Corynebacterium
Diphtheriae
Several species of the genus Corynebacterium are normal flora of
skin, upper respiratory tract (URT), urogenital and intestinal tract. The most
important member of the genus is C. diphtheriae the causative agent of diphtheria,
a localized inflammation of the throat with greyish white pseudomembrane and a
generalized toxemia due to the secretion and dissemination of a highly potent
toxin.
The name Corynebacterium
diphtheria is derived from Greek
word ‘Coryne’ – “Club shaped swellings” or“Knotted rod” ‘Diphthera’ – Leather.
• They are Gram positive slender rods, pleomorphic club shape
or coryneform bacterium Non – motile, non – sporing and
non – capsulated (Figure 7.9a & b).
• The bacilli are arranged in a characteristic
fashion in angular fashion resembling the letters V or L. This has been called
Chinese letter or cuneiform arrangement (Figure 7.10).
• They are club shaped due to the presence of metachromatic granules at one or both ends. These granules are composed of polymetaphosphates and represent energy storage depots.
• They are aerobic and facultative anaerobe.
Optimum temperature is 37°C and pH 7.2.
• They grow on the following media and show the
characteristic colony morphology (Table 7.5)
Toxin
• The pathogenicity is due to production of a very
powerful exotoxin by virulent strains of diphtheria bacilli.
• The
toxigenicity of diphtheria bacillus depends on the presence of a tox+ gene
which can be transferred from one bacterium to another by lysogenic
bacteriophages, of which beta phage is the most important.
Properties
The
diphtheria toxin is a heat – labile protein and has a molecular weight of about
62,000 Dalton. It consists of two fragments.
a. Fragment
A (24,000 Dalton) – It has all enzymatic activity.
b. Fragment
B (38,000 Dalton) – It is responsible for binding the toxin to the target
cells.
Mode of Action
The toxin
acts by inhibiting protein synthesis, specifically fragment A inhibits polypeptide
chain elongation in the presence of NAD by inactivating the elongation factor
(EF – 2) the toxin has special affinity for myocardium, adrenal gland and nerve
endings.
Source of
infection – Airborne droplets
Route of
entry – Upper respiratory tract
Incubation
period – 3–4 days
Site of
infection – Faucial (nasal, otitis, conjunctival, laryngeal, genital)
diphtheria is most commonly seen in children of 2–10years.
Faucial diphtheria is the most common type.
The infection is confined to humans only. The toxin has both local (flowchart
7.3) as well as systemic effects.
Systemic effects
The toxin
diffuses into the blood stream and causes toxemia. It has got affinity for
cardiac muscle, adrenal and nerve endings. It acts on the cells of these
tissues.
1. Laryngeal obstruction, asphyxia (it is a
condition of severe deficient supply of oxygen, causing suffocation).
2. Diphtheritic
myocarditis (inflammation of heart muscle), polyneuropathy (damage of multiple
peripheral nerves), paralysis of palatine (the top part of the inside of the
mouth) and ciliary muscles.
3. Degenerative changes in adrenal glands, kidney and liver may occur.
Specimen: Two swabs from the lesions are collected. One swab is used for smear preparationand other
swab for inoculation on culturemedia.
Direct microscopy: Smears
are stained with both Gram stain and
Albert stain.
a. Gram
Staining – Gram positive slender rods were observed.
b. Albert
staining – Club shaped with metachromatic granules were observed
Culture: The swabis inoculated on Loeffler’s serum slope, after overnight incubation at 37°C, the
plates were observed for characteristic colonies, which are identified by gram
staining
Diphtheria can be controlled by immunization. Three methods of immunization are available (Table 7.6).
The
specific treatment for diphtheria consists of administration of antitoxin with
dose of 20,000–100, 000 units of ADS intramuscularly and antibiotic therapy
using penicillin.
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