GUIDELINE for Tritrichomoniasis

Published: 01/01/2013
Last updated: [acf field='last_updated']
Last reviewed: [acf field='last_reviewed']

The Tritrichomoniasis guidelines were first published in the J Feline Med Surg 2013; 15: 647-649 by Tim Gruffydd-Jones et al. The present guidelines were updated by Séverine Tasker.


Tritrichomonas foetus is a protozoan organism that can cause predominantly large intestinal diarrhoea in cats. It is specific to cats, distinct from other Tritrichomonas species and not considered to be zoonotic. Infection is most common in young cats from multicat households, particularly pedigree breeding catteries. Affected cats show frequent foetid diarrhoea, often with mucus, fresh blood and straining, but generally remain bright and do not lose weight. Diagnosis of infection is based on direct microscopic examination of fresh faeces to view motile trophozoites. PCR testing is more sensitive, but can detect infections unrelated to diarrhoea, although a positive result in the presence of appropriate clinical signs is commonly used for diagnosis. A faecal loop can be used to collect faeces for diagnostic testing and can increase sensitivity. Treatment of choice is ronidazole, which should be used with care as it is an unlicensed drug for cats with a narrow safety margin. Ronidazole is not universally effective. Clinical signs are generally self-limiting in untreated cases but sometimes can take months to resolve.

Fig. 1 Tritrichomonas foetus, stained with Lugol’s iodine. Three anterior flagellae (

Fig. 1 Tritrichomonas foetus, stained with Lugol’s iodine. Three anterior flagellae (“tri”) can be seen, and an undulating membrane runs the length of the body; the trophozoites of Giardia spp. do not have the undulating membrane (Courtesy

Agent properties

Tritrichomonas foetus is a single-celled highly motile flagellate protozoan parasite (Fig. 1) that resides in the distal small intestine (ileum) and the large intestine (caecum and colon) of cats, where it can cause changes (Gookin et al., 1999; Gookin et al., 2001; Levy et al., 2001; Levy et al., 2003). It is distinct from Pentatrichomonas hominis, which infects humans (Levy et al., 2003). T. foetus is also recognized as a sexually transmitted parasite of the reproductive tract of cattle and an apathogenic commensal in the nasal cavities of pigs. T. foetus isolated from cats does not cause the same pathology as bovine isolates in experimental infection of cattle, and vice versa. Furthermore, studies have shown that feline strains are distinctly different from bovine and porcine strains, which are more closely related to each other (Dabrowska et al., 2019b; Pedraza-Diaz et al., 2019; Dabrowska et al., 2020). A new name of Tritrichomonas blagburni had been proposed for the feline species T. foetus (Walden et al., 2013), although this terminology is not yet widely accepted (Yao and Koster, 2015), and T. foetus will be used for the remainder of these guidelines.

During replication in the mucus of the intestine, trophozoites are produced by binary fission and excreted in the faeces. No oocyst form exists for T. foetus. Transmission occurs via the faecal-oral route. The trophozoites have very limited ability to survive outside the cat and do not persist in the environment but can remain viable for a few days in moist faeces (Singleton et al., 2019).


Prevalence studies have given variable results, depending upon the test used and population of cats sampled. Surveys based on PCR testing give the highest prevalence. It can be difficult to show an association between infection and signs of diarrhoea; the test detects infections that are not necessarily associated with the clinical picture. When comparing the prevalence in cats with clinical signs with that in healthy cats from the same background, there has not always been a clear difference. Infection is more common in cats from multicat environments, particularly from breeding colonies, and in some studies purebreds are at increased risk of infection (Yao and Koster, 2015) although reported breed associations vary in different studies (Hedgespeth et al., 2020). Groups can be affected, but also single cats within the household. Infection is generally more common in young cats, with most studies reporting increased levels of T. foetus infection in cats of 1 year of age or less (Kuehner et al., 2011; Yao and Koster, 2015). No sex predilection exists (Hedgespeth et al., 2020). A high degree of inbreeding has been hypothesised as a risk factor for T. foetus infection in cats (Hinney et al., 2019). A survey in Canada reported an association between infection and attendance at cat shows (Hosein et al., 2013). Review articles have summarised the varied T. foetus prevalences found worldwide (Yao and Koster, 2015; Bastos et al., 2019), with T. foetus reported in Europe, North America, Australia, New Zealand, Asia and South America.

