The Scoop on Poop--Maximizing the Diagnostic Yield of the Faecal Examination
World Small Animal Veterinary Association World Congress Proceedings, 2007
Stanley L. Marks, BVSc, PhD, DACVIM (Internal Medicine, Oncology), DACVN
University of California, Davis, School of Veterinary Medicine
Davis, CA, USA

Parasitic-associated diarrhoea in dogs and cats is one of the most common maladies facing small animal veterinarians; however, the diagnosis of these organisms can be challenging. Although immunologic and molecular assays are becoming increasingly available to aid in the diagnosis of protozoal infections, direct microscopic examination of faeces remains the mainstay of attaining a diagnosis in many animals. The techniques used most commonly include direct faecal smear (wet preparation) and a faecal floatation.

Collection and Storage of Faeces

Fresh faecal specimens (< 1 hr) should be examined whenever possible to maximize the likelihood of identifying a parasite. At least 5 g of faeces should be placed in a clean, dry, airtight container. If samples cannot be examined immediately, they should be refrigerated (up to 1 week) to preserve the integrity of ova, oocysts and cysts.1 Protozoal trophozoites must be examined right away in fresh faeces, and the specimen should not be refrigerated. One can preserve the viability of trophozoites for several hours by adding 3 mL of saline to 3-5 g of faeces.

Direct Wet Preparation

Direct wet preparations are used to evaluate the smear for the presence of trophozoites such as Giardia spp. and Tritrichomonas foetus. A small amount of faeces (peppercorn size) is placed on a warm slide and a drop of 0.9% saline is mixed with the faeces. It is important that the smear not be too thick, as trophozoites will be easily missed. After application of a coverslip, the smear is evaluated systematically for motile organisms using the 10X magnification, with confirmation at 40X magnification.

Stained Faecal Smear

The addition of iodine to the wet mount through the edge of the coverslip may aid in the visualization of internal structures of some protozoa. One must examine the direct wet preparation without any stain for motility first, because staining the preparation kills the organism. Methylene blue is useful for identifying trophozoites, particularly those of Entamoeba histolytica. Stained fecal smears are of little to no diagnostic value for the diagnosis of bacterial-associated diarrhea.

Faecal Flotation

Faecal floatations are indicated to find cysts, oocysts, and ova in faeces. Although standing (gravitational) flotation methods are easier and quicker to perform than centrifugation flotation, the latter has clearly superior sensitivity.2 Solutions used in centrifugation flotation methods include zinc sulfate and Sheather's sugar.

Procedure for Single Centrifugal Flotation3

1.  Prepare a faecal emulsion using 2-5 grams of faeces.

2.  Mix faeces with approximately 10 ml of floatation solution. For zinc sulfate solution, the optimal specific gravity is 1.18-1.20.

3.  Pour the mixture through a tea strainer into a beaker or faecal cup.

4.  Pour strained solution into a 15-ml centrifuge tube.

5.  Fill tube with floatation solution so that a slight positive meniscus forms.

6.  Place a coverslip on the tube, and put the tube in the centrifuge.

7.  Ensure that the centrifuge is balanced.

8.  Centrifuge at 1,200 rpm (280 x g) for 5 minutes.

9.  Remove the tube and let stand for 10 minutes.

10.  Remove the coverslips and place on a clean slide.

11.  Examine entire coverslip systematically at 100X magnification (10X objective). Use 40X objective lens to confirm diagnosis by visualizing internal structures and measuring the organism.

Parasitic Causes of Diarrhoea


Tritrichomonas foetus, the primary causative agent of bovine trichomoniasis, has recently been recognized as a protozoal pathogen in cats,4,5 although the organism has also been associated with diarrhoea in puppies. Infected cats are generally young, but have ranged in age from 3 months to 13 years (median 9 months). The prevalence of T. foetus infection at an international cat show was found to be 31% (36 out of 117 cats), with 28 out of 89 catteries affected.5 Co-infection by T. foetus and Giardia was common and was documented in 12% of cats. Misdiagnosis of Giardia is common in cats having T. foetus infection, and may explain why cats diagnosed with apparent Giardia infection do not respond to appropriate therapy.

