During June–August 2010, a total of 152 fecal samples were collected from the rectums of piglets (age 1–3 months; weight 6–24 kg), fattening pigs (age 3–4 months; weight 25–50 kg), and sows (age 1–2 years; weight 180–250 kg). The pigs were raised in 6 farrow-to-finish farms, 2 fattening farms, and 1 weaner indoor farm of central Italy (7 farms in the Umbria region and 2 farms in the Marche region). Pig fecal samples from 7 of the 9 farms were available for molecular analysis. Fecal samples from 21 pig farmers were collected from 5 of the 9 farms, 17 of which were available for molecular analysis.

Figure 1

Figure 1. . . . Dientamoeba fragilis trophozoites in a smear of pig feces after Giemsa staining, Italy, 2010–2011. Scale bar = 10 μm.

Microscopic diagnosis of D. fragilis was based on visualization of pleomorphic trophozoites, ranging in size from 4 µm to 20 µm, with fragmented chromatin and pale gray-blue finely vacuolated cytoplasm after Giemsa staining (Figure 1). DNA was extracted directly from 200 mg of feces by using the QIAamp DNA stool minikit (QIAGEN, Hilden, Germany). Reference D. fragilis DNA of genotype 1 (strains 379 and 1085) was used as a positive control.

A TaqMan real-time PCR that targets the 5.8 S ribosomal locus was performed in a LightCycler 480 apparatus (Roche Diagnostics GmbH, Mannheim, Germany) as described (11). For the 18S rRNA gene, a published assay (12) was used to amplify a 662-bp fragment, followed by amplification of a 366-bp fragment with newly designed primers DF322For (5′-GAGAAGGCGCCTGAGAGATA-3′) and DF687Rev (5′-TTCATACTGCGCTAAATCATT-3′). For the internal transcribed spacer 1 (ITS1) region, a nested PCR protocol was developed. In the primary reaction, the forward primer ssu2 (13) and the reverse primer Df-ITSRev (5′-GCGGGTCTTCCTATATAAACAAGAACC-3′) were used, whereas the forward primer Df-ITSnesFor (5′-ATACGTCCCTGCCCTTTGTA-3′) and the reverse primer Df-ITSnesRev (5′-GCAATGTGCATTCAAAGATCGAAC-3′) were used in the nested PCR. PCR products were purified and sequenced on both strands. The sequences were assembled by using SeqMan II (DNASTAR, Madison, WI, USA) and compared with those available in public databases by using BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi). Sequences from this study were submitted to GenBank under accession nos. JQ677147–JQ677168.

The microscopic examination showed that 52 of the 74 piglets, 11 of the 14 fattening pigs, and 8 of the 64 sows were positive for D. fragilis (Table 1). More trophozoites were observed in fecal samples from piglets, suggesting a higher susceptibility of young animals to infection (data not shown). The microscopic analysis also showed Blastocystis spp. (in 42% of pigs), Endolimax nana protozoa (32%), Iodoamoeba buetschli protozoa (25%), and other flagellates (4.5%). Of the 21 samples from pig farmers, 4 from farmers working on 2 farms were positive for D. fragilis by microscopy (Table 1).

Molecular techniques were applied to 38 pig fecal samples, specifically 24 samples positive by microscopy from 6 farms and 14 samples negative by microscopy from 2 farms, and to all 17 human fecal samples. A comparison of human and pig samples collected from the same farm was possible for farms 2, 3, and 5 (Table 2). Using real-time PCR, all 24 positive pig samples were amplified, with cycle threshold values ranging from 30 to 34, whereas none of the 14 negative samples were positive to this assay (Table 2). However, because no inhibition controls were run, false-negative results cannot be ruled out. Of the 17 human fecal samples, 13 were positive with cycle threshold values of 29–40. The sequence analysis of 15 amplified products (11 from pigs and 4 from humans) showed 100% homology with D. fragilis genotype 1 (Table 2). Genotype 2 was not found in any of the samples from pigs or humans.

Figure 2

Figure 2. . . . Multiple alignment of the 366-bp fragment of the 18S rRNA gene from Dientamoeba fragilis genotypes 1 and 2. Dot indicates identical nucleotides. Dashes indicate insertion or deletion. Nucleotide...

Next, a 366-bp fragment of the 18S rRNA gene was analyzed. In this fragment, genotypes 1 and 2 can be distinguished by 8 substitutions or insertions or deletions (Figure 2), which were further confirmed by sequencing the entire 18S rRNA gene from 2 reference isolates and 2 human isolates from this study. Amplification was obtained from 6 of the 24 positive pig samples and from 8 of the 17 human samples. Genotype 1 was identified in all samples (Figure 2). One human isolate (H7) showed a single nucleotide substitution in the fragment sequenced (Figure 2). Sequences from 3 microscopically negative pig samples (all from farm 1) had a high homology (96%) with Trichomitus batrachorum, a flagellate of reptiles, although the sequence could originate from T. rotunda, a flagellate of pigs that has not been described at the molecular level.

Last, we studied the more variable ITS1 locus. Amplification was obtained from 11 of the 24 pig samples (Table 2), but only 2 sequences could be clearly identified as D. fragilis. Four sequences showed homology (80%) with flagellates from different vertebrate classes whereas the remaining 5 sequences were excluded because of insufficient quality. The 2 D. fragilis sequences from pigs showed 100% homology with sequences from human isolates from the United Kingdom (Table 2), further supporting the presence of genotype 1 in these 2 hosts. A direct comparison of ITS1 sequences from humans and pigs from a single farm in Italy was not possible because D. fragilis was amplified from only 2 human samples from 2 farms from which no pig samples were available. The analysis of ITS1 from the 2 human isolates showed full identity to human isolates from the Netherlands and the United Kingdom (Table 2).

Considering the size of the world’s pig population (>1 billion), the close contact between pigs and humans in many parts of the world, and the difficulties in the proper management of pig fecal waste, the role of these animals as reservoirs of zoonotic pathogens must be carefully evaluated. We demonstrated that pigs are hosts of D. fragilis, on the basis of molecular analysis of 3 fragments in the ribosomal cluster. Sequence analyses of fragments of the 18S and 5.8S rRNA genes showed genotype 1 in isolates collected in the same farm from humans and pigs, suggesting the potential for zoonotic transmission of this parasite. If a transmissible cyst stage exists, then environmental contamination with pig feces should be considered a key factor in the transmission of this parasite. Pigs also are a fascinating animal model to elucidate the life cycle of this elusive parasite.