Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents

ABSTRACT Cervicovaginal inflammation, nonoptimal microbiota, T-cell activation, and hormonal contraceptives may increase HIV risk, yet associations between these factors and subclinical Candida colonization or hyphae are unknown. We collected cervicovaginal samples from 94 South African adolescents,...

Full description

Bibliographic Details
Main Authors: Anna-Ursula Happel, Melanie Gasper, Christina Balle, Iyaloo Konstantinus, Hoyam Gamieldien, Smritee Dabee, Katherine Gill, Linda-Gail Bekker, Jo-Ann S. Passmore, Heather B. Jaspan
Format: Article
Language:English
Published: American Society for Microbiology 2022-04-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.01626-21
_version_ 1811303498095001600
author Anna-Ursula Happel
Melanie Gasper
Christina Balle
Iyaloo Konstantinus
Hoyam Gamieldien
Smritee Dabee
Katherine Gill
Linda-Gail Bekker
Jo-Ann S. Passmore
Heather B. Jaspan
author_facet Anna-Ursula Happel
Melanie Gasper
Christina Balle
Iyaloo Konstantinus
Hoyam Gamieldien
Smritee Dabee
Katherine Gill
Linda-Gail Bekker
Jo-Ann S. Passmore
Heather B. Jaspan
author_sort Anna-Ursula Happel
collection DOAJ
description ABSTRACT Cervicovaginal inflammation, nonoptimal microbiota, T-cell activation, and hormonal contraceptives may increase HIV risk, yet associations between these factors and subclinical Candida colonization or hyphae are unknown. We collected cervicovaginal samples from 94 South African adolescents, aged 15 to 19 years, who were randomized to injectable norethisterone enanthate (Net-En), an etonorgesterol/ethinyl estradiol vaginal ring (NuvaRing), or oral contraceptives in the UChoose trial (NCT02404038) at baseline and 16 weeks post-randomization. We assessed cervicovaginal samples for subclinical Candida colonization (by quantitative PCR [qPCR]), hyphae (by Gram stain), microbiota composition (by 16S rRNA gene sequencing), cytokine concentrations (by Luminex), and cervical T-cell phenotypes and activation (by multiparameter flow cytometry). While hormonal contraceptive type did not influence incidence of Candida colonization or hyphae, hyphae presence was associated with significantly elevated concentrations of IL-22, IL-17A and IL-17F, all produced by Th17 cells, but not of other cytokines, such as IL-1β or IL-6, after adjustment for confounders. Subclinical Candida colonization was associated with reduced frequencies of Th17-like cells and elevated frequencies of CCR6-CCR10 T cells. Women with Candida hyphae were less likely to have bacterial vaginosis (BV). Persistent, subclinical colonization with Candida over 16 weeks was associated with significant increases in Th17-related cytokine concentrations and highly activated Th17-like and CCR6-CCR10 T-cell frequencies. These data suggest that vaginal Candida colonization and hyphae increase Th17-related cytokines, but not overall female genital tract inflammation in Sub-Saharan African adolescents. Persistent Candida colonization, even when asymptomatic, may increase Th17 cell frequencies and related cytokines and thereby could subsequently increase HIV risk, although the causal relationship requires confirmation. IMPORTANCE Sub-Saharan African female adolescents are globally at the highest risk of HIV acquisition, and genital inflammation, microbial dysbiosis, and cervical HIV target cell activation are thought to contribute to this risk. Previously, the relationship between these mucosal factors and subclinical vaginal Candida colonization or hyphae has not been described, and the role of HIV-susceptible Th17 cells in mediating anti-Candida immunity in the human female genital tract has not been clearly established. We show that presence of yeast hyphae was associated with increases in Th17 cell-related cytokines and the absence of microbial dysbiosis, and that persistent Candida colonization resulted in significant increases in Th17-related cytokines and highly activated Th17-like cell frequencies. Our results suggest that Th17 cells are important for anti-Candida immunity in the human female genital tract and that prolonged vaginal Candida colonization may contribute to increased HIV risk in Sub-Saharan African adolescents by increasing HIV target cell frequencies and activation.
first_indexed 2024-04-13T07:48:02Z
format Article
id doaj.art-677fd1cf332b4938be28d9bd84b16e31
institution Directory Open Access Journal
issn 2165-0497
language English
last_indexed 2024-04-13T07:48:02Z
publishDate 2022-04-01
publisher American Society for Microbiology
record_format Article
series Microbiology Spectrum
spelling doaj.art-677fd1cf332b4938be28d9bd84b16e312022-12-22T02:55:37ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972022-04-0110210.1128/spectrum.01626-21Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African AdolescentsAnna-Ursula Happel0Melanie Gasper1Christina Balle2Iyaloo Konstantinus3Hoyam Gamieldien4Smritee Dabee5Katherine Gill6Linda-Gail Bekker7Jo-Ann S. Passmore8Heather B. Jaspan9Department of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaSeattle Children’s Research Institute, Seattle, Washington, USADepartment of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaDepartment of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaDepartment of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaSeattle Children’s Research Institute, Seattle, Washington, USADesmond Tutu HIV Centre, University of Cape Town, Cape Town, South AfricaDesmond Tutu HIV Centre, University of Cape Town, Cape