BackgroundSemen is a critical vector for human immunodeficiency virus (HIV) sexual transmission and harbors seminal amyloid fibrils that can markedly enhance HIV infection. Semen-derived enhancer of viral infection (SEVI) is one of the best-characterized seminal amyloid fibrils. Due to their highly cationic properties, SEVI fibrils can capture HIV virions, increase viral attachment to target cells, and augment viral fusion. Some studies have reported that myricetin antagonizes amyloid β-protein (Aβ) formation; myricetin also displays strong anti-HIV activity in vitro.ResultsHere, we report that myricetin inhibits the formation of SEVI fibrils by binding to the amyloidogenic region of the SEVI precursor peptide (PAP248–286) and disrupting PAP248–286 oligomerization. In addition, myricetin was found to remodel preformed SEVI fibrils and to influence the activity of SEVI in promoting HIV-1 infection. Moreover, myricetin showed synergistic effects against HIV-1 infection in combination with other antiretroviral drugs in semen.ConclusionsIncorporation of myricetin into a combination bifunctional microbicide with both anti-SEVI and anti-HIV activities is a highly promising approach to preventing sexual transmission of HIV.Electronic supplementary materialThe online version of this article (10.1186/s12977-018-0432-3) contains supplementary material, which is available to authorized users.

Extended abstract of a paper presented at Microscopy and Microanalysis 2013 in Indianapolis, Indiana, USA, August 4 – August 8, 2013.

C17H15NO, monoclinic, C2/c (no. 15), a = 19.197(2) Å, b = 8.0719(8) Å, c = 16.6511(18) Å, α = 90°, β = 100.171(10)°, γ = 90°,V = 2539.6(5) Å3, Z = 8, Rgt(F) = 0.0416, wRref(F2) = 0.1107, T = 100(1) K.CCDC no.: 2020262

C19H20O8, triclinic, P 1 ‾ $P\bar{1}$ (no. 2), a = 7.0708(4) Å, b = 8.1261(4) Å, c = 16.1067(6) Å, α = 81.252(4)°, β = 81.500(4)°, γ = 77.890(4)°, V = 887.88(8) Å3, Z = 2, R gt (F) = 0.0418, wR ref(F 2) = 0.1158, T = 150 K.