Early events in the pathogenesis of foot-and-mouth disease in pigs; identification of oropharyngeal tonsils as sites of primary and sustained viral replication

PLoS One. 2014 Sep 3;9(9):e106859. doi: 10.1371/journal.pone.0106859. eCollection 2014.

Abstract

A time-course study was performed to elucidate the early events of foot-and-mouth disease virus (FMDV) infection in pigs subsequent to simulated natural, intra-oropharyngeal, inoculation. The earliest detectable event was primary infection in the lingual and paraepiglottic tonsils at 6 hours post inoculation (hpi) characterized by regional localization of viral RNA, viral antigen, and infectious virus. At this time FMDV antigen was localized in cytokeratin-positive epithelial cells and CD172a-expressing leukocytes of the crypt epithelium of the paraepiglottic tonsils. De novo replication of FMDV was first detected in oropharyngeal swab samples at 12 hpi and viremia occurred at 18-24 hpi, approximately 24 hours prior to the appearance of vesicular lesions. From 12 through 78 hpi, microscopic detection of FMDV was consistently localized to cytokeratin-positive cells within morphologically characteristic segments of oropharyngeal tonsil crypt epithelium. During this period, leukocyte populations expressing CD172a, SLA-DQ class II and/or CD8 were found in close proximity to infected epithelial cells, but with little or no co-localization with viral proteins. Similarly, M-cells expressing cytokeratin-18 did not co-localize with FMDV proteins. Intra-epithelial micro-vesicles composed of acantholytic epithelial cells expressing large amounts of structural and non-structural FMDV proteins were present within crypts of the tonsil of the soft palate during peak clinical infection. These findings inculpate the paraepiglottic tonsils as the primary site of FMDV infection in pigs exposed via the gastrointestinal tract. Furthermore, the continuing replication of FMDV in the oropharyngeal tonsils during viremia and peak clinical infection with no concurrent amplification of virus occurring in the lower respiratory tract indicates that these sites are the major source of shedding of FMDV from pigs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adenoids* / metabolism
  • Adenoids* / pathology
  • Adenoids* / virology
  • Animals
  • CD8-Positive T-Lymphocytes / metabolism
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Epithelial Cells / virology
  • Female
  • Foot-and-Mouth Disease Virus / physiology*
  • Foot-and-Mouth Disease* / metabolism
  • Foot-and-Mouth Disease* / pathology
  • Histocompatibility Antigens Class II / metabolism
  • Male
  • Swine
  • Swine Diseases* / metabolism
  • Swine Diseases* / pathology
  • Swine Diseases* / virology
  • Virus Replication*

Substances

  • Histocompatibility Antigens Class II

Grants and funding

This research was funded in part by ARS-CRIS Project 1940- 32000-057-00D and an interagency agreement with the Science and Technology Directorate of the U.S. Department of Homeland Security (award number HSHQDC-11-X-00189). CS is a recipient of a Plum Island Animal Disease Center Research Participation Program fellowship, administered by the Oak Ridge Institute for Science and Education (ORISE; www.orau.org) through an interagency agreement with the US Department of Energy. Additional funding was received from the National Pork Board (NPB project identification number: 11-174; www.pork.org), a government-owned corporation that administers a competitive peer-reviewed grants process with the objective to select and fund projects researching areas of importance to the pork industry. None of the contributing authors are employed by NPB, nor professionally evaluated by this entity. The funding received from NPB does not alter our adherence to PLOS ONE policies on sharing data and materials. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.