Corynebacterium diphtheriae: Difference between revisions
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Corynebacterium diphtheriae
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===Microbiology=== |
===Microbiology=== |
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*Non-spore-forming, pleomorphic, unencapsulated, nonmotile [[Stain::Gram-positive]] [[Shape::bacillus]] with clubbed ends |
*Non-spore-forming, [[Shape::pleomorphic]], unencapsulated, nonmotile [[Stain::Gram-positive]] [[Shape::bacillus]] with clubbed ends |
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*Needs to be cultured on special media, so notify the lab |
*Needs to be cultured on special media, so notify the lab |
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**On Loeffler medium, outgrows other throat flora by 12 to 18 hours |
**On Loeffler medium, outgrows other throat flora by 12 to 18 hours |
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*Classic "Chinese character" appearance on Gram stain (pallisading) of all [[Corynebacterium species|corynebacteria]] |
*Classic "Chinese character" appearance on Gram stain (pallisading) of all [[Corynebacterium species|corynebacteria]] |
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*Metachromatic granules on methylene blue |
*Metachromatic granules on methylene blue |
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*Four biovars: gravis, intermedius, mitis, and belfanti |
*Four biovars: ''gravis'', ''intermedius'', ''mitis'', and ''belfanti'' |
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**Based on morphology, fermentation, and hemolysis, but now more often based on PCR ribotyping |
**Based on morphology, fermentation, and hemolysis, but now more often based on PCR ribotyping |
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**Not clinically significant |
**Not clinically significant |
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*Exotoxin production is provided by the ''tox'' gene |
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**The gene is carried by bacteriophages, which convert non-toxigenic strains into toxigenic ones |
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**Toxin production is not necessary for the life cycle |
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===Pathophysiology=== |
===Pathophysiology=== |
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*Contains a polypeptide exotoxin that is cleaved into segment A, the active segment, and B, which binds receptors on susceptible cells (heparin-binding epidermal growth factor receptor) |
*Contains a polypeptide exotoxin that is cleaved into segment A, the active segment, and segment B, which binds receptors on susceptible cells (heparin-binding epidermal growth factor receptor) |
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*Segment A enters the cytosol after B binds, and inactivates mammalian tRNA translocase (elongation factor 2), which stops protein synthesis |
*Segment A enters the cytosol after B binds, and inactivates mammalian tRNA translocase (elongation factor 2), which stops protein synthesis |
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**Affects all cells, but heart, nerves, and kidneys are particularly sensitive |
**Affects all cells, but heart, nerves, and kidneys are particularly sensitive |
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*Mostly occurs in colder months |
*Mostly occurs in colder months |
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*Asymptomatic carriage is an important reservoir for the organism, with 3-5% carriage rates in endemic areas |
*Asymptomatic carriage is an important reservoir for the organism, with 3-5% carriage rates in endemic areas |
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**May also be carried by horses, cattle, and domestic cats |
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*Disease is rare in immunized populations |
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*Currently, the highest rates are seen in India, and particularly in Kerala state in people older than 10 years |
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*Maternal antibodies provide immunity until about 6 months |
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==Clinical Manifestations== |
==Clinical Manifestations== |
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===Cutaneous Diphtheria=== |
===Cutaneous Diphtheria=== |
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*Can also cause chronic non-healing ulcers with dirty-gray membrane, often with |
*Can also cause chronic non-healing ulcers with dirty-gray membrane, often with concomitant [[Staphylococcus aureus]] or [[Streptococcus pyogenes]] |
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*Generally not invasive and can cause immunity, but also contribute to the organism's reservoir |
