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Seroprevalence, predictors and estimated incidence of maternal and neonatal Herpes Simplex Virus Type 2 infection in semi-urban women in Kilifi, Kenya

BMC Infectious Diseases volume 11, Article number: 155 (2011) Cite this article

Abstract

Background

Herpes Simplex Virus type 2 (HSV-2) has public health importance as a leading cause of genital ulcers, a co-factor in HIV-1 acquisition and transmission and as a cause of neonatal herpes infections. Little is known of its epidemiology and burden in Coastal Kenya.

Methods

We screened plasma samples for HSV-2 infection from 826 women aged 15-34 years who participated in an HIV-1 survey in Kilifi in 2004. The sample comprised 563 women selected randomly from a demographic surveillance system (DSS) and 263 women who presented for voluntary counseling and testing (VCT). Predictors for HSV-2 seropositivity were determined using multivariate logistic regression. The incidence of HSV-2 infection and risk of neonatal herpes were estimated by a simple catalytic model fitted to age-seroprevalence data.

Results

HSV-2 prevalence was 32% in the DSS recruits vs. 44% in the VCT recruits (P < 0.001), while, HIV-1 prevalence was 8% in the DSS recruits vs. 12% in the VCT recruits (P = 0.12). Independent risk factors for HSV-2 infection in all women were: older age (30-34 years; odds ratio (OR) 10.5, 95% confidence interval (CI): 5.2 - 21.0), recruitment from VCT (OR 1.5, 95% CI: 1.1 - 2.1), history of genital ulcers (OR 1.7, 95% CI: 1.2 - 2.3) and HIV infection (OR 2.7, 95% CI: 1.6-4.6). Education beyond primary (OR 0.7, 95% CI: 0.5 - 0.9) was inversely associated with HSV-2 infection. In the DSS sample, HSV-2 incidence was estimated at 4 cases (95% CI: 3.3 - 4.4) per 100 women per year, 17 cases (95% CI: 16-18) per 1,000 pregnancies per year and 33 neonatal cases (95% CI: 31-36) per 100,000 births per year.

Conclusions

HSV-2 transmission is rapid following the onset of sexual activity and likely to result in a significant burden of genital ulcer disease. Nevertheless, the burden of neonatal HSV-2 can be predicted to be low. Educating young women about HSV-2 infection may help in reducing its burden in this semi-urban population.

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Background

Herpes Simplex Virus type 2 (HSV-2) infection among women of the general population worldwide is of considerable public health importance as a leading cause of genital ulcer disease [1, 2], neonatal herpes infections [3–6] and due to its role in enhancing HIV-1 acquisition and transmission [7–9].

Establishing the burden of HSV-2 infection can be difficult because incident cases and reactivations are often missed clinically [6, 10, 11], and vertical transmission is a rare occurrence in populations with low HSV-2 prevalence [12–15]. About 80% of neonatal herpes infections arise from primary genital HSV-2 infection, acquired late in pregnancy [3, 5, 6, 15], and can result in significant morbidity to the newborn child [4–6]. Reactivated HSV-2 infections are estimated to cause <5% of neonatal herpes transmission [5, 15]. Neonatal herpes infections can also be caused by HSV-1 infection in about 20% of the instances [5, 15]. In the USA, neonatal herpes incidence has been estimated as 1 case per 3200 live births in a study involving over 58000 live births born in the period 1982-1999 [3]. In Africa, there is no information on the proportion of pregnant women who acquire HSV during pregnancy or on the incidence or prevalence of neonatal HSV-2 infection[16].

Studies in the African continent have shown variation in HSV-2 prevalence across diverse populations of women, ranging from 22% among adults in Tanzania and 68% among adults in urban Kenya to 90% among commercial sex workers in Zaire [9, 17]. In Western Kenya, an HIV survey among women aged 13-34 years conducted in 2003-4 revealed an HSV-2 prevalence of 53% [18]. A more recent National AIDS Indicator survey among general population women aged 15 - 64 years estimated HSV-2 prevalence of 42% but data on the possible impact of maternal transmission of HSV-2 were not provided in that survey [19]. Prevalence data, however, provide information on the proportion of individuals infected and allow for an estimation of HSV-2 incidence. Hence, vertical transmission can be inferred [3, 14, 15].

In this study we explore the prevalence of and predictors associated with HSV-2 seropositivity, the estimated rate of infection and the potential risk of vertical transmission using two sample sets from within a well-enumerated population of semi-urban women from coastal Kenya, namely, (i) a random sample of the adult women population and (ii) self-selected women attending for voluntary counselling and testing (VCT).

