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A study on HIV, Syphilis, and Hepatitis B and C virus infections among female sex workers in the Republic of Congo



Female Sex Workers (FSWs) are considered to be at high risk for transmission of Sexually Transmitted Infections (STIs) and are defined as a priority of the national HIV/AIDS response in the Republic of Congo (RoC). However, no data are available regarding STIs in this group. This study aimed to determine the prevalences of HIV, syphilis and hepatitis B and C among FSWs in five cities in the country.


A cross-sectional study was conducted from November 2nd 2011 to May 15th 2012. Participants were recruited in Brazzaville, Pointe-Noire, Dolisie, Nkayi and Pokola using a respondent-driven sampling method.


A total of 805 FSWs were recruited with an average age of 28.31 ± 9.15 years. The overall prevalences of HIV, syphilis, HBV and HCV were 7.50%, 2.20%, 4.20% and 0.70%, respectively. The age groups 35–39 (20.51% [0%–36.93%], p = 0.0057) and greater than 40 years (16.67% [0%–34.93%], P = 0.016) were positively associated with behaviors at high risk of HIV infection. For syphilis, the most infected age group was the one greater than 40 years, at 6.25% ([1.06% –72.37%] p = 0.04). Pointe-Noire was the most infected city for syphilis and HBV, with 5.15% (p = 0.0061) and 4.22% (p˂0.001), respectively. No risk factors were associated with HCV infection. FSWs practicing in mobile prostitution sites had a significantly higher infection rate (2.1% [0%–11.09%] p = 0.04).


This study shows that the prevalence of HIV and other STIs in FSWs is high. Therefore, a combination of individual and structural interventions could reduce the risk of an STI “reservoir” among this population.

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HIV is responsible for one of the most destructive epidemics in recorded history. In 2015, UNAIDS reported 70% of the people living with HIV worldwide, 70% of new HIV infections and 66% of people dying from AIDS. Sub-Saharan Africa remains the most heavily affected region, and in this region, women represent more than 60% of HIV-infected persons [1]. Female sex workers (FSWs) are considered to be a high-risk group for the acquisition of HIV and other sexually transmitted infections (STIs). The relationship between sex work and HIV vulnerability has been recognized since the earliest days of the epidemic [2]. In countries with a generalized epidemic like the Republic of Congo (RoC), the HIV prevalence is consistently higher among FSWs than in the general population, and it was estimated that FSWs are 13.5 times more likely to be infected than other women [1]. To our knowledge, in Central Africa the burden of syphilis and hepatitis is not well described, with the exception of certain groups such as blood donors. Indeed, in the RoC approximately 7.5% and 0.5% of donors are affected by hepatitis B and C, respectively [3].

A systematic review of behavioral risk factors for STIs in FSWs in sub-Saharan Africa shows that the vulnerability of FSWs is inextricably linked to the realities of this “profession”. Accordingly, STI interventions for FSWs in the RoC are not guided by knowledge of country-specific risk factors, as recommended by UNAIDS in their practical guidelines for intensifying HIV prevention towards universal access [4]. The vulnerability for HIV as well as other STIs, such as syphilis and hepatitis viruses, in the FSW group is primarily the consequence of a high number of sexual partners and a high frequency of unprotected sex. Indeed, several previous studies have shown an association between STI prevalences among FSWs and inconsistent condom use as the main risk factor for HIV infection [46]. It has also been found that FSWs have a higher risk of contracting STIs from their non-paying partners than from their clients [2, 7].

In the RoC, FSWs have been identified as one of the highest-risk populations and priorities of national AIDS responses [8]. Unfortunately, there has been no study conducted in this group determining STI prevalences. Therefore, the current study aimed to determine prevalences of HIV, syphilis, and hepatitis B and C infections and to identify associated risk factors for these infections among FSWs in the RoC.


A cross sectional study was conducted from November 2nd 2011 to May 15th 2012in fixed and mobile FSW sites in five cities of the RoC, including Brazzaville, Pointe-Noire, Dolisie, Nkayi, and Pokola.

Data collection

Participants were recruited using the respondent-driven sampling technique, which has been shown to be reliable for conducting studies in hard to reach groups and samples [9]. Mapping was done to identify FSW sites, followed by the enumeration of FSWs at each site by trained interviewers in bars and nightclubs, with the help of neighborhood leaders, police officials, youth, and the associations of FSW against HIV/AIDS. The total number of FSWs and the number of sites per type of prostitution are shown in Table 1. The average number of FSWs per site was estimated to be 11.