*Generally not invasive and can cause immunity, but also contribute to the organism's reservoir |
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**Adult catch-up schedule would be Tdap followed 4 weeks later by Td followed 6 to 12 months later by another Td |
**Adult catch-up schedule would be Tdap followed 4 weeks later by Td followed 6 to 12 months later by another Td |
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*Adults should get a Tdap booster in adulthood at least once, and Td booster every 10 years |
*Adults should get a Tdap booster in adulthood at least once, and Td booster every 10 years |
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{{DISPLAYTITLE:''Corynebacterium diphtheriae''}} |
{{DISPLAYTITLE:''Corynebacterium diphtheriae''}} |
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[[Category:Gram-positive bacilli]] |
[[Category:Gram-positive bacilli]] |
Revision as of 01:22, 26 November 2020
Background
History
- Derived from the Greek word for leather
Microbiology
- Non-spore-forming, pleomorphic, unencapsulated, nonmotile Gram-positive bacillus with clubbed ends
- Needs to be cultured on special media, so notify the lab
- On Loeffler medium, outgrows other throat flora by 12 to 18 hours
- Classic "Chinese character" appearance on Gram stain (pallisading) of all corynebacteria
- Metachromatic granules on methylene blue
- Four biovars: gravis, intermedius, mitis, and belfanti
- Based on morphology, fermentation, and hemolysis, but now more often based on PCR ribotyping
- Not clinically significant
- Exotoxin production is provided by the tox gene
- The gene is carried by bacteriophages, which convert non-toxigenic strains into toxigenic ones
- Toxin production is not necessary for the life cycle
Pathophysiology
- Contains a polypeptide exotoxin that is cleaved into segment A, the active segment, and segment B, which binds receptors on susceptible cells (heparin-binding epidermal growth factor receptor)
- Segment A enters the cytosol after B binds, and inactivates mammalian tRNA translocase (elongation factor 2), which stops protein synthesis
- Affects all cells, but heart, nerves, and kidneys are particularly sensitive
- In the respiratory tract, causes the formation of a necrotic coagulum of fibrin, WBCs, RBCs, and epithelial cells
- Appears clinically as a pseudomembrane
Epidemiology
- Spread by droplets and direct contact, and via fomites
- Mostly occurs in colder months
- Asymptomatic carriage is an important reservoir for the organism, with 3-5% carriage rates in endemic areas
- May also be carried by horses, cattle, and domestic cats
- Disease is rare in immunized populations
- Currently, the highest rates are seen in India, and particularly in Kerala state in people older than 10 years
- Maternal antibodies provide immunity until about 6 months
Clinical Manifestations
Diphtheria
- Clinical syndrome of pharyngeal infection with systemic toxicity caused by C. diphtheriae and C. ulcerans
- Incubation period of 2 to 4 days
- Low-grade fever, hoarseness, pain, and laryngeal pseudomembrane that can cause stridor and obstruction
- Pseudomembrane starts white but later dirty gray with patches of green or black
- Bleeding if membrane is removed
- Can have a bullneck appearance
- Can also have serosanguineous nasal discharge and cervical lymphadenopathy
- Palatal paralysis and cranial nerve defects may cause dysphagia
- Systemic symptoms related to extent of local disease
Myocarditis
- 10-25% of cases
- Can range from acute heart failure and cardiogenic shock to more subacute heart failure and dilatation
- Can be monitored with AST (?and troponin?)
- ECG may show ST-T wave changes and first-degree heart block, which can progress to complete heart block
- Mortality is higher with ECG changes, and highest with AV blocks and LBBB
- Can be permanent
- Monitor for arrhythmias
Neurotoxicity
- Acutely, can manifest as paralysis of the soft palate and posterior pharynx, causing dysphagia
- Followed by cranial nerve defects
- After 10 days to 3 months, can develop a peripheral motor neuropathy from demyelination
- Generally fully resolves with time
Tubular Necrosis
- Caused by both the toxin itself and the septic shock
Complications and Prognosis
- Suffocation from aspiration of the pseudomembrane
- Rarely, bacteremia, endocarditis, and arthritis from hematogenous spread
- Mortality 3-12% even now, usually from asphyxiation or myocarditis, but is rare in immunized patients
Cutaneous Diphtheria
- Can also cause chronic non-healing ulcers with dirty-gray membrane, often with concomitant Staphylococcus aureus or Streptococcus pyogenes
- Generally not invasive and can cause immunity, but also contribute to the organism's reservoir
Asymptomatic Carrier State