Methods

Kilifi District is a largely rural district in Coastal Kenya, with an estimated population of 544,305 people (52% female)[20]. In the year 2000, the Kenya Medical Research Institute (KEMRI) - Wellcome Trust Research Programme defined and mapped a geographical area in Kilifi District for demographic surveillance and clinical and epidemiological research. The resultant Kilifi Demographic Surveillance System (DSS) monitors a population of around 240,000 residents [21]. Kilifi District has a birth rate of approximately 8,000 live births per year, perinatal mortality of 44 per 1000 live births [21] and about 4,000 women attend antenatal care at the district hospital per year [21]. Until 2003, in Kilifi, pregnant women were not routinely tested for HIV-1, and VCT services were not widely available. In 2004, a large HIV-1 survey was conducted at several semi-urban communities in and around Kilifi town and VCT services were strengthened.

In this study, we used data and serum samples of women aged 15-34 years who were participants of the 2004 HIV-1 survey and resided in Kilifi and Mtondia towns[21]. Kilifi and Mtondia areas are considered semi-urban, as they are not densely populated, have few paved roads and very few people have electricity.

Study participants were recruited (a) from the registers of the DSS by simple random sampling or (b) as they presented to a VCT-clinic supported by the study. The DSS participants were visited by local fieldworkers in their homes during daytime for recruitment into the HIV-1 study. Overall non-participation was approximately 30%, as has previously been reported when the DSS register is used for population sampling[22]. Non-participation was predominantly caused by women who were not present at the time of visiting the household. No records of refusal were kept for non-respondent women.

At recruitment, all volunteers were interviewed, counselled and educated about the HIV prevalence study prior to enrolment. Acceptance of HIV-1 testing was an enrolment criterion. All volunteers gave informed consent for storage of their blood samples and for more testing of those samples on other infections related to HIV. A survey questionnaire was administered through one on one interview for collection of data on socio-demographic characteristics, sexual exposure, medical history and knowledge of sexually transmitted disease (STD) / HIV-1 related infections. A medical history that focused on the past or present STDs was obtained. Medical care for prevalent sexually transmitted diseases was provided. Volunteers received pre- and post-HIV test counselling, and were tested for HIV-1 at the enrolment visit using two rapid test kits (Determine, Abbott Laboratories, Abbott Park, Illinois, USA; Unigold, Trinity Biotech plc, Bray, Ireland) in parallel. Discrepant rapid HIV-1 test results were resolved using an ELISA test (Genetic System HIV-1/2 plus O EIA, Bio-Rad Laboratories, Redmond, Washington, USA). Women who tested HIV-1 positive were offered a pregnancy test and referred for comprehensive HIV care, including Prevention of Mother to Child Transmission (PMCTC) services, as appropriate, at the District Hospital.

After testing for HIV-1, serum samples were stored for other tests related to HIV-1 infection. The Kenya National Ethical Review Committee approved this study.

Determination of HSV-2 antibody status

Approximately 10 ml of blood was collected from each study participant, and the serum was stored at -70°C. HSV-2 specific antibody status was determined for serum samples using the HerpeSelect 2 ELISA IgG (Focus Diagnostics, Cypress, California, USA) according to the manufacturer's protocol [23] with the following exception. The protocol recommends a cut off index value of 1.1 to determine HSV-2 infection. Due to a lower specificity of the HerpeSelect test on serum samples from African populations, we used a cut off value of > 3.5 to determine HSV-2 prevalence and incidence estimates [24–26].

Statistical analyses

(i) Analysis of predictors of HSV infection

We conducted the analyses using STATA version 10 (StataCorp, College Station, Texas, USA). Chi-squared and Fisher's exact tests were used to determine univariate associations with prevalent HSV-2 infection. Multivariate logistic regression was used to identify independent predictors of HSV-2 seropositive status. Variables were introduced sequentially into a multivariate model, beginning with those with the strongest univariate association (lowest p values) and including only those which provided a significantly improved fit to the data (a likelihood ratio test, LRT, P < 0.05). The correlation coefficient between two variables was used to determine whether to exclude a variable from analysis due to excessive colinearity (i.e., r2 > 0.2).

