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Systematic Review

Supplementation of Probiotics in Pregnant Women Targeting Group B Streptococcus Colonization: A Systematic Review and Meta-Analysis

by
Daniela Menichini
1,2,*,
Giuseppe Chiossi
2,
Francesca Monari
2,
Francesco De Seta
3 and
Fabio Facchinetti
2
1
Department of Biomedical, Metabolic and Neural Sciences, International Doctorate School in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, 41124 Modena, Italy
2
Unit of Obstetrics and Gynecology, Mother-Infant Department, University of Modena and Reggio Emilia, 41124 Modena, Italy
3
Institute for Maternal and Child Health “IRCCS Burlo Garofolo”, 34137 Trieste, Italy
*
Author to whom correspondence should be addressed.
Nutrients 2022, 14(21), 4520; https://doi.org/10.3390/nu14214520
Submission received: 4 October 2022 / Revised: 14 October 2022 / Accepted: 24 October 2022 / Published: 27 October 2022
(This article belongs to the Special Issue Role of Lactobacillus and Probiotics in Human Health and Diseases)
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Abstract

:
This systematic review and meta-analysis aimed to determine if probiotic supplementation in pregnancy reduced maternal Group B streptococcus (GBS) recto-vaginal colonization in pregnant women at 35–37 weeks of gestation. Electronic databases (i.e., PubMed, MEDLINE, ClinicalTrials.gov, ScienceDirect, and the Cochrane Library) were searched from inception up to February 2022. We included RCTs assessing the effects of probiotic supplementation in pregnancy on GBS recto-vaginal colonization. The primary outcome was GBS-positive recto-vaginal cultures performed at 35–37 weeks of gestation. Secondarily, we evaluated obstetric and short-term neonatal outcomes. A total of 132 publications were identified; 9 full-length articles were reviewed to finally include 5 studies. Probiotic supplementation reduced vaginal GBS colonization: the GBS positive culture rate was estimated at 31.9% (96/301) in the intervention group compared to 38.6% (109/282) in the control group (OR = 0.62, 95% CI 0.40–0.94, I2 4.8%, p = 0.38). The treatment started after 30 weeks of gestation and was more effective in reducing GBS colonization (OR 0.41, 95% CI 0.21–0.78, I2 0%, p = 0.55). Probiotic administration during pregnancy, namely in the third trimester, was associated with a reduced GBS recto-vaginal colonization at 35–37 weeks and a safe perinatal profile. Whether this new strategy could reduce the exposition of pregnant women to significant doses of antibiotics in labor needs to be evaluated in other trials.

1. Introduction

Group B streptococcus (GBS) is an important cause of maternal and neonatal morbidity and mortality worldwide. In Europe, the percentage of women colonized with GBS in pregnancy ranges from 1.5 to 30% and accounts for chorioamnionitis, cystitis, pyelonephritis, bacteremia, fever, and postpartum endometritis [1,2]. The presence of the pathogen in the maternal urinary tract at the time of delivery is the most important risk factor for neonatal GBS infection; alternatively, GBS can reach the amniotic fluid by ascending through the cervix with intact or ruptured membranes [3], especially in the cases of prolonged labor, premature rupture of membranes (PROM), or preterm birth (PTB) [4]. Less frequent GBS-related morbidities are represented by surgical wound infection after cesarean delivery, pelvic abscesses, pelvic septic thrombophlebitis, and osteomyelitis [5]. Approximately 98% of colonized newborns are asymptomatic while the early-onset symptomatic forms have a 1–3% incidence with a 50–60% neonatal mortality [6,7].
GBS is detected with universal culture screening at 35–37 weeks’ gestation; currently, antibiotic prophylaxis in active labor is the most effective intervention to counteract early neonatal infections in GBS-positive women [8]. Antibiotic prophylaxis is also effective when administered to women with risk factors for GBS colonization (i.e., labor <37 weeks, amniotic membrane rupture for ≥18 h, or intrapartum T > 38°C) and unknown GBS status [9].
However, the widespread use of intrapartum antibiotics likely affects the biodiversity of maternal and neonatal microbiota and is associated with mother and infant gut microbiota dysbiosis [10,11]. The vaginal microbiota has indeed been recognized as a novel factor by which maternal stress and perturbations may contribute to reprogramming the developing brain of the offspring, predisposing individuals to neurodevelopmental disorders [12].
Moreover, intrapartum antibiotic prophylaxis (IAP) may secondarily decrease the susceptibility to penicillin or ampicillin, the agents of choice used to prevent GBS disease [13,14]. Therefore, several strategies have been tested as alternatives. A small study showed that intrapartum vaginal flushing with chlorhexidine was as effective as ampicillin in preventing GBS transmission to neonates and also reduced the rate of neonatal E. coli colonization [15]. The WHO launched the first GBS maternal immunization program to develop a GBS vaccine but the results are not available yet [16]. Natural antibacterial phytochemicals (i.e., Carvacrol) have been shown to compromise the cell membrane integrity by inducing changes that lead to leakage of cytoplasmic contents such as lactate dehydrogenase enzymes and nucleic acids, demonstrating an additive–synergistic effect with clindamycin or penicillin [17]. In addition, plant-based compounds were used to inhibit the virulence properties and gene expression [18] of Streptococcus species; indeed, promising results have been reported regarding the synergistic effects of citral (citrus oil with anti-inflammatory and bactericidal properties) and phloretin (a polyphenolic chalcone that has many interesting biological properties, including inhibition of Gram-positive and Gram-negative bacteria) to combat the virulence of Streptococcus [19]. Finally, probiotics were studied to reduce GBS colonization rates at 35–37 weeks of gestation to prevent neonatal infections.
Probiotics are live microorganisms that, when administered in adequate amounts, confer a health benefit to the host [20]. Their supplementation is increasingly widespread and accepted globally due to their documented health benefits [21,22].
Research studies have proven that women with higher vaginal colonization of lactobacilli are more likely to have no detectable vaginal GBS [23,24,25]. Indeed, probiotics have the potential to maintain vaginal homeostasis through the occupation of niches that impede the expansion of other bacteria and the establishment of biofilms, the increase in lactic acid and production of other antimicrobial compounds, and the regulation of the local cervicovaginal mucosal immune responses [26,27,28]. Moreover, no major safety concerns were reported for probiotics [29] and a recently published systematic review and meta-analysis stated that probiotics and prebiotics in pregnancy and lactation were safe. Only one study that administered Lactobacillus rhamnosus and L. reuteri showed a higher risk of vaginal discharge and changes in stool consistency, but overall, no serious health concerns to the mother or infant have been raised regarding probiotic and prebiotic use [30].
On these grounds, we conducted a systematic review and meta-analysis to summarize the available evidence on the effects of probiotic supplementation to decrease maternal GBS recto-vaginal colonization.

