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. 2022 Oct 18;2022:6279343. doi: 10.1155/2022/6279343

An Initial Survey on the Prevalence of Group B Streptococcus (GBS) among Yemeni Pregnant Women in Sana'a City

Ibrahim Al-Subol 1,, Maha Abdul-Aziz 2, Abdullah A Almikhlafy 3, Talal Alqahtani 4
PMCID: PMC9596256  PMID: 36303949

Abstract

Background

Infection with group B Streptococcus (GBS) is still a neonatal life-threatening illness, especially in developing countries such as Yemen.

Objective

This study was aimed at determining the vaginal colonization rate and antibiotic susceptibility pattern of GBS among Yemeni pregnant women.

Methods

We conducted a cross-sectional study over a four-month period involving 210 pregnant women at the 35th to 39th gestational weeks who visited Gaza medical center in Sana'a city, Yemen. The collected vaginal swab specimen was inoculated in the Todd-Hewitt enrichment broth and incubated for 24 h and then subcultured on a 5% human blood agar plate. All positive cultures identified as GBS were subjected to antibiotic susceptibility tests using the disk diffusion method.

Results

Out of 210 recruited pregnant women, 23 (10.95%) were GBS vaginal carriers. All GBS isolates were sensitive to penicillin, ampicillin, levofloxacin, cefotaxime, and vancomycin.

Conclusion

Based on the study's results, approximately eleven out of every 100 pregnant women in Sana'a city are vaginally colonized by GBS. Beta-lactam antibiotics remain the drug of choice to treat and prevent GBS infections. A prenatal screening policy is urgently needed for Yemeni pregnant women.

1. Introduction

On January 1, 2016, the globe formally started implementing the United Nations sustainable development goals (SDGs). One of these 17 goals is enhancing mother, neonate, and child health and planning to end mother and child deaths from preventable diseases [1]. To achieve these goals, neonatal fatalities in each nation should be about 12 per 1000 live births by 2030 [2, 3]. Despite the falling in maternal mortality with substantial variation among countries [4, 5], it is still high especially in developing countries. In 2017, over 295 thousand women died while pregnant or after giving birth, and 94% of these avoidable fatalities occurred in poor and middle-income countries [6]. In low- and middle-income nations, infectious diseases continue to rank among the leading causes of preterm birth and newborn encephalopathy [7, 8], which are major causes of neonatal death and survivors' mental disorders [912]. Streptococcus agalactiae or group B Streptococcus (GBS) is spherical-shaped (coccus) Gram-positive pathobiont bacteria that is often found in the reproductive and gastrointestinal tracts of healthy women, and it can cause serious maternal and neonatal infections [13, 14]. Worldwide, there is a considerable variation in the prevalence of GBS maternal colonization, ranging from high (35%) in the Caribbean to a much lower prevalence (13% and 11%) in Southern and Eastern Asia, respectively [15]. At the regional level, the prevalence of GBS maternal colonization was 19.5% in Jordan [16], 15% in Saudi Arabia [17], 11.3% in Egypt [18], and 10.1% in the United Arab Emirates [19]. Infants born to mothers who are vaginally colonized by GBS are at high risk of acquiring bacteria and may develop life-threatening neonatal meningitis, pneumonia, and septic shock, and neurological deficits may result among survivors [2023]. Yemen is one of the least developed nations, and its people are vulnerable to a variety of illnesses, including neonatal infections. Up to date, no data regarding the prevalence of GBS among Yemeni pregnant women has been published. Therefore, this study was aimed at estimating the prevalence and antibiotic susceptibility pattern of GBS among pregnant women in Sana'a city, Yemen.

2. Methodology

2.1. Study Design, Population, and Setting

We conducted a 4-month cross-sectional study (from June to September 2019) to determine the prevalence of GBS maternal colonization and its antibiotic susceptibility profile among Yemeni pregnant women who attended the Gaza medical center in Sana'a city. Pregnant women who were not within the range of 35th-39th gestational weeks, on antibiotic therapy, diabetics, and those who had urinary tract infections were excluded.