(ii) The risk of primary maternal and neonatal HSV-2 infection

The incidence of maternal HSV-2 infection and risk of neonatal herpes were estimated using a simple catalytic model as described in [27]. In this model, the force of infection (i.e. per person incidence) was calculated by fitting age-stratified prevalence of specific antibodies to an exponential decay model by maximum likelihood. The assumption was made that seronegative status equates to the absence of HSV-2 infection (past or present), and that following infection there was no reversion to seronegativity. In other words we assumed the seronegative status is equated with being susceptible to infection. We further assumed that all women were seronegative at age 14 years and thereafter exposed to a force of infection (per year), λ, constant across all ages and unchanging over time (where λ > 0). Hence the proportion susceptible, s (a), at age a can be defined as

(1)

where 14 < a < 35. The proportion seropositive at age a, p(a), is therefore 1-s(a). We fit this model by maximum likelihood to our observed proportions remaining seronegative, S(i), representing r(i) seronegative individuals out of n(i) sampled for each single year of volunteer age, i = 15-34, to identify the value of the force of infection best supported by the data and estimate the 95% confidence intervals [27].

We made the assumption that the force of infection acting on pregnant women is equivalent to that estimated from our seroprevalence survey. If we now assume that the childbearing age range is 15-44 years, with average proportion susceptible derived from (1), and given a gestation period of 40 weeks, it follows that the average annual risk of primary maternal HSV-2 infections per pregnancy, I m , is

(2)

which for small λ approximates to

(3)

Assuming vertical HSV-2 infection only arises if a pregnant woman is shedding virus at the time of birth [6], that is, only for a primary or initial HSV-2 infection during the final 11 days of pregnancy [28], and that this transmission risk, v, is 50% [5, 15], then from equation (3) the risk of neonatal HSV per pregnancy,I n , is

(4)

The number of maternal infections per 1,000 pregnancies and neonatal infections per 100,000 live births can thus be defined from equations (3) and (4), respectively; the latter assuming there is no excess mortality attributable to HSV-2 infection.

Results

The sample comprised 826 women of median age 24 years (Interquartile range (IQR): 15-34 years), of whom 563 (68%) were selected by random sampling from the DSS (median age of 24 years; IQR 21-29), and 263 (32%) were individuals presenting to the VCT-clinic (median age 24 years; IQR 21-28). Details of demographic characteristics of these women in the two groups (DSS and VCT participants) are given in (Table 1).

Table 1 Characteristics of participating women from Kilifi, Kenya
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The two sampling groups differed in their marital status and religion (Table 1). Women attending VCT, when compared to the random sample from the DSS, were more likely to have used condoms, to have had casual sexual relationships, had more sexual partners in the previous year, and also to have genital ulcers (either presently or ever). The two groups did not differ significantly in HIV-1 prevalence (12% in VCT vs. 8% in DSS, P = 0.12), ethnic composition, educational level attained, or age distribution. There was a higher seroprevalence of HSV-2 in VCT-women compared with DSS-women (44% (115/263) vs. 32% (181/563), P < 0.001). Of 77 HIV-1 positive women, 50 (65%) were HSV-2 positive, compared to 33% (246/749) of HIV-1 negative women (p = 0.001).

Predictors of HSV-2 seropositivity

Significant associations from univariate analysis are detailed in Table 2. The probability of being HSV-2 seropositive was significantly higher in women who were of older age, were sampled from the VCT clinic, were ever married, were less educated, had causal partners in the last year, had ever had genital ulcers, or were HIV-1 antibody positive. Marital status was correlated (r2>0.2) with multiple factors (including educational status, HIV-1 status, religion, use of condoms and history of genital ulcers) and was dropped from further analysis. Factors shown to be independently associated with HSV-2 sero-positivity using multivariate logistic modelling are shown in Table 3. HSV-2 positive status was found to be associated with increasing age, recruitment from the VCT centre, history of genital ulcers and positive HIV-1 sero-status. Higher educational level was inversely associated with HSV-2 seropositivity. Separate multivariate models for DSS and VCT women were developed, which gave similar results to those of the full model, except that for DSS women the association with present genital ulcers was replaced with ever having had genital ulcers, and for VCT women the association with casual partners in the last year was lost. In the full model no factors significantly interacted with the association between study group (DSS vs. VCT) and HSV-2 status.

Table 2 Risk factors for HSV-2 in semi-urban women in Kilifi, Kenya: univariate analysis
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Table 3 Risk factors for HSV-2 in semi-urban women in Kilifi, Kenya: multivariate analysis (n = 826)
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Incidence estimates of maternal HSV-2 infection and estimated risk of neonatal herpes

The proportions of HSV-2 seronegative women recruited from the DSS declined from 94% in those aged 15-19 years to 47% in those aged >30 years. The corresponding proportions for VCT-women were 83% and 48%. In 30 DSS-women aged 15-16 years only 3% were HSV-2 seropositive. The fit of the maximum likelihood catalytic models to proportions seronegative by age and by source of recruitment (DSS or VCT) are shown in Figure 1. The estimated incidence of HSV-2 infection was 3.8 (95% CI: 3.3-4.4) per 100 seronegative women per year for DSS-participants (Table 4) and 5.7% (95% CI 4.7-6.8) per year for VCT participants.

