Next Article in Journal
Ciprofloxacin and Clinafloxacin Antibodies for an Immunoassay of Quinolones: Quantitative Structure–Activity Analysis of Cross-Reactivities
Next Article in Special Issue
Recent Advances on Microbiota Involvement in the Pathogenesis of Autoimmunity
Previous Article in Journal
Molecular Network-Based Drug Prediction in Thyroid Cancer
Previous Article in Special Issue
Bacteriocins and Bacteriophages: Therapeutic Weapons for Gastrointestinal Diseases?
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Interplay among Vaginal Microbiome, Immune Response and Sexually Transmitted Viral Infections

Maria Gabriella Torcia
Department of Clinical and Experimental Medicine, University of Firenze, 50139 Firenze, Italy
Int. J. Mol. Sci. 2019, 20(2), 266;
Submission received: 6 December 2018 / Revised: 7 January 2019 / Accepted: 8 January 2019 / Published: 11 January 2019


The vaginal ecosystem is important for women’s health and for a successful reproductive life, and an optimal host-microbial interaction is required for the maintenance of eubiosis. The vaginal microbiota is dominated by Lactobacillus species in the majority of women. Loss of Lactobacillus dominance promotes the colonization by anaerobic bacterial species with an increase in microbial diversity. Vaginal dysbiosis is a very frequent condition which affects the immune homeostasis, inducing a rupture in the epithelial barrier and favoring infection by sexually transmitted pathogens. In this review, we describe the known interactions among immune cells and microbial commensals which govern health or disease status. Particular attention is given to microbiota compositions which, through interplay with immune cells, facilitate the establishment of viral infections, such as Human Immunodeficiency Virus (HIV), Human Papilloma Virus (HPV), Herpes Simplex Virus 2 (HSV2).

1. The Vaginal Ecosystem

The vaginal mucosal ecosystem is comprised of a stratified squamous epithelium covered by a mucosal layer continuously lubricated by cervicovaginal fluid (CVF), which contains products of epithelial cells, such as mucins and antimicrobial molecules B-Defensin, Lipocalin, Elafine and secretory leukocyte protease inhibitor (SLPI) [1,2], IgA and IgG antibodies produced by mucosal plasma cells. CVF continuously lubricates epithelium, maintains the fluidity of the ecosystem and represents the first line of defense against exogenous pathogen colonization through the activity of mucins which entrap microbes and facilitate their binding to antibodies [3].
Cervicovaginal fluid also helps to contain the vaginal microbiota, microbial communities which exist in a mutualistic relationship with the host. The vaginal microbiota is unique in that, in many women, it is most often dominated by Lactobacillus species [4,5]. The latter produce lactic acid and bacteriocins, which contribute to prevent bacterial growth and, by maintaining a low vaginal pH (3.0–4.5), eventually favor Lactobacillus dominance. Moreover, Lactobacillus species adhere to epithelial surfaces, preventing the adhesion of bacteria able to infect epithelial cells, promote the autophagy of cells infected by viruses, bacteria or protozoa, facilitating their elimination [6], and modulate any inflammatory process that could have negative consequences, especially during pregnancy [7].
These activities are also necessary to prevent immune reactions against sperm. It is believed that the human behavior with sexual activities at any time during the menstrual cycle, as well as during gestation, may have contributed to select Lactobacillus species in the vaginal microbiota.
The detailed composition of vaginal microbiota and the relative abundance of the bacterial species has recently been defined through high-throughput 16s rRNA gene sequencing. At least five microbial communities, here referred as Community State Type (CST) were identified. Four CSTs are dominated by Lactobacillus (L.) species highly adapted to the vaginal environment [4,5]. In particular CST-I is dominated by Lactobacillus crispatus; CST-II by Lactobacillus gasseri; CST-III by Lactobacillus iners; CST-V by Lactobacillus jensenii. The CST-IV is comprised by polymicrobial communities, with prevalence of strictly anaerobic species of the order Gardnerella, Atopobium, Mobiluncus, Megasphoera Prevotella, Streptococcus, Mycoplasma, Ureaplasma, Dialister, Bacteroides, etc. [4,8,9]. The latter CST is very common in black and Hispanic women, ranging from 10% in United States [4] to 60% in South Africa [10]. The factors driving racial and geographic differences in cervicovaginal communities are not known yet, but could include changes in sexual behavior, hygienic practices, rectal colonization or even host genetics [11].
In many cases, a low vaginal pH may be maintained by microbes of CST-IV through the production of lactic acid [9], in this case, the presence of CST-IV is completely asymptomatic. However, loss of Lactobacillus dominance facilitates Bacterial Vaginosis (BV), the most common vaginal infection in reproductive-aged women [12,13], characterized by vaginal discharge, irritation, fishy odor and a vaginal pH often >4.5. Hormonal changes strongly affect the composition of vaginal microbiota during a woman’s life, in particular at menopausal age, when reduced estrogen levels decrease the glycogen availability with the consequent depletion in Lactobacillus species [14].
In addition to epithelial cells and microbiota, the vaginal ecosystem comprises also cells of innate and adaptive immunity as neutrophils, macrophages, classic dendritic cells, Langerhans cells, NK cells, T and B lymphocytes. [15]. CD3+ T lymphocytes, predominantly CD8+ lymphocytes, are distributed in the lamina propria of the cervix and vagina. In particular, in ectocervical mucosa they have an effector/memory (CD27 CD45RA) or effector phenotype (CD27CD45RA+); B cells are found as aggregates or follicular-like structures surrounded by T lymphocytes. Plasma cells, as well as a small number of macrophages CD68+ and dendritic cells, are distributed throughout the lamina propria. Dendritic cells and monocyte/macrophagic CD14+ cells represent the most prevalent antigen-presenting cells in the vaginal ecosystem. Immune cell trafficking and activation throughout the reproductive tract is tightly mediated by the expression of pattern recognition receptors (PRR) [16,17] and is regulated by endocrine signaling [18].

