In February and July 2014, intestinal contents were obtained from young nursing piglets with diarrhea on farms in Ohio, USA. PDCoV strains OH-FD22 and OH-FD100 were detected in samples by using a TaqMan quantitative reverse transcription RT-PCR (qRT-PCR) specific for the membrane gene (nt 23395–23466) as reported (7), or an RT-PCR specific for the PDCoV membrane gene (nt 23111–23651) based on the sequence of PDCoV strain (USA/Illinois121/2014; GenBank accession no. KJ481931), as described in the in situ hybridization method. The partial membrane gene sequences of OH-FD22 and OH-FD100 were identical to that of USA/Illinois121/2014. Samples were negative for PEDV, rotavirus groups A–C, transmissible gastroenteritis virus (TGEV)/porcine respiratory coronavirus (PRCV), and caliciviruses (noroviruses, sapoviruses, and St. Valerien–like viruses) by RT-PCR as reported (8). The samples were bacteriologically sterilized by using 0.22-μm syringe filters and then prepared as inoculum.

Near-term gnotobiotic pigs were delivered aseptically by hysterectomy from 2 specific pathogen–free sows (9). Seven 11- to 14-day-old pigs were randomly assigned to a PDCoV-inoculated group (pigs 1–5) or as negative controls (pigs 6 and 7). Pigs 1–3 and pigs 4 and 5 were inoculated orally with 8.8 log₁₀ genomic equivalents (GEs) of PDCoV strain OH-FD22 and 11.0 log₁₀ GEs of OH-FD100, respectively. Clinical signs were monitored hourly. Pig 2 was monitored for long-term clinical signs and virus shedding until day postinoculation (dpi) 23. Pigs were euthanized for pathologic examination at 24–48 h or >48 h after onset of clinical signs. All animal-related experimental protocols were approved by the Ohio State University Institutional Animal Care and Use Committee.

Fecal or rectal swab samples were prepared as described (8,9). Virus RNA was extracted by using the Mag-MAX Viral RNA Isolation Kit (Applied Biosystems, Foster City, CA, USA) according to the manufacturer’s instructions. Titers of virus shed in feces were determined by using the qRT-PCR and the OneStep RT-PCR Kit (QIAGEN, Valencia, CA, USA) as reported (7). A standard curve was generated by using the PCR amplicon (nt 23111–23651) of strain OH-FD22. The detection limit of the qRT-PCR was 10 GEs/reaction, which corresponded to 4.6 log₁₀ and 3.6 log₁₀ GEs/mL of PDCoV in fecal and serum samples, respectively.

Small and large intestinal tissues and other major organs (lung, liver, heart, kidney, spleen, and mesenteric lymph nodes) were examined. Mean jejunal ratios of villous height to crypt depth were measured as reported (8). For PDCoV RNA detection in formalin-fixed, paraffin-embedded tissues, a nonradioactive digoxigenin-labeled cDNA probe specific for the 541-bp virus membrane gene sequence (nt 23111–23651), amplified with the primers forward 5′-CGCGTAATCGTGTGATCTATGT-3′ and reverse 5′-CCGGCCTTTGAAGTGGTTAT-3′, was used for in situ hybridization as described (10). Reverse transcription was conducted at 50°C for 30 min, followed by denaturation at 94°C for 5 min; 35 cycles at 94°C for 40 s, 55°C for 40 s, and 72°C for 1 min; and final extension at 72°C for 7 min.

OH-FD22–infected pig 2 was immunized intramuscularly with OH-FD22 from the gnotobiotic pig–passaged intestinal contents that were semipurifed by sucrose gradient ultracentrifugation (11) and mixed with complete and incomplete Freund’s adjuvants at dpi 30 and dpi 44 (11). Immunofluorescence staining was performed on frozen or formalin-fixed, paraffin-embedded tissues as described (8,9) by using hyperimmune gnotobiotic pig antiserum against OH-FD22. Tissues from control pigs 6 and 7 and PEDV-infected gnotobiotic pigs (8) were used negative controls for in situ hybridization/immunofluorescence staining.