Figure 1
figure 1

Age-stratified proportions HSV-2 seronegative by age (years) and by study group for semi-urban women from Kilifi, coastal Kenya. Data are shown for a random sample from the demographic surveillance system, DSS (filled marker) and a sample attending the VCT clinic (open marker). The corresponding best fit catalytic model curves (solid for DSS and dashed line VCT) are based on maximum log likelihood estimates (MLE) of the HSV-2 force of infection ( 95% CL, MLE) of 3.8% per annum (3.3-4.4, -319.532) in DSS women and 5.7% per annum (4.7-6.8, -168.233) in VCT women respectively.

Full size image
Table 4 The estimated incidence of maternal and neonatal HSV-2 transmission in a random sample of 563 resident semi-urban women from Kilifi, Kenya
Full size table

Using estimates of the force of infection acting on women in the DSS, we estimate an average proportion seronegative of 58.6% (95% CI: 54.4-62.8) over the child-bearing age. Hence the estimated incidence of maternal infections derived from Equation 3 is 17.1 (95% CI: 15.7-18.3) cases per 1,000 pregnancies per year, and the estimated incidence of neonatal transmission derived from Equation 4 is 33 (95% CI: 31-36) per 100,000 pregnancies per year (Table 4).

Discussion

In this study we describe the serological epidemiology of prevalent HSV-2 infection among women of the semi-urban population of Kilifi, coastal Kenya, who were presumed to be either a relatively low risk group for HIV infection randomly selected from within a population under demographic surveillance or a self-selected presumed higher risk group for HIV infection recruited from a VCT-centre. Our aims were to characterize predictors of prevalent HSV-2 infection, estimate incidence of maternal HSV-2 infection within this population, and hence, indirectly, estimate the potential neonatal disease burden.

Overall, HSV-2 prevalence in DSS-women and VCT-women aged 15-34 years, at 32%, and 44%, respectively, is in the same range of the 42% national prevalence reported among Kenyan women from 15-64 years of age [19]. Similar to other studies, we found a rapid rise in HSV-2 seroprevalence from mid-late teenage years upwards coincident with onset of sexual activity [29]. Consistent with results of the national survey[19], we observed that HSV-2 prevalence increases with age. Analysis of factors associated with prevalent HSV-2 infection suggests a small but significantly higher proportion of women attending VCT with HSV-2 compared with the general population women selected through the DSS. However, the nature of the factors associated with prevalent HSV-2 infection in multivariate analysis appeared largely the same between the two groups.

Positive HIV-1 status was the strongest independent predictor of HSV-2 seropositivity, as reported elsewhere [29, 30]. HIV-1 infection increases the risk of acquisition of HSV-2, the frequency and severity and reactivations [31, 32]. Other variables associated with sexually transmitted diseases were also independently associated, but less strongly, with HSV-2 infection, including the presence of genital ulcers and having had a casual partner in the preceding 12 months.

Education beyond primary school (greater than year 8 in Kenyan schools), with a prevalence of 45% in this sample, was found to be inversely associated with HSV-2, with ~1.5 fold reduced likelihood of seropositivity. Similarly, a separate study has found that not finishing primary school was a significant predictor of HSV-2 prevalence among 469 women enrolled for an at-risk cohort of HIV-1 infection from nearby coastal areas [33]. Although education attainment has been inconsistently associated with HSV-2 sero-prevalence in prior studies [29, 34, 35], knowledge of HSV-2 infection among women in similar parts of East Africa has been very low [36]and the development of reproductive education programs, within the school curriculum, to increase awareness of HSV-2, is an intervention activity worth undertaking in Kenyan schools.

Using data from our prevalence study, we estimated the incidence of vertical transmission of HSV-2. The catalytic model we used was computed on the assumptions that HSV-2 shedding during delivery as a result of primary HSV-2 infection has a 50% risk of neonatal HSV-2 acquisition [5, 15], and the risk of a baby acquiring HSV-2 from an infected mother occurs at primary infection within 11 days [28] (the average duration of viral shedding) of delivery [3, 6, 37]. Kilifi has a birth rate of 8000 live births per year [21], hence it is estimated that about 3 cases of neonatal herpes will occur per year among pregnant women in this population.

Earlier studies in Kilifi, assumed that the large number of perinatal deaths, especially those occurring at home, where cause could not be established, may have been related to HIV and sexually transmitted infections [21, 38]. However, our data suggests that the burden of neonatal HSV-2 disease from maternal transmission is low and contributes insignificantly to the observed neonatal deaths in this region.

