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Impact of Herpes Simplex Virus Type 2 and Human Immunodeficiency Virus Dual Infection on Female Genital Tract Mucosal Immunity and the Vaginal Microbiome.
Keller, Marla J; Huber, Ashley; Espinoza, Lilia; Serrano, Myrna G; Parikh, Hardik I; Buck, Gregory A; Gold, Jeremy A; Wu, Yiqun; Wang, Tao; Herold, Betsy C.
Affiliation
  • Keller MJ; Departments of Medicine, Albert Einstein College of Medicine, Bronx, New York.
  • Huber A; Departments of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York.
  • Espinoza L; Present Affiliation: Department of Obstetrics, Gynecology and Reproductive Medicine, Stony Brook University School of Medicine, Stony Brook, New York.
  • Serrano MG; Departments of Medicine, Albert Einstein College of Medicine, Bronx, New York.
  • Parikh HI; Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond.
  • Buck GA; Center for Microbiome Engineering and Data Analysis, Virginia Commonwealth University, Richmond.
  • Gold JA; School of Medicine Research Computing, University of Virginia, Charlottesville.
  • Wu Y; Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond.
  • Wang T; Center for Microbiome Engineering and Data Analysis, Virginia Commonwealth University, Richmond.
  • Herold BC; Computer Science Department, Virginia Commonwealth University, Richmond.
J Infect Dis ; 220(5): 852-861, 2019 07 31.
Article in En | MEDLINE | ID: mdl-31111902
ABSTRACT

BACKGROUND:

Mechanisms linking herpes simplex virus type 2 (HSV-2) with human immunodeficiency virus (HIV) are not fully defined. We tested the hypothesis that HSV-2 and HIV dual infection is associated with cervicovaginal inflammation and/or vaginal dysbiosis.

METHODS:

Genital tract samples were obtained weekly over a 12-week period from 30 women seropositive (+) for HIV and HSV-2 and 15 women each who were seropositive for one or seronegative (-) for both viruses. Immune mediators, antimicrobial activity, and microbial composition and diversity were compared.

RESULTS:

Significant differences in the concentrations of interferon-γ (P = .002), tumor necrosis factor-α (P = .03), human beta defensin 1 (P = .001), secretory leukocyte protease inhibitor (P = .01), and lysozyme (P = .03) were observed across the 4 groups (Kruskal-Wallis). There were also significant differences in vaginal microbial alpha diversity (Simpson index) (P = .0046). Specifically, when comparing HIV-1+/HSV-2+ to HIV-1-/HSV-2- women, a decrease in Lactobacillus crispatus and increase in diverse anaerobes was observed. The number of genital HSV outbreaks was greater in HIV+ versus HIV- women (39 versus 12) (P = .04), but there were no significant differences when comparing outbreak to non-outbreak visits.

CONCLUSIONS:

Increased microbial diversity and cervicovaginal inflammation in HIV and HSV-2 dually infected women may adversely impact genital health and, in the absence of antiretroviral therapy, facilitate HIV shedding.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Vagina / Herpes Genitalis / HIV Infections / Herpesvirus 2, Human / Immunity, Mucosal / Microbiota / Genitalia, Female Limits: Adult / Female / Humans / Middle aged Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Vagina / Herpes Genitalis / HIV Infections / Herpesvirus 2, Human / Immunity, Mucosal / Microbiota / Genitalia, Female Limits: Adult / Female / Humans / Middle aged Language: En Year: 2019 Type: Article