Town, South AfricaDepartment of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaDepartment of Pathology, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South AfricaABSTRACT Cervicovaginal inflammation, nonoptimal microbiota, T-cell activation, and hormonal contraceptives may increase HIV risk, yet associations between these factors and subclinical Candida colonization or hyphae are unknown. We collected cervicovaginal samples from 94 South African adolescents, aged 15 to 19 years, who were randomized to injectable norethisterone enanthate (Net-En), an etonorgesterol/ethinyl estradiol vaginal ring (NuvaRing), or oral contraceptives in the UChoose trial (NCT02404038) at baseline and 16 weeks post-randomization. We assessed cervicovaginal samples for subclinical Candida colonization (by quantitative PCR [qPCR]), hyphae (by Gram stain), microbiota composition (by 16S rRNA gene sequencing), cytokine concentrations (by Luminex), and cervical T-cell phenotypes and activation (by multiparameter flow cytometry). While hormonal contraceptive type did not influence incidence of Candida colonization or hyphae, hyphae presence was associated with significantly elevated concentrations of IL-22, IL-17A and IL-17F, all produced by Th17 cells, but not of other cytokines, such as IL-1β or IL-6, after adjustment for confounders. Subclinical Candida colonization was associated with reduced frequencies of Th17-like cells and elevated frequencies of CCR6-CCR10 T cells. Women with Candida hyphae were less likely to have bacterial vaginosis (BV). Persistent, subclinical colonization with Candida over 16 weeks was associated with significant increases in Th17-related cytokine concentrations and highly activated Th17-like and CCR6-CCR10 T-cell frequencies. These data suggest that vaginal Candida colonization and hyphae increase Th17-related cytokines, but not overall female genital tract inflammation in Sub-Saharan African adolescents. Persistent Candida colonization, even when asymptomatic, may increase Th17 cell frequencies and related cytokines and thereby could subsequently increase HIV risk, although the causal relationship requires confirmation. IMPORTANCE Sub-Saharan African female adolescents are globally at the highest risk of HIV acquisition, and genital inflammation, microbial dysbiosis, and cervical HIV target cell activation are thought to contribute to this risk. Previously, the relationship between these mucosal factors and subclinical vaginal Candida colonization or hyphae has not been described, and the role of HIV-susceptible Th17 cells in mediating anti-Candida immunity in the human female genital tract has not been clearly established. We show that presence of yeast hyphae was associated with increases in Th17 cell-related cytokines and the absence of microbial dysbiosis, and that persistent Candida colonization resulted in significant increases in Th17-related cytokines and highly activated Th17-like cell frequencies. Our results suggest that Th17 cells are important for anti-Candida immunity in the human female genital tract and that prolonged vaginal Candida colonization may contribute to increased HIV risk in Sub-Saharan African adolescents by increasing HIV target cell frequencies and activation.https://journals.asm.org/doi/10.1128/spectrum.01626-21vaginal candidiasisSub-Saharan Africagenital inflammationHIV target cellsmucosal immunity
spellingShingle Anna-Ursula Happel
Melanie Gasper
Christina Balle
Iyaloo Konstantinus
Hoyam Gamieldien
Smritee Dabee
Katherine Gill
Linda-Gail Bekker
Jo-Ann S. Passmore
Heather B. Jaspan
Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
Microbiology Spectrum
vaginal candidiasis
Sub-Saharan Africa
genital inflammation
HIV target cells
mucosal immunity
title Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
title_full Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
title_fullStr Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
title_full_unstemmed Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
title_short Persistent, Asymptomatic Colonization with Candida is Associated with Elevated Frequencies of Highly Activated Cervical Th17-Like Cells and Related Cytokines in the Reproductive Tract of South African Adolescents
title_sort persistent asymptomatic colonization with candida is associated with elevated frequencies of highly activated cervical th17 like cells and related cytokines in the reproductive tract of south african adolescents
topic vaginal candidiasis
Sub-Saharan Africa
genital inflammation
HIV target cells
mucosal immunity
url https://journals.asm.org/doi/10.1128/spectrum.01626-21
work_keys_str_mv AT annaursulahappel persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT melaniegasper persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT christinaballe persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT iyalookonstantinus persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT hoyamgamieldien persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT smriteedabee persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT katherinegill persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT lindagailbekker persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT joannspassmore persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents
AT heatherbjaspan persistentasymptomaticcolonizationwithcandidaisassociatedwithelevatedfrequenciesofhighlyactivatedcervicalth17likecellsandrelatedcytokinesinthereproductivetractofsouthafricanadolescents