- C. diphtheriae not particularly invascive and can colonize the respiratory tract and skin
- Common in areas that do not vaccinate, as well as inner cities and rural areas
Differential Diagnosis
- Infectious mononucleosis
- Streptococcal or viral pharyngitis
- Vincent angina
- Acute epiglottitis
Diagnosis
- Clinical diagnosis based on:
- Mildly painful tonsilitis or pharyngitis with a membrane, especially if the memrane extends to the uvula and soft palate
- Adenopathy and cervical swelling, especially if assocaited with memranous pharyngitis and signs of systemic toxicity
- Hoarseness and stridor
- Palatal paralysis
- Serosanguineous nasal discharge with associated mucosal membrane
- Temperature not over 102.5ºF (39ºC)
- History of travel to endemic country
- Collected specimens from nose or throat, and any mucosal or cutaneous lesions
- Ideally collected from below the pseudomembrane
- Can also collect a piece of pseudomembrane
- Notify lab, who will use modified Tinsdale agar or cystine-tellurite blood agar
- Gram stain should show classic coryneform "Chinese letter" appearance
- PCR for the toxin gene exists
- Culture
- Tinsdale medium (contains teluride and cysteine), inhibits non-pathogenic Corynebacterium species
Management
Pharyngeal Diphtheria
- Supportive management, with a focus on airway protection
- Preemptive intubation is recommended in most situations
- May require tracheotomy if severe
- If concern for pharyngeal diphtheria, then need to treat presumptively with antitoxin and penicillin while awaiting confirmation of the diagnosis
- Start with with equine-derived diphtheria antitoxin (DAT)
- Prevents toxin from entering the cell
- First must rule out horse protein hypersensitivity
- History of allergy
- Scratch test: drop of 1:1000 dilution applied to superficial scratch; if no wheal in 15 minutes, inject 0.02 mL of 1:1000 dilution intracutaneously
- Epipen at the ready!
- Dose depends on duration of symptoms
- ≤48 hours: 20,000-40,000 units
- ≥3 days: 80,000-120,000 units, including anyone with neck swelling
- Nasopharyngeal: 40,000-80,000 units
- Diluted in 250-500 mL NS and infused over 60-120 minutes
- 10% risk of serum sickness
- Also treat with a 14-day course of an appropriate antibiotic
- Procaine penicillin G 600,000 units IM q12h (300,000 units if weight ≤10 kg)
- Can switch or oral penicillin once able to take oral medication
- Erythromycin 40 mg/kg/day (max 2 g) PO/IV divided qid
- Procaine penicillin G 600,000 units IM q12h (300,000 units if weight ≤10 kg)
- Test of cure should be done at least 24 hours after completing treatment, with two cultures from both nose and throat at least 24 hours apart
Cutaneous Diphtheria
- Treated with a 14-day course of antibiotics, as above
- Test of cure should be done at least 24 hours after completing treatment, with two cultures from cutaneous lesions at least 24 hours apart
Asymptomatic Carrier State
- Should be treated to prevent transmission to others
- Benzathine penicillin G 600,000 (<6 years) to 1,200,000 (≥6 years) units IM once, or erythromycin 40 mg/kg/day (max 1 g) for 7 to 10 days
- If cultures still positive after treatment, do another 10-day course of erythromycin (more effective than penicillin)
Prevention
Infection Control
- Contact precautions for cutaneous diphtheria, droplet precautions for pharyngeal diphtheria
- Must be in isolation until treatment is completed and until two negative cultures at 24 hour intervals
Prophylaxis
- Indicated for healthcare workers exposed to nasopharyngeal secretions, household contacts, other habitual close contacts, people sharing utensils or kitchen facilities, and childcare workers
- Indicated regardless of immunization status
- Procedure
- Monitor for symptoms for 7 days
- Collect culture specimens before treatment
- Antimicrobial prophylaxis with either benzathine penicillin G 600,000 (<30 kg) to 1,200,000 (≥30 kg) units IM once, or erythromycin 40 mg/kg/day (max 1 g) for 7 to 10 days
- Repeat culture after treatment, and repeat a 10-day course of erythromycin if still positive (more effective than penicillin)
- If previously vaccinated, give a Td/Tdap booster if it's been more than 5 years from last dose
- If not fully vaccinated, complete the vaccine series
Vaccination
- The available vaccine is against diphtheria toxin, so protects against the harmful effects of infection but does not directly prevent infection
- Asymptomatic carriage still occurs, though at a lower population level
- Diphtheria toxoid vaccine is given as a ≥3-dose series in childhood
- Typically in combination with others (e.g. DTaP-IPV-HiB at 2, 4, 6, and 18 months
- Adult catch-up schedule would be Tdap followed 4 weeks later by Td followed 6 to 12 months later by another Td
- Adults should get a Tdap booster in adulthood at least once, and Td booster every 10 years