Figure 1

Figure 1. Porcine deltacoronavirus (OH-FD22) particle detected in intestinal contents from a gnotobiotic pig. The sample was negatively stained with 3% phosphotungstic acid. Scale bar indicates 100 nm.

Acute, severe, watery diarrhea, vomiting, or both developed in all inoculated pigs. Clinical signs developed at hour postinoculation (hpi) 21–24, regardless of the inoculum strain or dose (Table 1). At hpi 96–120, pig 1 exhibited severe dehydration, loss of bodyweight, and lethargy. Pig 2, which was followed up longer, showed diarrhea until dpi 7. All inoculated pigs exhibited onset of clinical disease similar to that of infection with PEDV strain PC21A (6.3–9.0 log₁₀ GEs/pig) in gnotobiotic pigs (8). Immune electron microscopy with hyperimmune serum to PDCoV from a gnotobiotic pig showed only PDCoV particles in the intestinal contents (Figure 1). For pig-passaged OH-FD22 and OH-FD100 samples, RT-PCR results were negative for PEDV, rotavirus groups A–C, TGEV/PRCV, and caliciviruses. Detection of fecal virus shedding at hpi 24 coincided with onset of clinical signs (Table 1) in pigs 2–5. In pig 1, which showed only vomiting at hpi 24, fecal shedding occurred at hpi 48 at the onset of diarrhea.

Figure 2

Figure 2. Intestinal changes in gnotobiotic pigs inoculated with porcine deltacoronavirus (PDCoV) strains OH-FD22 (panels A, B, E, G, I, and J) and OH-FD100 (panels D and K). A) Intestine of pig 3...

Macroscopic examination showed that all infected pigs had PEDV-like lesions characterized by thin and transparent intestinal walls (proximal jejunum to colon) and accumulation of large amounts of yellow fluid in the intestinal lumen (Figure 2, panel A). The stomach was filled with curdled milk. Other internal organs appeared normal. Histologic lesions included acute diffuse, severe atrophic enteritis (Figure 2, panels B, D) and mild vacuolation of superficial epithelial cells in cecum and colon (Figure 2, panel E). The mean jejunal ratios of villous height to crypt depth of infected pigs 3–5 at hpi 72–120 ranged from 1.4 to 3.6 (Table 2), which were similar to those in gnotobiotic pigs experimentally infected with PEDV strain PC21A (8). Clinical signs or lesions did not develop in negative control pigs during the experiment (Figure 2, panels C, F).

In situ hybridization–positive or immunofluorescence-stained cells were observed mainly in the villous epithelium of small (duodenum to ileum) and large intestines (Table 2; Figure 2, panels G, I–K). Immunofluorescence was confined to the cytoplasm of villous epithelial cells (Figure 2, panel J) and was infrequently observed in crypt epithelial cells. No other internal organs of infected pigs showed in situ hybridization–positive or immunofluorescence-positive staining. In situ hybridization–positive or immunofluorescence-stained cells were not detected in negative control pigs (Figure 2, panels H, L) and PEDV-infected gnotobiotic pigs.

Under the experimental conditions used, no PDCoV-inoculated pigs at hpi 72–168 had detectable virus RNA (<3.6 log₁₀ GEs/mL) in serum. However, viremia was detected frequently in symptomatic PEDV-infected pigs (8,13).

Since 2013–2014, newly emerged PEDV and PDCoV have spread throughout the United States and caused a high number of pig deaths (1,2,6), but no studies of the pathogenicity of PDCoV have been reported. Our data confirm that PDCoV strains OH-FD22 and OH-FD100 are enteropathogenic and acutely infect the entire intestine. However, the jejunum and ileum are the primary sites of infection. PDCoV infection caused severe atrophic enteritis accompanied by severe diarrhea, vomiting, or both. These clinical and pathologic features in PDCoV-infected pigs resemble those of PEDV and TGEV infections. Differential diagnosis of PDCoV, PEDV, and TGEV is critical to control virus epidemic diarrhea on swine farms in the United States.