Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1
Defensins, RNases and cytokines are present at mucosal barriers, main ports of HIV entry, and are potential mediators of the resistant phenotype exhibited by HIV-1-exposed seronegative individuals (HESN) during sexual exposure. We aimed to determine the role of solublefactors in natural resistance t...
- Autores:
-
Aguilar Jiménez, Wbeimar
Feng, Zhimin
Russo, Aniello
Potenza, Nicoletta
Estrada, Hernando
Rugeles López, María Teresa
Weinberg, Aaron
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2016
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/1352
- Acceso en línea:
- https://hdl.handle.net/20.500.12494/1352
- Palabra clave:
- Antiviral
HIV-1
(Human immunodeficiency virus type 1)
RNases
Natural resistance
Exposed seronegative
individuals
HBDs
- Rights
- embargoedAccess
- License
- Licencia CC
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dc.title.spa.fl_str_mv |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
title |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
spellingShingle |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 Antiviral HIV-1 (Human immunodeficiency virus type 1) RNases Natural resistance Exposed seronegative individuals HBDs |
title_short |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
title_full |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
title_fullStr |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
title_full_unstemmed |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
title_sort |
Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1 |
dc.creator.fl_str_mv |
Aguilar Jiménez, Wbeimar Feng, Zhimin Russo, Aniello Potenza, Nicoletta Estrada, Hernando Rugeles López, María Teresa Weinberg, Aaron |
dc.contributor.advisor.none.fl_str_mv |
Zapata Builes, Wildeman |
dc.contributor.author.none.fl_str_mv |
Aguilar Jiménez, Wbeimar Feng, Zhimin Russo, Aniello Potenza, Nicoletta Estrada, Hernando Rugeles López, María Teresa Weinberg, Aaron |
dc.subject.spa.fl_str_mv |
Antiviral HIV-1 (Human immunodeficiency virus type 1) RNases Natural resistance Exposed seronegative individuals HBDs |
topic |
Antiviral HIV-1 (Human immunodeficiency virus type 1) RNases Natural resistance Exposed seronegative individuals HBDs |
description |
Defensins, RNases and cytokines are present at mucosal barriers, main ports of HIV entry, and are potential mediators of the resistant phenotype exhibited by HIV-1-exposed seronegative individuals (HESN) during sexual exposure. We aimed to determine the role of solublefactors in natural resistance to HIV-1 infection. Vaginal/endocervical/oral mucosal samples were taken from 60 HESN, 60 seropositive (SP) and 61 healthy controls (HC). Human neutrophil peptide 1 (hNP-1), human beta defensin (hBD) 2 and 3, RNases, MIP-1b and RANTES mRNA transcripts were quantified by qPCR and in vitro single-round, recombinant-based viral infectivity assay was used to evaluate the anti-HIV-1 activity of hBDs and RNases. HESN expressed significantly higher levels of hNP-1, hBDs mRNA in oral mucosa compared to HC (P < 0.05). In genital mucosa, significantly higher mRNA levels of MIP-1b, RANTES and RNases were found in HESN compared to HC (P < 0.05). HBDs and RNases inhibit HIV-1 replication, particularly R5 at entry, reverse transcription and nuclear import of the viral life cycle. hNP-1, hBDs, MIP-1b, RANTES and RNases, collectively could contribute to HIV-1 resistance during sexual exposure. Moreover, the inhibition of HIV-1 infection in vitro by hBDs and RNases suggests that they may be exploited as potential antiretrovirals. |
publishDate |
2016 |
dc.date.issued.none.fl_str_mv |
2016-03 |
dc.date.accessioned.none.fl_str_mv |
2017-08-24T14:35:41Z |
dc.date.available.none.fl_str_mv |
2017-03 2017-08-24T14:35:41Z |
dc.type.none.fl_str_mv |
Artículo |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.coarversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
publishedVersion |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12494/1352 |
dc.identifier.bibliographicCitation.spa.fl_str_mv |
Zapata, W., Aguilar Jimenez, W., Feng, Z., Weinberg, A., Russo, A., Potenza, N., Estrada, H., & Rugeles, M. (2016). Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1. Microbes Infect, 18, 211-219 |
url |
https://hdl.handle.net/20.500.12494/1352 |
identifier_str_mv |
Zapata, W., Aguilar Jimenez, W., Feng, Z., Weinberg, A., Russo, A., Potenza, N., Estrada, H., & Rugeles, M. (2016). Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1. Microbes Infect, 18, 211-219 |
dc.relation.isversionof.spa.fl_str_mv |
http://www.sciencedirect.com/science/article/pii/S1286457915002324?via%3Dihub |
dc.rights.cc.none.fl_str_mv |
Licencia CC |
dc.rights.accessrights.none.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
dc.rights.coar.none.fl_str_mv |
http://purl.org/coar/access_right/c_f1cf |
rights_invalid_str_mv |
Licencia CC http://purl.org/coar/access_right/c_f1cf |
eu_rights_str_mv |
embargoedAccess |
dc.publisher.spa.fl_str_mv |
Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000 |
dc.publisher.program.spa.fl_str_mv |
Medicina |
dc.publisher.place.spa.fl_str_mv |
Medellín |
institution |
Universidad Cooperativa de Colombia |
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spelling |
Zapata Builes, WildemanAguilar Jiménez, WbeimarFeng, ZhiminRusso, AnielloPotenza, NicolettaEstrada, HernandoRugeles López, María TeresaWeinberg, Aaron2017-08-24T14:35:41Z2017-032017-08-24T14:35:41Z2016-03https://hdl.handle.net/20.500.12494/1352Zapata, W., Aguilar Jimenez, W., Feng, Z., Weinberg, A., Russo, A., Potenza, N., Estrada, H., & Rugeles, M. (2016). Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1. Microbes Infect, 18, 211-219Defensins, RNases and cytokines are present at mucosal barriers, main ports of HIV entry, and are potential mediators of the resistant phenotype exhibited by HIV-1-exposed seronegative individuals (HESN) during sexual exposure. We aimed to determine the role of solublefactors in natural resistance to HIV-1 infection. Vaginal/endocervical/oral mucosal samples were taken from 60 HESN, 60 seropositive (SP) and 61 healthy controls (HC). Human neutrophil peptide 1 (hNP-1), human beta defensin (hBD) 2 and 3, RNases, MIP-1b and RANTES mRNA transcripts were quantified by qPCR and in vitro single-round, recombinant-based viral infectivity assay was used to evaluate the anti-HIV-1 activity of hBDs and RNases. HESN expressed significantly higher levels of hNP-1, hBDs mRNA in oral mucosa compared to HC (P < 0.05). In genital mucosa, significantly higher mRNA levels of MIP-1b, RANTES and RNases were found in HESN compared to HC (P < 0.05). HBDs and RNases inhibit HIV-1 replication, particularly R5 at entry, reverse transcription and nuclear import of the viral life cycle. hNP-1, hBDs, MIP-1b, RANTES and RNases, collectively could contribute to HIV-1 resistance during sexual exposure. Moreover, the inhibition of HIV-1 infection in vitro by hBDs and RNases suggests that they may be exploited as potential antiretrovirals.wildeman.zapatab@campusucc.edu.coUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Programa de Medicina, Medellín y Envigado, Colombia, 00000MedicinaMedellínhttp://www.sciencedirect.com/science/article/pii/S1286457915002324?via%3DihubAntiviralHIV-1(Human immunodeficiency virus type 1)RNasesNatural resistanceExposed seronegativeindividualsHBDsIdentification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1Artículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionLicencia 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