2. Materials and Methods

2.1. Search Strategy

The review protocol was established by two investigators (G.C. and D.M.) before the commencement of the study and was registered with the PROSPERO International Prospective Register of Systematic Reviews (registration no. 184589). The electronic databases MEDLINE, ClinicalTrials.gov, PROSPERO, and the Cochrane Central Register of Controlled Trials were searched from the inception of each database until February 2022 using the following terms: ‘GBS’, ‘group B streptococcus’, ‘colonization’, ‘probiotics’, ‘recto-vaginal colonization’, ‘GBS colonization’, and ‘randomized trial’. All manuscripts were reviewed for pertinent references. No language restrictions were applied.

2.2. Study Selection

Selection criteria included RCTs that evaluated the effects of probiotic supplementation in pregnancy on GBS recto-vaginal colonization. We included RCTs involving pregnant women receiving probiotics. The primary outcome was GBS-positive recto-vaginal cultures performed at 35–37 weeks’ gestation. Secondarily, we evaluated obstetric outcomes: preterm birth (PTB), preterm rupture of membranes (PROM), chorioamnionitis, and neonatal outcomes (neonatal infection and neonatal intensive care unit (NICU) admission).

2.3. Data Extraction and Risk-of-Bias Assessment

Data from each eligible study were extracted without modification of original data onto custom-made data collection forms. A two-by-two table was used to calculate the relative risk (OR). The summary measures were reported as OR with 95% CI; between-study heterogeneity was accounted for using random-effects meta-analyses. Subgroup analyses were performed according to the positive or unknown GBS baseline according to the gestational age at beginning of the treatment with probiotics (after 30 weeks or before 30 weeks) and to the duration of the treatment (less or more than 12 weeks). Data analysis was performed using Stata 15.1 (StataCorp, College Station, TX, USA).
We assessed the risk of bias in each included study using the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions [31]. Seven characteristics related to the risk of bias were assessed in each included trial because there is evidence that these issues are associated with biased estimates of treatment effect: (1) random sequence generation; (2) allocation concealment; (3) blinding of participants and personnel; (4) blinding of outcome assessment; (5) incomplete outcome data; (6) selective reporting; and (7) other bias. Review authors’ judgments were categorized as ‘low risk’, ‘high risk’, or ‘unclear risk’ of bias [31]. Publication bias was evaluated using a funnel plot. Our study was exempt from IRB approval because it collected and integrated publicly available research. The review was reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (see the Supplementary File S1).

3. Results

The flow diagram of the electronic search details and selection process is shown in Figure 1. A total of 132 publications were identified; of these, 123 were excluded according to the title or the abstract, while 9 full-length articles matched the inclusion criteria. After revision, three studies were excluded because they were non-RCTs and one was excluded because only the protocol was available. Thus, five eligible RCTs were finally included in the analysis. The main features of the included studies are summarized in Table 1.
As reported in Figure 2, most of the included studies were considered to have a low or unclear risk of bias. The blinding of participants and personnel was the most frequent bias among the included studies. All of the studies were exempt from selection bias thanks to the randomization, as well as from reporting bias.
The population was Caucasian in three studies [33,35,36] while one study also included Hispanic and other ethnicities [34]; the remnant one was conducted on Asian women [32]. The sample size ranged from 34 to 151 pregnant women. All of the included studies tested oral supplementation with probiotics. Probiotic strains were the same in four of the studies (Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 L) [32,33,34,35], while Lactobacillus jensenii Lbv116, Lactobacillus crispatus Lbv88, Lactobacillus rhamnosus Lbv96, and Lactobacillus gasseri Lbv150 were used in the remnant study [36]. Doses ranged from 1 ×108 CFU to 5.4 ×109 CFU daily. The duration of supplementation ranged from 2 to 12 weeks (Table 1). While three studies investigated women known to have GBS-positive cultures [32,33,36], the remnants included women with an unknown GBS status [34,35].
Probiotic supplementation caused a drop in vaginal GBS colonization: the GBS-positive culture rate was 31.9% (96/301) in the intervention group compared to 38.6% (109/282) in the placebo group (OR = 0.62, 95% CI 0.40–0.94, I2 4.8%, p = 0.38; Figure 3).
This positive result also was confirmed among women with a GBS-positive baseline that encountered a significant conversion to negative culture after probiotic treatment (OR = 0.41, 95%CI 0.21–0.78, I2 0%, p = 0.55; Figure 4).
The subgroup analysis showed that if the treatment was started after 30 weeks of gestation, it was more effective in reducing GBS colonization (OR 0.41, 95% CI 0.21–0.78, I2 0%, p = 0.55; Figure 5).
The duration of the treatment (less or more than 12 weeks) did not seem to alter the effect on GBS colonization because the stratified group showed positive trends toward the protective effect of probiotics (Figure 6).
The secondary outcomes were not meta-analyzed because they were reported in only a few studies; these outcomes are summarized in Table 2. Ming-Ho et al. [32] and Sharpe et al. [35] described fewer NICU admissions as well as lower rates of clinical chorioamnionitis and neonatal infections when probiotics were prescribed to pregnant mothers, although significance was not reached. No differences in intrapartum fever, preterm birth, or neonatal infections were reported in the other studies. Of note, none of the studies reported cases of adverse effects related to probiotics, neither for the mothers nor the babies.
No risk of publication bias was detected according to funnel plot (Figure 7).

