Figure 2
Figure 2. Accelerated replication of PVM in mouse bmEos from MyD88−/− mice. (A) Q-RT-PCR detection of virus titer in bmEos. Virus titer was determined in PVM-infected (filled symbols) and hiPVM-challenged (open symbols) wild-type (C57BL/6; circles) and MyD88−/− mouse bmEos (squares). Values shown are representative of 2 experiments performed in triplicate (data shown represent mean ± SEM); *P < .05. (B) Immunodetection of PVM in extracts of bmEos. PVM was detected at 9 days after inoculation of bmEos cultures on a Western blot probed with rabbit polyclonal anti-PVM N peptide antibody (αNPVM). Lanes 1 to 3 are extracts from bmEos from wild-type C57BL/6 mice; lanes 4 to 6, extracts from bmEos from MyD88−/− mice; lanes 1 and 4, from unchallenged bmEos (controls); lanes 2 and 5, from hiPVM-challenged bmEos; lanes 3 and 6, from PVM-infected bmEos. After probing with anti-PVM N antibody the blot was stripped and probed with anti–mouse GAPDH (αGAPDH) as a control for protein loading. Blot shown is single membrane, divided to omit intervening protein marker lanes.

Accelerated replication of PVM in mouse bmEos from MyD88−/− mice. (A) Q-RT-PCR detection of virus titer in bmEos. Virus titer was determined in PVM-infected (filled symbols) and hiPVM-challenged (open symbols) wild-type (C57BL/6; circles) and MyD88−/− mouse bmEos (squares). Values shown are representative of 2 experiments performed in triplicate (data shown represent mean ± SEM); *P < .05. (B) Immunodetection of PVM in extracts of bmEos. PVM was detected at 9 days after inoculation of bmEos cultures on a Western blot probed with rabbit polyclonal anti-PVM N peptide antibody (αNPVM). Lanes 1 to 3 are extracts from bmEos from wild-type C57BL/6 mice; lanes 4 to 6, extracts from bmEos from MyD88−/− mice; lanes 1 and 4, from unchallenged bmEos (controls); lanes 2 and 5, from hiPVM-challenged bmEos; lanes 3 and 6, from PVM-infected bmEos. After probing with anti-PVM N antibody the blot was stripped and probed with anti–mouse GAPDH (αGAPDH) as a control for protein loading. Blot shown is single membrane, divided to omit intervening protein marker lanes.

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