Studies in Europe have tended to sample cats with chronic diarrhoea, and T. foetus has indeed been detected in the faeces of up to 39% of cats in the UK, Austria, Germany, Greece, Italy, the Netherlands, Norway, Poland, Spain, Switzerland and Turkey (Gookin et al., 2004; Mardell and Sparkes, 2006; Dahlgren et al., 2007; Gunn-Moore and Tennant, 2007; Gunn-Moore et al., 2007; Steiner et al., 2007; Burgener et al., 2009; Frey et al., 2009; Holliday et al., 2009; Schrey et al., 2009; van Doorn et al., 2009; Xenoulis et al., 2010; Kuehner et al., 2011; Tysnes et al., 2011; Mostegl et al., 2012; Profizi et al., 2013; Paris et al., 2014; Dabrowska et al., 2015; Arranz-Solis et al., 2016; Ceplecha et al., 2017; Veronesi et al., 2019; Yildiz and Sursal, 2019).


The mechanism by which T. foetus induces diarrhoea is not clear. It resides in the mucus on the mucosal surface of the distal small and large intestine and adherence factors might be important. The organism can produce toxins and induces an inflammatory response in the colon. Cysteine protease CP30 has been identified as a potential virulence factor in T. foetus-induced adhesion-dependent cytotoxicity in the feline intestine and could be targeted for future treatment strategies (Gould et al., 2017).


Little is known about the immunity to Tritrichomonads. Infections generally resolve, which suggests that infected cats develop an effective immune response.

Clinical signs

Not all infections are associated with clinical signs. The parasite targets the large intestine, and the features of the diarrhoea are usually suggestive of colitis, with frequent passage of small quantities of liquid to semi-formed faeces, often with blood, mucus, flatulence and some straining. Clinical signs can wax and wane and the diarrhoea can be malodorous. In one study, the median duration of diarrhoea was 135 days (Xenoulis et al., 2013). Some affected cats develop faecal incontinence and perianal swelling. Sometimes anorexia and depression are reported (Xenoulis et al., 2013) but generally cats have reasonable body condition without systemic signs. Clinical signs can last for 5-24 months (Foster et al., 2004). The parasite has been found in the genital tract of cats but does not appear to be linked to reproductive disease, although a case of pyometra in association with T. foetus infection of the uterus has been reported (Dahlgren et al., 2007).  One report (Pazzini et al., 2018) documented the presence of T. foetus in the nasal cavity of a cat with chronic purulent nasal discharge, in association with Mycoplasma felis, although more work is required to elucidate the pathogenicity of the agent in this anatomical location.


Excellent online resources on the diagnosis of infection, which have been written for owners but also contain valuable information for veterinary surgeons, are available for further information on diagnosis (Gookin and Dybas accessed December 26th 2020).

Diagnostic methods available

Direct examination

The organism can be identified in fresh faeces (within 6 hours of collection (Hale et al., 2009)) by direct examination (wet mount preparation), which reveals the motile trophozoites. The single flagellum induces a jerky forward motion that can aid in differentiation from the trophozoites of Giardia species (which have a slow, falling-leaf movement). Faeces are suspended in saline and examined under light microscopy with a cover slip at x 200-400 magnification. If mucus is passed with the faeces, this represents a good sample for examination.  However, this method may miss infections and one study reported a sensitivity of 14.7% for trophozoite examination (Yao and Koster, 2015).


Diagnosis can be achieved by culturing the organism, for which the “InPouch” culture system is commonly used but culture on modified Diamond’s medium is also possible. Culture can take up to seven days to become positive. This method can yield false negative results if there is a delay in analysis. One study reported a sensitivity of 58.8% for the InPouch culture system (Yao and Koster, 2015).


Infection can also be diagnosed using PCR, which is now widely available in laboratories (Dabrowska et al., 2019a). PCR can be very sensitive and will detect the DNA of non-viable trophozoites too. However, PCR sensitivity can be affected by faecal inhibitors although most PCR labs will screen for inhibitors in assays by use of internal control PCRs. PCR has the disadvantage of being able to identify infections which may not be clinically relevant so detection of trophozoites in faecal smears or culture of the organism may be better tests for identifying cases for which treatment is indicated. However, a positive PCR result in the presence of suggestive signs is usually adequate for diagnosis.


Trophozoites can be present, but are difficult to identify, on histopathological examination of colonic biopsies (Yaeger and Gookin, 2005) and less invasive methods of diagnosis on faecal samples are preferred.