2. Interplay between Host and Vaginal Microbiota in Health and Disease

Interplay between the cervicovaginal microbiota and the cells of immune system is determinant to prevent infections by external pathogens and to maintain an immuno-tolerant environment, particularly during pregnancy. Sex hormones are key regulators of this interplay: they regulate the production of antimicrobial peptides (beta-defensin, alpha Defensin, SLPI) and of pro-inflammatory cytokines (IL-6, IL-8) by the vaginal epithelial cells to ensure, when necessary, survival of sperm and to prevent ascending infections [19]; estrogens in particular also contribute to select microbial populations. At prepuberal age, vaginal microbiota is dominated by anaerobic species of the Enterobacteriacee and/or Staphylococcacee family. At puberty, the increased concentrations of estrogens promote the accumulation of glycogen by mature epithelial cells. Maltotriose and alpha-dextrins, derived from alpha-amylase-mediated glycogen digestion are selective food for Lactobacillus species that use these products for the synthesis of lactic acid. The low pH, the maintenance of mucous viscosity and the prevention of bacterial binding on epithelial surfaces are all factors that favor Lactobacillus dominance [20].
When Lactobacillus dominance is lost and microbial diversity increases, changes in immune and epithelial homeostasis often appear, induced through multiple mechanisms, as: (a) production of pro-inflammatory cytokines and chemokines, (b) recruitment of immune cells (c) reduction in the viscosity of the CVF, due to the production of mucin-degrading enzymes (including sialidase, α-fucosidase, α-and β-galactosidase, N-acetyl-glucosaminidase, and glycine and arginine aminopeptidases [21,22]. Physical/chemical changes in vaginal ecosystem ultimately affect the barrier properties of both CVF and the genital epithelium and increase the risk of infection with sexually transmitted pathogens. In fact, vaginal dysbiosis was associated with increased risk of acquisition of Sexual Transmitted Infections (STI) such as Neisseria gonorrhoeae, Chlamydia trachomatis, Trichomonas vaginalis, Herpes Simplex Virus (HSV), Human Papilloma Virus (HPV), and Human Immunodeficiency Virus (HIV) [12,13]. Even in the absence of clinical symptomatology, women harboring CST-IV in vaginal microbiota may be at high risk of STI or of early pregnancy loss and pre-term delivery [20].
STI impose major health and economic burdens globally, in particular in low- and middle-income countries (LMICs) [23]. It is estimated that about 18.9 million people, of whom 48% aged 15 to 24 years, acquired a new STI every year [24]. This is likely an underestimation of the real incidence of STI, as they are often asymptomatic.
Sexually transmitted viral infections, the subject of this review, also represent a serious health problem globally. A total of 34 million people were living with HIV at the end of 2011. Worldwide prevalence of genital HPV infection is estimated at 440 million persons, causing 510,000 cases of cervical cancer and approximately 288,000 deaths [25]. An estimated 417 million people aged 15–49 (11%) worldwide have Herpes Simplex Virus type 2 (HSV-2) infection, and HSV-2 incidence was 23.6 million new cases per year [26]. Prevalence of HSV-2 infection was estimated to be highest in Africa (31.5%), followed by the Americas (14.4%). It increases with age, though the highest numbers of people newly-infected were adolescents [27].
Risk factors commonly associated with acquisition of STI include biological and behavioral factors, number of sexual partners, lack of information about transmission modalities, difficulty to access to prevention services and, as reported above, selected compositions of the vaginal microbiota [28]. Moreover, the epidemiology of these infections is extremely complicated by the fact that each of them increases the risk of contracting other STI.
Metagenomic studies largely contributed to define the microbial communities most frequently associated with these infections. The assessment of the interplay among microbial communities, immune cells reactivity and epithelial homeostasis has contributed to define the environment in which infections are established and, in particular for HPV infection, also the one that facilitates persistence of the pathogen. This information will be helpful for the development of new diagnostic assays as well as new therapeutic strategies based on the replacement of harmful microbial communities. The following sections describe in greater detail current knowledge on the interplay between vaginal microbiota, immune system and epithelial cells in the most prevalent sexually transmitted viral infections: HIV, HPV, HSV-2.

3. The Vaginal Microbiota and HIV Infection

The importance of understanding how bacterial communities modulate female genital health has come strongly into focus, in particular with the evolving knowledge about the influence of cervicovaginal microbiota on HIV acquisition. As known, the highest incidence of HIV infections, with an extraordinarily high number of infected women in reproductive age, is in the African continent and, particularly in the sub-Saharan regions.
Socio-economic factors largely contribute to such high incidence. The prevalence of CST-IV in the vaginal microbiota of African women, however, also suggested that this CST may affect the susceptibility to HIV infection. The molecular mechanisms that have been suggested are:
(A) A decrease in D-lactate concentrations and the lowering of virions trapping. In fact, d-lactate, the main metabolic product of numerous Lactobacillus species, including L. crispatus, contributes to trap virions by favoring hydrogen bridges between HIV surface proteins and carboxylic groups of mucins [29].
(B) CST-IV microbes produce enzymes that degrade the mucus included sialidase, α-fucosidase, α-and β-galactosidase, N-acetyl-glucosaminidase, and glycine and arginine aminopeptidases [21,22,30].
(C) Antigen-presenting cells activated by bacterial products, in particular LPS, produce cytokines and chemokines which increase the recruitment of activated CD4+ lymphocytes [10].
The first observations on the associations between defined microbial communities and HIV susceptibility were obtained in cross-sectional studies. These studies have a serious limitation since the recruited people were at “high risk” of infection (e.g., sex workers) and left the doubt that changes in the microbiome may be a consequence of HIV infection rather than a contributing cause [10,31,32,33]. Recently, however, these doubts have been resolved: a prospective study on a cohort of healthy HIV-uninfected black South African women who were monitored for incident HIV infection clearly showed that none of the women who acquired HIV had a L. crispatus dominant community [34]; in contrast, women belonging to CST-IV experienced up to four-fold greater rates of HIV acquisition during follow-up compared to women of the CST-I, dominated by L. crispatus [34]. In particular, a subgroup of CST-IV dominated by Prevotella bivia, Prevotella melaninogenica, Veillonella montpellierensis, Mycoplasma species, and Sneathia sanguinegens was identified as the cervicotype with significantly higher risk of HIV acquisition [34]. Recent observations expanded the number of bacterial taxa associated with increased risk of HIV acquisition: in addition to Prevotella species, Parvimonas species type 1 and type 2, Gemella asaccharolytica, Eggerthella species type 1 and vaginal Megasphaera species were significantly associated with HIV acquisition [35].
The mechanisms underlying the increased HIV susceptibility likely reside in the ability of the bacterial taxa to induce a strong inflammation in the cervicovaginal environment with elevated concentrations of IL-17, IL-23 and IL-1β and high recruitment of CCR5+ CD4 T cells, the primary target of HIV infection. These cells also show an activated phenotype (HLA-DR+CD38+) and thus they are highly permissive for viral replication [34]. High numbers of activated γδ CD4 T lymphocytes expressing the Vδ2 chain, which potentially are targets of HIV and permissive for its replication, were also found increased in women with vaginal microbiota not dominated by Lactobacillus species [36], thus defining a framework where selected microbial communities are closely linked with immune activation and HIV infection.
Such knowledge also suggests that, in addition to vaccines, strategies to prevent HIV infection may include the stable colonization of vaginal microbiota with non-dangerous bacterial taxa to limit inflammation and T-cell recruitment. Since vaginal dysbiosis may undermine the efficacy of locally administered antiviral drugs [37], changes in vaginal microbiota will also improve the efficacy of these drugs.

