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Watery Diarrhea: V. Cholerae/Cholera Toxin

by John Fisher, MD
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    00:00 So let's talk about cholera caused by <i>Vibrio cholerae</i> which is really the prototype of watery diarrhea and it's got a prototypic AB toxin. The A subunit is what's causing the disease. The B subunit is really what binds the toxin to the GI epithelium. So, here's what happens. This B subunit is trying to bind the gastrointestinal mucosa, small bowel, and it forms a pentameric ring and binds the toxin to an enterocyte receptor and that enterocyte receptor is a GM1 ganglioside on the mucosal cell surface and what that B subunit does in its pentameric ring is actually forms a pore in the cell and that allows the active component of the toxin to get in.

    01:09 Now, cholera, it seems kind of complicated if you look at the slide but let me sort of gradually walk you through it so you know that the B subunit causes this pore and binds the cholera toxin to the cell and then the toxin enters the cell and it actually enters the endoplasmic reticulum retrograde. The toxin then interacts with ADP-ribosylation factor to activate the stimulatory protein GS alpha and what that does is stimulates the release of adenylyl cyclase and so what you get is marked increases in the cell of cyclic AMP and if you get large increases of cyclic AMP, what that does is cause the release of chloride ions into the lumen and of course sodium follows chloride and what you get is a massive watery osmotic diuresis and in summary that's the way cholera toxin works. So the typical patient with cholera has unbelievably severe frequent watery diarrhea up to a liter an hour and the stool is essentially liquid without much odor after a few stools and has no blood, no pus and the stool has been described as appearing like rice water but with 1 liter an hour of diarrhea you can imagine how rapidly somebody becomes dehydrated and of course their blood pressure takes a nosedive. So they may lose up to 6 liters in an hour in the most severe cases and the organisms are present in the stool, you can actually see them on a gram stain and patients have lost more than 10% of their body weight and obviously that leads to dehydration and shock, death within 12 hours or less, occasionally within 2 to 3 hours. So we've got to take fast action if we're trying to treat somebody with cholera and so what we got to do is rapidly replace fluids. If they have a milder version we can try oral with sodium chloride and some sugar but more often than not they will need IV fluids and the classic one used is Ringer's lactate because it's got sodium, potassium chloride and similar concentrations as plasma plus some calcium and some lactate and we got to kill the bug and so for that we use azithromycin or a fluoroquinolone.


    About the Lecture

    The lecture Watery Diarrhea: V. Cholerae/Cholera Toxin by John Fisher, MD is from the course Gastrointestinal Infections.


    Included Quiz Questions

    1. Rice water appearance
    2. Malodorous
    3. Bloody
    4. Mucousy
    5. Purulent
    1. Creates a pore in the intestinal mucosal cell wall to allow active toxin to enter the cell
    2. It is the active toxic component of the pathogen
    3. Enters the endoplasmic reticulum
    4. Releases sodium ions into the intestinal lumen
    5. Binds to cyclic AMP
    1. Causes osmotic diuresis
    2. Flattens the intestinal brush border
    3. Acts as a bulk forming laxative
    4. Stimulates intestinal peristalsis
    5. The bacteria invades the mucosa and causes inflammatory diarrhea
    1. Hypovolemic shock
    2. Toxic shock
    3. Cardiogenic shock
    4. Fulminant liver failure
    5. Cardiorespiratory failure
    1. Azithromycin and rapid intravenous electrolyte and fluid replacement
    2. Clindamycin and oral hydrataion
    3. Fosfomycin and gentle intravenous fluid replacement
    4. Only rapid intravenous hydration is neccessary to hydrate the patient and wash out the bacteria
    5. Flouroquinolone and anti-diarrheal medications

    Author of lecture Watery Diarrhea: V. Cholerae/Cholera Toxin

     John Fisher, MD

    John Fisher, MD


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