2.2. Sample Size

The sample was calculated using OpenEpi.com (an open-source web tool) based on an expected prevalence of 15% (according to other regional previous studies) at a confidence level of 95% and an accepted marginal error of 5%. Thus, the calculated sample was 196 and our study involved 210 participants.

2.3. Specimen and Data Collection

After the participant consent, a trained nurse carried out vaginal swabbing according to CDC recommendations [24]. The collected specimens were inoculated into Amies transport medium, properly labeled, and transferred immediately to the microbiology laboratory. A structured questionnaire in Arabic that includes information regarding age, education level, previous gestations, previous miscarriages, previous antibiotic use, diabetes, and other chronic diseases was used via face-to-face interview for each participant.

2.4. Bacterial Isolation and Identification

The collected specimens were inoculated into the Todd-Hewitt broth containing gentamicin (8 μg/mL) and nalidixic acid (15 μg/mL) and incubated at 37°C for 24 h. In the next day, the incubated Todd-Hewitt broths were subcultured on 5% human blood agar plates and incubated at 37°C for 24 h. The isolated pure colonies were identified as GBS by the following criteria: colony morphology, Gram staining, hemolysis, catalase, and CAMP test [25].

2.5. Antibiotic Susceptibility Testing

Antibiotic susceptibility testing for penicillin (10 U), ampicillin (10 μg), levofloxacin (5 μg), cefotaxime (30 μg), clindamycin (2 μg), vancomycin (30 μg), and tetracycline (30 μg) was performed for all GBS isolates using the disk diffusion method on the Mueller-Hinton agar containing 5% human blood according to CLSI guideline [26].

2.6. Data Analysis

The results were tabulated and analyzed by IBM SPSS Statistics version 23 for Windows® (IBM Corp., Armonk, NY, USA). Descriptive statistics included frequencies and cross-tabulation; however, the significance of differences was tested by chi-square and Fisher's exact tests. The significance level (P value) of less than 0.05 was considered significant.

2.7. Research Ethics

The approval to conduct this study was obtained from medical research ethics committee of the University of Science and Technology, NO (ECA/UST191).

3. Results

The mean age of 210 participant pregnant women was 26.14 ± 5.28 years ranging from 16 to 38 years. The results of this study showed that 23 pregnant women (10.95%) with 95% CI (6.95 to 14.95%) were GBS vaginal colonized. The mean age of pregnant women with positive GBS vaginal colonization was 26.47 ± 6.5 years, whereas it was 26.1 ± 5.12 years for the rest negative participants. The mean gestational age of pregnant women with positive GBS vaginal colonization was 37.17 ± 1.34 weeks, whereas it was 36.91 ± 1.08 weeks for the rest negative participants, and therefore, there was no correlation between participants' age or gestational age and GBS vaginal colonization. Statistical analysis of the variables (gravida, previous abortions, and educational level) showed that there were no statistical significant differences (P˃0.05) between different groups of participants as shown in (Table 1).

Table 1.

Relationship between independent variables and GBS vaginal colonization rate among Yemeni pregnant women in Sana'a city.

Variables Vaginal colonization Total P value
Yes No
N % N %
Gravida 0 2 18.20% 9 81.80% 11 0.517
1 5 12.50% 35 87.50% 40
2 3 5.80% 49 94.20% 52
3 or more 13 12.10% 94 87.90% 107
Abortions No 17 11.30% 134 88.70% 151 0.82
Yes 6 10.20% 53 89.80% 59
Educational level Illiterate 8 14.80% 46 85.20% 54 0.565
Preparatory 7 8.60% 74 91.40% 81
Secondary 8 11.60% 61 88.40% 69
University 0 0.00% 6 100.00% 6

All 23 GBS isolates were undergone antibiotic susceptibility testing which showed that all isolates were sensitive to penicillin, ampicillin, levofloxacin, cefotaxime, and vancomycin, while the sensitivity to clindamycin and tetracycline decreased to be 82.8% and 30.5%, respectively (Table 2).

Table 2.

Antibiotic susceptibility profile of the 23 vaginal GBS isolates from Yemeni pregnant women in Sana'a city.

