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Vaginal colonisation of women in labour with potentially pathogenic bacteria: a cross sectional study at three primary health care facilities in Central Uganda

Abstract

Background

Potentially pathogenic bacteria that colonise the lower genital tract of women in labour can be passed to the baby during birth. While many babies become colonised with these bacteria after delivery, a few develop neonatal infections. The lower genital tract is a reservoir for potential pathogens and a source of infection for neonates. We determined the prevalence of vaginal colonisation of potentially pathogenic bacteria among women in labour in Central Uganda and identified potential risk factors associated with this colonisation.

Methods

We conducted a cross sectional study at three primary health care facilities and collected vaginal swabs from HIV-1 negative women in labour. Specimens were cultured on different selective microbiological media, and biochemical tests were used to classify bacterial isolates on the species level. Multivariable logistic regression analyses were used to estimate the association between relevant exposures and colonisation with potentially pathogenic bacteria.

Results

We recruited 1472 women in labour whose mean age was 24.6 years (standard deviation [SD] 4.9). Of these, 955 (64.9%; 95% Confidence Interval [CI] 62.4, 67%) were vaginally colonised with at least one potentially pathogenic bacterial species. The most commonly isolated species were Escherichia coli (n = 508; 34.5%), Klebsiella pneumoniae (n = 144; 9.8%) and Staphylococcus aureus (n = 121; 8.2%). Results from exploratory multivariable regression analyses indicated that having had ≥5 previous pregnancies (adjusted odds ratio [aOR] 0.59; 95% CI 0.35, 0.97) or being ≥30 years old (aOR 1.52; 95% CI 1.03, 2.23) could be associated with vaginal colonisation with any potentially pathogenic bacteria, as well as with vaginal colonisation with S. aureus (aOR 0.33; 95% CI 0.12, 0.88, and aOR 2.17; 95% CI 1.17, 4.00, respectively). Possession of domestic animals in a household (aOR 0.57; 95% CI 0.35, 0.92) could be associated with vaginal colonisation with E. coli.

Conclusions

Two-thirds of HIV-1 negative women in labour were vaginally colonised by potentially pathogenic bacteria, mainly E. coli, K. pneumoniae, and S. aureus.

Peer Review reports

Background

The normal lower genital tract is inhabited by a number of different bacteria that live in well-balanced populations. In healthy women of reproductive age, the primary bacteria colonising the vagina are of the genus Lactobacillus [1]. They reduce the pH of the vagina to between 2 and 4, which helps to inhibit growth of pathogenic bacteria [2]. During pregnancy, physiological changes alter the homeostasis of the vaginal environment. These changes are complex and not fully understood, but they generally lead to a reduction in the Lactobacillus population and, thereby, facilitating the growth of potentially pathogenic bacteria such as Staphylococcus aureus and members of the Enterobacteriaceae family [3].

During vaginal delivery, a newborn comes into direct contact with the mother’s flora in the lower genital tract. Eventually, the baby’s umbilicus, mucous membranes and parts of the skin may be colonised with bacteria that are potentially pathogenic for the neonate [4]. This colonisation process is known as seeding, and it has implications for long term neonatal health outcomes [5]. The potentially pathogenic bacteria that are seeded to the baby often include S. aureus, group B Streptococcus (GBS), group A Streptococcus (GAS), Enterococcus spp., Klebsiella pneumoniae, Escherichia coli, Enterobacter spp., Pseudomonas spp. and Citrobacter spp. [6].

Severe infections account for 26% of neonatal deaths globally [7] and they are the leading cause of mortality among newborns in sub Saharan Africa [8]. The lower genital tract of women is an important source of pathogens causing life-threatening infections including bacteremia, meningitis, pneumonia and arthritis during the first week of life [9, 10] [11]. We conducted a cross-sectional study among women in labour at three primary health care facilities in the Central region of Uganda to estimate the prevalence and improve our understanding of the aetiology and risk factors associated with vaginal colonisation by potentially pathogenic bacteria.

