Differential sexual network connectivity offers a parsimonious explanation for population-level variations in the prevalence of bacterial vaginosis: a data-driven, model-supported hypothesis
The prevalence of bacterial vaginosis (BV) and vaginal microbiota types varies dramatically between different populations around the world. Understanding what underpins these differences is important, as high-diversity microbiotas associated with BV are implicated in adverse pregnancy outcomes and enhanced susceptibility to and transmission of sexually transmitted infections.
We hypothesize that these variations in the vaginal microbiota can, in part, be explained by variations in the connectivity of sexual networks. We argue: 1) Couple-level data suggest that BV-associated bacteria can be sexually transmitted and hence high sexual network connectivity would be expected to promote the spread of BV-associated bacteria. Epidemiological studies have found positive associations between indicators of network connectivity and the prevalence of BV; 2) The relationship between BV prevalence and STI incidence/prevalence can be parsimoniously explained by differential network connectivity; 3) Studies from other mammals are generally supportive of the association between network connectivity and high-diversity vaginal microbiota.
To test this hypothesis, we propose a combination of empirical and simulation-based study designs.
KeywordsBacterial vaginosis Microbiome Sexual network connectivity Concurrency STI HIV
Community State Type
There is little consensus as to why the proportion of reproductive-age women with particular CSTs, and in particular those with BV-VMB, varies so dramatically between different populations . Some have postulated that genetic differences between populations (such as differences in innate and adaptive immune systems, the composition and quantity of vaginal secretions, and ligands on epithelial cell surfaces [4, 9]) may be responsible. Others have argued that the prevalence of practices known to influence the VMB may be responsible: including use of vaginal douching, nutrition, smoking, personal hygiene, methods of birth control, and sexual behaviors [10, 11, 12].
Both BV and some L. iners-dominated VMBs have been associated with various adverse outcomes, including enhanced susceptibility to STIs such as HIV, enhanced transmission of HIV, pelvic inflammatory disease and a range of adverse pregnancy outcomes [13, 14, 15]. One meta-analysis found that BV-VMB increased the risk of HIV acquisition by 60% (relative risk 95% CI 1.2–2.1) . In populations where the prevalence of BV is over 30%, this may translate into 15% of HIV infections being attributable to BV-VMB . Similar lines of reasoning suggest that BV-VMB may explain a considerable proportion of the differential spread of other STIs between different populations [17, 18, 19, 20, 21, 22, 23].
We hypothesize that variations in sexual network connectivity may be at least partially responsible for variations in the prevalence of BV-VMB between different populations, and below we present three types of evidence in support of this thesis:
Individual and couple-level data
Correlation of bacterial species between vagina and penile skin and male urethra from couples with bacterial vaginosis and couples without bacterial vaginosis in cross sectional study by Zozaya et al.  Only the top 13 most correlated species are shown
Couples with BV (n = 65)
Couples without BV (n = 31)
Couple studies have found high rates of concordance (up to 100%) for various BVAB (including biofilm forming G. vaginalis ) in women’s VMB and the coronal sulci/distal urethras of their male partners [36, 37, 38, 39, 40, 41] or the vaginas of their female partners . A study of the genital microbiomes of 165 men and their partners in Rakai, Uganda found that the penile microbiomes could be segregated into two main groups - a BV and a non-BV-type group . The BV-type group had a higher prevalence and abundance of BV associated bacteria. The female partners of this group were also more likely to have BV  as assessed by Nugent’s scoring (the women in this study did not have their vaginal microbiomes characterized molecularly). Two studies that simultaneously characterized the genital microbiomes of women and their male partners found a strong intra-couple correlation for the presence or absence of individual bacterial species [39, 44]. In both studies, concentrations of BVAB were low or undetectable in women without BV and their partners but abundant and concordant at a species level for women with BV and their partners coronal sulci (and to a lesser extent urethra) [39, 44]. Other studies have established a high degree of concordance of oligotype and phenotype (such a biofilm forming or not) of G. vaginalis and other BVAB between monogamous partners [36, 45, 46]. In one of these studies, for example, all women with BV had evidence of a biofilm- forming G. vaginalis vaginal infection as did all their male partners in their urine . Women who have sex with women have also been shown to have a high degree of concordance for BV status and this has been linked to practices that transmit vaginal fluid between women [47, 48].