Interestingly, our estimate of the incidence of neonatal herpes is similar to the estimate of 1 case per 3200 live births from the USA [3]. However, most births in Kilifi district occur at home and options for appropriate interventions while mothers experience acute HSV-2 infections prior to birth are very limited. Where possible, prevention programmes aiming to reduce the burden of HIV-1 infections in women need to include information on HSV-2 infection. Pregnant women should be counselled to use condoms and avoid unprotected oral-genital contact during the last trimester of pregnancy and be advised to report to a referral health facility when signs of genital herpes infection are noted prior to delivery [14].

There are several limitations to this study. First, during the 2004 HIV-1 survey, records of women refusing participation in the HIV-1 survey were not kept. Therefore, we were unable to establish whether individuals who refused and those who participated in the study differed in characteristics. Second, this was a cross sectional study restricted to women only. Hence, the analysis of predictors of prevalent HSV-2 infection only established associations and could not make causal inferences. Third, we did not conduct any biological measurements of other common sexually transmitted diseases (e.g. syphilis) or perform visual inspection for the presence of genital ulcers. Lastly, we based our catalytic model on assumptions that HSV-2 incidence is independent of age (or time), even though, the risk for HSV-2 infection increases with age. In this study, including age-dependence in the rate of infection did not significantly improve the model fit. Furthermore, the data appear to follow a linear cumulative hazard from which we deduced that there was no good evidence for age (or time) dependence in HSV-2 incidence. We also, may have underestimated the burden of neonatal herpes infection as HSV-2 acquisition due to reactivated HSV-2 infections were not included in the model (considered to have less than 5% risk of neonatal herpes infections transmission), and HSV-1 infections in this study population were not measured.

Conclusions

In summary, the existing burden of HSV-2 infection in the Kilifi semi-rural population is similar to national HSV-2 prevalence estimates in Kenya. HSV-2 transmission is rapid following the onset of sexual activity. Women infected with HSV-2 have an increased risk of acquiring HIV-1, and HSV-2 infection may remain a driving force behind the HIV-1 epidemic in this semi-urban population. Mother to child herpes transmission is unlikely to be a significant public health problem in this population. Educating young women about HSV-2 infection may help in reducing its burden in this semi-urban population.

References

  1. 1.

    Corey L, Handsfield HH: Genital herpes and public health: addressing a global problem. Jama. 2000, 283 (6): 791-794. 10.1001/jama.283.6.791.

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Gupta R, Warren T, Wald A: Genital herpes. Lancet. 2007, 370 (9605): 2127-2137. 10.1016/S0140-6736(07)61908-4.

    Article  PubMed  Google Scholar 

  3. 3.

    Brown ZA, Wald A, Morrow RA, Selke S, Zeh J, Corey L: Effect of serologic status and cesarean delivery on transmission rates of herpes simplex virus from mother to infant. Jama. 2003, 289 (2): 203-209. 10.1001/jama.289.2.203.

    Article  PubMed  Google Scholar 

  4. 4.

    O'Riordan DP, Golden WC, Aucott SW: Herpes simplex virus infections in preterm infants. Pediatrics. 2006, 118 (6): e1612-1620. 10.1542/peds.2005-1228.

    Article  PubMed  Google Scholar 

  5. 5.

    Brown ZA, Selke S, Zeh J, Kopelman J, Maslow A, Ashley RL, Watts DH, Berry S, Herd M, Corey L: The acquisition of herpes simplex virus during pregnancy. The New England journal of medicine. 1997, 337 (8): 509-515. 10.1056/NEJM199708213370801.

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Brown ZA, Benedetti J, Ashley R, Burchett S, Selke S, Berry S, Vontver LA, Corey L: Neonatal herpes simplex virus infection in relation to asymptomatic maternal infection at the time of labor. The New England journal of medicine. 1991, 324 (18): 1247-1252. 10.1056/NEJM199105023241804.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Bollen LJ, Whitehead SJ, Mock PA, Leelawiwat W, Asavapiriyanont S, Chalermchockchareonkit A, Vanprapar N, Chotpitayasunondh T, McNicholl JM, Tappero JW, Shaffer N, Chuachoowong R: Maternal herpes simplex virus type 2 coinfection increases the risk of perinatal HIV transmission: possibility to further decrease transmission?. Aids. 2008, 22 (10): 1169-1176. 10.1097/QAD.0b013e3282fec42a.

    Article  PubMed  Google Scholar 

  8. 8.