Methods

Study design and setting

This cross-sectional study was conducted between July 2016 and July 2018 in three primary health care facilities in Central Uganda: Mukono Health Centre IV, Kawaala Health Centre III, and Kitebi Health Centre III. These three health care facilities have a combined monthly average of 2400 antenatal visits and 1200 deliveries. The three health facilities mostly deliver women who are considered to have low risk of obstetric complications. The women who are likely to have complicated deliveries are usually referred to tertiary hospitals. The HIV prevalence among women in reproductive age in Uganda is approximately 8% [12]. The Mukono Health Centre IV is located within Mukono district, which has a largely rural population of around 60,000 people and is located around 25 km from Uganda’s capital city, Kampala, while the Kitebi Health Centre III and the Kawaala Health Centre III are located in Kampala, which has a population of approximately 1.5 million people. The study was nested within an ongoing randomised controlled trial aimed at assessing the effectiveness of a single application of 4% chlorhexidine solution on the umbilical cord stump for the prevention of omphalitis and severe illness in HIV-1 unexposed newborns [13].

Participants

We included women who became enrolled in the above-mentioned randomised controlled trial, who were HIV-1 negative, who gave birth during the daytime on a weekday, who gave consent to participate in the study before (orally) and within 12 h (written) after giving birth, and who gave birth to babies who had the following characteristics: birth weights of > 1.5 kg, no severe congenital anomalies, no obvious signs of cord stump infection, and no severe illness requiring hospitalisation at birth [13]. The randomised controlled trial aims to recruit 4760 newborns, and we enrolled 1472 of these into the present study. With this sample size we would obtain a very high (0.7 to 2.6%) absolute precision, i.e. the difference between the upper limit and the lower limit of the 95% confidence interval (CI) for prevalence values ranging from 2 to 50%. Demographic characteristics of the study participants were collected through interviews, as described below, and can be found listed in Table 1.

Table 1 Distribution of characteristics of study participants at the three study sites

Data collection and consent

Trained research nurses obtained verbal consent to collect specimens from women in labour, and after giving birth, obtained written informed consent to allow for the use of the collected specimens and data. Socio-demographic and clinical data were collected by using structured electronic questionnaires on mobile phones based on the Open Data Kit (ODK) software [14]. Distribution of relevant characteristics we collected can be found listed in Table 1. These include exposures associated with vaginal colonisation of mother, including premature rupture of membranes (PROM), defined as breakage of membranes of the amniotic sac before labour onset [15], prolonged labour, defined as labour beyond 24 h, parity, maternal level of education, maternal age, hospitalisation during pregnancy, marital status, antenatal care attendance, possession of domestic animals in the household, having been pregnant multiple times (multigravidity) and socioeconomic data.

Specimen collection and transportation

Trained midwives collected vaginal swab specimens from the women during labour, by using Regular Rayon sterile swabs pre-packed with Amies Agar Gel without Charcoal transport medium (Copan Diagnostics Inc., Murrieta, CA). The swab was first carefully inserted into the vagina about halfway between the introitus and cervix. This way, contamination from the cervical mucus was avoided. The swab was then gently pressed towards the vaginal walls and rotated to ensure that it was thoroughly coated. The midwives took caution when removing the swab to avoid contact with the skin and the anal area. The vaginal swabs were immediately stored in the Amies transport medium in a specimen transport cooler. The coolers were subsequently transported within 24 h to MBN Clinical Laboratories where the specimens immediately underwent microbiological analyses [16].

Microbiological analyses

Primary inoculation of the vaginal swabs was done on 5% sheep blood agar (BioLab Zrt., Budapest, Hungary) and on MacConkey agar (BioLab Zrt.), followed by aerobic incubation between 35 °C–37 °C for 18–24 h. The blood agar plates were further incubated for a total of 72 h to allow development of slow growing bacterial colonies. From these plates, we picked and streaked one representative of each morphologically distinct colony onto new agar plates and used colonies from this sub-culture for further species identification and characterisation.

Bacterial species identification was performed by using conventional microbiological techniques.

Gram-positive bacterial identification: Staphylococcus aureus species was identified based on positive catalase, coagulase and DNase tests. Beta-haemolytic Streptococci were identified by having distinct colony characteristics, having transparent haemolytic zones around colonies grown on blood agar plates, being Gram stain positive and being negative in the catalase test. The beta-haemolytic colonies were further Lancefield grouped into different species/groups (Streptococcus A-D) using the Streptococcal Grouping Kit (Oxoid Ltd., Basingstoke, Hants, UK). Enterococcus species were identified by being positive in the bile esculin test [17].

Gram-negative bacteria identification: These were identified biochemically based on lactose fermentation, triple sugar iron agar, sulfur-indole-motility, citrate and urease tests [17].

