Bacterial vaginosis, vaginal flora patterns and vaginal hygiene practices in patients presenting with vaginal discharge syndrome in The Gambia, West Africa

Background Bacterial vaginosis (BV) – a syndrome characterised by a shift in vaginal flora – appears to be particularly common in sub-Saharan Africa, but little is known of the pattern of vaginal flora associated with BV in Africa. We conducted a study aimed at determining the prevalence of BV and patterns of BV-associated vaginal micro-flora among women with vaginal discharge syndrome (VDS) in The Gambia, West Africa. Methods We enrolled 227 women with VDS from a large genito-urinary medicine clinic in Fajara, The Gambia. BV was diagnosed by the Nugent's score and Amsel's clinical criteria. Vaginal swabs were collected for T vaginalis and vaginal flora microscopy, and for Lactobacillus spp, aerobic organisms, Candida spp and BV-associated bacteria (Gardnerella vaginalis, anaerobic bacteria, and Mycoplasma spp) cultures; and cervical swabs were collected for N gonorrhoeae culture and C trachomatis PCR. Sera were tested for HIV-1 and HIV-2 antibodies. Sexual health history including details on sexual hygiene were obtained by standardised questionnaire. Results BV prevalence was 47.6% by Nugent's score and 30.8% by Amsel's clinical criteria. Lactobacillus spp were isolated in 37.8% of women, and 70% of the isolates were hydrogen-peroxide (H202)-producing strains. Prevalence of BV-associated bacteria were: G vaginalis 44.4%; Bacteroides 16.7%; Prevotella 15.2%; Peptostretococcus 1.5%; Mobiluncus 0%; other anaerobes 3.1%; and Mycoplasma hominis 21.4%. BV was positively associated with isolation of G vaginalis (odds-ratio [OR] 19.42, 95%CI 7.91 – 47.6) and anaerobes (P = 0.001 [OR] could not be calculated), but not with M hominis. BV was negatively associated with presence of Lactobacillus (OR 0.07, 95%CI 0.03 – 0.15), and H2O2-producing lactobacilli (OR 0.12, 95% CI 0.05 – 0.28). Presence of H2O2-producing lactobacilli was associated with significantly lower prevalence of G vaginalis, anaerobes and C trachomatis. HIV prevalence was 12.8%. Overall, there was no association between BV and HIV, and among micro-organisms associated with BV, only Bacteroides spp. and Prevotella spp. were associated with HIV. BV or vaginal flora patterns were not associated with any of the factors relating to sexual hygiene practices (vaginal douching, menstrual hygiene, female genital cutting). Conclusion In this population, BV prevalence was higher than in corresponding populations in industrialised countries, but the pattern of vaginal micro-flora associated with BV was similar. BV or vaginal flora patterns were not associated with HIV nor with any of the vaginal hygiene characteristics.


Background
Bacterial vaginosis (BV) is a poly-microbial syndrome characterised by a shift in vaginal flora from a predominant population of lactobacilli to their gradual or total replacement with anaerobes such as Gardnerella vaginalis, Prevotella, Bacteroides and Mobiluncus species (spp), and with other bacteria including Mycoplasma and Ureaplasma species [1]. BV is one of the most frequent conditions encountered in sexually transmitted diseases (STD), genitourinary medicine (GUM) or other reproductive health clinics throughout the world. BV has been strongly associated with poor pregnancy outcomes such as preterm delivery of low-birth-weight infants [2] and several studies have now established associations between BV and HIV [3][4][5]. BV appears to be particularly common in sub-Saharan Africa where several studies have reported high prevalence rates, ranging from 20-49% among women presenting to STD clinics with vaginal discharge [6][7][8], from 21-52% among pregnant women attending antenatal clinics [9][10][11], and from 37-51% in community-based studies [3,12]. These are very much higher than the rates reported from industrialised countries, 13% in GUM clinic attenders in the UK [13], 11% in gynaecology clinic attendees in London [14], and 15% to 30% in studies of non-pregnant women in USA [15].
The reasons for these disparities are not entirely clear, but may arise in part through the use of different case definitions for BV, and because the pattern of vaginal microflora associated with this condition may differ in different populations. Earlier African studies have relied on the Amsel's clinical definition of BV [16], whilst more recent studies have adopted the microbiological Nugent's scoring technique [17]. The latter method relies on the identification of categories of vaginal micro-flora based on quantitative assessment of a vaginal Gram-stained smear. The Nugent's method has been extensively validated in industrialised countries where numerous vaginal flora studies have been conducted [1], but little is known of the pattern of vaginal micro-flora associated with BV in Africa. The characterisation of vaginal micro-flora is an important step in understanding the pattern of flora associated with BV. This information may help investigate the significance of this condition in clinical pathology and for targeting treatment. In particular, it is important to know whether vaginal flora changes may enhance HIV acquisition as suggested [5], and to unravel some of the factors that influence such changes, as these could be perhaps modified. Behavioural factors such as vaginal douching or menstrual hygiene practices have been suggested as important factors that might influence vaginal flora composition [18], but little data is available from African populations [19,20].
We have conducted a study aiming at determining the prevalence of BV among women self-presenting with vaginal discharge at a GUM clinic in Fajara, The Gambia. We report here on the vaginal micro-flora patterns and vaginal hygiene practices found in these patients and associations with their HIV serostatus.