Antibiotic agent Antibiotic susceptibility pattern
No. (%) of isolates
S I R
Penicillin G 10 IU 23 (100%) 0 (0%) 0 (0%)
Ampicillin 10 μg 23 (100%) 0 (0%) 0 (0%)
Levofloxacin 5 μg 23 (100%) 0 (0%) 0 (0%)
Cefotaxime 30 μg 23 (100%) 0 (0%) 0 (0%)
Vancomycin 30 μg 23 (100%) 0 (0%) 0 (0%)
Clindamycin 2 μg 19 (82.80%) 2 (8.60%) 2 (8.60%)
Tetracycline 30 μg 7 (30.50%) 5 (21.70%) 11 (47.80%)

S = sensitive, I = intermediate, R = resistant.

4. Discussion

At the community level in Yemen, no research has been carried out to determine the frequency and burden of neonatal infections. According to United States Agency for International Development (USAID) estimates, Yemen still has high under-5 children, infants, and newborns mortality rates (59.6, 45.7, and 28.1 deaths per 1,000 live births, respectively), with an essential portion of this mortality being caused by infectious diseases [27]. Our recent study reported a high proportion of culture-confirmed neonatal sepsis, accounting for two-thirds (77.38%) of neonates admitted to the referral hospitals in Sana'a city [28].

Although prenatal screening for pregnant women is important and beneficial, no official Yemeni guidelines regarding GBS in pregnant women have been established. This cross-sectional study was conducted on 210 Yemeni pregnant women to investigate the prevalence of vaginal colonization by GBS for the first time in Yemen. The present study revealed that 10.95% of Yemeni pregnant women were vaginally colonized by GBS. Given the absence of prenatal screening procedures for Yemeni pregnant women and the resulting lack of access by colonized mothers to antibiotic prophylaxis, this colonization rate entails significant risks. This result is consistent with the findings of several similar studies from developing countries where the GBS vaginal colonization ranged from 10% to 15%. For instance, it was 15% in Bangladesh [29], 10.4% in Ethiopia [30], and 14% in Cameroon [31]. However, GBS vaginal colonization in other countries was reported to be less than that of ours. For example, it was 8.2% in China [32], 7.6% in Saudi Arabia [33], and 2% in India [34], whereas higher colonization rates were reported in other countries, such as 26% in Brazil [35], 19.5% in Jordan [16], and 30.9% in South Africa [36]. The variation of colonization rates among different studies may be attributed to several factors, such as different specimen collection sites (vaginal, rectal, or both), different sample sizes, different personal hygiene practices, different sexual behaviors, antibiotic use, religion and culture beliefs, and different ways to isolate bacteria. The low prevalence in our study may be attributed to the fact that we were unable to persuade the participant to allow us to take a rectal swab. In our study, the relationship between variables (gravida, previous abortions, and educational level) and GBS vaginal colonization was insignificant (P˃0.05) (Table 1). This finding conforms to other research findings, such as [13, 16, 37, 38]. Regarding antibiotic resistance, many earlier studies have been performed to find out the sensitivity of GBS to various antibiotics [24, 39, 40]. Our results showed that all isolates were sensitive to penicillin, ampicillin, levofloxacin, cefotaxime, and vancomycin. These findings are close to the findings of other studies, such as [41] done in Nigeria, [42] in Saudi Arabia, and [30] in Ethiopia. Generally, penicillin is yet the drug of choice for prophylaxis and treatment against GBS colonization and infections. Thus, our result is consistent with other research results concerned with GBS sensitivity to penicillin [30, 39, 42, 43], whereas our result is inconsistent with the Ethiopian study result where the highest resistance was observed against penicillin [44]. Women who were penicillin-allergic clindamycin is recommended for GBS prophylaxis during labor [24]. During the last 10 years, GBS strains had exhibited resistance to other antibiotics, including erythromycin and clindamycin [45]. Clindamycin and/or erythromycin resistant GBS has already been notified earlier, ranging from 0.7% to 51.3% for erythromycin and from 1.7 to 50% for clindamycin [46, 47]. In the current study, the GBS clindamycin resistance level was 8.6%, and this is close to clindamycin resistance level (5.1%) in Saudi Arabia [42]. The different antibiotic sensitivity patterns of GBS among different studies may be attributed to different antibiotic practices and different mutated GBS strains.