Table 1 Total number of different type of prostitution and FSW per sites

In the absence of baseline data on HIV prevalence in this population, the required sample size was calculated using the following formula and by taking as reference the mean of the ratio “HIV prevalence in this population/HIV prevalence among those aged 15–49 in Central Africa,” which was estimated at 18.7%:

n = [zα 2*p*(1-p)/e2]*d. Where zα = reduced risk α = 5%; e: margin of error which is set at 0.05, p: estimated prevalence of HIV infection among FSWs; d: FSWs Inclusion Interval.

The prevalence of HIV among people aged 15 to 49 years is 3.20%. By applying a sampling interval of 3 and by taking into account a predicted refusal rate of 15%, the sample size was estimated at 845 as described in Table 2. The total number of sites necessary to achieve the estimated sample size was calculated by taking into account the average number of FSWs by site according to the mapping results as described in Table 1.

Table 2 Distribution of sex worker prostitution sites by cities

The total number of sites required to reach the estimated sample size was calculated by taking into account the average number of FSW per site according to the mapping results, which was 11. Thus, the total number of sites needed to reach the required sample size was estimated at 62. Table 3 shows the distribution of sites by city and by category according to the distribution of these variables in the population as a whole.

Table 3 Number of selected sites per cities

FSWs attending each site were invited, in groups of 20, to attend a workshop dedicated to STI education and data collection for the study. At the second visit, the workshop was organized as beneficial for the FSWs. Each workshop started with a presentation of the objectives, activities and expected results, followed by asking for willingness to participate in the study and an invitation for individual face-to-face interviews. Questionnaires were administered using an individual questionnaire adapted from one developed by Family Heath International for behavioral surveys [10]. FSWs who agreed to participate in the study were then asked to provide consent.

FSWs were defined as adults or young females who received goods in exchange for sexual services, either regularly or occasionally, and who may or may not consciously define those activities as income-generating [11].

Laboratory procedures

Five milliliters (5 mL) of whole blood were collected in EDTA tubes. Plasma was then obtained after centrifuging for 10 min at 5000 rev/min and kept at −20 °C before transfer to the Molecular Biology Unit of Laboratoire National de Santé Publique (LNSP) in Brazzaville, where all the HIV, HCV, HBV and syphilis tests were performed. Plasma specimens were screened for HIV and HCV antibodies and the surface hepatitis B antigen (AgHBs) using ELISA tests (Bio-Rad Genscreen HIV1/2 Ag-Ac Ultra, Bio-Rad Monolisa HCV and Bio-Rad Monolisa HBV Ultra, Marne la Coquette, France, respectively). The following algorithm was used to detect antibodies against HIV: the ELISA-positive samples were confirmed by the Western blot (New LAV Blot I, Bio-Rad, Marnes la Coquette, France). The Rapid Plasma Reagine (RPR) test (BioScan, BHA BIO-TECH India) was first used to detect syphilis infection, and active syphilis was identified by testing the RPR-positive samples with the TPHA test (Biotech TPHA test kit, UK).

Data analysis

All data were entered into Cs Pro version 4.0 and then transferred to SPSS 17.0 software for statistical analysis. Differences with a p-value of <0.05 were considered statistically significant. The analyzed variables included the prevalences of syphilis, HIV, Hepatitis B and C. The prevalence’s of these infections were tested for associations with cities (Brazzaville, Pointe-Noire, Dolisie, Nkayi and Pokola), age group (<20, 20–24, 25–29, 30–34, 35–39 and >40 years old), age of first sex (<15 and > 15 years old), drug use and unprotected sex. Differences between proportional data were compared using the chi-square test, a multivariable logistic regression model was used and the magnitude of associations was assessed using odds ratios with respective 95% CIs.


Out of a total of 852 FSWs interviewed, 805 (94.4%) were enrolled, including 35.6% (n = 287) in Brazzaville, 28.9% (n = 233) in Pointe-Noire, 11.5% (n = 93) in Dolisie, 11.6% (n = 94) in Nkayi and 12.17% (n = 98) in Pokola. The percentages of FSWs originally from the RoC, the Democratic Republic of Congo (DRC) and other countries were, respectively, 59.2%, 38.8%, and 2%.