4. Discussion

GBS colonizes approximately 20% of pregnant women and represents the most important risk factor for neonatal early-onset sepsis (EOS) with a high rate of morbidity and mortality.
This systematic review and meta-analysis was conducted to determine if probiotic supplementation in pregnancy reduced maternal GBS recto-vaginal colonization in pregnant women at 35–37 weeks of gestation.
We found that women receiving probiotic supplementation in pregnancy, when compared to those receiving placebo, had lower GBS positive recto-vaginal cultures at universal screening performed at 35–37 weeks gestation. These findings also were confirmed among known GBS-positive women who reached a higher conversion to a negative culture [32,36]. A subanalysis showed that this effect was amplified when treatment began after the 30th week of gestation, meaning that proximity to delivery could play a key role, while the long duration of the treatment did not improve the effects.
Such an effect was observed across all studies and was independent of the study effect size as indicated by the low between-study heterogeneity in the treatment effect (I-squared of 4.8%) and the low between-study variance (tau-squared of 0.01).
The composition of probiotics in primary studies included Lactobacillus spp., which have shown anti-GBS activity “in vitro” [37]. Indeed, Lactobacillus cells have been demonstrated to be able to interact and aggregate with Streptococcus cells and kill the GBS, underlining the importance of bacterial co-aggregation as an antimicrobial mechanism against pathogens [37]. Afterward, Lactobacilli compete with Streptococcus for adhesion to vaginal mucosa cells and nutrients and produce antimicrobial substances (hydrogen peroxide, lactic acid, and bacteriocins) that affect GBS replication; they can also counteract other pathogens such as C. vaginalis and N. gonorrheae as demonstrated in bacterial co-aggregation studies [38,39,40].
In three of the included studies, probiotic administration did not significantly reduce GBS recto-vaginal colonization [33,34,35]. The short duration of the intervention (3 weeks) may account for such results in the study by Olsen et al. [33], while the probiotic composition, compliance, and population baseline characteristics may have played a role in the studies by Sharpe et al. [35] and Aziz et al. [34].
Regarding safety concerns, probiotics are generally considered safe and well tolerated. Current data suggest that probiotic supplementation is rarely systemically absorbed when used by healthy individuals. One meta-analysis of several randomized controlled trials conducted with women during the third trimester did not report an increase in adverse neonatal outcomes [41]. We confirmed these findings supporting maternal probiotic administration, which did not worsen short-term neonatal health (NICU admission or sepsis). Furthermore, according to a recently published meta-analysis and systematic review, probiotic products have other clinical benefits during or after pregnancy such as preventing or treating gestational diabetes [42], mastitis [43], preterm birth [44], and infantile atopic dermatitis [45].
Therefore, these products may contribute to improving the health of pre-pregnant, pregnant, and postpartum patients and their children in specific situations, and their benefits may outweigh the documented minimal risks.
Our meta-analysis demonstrated that probiotic supplementation was also associated with a significant reduction in emergency cesarean sections [33]. However, the trial was not equipped for this secondary outcome and the finding has not been confirmed in another RCT [36].
Interestingly, another study reported that prenatal probiotics significantly reduced the incidence of bacterial vaginosis, increased colonization with vaginal Lactobacillus and intestinal Lactobacillus rhamnosus, altered immune markers in serum and breast milk, and improved maternal glucose metabolism, resulting in significantly higher counts of Bifidobacterium and Lactococcus lactis (healthy intestinal flora) in neonatal stool [46].
It is nowadays recognized that the maternal microbiota influences the colonization in the infant. Recent studies suggested that this mechanism begins before delivery during intrauterine life. Indeed, during gestation, the fetus can encounter microorganisms of maternal origin. In fact, fragments of bacterial DNA have been found in the umbilical cord, in the amniotic fluid, and even in the meconium [47].
Their presence is made possible by the fact that during gestation, the maternal gut becomes more permeable, which favors bacterial translocation. Commensal microbes translocate from the maternal gut to the placenta or fetal gut during pregnancy. These microbes impact the development of fetal immunity via various mechanisms including epigenetic changes, the release of short-chain fatty acids, and alteration of the cytokine environment. This aspect is of fundamental importance because if the mother is in conditions of eubiosis, the contact of the fetus with the correct bacterial strains will create a very favorable condition for the newborn gut. If, on the other hand, the mother has an altered microbiota, it is possible to witness the passage from the maternal bloodstream through the placenta to the fetus of different bacterial strains that could lead to greater exposure of the newborn to diseases [48].
This reinforces the importance of maintaining a healthy maternal microbiota not only in the proximity of childbirth, but also throughout the entire pregnancy and even during breastfeeding thanks to healthy lifestyles and the use of probiotics.
A recent systematic review and meta-analysis [49] that also included non-randomized and quasi-experimental clinical studies reported the efficacy of probiotic intervention in reducing the rate of GBS-positive women, although with less strength of the evidence (few placebo-controlled studies). Moreover, our evaluation, which included RCTs only, provided additional information. Indeed, the efficacy of probiotics seems to be related to third-trimester supplementation with respect to treatment implemented long before parturition. Finally, we also provided some insights into neonatal health.
Supporting these promising data on probiotics and neonatal health, a recent multi-center study was conducted on infants (up to 32 weeks’ gestation) admitted to 289 neonatal intensive care units (NICUs) receiving probiotics during the first postnatal days. Several adverse outcomes were evaluated: necrotizing enterocolitis (NEC), bloodstream infections, meningitis, and death. The authors reported a decrease in the odds of NEC and death but concluded that little is known about the doses of particular strains and the mechanism of action that determine which treatment produces the maximum safety and efficacy [50].
The strengths of our study included the comprehensive search strategy of including only RCTs with no language restrictions and the low degree of heterogeneity in the included studies. The limitations primarily related to the low number of studies included in the meta-analysis and the quality of the studies, as some of them were judged to have an unclear risk of bias. In particular, the study by Aziz et al. [34], which had the highest risk of bias, was also the most numerous one, thus it primarily drove the others included in the meta-analysis. Moreover, since probiotics are not treated as medicines, the different strains at different dosages and different routes of administration are not well regulated by governing agencies in most countries. In addition, compliance with treatment was not adequately addressed across the surveys, as only Olsen et al. [33] identified that fully compliant women had a significant increase in the quantity of vaginal commensal bacteria.