5. Conclusion

In Yemen where prenatal screening is not a routine besides boor awareness of the importance of antibiotic intrapartum prophylaxis, 11% of Yemeni pregnant women are GBS vaginal colonized. Fortunately, in our region, all GBS isolates were sensitive to beta-lactam antibiotics; thus, penicillin remains the first choice for treatment and prophylaxis at the prenatal period of mothers who carry these bacteria and are not penicillin allergic. From the context of what was stated in the results, we recommend an official routine prenatal screening for Yemeni pregnant women in order to take appropriate preventive measures and prevent potentially life-threatening infections of newborns.

6. Limitation

One limitation of our study was that the GBS isolates were not subjected to serotyping due to the lack of the required GBS serotyping kit in the Yemeni market.

Acknowledgments

We would like to thank the participants. We equally thank the I lab and Gaza center staffs for providing assistance with specimen collection and microbiological procedures.

Data Availability

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Disclosure

The earlier version of this manuscript was previously posted as a preprint on the Research Square platform [48].

Conflicts of Interest

We declare that we have no competing interests.

References

  • 1.UN. 17 Goals to Transform Our World United Nations: United Nations. 2021. November 2021. https://www.un.org/sustainabledevelopment/
  • 2.Lawn J. E., Blencowe H., Oza S., et al. Every newborn: progress, priorities, and potential beyond survival. The Lancet . 2014;384(9938):189–205. doi: 10.1016/S0140-6736(14)60496-7. [DOI] [PubMed] [Google Scholar]
  • 3.Chou D., Daelmans B., Jolivet R., Kinney M., Say L. Every Newborn Action Plan (ENAP) and Ending Preventable Maternal Mortality (EPMM) working groups. Ending preventable maternal and newborn mortality and stillbirths. BMJ . 2015;351:p. 4255. doi: 10.1136/bmj.h4255. [DOI] [PubMed] [Google Scholar]
  • 4.Alkema L., Chou D., Hogan D., et al. Global, regional, and national levels and trends in maternal mortality between 1990 and 2015, with scenario-based projections to 2030: a systematic analysis by the UN Maternal Mortality Estimation Inter-Agency Group. The Lancet . 2016;387(10017):462–474. doi: 10.1016/S0140-6736(15)00838-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.WHO. Maternal mortality: World Health Organization. 2021. November 2021 https://www.who.int/news-room/fact-sheets/detail/maternal-mortality.
  • 6.WHO. Trends in maternal mortality 2000 to 2017: estimates by WHO, UNICEF, UNFPA, World Bank Group and the United Nations Population Division . 2019. https://apps.who.int/iris/handle/10665/327595 .
  • 7.Liu L., Oza S., Hogan D., et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities: an updated systematic analysis. The Lancet . 2015;385(9966):430–440. doi: 10.1016/S0140-6736(14)61698-6. [DOI] [PubMed] [Google Scholar]
  • 8.Murray C. J., Vos T., Lozano R., et al. Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. The Lancet . 2012;380(9859):2197–2223. doi: 10.1016/S0140-6736(12)61689-4. [DOI] [PubMed] [Google Scholar]
  • 9.Say L., Chou D., Gemmill A., et al. Global causes of maternal death: a WHO systematic analysis. The Lancet Global Health . 2014;2(6):e323–e333. doi: 10.1016/S2214-109X(14)70227-X. [DOI] [PubMed] [Google Scholar]
  • 10.Seale A. C., Blencowe H., Zaidi A., et al. Neonatal severe bacterial infection impairment estimates in South Asia, sub-Saharan Africa, and Latin America for 2010. Pediatric Research . 2013;74(S1):73–85. doi: 10.1038/pr.2013.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Blencowe H., Lee A. C., Cousens S., et al. Preterm birth-associated neurodevelopmental impairment estimates at regional and global levels for 2010. Pediatric Research . 2013;74(S1):17–34. doi: 10.1038/pr.2013.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Lee A. C., Kozuki N., Blencowe H., et al. Intrapartum-related neonatal encephalopathy incidence and impairment at regional and global levels for 2010 with trends from 1990. Pediatric Research . 