Study population and sample collection
This study was part of a WHO-sponsored evaluation of STI syndromic management and of a novel rapid diagnostic test for BV conducted at the GUM clinic of the Medical Research Council (MRC) in Fajara, The Gambia. Study details have been reported elsewhere [21]. Briefly, consecutive and consenting women aged 18 and over, attending the MRC clinic with self-reported symptoms of vaginal discharge and/or vaginal itching were included in the study. Pregnant women were excluded because it was anticipated that their vaginal flora might differ substantially from that of other women attending the clinic. A standardised questionnaire elicited socio-demographic characteristics, reproductive and sexual health history including vaginal douching and menstrual hygiene practices, and current STD symptoms. Women underwent genital examination during which vaginal and cervical swabs were collected. The first vaginal swab was used for aerobic and anaerobic cultures; the second swab was used for direct wet mount microscopy, detection of fishy amine odour ("whiff" test) when mixed with 10% potassium hydroxide (KOH) preparation, and vaginal pH determination (range 4.0-7.0); the third swab was rolled onto a slide for Gram staining; two cervical swabs were collected for Neisseria gonorrhoeae culture on modified Thayer-Martin media, and for Chlamydia trachomatis polymerase chain reaction (PCR) testing using an in-house method [22]. A blood sample was collected for HIV testing as routinely offered at the GUM clinic. Serological diagnosis of HIV infection was done according to a strategy described elsewhere [23]. In brief, sera were screened by the ICEHIV-1.O.2 (Murex Diagnostics Ltd, Dartford, UK) and reactive samples were retested by type-specific ELISAs: Wellcozyme HIV recombinant -1 (Murex) for HIV-1, and ICE-HIV-2 test (Murex) for HIV-2. Samples clearly positive in one type were assigned the corresponding serological status; samples positive in both ELISAs were further tested by a synthetic peptide-based strip method, Pepti-Lav 1-2 (Sanofi Diagnostics Pasteur, Marne-La-Coquette, France).
Treatment was given to all women according to the Gambian government syndromic management protocols covering all likely vaginal and cervical infections. This included a single dose of 2.0 g of metronidazole to cover Trichomonas vaginalis (TV) and BV. HIV-infected patients were referred internally to our specialist clinic and managed according to local standard guidelines. The wet preparations were examined microscopically for  the presence of motile TV, yeast cells, and 'clue cells'. Vaginal smear slides were heat fixed, Gram-stained and examined for vaginal flora categories using the Nugent's method [17]. The method involves assigning a score between 0 and 10 based on quantitative assessment of the Gram-stain for three different bacterial morphotypes: (i) large Gram-positive rods (indicative of Lactobacillus spp), (ii) small Gram-negative or variable rods (indicative of Gardnerella, Bacteroides and other anaerobic bacteria), and (iii) curved, Gram-variable rods (indicative of Mobiluncus spp). Scores between 0 and 3 represent 'normal vaginal flora', between 4 and 6 'intermediate vaginal flora', and scores between 7 and 10 are considered diagnostic for 'BV'.

