Fastideous growth needs. Requires
enrichments for growth.
Habitat
- Mucous membranes of the respiratory
tract in humans.
Source
- The patient's own mucous membranes
or transmitted patient-to-patient.
Epidemiology
- Haemophilus parainfluenzae
and nonencapsulated H. influenzae typically colonize the upper respiratory
tract in humans within the first few months of life. These bacteria typically
cause sinusitis, otitis media (def),
bronchitis(def),
and pneumonia (def).
- Encapsulated H. influenzae,
primarily H. influenzae type b, is uncommon as normal flora of the
upper respiratory tract but can be a common cause of serious infection in
children.
- Until immunization of children
against H. influenzae type b became routine in developed countries,
this bacterium was the most common cause of pneumonia, septicemia(def),
meningitis (def),
and epiglottitis (def)
in children under the age of four. Immunization has reduced the incidence
of systemic infection by this bacterium 95%.
Clinical Disease
- Haemophilus influenzae
does not cause influenza. Influenza
is a viral infection.
- Haemophilus parainfluenzae
and nonencapsulated H. influenzae typically cause sinusitis, otitis
media (def),
bronchitis (def),
and pneumonia (def).
- H. influenzae type b
is the most common cause of pneumonia, septicemia (def),
meningitis (def),
epiglottitis (def),
and cellulitis in children under the age of four who are not immunized.
Pathogenicity
- In the outer membrane of the gram-negative
cell wall, the lipopolysaccharide functions as an endotoxin . Endotoxin, especially
when in the blood, can lead to inflammation, high fever, hypotension, capillary
damage, intravascular coagulation, tissue degradation, and irreversible shock.
Death is a result of what is called the shock cascade (see
Fig. 1). It also impairs ciliary function leading to damage to the respiratory
epithelium.
- Pili (def)
and a variety of cell wall adhesins (def)
enable the bacterium to colonize the oropharynx and respiratory epithelium.
- A capsule of polyribitol phosphate
enables encapsulated strains to resist phagocytosis.
- Immunoglobulin A1 proteases degrade
the IgA antibodies (def)
found in mucous to protect mucous membranes.
Treatment
- Typically treated with broad-spectrum
cephalosporins, azrithromycin, or fluroquinolones* (see
antibiotic table).
- Prevented by active
immunization (def)
with a conjugate capsular vaccine containing polyribitol phosphate capsular
material from H. influenzae type b.
*Drugs may change with time.
For a more detailed article on Haemophilus
influenzae infections, see
Haemophilus influenzae
Infections, by Mark R Schleiss, MD, Associate Professor, Department of Pediatrics,
Division of Infectious Diseases, University of Cincinnati and Children's Hospital
Research Foundation.
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Updated: Feb. 11, 2005
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