Identification of Pentatrichomonas hominis in feline fecal samples by polymerase chain reaction assay

• Published in: Veterinary parasitology 2007-04, Vol.145 (1), p.11-15
• Main Authors: Gookin, Jody L., Stauffer, Stephen H., Levy, Michael G.
• Format: Article
• Language: English
• Subjects: Animals; Cat Diseases - diagnosis; Cat Diseases - parasitology; cats; Cats - parasitology; Diarrhea; disease detection; disease prevalence; feces; Feces - parasitology; mixed infection; molecular systematics; pathogen identification; Pentatrichomonas hominis; polymerase chain reaction; Polymerase Chain Reaction - methods; Polymerase Chain Reaction - veterinary; protozoal infections; ribosomal DNA; RNA, Protozoan - analysis; RNA, Protozoan - genetics; RNA, Ribosomal, 16S - genetics; RNA, Ribosomal, 18S - genetics; Trichomonadida - genetics; Trichomonadida - isolation & purification; Trichomonas; Trichomonas Infections - diagnosis; Trichomonas Infections - veterinary; trichomoniasis; Tritrichomonas foetus
• ISSN: 0304-4017; 1873-2550
• DOI: 10.1016/j.vetpar.2006.10.020

Pentatrichomonas hominis is considered to be a commensal protozoan of the vertebrate digestive tract. On the basis of light microscopic examination of feces, some investigators presumptively identified P. hominis as a causative agent of feline diarrhea. However, molecular identification of P. hominis infection in the cat has not been reported. Another trichomonad, Tritrichomonas foetus, is recognized as an intestinal pathogen in cats and often presumptively diagnosed on the basis of the presence of trichomonads in diarrheic feces. It is of importance to determine if cats are natural hosts for P. hominis, as the presence of this organism could result in inaccurate assumption of T. foetus infection. In this study, we used a species-specific PCR assay to identify P. hominis 18S rRNA genes in fecal samples collected from a convenience population of cats in which a high prevalence of T. foetus infection had been previously identified (cat show) or suspected (submitted for T. foetus diagnostic testing). The prevalence of T. foetus infection in these samples was 31% and 28.6%, respectively. P. hominis infection was identified by PCR of DNA extracted from feces of five cats (1.9% and 2.1% of fecal samples, respectively). All cats in which P. hominis was identified were also infected with T. foetus. PCR identification of P. hominis infection in the cat should facilitate future studies to determine the pathogenicity of this species and enable differentiation of P. hominis from other known or as-yet unidentified species of trichomonads that may infect cats.