Gag-Protease Sequence Evolution Following Protease Inhibitor Monotherapy Treatment Failure in HIV-1 Viruses Circulating in East Africa.

Around 2.5 million HIV-infected individuals failing first-line therapy qualify for boosted protease inhibitor (bPI)-based second-line therapy globally. Major resistance mutations are rarely present at treatment failure in patients receiving bPI and the determinants of failure in these patients remain unknown. There is evidence that Gag can impact PI susceptibility. Here, we have sequenced Gag-Protease before and following failure in 23 patients in the SARA trial infected with subtypes A, C, and D viruses. Before bPI, significant variation in Protease and Gag was observed at positions previously associated with PI exposure and resistance including Gag mutations L449P, S451N, and L453P and Protease K20I and L63P. Following PI failure, previously described mutations in Protease and Gag were observed, including those at the cleavage sites such as R361K and P453L. However, the emergence of clear genetic determinants of therapy failure across patients was not observed. Larger Gag sequence datasets will be required to comprehensively identify mutational correlates of bPI failure across subtypes

Observation of the screening signature in the lateral photovoltage of electrons in the Quantum Hall regime

The lateral photovoltage generated in the plane of a two-dimensional electron system (2DES) by a focused light spot, exhibits a fine-structure in the quantum oscillations in a magnetic field near the Quantum Hall conductivity minima. A double peak structure occurs near the minima of the longitudinal conductivity oscillations. This is the characteristic signature of the interplay between screening and Landau quantization.Comment: 4 pages, 4 figures, to be published in Phys. Rev.

Impact of the N348I Mutation in HIV-1 Reverse Transcriptase on Nonnucleoside Reverse Transcriptase Inhibitor Resistance in Non-Subtype B HIV-1▿

We investigated the effect of N348I alone and with M184V on nonnucleoside reverse transcriptase inhibitor (NNRTI) drug susceptibility and replicative capacity in B and non-B HIV-1 isolates. N348I reduced the susceptibility to all NNRTI drugs across subtypes. The replication capacity of all viruses in a variety of cell lines was impaired by N348I. Interestingly, the N348I and M184V double mutation compensated for the reduced NNRTI drug susceptibility observed in the N348I single mutant and marginally improved viral replicative capacity

Structural investigation of the stability in temperature of some high entropy / multi major components alloys as a function of their electronic structure

High Entropy Alloys (HEA) can be classified in three domains according to their e/a and r values, with e/a, the number of itinerant valence electrons and r the average radius for a 12 nearest atoms neighborhood. The phase composition, thermal stability and possible phase transformations of a series of HEA alloys, CoCrzFeNi-XY (with X and Y = Al, Cu, Pd, Ru, Ti and z = 0 or 1), selected according to their e/a ratio were investigated in cast conditions (T0), after 3 h homogenization at 1100 °C (T1) and after 3 h annealing at 700 °C (T3). When observing the behavior of the different Domains of HEAs as classified by electronic structure it is observed that for the alloys from Domain I which contain fcc structures, the microstructure transforms from multi-to almost single-phase under homogenization (T1). In Domain III alloys containing cubic (bcc and/or B2) structures, very small multi-structural changes are observed. Alloys in Domain II have a mixed structure, i.e. several different structures in the diffraction pattern, which changes during heat treatments

Structural investigation of the stability in temperature of some high entropy alloys as a function of their electronic structure

International audienceHigh Entropy Alloys (HEA) can be classified in three domains according to their e/a and r values, with e/a, the number of itinerant valence electrons and r the average radius for a 12 nearest atoms neighborhood. The phase composition, thermal stability and possible phase transformations of a series of HEA alloys, CoCrzFeNi-XY (with X and Y = Al, Cu, Pd, Ru, Ti and z=0 or 1), selected according to their e/a ratio were investigated in cast conditions (T0), after 3 hours homogenization at 1100°C (T1) and after 3 hours annealing at 700°C (T3). It is observed that for the alloys from domain I which contains fcc structures, the microstructure transforms from multi-to almost single-phase under homogenization (T1). In domain III alloys contains cubic (bcc and/or B2) structures very small multi-structural changes are observed. Alloys in domain II have mixed structure, i.e. several different structures in the diffraction pattern, which changes during heat treatments