Sampling for diagnosis

Diarrhoeic mucoid faecal samples are said to be preferable (rather than solid faecal) samples to increase sensitivity of T. foetus testing for all direct diagnostic methods. Colonic flushing used to be the favoured technique to obtain samples for testing; this could be performed in a conscious cat by inserting a lubricated soft 8-12 French catheter into the cat’s rectum and colon and flushing with ~10 ml of warm sterile saline followed by aspiration of as much of the fluid as possible for submission following centrifugation or sedimentation with disposal of the supernatant. An online video of this technique is available at (Gookin accessed December 26th 2020). However, a study (Hedgespeth et al., 2020) that used PCR for diagnosis of T. foetus infection reported that faecal samples collected by insertion of a faecal loop into the rectum were significantly more likely to yield positive results than samples collected by colonic flush. Of course, a causal association with collection technique cannot be proven and further studies are required, but these results do suggest that faecal loops should be considered for optimal collection of samples. It is possible that faecal loops allow collection from the surface of the colonic mucosa where trichomonads adhere to mucus and the epithelial lining.

Treatment and Management

The treatment of choice is ronidazole, a nitroimidazole related to metronidazole, which is the only drug with demonstrated efficacy against T. foetus (Grellet et al., 2017; Hinney et al., 2019; Morgan, 2019), although published evidence is limited (Hinney et al., 2019; Morgan, 2019). A report has casted doubt on the efficacy of treatment (Hedgespeth et al., 2020) as previous ronidazole treatment was not associated with positive or negative PCR results for T. foetus, but it is still commonly used. Ronidazole is not licensed for use in cats. Informed signed owner consent should be obtained before use. It can be obtained as a powder and formulated in capsules, and tablets are now available from specialist veterinary pharmaceutical companies. There has been recent debate about the appropriate dose; currently 30 mg/kg daily orally for 2 weeks is recommended. This dosage is lower than some previous recommendations but reduces the risk of side effects, which comprise neurotoxic signs (as with high doses of metronidazole) such as lethargy, inappetence, ataxia, seizures and/or tremors. Accurate weight measurement of the cat to be treated is important to ensure appropriate doses are given. Ronidazole is teratogenic so cannot be given to pregnant or nursing queens and must be handled with gloves by owners. It can take several weeks for cats to respond to treatment since elimination of infection does not always occur (Bastos et al., 2019). Relapses following treatment or treatment failure can occur in up to 25% of treated cats (Holliday et al., 2009; Bell et al., 2010; Grellet et al., 2017); treatment failure does not appear to be more likely in multicat households (Hedgespeth et al., 2020). Preliminary data suggest that the addition of a probiotic to ronidazole therapy could reduce the likelihood of T. foetus relapse (Lalor and Gunn-Moore, 2012). The diarrhoea will usually resolve spontaneously even in untreated cats although this can take several months or longer.

Tinidazole has been used by some (Gookin et al., 2007; Pennisi et al., 2012) as an alternative to ronidazole with variable results.  One of these showed effective treatment of concurrent tritrichomonas and giardia infections with tinidazole in FIV infected cats (Pennisi et al., 2012).

To reduce risk of reinfection and transmission, litter tray hygiene should be very good with frequent emptying and cleaning of trays and, if possible, infected cats should be isolated. Minimising stress and avoiding high densities in multicat households can also be important to minimise infection (Bastos et al., 2019).  Tritrichomonads are said to be easily killed in the environment with most disinfectants, so regular cleaning of “infected” households is important.

A key unanswered question, when infection is identified in a group of cats, is which cats should be treated – all animals in a group or just cats with diarrhoea. A reasonable approach is to treat only cats that are showing signs and are positive on faecal smears. Additionally, it should be remembered that co-infections with other intestinal pathogens can occur especially in multicat households (Paris et al., 2014; Zanzani et al., 2016), which can complicate diagnosis and response to treatment.

Excellent online resources on the treatment of T. foetus infection are available at (Gookin and Dybas accessed December 26th 2020). These guidelines have been written for owners but contain excellent information for veterinarians, and consultation and reference to these guidelines is suggested if ronidazole is to be used or if further information on treatment of T. foetus is required.


