Corynebacterium diphtheriae (Diphtheria)

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Corynebacterium diphtheriae (Diphtheria)

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pii bw2 2.0

Bacterial structure and functions
Staphylococcus aureus
Streptococcus pyogenes (Group A Strep)
Enterococcus
Neisseria meningitidis
Neisseria gonorrhoeae
Listeria monocytogenes
Corynebacterium diphtheriae (Diphtheria)
Bacillus anthracis (Anthrax)
Escherichia coli
Salmonella typhi (typhoid fever)
Salmonella (non-typhoidal)
Shigella
Yersinia pestis (Plague)
Yersinia enterocolitica
Klebsiella pneumoniae
Enterobacter
Bordetella pertussis (Whooping cough)
Pseudomonas aeruginosa
Vibrio cholerae (Cholera)
Haemophilus influenzae
Mycobacterium tuberculosis (Tuberculosis)
Mycobacterium leprae
Chlamydia pneumoniae
Chlamydia trachomatis
Rickettsia rickettsii (Rocky Mountain spotted fever) and other Rickettsia species
Coxiella burnetii (Q fever)
Clostridium botulinum (Botulism)
Clostridium difficile (Pseudomembranous colitis)
Clostridium perfringens
Clostridium tetani (Tetanus)
Bacteroides fragilis
Treponema pallidum (Syphilis)
Borrelia burgdorferi (Lyme disease)
Leptospira
Candida
Mycoplasma pneumoniae
Malassezia (Tinea versicolor and Seborrhoeic dermatitis)
Aspergillus fumigatus
Cryptococcus neoformans
Mucormycosis
Sporothrix schenckii
Histoplasmosis
Blastomycosis
Coccidioidomycosis and paracoccidioidomycosis
Leishmania
Pediculus humanus and Phthirus pubis (Lice)
Sarcoptes scabiei (Scabies)
Toxoplasma gondii (Toxoplasmosis)
Babesia
Giardia lamblia
Trypanosoma cruzi (Chagas disease)
Trichomonas vaginalis
Enterobius vermicularis (Pinworm)
Toxocara canis (Visceral larva migrans)
Viral structure and functions
Adenovirus
Cytomegalovirus
Epstein-Barr virus (Infectious mononucleosis)
Herpes simplex virus
Human herpesvirus 6 (Roseola)
Human herpesvirus 8 (Kaposi sarcoma)
Varicella zoster virus
Human papillomavirus
Ebola virus
Dengue virus
Zika virus
Influenza virus
Measles virus
Respiratory syncytial virus
Coxsackievirus
Rhinovirus
HIV (AIDS)
Eastern and Western equine encephalitis virus
Antimetabolites: Sulfonamides and trimethoprim
Antituberculosis medications
Cell wall synthesis inhibitors: Cephalosporins
Cell wall synthesis inhibitors: Penicillins
DNA synthesis inhibitors: Fluoroquinolones
DNA synthesis inhibitors: Metronidazole
Mechanisms of antibiotic resistance
Miscellaneous cell wall synthesis inhibitors
Miscellaneous protein synthesis inhibitors
Protein synthesis inhibitors: Aminoglycosides
Protein synthesis inhibitors: Tetracyclines
Azoles
Herpesvirus medications
Anatomy of the pelvic girdle

Transcript

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Corynebacterium diphtheriae or just C. diphtheriae takes its name from the Greek;. “Coryne” that means club, and “diphtheriae,” which means leather.

So to sum this up, C. diphtheriae is a club-looking bacteria that causes diphtheria, an infection with a characteristic tough leathery membrane that forms in the pharynx.

C diphtheria has four main subspecies; C. diphtheriae mitis, C. diphtheriae Intermedius, C. diphtheriae Gravis, and C. diphtheriae Belfanti.

OK, now, C. diphtheriae has a thick peptidoglycan cell wall that takes in purple dye when Gram-stained - so it’s a gram-positive bacteria.

It is aerobic, which means it requires oxygen to grow, and it doesn’t form spores.

Now, when stained with Albert’s stain, these bacteria demonstrate some unique features.

They look like green, club-shaped bacteria with metachromatic granules, which are these dark blue dots made of phosphate, located at the bacterial poles.

When many, and clustered together, these bacteria seem to be arranged in a characteristic pattern that resembles Chinese letters.

Finally, C. diphtheriae is a fastidious bacteria.

This means it can only grow on special nutrients-enriched media.

The medium commonly used to grow this bug is cysteine-tellurite blood agar on which C. diphtheriae grow into black colonies.

Alright, any of the C. diphtheriae subspecies can be either toxigenic or not, depending on whether or not they produce the diphtheria toxin, or DT for short.

DT is a cytotoxic protein, where cytotoxic means it causes damage to host cells.

In fact, all the C. diphtheriae subspecies start out as non-toxigenic, but they become toxigenic after they’re infected by a beta-bacteriophage.

This is a kind of virus that attaches to bacteria and merges its own genome with the bacteria’s.

The beta-bacteriophage genome contains tox-genes, which code for diphtheria toxin production.

Following this, C. diphtheriae can make DT, and, in turn, cause diphtheria.

Now, DT has two main subunits, A and B, joined by a disulfide bond, with each of the subunits playing a specific role in the invasion and destruction to the host's cells.

The B subunit, which is the Bigger portion of DT complex, helps Binding to the host’s cell membrane.

After attaching to the host’s cells, the whole DT complex gets slowly engulfed by the cell membrane, which invaginates to form a sac on its inner side.

The sac then separates from the actual cell membrane forming a vesicle called an endosome.

Within the host’s cell cytoplasm, the medium inside the endosome becomes more acidic, and as a consequence, the disulfide bond holding the two subunits together becomes weak and eventually break, separating the subunits.

The A subunit then diffuses through the endosome membrane into the cytoplasm, where it goes straight to the ribosomes.

Here, it interferes with cell protein synthesis.

This happens because the A subunit has an ADP-ribose group, which attaches to the elongation factor - EF2, an important ribosomal protein that joins amino acids together during protein synthesis.

This process is called EF2 ADP-ribosylation, and it results in complete deactivation of the EF2, which stops protein synthesis, leading to cell death.

Ok, now, C. diphtheriae mainly causes diphtheria in unvaccinated or immunocompromised people.

Most often, the bacteria can be transmitted from one person to another mainly by respiratory droplets, following coughing or sneezing, in which case it causes pharyngeal diphtheria, but they can also enter the body through open lesions on the skin, causing cutaneous diphtheria.

Following inhalation of infected respiratory droplets, C. diphtheriae attaches to the pharyngeal epithelial cells, where they release DT toxin.

This causes local inflammation that leads to necrosis of pharyngeal tissue, and neck swelling.

The necrotic tissue builds up over the pharynx and larynx forming a gray adherent leathery membrane, commonly referred to as a pseudomembrane.

In some cases, a portion of this pseudomembrane can detach and get lodged into the trachea or bronchi, and when it is big enough, it can block the airways completely, causing death by asphyxiation.