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. Author manuscript; available in PMC: 2015 May 8.
Published in final edited form as: J Gen Virol. 2008 Apr;89(0 4):1043–1048. doi: 10.1099/vir.0.83195-0

Table 1.

Temporal appearance of high frequency mutations during disease progression in vivo

Mutation
R1 S55L D135G Q138R R127K* G110D* V105A* S55P* R143H* G134D V112A
Group B B A A A A A A A A A
Days p.i.§ Inoc Inoc Inoc Inoc 118 201 754 754 754 Inoc 35
*

Mutations most frequently observed in the background of D135G/Q138R.

Mutation most frequently observed in the background of G134D.

Group assignment of high frequency mutations is based on previous phylogenetic and cluster analyses of Rev populations observed in vivo (Baccam et al., 2003). Variants in Group A have overall higher Rev activity than variants in Group B.

§

The first day post-inoculation each high frequency Rev mutation was observed at greater than 50 % frequency in the sampled population.