4. The Vaginal Microbiota and HPV Infection

Infection with HPV is the most common viral infection of the reproductive tract and high-risk (HR) genital HPVs are central etiological agents in the development of cervical cancer and of its premalignant precursor, cervical intraepithelial neoplasia (CIN) [38]. HR-HPV genotypes 16, 18, 31, 33, and 35 are the most diffuse worldwide. Other HR genotypes are HPV 39, 45, 51, 52, 56, 58, 66 and 69 [39]. Generally, HPV infects the basal layer of the cervical squamous epithelium, where viral genomes persist as episomes at low-copy numbers [40]. High copies of virions are produced upon differentiation of epithelial cells and the new progeny of virions may be released from the epithelial surface. Infection of stem cell-like cells of the basal layer ensures persistence of infection [41].
The oncogenic activity of HR-HPVs is based on the functional properties of their E6 and E7 proteins [42]. These proteins inactivate p53 and retinoblastoma protein, respectively, and lead to the inhibition of apoptosis and to cell cycle progression of cells at the basal and differentiated layers of cervical epithelium. Viral integration with genetic alterations ultimately may induce uncontrolled cell proliferation [43,44]. At the histological level, different grades of squamous intraepithelial lesions are the result of persistent HR-HPV infection and, if undetected and untreated, they may lead to high-grade lesions and cancer in an average of 5 to 15 years [45].
The immune response to acute HPV infections is initially mediated by mucosal NK cells [46,47] and by epithelial cells which produce antimicrobial peptides with reported anti-viral effects [48]. However, HR-HPVs have evolved molecular strategies to escape innate and adaptive immunity [49,50,51,52]. HR-HPV infection never associates with a marked pro-inflammatory environment [53,54,55]. A rather high number of CD4+ CD25+ regulatory T cells and the presence of activated TH2 cells were reported in HR-HPV persistent infections and associated with the suppression of cytotoxic functions, induction of T cell anergy [56,57]. Consequently, virus-induced immune suppression may be responsible for increased infection with other sexually transmitted diseases such as Chlamydia trachomatis infection [58,59].
Emerging data support the notion that the vaginal microbiome is involved in the natural history of the disease [46].
Since HPV infections, even with HR genotypes, may be transient and more than 50% of them are cleared within six months while almost 90% are cleared within two years, we believe it is critical to consider data obtained in longitudinal studies and to devote special attention to the context in which they were obtained [4,46]. The first longitudinal study observed a cohort of 32 North American sexually active and premenopausal women over the course of 16 weeks using self-sampling at twice-weekly intervals [14]. A total of 930 samples of cervicovaginal mucous were obtained and microbiota studies revealed that women with CSTs III (dominance of L. iners) or with a subtype of CST-IV with a high proportion of Atopobium, Prevotella, Gardnerella species were most likely to be HPV positive and had the slowest rate of infection clearance.
In a subsequent survey, Di Paola et al. [30] used cervicovaginal samples collected in a study for HR-HPV screening program in Italy. A total of 55/1029 samples were positive for HR-HPV at the baseline screening. The authors used the results of the second HR-HPV screening performed after one year to stratify the baseline sampling in Clearance group, with no evidence of HR-HPV DNA after one year; the Persistence group, HR-HPV+ with at least one of the HPV-DNA genotypes of the baseline sampling after one year. A group of cervicovaginal samples from women negative for HR-HPV (HR-HPV) infections was included as a control. The results of this study showed that a subgroup of CST-IV dominated by strictly anaerobic species (Gardnerella, Prevotella, Atopobium, Megasphoera) was prevalent in the Persistence group, compared with either the Clearance or Control group. Odds ratio analysis confirmed that this CST may be a risk factor for the persistence of HR-HPV infection.
In agreement with previous reports [60,61], a significant enrichment in Sneathia and Megasphaera was found in the group of HR-HPV+ women, compared to HR-HPV controls, while the Atopobium genus was significantly enriched in Persistence group, compared to the other groups.
Although the association of bacterial vaginosis with higher rates of HPV infection and persistence has been known from a long time [62], metagenomic data revealed that selected microbiota compositions increase the risk of infection, even in the total absence of clinical symptomatology. While it is quite clear that some microbial communities favor HPV infection by modifying the barrier effect of cervical mucus and of stratified epithelium, the effects of microbiota-related immunological changes on the outcomes of HPV infection are not elucidated yet. This may depend on the impact of HPV infection on the host’s immune defenses [53,54], and on the mucosal metabolism which can also affect the composition of the vaginal microbiota. Therefore, the immunological signature of HPV infection on vaginal microbiota has to be further elucidated and more data are needed to have a full understanding of how HPV infections are modulated by the vaginal environment.
Persistent infection with HR-HPV is a necessary, but not sufficient, condition for the development of cervical cancer. As soon as the establishment of HR-HPV infection occurs, cellular changes can be observed in the cervical exfoliated cells. Persistent infections can result in different grades of squamous intraepithelial lesions that ultimately lead to high-grade lesions and cancer in an average of 5 to 14 years if undetected and untreated [45].
Recently, much attention has been given to the role of vaginal microbiota in the progression of epithelial lesions up to carcinogenesis. Drago et al. [63] found a strong correlation between Ureaplasma parvum-HPV co-infection and CIN1. Mitra et al. [64] have studied a cohort of 169 women with different degrees of cervical lesions and showed that increasing severity of cervical lesions was associated with higher vaginal microbiome diversity and decreased relative abundance of Lactobacillus species. CST-IV was associated with increasing disease severity, irrespective of HPV status. [61,65]. In particular, Atopobium vaginae and Lactobacillus iners were associated with an increased risk of neoplastic progression in HPV+ women [61], while Sneathia sanguinegens [54,61,64] and other Fusobacterial species [61], Anaerococcus tetradius and Peptostreptococcus anaerobius [64], were shown to be associated with an increase in disease severity. Novel bacterial taxa (Shuttleworthia, Gemella and Olsenella) and Streptococcus agalactiae were found enriched in HPV+ women with low- and high-grade cervical dysplasia (LGD, HGD), invasive cervical carcinoma (ICC) [54]. Sneathia spp. was the only taxon significantly enriched both in HPV+ women without lesions of any grade and in women with precancerous lesions and cervical cancer, suggesting that this taxon may represent a metagenomic marker for CIN progression. In particular, Sneathia spp. were found enriched in precancerous groups, and invasive cervical cancer, particularly in subjects of Hispanic ethnicity [54].
The molecular mechanisms through which bacteria of CST-IV may favor neoplastic progression are: (a) they produce high levels of nitrosamines which are known carcinogens; (b) they induce DNA oxidative damage [66].
While HPV infection or clearance is not marked by a pro-inflammatory environment, patients with cervical dysplasia and ICC were shown to have an increase in pro-inflammatory cytokines and chemokines (TNF-α, TNF-β, MIP-1α, GM-CSF), as well as an increase in cytokines related to adaptive immune responses (IL-2, IL-4, SCD40L). [67]. Moreover, the concentrations of the immunomodulating cytokine IL-10 were found to be increased in the ICC group. However, no direct association between the increased concentrations of cytokines and chemokines and the microbiota composition was revealed. Only the concentration of IL36γ was always elevated in patients with carcinoma, suggesting a direct or indirect role of this cytokine in the carcinogenetic process [54]. These data strongly suggest that, similar to other mucosal sites, chronic genital inflammation may promote carcinogenesis.
In the future it is highly likely that metabolomic studies, using nuclear magnetic resonance and mass spectroscopy, may better define the association of vaginal microbiota composition in health and disease states. A better definition of the effects of individual bacterial species, such as L. iners, A. vaginae, and Sneathia species, on epithelial and immune cell functions is desirable. In fact, if the responsibility of a single bacterial species in HPV disease is defined, it will be possible to identify patients at higher risk using microchip array or metabolomic technologies. Moreover, it will be possible to develop new therapeutic strategies based on pre/probiotics, in order to manipulate the vaginal microbiota composition.