Sociodemographic information, history in sex work, knowledge of STIs and sexual behavior characteristics

The average age of the participants was 28.3 ± 9.1 years old (ranging from 18 to 66 years). FSWs spent an average of 19.7 ± 4.5 years in sex work. Among the FSWs interviewed, 8.6% were unschooled, 24.6% had primary education and 66.9% had secondary education. Approximately 18.7% of FSWs were sharing life with a partner versus 81.3% who were living alone. The percentage of FSWs using home-based sex work was 31.6%, while 58.2% were using establishment-based sex work and 2.2% mixed the two types of sex work.

Prevalences of HIV, Syphilis, HBV and HCV

The highest prevalences of HIV were observed in the cities of Pointe-Noire (12.8%) and Dolisie (7.5%), which also had prevalences of active syphilis of 5.1% and 2.1%, respectively. Concerning HBV and HCV, the highest prevalences were found in Ponte-Noire (7.3% and 14.1%, respectively), followed by Brazzaville for HCV (7.3%) and Nkayi for HBV (6.3%). In all 5 cities together, the prevalences of HIV, syphilis, HBV and HCV were 7.5%, 2.2%, 4.2% and 0.7% respectively, as described in Table 4.

Table 4 prevalence of HIV, syphilis (passive and active) and hepatitis B and C depending on cities

Factors associated with HIV, Syphilis, HBV and HCV status

Risk factors were investigated and multivariable analyses showed that the risk of contracting HIV and syphilis infections increased with age, specifically with age greater than 34 and 40 years (COR = 4.72 CI: 1.57 –14.15; p <0.005 and COR = 8.76 CI: 1.06 to 72.3; p = 0.044, respectively). Additionally, prevalences of syphilis and hepatitis B were significantly higher for FSWs living in the city of Pointe-Noire (COR = 14.19 [2.13-94.45]; p = 0.006 and COR = 6.61 [2.21–19.75; p = 0.0007 respectively]), and practicing mobile prostitution was associated with a greater risk of syphilitic infection (COR = 0.1 [0.01–0.91]; p = 0.014).

Other factors, including drug use, age at first sexual intercourse, the systematic use of condoms or type of prostitution, were not associated with the occurrence of these infections (Table 5).

Table 5 VIH, syphilis, hepatitis B and C infections associated with sociodemographic factors


This first report on the prevalences of HIV, syphilis, HBV and HCV among FSWs in the RoC shows that the prevalence of HIV among FSWs is 7.5%, significantly higher than those among other women and in the general population [8]. Regarding the cities of Brazzaville, Dolisie and Pointe-Noire, prevalences of 4.9%, 7.5%, and 12.8% were reported, and these are above the national average (3.2%). This prevalence is lower than those reported in studies conducted in sub-Saharan countries. Indeed, in West Africa, prevalences of 33.7% and 22.9% were found in Cote d’Ivoire and Senegal, respectively [12, 13], whereas in Rwanda (East Africa) the HIV prevalence among FSWs was 59.8% [14]. In central Africa, where few studies are available, it was reported that 23.6% and 23.3% of FSWs were HIV-infected in Cameroon and the DRC (Democratic Republic of the Congo), respectively [15]. In the context of the RoC, these results suggest that, even in the context of a generalized epidemic, HIV infection remains hyper-endemic among FSWs and spreads to the general population through clients (customers) and regular partners [2], showing a role played by FSW partners as a potential bridge to the general population [16].

In this study, ages ranging beyond 34 years were positively associated with HIV infection in this population. This observation was reported in others studies assessing prevalence rates in Africa and abroad. Indeed, most of the HIV-reactive FSWs were reportedly in the 30–39-year-old age group in studies conducted in India, Burkina-Faso and Nigeria [1719].

The current study has reported a relatively low prevalence of HCV among FSWs (0.74%). Literature data suggests a wide disparity of results in this population. In fact, while less than 1% among FSWs in Italy, the rate increases up to 74% among FSWs who inject drugs in China [20, 21]. Although in this study the use of drugs was almost nonexistent, it is unclear whether the low prevalence found in the present study reflects the real epidemic of HCV in this population in the RoC. Several studies conducted among non-injection drug users have established that the prevalence of HCV infection in this population was comparable to that observed in the general population. This observation has lead to the conclusion that sexual transmission is not necessarily a preferred route of transmission for HCV infection [2123].