The prognosis for T. foetus infection is usually good and in 88% of cats with diarrhoea, faecal consistency returns to normal spontaneously, but it occurs after 2 years of infection with a mean duration of diarrhoea of 135 days (Foster et al., 2004; Bastos et al., 2019).

Zoonotic risk

T. foetus is not considered to be zoonotic but good hygiene practice should be applied when handling infected cats and their faeces, particularly by immunosuppressed individuals (Singleton et al., 2019).


ABCD Europe gratefully acknowledges the support of Boehringer Ingelheim (the founding sponsor of the ABCD), Virbac, IDEXX GmbH and MSD Animal Health.


Arranz-Solis D, Pedraza-Diaz S, Miro G, Rojo-Montejo S, Hernandez L, Ortega-Mora LM, Collantes-Fernandez E (2016): Tritrichomonas foetus infection in cats with diarrhea from densely housed origins. Veterinary Parasitology 221118-122.

Bastos BF, Almeida FM, Brener B (2019): What is known about Tritrichomonas foetus infection in cats? Rev Bras Parasitol Vet 28(1), 1-11.

Bell ET, Gowan RA, Lingard AE, Mccoy RJ, Slapeta J, Malik R (2010): Naturally occurring Tritrichomonas foetus infections in Australian cats: 38 cases. J Feline Med Surg 12(12), 889-898.

Burgener IA, Frey CF, Kook PH, Gottstein B (2009): Tritrichomonas fetus: A new intestinal parasite in Swiss cats. Schweizer Archiv für Tierheilkunde 151(8), 383-389.

Ceplecha V, Svobodova V, Lendon C, Husnik R, Horackova K, Svoboda M (2017): A survey of feline trichomonosis suggests a low incidence of Tritrichomonas blagburni among cats in the Czech Republic. Veterinarni Medicina 62269-273.

Dabrowska J, Karamon J, Kochanowski M, Jedryczko R, Cencek T (2015): Tritrichomonas foetus infection in cat – first detection in Poland. Acta Parasitologica 60(4), 605-608.

Dabrowska J, Karamon J, Kochanowski M, Gottstein B, Cencek T, Frey CF, Muller N (2019a): Development and comparative evaluation of different LAMP and PCR assays for coprological diagnosis of feline tritrichomonosis. Vet Parasitol 27317-23.

Dabrowska J, Karamon J, Kochanowski M, Sroka J, Zdybel J, Cencek T (2019b): Tritrichomonas foetus as a Causative Agent of Tritrichomonosis in Different Animal Hosts. J Vet Res 63(4), 533-541.

Dabrowska J, Keller I, Karamon J, Kochanowski M, Gottstein B, Cencek T, Frey CF, Muller N (2020): Whole genome sequencing of a feline strain of Tritrichomonas foetus reveals massive genetic differences to bovine and porcine isolates. International Journal for Parasitology 50(3), 227-233.

Dahlgren SS, Gjerde B, Pettersen HY (2007): First record of natural Tritrichomonas foetus infection of the feline uterus. J Small Anim Pract 48(11), 654-657.

Foster DM, Gookin JL, Poore MF, Stebbins ME, Levy MG (2004): Outcome of cats with diarrhea and Tritrichomonas foetus infection. J Am Vet Med Assoc 225(6), 888-892.

Frey CF, Schild M, Hemphill A, Stunzi P, Muller N, Gottstein B, Burgener IA (2009): Intestinal Tritrichomonas foetus infection in cats in Switzerland detected by in vitro cultivation and PCR. Parasitol Res 104(4), 783-788.

Gookin JL, Levy MG, Law JM, Papich MG, Poore MF, Breitschwerdt EB (2001): Experimental infection of cats with Tritrichomonas foetus. Am J Vet Res 62(11), 1690-1697.

Gookin J, Stebbins M, Hunt E, Bulone K, Fulton M, Hochel R, Talaat M, Poore M, Levy M (2004): Prevalence and risk factors for feline Tritrichomonas foetus and Giardia infection. Journal of Clinical Microbiology 422707-2710.

Gookin JL, Stauffer SH, Coccaro MR, Poore MF, Levy MG, Papich MG (2007): Efficacy of tinidazole for treatment of cats experimentally infected with Tritrichomonas foetus. Am J Vet Res 68(10), 1085-1088.

Gookin JL, Breitschwerdt EB, Levy MG, Gager RB, Benrud JG (1999): Diarrhea associated with trichomonosis in cats. J Am Vet Med Assoc 215(10), 1450-1454.

