| Literature DB >> 30084033 |
Fangyuan Yin1, Junlong Liu1, Shandian Gao1, Aihong Liu1, Shuaiyang Zhao1, Sitong Li1, Jinming Wang1, Youquan Li1, Jianxun Luo1, Guiquan Guan2, Hong Yin3,4.
Abstract
Theileria annulata is the pathogen of bovine tropical theileriosis. It is extremely harmful to the cattle industry, with huge economic losses. The toll-like receptor (TLR) and NOD-like receptor (NLR) signaling pathways are crucial for resistance to infection of the protozoa, such as Plasmodium falciparum, Toxoplasma gondii, and Trypanosoma cruzi. However, the role of these immune-related pathways is unclear during T. annulata infection. In the present study, peripheral blood mononuclear cells and serum were separated from blood samples of calves infected with homogenized tick supernatants carrying T. annulata sporozoites at 12 h, 24 h, 36 h, 48 h, 72 h, 96 h, 120 h, 144 h and 168 h postinoculation. The Custom RT2 Profiler PCR Array was used to explore the mRNA levels of 42 TLR and NLR signaling pathway relevant genes. The TLR1, TLR6, TLR10, NLRP1, and MyD88 genes and their downstream signaling molecules significantly differed after the T. annulata infection in comparison with that of preinfection from 72 h to 168 h postinoculation. The serum concentrations of IL-6, IL-1β, and TNFα were significantly increased at 96 h and 168 h postinfection. These findings provided novel information to help determine the mechanisms of TLR and NLR signaling pathway involvement in protection against T. annulata infection.Entities:
Keywords: Innate immunity; NLRs; PCR array; TLRs; Theileria annulata
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Year: 2018 PMID: 30084033 DOI: 10.1007/s00436-018-6026-0
Source DB: PubMed Journal: Parasitol Res ISSN: 0932-0113 Impact factor: 2.289