STIs are transmitted along sexual networks, and as a result, the amount of connectivity between individuals in the network determines the speed and extent of STI spread in the network [49, 50, 51]. Network connectivity is a complex concept that can be characterized by a multi-dimensional array of metrics, including the number of partners per unit time, prevalence of concurrent partnering, size of core groups, type of sex, size of sexual network, length of gaps between partnerships, degree and type of homophily and relations between core and non-core groups [50, 52, 53, 54, 55, 56, 57]. We will confine our further consideration of network connectivity to number of partners per unit time and partner concurrency (partnerships overlapping in time). Both of these variables have clear definitions, have multiple prevalence estimates from around the world and have been found to be risk factors for most major STIs, including BV at the individual level [24, 52, 58, 59, 60, 61]. We acknowledge however that these variables are measures of local sexual networks. Future work could benefit from incorporating better measures of global sexual network connectivity such as the size of the forward reachable set. Since sexual network connectivity is a population-level property, ecological studies are also necessary to explore the possible explanations for variations in STI prevalence [50, 62]. Although not all studies have reached this conclusion, [63, 64] studies have generally found a positive association between STI prevalence and the prevalence of partner concurrency and/or numbers of partners per unit time [50, 52, 58, 65, 66, 67].
Enhanced network connectivity may play a particularly important role in facilitating the spread of the BV-associated G. vaginalis and T. vaginalis, because of their relatively short periods of colonization in men . T. vaginalis colonizes men for only 6 weeks (and women for 60 weeks) [69, 70]. This gender gap in colonization-duration means that T. vaginalis would go extinct in a serial monogamous population with at least 7 weeks between consecutive partners of men . Concurrency enables T. vaginalis to bypass this bottleneck and thereby could facilitate the spread of T. vaginalis and indirectly BV (because T. vaginalis predisposes to BV ). Similarly, G. vaginalis – one of the likely driver species of BV [72, 73] – has been shown to be well adapted to long-term colonization of the high glycogen vaginal environment  but poorly suited to long-term urethral colonization in men . G. vaginalis thus colonizes men for under 3 months but persists long term in women [36, 75]. One study, for example, found an identical strain of biofilm forming G. vaginalis persisting in one woman’s vagina for 15 years . If the BVAB (or at least a number of the keystone species responsible for BV) have a duration of colonization in the male that is as short as that of G. vaginalis, then this would result in a break of transmission of BVAB in populations with serial monogamy and gaps of a few months between sexual relationships. The illustration in Fig. 2 would then need to be adapted as ‘B’ would no longer be able to transmit the BVAB to his new partner at T3 if the time gap since his previous relationship was long enough to have removed the BVAB from his penile microbiome.
An individual-based network model of BV transmission
To demonstrate the interacting effects of higher sexual network connectivity and a shorter duration of colonization in men more explicitly, we developed a simple, didactic individual-based model representing two adjacent but entirely separate communities (see Additional file 1: NetworkModelDescription for a detailed description of the model). In the first community only serially monogamous relationships can be formed. In the second, both men and women remain available to form new relationships, regardless of the number of relationships they are already engaged in. In both communities, the duration of BVAB colonization is set to a fixed period of 6 weeks in men and 60 weeks in women. Additional file 2: NetworkMovie shows model output over 10 years with populations of 250 people in each community. In the community where concurrent relationships were allowed, the prevalence of partner concurrency varied between 2 and 11% over the 10-year simulation period, and by the end of it, 42% more relationships had been formed, compared to the community with lower network connectivity. The prevalence of BV-VMB plateaued around 55% in the high connectivity network and around 15% in the low connectivity network (a relative difference of 267%). This is an example based in heterosexual couplings and certainly future models should include partnerships between women as well.
Additional file 2: A movie file illustrating the main findings of the Netlogo model of BV transmission. (MP4 60657 kb)
Epidemiological studies confirm that concurrency and partner number are risk factors for BV
Epidemiological studies have shown number of partners per unit time to be a risk factor for BV-VMB [24, 76, 77]. Partner concurrency has also been shown to be an independent risk factor for BV in a longitudinal study of 3620 women followed up quarterly for 5 visits . In the Rakai study mentioned above, men with extramarital partners were also found to be more likely to have the BV-type penile microbiome than men with no extramarital partners . Finally, an ecological study found associations at the level of countries between the prevalence of male concurrency and the prevalence of BV among women . The same association was found at the level of ethnic groups within countries .
