Engineering of Lactobacillus jensenii To Secrete RANTES and a CCR5 Antagonist Analogue as Live HIV-1 Blockers

被引:46
|
作者
Vangelista, Luca [1 ]
Secchi, Massimiliano [1 ]
Liu, Xiaowen [2 ]
Bachi, Angela [3 ]
Jia, Letong [2 ]
Xu, Qiang [2 ]
Lusso, Paolo [1 ,4 ]
机构
[1] Ist Sci San Raffaele, Div Immunol Transplantat & Infect Dis, I-20132 Milan, Italy
[2] Osel Inc, Santa Clara, CA 95054 USA
[3] Ist Sci San Raffaele, Unit Biol Mass Spectrometry, I-20132 Milan, Italy
[4] Univ Cagliari, Sch Med, I-09124 Cagliari, Italy
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CYANOVIRIN-N; MICROBICIDE DEVELOPMENT; INACTIVATING PROTEIN; VAGINAL MICROBICIDES; BACTERIAL VAGINOSIS; COMMENSAL BACTERIA; FUSION INHIBITORS; RATIONAL DESIGN; 2-DOMAIN CD4;
D O I
10.1128/AAC.01492-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The development of effective microbicides for the prevention of HIV-1 sexual transmission represents a primary goal for the control of AIDS epidemics worldwide. A promising strategy is the use of bacteria belonging to the vaginal microbiota as live microbicides for the topical production of HIV-1 inhibitors. We have engineered a human vaginal isolate of Lactobacillus jensenii to secrete the anti-HIV-1 chemokine RANTES, as well as C1C5 RANTES, a mutated analogue that acts as a CCR5 antagonist and therefore is devoid of proinflammatory activity. Full-length wild-type RANTES and C1C5 RANTES secreted by L. jensenii were purified to homogeneity and shown to adopt a correctly folded conformation. Both RANTES variants were shown to inhibit HIV-1 infection in CD4(+) T cells and macrophages, displaying strong activity against HIV-1 isolates of different genetic subtypes. This work provides proof of principle for the use of L. jensenii-produced C1C5 RANTES to block HIV-1 infection of CD4(+) T cells and macrophages, setting the basis for the development of a live anti-HIV-1 microbicide targeting CCR5 in an antagonistic manner.
引用
收藏
页码:2994 / 3001
页数:8
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