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Infection of ectocervical tissue explants with HIV-1BaL.

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posted on 2017-05-19, 17:39 authored by Andrea Introini, Stéphanie Boström, Frideborg Bradley, Anna Gibbs, Axel Glaessgen, Annelie Tjernlund, Kristina Broliden

Infection of ectocervical explants with HIV-1BaL was independently performed after seminal plasma (SP) 25% treatment (post-SP,red), or in the presence of SP25% (SP-mix, blue) (see S1B Fig). In selected experiments, explants infected in the presence of SP were treated with lamivudine (3TC) 10μM throughout culture time. A) Kinetics of HIV-1BaL replication in explants treated with SP (colored line) or culture medium (CM) (black line). Virus replication was evaluated as p24gag concentration in explant culture medium over 18 days. Represented are mean values with s.e.m. (n = 9 for post-SP; n = 8 for SP-mix; n = 3 for SP-mix+3TC). B) Cumulative p24gag production over culture time. Lines connect measurements obtained from donor-matched explants. C) N-fold change in cumulative p24gag production in SP-treated explants compared to donor-matched untreated explants. Bars indicate median values. p<0.05 denotes a significant difference with CM (Wilcoxon signed rank test). D) HIV-1 DNA quantification in explants infected with a mix of HIV and SP or CM, cultured in the presence or the absence of 3TC, and harvested at the end of culture (day18). HIV-1 DNA copy numbers were normalized to the amount of the single-copy gene HBB. Lines connect measurements obtained from donor-matched explants. E) N-fold change in HIV-1 DNA copy numbers in SP-treated explants compared to donor-matched untreated explants. The bar indicates median value. p<0.05 denotes a significant difference with CM (Wilcoxon signed rank test).

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