5. Herpes Simplex Virus Type-2 (HSV-2)

Herpes simplex virus type-2 (HSV-2) is a common STI worldwide and the leading cause of genital ulcer disease [27]. Most HSV-2 infections are asymptomatic, with >80% of HSV-2 seropositive individuals asymptomatically shedding virus. More women are infected with HSV-2 than men; in 2012 it was estimated that 267 million women and 150 million men were living with the infection. This is because sexual transmission of HSV is more efficient from men to women than from women to men [26].
After infection by sexual transmission, virus replication initiates in genital keratinocytes and may spread to thousands of cells. Then, the virus invariably enters the neuron to reach the dorsal root ganglia where lifelong latency is established [68]. Virus periodically reactivates within the ganglia and travels back down the neuron leading to either asymptomatic, low titer shedding, or less commonly recurrent ulcers which are typically associated with prolonged high titer shedding [69,70,71].
The first two studies examining the associations between HSV-2 and vaginal microbiota were published in 2003 [72,73]. The main data emerging from these studies was that lack of Lactobacillus protective species and a history of BV was significantly associated with HSV-2 seropositivity [72]. Additionally, prospective studies confirmed the association between prevalent HSV-2 infection and BV [74,75]. In the case of HSV-2 infection, the association with vaginal dysbiosis is bi-directional. HSV-2 infection indeed seems to increase the occurrence of dysbiosis by multiple mechanisms: (a) the intermittent HSV-2 reactivation also leads to immune activation in the genital environment favouring changes in microbiota composition [76]; (b) increased iron availability which facilitates the growth of Gardnerella vaginalis [77]. In the same way, BV increases genital shedding of HSV-2 [73,78,79].
HSV2 infection was extensively studied because it represents a high risk factor for HIV acquisition [80]. This increased risk may occur because HSV-2 reactivation disrupts the epithelial barrier and recruits activated CD4 cells, which are target cells for HIV infection, into the lesion. Moreover, it has been shown that the HSV regulatory proteins ICP0, ICP4, VP16 upregulate HIV replication and increase the frequency and the titer of mucosal HIV shedding. This may occur during both clinical and asymptomatic HSV reactivation. [81,82].
Microbiota-HSV2 interactions and the corresponding changes in vaginal immunity were recently studied through NGS technologies in a group of 51 African Caribbean and other black (ACB) HIV women [83]. The authors found that HSV-2 infection was associated with an increased number of mucosal CD4+ T-cell subsets without significant alterations in local proinflammatory cytokines; selected cytokines or antimicrobial peptides (MIP-3α, IL-6, IL-8, LL-37, and HNP1-3), associated with the number of CD4+ T cells and these were distinct from cytokines usually associated with CST-IV, suggesting that HSV-2 and vaginal CST-IV enhance HIV susceptibility through independent mucosal immune mechanisms.
In murine experimental models of HSV-2 infection, Oh et al. investigated the mechanisms by which commensal bacteria elicit immune protection against HSV-2 infection of the vaginal mucosa [84]. The authors demonstrated that vaginal dysbiosis, like that induced by antibiotic therapy, affects the T-cell mediated adaptive immune response inducing a marked suppression. The molecular mechanisms at the basis of immune-suppression relied on high concentrations of IL-33, an alarmin secreted by damaged epithelial cells in the vaginal environment [85] after antibiotic treatment.
IL33 strongly inhibits the IFN-γ secretion by activated mucosal T cells, limiting the recruitment of T cells which is required to clear viral infection. The suppressive effects of IL33 are also mediated by a recruitment of innate lymphocytes type 2 and eosinophils into vaginal tissue, which contributes to suppression of antiviral immunity against mucosal HSV-2 infection by producing cytokines interfering with a TH-1 response [86]. Interestingly, protease activity by commensal bacteria resistant to antibiotic-treatment is likely responsible for epithelial damage and IL-33 secretion. Thus, in the case of HSV-2 infection a complex interplay among the virus, immune cells, and microbiota occurs, and it likely increases the susceptibility to other sexually transmitted diseases, including HIV.

6. Gaps and Challenges

Despite recent advances, significant gaps in knowledge concerning the vaginal microbiota have yet to be solved. Prevention strategies of sexually transmitted viral infection should be mainly based on the prevention and or treatment of recurrent BV. Treatment with oral or vaginal metronidazole or clindamycin is typically efficacious in the short term (as defined by Nugent or Amsel criteria) but recurrence rates are high [87]. An efficient strategy in the longer term may specifically target pathobionts or BV-associated anaerobs, while sparing Lactobacillus species or colonizing vaginal microbiota with appropriate probiotics. Common vaginal strains as L. gasseri and L. crispatus have been used in recurrent BV with moderate results; indeed, few randomized trials only (all including Lactobacillus rhamnosus) showed lower rates of recurrent BV in the probiotic group [88]. Hormonal therapy offers a potential approach to promote Lactobacillus dominant communities [89] while treatments to maintain vaginal acidity were not able to promote a healthy vaginal microbiota [90]. Treatments specifically targeting dysbiosis-associated anaerobes or pathobionts while sparing Lactobacillus species combined with biofilm disrupting agents, systemic or topical estrogen, and/or Lactobacillus-containing vaginal pro- or synbiotics might be more efficacious in the longer term.
The definition of cervicovaginal bacteria which mediate immunomodulatory mechanisms will help to identify molecules and to set up therapeutic strategies for infections that take advantage from a vaginal inflammatory environment. Finally, even when effective diagnostic tools are developed, it will be necessary to define the “harmful” levels of cervicovaginal inflammation, the appropriate "timing" of the therapeutic intervention and which women to target. We are confident that the progress achieved in recent years will make it possible to find the optimum solutions for these issues.


This research was funded by ITT, Regione Toscana, 62042012” and Ente Cassa di Risparmio, Firenze.

Conflicts of Interest

The author declares no conflict of interest.


CVFCervicovaginal fluid
CSTCommunity State Type
STISexually transmitted infections
HIVHuman immunodeficiency virus
HR-HPVHigh risk human papilloma virus
HSV2Herpes simplex virus 2


