PROGRAM |
DISCIPLINE |
HEALTH THEMES |
|
---|---|---|---|
Disease Elimination | Life Sciences | HIV + AIDS; Sexual + Reproductive Health; Sexually Transmitted Infections (STI's) |
The composition of the vaginal microbiota can influence the transmission of pathogens such as HIV. Women colonised with optimal vaginal bacterial communities, typically dominated by beneficial Lactobacillus spp., have a decreased risk of acquiring and transmitting HIV compared to women colonised with non-optimal microbiota.
A non-optimal vaginal microbiota is characterised by a depletion of beneficial Lactobacillus spp. and high relative abundance of non-beneficial bacterial species, as exemplified by bacterial vaginosis (BV), which is a common form of vaginal dysbiosis in women of reproductive age that occurs in up to 55 per cent of women in sub- Saharan Africa where HIV predominates (McKinnon et al 2019 AIDS Res Hum Retroviruses 25(3)).
Non-optimal vaginal microbiota increase local pro-inflammatory cytokines, recruit activated HIV target cells and disrupt cervicovaginal epithelial barrier integrity that together drive increased risk of HIV acquisition. While studies have described the association between the vaginal microbiota and increased susceptibility to HIV and sexually transmitted infections (STIs), relatively little is known about how the microbiota and its metabolites act on the epithelium to mediate this effect. Major distinguishing features of women colonised with optimal vaginal microbiota compared to women with BV are a dramatic increase in the levels of lactic acid and depletion of short chain fatty acids, suggesting a role for these metabolites as effector molecules of vaginal bacteria and the mucosal environment.
Projects are available to determine the direct anti-HIV and bactericidal mechanisms of vaginal microbiota metabolites (VMBs), their immune modulatory and barrier promoting effects on cervicovaginal epithelial cells (Hearps et al, 2017 Mucosal Immunol 10:1480; Delgado-Diaz and Jesaveluk et al, 2022 Microbiome 10:141), and how these metabolites modulate HIV transmigration through cervicovaginal epithelium as well as their role in shifting vaginal microbiota composition. These studies underpin an exciting program at Burnet to advance antibiotic-sparing strategies to optimise the vaginal microbiota and dampen genital inflammation to decrease susceptibility to HIV, and other STIs as well as adverse reproductive health outcomes.
Contact
Professor Gilda Tachedjian
Head, Life Sciences Discipline; Head, Retroviral Biology and Antivirals Laboratory
gilda.tachedjian@burnet.edu.au
Dr Anna Hearps
Deputy Program Director, Disease Elimination
anna.hearps@burnet.edu.au
Dr Lindi Masson
Senior Research Fellow
lindi.masson@burnet.edu.au
Dr Joshua Hayward
Senior Research Officer
joshua.hayward@burnet.edu.au
Dr Paula Ellenberg
Laboratory Manager
paula.ellenberg@burnet.edu.au
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When you study at Burnet, you broaden your impact working across our three Institute-wide programs: Disease Elimination; Health Security and Pandemic Preparedness; Maternal, Child and Adolescent Health.
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