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Materials and Supplies
Floatation Fecal Analysis Method 1. Mix up the flotation solution. It should be saturated. This means that you dissolve as much solid in the water as it will hold. You can use a variety of chemicals including salt or sugar. Saturated sugar is prepared by dissolving a pound (454 grams) of sugar in 1 1/2 cups (355 ml) of water, and saturated salt takes a pound (454 grams) of salt in 4 4/5 cups (1140ml ) of water. If there are salts left in the bottom of the liquid, pour off the saturated liquid into a new container. Specific gravity should be approximately 1.20. 2. Collect fresh feces. Use an old pill bottle or a small jar for each animal. If not examined immediately, be sure to label the container with the date, time and animal that provided the specimen and keep it in a cool place. 3. Place 2 or 3 fresh beans into a test tube and pour in just enough flotation solution to cover them. 4. Mash them up in the liquid with your stirring rod. Add more of the solution and pour it through the strainer to remove the large particles. Pour the strained liquid into a clean test tube. 5. Next, fill up the test tube to the very top with more liquid. Place a microscope coverslip over the top. There should be no air between the coverslip and the liquid. Over time (20-30 minutes) the eggs will float up to the top and adhere to the glass plate. 6. Carefully remove the coverslip and lower it at an angle over a microscope slide with the sample sandwiched between both pieces of glass. 7. Examine the specimen for worm eggs and coccidia oocysts. Start with the lowest power (40X) on your microscope and increase magnification if you see something interesting. An illustrated chart would be helpful in identifying them. Note, you will also be looking at other debris. Do not confuse it with parasites. Modified Stoll's Fecal Analysis Method This method is more accurate than the simple
floatation method, but does require a centrifuge (preferably a swinging bucket
style).
1. 5 grams of feces is diluted with a measured quantity of regular tap water to a final quantity of 100 grams: 5 grams feces plus 95 ml water. 2. The fecal sample is dispersed evenly in the water, then 10 ml of the fecal slurry is decanted into a graduated centrifuge tube. This represents 10% of the original fecal sample (0.5 grams). 3. This sample is pelleted by centrifugation, the supernatant discarded, then the flotation solution is added to the centrifuge tube and mixed thoroughly. The tube is placed into the centrifuge, a slightly bulging meniscus is formed by adding several drops of additional flotation solution to the tube, and a coverslip is secured onto the meniscus and centrifuge tube. Centrifuge for 10 minutes at approximately 2000rpm. 4. Remove the coverslip after centrifugation and count all strongyle-type eggs that are recovered. We count only the strongyle-type eggs and make a notation if other parasitic structures are present. Based on this count of all strongyle-type eggs present in 10% of the original fecal sample, we establish the EPG by a simple multiplication constant of 2.
Video of live strongyloides (short - 294k) Strongyle oocyst (top) and Nematodirus oocyst (bottom) Anyone know what this is? Capillaria? One egg found in llama. Unidentified worm found in feces (different llama) after treatment with fenbendazole. Length is about a half inch. Not what I would expect from an intestinal worm. What would intestinal parasites do with antenna? |
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