In this study, the prevalence of HBV was found to be 4.24%, lower than the prevalence reported in blood donors, where 7.5% of samples were hepatitis B surface antigen positive [3]. This low prevalence in this population in the RoC may be partly explained by the relatively low level of injection drug use, which was shown to be a risk factor for contamination among FSWs [24]. Additionally, the practice of anal sex by FSWs has also been shown to increase the probability of HBV infection [25]. In the current study, anal sexual intercourse was not documented. Therefore, the hypothesis that HBV is sexually transmitted in FSWs, including the correlation of exposure periods, should be investigated in the context of the RoC.

Little is known regarding syphilis infections in Africa in the subpopulation of FSWs. The current study reports a prevalence of 2.23% for this infection. This prevalence varies from one locality to another. Indeed, in Sudan the prevalence ranges from 1.5% to 8.9%, depending on the region of the country, and it was observed that the HIV and syphilis prevalences were similar [26]. The reason for this variability, especially of the larger vulnerability of FSWs living in the city of Pointe-Noire compared with other localities, remains unexplained. However, Pointe-Noire is a port city with significant economic activity, and has a significant epidemiological situation, as suggested by the data from FSWs in this study as well as data reported for other subgroups of the population (2009 Esic inquiry, investigation of HIV in pregnant women, 2012). The reasons for this feature are still unknown.

In this study, FSWs living in the city of Pointe-Noire were highly infected with HIV and hepatitis B virus in comparison with those living in Brazzaville. The reason for this difference is unknown.

Limitations of the study

Certain limitations were noted in this study. The cross-sectional study design based on the respondent-driven sampling method, which is not necessarily representative of the FSW population, may be the origin of certain deficiencies, in particular as related to data concerning risk behaviors obtained on the basis of a questionnaire as this information is inherently difficult to verify. The existence of certain eligibility criteria may reduce the generalization of these data to all FSWs in the RoC. Additionally, the use of serological tests can introduce the possibility of false test results. For example, these tests cannot detect very recent infections, thus reducing their sensitivity, despite their sensitivity and specificity generally above 90% [27, 28].


Despite HIV prevention programs being implemented that focus on them, FSWs remain a very high risk group and an important contributor to population-level HIV transmission in the RoC. This study was the first one assessing HIV, syphilis, HBV and HCV prevalences among FSWs. There is therefore an urgent need to put in place a second-generation STD surveillance system that can help document incremental outcomes and the impact of interventions for this specific population.



Female Sex Workers


Hepatitis B virus


Hepatitis C virus


Human Immunodeficiency Virus.


Republic of Congo


  1. 1.

    UNAIDS. Global report: UNAIDS report on the global Aids epidemic | 2012. Geneva: 2012.

  2. 2.

    Minichiello V, Rahman S, Hussain R. Epidemiology of sexually transmitted infections in global indigenous populations: data availability and gaps. Int J STD AIDS. 2013;24(10):759–68.

    Article  PubMed  Google Scholar 

  3. 3.

    Angounda BM, Bokilo Dzia A, Niama FR, Ahombo G, Boumba LMA, Moukassa D, Ennaji MM, Ibara J-R. Seroprevalence of markers and Risk factors of Hepatitis B Virus among blood donors in Brazzaville, Congo. Int J Innov and Sc Res. 2015;20(1):171–9.

    Google Scholar 

  4. 4.

    World Health Organization. Sexually Transmitted Infections (STIs): The Importance of a Renewed Commitment to STI Prevention and Control in Achieving Global Sexual and Reproductive Health. Geneva: World Health Organization; 2013. Available from: Accessed 20 Aug 2015.

  5. 5.

    Dupin N1. Sexually transmitted infections in France in 2009. Rev Prat. 2010;60(4):520–5.

    Google Scholar 

  6. 6.

    Han L, Zhou C, Li Z, Poon AN, Rou K, Fuller S, Li Y, Shen L, Kang D, Huang L, Liao M, Fu X, Shepard C, Wu Z, Bulterys M. Differences in risk behaviours and HIV/STI prevalence between low-fee and medium-fee female sex workers in three provinces in China. Sex Transm Infect. 2016;92(4):309–15.