Microbiological methods for vaginal flora assessment
Vaginal swabs were directly inoculated at the clinic onto: (i) Columbia blood agar plates, which were incubated aerobically at 37°C for 24 to 48 hours to isolate aerobic bacteria, including lactobacilli; (ii) Columbia human blood bi-layer agar plates, which were incubated microaerophilically at 36°C and read after 48 to 72 hours for Gardnerella vaginalis isolation; (iii) Columbia-base lake horse blood kanamycin agar plates, which were incubated anaerobically at 36°C for 48 to 72 hours to isolate anaerobic bacteria; (iv) Mycoplasma broths incubated for 48 hrs then sub-cultured onto Mycoplasma agar, and incubated micro-aerophilically for 48 to 72 hours; (v) Mann Rogosa Sharpe (MRS) medium, which was used for the isolation of Lactobacillus spp after incubation in CO 2 at 37°C for 48 hours; and (vi) Sabouraud's agar plates, which were incubated micro-aerophilically at 36°C 24 to 48 hour to isolate Candida spp.
Growth of bacterial isolates was graded as confluent (heavy growth), semi-confluent (moderate pure to mixed growth of bacteria with visible separate single colonies); and scanty (occasional single isolated colonies).

Presumptive identification procedures
Lactobacilli and other aerobic flora Lactobacilli were presumptively identified by their ability to grow well on MRS, Gram stain microscopy and catalase reaction. Isolates were further tested for their ability to produce hydrogen peroxide (H 2 O 2 ) using a 2,3 tetramethyl benzedine method [24], and classified as positive when they produced blue coloration. The level of H 2 O 2 production was determined by visually grading the intensity of the blue colour produced into low, moderate and high categories.
Coliform spp were identified as Gram-negative lactose fermenting rods; Staphylococcus spp were identified by their characteristic colony and Gram stain morphology, then tested for coagulase production (slide test); Gram-positive beta-haemolytic Streptococcus spp isolates were further typed using a rapid latex test according to the manufacturer's instructions (Streptex, Murex Biotech Ltd, Darford Kent, UK).
Candida spp were identified as colonies with typical yeastlike morphology and by characteristic morphology on a wet preparation examination (presence of budding cells and/or pseudo-hyphae).

BV-associated bacteria
Gardnerella vaginalis was identified by beta-haemolytic appearance of the colonies on human blood bilayer agar plate but not on sheep blood agars, Gram stain morphology (Gram-variable pleiomorphic coccobacilli mostly forming clumps) and negative catalase and oxidase reactions.
Suspected anaerobic isolates were sub-cultured onto Columbia blood agar without antibiotics and incubated in aerobic and anaerobic conditions. Strict anaerobes were further identified by Gram staining and antibiotic susceptibility to erythromycin, rifampicin, colistin, penicillin, kanamycin and vancomycin (Oxoid Discs, Unipath, Basinstoke, Hampshire UK). Gram-negative anaerobic bacilli were tested and the isolates which grew on bile medium and hydrolysed aesculin were identified as Bacteroides spp. Isolates which failed to grow on bile or hydrolyse aesculin were identified as Prevotella spp [25].
Mycoplasma spp were identified as typical "fried egg" colonies and stained with Diene's stain. They were further presumptively identified as Mycoplasma hominis by colonial appearance and staining characteristics with a permanent diffused light blue periphery and a darkly blue centre [25].

Diagnosis of bacterial vaginosis
The gold standard microbiological definition of BV was a score of 7-10 by the Nugent's method described above. Amsel's clinical criteria were also used to make a clinical diagnosis of BV, which included the presence of any three of the following; (i) homogeneous grey adherent vaginal discharge; (ii) vaginal fluid pH ≥ 4.6; (iii) release of fishy amine odour when 10% potassium hydroxide (KOH) solution was added to a sample of vaginal fluid (the "whiff" test); and (iv) the presence of 'clue cells' representing over 20% of vaginal epithelial cells on wet-prep microscopic examination [16].
Ten percent random quality control checks were carried out on the microscopist by an experienced BV microscopist, for Nugent's score and wet preparation readings for 'clue cells'.