5. Conclusions

Preventing maternal GBS colonization has an important impact on the health of the newborn because it may avoid the 1–3% of early-onset symptomatic forms [6,7]. It also has an impact on women’s exposure to IAP, which has potential perinatal microbiological sequelae of exposure for the mother and the newborn. Thus, primary prevention strategies for GBS colonization are increasingly urgent; probiotics, with their antagonistic activities against GBS, are promising. This systematic review and meta-analysis demonstrated that the administration of probiotics during pregnancy, namely in the third trimester, was associated with a reduced GBS recto-vaginal colonization at 35–37 weeks and a safe perinatal profile. Probiotics also may be useful to counteract GBS colonization when it is already established, showing a considerable negativization rate in GBS-positive women. Whether this new strategy could reduce the exposure of pregnant women to significant doses of antibiotics in labor needs to be further investigated. Future double-blind randomized controlled trials with larger and more diverse samples are required.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/nu14214520/s1, Supplementary File S1: The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. Ref. [51] in Supplementary Materials.

Author Contributions

D.M., F.D.S. and F.F. conceived of the presented idea; D.M., F.M. and G.C. performed the literature search and screened the articles for inclusion; G.C. performed the statistical analysis. All authors discussed the results and contributed to the final manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study was based on secondary data so ethics approval was not required.

Informed Consent Statement

Patient consent was not applicable because this study was based on secondary data.

