<p>(A) RD (left) or Jurkat (right) cells were infected with EV71-02363 mutants at 1 CCID<sub>50</sub> per cell for 1 h, then washed, cultured, and harvested at the indicated days (d) post-infection. (B, C) EV71 replication in Jurkat cells incubated with anti-PSGL-1 mAb and isotype control. Cells were pretreated with antibodies for 1 h and then infected with 1 CCID<sub>50</sub> per cell for 1 h, washed, cultured, and harvested at 3 days (d) post-infection. Viral titers are expressed as the mean, and error bars indicate s. d. for triplicate samples. (B) EV71-02363. (C) EV71-1095. Although arise in viral titer was observed for EV71-1095-EE at day 3 (asterisk), the recovered viruses were VP1-145E to G revertants.</p
<p>Viruses were produced by co-transfection of 293T cells with combinations of Env deficient backbon...
<p>(A) 293T, HeLa, NP2 and GHOST cells were transfected with four different plasmids (WT, ΔVpu, L30E...
<p>(<b>A</b>) Detection of EV71 genome, vimentin and ser 82-p vimentin distribution in virus infecte...
<p>Jurkat cells were transfected with the indicated molecular clones. At 2-day intervals the cells w...
<p>(A) Jurkat cells were transfected with the indicated molecular clones. At 2-day intervals the cel...
<p>Cell lines (293T, HeLa, NP2 and GHOST) were transfected with equal amount of wild-type pNL-AD8 (W...
<p>(A) HT29 cells were seeded on culture plates and infected with EV71 at the MOI of 1. Cell morphol...
<p>(A) pNL4-3 plasmids with mutations in <i>pol, env</i>-<i>nef</i> or both were constructed (marked...
<p>(A) Percentage of infected macrophages following infection with VSV-G pseudotyped WT virus (NHGca...
<p>(A) RD-A cells infected with EV71 virus at the MOI of 0, 1, 5 and 10 for 12 h were trypsinized an...
<p><b>(A)</b> A sequencing chromatogram of the mutated H-I loop region. <b>(B)</b> Viral titers in t...
(A) Jurkat cells were infected as in Fig. 2 with RT- NL4-3virions (Vpr) lacking Vpr (Δ) or containin...
<p>Peripheral blood mononuclear cells (PBMC) were prepared from blood of healthy donors. The experim...
Cellular mutants defective in the expression of viral polypeptides were isolated from the Friend ery...
<p>(A) 3X10<sup>5</sup> CEM-SS cells were infected with viral titers equivalent to 5 ng of p24 of VS...
<p>Viruses were produced by co-transfection of 293T cells with combinations of Env deficient backbon...
<p>(A) 293T, HeLa, NP2 and GHOST cells were transfected with four different plasmids (WT, ΔVpu, L30E...
<p>(<b>A</b>) Detection of EV71 genome, vimentin and ser 82-p vimentin distribution in virus infecte...
<p>Jurkat cells were transfected with the indicated molecular clones. At 2-day intervals the cells w...
<p>(A) Jurkat cells were transfected with the indicated molecular clones. At 2-day intervals the cel...
<p>Cell lines (293T, HeLa, NP2 and GHOST) were transfected with equal amount of wild-type pNL-AD8 (W...
<p>(A) HT29 cells were seeded on culture plates and infected with EV71 at the MOI of 1. Cell morphol...
<p>(A) pNL4-3 plasmids with mutations in <i>pol, env</i>-<i>nef</i> or both were constructed (marked...
<p>(A) Percentage of infected macrophages following infection with VSV-G pseudotyped WT virus (NHGca...
<p>(A) RD-A cells infected with EV71 virus at the MOI of 0, 1, 5 and 10 for 12 h were trypsinized an...
<p><b>(A)</b> A sequencing chromatogram of the mutated H-I loop region. <b>(B)</b> Viral titers in t...
(A) Jurkat cells were infected as in Fig. 2 with RT- NL4-3virions (Vpr) lacking Vpr (Δ) or containin...
<p>Peripheral blood mononuclear cells (PBMC) were prepared from blood of healthy donors. The experim...
Cellular mutants defective in the expression of viral polypeptides were isolated from the Friend ery...
<p>(A) 3X10<sup>5</sup> CEM-SS cells were infected with viral titers equivalent to 5 ng of p24 of VS...
<p>Viruses were produced by co-transfection of 293T cells with combinations of Env deficient backbon...
<p>(A) 293T, HeLa, NP2 and GHOST cells were transfected with four different plasmids (WT, ΔVpu, L30E...
<p>(<b>A</b>) Detection of EV71 genome, vimentin and ser 82-p vimentin distribution in virus infecte...