Statistical methods
Frequency tables were produced to describe the prevalence of genital infections and of micro-flora isolates. Bacteroides, Prevotella, Peptostreptococcus and other anaerobic isolates were grouped as 'anaerobes'. Chi-square tests were used to examine the association between isolates and BV diagnosis by Nugent's score and Amsel's clinical criteria in univariate analyses. Logistic regression was used to estimate the association between each isolate and diagnosis of BV by one method adjusted for (i.e. within categories of) BV diagnosis by the other method; and to test whether the observed associations were different between categories of the other method (i.e. testing for interaction). Chi-square and Fisher's Exact (for small numbers) tests were used to examine associations between categorical variables such as: isolation of lactobacilli, particularly H 2 O 2 -producing strains and G vaginalis, anaerobic isolates, Mycoplasma hominis, as well as N gonorrhoeae, C trachomatis, Candida spp or T vaginalis; HIV and each of the vaginal flora micro-organisms mentioned above, and with BV (Nugent's score 7-10); HIV and vaginal hygiene variables; and between BV and vaginal hygiene variables.

Ethical issues
The study was approved by the Ethical Committees of the MRC Gambia and the London School of Hygiene & Tropical Medicine, and by the Ethics Review Board of the World Health Organisation.

Results
Two hundred and thirty women were enrolled in the study over a four-month period in 2000, but data of three women were subsequently excluded because the women had not reported any symptoms consistent with our case definition of vaginal discharge syndrome. The denominators used in subsequent analyses vary slightly depending on completeness of microbiological investigations.
The median age of the patients was 26 years (range 18-50), 71% of women were married, and a majority of women (84%) reported only one sexual partner in the last three months. Antibiotic use prior to attending the clinic was reported by 18% of patients.  4 Anaerobic isolates were found in 21 samples out of 66; 5 women had more than 1 anaerobic isolate in which case the highest level of growth was used for the significance test. 5 Anaerobic Gram-negative rods, anaerobic Gram-positive or pigmented anaerobes.

Clinical and aetiological findings
The prevalence of cervical infections was 6.3% (

Vaginal flora cultures
Results of vaginal flora cultures for aerobic, micro-aerophilic and anaerobic bacteria as well as cultures for Mycoplasma are shown in Table 1. Variations in the denominators for the types of bacteria isolated were due to cases of either contamination or growth failure. The lower number of anaerobic cultures performed (n = 66) was due to a breakdown in the supply of anaerobic Gas-Packs. We defined two unidentified Gram-positive anaerobic isolates as 'Other' anaerobic isolates.
Gardnerella vaginalis, lactobacilli, streptococci and Mycoplasma spp were present as confluent or semi-confluent growth. Mobiluncus spp were not isolated. Staphylococcus spp, and Coliforms spp were mostly present in scanty num-  9 Not possible to calculate OR relative to normal flora due to lack of anaerobic isolation in normal subjects. 10 Not possible to fit model due to lack of anaerobic isolation in normal subjects.
bers. Bacteroides and Prevotella spp were present in semiconfluent to confluent numbers.

Associations between bacterial vaginosis and vaginal flora
Patterns of micro-flora isolates according to BV diagnosis by Nugent's score and Amsel's clinical criteria are summarised in . G vaginalis and the anaerobes were strongly associated with BV diagnosis by both Nugent's score and Amsel's criteria. G vaginalis remained significantly associated with BV diagnosis by either method, within the diagnosis categories of the other method. It was not possible to compare the prevalence of anaerobes across the three Nugent categories within Amsel's diagnosis using a likelihood ratio test due to the lack of anaerobic isolation in normal subjects. M hominis was more common in women with BV by both Nugent's and Amsel's criteria but the association was not statistically significant. Coliform spp, staphylococci and streptococci were not significantly associated with BV by either Nugent's score or Amsel's criteria (data not shown).
The associations between the presence of lactobacilli, including the presence of H 2 O 2 producing lactobacilli strains, and the isolation of other vaginal or cervical organisms are shown in Table 3. There were significant 2 to 4 fold decreases in colonisation by G vaginalis or anaerobes in the presence of H 2 O 2 -producing lactobacilli (P < 0.001 and P = 0.016 respectively). M hominis isolation was less prevalent in the presence of H 2 O 2 -producing lactobacilli, but this was not statistically significant. Overall there was no significant difference for Candida isolates (P = 0.108) but the lowest prevalence was observed when no lactobacilli were isolated. Detection of C trachomatis was significantly reduced (p = 0.024) in the presence of H 2 O 2producing lactobacilli strains, whilst N gonorrhoeae was isolated more frequently in the absence of lactobacilli, although this was not statistically significant.