Data Availability Statement

The data are available upon reasonable request from the corresponding author (D.M.; email: [email protected]).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Barcaite, E.; Bartusevicius, A.; Tameliene, R.; Kliucinskas, M.; Maleckiene, L.; Nadisauskiene, R. Prevalence of maternal group B streptococcal colonisation in European countries. Acta Obs. Gynecol. Scand. 2008, 87, 260–271. [Google Scholar] [CrossRef] [PubMed]
  2. Hall, J.; Hack Adams, N.; Bartlett, L.; Seale, A.; Lamagni, T.; Bianchi-Jassir, F.; Lawn, E.J.; Baker, C.J.; Cutland, C.; Heath, P.T.; et al. Maternal Disease With Group B Streptococcus and Serotype Distribution Worldwide: Systematic Review and Meta-analyses. Clin. Infect. Dis. 2017, 65, S112–S124. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Al-Kadri, H.; Bamuhair, S.; Al Johani, S.; Al-Buriki, N.; Tamim, H. Maternal and neonatal risk factors for early-onset group B streptococcal disease: A case control study. Int. J. Womens Health 2013, 5, 729–735. [Google Scholar] [CrossRef] [Green Version]
  4. Bianchi-Jassir, F.; Seale, A.; Kohli-Lynch, M.; Lawn, J.; Baker, C.; Bartlett, L.; Cutland, C.; Gravett, M.G.; Heath, P.T.; Ip, M.; et al. Preterm Birth Associated With Group B Streptococcus Maternal Colonization Worldwide: Systematic Review and Meta-analyses. Clin. Infect. Dis. 2017, 65, S133–S142. [Google Scholar] [CrossRef] [Green Version]
  5. Collin, M.; Shetty, N.; Guy, R.; Nyaga, V.; Bull, A.; Richards, M.; van der Kooi, T.; Koek, M.B.G.; De Almeida, M.; Roberts, S.A.; et al. Group B Streptococcus in surgical site and non-invasive bacterial infections worldwide: A systematic review and meta-analysis. Int. J. Infect. Dis. 2019, 83, 116–129. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Baker, C.; Edwards, M. Group B Streptococcal Infections. In Infectious Diseases of the Fetus and Newborn Infant, 4th ed.; Remington, J., Klein, J.O., Eds.; WB Saunders: Philadelphia, PA, USA, 1995; pp. 980–1054. [Google Scholar]
  7. Demianczuk, N.; Halperin, S.; McMillan, D. Prevention of perinatal group B streptococcal infection: Management strategies. Can. J. Infect. Dis. 1997, 8, 68–70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Verani, J.; McGee, L.; Schrag, S.J. Prevention of perinatal group B streptococcal disease-revised guidelines from CDC. MMWR. Recommendations and reports: Morbidity and mortality weekly report Recommendations and reports. Centers Dis. Control Prev. 2010, 59, 1–32. [Google Scholar]
  9. ACOG Committee. Committee Opinion No. 797. Obstet Gynecol. 2020, 135, 978–979. [Google Scholar] [CrossRef]
  10. Zimmermann, P.; Curtis, N. Effect of intrapartum antibiotics on the intestinal microbiota of infants: A systematic review. Arch. Dis. Child.-Fetal Neonatal Ed. 2020, 105, 201–208. [Google Scholar] [CrossRef]
  11. Tapiainen, T.; Koivusaari, P.; Brinkac, L.; Lorenzi, H.; Salo, J.; Renko, M.; Pruikkonen, H.; Pokka, T.; Li, W.; Nelson, K.; et al. Impact of intrapartum and postnatal antibiotics on the gut microbiome and emergence of antimicrobial resistance in infants. Sci. Rep. 2019, 9, 10635. [Google Scholar] [CrossRef] [Green Version]
  12. Jašarević, E.; Howerton, C.L.; Howard, C.D.; Bale, T.L. Alterations in the Vaginal Microbiome by Maternal Stress Are Associated With Metabolic Reprogramming of the Offspring Gut and Brain. Endocrinology 2015, 156, 3265–3276. [Google Scholar] [CrossRef]
  13. Back, E.E.; O’Grady, E.J.; Back, J.D. High rates of perinatal group B Streptococcus clindamycin and erythromycin resistance in an Upstate New York Hospital. Antimicrob. Agents Chemother. 2012, 56, 739–742. [Google Scholar] [CrossRef] [Green Version]
  14. Spaetgens, R. Perinatal antibiotic usage and changes in colonization and resistance rates of group B streptococcus and other pathogens. Obstet. Gynecol. 2002, 100, 525–533. [Google Scholar]
  15. Facchinetti, F.; Piccinini, F.; Mordini, B.; Volpe, A. Chlorhexidine vaginal flushings versus systemic ampicillin in the prevention of vertical transmission of neonatal group B streptococcus, at term. J. Matern. Fetal Neonatal Med. 2002, 11, 84–88. [Google Scholar] [CrossRef]
  16. World Health Organization. WHO Preferred Product Characteristics for Group B Streptococcus Vaccines. In Initiative for Vaccine Research (IVR) of the Department of Immunization, Vaccines and Biologicals; Vaccines and BiologicalsCH-1211; World Health Organization Department of Immunization: Geneva, Switzerland, 2014; pp. 5–16. [Google Scholar]
  17. Wijesundara, N.M.; Lee, S.F.; Cheng, Z.; Davidson, R.; Rupasinghe, H.P.V. Carvacrol exhibits rapid bactericidal activity against Streptococcus pyogenes through cell membrane damage. Sci. Rep. 2021, 11, 1487. [Google Scholar] [CrossRef]
  18. Khan, R.; Adil, M.; Danishuddin, M.; Verma, P.K.; Khan, A.U. In vitro and in vivo inhibition of Streptococcus mutans biofilm by Trachyspermum ammi seeds: An approach of alternative medicine. Phytomedicine 2012, 19, 747–755. [Google Scholar] [CrossRef]