Network connectivity is a parsimonious explanation for the association between the prevalence of BV and STIs
It has been argued that certain racial groups such as ‘black populations’  tend to have a higher prevalence of BV and that this is due to biological differences in susceptibility to BV [4, 9, 79]. The available evidence, however, suggests that populations (irrespective of race) with high network connectivity have a higher BV prevalence. (i) Black populations with low risk behavior as established by low prevalence of HIV and other STIs have low prevalences of BV [80, 81]. (ii) Populations with high network connectivity (as deduced by high STI prevalences) have high BV prevalences regardless of ethnicity. This has been most clearly established in sex workers where sex workers from all ethnic groups with available data have high BV prevalences [2, 28, 29]. BV prevalences have also been found to vary between non-black ethnic/racial groups within Canada, Peru, China and Spain . In the case of Canada and Peru, the high BV-prevalence ethnic groups were also found to have higher prevalences of other STIs suggesting a common risk factor may be responsible . (iii) The available evidence suggests that prior to sexual debut, there are no differences in VMB between ethnic groups but that differences only emerge post debut [82, 83]. (iv) In a longitudinal study, white women with black partners had the same BV prevalence as black women  and black women with white partners had the same BV prevalence as white women (C Kenyon’s unpublished data). (v) The VMBs from all racial/ethnic groups profiled thus far include all the major CSTs. It is merely the proportionate mix of CSTs that varies between ethnic groups [1, 85]. (vi) We have been unable to find any published studies that have established evidence of genetic differences in susceptibility to particular VMBs by race/ethnic group.
Populations with a higher prevalence of BV also tend to have a higher prevalence of other STIs . This association has been shown between BV and HIV prevalence at the level of world regions , countries  and ethnic groups within countries (Fig. 1) . These positive associations between STIs and BV could be due to a common underlying risk factor (such as network connectivity ) Alternatively, they could be explained by these STIs enhancing the probability of transition to BV . However, this explanation begs the question, why did these populations have higher STI prevalences? A possible answer is that they have poorer STI treatment services . The correlation between STI prevalence and quality of STI services is, however, weak or absent . Furthermore, this does not explain the strong correlation between the incurable STI, herpes simplex virus-2 (HSV-2), and BV and other STIs [88, 89]. These considerations lead us to predict that the most parsimonious explanation for why the prevalence of BV and various STIs is higher in certain populations than others is that these populations have more densely connected sexual networks. High network connectivity would be expected to not only directly facilitate the spread of BVAB and other STIs, but also to do so indirectly via the positive feedback resulting from BV and STIs enhancing the spread of one another. BV for example has been shown to enhance susceptibility to chlamydia [17, 21], gonorrhoea , HIV [23, 90, 91], HSV-2 [18, 19] and T. vaginalis [17, 21, 22]. HSV-2 and T. vaginalis have in turn been found to increase the risk for development of BV and acquisition of other STIs [17, 20, 21, 23].
Data from animal studies
Results from vaginal microbiome profiling in other animals are compatible with the hypothesis that differences in sexual network connectivity influence vaginal microbiomes. A study that compared the sympatric mice, Peromyscus californius and Peromyscus maniculatus found that the socially and genetically promiscuous P. maniculatus had greater vaginal microbiome diversity (a key feature of a BV-VMB) than the monogamous P. californius . Likewise a study that compared the vaginal microbiomes of 9 primate species with different mating behaviors found that vaginal microbial diversity was strongly correlated with host-specific socioecologic factors such as female and male promiscuity . Unlike the gut microbiome the vaginal microbiome showed little congruence with host phylogeny or diet . The authors concluded that differences in sexual behavior were key determinants of the degree of vaginal microbial diversity.
Empirical and simulation-based hypothesis tests
Testing the network-connectivity-VMB hypothesis would ideally involve longitudinal studies that follow up sympatric sub-populations with high and low STI prevalence from the time of sexual debut. Critically these studies should characterize the vaginal and penile microbiomes of sexual partners at frequent intervals. This, combined with detailed behavioral data, should enable researchers to ascertain if differences in network connectivity are responsible for the differential spread of BVAB in the high and low STI prevalence populations. The longitudinal study design should also provide better insights into the interactions between sexual behaviour, genital microbiomes and STIs. The importance of these longitudinal couple studies for the BV-network connectivity hypothesis cannot be overstated. We have shown evidence of a strong correlation between penile skin microbiota and the partner’s VMB. Longitudinal studies are however required to establish that these penile microbiota can be sexually transmitted to the man’s next partner and result in changes in her VMB.