Discussion
The main objective of this study was to determine the prevalence of BV and the pattern of vaginal micro-flora among women with vaginal discharge syndrome in an
Using Nugent's score as the gold standard, a BV prevalence of 47.6% was found in this population. This compares to the range (20-49%) reported from other African populations attending STI clinics: 20-23% in Burkina Faso [7] and Malawi [27], 37% in Tanzania [8] and 49% in Kenya [6]. High prevalence of BV (21-29%) has also been observed among pregnant women in Kenya and South Africa [9,11,28], The reasons for higher BV rates in African populations are not known. High BV rates have been reported among African-American women [15], although it has been argued that levels of education and other  socio-economic factors were confounding these associations [15,29]. Lifestyle practices such as vaginal douching have also been associated with an increased prevalence of BV [15,18,19], although, the direction of causality is again uncertain, since most studies have been of cross-sectional nature and many potentially confounding factors such as educational, socio-economical and behavioural factors have not always been entirely controlled for. We did not find any association between BV or vaginal micro-organisms and vaginal hygiene practices such as douching before or after sex, the nature of douching compounds used, the source of the water, or with menstrual sanitary protection. This finding perhaps owes to the fact that a very large proportion of women reported these practices, thus any relatively small association with BV would be hard to find with our sample size. On the other hand, additional possible explanations for the high prevalence or incidence of BV in African populations have to be sought -the role of hormonal factors should be explored. An association between BV and HIV has been reported in several studies [3,4,30], possibly influenced by vaginal hygiene practices [18,20,31]. However, as in our study, not all studies reporting on douching, BV and HIV have found associations between these factors [19]. The relationship between HIV, risk for BV or other STIs is complex, and could be contributed to by high risk sexual behaviour. Our study population consisted only of symptomatic women attending a GUM clinic, thus highrisk behaviours may have blurred any possible association. To our knowledge, this study is one of the first to report on female genital cutting in relation to HIV and vaginal flora in Africa. We did not find any significant impact of circumcision on vaginal flora or HIV serostatus.
A comparison of vaginal micro-flora isolates with Nugent's score showed significant positive associations between a diagnosis of BV and the isolation of G vaginalis, a significant positive association with anaerobes, and a significant negative association with the presence of lactobacilli. These findings are not surprising, since the method employed for the Nugent's score is based on the observation of BV-associated bacterial morphotypes. Nonetheless there have been no reports of vaginal micro flora culture studies in African population aimed at exploring the patterns of BV-associated flora. This study has demonstrated similar vaginal bacterial isolates to those found in the United States [32,33]. These studies found a strong association between BV and the isolation of G vaginalis, anaerobic gram-negative rods belonging to the genera Prevotella, Porphyromonas and Bacteroides, Peptostreptococcus spp, M hominis, Ureaplasma urealyticum, and often Mobiluncus spp.
A lower concentration of facultative species of Lactobacillus among women with BV in comparison to women with a normal flora was noted in this study. Lactobacilli are reported to play an important role in the maintenance of normal vaginal flora [34,35] through the provision of defence mechanisms against pathogenic organisms via hydrogen peroxide (H 2 0 2 ) production and the maintenance of an acidic microenvironment generated by lactic acid production. A low pH has been shown to have a direct microbicidal and virucidal effect [36]. Hydrogen peroxide, which is produced by some lactobacilli strains, also has a direct antimicrobial effect. H 2 O 2 can inhibit the growth of Bacteroides, Gardnerella, Mobiluncus, Mycoplasma and other vaginal organisms by acting directly on these organisms using its toxic effect, or by reacting with halide ions in the presence of vaginal peroxidase as part of the H 2 O 2 -halide peroxidase antibacterial system. Lactobacilli can also adhere onto vaginal epithelial cells [37] thus blocking the attachment of any pathogenic BV-associated bacteria onto these cells, Lactobacilli are known to produce biosurfactant, bacteriocins and coaggregation molecules [38], all of which contribute to the maintenance of a healthy vaginal micro-environment.
In our study, a large proportion of lactobacilli isolates (70%) were H 2 O 2 producers. These isolates were associated with a significantly lower prevalence of G vaginalis, anaerobes and C trachomatis, with trends of lower prevalence of N gonorrhoeae and M hominis, suggesting a protective effect of vaginal/cervical colonisation conferred by these lactobacilli strains. The absence of H 2 0 2 -producing lactobacilli was not associated with growth of Candida spp. This is different from the findings observed in a study conducted by Hillier et al [35], in which significant associations between H 2 O 2 production and protection against BV and other STI as well as protection against symptomatic candidiasis were reported.
