Rotavirus NSP4 triggers secretion of proinflammatory cytokines from macrophages via Toll-Like Receptor 2

Yi Ge, Ashley Scott Mansell, James E Ussher, Anna E S Brooks, Kristy Manning, Carol J H Wang, John A Taylor

Research output: Contribution to journalArticleResearchpeer-review

43 Citations (Scopus)

Abstract

Nonstructural protein 4 (NSP4), encoded by rotavirus, exhibits various properties linked to viral pathogenesis, including enterotoxic activity. A recent study (O. V. Kavanagh et al., Vaccine 28:3106-3111, 2010) indicated that NSP4 also has adjuvant properties, suggesting a possible role in the innate immune response to rotavirus infection. We report here that NSP4 purified from the medium of rotavirus-infected Caco-2 cells triggers the secretion of proinflammatory cytokines from macrophage-like THP-1 cells and nitric oxide from murine RAW 264.7 cells. Secretion is accompanied by the stimulation of p38 and JNK mitogen-activated protein kinases (MAPKs) and nuclear factor NF-kappaB. NSP4 triggered the secretion of cytokines from murine macrophages derived from wild-type but not MyD88(-/-) or Toll-like receptor 2 (TLR2(-/-)) mice and induced secretion of interleukin-8 (IL-8) from human embryonic kidney cells transfected with TLR2 but not TLR4. Our studies identify NSP4 as a pathogen-associated molecular pattern (PAMP) encoded by rotavirus and provide a mechanism for the production of proinflammatory cytokines associated with the clinical symptoms of infection in humans and animals.
Original languageEnglish
Pages (from-to)11160 - 11167
Number of pages8
JournalJournal of Virology
Volume87
Issue number20
DOIs
Publication statusPublished - 2013

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