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. 2024 Aug 21;12(10):e00829-24. doi: 10.1128/spectrum.00829-24

Fig 4.

Images and graphs compare fluorescence, VSV-GFP titer, and mRNA levels of VSV, SeV, EV71, and ZIKV in CRISPR V2 and A2B1 knockout cells at various post-infection times. Bar graphs plot the effect of A2B1 levels on VSV, SeV, EV71,and ZIKV mRNA expression.

HnRNP A2B1 upregulation of viral replication is conserved among RNA viruses. (A) WT and A2B1-/- THP-1 cells were infected with VSV-GFP at an MOI of 10 for 24 h. Green fluorescence was observed with a fluorescence microscope, and cells were observed with an inverted microscope (left). The relative fluorescence intensity was calculated using Image J software (light). (B) WT and A2B1-/- THP-1 cells were infected with VSV-GFP virus at an MOI of 10 for the indicated time points. VSV-GFP virus titers in cell culture supernatant were measured with TCID50. (C) WT and A2B1-/- THP-1 cells were infected at an MOI of 10 with VSV-GFP, SeV, EV71, or Zika for 12 h and 24 h, respectively. Viral mRNA levels were analyzed with RT-qPCR. (D) MEF cells were transfected with HA-tagged A2B1 for 24 h and then were infected at an MOI of 10 with VSV-GFP, SeV, EV71, or ZIKV for 12 h and 24 h, respectively. Viral mRNA levels were analyzed with RT-qPCR. Data were obtained from three independent experiments (n = 3). *P < 0.05, **P < 0.01, ***P < 0.001, ns, not significant.