In addition to empirical research, simulation-based study designs would also be useful to test aspects of the hypothesis presented here. Previous modeling studies have found that relatively small increases in network connectivity can lead to non-linear increases in HIV/STI spread . If this applies to BV as well, then more connected sexual networks would be expected to facilitate the rapid spread of BVAB and various other STIs soon after sexual debut. Our own individual-based model of BVAB transmission provides a fitting illustration of the strong, non-linear effect of higher network connectivity, even in the absence of other STIs. The addition of a few key features could turn this didactic tool into a rigorous framework that unifies relevant knowledge of the microbiology, epidemiology and sociology of BV and other STI co-infections. In line with current insights from molecular microbiology, vaginal and penile microbiomes should be classified into at least five CSTs . Furthermore, interactions with various STI co-infections – most notably chlamydia, gonorrhoea, T. vaginalis, HSV-2 and HIV – should be modelled explicitly, and other non-infectious causal factors (such as douching, smoking, diet) on the pathway to develop BV should be included as well. Lastly, the model should allow for more heterogeneity in sexual activity levels, as well as more structure in the network (for example, a non-random age-mixing pattern, and clustering of a high-risk core group within the network, and same sex partnerships). Besides the obvious advantages of being relatively fast and inexpensive, simulation studies can quantify the effect of uncertainty surrounding behavioral and biological parameters on the main outcomes measures.
If confirmed by empirical and simulated data, the network connectivity approach would offer a new paradigm for conceptualizing how differences in VMB emerge. If the proportion of a population that has BV is a population-level-property that is partially determined by network connectivity, then this introduces new options for prevention of BV and BV-associated adverse health outcomes such as adverse pregnancy outcomes and transmission of other STIs including HIV. It suggests that interventions that have been shown to reduce network connectivity may result in reductions in the prevalence of these VMBs. Because BV-VMBs may be responsible for a large proportion of the population attributable fraction of HIV and other STIs  and the spread of these STIs is also directly enhanced by network connectivity, small reductions in connectivity could translate into large declines in STI incidence. Uganda’s ‘Zero Grazing’ campaign  and similar processes elsewhere in Africa , which resulted in dramatic declines in side-partners and hence network connectivity, could be viewed as providing guidance for this approach. A better appreciation for the network connectivity would also help us unravel the disparities between ethnic groups that we see in BV, STIs and reproductive outcomes.
We would like to thank Tania Crucitti, Leigh Johnson and discussants at the University of Cape Town Public Health Seminar Series for helpful comments on an earlier draft of the paper.
Availability of data and materials
The model of BV transmission including all code used is available in Additional file 3.
CK conceptualized the paper. WD created the model. CK, WD and RB played a role in writing, editing and approving the final version.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- 1.van de Wijgert JH, Borgdorff H, Verhelst R, Crucitti T, Francis S, Verstraelen H, et al. The vaginal microbiota: what have we learned after a decade of molecular characterization? PLoS One. 2014;9(8):e105998. https://doi.org/10.1371/journal.pone.0105998 PubMed PMID: 25148517; PubMed Central PMCID: PMCPMC4141851.CrossRefPubMedPubMedCentralGoogle Scholar
- 2.Jespers V, Crucitti T, Menten J, Verhelst R, Mwaura M, Mandaliya K, et al. Prevalence and correlates of bacterial vaginosis in different sub-populations of women in sub-Saharan Africa: a cross-sectional study. PLoS One. 2014;9(10):e109670. https://doi.org/10.1371/journal.pone.0109670 Epub 2014/10/08. PubMed PMID: 25289640; PubMed Central PMCID: PMCPMC4188821.CrossRefPubMedPubMedCentralGoogle Scholar
- 3.Lennard K, Dabee S, Barnabas SL, Havyarimana E, Blakney A, Jaumdally SZ, et al. Microbial composition predicts genital tract inflammation and persistent bacterial vaginosis in adolescent South African women. Infect Immun. 2017. https://doi.org/10.1128/IAI.00410-17 Epub 2017/10/19. PubMed PMID: 29038128.