Gookin J (accessed December 26th 2020): T. foetus Diagnostic Laboratory

Gookin J, Dybas D (accessed February 21st 2024): An owner’s guide to diagnosis and treatment of cats infected with Tritrichomonas foetus

Gould EN, Giannone R, Kania SA, Tolbert MK (2017): Cysteine protease 30 (CP30) contributes to adhesion and cytopathogenicity in feline Tritrichomonas foetus. Vet Parasitol 244114-122.

Grellet A, Makhlouf SE, Desquilbet L, Hovhannessian F, Boogaerts C, Dore V, Anthony M, Espana B, Prouillac C, Kirilov P, Polack B, Perrot S (2017): Efficacy of guar gum-based ronidazole capsules as a treatment for Tritrichomonas foetus infection in cats. J Feline Med Surg 19(2), 177-184.

Gunn-Moore D, Tennant B (2007): Tritrichomonas foetus diarrhoea in cats. Vet Rec 160(24), 850-851.

Gunn-Moore DA, McCann TM, Reed N, Simpson KE, Tennant B (2007): Prevalence of Tritrichomonas foetus infection in cats with diarrhoea in the UK. J Feline Med Surg 9(3), 214-218.

Hale S, Norris JM, Slapeta J (2009): Prolonged resilience of Tritrichomonas foetus in cat faeces at ambient temperature. Vet Parasitol 166(1-2), 60-65.

Hedgespeth BA, Stauffer SH, Robertson JB, Gookin JL (2020): Association of fecal sample collection technique and treatment history with Tritrichomonas foetus polymerase chain reaction test results in 1717 cats. Journal of Veterinary Internal Medicine 34(2), 734-741.

Hinney B, Christen I, Jahne S, Gaisbauer S, Schrammel N, Markl A, Joachim A, Kunzel F (2019): Efficacy and safety of ronidazole treatment against Tritrichomonas foetus in a cat colony with multiple disorders. Vet Parasitol Reg Stud Reports 18100344.

Holliday M, Deni D, Gunn-Moore DA (2009): Tritrichomonas foetus infection in cats with diarrhoea in a rescue colony in Italy. J Feline Med Surg 11(2), 131-134.

Hosein A, Kruth SA, Pearl DL, Richardson D, Maggs JC, Peach HA, Peregrine AS (2013): Isolation of Tritrichomonas foetus from cats sampled at a cat clinic, cat shows and a humane society in southern Ontario. J Feline Med Surg 15(8), 706-711.

Kuehner KA, Marks SL, Kass PH, Sauter-Louis C, Grahn RA, Barutzki D, Hartmann K (2011): Tritrichomonas foetus infection in purebred cats in Germany: Prevalence of clinical signs and the role of co-infection with other enteroparasites. J Feline Med Surg 13(4), 251-258.

Lalor S, Gunn-Moore D (2012): Effects of concurrent ronidazole and probiotic therapy in cats with Tritrichomonas foetus-associated diarrhoea. (Abstract). J Feline Med Surg 14651.

Levy MG, Gookin JL, Poore MF, Litaker RW, Dykstra M (2001): Information on parasitic gastrointestinal tract infections in cats. J Am Vet Med Assoc 218(2), 194-195.

Levy MG, Gookin JL, Poore M, Birkenheuer AJ, Dykstra MJ, Litaker RW (2003): Tritrichomonas foetus and not Pentatrichomonas hominis is the etiologic agent of feline trichomonal diarrhea. J Parasitol 89(1), 99-104.

Mardell EJ, Sparkes AH (2006): Chronic diarrhoea associated with Tritrichomonas foetus infection in a British cat. Vet Rec 158(22), 765-766.

Morgan GB (2019): An evaluation of the use of ronidazole for the treatment of Tritrichomonas foetus in cats. Vet Evidence 4(4).

Mostegl MM, Wetscher A, Richter B, Nedorost N, Dinhopl N, Weissenbock H (2012): Detection of Tritrichomonas foetus and Pentatrichomonas hominis in intestinal tissue specimens of cats by chromogenic in situ hybridization. Vet Parasitol 183(3-4), 209-214.

Paris JK, Wills S, Balzer HJ, Shaw DJ, Gunn-Moore DA (2014): Enteropathogen co-infection in UK cats with diarrhoea. Bmc Veterinary Research 10.