    Abu-Raddad LJ, Magaret AS, Celum C, Wald A, Longini IM, Self SG, Corey L: Genital herpes has played a more important role than any other sexually transmitted infection in driving HIV prevalence in Africa. PloS one. 2008, 3 (5): e2230-10.1371/journal.pone.0002230.

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Corey L, Wald A, Celum CL, Quinn TC: The effects of herpes simplex virus-2 on HIV-1 acquisition and transmission: a review of two overlapping epidemics. Journal of acquired immune deficiency syndromes (1999). 2004, 35 (5): 435-445. 10.1097/00126334-200404150-00001.

    Article  Google Scholar 

  10. 10.

    Mertz GJ, Benedetti J, Ashley R, Selke SA, Corey L: Risk factors for the sexual transmission of genital herpes. Ann Intern Med. 1992, 116 (3): 197-202.

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Schillinger JA, McKinney CM, Garg R, Gwynn RC, White K, Lee F, Blank S, Thorpe L, Frieden T: Seroprevalence of herpes simplex virus type 2 and characteristics associated with undiagnosed infection: New York City, 2004. Sex Transm Dis. 2008, 35 (6): 599-606. 10.1097/OLQ.0b013e3181666fb1.

    Article  PubMed  Google Scholar 

  12. 12.

    Corey L, Wald A: Maternal and neonatal herpes simplex virus infections. N Engl J Med. 2009, 361 (14): 1376-1385. 10.1056/NEJMra0807633.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Poeran J, Wildschut H, Gaytant M, Galama J, Steegers E, van der Meijden W: The incidence of neonatal herpes in The Netherlands. J Clin Virol. 2008, 42 (4): 321-325. 10.1016/j.jcv.2008.02.004.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Mindel A, Taylor J, Tideman RL, Seifert C, Berry G, Wagner K, Page J, Marks C, Trudinger B, Cunningham A: Neonatal herpes prevention: a minor public health problem in some communities. Sex Transm Infect. 2000, 76 (4): 287-291. 10.1136/sti.76.4.287.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Ades AE, Peckham CS, Dale GE, Best JM, Jeansson S: Prevalence of antibodies to herpes simplex virus types 1 and 2 in pregnant women, and estimated rates of infection. J Epidemiol Community Health. 1989, 43 (1): 53-60. 10.1136/jech.43.1.53.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Mullick S, Watson-Jones D, Beksinska M, Mabey D: Sexually transmitted infections in pregnancy: prevalence, impact on pregnancy outcomes, and approach to treatment in developing countries. Sex Transm Infect. 2005, 81 (4): 294-302. 10.1136/sti.2002.004077.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Weiss HA, Buve A, Robinson NJ, Van Dyck E, Kahindo M, Anagonou S, Musonda R, Zekeng L, Morison L, Carael M, Laga M, Hayes RJ: The epidemiology of HSV-2 infection and its association with HIV infection in four urban African populations. Aids. 2001, 15 (Suppl 4): S97-108.

    Article  PubMed  Google Scholar 

  18. 18.

    Amornkul Pauli, Vandenhoudt Hilde, Nasokho Peter, Odhiambo Frank, Mwaengo Dufton, Hightower Allen, Buve Anne, Misore Ambrose, Vulule John, Vitek Charles, Glynn Judith, Greenberg Alan, Slutsker Laurence, Kevin M, De C: HIV Prevalence and Associated Risk Factors among Individuals Aged 13-34 Years in Rural Western Kenya. PLoS One. 2009, 4 (7): e6470-10.1371/journal.pone.0006470.

    Article  PubMed  PubMed Central  Google Scholar 

  19. 19.

    GOK: National AIDS and STI Control Programme, 2007 Kenya AIDS Indicator Survey, Official Report. Official KAIS report. 2009

    Google Scholar 

  20. 20.

    GOK: Effective management for sustainable economic growth and poverty reduction. Kilifi District Development Plan 2002-2008. Government Printers Nairobi. 2002

    Google Scholar 

  21. 21.

    Bauni EK, Gatakaa H, Williams TN, Nokes DJ, Tsofa BK, JA S: Abstract. 2007, Perinatal and Neonatal mortality among the Mijikenda Community of Kilifi District, 5th UAPS Ghana,

    Google Scholar 

  22. 22.

    Papo JK, Bauni EK, Sanders EJ, Brocklehurst P, Jaffe HW: Exploring the condom gap: is supply or demand the limiting factor - condom access and use in an urban and a rural setting in Kilifi district, Kenya. Aids. 2011, 25 (2): 247-255. 10.1097/QAD.0b013e328341b9b8.

