Histidine-Rich Glycoprotein Inhibits HIV-1 Infection in a pH-Dependent Manner
Author(s) -
Ezequiel Dantas,
Fernando Erra Díaz,
Pehuén Pereyra Gerber,
Augusto Varese,
Diana Jerusalinsky,
Alberto L. Epstein,
Hernán Garcı́a Rivello,
Ana Jaén,
Julieta Pandolfi,
Ana Ceballos,
Matías Ostrowski,
Juan Sabatté,
Jorge Geffner
Publication year - 2018
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01749-18
Subject(s) - biology , glycoprotein , histidine , virology , human immunodeficiency virus (hiv) , plasma protein binding , microbiology and biotechnology , biochemistry , amino acid
Vaginal intercourse represents a high-risk route for HIV-1 transmission. The efficiency of male-to-female HIV-1 transmission has been estimated to be 1 in every 1,000 episodes of sexual intercourse, reflecting the high degree of protection conferred by the genital mucosa. However, the contribution of different host factors to the protection against HIV-1 at mucosal surfaces remains poorly defined. Here, we report for the first time that acidic values of pH enable the plasma protein histidine-rich glycoprotein (HRG) to strongly inhibit HIV-1 infection. Because cervicovaginal secretions usually show low pH values, our observations suggest that HRG might represent a constitutive antiviral mechanism in the vaginal mucosa. Interestingly, infection by other viruses, such as respiratory syncytial virus and herpes simplex virus 2, was also markedly inhibited by HRG at low pH values, suggesting that extracellular acidosis enables HRG to display broad antiviral activity.
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