  19. Adil, M.; Baig, M.H.; Rupasinghe, H.V. Impact of citral and phloretin, alone and in combination, on major virulence traits of Streptococcus pyogenes. Molecules 2019, 24, 4237. [Google Scholar] [CrossRef] [Green Version]
  20. Hill, C.; Guarner, F.; Reid, G.; Gibson, G.R.; Merenstein, D.J.; Pot, B.; Morelli, L.; Canani, R.B.; Flint, H.J.; Salminen, S.; et al. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic. Nat. Rev. Gastroenterol. Hepatol. 2014, 11, 506–514. [Google Scholar] [CrossRef] [Green Version]
  21. Chin-Lee, B.; Curry, W.J.; Fetterman, J.; Graybill, M.A.; Karpa, K. Patient experience and use of probiotics in community-based health care settings. Patient Prefer. Adherence 2014, 8, 1513–1520. [Google Scholar]
  22. Betz, M.; Uzueta, A.; Rasmussen, H.; Gregoire, M.; Vanderwall, C.; Witowich, G. Knowledge, use and perceptions of probiotics and prebiotics in hospitalised patients. Nutr. Diet. 2015, 72, 261–266. [Google Scholar] [CrossRef]
  23. Rosen, G.H.; Randis, T.M.; Desai, P.V.; Sapra, K.J.; Ma, B.; Gajer, P.; Humphrys, M.; Ravel, J.; Gelber, S.E.; Ratner, A.J. Group B Streptococcus and the Vaginal Microbiota. J. Infect. Dis. 2017, 216, 744–751. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Altoparlak, U.; Kadanali, A.; Kadanali, S. Genital flora in pregnancy and its association with group B streptococcal colonization. Int. J. Gynecol. Obstet. 2004, 87, 245–246. [Google Scholar] [CrossRef] [PubMed]
  25. Whitney, C.; Daly, S.; Limpongsanurak, S.; Festin, M.; Thinn, K.; Chipato, T.; Lumbiganon, P.; Sauvarin, J.; Andrews, W.; Tolosa, J.E.; et al. The International Infections in Pregnancy Study: Group B streptococcal colonization in pregnant women. J. Matern. Neonatal Med. 2004, 15, 267–274. [Google Scholar] [CrossRef] [PubMed]
  26. Tachedjian, G.; Aldunate, M.; Bradshaw, C.S.; Cone, R.A. The role of lactic acid production by probiotic Lactobacillus species in vaginal health. Res. Microbiol. 2017, 168, 782–792. [Google Scholar] [CrossRef]
  27. Petrova, M.I.; Imholz, N.C.E.; Verhoeven, T.L.A.; Balzarini, J.; Van Damme, E.J.M.; Schols, D.; Vanderleyden, J.; Lebeer, S. Lectin-Like Molecules of Lactobacillus rhamnosus GG Inhibit Pathogenic Escherichia coli and Salmonella Biofilm Formation. PLoS ONE 2016, 11, e0161337. [Google Scholar] [CrossRef] [Green Version]
  28. Allonsius, C.N.; Vandenheuvel, D.; Oerlemans, E.F.M.; Petrova, M.I.; Donders, G.G.G.; Cos, P.; Delputte, P.; Lebeer, S. Inhibition of Candida albicans morphogenesis by chitinase from Lactobacillus rhamnosus GG. Sci. Rep. 2019, 2900, 1–12. [Google Scholar] [CrossRef]
  29. Wijgert, J.; Verwijs, M. Lactobacilli-containing vaginal probiotics to cure or prevent bacterial or fungal vaginal dysbiosis: A systematic review and recommendations for future trial designs. BJOG An Int. J. Obstet. Gynaecol. 2020, 127, 287–299. [Google Scholar] [CrossRef]
  30. Sheyholislami, H.; Connor, K.L. Are Probiotics and Prebiotics Safe for Use during Pregnancy and Lactation? A Systematic Review and Meta-Analysis. Nutrients 2021, 13, 2382. [Google Scholar] [CrossRef]
  31. Higgins, J.P.; Green, S. (Eds.) Cochrane Handbook for Systematic Reviews of Interventions Version 5.1.0; The Cochrane Collaboration: London, UK; John Wiley & Sons Ltd.: Hoboken, NJ, USA, 2011. [Google Scholar]
  32. Ho, M.; Chang, Y.Y.; Chang, W.C.; Lin, H.C.; Wang, M.H.; Lin, W.C.; Wang, M.H.; Lin, W.C.; Chiu, T.H. Oral Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14 to reduce Group B Streptococcus colonization in pregnant women: A randomized controlled trial. Taiwan J. Obstet. Gynecol. 2016, 55, 515–518. [Google Scholar] [CrossRef] [Green Version]
  33. Olsen, P.; Williamson, M.; Traynor, T.; Georgiou, C. The impact of oral probiotics on vaginal Group B Streptococcal colonisation rates in pregnant women: A pilot randomised control study. Women Birth 2017, 31, 31–37. [Google Scholar] [CrossRef] [Green Version]
  34. Aziz, N.; Spiegel, A.; Bentley, J.; Yoffe, P.; Klikoff, A.; Ehrlich, K.; El-Sayed, Y.; Norton, M.; Taslimi, M. Evaluation of Probiotic Oral Supplementation Effects on Group B Streptococcus Rectovaginal Colonization in Pregnant Women: A Randomized Double-Blind Placebo-Controlled Trial. Am. J. Obstet. Gynecol. 2018, 218, S509–S510. [Google Scholar] [CrossRef] [Green Version]
  35. Sharpe, M.; Shah, V.; Freire-Lizama, T.; Cates, E.; McGrath, K.; David, I.; Cowan, S.; Letkeman, J.; Steward-Wilson, E. Effectiveness of oral intake of Lactobacillus rhamnosusGR-1 and Lactobacillus reuteri RC-14 on Group B Streptococcus colonization during pregnancy: A midwifery-led double-blind randomized controlled pilot trial. J. Matern. Neonatal Med. 2019, 34, 1814–1821. [Google Scholar] [CrossRef] [PubMed]