- 7.Wertz J, Isaacs-Cosgrove N, Holzman C, Marsh TL. Temporal Shifts in Microbial Communities in Nonpregnant African-American Women with and without Bacterial Vaginosis. Interdiscip Perspect Infect Dis. 2008;2008:181253. https://doi.org/10.1155/2008/181253 Epub 2008/01/01. PubMed PMID: 19277101; PubMed Central PMCID: PMCPMC2648625.CrossRefPubMedGoogle Scholar
- 8.Santiago GL, Cools P, Verstraelen H, Trog M, Missine G, El Aila N, et al. Longitudinal study of the dynamics of vaginal microflora during two consecutive menstrual cycles. PLoS One. 2011;6(11):e28180. https://doi.org/10.1371/journal.pone.0028180 Epub 2011/12/06. PubMed PMID: 22140538; PubMed Central PMCID: PMCPMC3227645.CrossRefPubMedGoogle Scholar
- 11.Bradshaw CS, Brotman RM. Making inroads into improving treatment of bacterial vaginosis - striving for long-term cure. BMC Infect Dis. 2015;15:292. https://doi.org/10.1186/s12879-015-1027-4 Epub 2015/07/30. PubMed PMID: 26219949; PubMed Central PMCID: PMC4518586.CrossRefPubMedPubMedCentralGoogle Scholar
- 12.Callahan BJ, DiGiulio DB, Goltsman DSA, Sun CL, Costello EK, Jeganathan P, et al. Replication and refinement of a vaginal microbial signature of preterm birth in two racially distinct cohorts of US women. Proc Natl Acad Sci U S A. 2017;114(37):9966–71. https://doi.org/10.1073/pnas.1705899114 Epub 2017/08/30. PubMed PMID: 28847941; PubMed Central PMCID: PMCPMC5604014.CrossRefPubMedPubMedCentralGoogle Scholar
- 13.Bautista CT, Wurapa E, Sateren WB, Morris S, Hollingsworth B, Sanchez JL. Bacterial vaginosis: a synthesis of the literature on etiology, prevalence, risk factors, and relationship with chlamydia and gonorrhea infections. Mil Med Res. 2016;3:4. https://doi.org/10.1186/s40779-016-0074-5 Epub 2016/02/16. PubMed PMID: 26877884; PubMed Central PMCID: PMCPMC4752809.CrossRefPubMedPubMedCentralGoogle Scholar
- 15.Vaneechoutte M. Lactobacillus iners, the unusual suspect. Res Microbiol. 2017. https://doi.org/10.1016/j.resmic.2017.09.003 Epub 2017/09/28. PubMed PMID: 28951208.
- 16.Atashili J, Poole C, Ndumbe PM, Adimora AA, Smith JS. Bacterial vaginosis and HIV acquisition: a meta-analysis of published studies. AIDS. 2008;22(12):1493–501. https://doi.org/10.1097/QAD.0b013e3283021a37 Epub 2008/07/11. PubMed PMID: 18614873; PubMed Central PMCID: PMCPMC2788489.CrossRefPubMedPubMedCentralGoogle Scholar
- 20.Esber A, Vicetti Miguel RD, Cherpes TL, Klebanoff MA, Gallo MF, Turner AN. Risk of bacterial vaginosis among women with herpes simplex virus type 2 infection: a systematic review and meta-analysis. J Infect Dis. 2015;212(1):8–17. https://doi.org/10.1093/infdis/jiv017 PubMed PMID: 25589333.CrossRefPubMedGoogle Scholar
- 21.Kaul R, Nagelkerke NJ, Kimani J, Ngugi E, Bwayo JJ, Macdonald KS, 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(11):1692–7. https://doi.org/10.1086/522006 PubMed PMID: 18008255.CrossRefPubMedGoogle Scholar
- 22.Rathod SD, Krupp K, Klausner JD, Arun A, Reingold AL, Madhivanan P. Bacterial vaginosis and risk for Trichomonas vaginalis infection: a longitudinal analysis. Sex Transm Dis. 2011;38(9):882–6. https://doi.org/10.1097/OLQ.0b013e31821f91a1 Epub 2011/08/17. PubMed PMID: 21844747; PubMed Central PMCID: PMCPMC3156984.CrossRefPubMedPubMedCentralGoogle Scholar