    Article  PubMed  Google Scholar 

  7. 7.

    Kinoshita-Moleka R, Smith JS, Atibu J, Tshefu A, Hemingway-Foday J, Hobbs M, Bartz J, Koch MA, Rimoin AW, Ryder RW. Low prevalence of HIV and other selected sexually transmitted infections in 2004 in pregnant women from Kinshasa, the Democratic Republic of the Congo. Epidemiol Infect. 2008;136(9):1290–6. Epub 2007 Nov 21.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    CNLS Congo-Brazzaville. Cadre Stratégique National de Lutte contre le VIH/Sida 2009–2013. Available at: Accessed 14 Dec 2011.

  9. 9.

    Wejnert C. An empirical test of Respondent Driven Sampling: Point estimates, variance, degree measures and out-of-equilibrium data. Cyprian Wejnert Sociol Methodol. Sociol Methodol. 2009;39(1):73–116.

    Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Family Health International. Behavioral surveillance survey: guidelines for repeated behavioral survey in populations at risk. Available on: Accessed 14 Dec 2011.

  11. 11.

    ONUSIDA. Le VIH et le commerce du sexe – note d’orientation de l’ONUSIDA. Genève: 2009.

  12. 12.

    Nouaman MN, Meless DG, Coffie PA, Arrivé E, Tchounga BK, Ekouévi DK, Anoma C, Eholié SP, Dabis F, Jaquet A, with the IeDEA West Africa collaboration. Oral health and HIV infection among female sex workers in Abidjan, Côte d’Ivoire. BMC Oral Health. 2015;15:154.

    Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Kane CT, Diawara S, Ndiaye HD, Diallo PA, Wade AS, Diallo AG, Belec L, Mboup S. Concentrated and linked epidemics of both HSV-2 and HIV-1/HIV-2 infections in Senegal: public health impacts of the spread of HIV. Int J STD AIDS. 2009;20(11):793–6. doi:10.1258/ijsa.2008.008414.

    Article  PubMed  Google Scholar 

  14. 14.

    Braunstein SL, Ingabire CM, Geubbels E, Vyankandondera J, Umulisa M-M, Gahiro E, Uwineza M, Tuijn CJ, Nash D, van de Wijgert JHHM. High Burden of Prevalent and Recently Acquired HIV among Female Sex Workers and Female HIV Voluntary Testing Center Clients in Kigali, Rwanda. PLoS One. 2011;6(9):e24321.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Papworth E, Ceesay N, An L, Thiam-Niangoin M, Ky-Zerbo O, Holland C, Dramé FM, Grosso A, Diouf D, Baral SD. Epidemiology of HIV among female sex workers, their clients, men who have sex with men and people who inject drugs in West and Central Africa. J Int AIDS Soc. 2013;16(4Suppl3):18751. doi:10.7448/IAS.16.4.c18751. Published online 2013 December 2.

    PubMed  PubMed Central  Google Scholar 

  16. 16.

    Shah NS, Shiraishi RW, Subhachaturas W, et al. Bridging Populations—Sexual Risk Behaviors and HIV Prevalence in Clients and Partners of Female Sex Workers, Bangkok, Thailand. 2007. J Urban Health. 2011;8(3):533–44.

    Article  Google Scholar 

  17. 17.

    Praseeda SD, Anuradha D, Jayanthi SS. Study of Hbv& HcvInfection in Female Sex Workers & Their Co-Infection With Hiv. J Clin and Diag Res. 2013;7(2):234–7.

    Google Scholar 

  18. 18.

    Traore IT, Hema NM, Sanon A, Some F, et al. HIV risk and behaviour among part-time versus professional FSW: baseline report of an interventional cohort in Burkina Faso. Sex Transm Infect. 2016. doi:10.1136/sextrans-2015-052038 [Epub ahead of print].

    PubMed  Google Scholar 

  19. 19.

    Zermiani M, Mengoli C, Rimondo C, Galvan U, Cruciani M, Serpelloni G. Prevalence of Sexually Transmitted Diseases and Hepatitis C in a Survey of Female Sex Workers in the North-East of Italy. Open AIDS J. 2012;6:60–4.