  1. King, A.E.; Critchley, H.O.D.; Kelly, R.W. Innate immune defences in the human endometrium. Reprod. Biol. Endocrinol. 2003, 1, 116. [Google Scholar] [CrossRef] [PubMed]
  2. King, A.E.; Wheelhouse, N.; Cameron, S.; McDonald, S.E.; Lee, K.-F.; Entrican, G.; Critchley, H.O.; Horne, A.W. Expression of secretory leukocyte protease inhibitor and elafin in human fallopian tube and in an in-vitro model of Chlamydia trachomatis infection. Hum. Reprod. 2009, 24, 679–686. [Google Scholar] [CrossRef] [PubMed]
  3. Chen, A.; McKinley, S.A.; Wang, S.; Shi, F.; Mucha, P.J.; Forest, M.G.; Lai, S.K. Transient antibody-mucin interactions produce a dynamic molecular shield against viral invasion. Biophys. J. 2014, 106, 2028–2036. [Google Scholar] [CrossRef] [PubMed]
  4. Ravel, J.; Gajer, P.; Abdo, Z.; Schneider, G.M.; Koenig, S.S.K.; McCulle, S.L.; Karlebach, S.; Gorle, R.; Russell, J.; Tacket, C.O.; et al. Vaginal microbiome of reproductive-age women. Proc. Natl. Acad. Sci. USA 2011, 108, 4680–4687. [Google Scholar] [CrossRef] [PubMed]
  5. Kroon, S.J.; Ravel, J.; Huston, W.M. Cervicovaginal microbiota, women’s health, and reproductive outcomes. Fertil Steril. 2018, 110, 327–336. [Google Scholar] [CrossRef] [PubMed]
  6. Ghadimi, D.; de Vrese, M.; Heller, K.J.; Schrezenmeir, J. Lactic acid bacteria enhance autophagic ability of mononuclear phagocytes by increasing Th1 autophagy-promoting cytokine (IFN-gamma) and nitric oxide (NO) levels and reducing Th2 autophagy-restraining cytokines (IL-4 and IL-13) in response to Mycobacteriu. Int. Immunopharmacol. 2010, 10, 694–706. [Google Scholar] [CrossRef] [PubMed]
  7. Aldunate, M.; Srbinovski, D.; Hearps, A.C.; Latham, C.F.; Ramsland, P.A.; Gugasyan, R.; Cone, R.A.; Tachedjian, G. Antimicrobial and immune modulatory effects of lactic acid and short chain fatty acids produced by vaginal microbiota associated with eubiosis and bacterial vaginosis. Front. Physiol. 2015, 6, 164. [Google Scholar] [CrossRef]
  8. Fredricks, D.N.; Fiedler, T.L.; Marrazzo, J.M. Molecular identification of bacteria associated with bacterial vaginosis. N. Engl. J. Med. 2005, 353, 1899–1911. [Google Scholar] [CrossRef]
  9. Gajer, P.; Brotman, R.M.; Bai, G.; Sakamoto, J.; Schutte, U.M.E.; Zhong, X.; Koenig, S.S.; Fu, L.; Ma, Z.S.; Zhou, X.; et al. Temporal dynamics of the human vaginal microbiota. Sci. Transl. Med. 2012, 4, 132ra52. [Google Scholar] [CrossRef]
  10. Anahtar, M.N.; Byrne, E.H.; Doherty, K.E.; Bowman, B.A.; Yamamoto, H.S.; Soumillon, M.; Padavattan, N.; Ismail, N.; Moodley, A.; Sabatini, M.E.; et al. Cervicovaginal bacteria are a major modulator of host inflammatory responses in the female genital tract. Immunity 2015, 42, 965–976. [Google Scholar] [CrossRef]
  11. Muzny, C.A.; Schwebke, J.R. Pathogenesis of Bacterial Vaginosis: Discussion of Current Hypotheses. J. Infect. Dis. 2016, 214, S1–S5. [Google Scholar] [CrossRef] [PubMed]
  12. Kenyon, C.; Colebunders, R.; Crucitti, T. The global epidemiology of bacterial vaginosis: A systematic review. Am. J. Obstet. Gynecol. 2013, 209, 505–523. [Google Scholar] [CrossRef]
  13. Van de Wijgert, J.H.H.M.; Jespers, V. The global health impact of vaginal dysbiosis. Res. Microbiol. 2017, 168, 859–864. [Google Scholar] [CrossRef]
  14. Brotman, R.M.; Shardell, M.D.; Gajer, P.; Fadrosh, D.; Chang, K.; Silver, M.I.; Viscidi, R.P.; Burke, A.E.; Ravel, J.; Gravitt, P.E. Association between the vaginal microbiota, menopause status, and signs of vulvovaginal atrophy. Menopause 2014, 21, 450–458. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Lee, S.K.; Kim, C.J.; Kim, D.-J.; Kang, J.-H. Immune cells in the female reproductive tract. Immune Netw. 2015, 15, 16–26. [Google Scholar] [CrossRef] [PubMed]
  16. Aflatoonian, R.; Fazeli, A. Toll-like receptors in female reproductive tract and their menstrual cycle dependent expression. J. Reprod. Immunol. 2008, 77, 7–13. [Google Scholar] [CrossRef]
  17. Hart, K.M.; Murphy, A.J.; Barrett, K.T.; Wira, C.R.; Guyre, P.M.; Pioli, P.A. Functional expression of pattern recognition receptors in tissues of the human female reproductive tract. J. Reprod. Immunol. 2009, 80, 33–40. [Google Scholar] [CrossRef] [Green Version]
  18. Yeaman, G.R.; Collins, J.E.; Fanger, M.W.; Wira, C.R.; Lydyard, P.M. CD8+ T cells in human uterine endometrial lymphoid aggregates: Evidence for accumulation of cells by trafficking. Immunology 2001, 102, 434–440. [Google Scholar] [CrossRef]
  19. Wira, C.R.; Fahey, J.V.; Rodriguez-Garcia, M.; Shen, Z.; Patel, M.V. Regulation of mucosal immunity in the female reproductive tract: The role of sex hormones in immune protection against sexually transmitted pathogens. Am. J. Reprod. Immunol. 2014, 72, 236–258. [Google Scholar] [CrossRef]
  20. Amabebe, E.; Anumba, D.O.C. The Vaginal Microenvironment: The Physiologic Role of Lactobacilli. Front. Med. 2018, 5, 181. [Google Scholar] [CrossRef]
  21. Olmsted, S.S.; Meyn, L.A.; Rohan, L.C.; Hillier, S.L. Glycosidase and proteinase activity of anaerobic gram-negative bacteria isolated from women with bacterial vaginosis. Sex. Transm. Dis. 2003, 30, 257–261. [Google Scholar] [CrossRef] [PubMed]
  22. Moncla, B.J.; Chappell, C.A.; Mahal, L.K.; Debo, B.M.; Meyn, L.A.; Hillier, S.L. Impact of bacterial vaginosis, as assessed by nugent criteria and hormonal status on glycosidases and lectin binding in cervicovaginal lavage samples. PLoS ONE 2015, 10, e0127091. [Google Scholar] [CrossRef] [PubMed]
  23. World Health Organization. Global Incidence and Prevalence of Selected Sexually Transmitted Infections—2008; World Health Organization: Geneva, Switzerland, 2012. [Google Scholar]
  24. Weinstock, H.; Berman, S.; Cates, W.J. Sexually transmitted diseases among American youth: Incidence and prevalence estimates, 2000. Perspect. Sex. Reprod. Health 2004, 36, 6–10. [Google Scholar] [CrossRef]
  25. Saslow, D.; Boetes, C.; Burke, W.; Harms, S.; Leach, M.O.; Lehman, C.D.; Morris, E.; Pisano, E.; Schnall, M.; Sener, S.; et al. American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. CA Cancer J. Clin. 2007, 57, 75–89. [Google Scholar] [CrossRef] [PubMed]