Reference strains S. aureus ATCC 25923 for gram-positive bacteria, and E. coli ATCC 25922 and P. aeruginosa ATCC 27853 for gram-negative bacteria were regularly included in the identification pipeline to control the quality of the microbiological procedures

Main outcome and exposure definitions

The study’s main outcome was vaginal colonisation with potentially pathogenic bacteria. Colonisation with potential pathogenic bacteria was defined as isolation of at least one of the following types of bacteria from the vaginal swab; S. aureus, E. coli, K. pneumoniae, group A Streptococcus (GAS), group B Streptococcus (GBS), Enterococcus spp., Pseudomonas spp., Enterobacter spp., Citrobacter spp., Proteus spp. and/or Acinetobacter spp. These bacteria are known to cause infections in newborns. Other bacteria that were isolated which we considered to represent commensal strains since they rarely are found associated with newborn infections included Candida spp., Micrococcus spp., Corynebacterium spp., Lactobacillus spp., Bacillus spp., Bukolderia spp., Serratia spp. and coagulase-negative Staphylococcus. Such isolates were not included in the analyses.

In the statistical analyses, described below, we tested for associations between different exposures and 4 different outcomes, including colonization with any potential pathogen, with E. coli, with S. aureus, and with K. pneumoniae. In those analyses, we tested exposures that other studies have found to be associated with maternal colonization with potentially pathogenic bacteria [18,19,20,21], including: Maternal level of education, maternal age, hospitalisation during pregnancy, marital status, number of previous pregnancies, antenatal tetanus toxoid vaccination, number of antenatal care visits, hospitalisations during pregnancy, possession of domestic animals at home, and socioeconomic status. Socioeconomic status was represented by a wealth index variable which was generated by performing principal component analysis on data about household ownership of cupboards, radios, televisions, a mobile phone, refrigerator, motor cycle, car, ownership of a house and/or land, and presence of cemented walls, type of toilet, and three or more rooms in the house. Five quintiles of the wealth index variables were generated with the poorest belonging to quintile 1, and the least poor to quintile 5.

Statistical analysis

The data were analysed by using STATA 15.0 (StataCorp LLC, College Station, TX, USA). To obtain an estimate of the overall vaginal colonisation prevalence, we divided the number of women who had a positive vaginal culture for one or more potential pathogens by the total number of enrolled women in the study. To explore the associations between the above-mentioned outcomes and exposures, we performed bivariable (unadjusted) and multivariable (adjusted) logistic regression analyses where we estimated odds ratios (OR) and 95% confidence intervals (CIs) for each exposure. For each tested model we used the estat vif command in STATA to ensure there was little potential multicollinearity between the independent variables in the model, as indicated by one or more variance inflation factor estimates of > 10. None of our models appeared to have potential multicollinearity issues.

Results

We recruited a total of 1472 women including 545 (37.0%) from Kawaala Health Centre III, 524 (36%) from Kitebi Health Centre III and 403 (27%) from Mukono Health Centre IV. The characteristics of these women are listed in Table 1. All but 3 (0.2%) of the women had vaginal deliveries. The mean age of the participants was 24.6 (standard deviation 4.9) years, 1172 (80%) were married or cohabiting, 1295 (88%) earned less than 30 US dollars per month, 185 (15.8%) had other sexual partners and 488 (33%) had at least a primary education. Only 6 (0.41%) of the women experienced PROM and 14 (0.9%) prolonged labour.

Vaginal colonisation

Of the 1472 recruited women, 955 (64.9%; 95% CI 62.4, 67.3%) were colonised with at least one potential bacterial pathogen. Of the 955 colonised women, 878 were colonised with one potentially pathogenic bacteria, 69 were colonised with two potential pathogens while the remaining three women were colonised with three potential bacterial pathogens (Table 2). A total of 1025 potentially pathogenic bacterial pathogens were isolated from the colonised women. Overall, the most frequently isolated potential bacterial pathogens were E. coli (n = 508; 34.5%), K. pneumoniae (n = 145; 9.9%) and S. aureus (n = 121; 8.2%). There were no major differences in proportions of women colonised by potentially pathogenic bacteria between the three study sites (Table 3).