- 25.Bradshaw CS, Vodstrcil LA, Hocking JS, Law M, Pirotta M, Garland SM, et al. Recurrence of Bacterial Vaginosis Is Significantly Associated With Posttreatment Sexual Activities and Hormonal Contraceptive Use. Clin Infect Dis. 2013;56(6):777–86. https://doi.org/10.1093/Cid/Cis1030 PubMed PMID: WOS:000315630800009.CrossRefPubMedGoogle Scholar
- 30.Brotman RM, Ravel J, Cone RA, Zenilman JM. Rapid fluctuation of the vaginal microbiota measured by Gram stain analysis. Sex Transm Infect. 2010;86(4):297–302. https://doi.org/10.1136/sti.2009.040592 Epub 2010/07/28. PubMed PMID: 20660593; PubMed Central PMCID: PMCPMC3534767.CrossRefPubMedPubMedCentralGoogle Scholar
- 35.Sanchez S, Garcia PJ, Thomas KK, Catlin M, Holmes KK. Intravaginal metronidazole gel versus metronidazole plus nystatin ovules for bacterial vaginosis: a randomized controlled trial. Am J Obstet Gynecol. 2004;191(6):1898–906. https://doi.org/10.1016/j.ajog.2004.06.089 Epub 2004/12/14. PubMed PMID: 15592270.CrossRefPubMedGoogle Scholar
- 36.Swidsinski A, Doerffel Y, Loening-Baucke V, Swidsinski S, Verstraelen H, Vaneechoutte M, et al. Gardnerella biofilm involves females and males and is transmitted sexually. Gynecol Obstet Investig. 2010;70(4):256–63. https://doi.org/10.1159/000314015 Epub 2010/11/06. PubMed PMID: 21051845.CrossRefGoogle Scholar
- 37.Balashov SV, Mordechai E, Adelson ME, Gygax SE. Identification, quantification and subtyping of Gardnerella vaginalis in noncultured clinical vaginal samples by quantitative PCR. J Med Microbiol. 2014;63(Pt 2):162–75. https://doi.org/10.1099/jmm.0.066407-0 Epub 2013/11/10. PubMed PMID: 24200640.CrossRefPubMedGoogle Scholar
- 39.Zozaya M, Ferris MJ, Siren JD, Lillis R, Myers L, Nsuami MJ, et al. Bacterial communities in penile skin, male urethra, and vaginas of heterosexual couples with and without bacterial vaginosis. Microbiome. 2016;4:16. https://doi.org/10.1186/s40168-016-0161-6 Epub 2016/04/20. PubMed PMID: 27090518; PubMed Central PMCID: PMCPMC4835890.CrossRefPubMedPubMedCentralGoogle Scholar
- 40.Nelson DE, Dong Q, Van der Pol B, Toh E, Fan B, Katz BP, et al. Bacterial communities of the coronal sulcus and distal urethra of adolescent males. PLoS One. 2012;7(5):e36298. https://doi.org/10.1371/journal.pone.0036298 PubMed PMID: 22606251; PubMed Central PMCID: PMC3350528.CrossRefPubMedPubMedCentralGoogle Scholar
- 41.Nelson DE, Van Der Pol B, Dong Q, Revanna KV, Fan B, Easwaran S, et al. Characteristic male urine microbiomes associate with asymptomatic sexually transmitted infection. PLoS One. 2010;5(11):e14116. https://doi.org/10.1371/journal.pone.0014116 Epub 2010/12/03. PubMed PMID: 21124791.CrossRefPubMedPubMedCentralGoogle Scholar
- 42.Marrazzo JM, Antonio M, Agnew K, Hillier SL. Distribution of genital lactobacillus strains shared by female sex partners. J Infect Dis. 2009;199(5):680–3. https://doi.org/10.1086/596632 Epub 2009/02/10. PubMed PMID: 19199538; PubMed Central PMCID: PMC3291173.CrossRefPubMedPubMedCentralGoogle Scholar
- 43.Liu CM, Hungate BA, Tobian AA, Ravel J, Prodger JL, Serwadda D, et al. Penile Microbiota and Female Partner Bacterial Vaginosis in Rakai, Uganda. MBio. 2015;6(3):e00589. https://doi.org/10.1128/mBio.00589-15 PubMed PMID: 26081632; PubMed Central PMCID: PMCPMC4471566.CrossRefPubMedPubMedCentralGoogle Scholar