  26. McQuillan, G.; Kruszon-Moran, D.; Flagg, E.W.; Paulose-Ram, R. Prevalence of Herpes Simplex Virus Type 1 and Type 2 in Persons Aged 14–49: United States, 2015–2016. NCHS Data Brief. 2018, 304, 1–8. [Google Scholar]
  27. Looker, K.J.; Garnett, G.P.; Schmid, G.P. An estimate of the global prevalence and incidence of herpes simplex virus type 2 infection. Bull. World Health Organ. 2008, 86, 805–812. [Google Scholar] [CrossRef] [PubMed]
  28. Nardis, C.; Mosca, L.; Mastromarino, P. Vaginal microbiota and viral sexually transmitted diseases. Ann. Ig. 2013, 25, 443–456. [Google Scholar] [PubMed]
  29. Nunn, K.L.; Wang, Y.-Y.; Harit, D.; Humphrys, M.S.; Ma, B.; Cone, R.; Ravel, J.; Lai, S.K. Enhanced Trapping of HIV-1 by Human Cervicovaginal Mucus Is Associated with Lactobacillus crispatus-Dominant Microbiota. MBio 2015, 6. [Google Scholar] [CrossRef]
  30. Di Paola, M.; Sani, C.; Clemente, A.M.; Iossa, A.; Perissi, E.; Castronovo, G.; Tanturli, M.; Rivero, D.; Cozzolino, F.; Cavalieri, D.; et al. Characterization of cervico-vaginal microbiota in women developing persistent high-risk Human Papillomavirus infection. Sci. Rep. 2017, 7, 10200. [Google Scholar] [CrossRef] [PubMed]
  31. Schellenberg, J.J.; Links, M.G.; Hill, J.E.; Dumonceaux, T.J.; Kimani, J.; Jaoko, W.; Wachihi, C.; Mungai, J.N.; Peters, G.A.; Tyler, S.; et al. Molecular definition of vaginal microbiota in East African commercial sex workers. Appl. Environ. Microbiol. 2011, 77, 4066–4074. [Google Scholar] [CrossRef]
  32. Martin Harold, L.J.; Richardson, B.A.; Nyange, P.M.; Lavreys, L.; Hillier, S.L.; Chohan, B.; Mandaliya, K.; Ndinya-Achola, J.O.; Bwayo, J.; Kreiss, J. Vaginal Lactobacilli, Microbial Flora, and Risk of Human Immunodeficiency Virus Type 1 and Sexually Transmitted Disease Acquisition. J. Infect. Dis. 1999, 180, 1863–1868. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Atashili, J.; Poole, C.; Ndumbe, P.M.; Adimora, A.A.; Smith, J.S. Bacterial vaginosis and HIV acquisition: A meta-analysis of published studies. AIDS 2008, 22, 1493–1501. [Google Scholar] [CrossRef] [PubMed]
  34. Gosmann, C.; Anahtar, M.N.; Handley, S.A.; Farcasanu, M.; Abu-Ali, G.; Bowman, B.A.; Padavattan, N.; Desai, C.; Droit, L.; Moodley, A.; et al. Lactobacillus-Deficient Cervicovaginal Bacterial Communities Are Associated with Increased HIV Acquisition in Young South African Women. Immunity 2017, 46, 29–37. [Google Scholar] [CrossRef] [PubMed]
  35. McClelland, R.S.; Lingappa, J.R.; Srinivasan, S.; Kinuthia, J.; John-Stewart, G.C.; Jaoko, W.; Richardson, B.A.; Yuhas, K.; Fiedler, T.L.; Mandaliya, K.N.; et al. Evaluation of the association between the concentrations of key vaginal bacteria and the increased risk of HIV acquisition in African women from five cohorts: A nested case-control study. Lancet Infect. Dis. 2018, 18, 554–564. [Google Scholar] [CrossRef]
  36. Alcaide, M.L.; Strbo, N.; Romero, L.; Jones, D.L.; Rodriguez, V.J.; Arheart, K.; Martinez, O.; Bolivar, H.; Podack, E.R.; Fischl, M.A.; et al. Bacterial Vaginosis Is Associated with Loss of Gamma Delta T Cells in the Female Reproductive Tract in Women in the Miami Women Interagency HIV Study (WIHS): A Cross Sectional Study. PLoS ONE 2016, 11, e0153045. [Google Scholar] [CrossRef] [PubMed]
  37. Velloza, J.; Heffron, R. The Vaginal Microbiome and its Potential to Impact Efficacy of HIV Pre-exposure Prophylaxis for Women. Curr. HIV/AIDS Rep. 2017, 14, 153–160. [Google Scholar] [CrossRef] [PubMed]
  38. Fitzmaurice, C.; Dicker, D.; Pain, A.; Hamavid, H.; Moradi-Lakeh, M.; MacIntyre, M.F.; Allen, C.; Hansen, G.; Woodbrook, R.; Wolfe, C.; et al. The Global Burden of Cancer 2013. JAMA Oncol. 2015, 1, 505–527. [Google Scholar] [CrossRef] [Green Version]
  39. De Villiers, E.-M.; Fauquet, C.; Broker, T.R.; Bernard, H.-U.; zur Hausen, H. Classification of papillomaviruses. Virology 2004, 324, 17–27. [Google Scholar] [CrossRef] [Green Version]
  40. Doorbar, J. Molecular biology of human papillomavirus infection and cervical cancer. Clin. Sci. 2006, 110, 525–541. [Google Scholar] [CrossRef]
  41. Egawa, N.; Egawa, K.; Griffin, H.; Doorbar, J. Human Papillomaviruses; Epithelial Tropisms, and the Development of Neoplasia. Viruses 2015, 7, 3863–3890. [Google Scholar] [CrossRef] [Green Version]
  42. Zur Hausen, H. Papillomaviruses and cancer: From basic studies to clinical application. Nat. Rev. Cancer 2002, 2, 342–350. [Google Scholar] [CrossRef] [PubMed]
  43. De Marco, F. Oxidative stress and HPV carcinogenesis. Viruses 2013, 5, 708–731. [Google Scholar] [CrossRef] [PubMed]
  44. Doorbar, J.; Quint, W.; Banks, L.; Bravo, I.G.; Stoler, M.; Broker, T.R.; Stanley, M.A. The biology and life-cycle of human papillomaviruses. Vaccine 2012, 30, F55–F70. [Google Scholar] [CrossRef] [PubMed]
  45. Woodman, C.B.J.; Collins, S.I.; Young, L.S. The natural history of cervical HPV infection: Unresolved issues. Nat. Rev. Cancer 2007, 7, 11–22. [Google Scholar] [CrossRef] [PubMed]
  46. Mitra, A.; MacIntyre, D.A.; Marchesi, J.R.; Lee, Y.S.; Bennett, P.R.; Kyrgiou, M. The vaginal microbiota, human papillomavirus infection and cervical intraepithelial neoplasia: What do we know and where are we going next? Microbiome 2016, 4, 58. [Google Scholar] [CrossRef] [PubMed]
  47. Stanley, M.A. Epithelial cell responses to infection with human papillomavirus. Clin. Microbiol. Rev. 2012, 25, 215–222. [Google Scholar] [CrossRef] [PubMed]
  48. Yarbrough, V.L.; Winkle, S.; Herbst-Kralovetz, M.M. Antimicrobial peptides in the female reproductive tract: A critical component of the mucosal immune barrier with physiological and clinical implications. Hum. Reprod. 2015, 21, 353–377. [Google Scholar] [CrossRef]
  49. Guess, J.C.; McCance, D.J. Decreased migration of Langerhans precursor-like cells in response to human keratinocytes expressing human papillomavirus type 16 E6/E7 is related to reduced macrophage inflammatory protein-3alpha production. J. Virol. 2005, 79, 14852–14862. [Google Scholar] [CrossRef]
  50. Karim, R.; Meyers, C.; Backendorf, C.; Ludigs, K.; Offringa, R.; van Ommen, G.-J.B.; Melief, C.J.; van der Burg, S.H.; Boer, J.M. Human papillomavirus deregulates the response of a cellular network comprising of chemotactic and proinflammatory genes. PLoS ONE 2011, 6, e17848. [Google Scholar] [CrossRef]
