2018
DOI: 10.1016/j.micpath.2018.09.023
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Molecular cloning of porcine 2′,5′-oligoadenylate synthetase-like protein and its role in porcine reproductive and respiratory syndrome virus infection

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Cited by 10 publications
(4 citation statements)
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“…For example, 2′-5′-oligoadenylate synthetase like (OASL) and interferon alpha inducible protein 6 (IFI6) were significantly up-regulated in the TC-Infection group at both transcriptome and proteome datasets, which were involved in immune response during virus infection. In particular, OASL not only inhibits PRRSV replication but also activates interferon-β production ( Wang et al, 2018 ). Furthermore, 256 genes belonging to both DEGs and DEPs in LW pigs ( Figure 4B , Supplementary Figure S5C ).…”
Section: Resultsmentioning
confidence: 99%
“…For example, 2′-5′-oligoadenylate synthetase like (OASL) and interferon alpha inducible protein 6 (IFI6) were significantly up-regulated in the TC-Infection group at both transcriptome and proteome datasets, which were involved in immune response during virus infection. In particular, OASL not only inhibits PRRSV replication but also activates interferon-β production ( Wang et al, 2018 ). Furthermore, 256 genes belonging to both DEGs and DEPs in LW pigs ( Figure 4B , Supplementary Figure S5C ).…”
Section: Resultsmentioning
confidence: 99%
“…The MARC-145 cells were infected with PRRSV (MOI = 1.0) at 37 °C for 1 h, followed by discarding the supernatant and culturing the cells in DMEM (2% FBS) at 37 °C for another 18 h. After three washes with DMEM, 24-well plates were added with fresh DMEM containing different concentrations of Gel-FeS NPs (0, 85.0, 170.0, 255.0, and 340.0 µg/mL). After incubation for 15, 30, 45 and 60 min, the PRRSV supernatant samples were collected, followed by adding fresh DMEM and collecting the cell lysate by freezing and thawing three times [ 63 ]. Finally, a plaque assay was performed to determine the virus content of the corresponding samples.…”
Section: Methodsmentioning
confidence: 99%
“…Briefly, monolayer cell plates were infected with PRRSV (MOI = 0.01) for 1 h in an incubator at 37 °C and further cultured with fresh DMEM (containing 2% fetal bovine serum) for another 17 h. Then, Rhe@AgNPs (S- and L-Rhe/Ag) with a concentration of 8.0 µg/mL and 16.0 µg/mL were added to the 24-well plate and cultured for 15, 30, 45, and 60 min, respectively. Finally, the supernatant was collected [ 43 ], and the virus content in the corresponding samples was determined by the TCID 50 assay [ 41 ].…”
Section: Experimental Partmentioning
confidence: 99%