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...

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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
id COOPER2_fa0f3a22ea930986a0656e2145c0421d
oai_identifier_str oai:repository.ucc.edu.co:20.500.12494/1352
network_acronym_str COOPER2
network_name_str Repositorio UCC
repository_id_str
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
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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. 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