    Article  PubMed  Google Scholar 

  23. 23.

    Diagnostics F: Enzyme-linked immunosorbent assay (ELISA) for the qualitative detection of human IgG class antibodies to HSV-2; For in vitro Diagnostic Use. Package insert, Product Code EL0920G. 2007, Cypress, California, USA

    Google Scholar 

  24. 24.

    Ashley-Morrow R, Nollkamper J, Robinson NJ, Bishop N, Smith J: Performance of focus ELISA tests for herpes simplex virus type 1 (HSV-1) and HSV-2 antibodies among women in ten diverse geographical locations. Clin Microbiol Infect. 2004, 10 (6): 530-536. 10.1111/j.1469-0691.2004.00836.x.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    LeGoff J, Mayaud P, Gresenguet G, Weiss HA, Nzambi K, Frost E, Pepin J, Belec L: Performance of HerpeSelect and Kalon assays in detection of antibodies to herpes simplex virus type 2. J Clin Microbiol. 2008, 46 (6): 1914-1918. 10.1128/JCM.02332-07.

    Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Morrow RA, Friedrich D, Krantz E: Performance of the Focus and Kalon Enzyme-Linked Immunosorbent Assays for Antibodies to Herpes Simplex Virus Type 2 Glycoprotein G in Culture-Documented Cases of Genital Herpes. J Clin Microbiol. 2003, 41 (11): 5212-5214. 10.1128/JCM.41.11.5212-5214.2003.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Cutts FT, Vynnycky E: Modelling the incidence of congenital rubella syndrome in developing countries. Int J Epidemiol. 1999, 28 (6): 1176-1184. 10.1093/ije/28.6.1176.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Corey L, Adams HG, Brown ZA, Holmes KK: Genital herpes simplex virus infections: clinical manifestations, course, and complications. Ann Intern Med. 1983, 98 (6): 958-972.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Watson-Jones D, Weiss HA, Rusizoka M, Baisley K, Mugeye K, Changalucha J, Everett D, Balira R, Knight L, Ross D, Hayes RJ: Risk factors for herpes simplex virus type 2 and HIV among women at high risk in northwestern Tanzania: preparing for an HSV-2 intervention trial. J Acquir Immune Defic Syndr. 2007, 46 (5): 631-642. 10.1097/QAI.0b013e31815b2d9c.

    Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Kapiga SH, Sam NE, Bang H, Ni Q, Ao TT, Kiwelu I, Chiduo S, Ndibe U, Seage G, Coplan P, Shao J, Rosenberg ZF, Essex M: The role of herpes simplex virus type 2 and other genital infections in the acquisition of HIV-1 among high-risk women in northern Tanzania. J Infect Dis. 2007, 195 (9): 1260-1269. 10.1086/513566.

    Article  PubMed  Google Scholar 

  31. 31.

    Van de Perre P, Segondy M, Foulongne V, Ouedraogo A, Konate I, Huraux JM, Mayaud P, Nagot N: Herpes simplex virus and HIV-1: deciphering viral synergy. Lancet Infect Dis. 2008, 8 (8): 490-497. 10.1016/S1473-3099(08)70181-6.

    CAS  Article  PubMed  Google Scholar 

  32. 32.

    Rebbapragada A, Wachihi C, Pettengell C, Sunderji S, Huibner S, Jaoko W, Ball B, Fowke K, Mazzulli T, Plummer FA, Kaul R: Negative mucosal synergy between Herpes simplex type 2 and HIV in the female genital tract. Aids. 2007, 21 (5): 589-598. 10.1097/QAD.0b013e328012b896.

    Article  PubMed  Google Scholar 

  33. 33.

    Okuku HS, Sanders EJ, Nyiro J, Ngetsa C, Ohuma E, McClelland R, Price M, Graham S: Factors Associated with Herpes Simplex Virus Type 2 Prevalence and Incidence in a Cohort of High-risk Men and Women in Coastal Kenya. Sex Transm Dis. 2010, (under review)

    Google Scholar 

  34. 34.

    Kebede Y, Dorigo-Zetsma W, Mengistu Y, Mekonnen Y, Schaap A, Wolday D, Sanders EJ, Messele T, Coutinho RA, Dukers NH: Transmission of herpes simplex virus Type 2 among factory workers in Ethiopia. J Infect Dis. 2004, 190 (2): 365-372. 10.1086/422038.

    Article  PubMed  Google Scholar 

  35. 35.