Clinical Signs

T. foetus infection in kittens can be associated with a chronic or recurrent large intestinal diarrhoea characterized by increased mucous, tenesmus, occasional haematochezia, and increased frequency. The anus is frequently red, swollen, and painful, and faecal incontinence is not uncommon. Most animals are otherwise healthy with a normal appetite. Tritrichomonas foetus can also be cultured from the faeces of asymptomatic animals, many of whom will not develop diarrhoea.


1. Multiple Direct Wet Preparations on Diarrhoeic Faecal Specimens

Direct faecal smears are performed to evaluate for the presence of Tritrichomonas foetus trophozoites. The sensitivity of direct faecal smear examination for diagnosis of T. foetus is relatively low in cats with spontaneous disease (14%). T. foetus can be distinguished from Giardia based on morphology and motility. Giardia trophozoites have a concave ventral disc and motility mimicking a falling leaf, whereas trichomonads are spindle-shaped, have an undulating membrane that courses the entire length of the body, and move in a more irregular and jerky fashion. T. foetus does not have a cyst stage, underscoring the limitations of faecal flotation for diagnosing this organism.

2. Faecal Cultures Performed with an InPouch TF Kit

A commercially-available system marketed for diagnosis of T. foetus infection in cattle and cats (InPouch TF, Biomed Diagnostics, White City, Oregon) is more sensitive than the direct wet preparation.Approximately 0.05 grams (less than a peppercorn) of freshly voided faeces can be placed in the InPouch for culture, or alternatively, a saline-moistened cotton-tipped swab can be placed in the rectum and then gently agitated in the InPouch for culture. The InPouch should be incubated at 37° C for 24 h, followed by storage at room temperature in an upright position in the dark and examined q 48 hours for up to 10 days for motile trophozoites using a 20 or 40X objective. The InPouches can also be stored at room temperature for the entire incubation period if one does not have access to an incubator; however, a brief incubation period usually results in more rapid growth of the trophozoites and a potentially earlier diagnosis. The media in the InPouch does not support the growth of Giardia or Pentatrichomonas hominis according to the manufacturer.

3. Single Tube Nested PCR of DNA Extracted from Faeces

A sensitive and specific single-tube nested PCR from feline or canine faeces has been described.6 The PCR test is more sensitive than faecal culture and tested positive in 55% of cultures that were negative for T. foetus, even when faeces were normal.

4. Histopathology and Immunohistopathology

Histopathologic changes in colonic mucosal biopsies from infected cats have revealed a lymphoplasmacytic colitis with a significant neutrophilic component.7 The intestinal epithelium is frequently attenuated, and immunohistochemistry can be utilized to detect the trichomonads on the surface epithelium and within crypts.


Ronidazole, a nitroimidazole similar in structure to metronidazole, has been shown to be highly effective at eradicating T. foetus from cats in preliminary studies.8 The drug is administered at a dose of 30mg/kg BID for approximately 10-14 days. The drug has been associated with anorexia and reversible neurologic side effects in a small number of cats.9 Newer and more effective nitroimidazoles are currently being investigated following recent reports of recurrent infections in some cats following administration of ronidazole.

Cryptosporidium SPP.

Infection with the ubiquitous protozoan parasites, Cryptosporidium parvum and C. felis, in puppies and kittens can cause a spectrum of disease ranging from asymptomatic carrier state to mild, transient diarrhoea, or prolonged severe life-threatening malabsorption syndrome or inflammatory bowel disease.10,11


The laboratory detection of this ubiquitous protozoan parasite in diarrheic animals is difficult, predominantly because the organism is so small (average 4.6 × 4.0 μm) and difficult to find in faecal specimens via light microscopy,and because faecal shedding may be intermittent. Immunofluorescent detection procedures are more sensitive and specific than acid-fast stains, and are generally the method of choice for morphological diagnosis in humans. The newer enzyme immunoassays designed to detect Cryptosporidium antigens in faeces, have proven more sensitive than microscopic techniques. The ProSpecT Microplate ELISA is one of the most sensitive diagnostic tests (89% sensitivity) for Cryptosporidium spp., however, the ProSpecT Rapid ELISA is highly insensitive (15% sensitivity) and should not be utilized.12


Eradication of this parasite has proven difficult, and many putatively effective drugs are either toxic or ineffective. The aminoglycoside, paromomycin, is potentially nephrotoxic and ototoxic, and should not be used in animals with compromised renal function. A recent prospective blinded study completed by the author failed to show any benefit for tylosin in naturally infected kittens. Azithromycin is used in humans for management of Cryptosporidiosis, and appears safe in dogs and cats when administered at a dosage of 7-10 mg/kg BID for 7 days; however, its efficacy is unknown.

