Corynebacterium - The Club-Shaped Invaders
- Gram-positive, non-motile, club-shaped (coryneform) rods arranged in V/Y shapes or palisades.
- Contain metachromatic (Babes-Ernst) granules.
- Pathogenesis (C. diphtheriae): Diphtheria toxin, an A-B exotoxin, inhibits protein synthesis by ADP-ribosylating Elongation Factor 2 (EF-2).
- Clinical Triad: Pharyngitis with thick, gray pseudomembrane, "bull neck" (cervical lymphadenopathy), and low-grade fever.
- Systemic: Myocarditis, arrhythmias, and neuropathies.
- Diagnosis: Culture on Tellurite agar (black colonies) or Loeffler medium. Toxin detection via Elek test or PCR.
- Treatment: Antitoxin (most critical) + Erythromycin or Penicillin.
- Prevention: DTaP/Tdap toxoid vaccine.
⭐ The gene encoding the diphtheria toxin (tox) is introduced into C. diphtheriae by a lysogenic bacteriophage (β-prophage).

Diphtheria Toxin - The Protein Assassin
An A-B polypeptide exotoxin that irreversibly inhibits protein synthesis.
- Source: The tox gene is acquired via lysogenic conversion from a temperate β-prophage.
- Mechanism of Action:
- B (Binding) subunit attaches to the Heparin-Binding EGF-like growth factor (HB-EGF) receptor, which is abundant on cardiac and nerve cells.
- A (Active) subunit enters the cell cytoplasm.
- It catalyzes the ADP-ribosylation of Elongation Factor 2 (EF-2).
- This inactivation of EF-2 halts polypeptide chain elongation, leading to cell death.

⭐ The systemic effects (e.g., myocarditis, arrhythmias, neuropathies) are the direct result of toxin dissemination and its action on cells expressing the HB-EGF receptor. This is distinct from the local tissue necrosis that forms the pharyngeal pseudomembrane.
Diphtheria Clinical - From Grey Neck to Failing Heart
- Respiratory Diphtheria (Local Toxin)
- Presents 2-5 days post-exposure with sore throat, malaise, and low-grade fever.
- Hallmark: A dense, grey, adherent pseudomembrane forms over the tonsils and pharynx; bleeds if dislodged.
- Severe cases develop a "bull neck" from massive cervical adenopathy and edema, which can compromise the airway.

- Systemic Toxin Complications
- Myocarditis (1-2 wks): The most common cause of mortality. Can cause arrhythmias, heart block, and acute heart failure.
- Neuropathy (wks-mos): A progressive, symmetric polyneuropathy. Often starts with paralysis of the soft palate and diaphragm.
⭐ The diphtheria exotoxin irreversibly inactivates Elongation Factor-2 (EF-2) via ADP-ribosylation, which halts protein synthesis and causes cell death, especially in the heart and nerves.
Lab & Treatment - Tinsdale, Toxoids & Triage
-
Lab Diagnosis
- Culture on Tinsdale agar → black colonies with brown halos.
- Loeffler's medium → metachromatic (blue/red) granules.
- Elek test → detects toxin production (in vitro precipitation line).
-
Treatment & Prevention
- Triage Priority: Administer diphtheria antitoxin immediately on suspicion.
- Antibiotics: Penicillin G or erythromycin.
- Prevention: DTaP vaccine (diphtheria toxoid).
⭐ Crucial step: Antitoxin administration should NOT be delayed for lab confirmation. It neutralizes circulating toxin only.

High‑Yield Points - ⚡ Biggest Takeaways
- Gram-positive, club-shaped rods arranged in V or Y shapes ("Chinese letters").
- C. diphtheriae causes diphtheria via an exotoxin that inhibits protein synthesis by ADP-ribosylating EF-2.
- Presents with a grayish-white pseudomembrane in the pharynx and a "bull neck" due to lymphadenopathy.
- Systemic complications include myocarditis and neuropathy.
- Grows on tellurite agar (black colonies) and Loeffler's medium.
- The toxoid vaccine (in DTaP) is key for prevention.
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