  51. Sperling, T.; Oldak, M.; Walch-Ruckheim, B.; Wickenhauser, C.; Doorbar, J.; Pfister, H.; Malejczyk, M.; Majewski, S.; Keates, A.C.; Smola, S. Human papillomavirus type 8 interferes with a novel C/EBPbeta-mediated mechanism of keratinocyte CCL20 chemokine expression and Langerhans cell migration. PLoS Pathog. 2012, 8, e1002833. [Google Scholar] [CrossRef]
  52. Hong, S.; Laimins, L.A. The JAK-STAT transcriptional regulator, STAT-5, activates the ATM DNA damage pathway to induce HPV 31 genome amplification upon epithelial differentiation. PLoS Pathog. 2013, 9, e1003295. [Google Scholar] [CrossRef] [PubMed]
  53. Clifford, G.M.; Rana, R.K.; Franceschi, S.; Smith, J.S.; Gough, G.; Pimenta, J.M. Human papillomavirus genotype distribution in low-grade cervical lesions: Comparison by geographic region and with cervical cancer. Cancer Epidemiol. Biomark. Prev. 2005, 14, 1157–1164. [Google Scholar] [CrossRef] [PubMed]
  54. Laniewski, P.; Barnes, D.; Goulder, A.; Cui, H.; Roe, D.J.; Chase, D.M.; Herbst-Kralovetz, M.M. Linking cervicovaginal immune signatures, HPV and microbiota composition in cervical carcinogenesis in non-Hispanic and Hispanic women. Sci. Rep. 2018, 8, 7593. [Google Scholar] [CrossRef] [PubMed]
  55. Shannon, B.; Yi, T.J.; Perusini, S.; Gajer, P.; Ma, B.; Humphrys, M.S.; Thomas-Pavanel, J.; Chieza, L.; Janakiram, P.; Saunders, M.; et al. Association of HPV infection and clearance with cervicovaginal immunology and the vaginal microbiota. Mucosal Immunol. 2017, 10, 1310–1319. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Bordignon, V.; Di Domenico, E.G.; Trento, E.; D’Agosto, G.; Cavallo, I.; Pontone, M.; Pimpinelli, F.; Mariani, L.; Ensoli, F. How Human Papillomavirus Replication and Immune Evasion Strategies Take Advantage of the Host DNA Damage Repair Machinery. Viruses 2017, 9, 390. [Google Scholar] [CrossRef] [PubMed]
  57. Bonin, C.M.; Padovani, C.T.J.; da Costa, I.P.; Avila, L.S.; Ferreira, A.M.T.; Fernandes, C.E.S.; dos Santos, A.R.; Tozetti, I.A. Detection of regulatory T cell phenotypic markers and cytokines in patients with human papillomavirus infection. J. Med. Virol. 2019, 91, 317. [Google Scholar] [CrossRef] [PubMed]
  58. Smith, J.S.; Munoz, N.; Herrero, R.; Eluf-Neto, J.; Ngelangel, C.; Franceschi, S.; Bosch, F.X.; Walboomers, J.M.; Peeling, R.W. Evidence for Chlamydia trachomatis as a human papillomavirus cofactor in the etiology of invasive cervical cancer in Brazil and the Philippines. J. Infect. Dis. 2002, 185, 324–331. [Google Scholar] [CrossRef] [PubMed]
  59. Alberts, C.J.; Schim van der Loeff, M.F.; Papenfuss, M.R.; da Silva, R.J.C.; Villa, L.L.; Lazcano-Ponce, E.; Nyitray, A.G.; Giuliano, A.R. Association of Chlamydia trachomatis infection and herpes simplex virus type 2 serostatus with genital human papillomavirus infection in men: The HPV in men study. Sex. Transm. Dis. 2013, 40, 508–515. [Google Scholar] [CrossRef]
  60. Gao, W.; Weng, J.; Gao, Y.; Chen, X. Comparison of the vaginal microbiota diversity of women with and without human papillomavirus infection: A cross-sectional study. BMC Infect. Dis. 2013, 13, 271. [Google Scholar] [CrossRef]
  61. Audirac-Chalifour, A.; Torres-Poveda, K.; Bahena-Roman, M.; Tellez-Sosa, J.; Martinez-Barnetche, J.; Cortina-Ceballos, B.; López-Estrada, G.; Delgado-Romero, K.; Burguete-García, A.I.; Cantú, D.; et al. Cervical Microbiome and Cytokine Profile at Various Stages of Cervical Cancer: A Pilot Study. PLoS ONE 2016, 11, e0153274. [Google Scholar] [CrossRef]
  62. Gillet, E.; Meys, J.F.; Verstraelen, H.; Bosire, C.; De Sutter, P.; Temmerman, M.; Broeck, D.V. Bacterial vaginosis is associated with uterine cervical human papillomavirus infection: A meta-analysis. BMC Infect. Dis. 2011, 11, 10. [Google Scholar] [CrossRef]
  63. Drago, F.; Herzum, A.; Ciccarese, G.; Dezzana, M.; Casazza, S.; Pastorino, A.; Bandelloni, R.; Parodi, A. Ureaplasma parvum as a possible enhancer agent of HPV-induced cervical intraepithelial neoplasia: Preliminary results. J. Med. Virol. 2016, 88, 2023–2024. [Google Scholar] [CrossRef] [PubMed]
  64. Mitra, A.; MacIntyre, D.A.; Lee, Y.S.; Smith, A.; Marchesi, J.R.; Lehne, B.; Bhatia, R.; Lyons, D.; Paraskevaidis, E.; Li, J.V.; et al. Cervical intraepithelial neoplasia disease progression is associated with increased vaginal microbiome diversity. Sci. Rep. 2015, 5, 16865. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Oh, H.Y.; Kim, B.-S.; Seo, S.-S.; Kong, J.-S.; Lee, J.-K.; Park, S.-Y.; Hong, K.M.; Kim, H.K.; Kim, M.K. The association of uterine cervical microbiota with an increased risk for cervical intraepithelial neoplasia in Korea. Clin. Microbiol. Infect. 2015, 21, 674.e1–674.e9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Piyathilake, C.J.; Ollberding, N.J.; Kumar, R.; Macaluso, M.; Alvarez, R.D.; Morrow, C.D. Cervical Microbiota Associated with Higher Grade Cervical Intraepithelial Neoplasia in Women Infected with High-Risk Human Papillomaviruses. Cancer Prev. Res. 2016, 9, 357–366. [Google Scholar] [CrossRef] [PubMed]
  67. Mhatre, M.; McAndrew, T.; Carpenter, C.; Burk, R.D.; Einstein, M.H.; Herold, B.C. Cervical intraepithelial neoplasia is associated with genital tract mucosal inflammation. Sex. Transm. Dis. 2012, 39, 591–597. [Google Scholar] [CrossRef] [PubMed]
  68. Thellman, N.M.; Triezenberg, S.J. Herpes Simplex Virus Establishment, Maintenance, and Reactivation: In Vitro Modeling of Latency. Pathogens 2017, 6, 28. [Google Scholar] [CrossRef]
  69. Beyrer, C.; Jitwatcharanan, K.; Natpratan, C.; Kaewvichit, R.; Nelson, K.E.; Chen, C.Y.; Weiss, J.B.; Morse, S.A. Molecular methods for the diagnosis of genital ulcer disease in a sexually transmitted disease clinic population in northern Thailand: Predominance of herpes simplex virus infection. J. Infect. Dis. 1998, 178, 243–246. [Google Scholar] [CrossRef]
  70. Johnston, C.; Corey, L. Current Concepts for Genital Herpes Simplex Virus Infection: Diagnostics and Pathogenesis of Genital Tract Shedding. Clin. Microbiol. Rev. 2016, 29, 149–161. [Google Scholar] [CrossRef]