- 44.Zozaya-Hinchliffe M, Lillis R, Ferris M, Taylor S, Martin DH. Carriage of bacterial vaginosis-associated species by male sexual partners. American Society of Microbiology 108th General Meeting; 2008.Google Scholar
- 45.Eren AM, Zozaya M, Taylor CM, Dowd SE, Martin DH, Ferris MJ. Exploring the diversity of Gardnerella vaginalis in the genitourinary tract microbiota of monogamous couples through subtle nucleotide variation. PLoS One. 2011;6(10):e26732. https://doi.org/10.1371/journal.pone.0026732 Epub 2011/11/03. PubMed PMID: 22046340; PubMed Central PMCID: PMCPMC3201972.CrossRefPubMedPubMedCentralGoogle Scholar
- 49.Aral SO, Leichliter JS, Blanchard JF. Overview: the role of emergent properties of complex systems in the epidemiology and prevention of sexually transmitted infections including HIV infection. Sex Transm Infect. 2010;86(Suppl 3):iii1–3. https://doi.org/10.1136/sti.2010.047373 Epub 2010/12/01. 86/Suppl_3/iii1. PubMed PMID: 21098053.CrossRefPubMedGoogle Scholar
- 50.Morris M, Goodreau S, Moody J. Sexual networks, concurrency and STD/HIV. In: Holmes KK, editor. Sexually transmitted diseases. 4th ed. New York: McGraw-Hill Medical; 2008. p. xxv–2166.Google Scholar
- 51.Kenyon C, Delva W. It’s the network, stupid: a population’s sexual network connectivity determines. F1000Res. 2018. https://f1000research.com/articles/7-1880/v1.
- 55.Maughan-Brown B, Kenyon C, Lurie MN. Partner age differences and concurrency in South Africa: implications for HIV-infection risk among young women. AIDS Behav. 2014;18(12):2469-76. https://doi.org/10.1007/s10461-014-0828-6
- 57.Kraut-Becher J, Eisenberg M, Voytek C, Brown T, Metzger DS, Aral S. Examining racial disparities in HIV: lessons from sexually transmitted infections research. J Acquir Immune Defic Syndr. 2008;47(Suppl 1):S20–7. https://doi.org/10.1097/QAI.0b013e3181605b95 Epub 2008/04/09. PubMed PMID: 18301130.CrossRefPubMedGoogle Scholar
- 58.Kenyon CR, Buyze J, Klebanoff M, Brotman RM. Association between bacterial vaginosis and partner concurrency: a longitudinal study. Sex Transm Infect. 2016. https://doi.org/10.1136/sextrans-2016-052652 PubMed PMID: 27645157.
- 60.Koumans EH, Farley TA, Gibson JJ, Langley C, Ross MW, McFarlane M, et al. Characteristics of persons with syphilis in areas of persisting syphilis in the United States: sustained transmission associated with concurrent partnerships. Sex Transm Dis. 2001;28(9):497–503 Epub 2001/08/24. PubMed PMID: 11518865.CrossRefGoogle Scholar
- 62.Aral SO, Padian NS, Holmes KK. Advances in multilevel approaches to understanding the epidemiology and prevention of sexually transmitted infections and HIV: an overview. J Infect Dis. 2005;191(Suppl 1):S1–6. https://doi.org/10.1086/425290 Epub 2005/01/01. PubMed PMID: 15627219.CrossRefPubMedGoogle Scholar
- 65.Kenyon C. Strong associations between national prevalence of various STIs suggests sexual network connectivity is a common underpinning risk factor. BMC Infect Dis. 2017;17(1):682. https://doi.org/10.1186/s12879-017-2794-x Epub 2017/10/14. PubMed PMID: 29025419; PubMed Central PMCID: PMCPMC5639489.CrossRefPubMedPubMedCentralGoogle Scholar
- 68.Kenyon CR. Bypassing the ‘rapid-clearance-in-males-buffer’: a fourth mechanism to explain how concurrency enhances STI spread. Int J STD AIDS. 2017. https://doi.org/10.1177/0956462417706246 PubMed PMID: 28457203.