Table 2 Number and percentage of women colonised with more than one potentially pathogenic bacterial isolates
Table 3 Distribution of bacterial isolates from study participants across the three study sites

Exposures associated with vaginal colonisation

In the statistical analyses to identify exposures that are potentially associated with colonization with different pathogens, we found that having ≥5 previous pregnancies (aOR 0.59; 95% CI 0.35, 0.97) and maternal age of ≥30 years (aOR 1.52; 95% CI 1.03, 2.23) were associated with vaginal colonisation of women in labour with any potentially pathogenic bacteria (Table 4). Focusing these analyses on the three most commonly isolated potential pathogenic bacteria, we found that maternal age of ≥30 years (aOR 2.17; 95% CI 1.17, 4.00) and a history of at least 5 previous pregnancies (aOR 0.33; 95% CI 0.12, 0.88) were associated with S. aureus vaginal colonisation (Table 5). We found that possession of domestic animals in a household (aOR 0.57; 95% CI 0.35, 0.92) could be associated with vaginal colonisation by E. coli (Table 6). We found no exposures significantly associated with colonisation by E. coli (Table 6) and K. pneumoniae (Table 7).

Table 4 Exposures associated with vaginal colonisation with any potentially pathogenic bacteria of women in labour at three study sites (N = 1472)
Table 5 Exposures associated with vaginal S. aureus colonisation of women in labour at three study sites (N = 1472)
Table 6 Exposures associated with vaginal E. coli colonisation of women in labour at three study sites (N = 1472)
Table 7 Exposures associated with vaginal K. pneumoniae colonisation of women in labour at three study sites (N = 1472)

Discussion

We studied the prevalence of different potentially pathogenic bacteria colonising the vagina of women in labour at three primary health care facilities in Central Uganda and evaluated the association between potential risk factors and colonisation with these bacteria.

Sixty-five percent (65%) of the study participants were colonised by at least one potential bacterial pathogen. The prevalence of women colonised with potential pathogens in our study was higher than that reported in a similar study in Bangladesh [22]. This differences in colonisation prevalence may be due to several reasons, including differences in ethnic and geographical settings, that our study women were colonised with a wider range of pathogen species and the small sample size in the Bangladesh study. E. coli, K. pneumoniae and S. aureus were the most commonly isolated species. We found that the prevalences of individual potentially pathogenic bacteria were similar to those reported in other studies— E. coli was the predominant potential pathogen with a proportion similar to a study in Iran [23]. The proportion of K. pneumoniae isolates we found is similar to that reported in Nigeria [24] and Bangladesh [22]. Another study reported a prevalence of S. aureus vaginal colonisation in pregnant women similar to ours [25]. The bacteria that colonise the vagina of women in labour play an important role in newborn health such as defining their early gut microbiota [26]. A recent study has demonstrated that maternal vaginal colonisation with E. coli or S. aureus is significantly associated with pathogens isolated from the blood of neonates with early-onset sepsis [27].

In our study, the prevalence of vaginal GBS colonisation was only 0.2%, which is lower than what similar studies have reported [28, 29]. The difference could be a result of the methodological differences between our study and the other studies. We did not use the Todd Hewitt medium for GBS isolation, and did not collect anal swabs in our study, which could potentially have underestimated the GBS prevalence. The difference could also result from the fact that we use culture-based techniques to detect GBS instead of the more sensitive PCR based methods. However, vaginal colonisation varies greatly across geographical settings and a systematic review of studies from 85 countries indicates that East Africa and southern Asia have the lowest prevalence of maternal vaginal GBS colonisation compared to other regions [30]. Generally, we observed that there were no major differences in proportions of women colonised by potentially pathogenic bacteria between the study sites. This is an important finding because it indicates that this was a well-conducted large study and its findings are generalizable.

We found that women 30 years or more of age appeared more likely to be vaginally colonised with any potentially pathogenic bacteria and particularly with S. aureus compared to women who were 20–24 years in our study. Similar observations have been made in other studies [19, 21], where they found that older women were more often colonised than younger women. Vaginal colonisation rates during pregnancy may be attributed to several factors such as gestational age, mother’s age and parity. The association we observed could possibly be due to the fact that the majority of the women aged ≤30 years in our study were multipara and multigravida. We also found that women who had had at least 5 previous pregnancies appeared less likely to be colonised with these organisms than primigravida women. In contrast, studies in Thailand [31], Trinidad [19] and India [32] found multigravida women were more often colonised than primigravida women. These differences are difficult to explain, and given the exploratory nature of these analyses, further studies would be needed to confirm these results.