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Tang Z, Zhang C, Li X, Liu Y, Su S, Zhou Y, Shen Z. HIV risk among female sex workers with different patterns of drug use behaviors in Southwest China: a cross-sectional study. AIDS Care. 2015;27(3):293–300.

    Article  PubMed  Google Scholar 

  21. 21.

    Forbi JC, Onyemauwa N, Gyar SD, Oyeleye AO, Entonu P, Agwale SM. High prevalence of hepatitis B virus among female sex workers in Nigeria. Rev Inst Med Trop S Paulo. 2008;50(4):219–21.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Thuy NTT, Nhung VT, Van Thuc N, et al. HIV infection and risk factors among female sex workers in southern Vietnam. AIDS. 1998;12:425–32.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Dunkle KL, Beksinska ME, Rees VH, et al. Risk factors for HIV infection among sex workers in Johannesburg, South Africa. Int J STD AIDS. 2005;16:256–61.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Weir SS, Roddy RE, Zekeng L, et al. Association between condom use and HIV infection: a randomized study of self-reported condom use measures. J Epidemiol Community Health. 1999;53:417–22.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Lange WR, Cone EJ, Snyder FR. The association of hepatitis B virus in parental drug abusers, 1971 to 1972 and 1986 to 1987. Arch Intern Med. 1990;150:365–8.

  26. 26.

    Elhadi M, Elbadawi A, Abdelrahman S, Mohammed I, Bozicevic I, Hassan EA, Elmukhtar M, Ahmed S, Abdelraheem MS, Mubarak N, Elsanousi S, Setayesh H. Integrated bio-behavioural HIV surveillance surveys among female sex workers in Sudan, 2011–2012. Sex Transm Infect. 2013;89 Suppl 3:iii17–22.

    Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Hwang SH, Oh HB, Kim HS, Lee EY. Evaluation of HBs Ag, HCV and HIV Ag-Ab Assays using Bio-Rad Elite Microplate Analyzer. Korean J Lab Med. 2006;26(6):436–41.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Sano T, Kondo M, Yoshimura Y, Tachikawa N, Sagara H, Itoda I, Yamanaka K, Sudo K, Kato S, Imai M. Evaluation of a new vesion of the human immunodeficiency virus antigen and antibody combination assay with improved sensitivity in HIV-1 p24 antigen detection. Kansenshogaku Zasshi. 2013;87(4):415–23.

    Article  PubMed  Google Scholar 

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The authors acknowledge the following groups and individuals for their contributions to this study: the FSWs, the health Directors of regions covered by the study, members of the national ethics committee, the team leader of the Project for Fighting AIDS and for Health in the Word Bank country Office, and the Director of the National Center for Blood Transfusion.


The study was supported by the Project for Fighting AIDS and for Health and co-sponsored by the RoC Government and the World Bank.

Availability of data and materials

The data generated and analyzed in this study are not publicly available for ethical reasons. However, they may be available from the corresponding author upon request.

Authors’ contributions

FRN, DL, FFM, ESBK, FKM and YI conceived and designed the study, organized the data collection and finalized the manuscript. LBNC, EMK, IL and PIM performed HIV, HBV, HCV and syphilis testing. DLR, ASPDB, AL and FM participated in the design of the study; RFN and FFM drafted the manuscript, KSC and EBMK reviewed the final draft of the manuscript; MFP and HJP coordinated the study. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not Applicable. This is an anonymous and uncorrelated study and does not include individual identifying information.

Ethics approval and consent to participate

The study protocol was revised and approved by the Comité d’Ethique de Recherche en Sciences de la Santé (CERSSA) from the Ministère de la Recherche scientifique et de l’Inovation Technologique (04/DGRST/CERSSA). The signed informed consent forms were obtained from FSWs after receiving explanations regarding the study in French and in both national languages (Lingala and Mutukutuba). FSWs who did not give their approved consent were not included in the study, although they were invited to participate in the workshop.

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Correspondence to Fabien Roch Niama.

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Niama, F., Loukabou Bongolo, N.C., Mayengue, P.I. et al. A study on HIV, Syphilis, and Hepatitis B and C virus infections among female sex workers in the Republic of Congo. Arch Public Health 75, 21 (2017).

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  • Female Sex Workers
  • HIV
  • HBV
  • HCV
  • Republic of Congo