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. 2011 Nov 1;7(9):1345–1356. doi: 10.7150/ijbs.7.1345

Figure 1.

Figure 1

Functional characterization of the recombinant AcNPV-LC3 baculovirus and schedule of immunization. AcNPV-LC3 baculovirus was generated by cloning the sequence of the E. histolytica Gal-lectin LC3 fragment into the pBlueCMV transfer plasmid downstream of the CMV promoter sequence (A). Ability of AcNPV-LC3 to drive the expression of LC3 in mammalian cells was carried out by Western blot on transduced HepG2 cells extract using a rabbit polyclonal anti-Gal-lectin heavy subunit antiserum. A band of the expected LC3 molecular weight of 50 kDa was observed in the transduced cells (B, line 3). No band was observed in non-transduced cells extract (B, line 2). Details on schedule immunization (oral and nasal routes), intraportal challenge with amoeba and sacrifice of hamsters is shown in C.