In previous studies [39,40], M hominis and Ureaplasma urealyticum have been associated with BV, although not in all cases [41]. In our study, there appears to be some association between M hominis and BV, defined either by Nugent's score or Amsel's criteria, but these were not statistically significant. This observed difference may be due to the different detection protocols employed by different researchers.
Other bacteria that have been isolated in this study included Staphylococcus spp (38.4%), Coliform spp (20.0%)and Streptococcus spp (38.4%) but they were not associated with any particular vaginal microflora. Most of the staphylococci isolates were coagulase-negative, which are perceived to be normal commensal organisms. Most streptococci were found to belong to group B, an organism which can be highly pathogenic, particularly at time of delivery when it has been associated with neonatal sepsis and premature delivery [42]. The high prevalence of Group B streptococci seen in this study was similar to that reported in previous work done in The Gambia [43]. The latter study, however, failed to demonstrate any association between isolation of Group B streptococci and disease manifestation in neonates. Thus, the high prevalence of group B streptococci isolates reported in this study may not pose any significant clinical problem in this setting.
Several logistical problems have arisen in the course of this study, which may limit interpretation of the data on vaginal flora patterns. First, Mobiluncus spp, were not isolated despite observing Mobiluncus-like organisms in some of the vaginal Gram-stained smears. This finding could be attributed to a low prevalence of Mobiluncus in our population, or to an inadequate isolation procedure, which will warrant further investigation. Second, our adoption of a 48-hours incubation period for broth-and agar-Mycoplasma culture procedures did not favour the isolation of Ureaplasma urealyticum, as the latter is sensitive to the metabolic by-products generated during extended incubation periods. This may have been partly responsible for the lack of Ureaplasma isolation in this study. Finally, there was a low-recovery rate for a significant number of stored isolates. Optimum storage procedures are not easy to maintain in tropical climates. These logistical problems with fastidious organisms may explain why it is difficult to attempt studies of vaginal flora in developing countries.
Another possible limitation of our study was the absence of inclusion of women who did not complain of vaginal discharge syndrome, which would have allowed a more comprehensive description of patterns of vaginal flora in symptomatic and symptomless women. Our study shows, however, that the pattern of organisms cultured in BV in this environment is similar to what has been reported in corresponding populations in industrialised countries, and therefore suggest that different vaginal flora patterns are not the major explanation behind the higher prevalence of BV in Africa.
In most STI or GUM clinics in industrialised countries, routine BV diagnosis is made using Nugent's score or Amsel's clinical criteria. In resource-poor settings good microscopy is not often available, and clinicians rely on clinical judgement or may apply all or part of the Amsel's clinical criteria. This study found there was an association between Amsel's criteria and Nugent's score, a strong correlation between Amsel's diagnosis and the presence of G vaginalis and anaerobes, and a negative correlation with the presence of lactobacilli. However, as shown in Figure  1, a large number of true BV cases (by Nugent's score) were missed by the Amsel's method, limiting its utility as a BV diagnostic method. The Amsel's method can be highly subjective with regards the description of the discharge and the olfactive component ('whiff' test); the wet mount microscopy depends on the experience of the microscopist and can represent a further subjective element, particularly when performed under pressing clinical conditions [1]. Despite regular supervision and the use of the same clinician and microscopist throughout the study (which insured internal consistency of our results), the discrepancies we found between the Amsel's criteria and the accepted gold standard diagnosis (Nugent's method) in this study appear to preclude the use of this method under routine clinical conditions in our setting.
Our study found that where Gram-staining led to a classification of 'intermediate flora' by Nugent's score, this was reflected in the microbiological findings, which were 'intermediate' quantitatively and qualitatively between 'normal' and 'BV' categories (table 2 and figure 1) and distinct from them. This supports the validity of the classification and could indicate that the 'intermediate' flora precedes the development or follow the resolution of frank BV. Longitudinal studies are required to elucidate this phenomenon.

Conclusion
In this population, BV prevalence was higher than in corresponding populations in industrialised countries, but the pattern of vaginal micro-flora associated with BV was similar. BV or vaginal flora patterns were not associated with HIV nor with any of the vaginal hygiene characteristics. Further studies on the public health significance of BV in this kind of setting are needed to determine future strategies for intervention