    Tobian AA, Charvat B, Ssempijja V, Kigozi G, Serwadda D, Makumbi F, Iga B, Laeyendecker O, Riedesel M, Oliver A, Chen MZ, Reynolds SJ, Wawer MJ, Gray RH, Quinn TC: Factors associated with the prevalence and incidence of herpes simplex virus type 2 infection among men in Rakai, Uganda. J Infect Dis. 2009, 199 (7): 945-949. 10.1086/597074.

    Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Tassiopoulos KK, Seage G, Sam N, Kiwelu I, Shao J, Ao TT, Essex M, Coplan P, Rosenberg Z, Hughes M, Kapiga S: Predictors of herpes simplex virus type 2 prevalence and incidence among bar and hotel workers in Moshi, Tanzania. J Infect Dis. 2007, 195 (4): 493-501. 10.1086/510537.

    Article  PubMed  Google Scholar 

  37. 37.

    Brown ZA, Gardella C, Wald A, Morrow RA, Corey L: Genital herpes complicating pregnancy. Obstet Gynecol. 2005, 106 (4): 845-856. 10.1097/01.AOG.0000180779.35572.3a.

    Article  PubMed  Google Scholar 

  38. 38.

    English M, Muhoro A, Aluda M, Were S, Ross A, Peshu N: Outcome of delivery and cause-specific mortality and severe morbidity in early infancy: a Kenyan District Hospital birth cohort. Am J Trop Med Hyg. 2003, 69 (2): 228-232.

    PubMed  Google Scholar 

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Acknowledgements

This paper is published with the permission of the Director of KEMRI. We are grateful to the study volunteers. We acknowledge the work of KEMRI counsellors during the HIV-1 survey in 2004, the Demographic Surveillance System for supporting this study and staff of Kilifi District Hospital for providing comprehensive HIV care. We are grateful to the International AIDS Vaccine Initiative (IAVI) for supporting HIV-1 research at KEMRI-Kilifi. This work was made possible in part by the generous support of the American people through the United States Agency for International Development (USAID). The contents are the responsibility of the study authors and do not necessarily reflect the views of USAID or the United States Government.

Joyce U. Nyiro was supported by KEMRI-UCSF Infectious Disease Research Training Program (Grant # 5 D43 TW007388).

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    Affiliations

    1. Centre for Geographic Medicine Research-Coast, Kenya Medical Research Institute, Kilifi, Kenya

      Joyce U Nyiro, Eduard J Sanders, Caroline Ngetsa, Steve Wale, Ken Awuondo & D James Nokes

    2. Centre for Clinical Vaccinology & Tropical Medicine, University of Oxford, Oxford, UK

      Eduard J Sanders

    3. Kenya Medical Research Institute/ Centre for Microbiology Research, Nairobi, Kenya

      Elizabeth Bukusi

    4. International AIDS Vaccine Initiative, New York, New York, USA

      Matthew A Price & Pauli N Amornkul

    5. School of Life Sciences, University of Warwick, Coventry, UK

      D James Nokes

    Authors
    1. Joyce U Nyiro
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    2. Eduard J Sanders
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    3. Caroline Ngetsa
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    4. Steve Wale
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    5. Ken Awuondo
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    6. Elizabeth Bukusi
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    7. Matthew A Price
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    8. Pauli N Amornkul
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    9. D James Nokes
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    Correspondence to Joyce U Nyiro.

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    The authors declare that they have no competing interests.

    Authors' contributions

    JUN designed, implemented the study, performed initial analysis and drafted the manuscript; EJS designed the HIV-1 study and revised the manuscript; CN performed HSV-2 laboratory testing and revised the manuscript; SW collected samples, conducted VCT counselling and revised the manuscript; KA performed HSV-2 laboratory testing and revised the manuscript; EB Revised the manuscript; MAP designed the HIV-1 study and revised the manuscript; PNA designed the study and revised the manuscript; DJN performed data analysis and revised the manuscript. All authors read and approved the final manuscript.

    Joyce U Nyiro, Eduard J Sanders, Caroline Ngetsa, Steve Wale, Ken Awuondo, Elizabeth Bukusi, Matthew A Price, Pauli N Amornkul and D James Nokes contributed equally to this work.

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    Nyiro, J.U., Sanders, E.J., Ngetsa, C. et al. Seroprevalence, predictors and estimated incidence of maternal and neonatal Herpes Simplex Virus Type 2 infection in semi-urban women in Kilifi, Kenya. BMC Infect Dis 11, 155 (2011). https://doi.org/10.1186/1471-2334-11-155

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    Keywords

    • Genital Ulcer
    • Demographic Surveillance System
    • Neonatal Herpes
    • General Population Woman
    • Neonatal Herpes Infection

    BMC Infectious Diseases

    ISSN: 1471-2334

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