- 69.Van Der Pol B, Williams JA, Orr DP, Batteiger BE, Fortenberry JD. Prevalence, incidence, natural history, and response to treatment of trichomonas vaginalis infection among adolescent women. J Infect Dis. 2005;192(12):2039–44. https://doi.org/10.1086/498217 Epub 2005/11/17. PubMed PMID: 16288365.CrossRefGoogle Scholar
- 70.Hobbs MM, Seña AC, Swygard H, Schwebke J. Trichomonas vaginalis and trichomoniasis. Sex Transm Dis. 2008;12:771–93.Google Scholar
- 71.Brotman RM, Bradford LL, Conrad M, Gajer P, Ault K, Peralta L, et al. Association between Trichomonas vaginalis and vaginal bacterial community composition among reproductive-age women. Sex Transm Dis. 2012;39(10):807–12. https://doi.org/10.1097/OLQ.0b013e3182631c79 PubMed PMID: 23007708; PubMed Central PMCID: PMCPMC3458234.CrossRefPubMedPubMedCentralGoogle Scholar
- 82.Hickey RJ, Zhou X, Settles ML, Erb J, Malone K, Hansmann MA, et al. Vaginal microbiota of adolescent girls prior to the onset of menarche resemble those of reproductive-age women. MBio. 2015;6(2). https://doi.org/10.1128/mBio.00097-15 PubMed PMID: 25805726; PubMed Central PMCID: PMCPMC4453513.
- 85.Zhou X, Hansmann MA, Davis CC, Suzuki H, Brown CJ, Schutte U, et al. The vaginal bacterial communities of Japanese women resemble those of women in other racial groups. FEMS Immunol Med Microbiol. 2010;58(2):169–81. https://doi.org/10.1111/j.1574-695X.2009.00618.x Epub 2009/11/17. PubMed PMID: 19912342; PubMed Central PMCID: PMCPMC2868947.CrossRefPubMedGoogle Scholar
- 86.Aral SO, Over M, Manhart L, Holmes KK. Sexually Transmitted Infections. In: Jamison DT, Mosley WH, editors. Disease control priorities in developing countries: health policy responses to epidemiological change. 2. Washington (DC): World Bank; 2006. p. 653–89.Google Scholar
- 87.Kenyon CR, Osbak K, Tsoumanis A. The Global Epidemiology of Syphilis in the Past Century - A Systematic Review Based on Antenatal Syphilis Prevalence. PLoS Negl Trop Dis. 2016;10(5):e0004711. https://doi.org/10.1371/journal.pntd.0004711 PubMed PMID: 27167068; PubMed Central PMCID: PMCPMC4864207.CrossRefPubMedPubMedCentralGoogle Scholar
- 91.Cohen CR, Lingappa JR, Baeten JM, Ngayo MO, Spiegel CA, Hong T, et al. Bacterial vaginosis associated with increased risk of female-to-male HIV-1 transmission: a prospective cohort analysis among African couples. PLoS Med. 2012;9(6):e1001251. https://doi.org/10.1371/journal.pmed.1001251 Epub 2012/06/30. PubMed PMID: 22745608; PubMed Central PMCID: PMCPMC3383741.CrossRefPubMedPubMedCentralGoogle Scholar
- 93.Yildirim S, Yeoman CJ, Janga SC, Thomas SM, Ho M, Leigh SR, et al. Primate vaginal microbiomes exhibit species specificity without universal Lactobacillus dominance. ISME J. 2014;8(12):2431–44. https://doi.org/10.1038/ismej.2014.90 Epub 2014/07/19. PubMed PMID: 25036926; PubMed Central PMCID: PMCPMC4260710.CrossRefPubMedPubMedCentralGoogle Scholar
- 94.Kirby D. Changes in sexual behaviour leading to the decline in the prevalence of HIV in Uganda: confirmation from multiple sources of evidence. Sex Transm Dis. 2008;84(Suppl 2):ii35–41.Google Scholar
- 95.Halperin D, Mugurungi O, Hallett T, Muchini B, Campbell B, Magure T, et al. A surprising prevention success: why did the HIV epidemic decline in Zimbabwe? PLoS Med. 2011;8(2):e1000414. https://doi.org/10.1371/journal.pmed.1000414 Epub 2011/02/25. PubMed PMID: 21346807.CrossRefPubMedPubMedCentralGoogle Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.