More surprising was the finding that women living with domestic animals at home were less likely to be colonised by E. coli than those who did not live with animals. Normally, living with animals would be considered an important risk factor for infection with E. coli [33, 34]. Further studies would be needed to identify the underlying reasons for why these women appeared to be protected. Few women in our study experienced premature rupture of membranes (PROM), which is an important risk factor for neonatal infections [35]. The low prevalence of PROM among the participants in our study is probably a result of the pre-delivery screening that is being done at our three health facilities, where women who are considered to be at risk of experiencing PROM or other complications during delivery are early on referred to tertiary hospitals.

One of the limitations of this study is that we only enrolled HIV-1 negative women. Nevertheless, we are confident that these findings are generalisable to the majority of women in reproductive age in Uganda because 92% of women of reproductive age in Uganda are HIV-1 negative. Since we used traditional microbiological methods to identify the different potential pathogenic bacteria, our prevalence estimates are probably lower than they would have been if we instead had used molecular profiling methods, such as PCR, to detect colonization.

Conclusion

We found that among HIV-1 negative women in labour at health facilities in Central Uganda, almost two-thirds had vaginal colonisation by potentially pathogenic bacteria, mainly E. coli, K. pneumoniae, and S. aureus. This is of concern since exposures to pathogenic bacteria during birth is likely to increase the risk of newborn infections. We have also identified exposures that appear to be associated with colonisation with these potentially pathogenic organisms. Further studies are needed to evaluate the virulence of the potential pathogens and the risk of neonatal infections associated with this colonisation.

Availability of data and materials

Datasets used for this study can be obtained through a reasonable request from the principal investigator of the chlorhexidine trial (VN) nankabirwav@gmail.com and the corresponding author.

Abbreviations

CI:

Confidence interval

CISMAC:

Centre for intervention science in maternal and child health

GAS:

Group A Streptococcus

GBS:

Group B Streptococcus

HIV-1:

Human immunodeficiency virus type 1

NORHED:

Norwegian programme for capacity development in higher education and research for development

ODK:

Open data kit

OR:

Odds ratio

PCR:

Polymerase chain reaction

PROM:

Premature rupture of membranes

SD:

Standard deviation

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Acknowledgements

We thank all the women who participated in our study and the midwives at Kawaala Health Centre III, Kitebi Health Centre III and Mukono Health Centre IV for their cooperation. Special thanks to the CISMAC research nurses for their hard work and commitment. We acknowledge the MBN microbiology team, including Emmanuel Aboce, Mango Wandera Dennis and Sheila Tumwesigye for their excellent work.

Funding

This work was funded by the Research Council of Norway through its Centre of Excellence scheme and the University of Bergen (UiB), Norway to the Centre for Intervention Science in Maternal and Child Health (CISMAC; project number 223269) and its funding of the parent Chlorhexidine trial. The Norwegian programme for capacity development in higher education and research for development (NORHED) through the Survival Pluss project (Project Number; UGA-13-0030) partly funded this work. The Research Council of Norway and NORHED played no role in design, analysis or interpretation of the study findings.

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Authors

Contributions

JT, VN, HS, JKT, and FB conceived the study. JT, VN, FB, HS and ON designed the study. JT and FB led the microbiology testing and results interpretation. HSt, VN and HS prepared the Chlorhexidine trial dataset for analysis. JT, DM, and HSt analysed the data. JT wrote the first draft of manuscript. All authors reviewed the manuscript, approved and agreed to submit the final version of the manuscript.

Corresponding author

Correspondence to Josephine Tumuhamye.

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Ethics approval and consent to participate

Informed consent was obtained for both the interview and specimen storage. Ethical approval was obtained from the Research and Ethics Review Committee of School of Medicine, SOMREC, Makerere University (REC 2015–118) and from the Uganda National Council of Science and Technology (HS 1927).

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Not applicable

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Authors declare no competing interests.

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Tumuhamye, J., Steinsland, H., Tumwine, J.K. et al. Vaginal colonisation of women in labour with potentially pathogenic bacteria: a cross sectional study at three primary health care facilities in Central Uganda. BMC Infect Dis 20, 98 (2020). https://doi.org/10.1186/s12879-020-4821-6

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Keywords

  • Potentially pathogenic bacteria
  • Vaginal colonisation
  • Labour
  • Escherichia coli
  • Klebsiella pneumoniae
  • Staphylococcus aureus
  • Uganda