Pazzini L, Mugnaini L, Mancianti F, Ressel L (2018): Tritrichomonas foetus and Mycoplasma felis coinfection in the upper respiratory tract of a cat with chronic purulent nasal discharge. Veterinary Clinical Pathology 47(2), 294-296.

Pedraza-Diaz S, Arranz-Solis D, Gomez-Couso H, Fuschs L, Fort M, Rengifo-Herrera C, Navarro-Lozano V, Ortega-Mora LM, Collantes-Fernandez E (2019): Multilocus analysis reveals further genetic differences between Tritrichomonas foetus from cats and cattle. Vet Parasitol 276108965.

Pennisi MG, Napoli E, Ingra LAM (2012): Pilot study on efficancy and safety of tinidazole against natural Tritrichomonas foetus infection (abstract). J Feline Med Surg 14657.

Profizi C, Cian A, Meloni D, Hugonnard M, Lambert V, Groud K, Gagnon AC, Viscogliosi E, Zenner L (2013): Prevalence of Tritrichomonas foetus infections in French catteries. Vet Parasitol 196(1-2), 50-55.

Schrey C, Mundhenk L, Gruber A, Henning K, Frey C (2009): Tritrichomonas foetus as a cause of diarrhoea in three cats. Kleintierpraxis 54(2), 93-96.

Singleton DA, Arsevska E, Smyth S, Barker EN, Jewell C, Brant B, Sanchez-Vizcaino F, Dawson S, Pinchbeck GL, Noble PJM, Jones PH, Radford AD (2019): Small animal disease surveillance: gastrointestinal disease, antibacterial prescription and Tritrichomonas foetus. Vet Rec 184(7), 211-216.

Steiner JM, Xenoulis PG, Read SA, Suchodolski JS, Globokar M, Huisinga E, Thucre S (2007): Identification of Tritrichomonas foetus DNA in feces from cats with diarrhea from Germany and Austria. Journal of Veterinary Internal Medicine 21(3), 649.

Tysnes K, Gjerde B, Nodtvedt A, Skancke E (2011): A cross-sectional study of Tritrichomonas foetus infection among healthy cats at shows in Norway. Acta Veterinaria Scandinavica 53.

van Doorn DCK, de Bruin MJ, Jorritsma RA, Ploeger HW, Schoormans A (2009): Prevalence of Tritrichomonas foetus among Dutch cats. Tijdschrift Voor Diergeneeskunde 134(17), 698-700.

Veronesi F, Gazzonis AL, Napoli E, Brianti E, Persichetti MF, Santoro A, Zanzani SA, Olivieri E, Diaferia M, Giannetto S, Pennisi MG, Manfredi MT (2019): Corrigendum to “Cross-sectional survey on Tritrichomonas foetus infection in Italian cats” [Vet. Parasitol. Reg. Stud. Rep.] 6C (2016) 14-19]. Vet Parasitol Reg Stud Reports 16100284.

Walden HS, Dykstra C, Dillon A, Rodning S, Givens D, Bird R, Newton J, Lindsay D (2013): A new species of Tritrichomonas (Sarcomastigophora: Trichomonida) from the domestic cat (Felis catus). Parasitology Research 112(6), 2227-2235.

Xenoulis PG, Saridomichelakis MN, Read SA, Suchodolski JS, Steiner JM (2010): Detection of Tritrichomonas foetus in cats in Greece. J Feline Med Surg 12(10), 831-833.

Xenoulis PG, Lopinski DJ, Read SA, Suchodolski JS, Steiner JM (2013): Intestinal Tritrichomonas foetus infection in cats: a retrospective study of 104 cases. J Feline Med Surg 15(12), 1098-1103.

Yaeger MJ, Gookin JL (2005): Histologic features associated with Tritrichomonas foetus-induced colitis in domestic cats. Vet Pathol 42(6), 797-804.

Yao CQ, Koster LS (2015): Tritrichomonas foetus infection, a cause of chronic diarrhea in the domestic cat. Veterinary Research 46.

Yildiz K, Sursal N (2019): The first report of Tritrichomonas foetus in cats from Turkey. Israel J Vet Med 74127-133.

Zanzani SA, Gazzonis AL, Scarpa P, Olivieri E, Balzer HJ, Manfredi MT (2016): Coinfection with Tritrichomonas foetus and Giardia duodenalis in Two Cats with Chronic Diarrhea. Case Rep Vet Med 20165705168.