  36. Farr, A.; Sustr, V.; Kiss, H.; Rosicky, I.; Graf, A.; Makristathis, A.; Makristathis, A.; Petricevic, L. Oral probiotics to reduce vaginal group B streptococcal colonization in late pregnancy. Sci. Rep. 2020, 10, 19745. [Google Scholar] [CrossRef] [PubMed]
  37. Marziali, G.; Foschi, C.; Parolin, C.; Vitali, B.; Marangoni, A. In-vitro effect of vaginal lactobacilli against group B Streptococcus. Microb. Pathog. 2019, 136, 103692. [Google Scholar] [CrossRef]
  38. De Gregorio, P.R.; Tomás, M.S.J.; Terraf, M.C.L.; Nader-Macías, M.E.F. In vitro and in vivo effects of beneficial vaginal lactobacilli on pathogens responsible for urogenital tract infections. J. Med. Microbiol. 2014, 63, 685–696. [Google Scholar] [CrossRef]
  39. do Carmo, M.S.; Noronha, F.M.F.; Arruda, M.O.; da Silva Costa, Ê.P.; Bomfim, M.R.Q.; Monteiro, A.S.; Ferro, T.A.F.; Fernandes, E.S.; Giron, J.A.; Monteneiro-Neto, V. Lactobacillus fermentum ATCC 23271 displays in vitro inhibitory activities against Candida spp. Front. Microbiol. 2016, 7, 1722. [Google Scholar] [CrossRef] [Green Version]
  40. Foschi, C.; Salvo, M.; Cevenini, R.; Parolin, C.; Vitali, B.; Marangoni, A. Vaginal Lactobacilli Reduce Neisseria gonorrhoeae Viability through Multiple Strategies: An in Vitro Study. Front. Cell Infect. Microbiol. 2017, 7, 502. [Google Scholar] [CrossRef] [Green Version]
  41. Elias, J.; Bozzo, P.; Einarson, A. Are probiotics safe for use during pregnancy and lactation? Can. Fam. Physician 2011, 57, 299–301. [Google Scholar]
  42. Chen, X.; Jiang, X.; Huang, X.; He, H.; Zheng, J. Association between Probiotic Yogurt Intake and Gestational Diabetes Mellitus: A Case-Control Study. Iran. J. Public Health 2019, 48, 1248–1256. [Google Scholar] [CrossRef]
  43. Fernández, L.; Cárdenas, N.; Arroyo, R.; Manzano, S.; Jiménez, E.; Martín, V.; Rodríguez, J.M. Prevention of Infectious Mastitis by Oral Administration of Lactobacillus salivarius PS2 During Late Pregnancy. Clin. Infect. Dis. 2016, 62, 568–573. [Google Scholar] [CrossRef] [Green Version]
  44. Kriss, J.L.; Ramakrishnan, U.; Beauregard, J.L.; Phadke, V.K.; Stein, A.D.; Rivera, J.A.; Omer, S.B. Yogurt consumption during pregnancy and preterm delivery in Mexican women: A prospective analysis of interaction with maternal overweight status. Matern. Child. Nutr. 2018, 14, e12522. [Google Scholar] [CrossRef] [PubMed]
  45. Celik, V.; Beken, B.; Yazicioglu, M.; Ozdemir, P.G.; Sut, N. Do traditional fermented foods protect against infantile atopic dermatitis. Pediatr. Allergy Immunol. 2019, 30, 540–546. [Google Scholar] [CrossRef] [PubMed]
  46. VandeVusse, L.; Hanson, L.; Safdar, N. Perinatal Outcomes of Prenatal Probiotic and Prebiotic Administration. J. Perinat. Neonatal Nurs. 2013, 27, 288–301. [Google Scholar] [CrossRef]
  47. McDonald, B.; McCoy, K.D. Maternal microbiota in pregnancy and early life. Science 2019, 365, 984–985. [Google Scholar] [CrossRef] [PubMed]
  48. Rodriguez, D.A.; Peña Vélez, R.; Toro Monjaraz, E.M.; Ramirez Mayans, J.; MacDaragh Ryan, P. The Gut Microbiota: A Clinically Impactful Factor in Patient Health and Disease. SN Compr. Clin. Med. 2019, 1, 188–199. [Google Scholar] [CrossRef] [Green Version]
  49. Hanson, L.; VandeVusse, L.; Malloy, E.; Garnier-Villarreal, M.; Watson, L.; Fial, A.; Forgie, M.; Nerdini, K.; Safdar, N. Probiotic interventions to reduce antepartum Group B streptococcus colonization: A systematic review and meta-analysis. Midwifery 2022, 105, 103208. [Google Scholar] [CrossRef]
  50. Gray, K.D.; Messina, J.A.; Cortina, C.; Owens, T.; Fowler, M.; Foster, M.; Gbadegesin, S.; Clark, R.H.; Benjamin, D.K., Jr.; Zimmerman, K.O.; et al. Probiotic Use and Safety in the Neonatal Intensive Care Unit: A Matched Cohort Study. J. Pediatr. 2020, 222, 59–64.e1. [Google Scholar] [CrossRef]
  51. Moher, D.; Liberati, A.; Tetzlaff, J.; Altman, D.G.; The PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. PLoS Med. 2009, 6, e1000097. [Google Scholar] [CrossRef]
Nutrients 14 04520 g001 550
Figure 1. Flow diagram of the study search process.
Figure 1. Flow diagram of the study search process.
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Nutrients 14 04520 g002 550
Figure 2. Assessment of bias risk. (A) Summary of risk of bias for each trial. A plus sign indicates a low risk of bias; a minus sign indicates a high risk of bias; a question mark indicates an unclear risk of bias. Aziz, 2018 [34], Farr, 2020 [36], Ming-Ho, 2016 [32], Olsen, 2017 [33], Sharpe, 2019 [35]. (B) Risk of bias graph for each risk of bias item presented as percentages across all included studies.
Figure 2. Assessment of bias risk. (A) Summary of risk of bias for each trial. A plus sign indicates a low risk of bias; a minus sign indicates a high risk of bias; a question mark indicates an unclear risk of bias. Aziz, 2018 [34], Farr, 2020 [36], Ming-Ho, 2016 [32], Olsen, 2017 [33], Sharpe, 2019 [35]. (B) Risk of bias graph for each risk of bias item presented as percentages across all included studies.