Giardia SPP.

Giardia infection in adult dogs and cats is often subclinical or associated with a transient softening of the stool early in the infection; however, acute diarrhoea tends to occur in puppies and kittens shortly after infection.


Microscopic diagnosis of Giardia infection can be difficult, because cysts and trophozoites may be shed intermittently and because cysts are so delicate. Many artifacts (grass pollen, yeast, etc.) mimic to varying degrees the morphology of Giardia cysts, and care must be exercised in differentiating these from Giardia. Direct fluorescent antibody assay (DFA,) is often the standard against which other tests for Giardia are measured. The Merifluor® Cryptosporidium/Giardia assay (Meridian Diagnostics, Inc., Cincinnati, Ohio) uses a fluorescein isothiocyanate (FITC)-labeled monoclonal antibody directed against cell wall antigens of Giardia cysts in the stool; however, a fluorescent microscope is necessary to perform this test. Enzyme immunoassays are relatively simple to perform and do not require morphological identification of the cyst or oocyst,13 thus saving technician time and potentially avoiding false negative interpretations. A novel SNAP® Giardia Test Kit (IDEXX Laboratories, Inc., Westbrook, Maine) for detection of GCWP 1 in canine and feline faeces was recently released, and shown to have a sensitivity of 85.3% in cats when compared to the DFA test. The sensitivity improved to 97.8% when the test was used in parallel with faecal flotation, underscoring the value of this immunoassay in the clinical setting.14


Metronidazole was shown to be highly effective and safe when given at 25 mg/kg PO q12h for 7 days to cats with experimental infections,15 although it is less effective in dogs with eradication of the organism occurring in 67% of treated dogs. Albendazole is also relatively effective when dosed at 25 mg/kg BID for 5 days; however, the drug has been associated with pancytopenia and is teratogenic. A recent trial evaluating the efficacy of fenbendazole in cats co-infected with Cryptosporidium parvum revealed that the drug was safe; however, it was relatively ineffective (50%) in cats co-infected with Cryptosporidium.16 Fenbendazole is the author's first drug of choice for treating infected puppies and kittens. Drontal Plus was shown to be relatively safe and effective in experimentally infected kittens and naturally infected puppies when given at twice the recommended dose. The dose of febantel used was 56.5mg/kg.17 Prevention of reinfection by decontaminating the environment18 and bathing the animal to clean cysts from the coat are important strategies in the management of infected animals.


1.  Lappin MR, et al. Infectious diseases of the dog and cat, Ed 2. 1998;437-441.

2.  Dryden MW, et al. Vet Ther 2005;6(1):14-28.

3.  Dryden MW, et al. Vet Ther 2006;7(1):4-14.

4.  Gookin JL, et al. J Am Vet Med Assoc 215 (10):1450-1454, 1999.

5.  Gookin JL, et al. J Clin Microbiol 2004;42 (6):2707-2710.

6.  Gookin JL, et al. J Clin Microbiol 40(11):4126-30, 2002.

7.  Yaeger MJ, et al. Vet Pathol 2005;42(6):797-804.

8.  Gookin JL, et al. J Vet Intern Med 2006;20(3):536-43.

9.  Rosado TW, et al. J Vet Int Med (In Press).

10. Current WL. J Am Vet Med Assoc 1985;187:1334-1338.

11. Lappin MR, et al. Feline Practice 25:10-13, 1997.

12. Marks SL, et al. J Am Vet Med Assoc 2004;225:1549-1553.

13. Boone JH, et al. J Clin Microbiol 1999;37:611-614.

14. Mekaru S, et al. J Vet Int Med (In Press).

15. Scorza AV, et al. J Feline Med Surg. 2004;6(3):157-60.

16. Keith CL, et al. Am J Vet Res 2003;64(8):1027-9.

17. Scorza AV, et al. J Vet Int Med, Abstract, 2004;18(3):388.

18. Zimmer JF, et al. J Am Anim Hosp Assoc 1988;24:379-385.

Speaker Information
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Stanley L. Marks, BVSc, PhD, DACVIM (Internal Medicine, Oncology), DACVN
University of California, Davis, School of Veterinary Medicine
California, USA

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