  71. Brankin, A.E.; Tobian, A.A.R.; Laeyendecker, O.; Suntoke, T.R.; Kizza, A.; Mpoza, B.; Kigozi, G.; Nalugoda, F.; Iga, B.; Chen, M.Z.; et al. Aetiology of genital ulcer disease in female partners of male participants in a circumcision trial in Uganda. Int. J. STD AIDS 2009, 20, 650–651. [Google Scholar] [CrossRef] [Green Version]
  72. Evans, B.A.; Kell, P.D.; Bond, R.A.; MacRae, K.D.; Slomka, M.J.; Brown, D.W.G. Predictors of seropositivity to herpes simplex virus type 2 in women. Int. J. STD AIDS 2003, 14, 30–36. [Google Scholar] [CrossRef] [PubMed]
  73. Cherpes, T.L.; Meyn, L.A.; Krohn, M.A.; Hillier, S.L. Risk factors for infection with herpes simplex virus type 2: Role of smoking, douching, uncircumcised males, and vaginal flora. Sex. Transm. Dis. 2003, 30, 405–410. [Google Scholar] [CrossRef] [PubMed]
  74. Kaul, R.; Nagelkerke, N.J.; Kimani, J.; Ngugi, E.; Bwayo, J.J.; Macdonald, K.S.; Rebbaprgada, A.; Fonck, K.; Temmerman, M.; Ronald, A.R.; et al. Prevalent herpes simplex virus type 2 infection is associated with altered vaginal flora and an increased susceptibility to multiple sexually transmitted infections. J. Infect. Dis. 2007, 196, 1692–1697. [Google Scholar] [CrossRef]
  75. Masese, L.; Baeten, J.M.; Richardson, B.A.; Bukusi, E.; John-Stewart, G.; Jaoko, W.; McClelland, R.S. Incident herpes simplex virus type 2 infection increases the risk of subsequent episodes of bacterial vaginosis. J. Infect. Dis. 2014, 209, 1023–1027. [Google Scholar] [CrossRef] [PubMed]
  76. Van de Perre, P.; Segondy, M.; Foulongne, V.; Ouedraogo, A.; Konate, I.; Huraux, J.-M.; Mayaud, P.; Nagot, N. Herpes simplex virus and HIV-1: Deciphering viral synergy. Lancet Infect. Dis. 2008, 8, 490–497. [Google Scholar] [CrossRef]
  77. Piot, P.; Van Dyck, E.; Totten, P.A.; Holmes, K.K. Identification of Gardnerella (Haemophilus) vaginalis. J. Clin. Microbiol. 1982, 15, 19–24. [Google Scholar] [PubMed]
  78. Cherpes, T.L.; Melan, M.A.; Kant, J.A.; Cosentino, L.A.; Meyn, L.A.; Hillier, S.L. Genital tract shedding of herpes simplex virus type 2 in women: Effects of hormonal contraception, bacterial vaginosis, and vaginal group B Streptococcus colonization. Clin. Infect. Dis. 2005, 40, 1422–1428. [Google Scholar] [CrossRef]
  79. Cherpes, T.L.; Hillier, S.L.; Meyn, L.A.; Busch, J.L.; Krohn, M.A. A delicate balance: Risk factors for acquisition of bacterial vaginosis include sexual activity, absence of hydrogen peroxide-producing lactobacilli, black race, and positive herpes simplex virus type 2 serology. Sex. Transm. Dis. 2008, 35, 78–83. [Google Scholar] [CrossRef]
  80. Looker, K.J.; Elmes, J.A.R.; Gottlieb, S.L.; Schiffer, J.T.; Vickerman, P.; Turner, K.M.E.; Boily, M.C. Effect of HSV-2 infection on subsequent HIV acquisition: An updated systematic review and meta-analysis. Lancet Infect. Dis. 2017, 17, 1303–1316. [Google Scholar] [CrossRef]
  81. Heng, M.C.; Heng, S.Y.; Allen, S.G. Co-infection and synergy of human immunodeficiency virus-1 and herpes simplex virus-1. Lancet 1994, 343, 255–258. [Google Scholar] [CrossRef]
  82. Mbopi-Keou, F.X.; Gresenguet, G.; Mayaud, P.; Weiss, H.A.; Gopal, R.; Matta, M.; Paul, J.L.; Brown, D.W.; Hayes, R.J.; Mabey, D.C.; et al. Interactions between herpes simplex virus type 2 and human immunodeficiency virus type 1 infection in African women: Opportunities for intervention. J. Infect. Dis. 2000, 182, 1090–1096. [Google Scholar] [CrossRef]
  83. Shannon, B.; Gajer, P.; Yi, T.J.; Ma, B.; Humphrys, M.S.; Thomas-Pavanel, J.; Chieza, L.; Janakiram, P.; Saunders, M.; Tharao, W.; et al. Distinct Effects of the Cervicovaginal Microbiota and Herpes Simplex Type 2 Infection on Female Genital Tract Immunology. J. Infect. Dis. 2017, 215, 1366–1375. [Google Scholar] [CrossRef] [Green Version]
  84. Oh, J.E.; Kim, B.-C.; Chang, D.-H.; Kwon, M.; Lee, S.Y.; Kang, D.; Kim, J.Y.; Hwang, I.; Yu, J.W.; Nakae, S.; et al. Dysbiosis-induced IL-33 contributes to impaired antiviral immunity in the genital mucosa. Proc. Natl. Acad. Sci. USA 2016, 113, E762–E771. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Cayrol, C.; Girard, J.-P. IL-33: An alarmin cytokine with crucial roles in innate immunity, inflammation and allergy. Curr. Opin. Immunol. 2014, 31, 31–37. [Google Scholar] [CrossRef] [PubMed]
  86. Ebbo, M.; Crinier, A.; Vely, F.; Vivier, E. Innate lymphoid cells: Major players in inflammatory diseases. Nat. Rev. Immunol. 2017, 17, 665–678. [Google Scholar] [CrossRef] [PubMed]
  87. Bradshaw, C.S.; Brotman, R.M. Making inroads into improving treatment of bacterial vaginosis—Striving for long-term cure. BMC Infect. Dis. 2015, 15, 292. [Google Scholar] [CrossRef] [PubMed]
  88. Anukam, K.C.; Osazuwa, E.; Osemene, G.I.; Ehigiagbe, F.; Bruce, A.W.; Reid, G. Clinical study comparing probiotic Lactobacillus GR-1 and RC-14 with metronidazole vaginal gel to treat symptomatic bacterial vaginosis. Microbes Infect. 2006, 8, 2772–2776. [Google Scholar] [CrossRef]
  89. Van de Wijgert, J.H.H.M.; Verwijs, M.C.; Turner, A.N.; Morrison, C.S. Hormonal contraception decreases bacterial vaginosis but oral contraception may increase candidiasis: Implications for HIV transmission. AIDS 2013, 27, 2141–2153. [Google Scholar] [CrossRef]
  90. Decena, D.C.D.; Co, J.T.; Manalastas, R.M.J.; Palaypayon, E.P.; Padolina, C.S.; Sison, J.M.; Dancel, L.A.; Lelis, M.A. Metronidazole with Lactacyd vaginal gel in bacterial vaginosis. J. Obstet. Gynaecol. Res. 2006, 32, 243–251. [Google Scholar] [CrossRef]

Share and Cite

MDPI and ACS Style

Torcia, M.G. Interplay among Vaginal Microbiome, Immune Response and Sexually Transmitted Viral Infections. Int. J. Mol. Sci. 2019, 20, 266.

AMA Style

Torcia MG. Interplay among Vaginal Microbiome, Immune Response and Sexually Transmitted Viral Infections. International Journal of Molecular Sciences. 2019; 20(2):266.

Chicago/Turabian Style

Torcia, Maria Gabriella. 2019. "Interplay among Vaginal Microbiome, Immune Response and Sexually Transmitted Viral Infections" International Journal of Molecular Sciences 20, no. 2: 266.

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop