Porcine hemagglutinating encephalomyelitis virus infection in vivo and ex vivo

• Published in: Journal of virology 2021-05, Vol.95 (12)
• Main Authors: Mora-Díaz, Juan Carlos, Piñeyro, Pablo E, Rauh, Rolf, Nelson, William, Sankoh, Zianab, Gregg, Edward, Carrillo-Ávila, José Antonio, Shen, Huigang, Nelli, Rahul K, Zimmerman, Jeffrey J, Giménez-Lirola, Luis G
• Format: Article
• Language: English
• Subjects: Pathogenesis and Immunity
• ISSN: 0022-538X; 1098-5514
• DOI: 10.1128/JVI.02335-20

Porcine hemagglutinating encephalomyelitis virus (PHEV) is a Betacoronavirus that causes vomiting and wasting disease and/or encephalomyelitis in suckling pigs. This study characterized PHEV infection, pathogenesis, and immune response in caesarean-derived, colostrum-deprived (CDCD) neonatal pigs. Infected animals developed mild respiratory, enteric, and neurological clinical signs between 2 to 13 days post oronasal inoculation (dpi). PHEV did not produce viremia, but virus shedding was detected in nasal secretions (1-10 dpi) and feces (2-7 dpi) by RT-qPCR. Viral RNA was detected in all tissues except liver, but the detection rate and RT-qPCR Ct values decreased over time. The highest concentration of virus was detected in inoculated piglets necropsied at 5 dpi in turbinate and trachea, followed by tonsils, lungs, tracheobronchial lymph nodes, and stomach. The most representative microscopic lesions were gastritis lymphoplasmacytic, moderate, multifocal, with perivasculitis, and neuritis with ganglia degeneration. A moderate inflammatory response, characterized by increased levels of IFN-α in plasma (5 dpi) and infiltration of T lymphocytes and macrophages was also observed. Increased plasma levels of IL-8 were detected at 10 and 15 dpi, coinciding with the progressive resolution of the infection. Moreover, a robust antibody response was detected by 10 dpi. An air-liquid CDCD-derived porcine respiratory cells culture (ALI-PRECs) system showed virus replication in ALI-PRECs and cytopathic changes and disruption of ciliated columnar epithelia, thereby confirming the tracheal epithelia as a primary site of infection for PHEV. Among the ∼46 virus species in the Family (2019), many of which are important pathogens of humans and 6 of which are commonly found in pigs, porcine hemagglutinating encephalomyelitis remains one of the least researched. The present study provided a comprehensive characterization of the PHEV infection process and immune responses using CDCD neonatal pigs. Moreover, we used an porcine respiratory cells culture (ALI-PRECs) system resembling the epithelial lining of the tracheobronchial region of the porcine respiratory tract to demonstrate that the upper respiratory tract is a primary site of PHEV infection. This study provides a platform for further multidisciplinary studies of coronavirus infections.