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Nutrients 14 04520 g003 550
Figure 3. Forest plot for the GBS colonization. Ming-Ho, 2016 [32], Olsen, 2017 [33], Aziz, 2018 [34], Sharpe, 2019 [35], Farr, 2020 [36].
Figure 3. Forest plot for the GBS colonization. Ming-Ho, 2016 [32], Olsen, 2017 [33], Aziz, 2018 [34], Sharpe, 2019 [35], Farr, 2020 [36].
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Nutrients 14 04520 g004 550
Figure 4. Forest plot for the GBS colonization according to positive or unknown GBS baseline. Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
Figure 4. Forest plot for the GBS colonization according to positive or unknown GBS baseline. Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
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Figure 5. Forest plot for the GBS colonization according to the gestational age at beginning of the treatment with probiotics (after 30 weeks or before 30 weeks). Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
Figure 5. Forest plot for the GBS colonization according to the gestational age at beginning of the treatment with probiotics (after 30 weeks or before 30 weeks). Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
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Figure 6. Forest plot for the GBS colonization according to the duration of treatment with probiotics (less than 12 weeks or more than 12 weeks). Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
Figure 6. Forest plot for the GBS colonization according to the duration of treatment with probiotics (less than 12 weeks or more than 12 weeks). Ming-Ho, 2016 [32], Olsen, 2017 [33], Farr, 2020 [36], Aziz, 2018 [34], Sharpe, 2019 [35].
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Figure 7. Publication bias.
Figure 7. Publication bias.
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Table
Table 1. Study and population characteristics.
Table 1. Study and population characteristics.
StudyCountryEthnicityProbiotic/
Placebo		InterventionDosesTime
Ming-Ho, 2016 [32]ChinaAsian49/50L. rhamnosus GR-1 and L. reuteri RC-142 × 109 CFU/day from 35–37 weeks until delivery2 weeks
Olsen, 2017 [33]AustraliaCaucasian21/13L. rhamnosus GR-1 and L. reuteri RC-141 × 108 CFU (108 viable strains) for three weeks/until delivery3 weeks
Aziz, 2018 [34]USACaucasian
Hispanic
Other		125/126L. rhamnosus GR-1 and L. reuteri RC-145.4 × 109 CFU daily in capsule started at 28 weeks12 weeks
Sharpe, 2019 [35]CanadaCaucasian73/66L. rhamnosus GR-1 and L. reuteri RC-145 × 109 daily started at 23–25th week12 weeks
Farr, 2020 [36]AustriaCaucasian33/27L. jensenii Lbv116; L. crispatus Lbv88;
L. rhamnosus Lbv96; L. gasseri Lbv150		4 × 109 CFU daily
oral intake started between 32–36 weeks		2 weeks
CFU: colony-forming unit.
Table
Table 2. Secondary outcomes in the probiotic and control/placebo groups.
Table 2. Secondary outcomes in the probiotic and control/placebo groups.
StudyNMaternalLabor and DeliveryIntervention
Ming-Ho, 2016 [32]99Intrapartum fever:
Placebo: 0/50
Probiotic: 1/49 (2.0%)		N/ANICU admission
Placebo: 0/50
Probiotic: 1/49 (2.0%)
Olsen, 2017 [33]34PTB
Control: 0/13
Probiotic: 0/21		Emergency CS
Control: 5/13 (38.5%)
Probiotic: 0/21 *		Neonatal allergies ª
Control:0/13
Probiotic: 0/21
Aziz, 2018 [34]251PTB
Placebo: 3/121 (2.5%)
Probiotic: 4/116 (3.5%)		Chorioamnionitis
Placebo: 4/116 (3.5%)
Probiotic: 5/113 (4.4%)		Neonatal infections
Placebo: 2/121 (1.7%)
Probiotic: 4/115 (3.5%)
Sharpe, 2019 [35]139N/AIntrapartum infections
Placebo: 3/56 (5.3%)
Probiotic: 4/57 (7.0%)		NICU admission
Placebo: 3/56 (5.3%)
Probiotic: 0/57
Farr, 2020 [36]60PTB
Placebo: 1/41 (2.4%)
Probiotic: 4/41 (9.8%)		Cesarean section
Placebo: 22/41 (53.7%)
Probiotic: 22/41 (53.7%)		Neonatal sepsis
Placebo: 0/41
Probiotic: 0/41
ª Asthma, rhinitis, or eczema. * Significant values (p < 0.05).
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Menichini, D.; Chiossi, G.; Monari, F.; De Seta, F.; Facchinetti, F. Supplementation of Probiotics in Pregnant Women Targeting Group B Streptococcus Colonization: A Systematic Review and Meta-Analysis. Nutrients 2022, 14, 4520. https://doi.org/10.3390/nu14214520

AMA Style

Menichini D, Chiossi G, Monari F, De Seta F, Facchinetti F. Supplementation of Probiotics in Pregnant Women Targeting Group B Streptococcus Colonization: A Systematic Review and Meta-Analysis. Nutrients. 2022; 14(21):4520. https://doi.org/10.3390/nu14214520

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Menichini, Daniela, Giuseppe Chiossi, Francesca Monari, Francesco De Seta, and Fabio Facchinetti. 2022. "Supplementation of Probiotics in Pregnant Women Targeting Group B Streptococcus Colonization: A Systematic Review and Meta-Analysis" Nutrients 14, no. 21: 4520. https://doi.org/10.3390/nu14214520

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