2013;74(S1):50–72. doi: 10.1038/pr.2013.206. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Darabi R., Tadi S., Mohit M., et al. The prevalence and risk factors of group B Streptococcus colonization in Iranian pregnant women. Electronic Physician . 2017;9(5):4399–4404. doi: 10.19082/4399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Shabayek S., Spellerberg B. Group B streptococcal colonization, molecular characteristics, and epidemiology. Frontiers in Microbiology . 2018;9:p. 437. doi: 10.3389/fmicb.2018.00437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Russell N. J., Seale A. C., O'Driscoll M., et al. Maternal colonization with group B Streptococcus and serotype distribution worldwide: systematic review and meta-analyses. Clinical infectious diseases: an official publication of the Infectious Diseases Society of America . 2017;65(supplement_2):S100–SS11. doi: 10.1093/cid/cix658. Epub 2017/11/09. eng. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Clouse K., Shehabi A., Suleimat A. M., et al. High prevalence of group B Streptococcus colonization among pregnant women in Amman, Jordan. BMC Pregnancy and Childbirth . 2019;19(1):p. 177. doi: 10.1186/s12884-019-2317-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Mohamed A. M., Khan M. A., Faiz A., et al. Group B Streptococcus colonization, antibiotic susceptibility, and serotype distribution among Saudi pregnant women. Infection & Chemotherapy . 2020;52(1):70–81. doi: 10.3947/ic.2020.52.1.70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Wassef M., Ghaith D., Abdella R. M., Kamel M. Rapid screening for group B Streptococcus in near-term pregnant women by Granada™ biphasic broth. The Journal of Maternal-Fetal & Neonatal Medicine . 2017;30(13):1540–1543. doi: 10.1080/14767058.2016.1199679. [DOI] [PubMed] [Google Scholar]
  • 19.Amin A., Abdulrazzaq Y., Uduman S. Group B streptococcal serotype distribution of isolates from colonized pregnant women at the time of delivery in United Arab Emirates. Journal of Infection . 2002;45(1):42–46. doi: 10.1053/jinf.2001.0990. [DOI] [PubMed] [Google Scholar]
  • 20.Hall J., Adams N. H., Bartlett L., et al. Maternal disease with group B Streptococcus and serotype distribution worldwide: systematic review and meta-analyses. Clinical Infectious Diseases . 2017;65(supplement_2):S112–S124. doi: 10.1093/cid/cix660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Seale A. C., Blencowe H., Bianchi-Jassir F., et al. Stillbirth with group B Streptococcus disease worldwide: systematic review and meta-analyses. Clinical Infectious Diseases . 2017;65(supplement_2):S125–S132. doi: 10.1093/cid/cix585. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Madrid L., Seale A. C., Kohli-Lynch M., et al. Infant group B streptococcal disease incidence and serotypes worldwide: systematic review and meta-analyses. Clinical Infectious Diseases . 2017;65(supplement_2):S160–S172. doi: 10.1093/cid/cix656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Seale A. C., Bianchi-Jassir F., Russell N. J., et al. Estimates of the burden of group B streptococcal disease worldwide for pregnant women, stillbirths, and children. Clinical Infectious Diseases . 2017;65(supplement_2):S200–S219. doi: 10.1093/cid/cix664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Verani J. R., McGee L., Schrag S. J. Prevention of perinatal group B streptococcal disease: revised guidelines from CDC, 2010 . 2010. https://www.cdc.gov/Mmwr/preview/mmwrhtml/rr5910a1.htm . [PubMed]
  • 25.Cheesbrough M. District laboratory practice in tropical countries. IJMS . 2018;1(1):65–68. doi: 10.32441/ijms.v1i1.47. [DOI] [Google Scholar]
  • 26.Patel J. B., Cockerill F., Bradford P. A. Performance Standards for Antimicrobial Susceptibility Testing: Twenty-Fifth Informational Supplement . Clinical and Laboratory Standards Institute; 2015. [Google Scholar]
  • 27.Health: Fact sheet: Yemen. U.S. Agency for International Development. (2022, April 22) September 2022, https://www.usaid.gov/yemen/fact-sheets/health-fact-sheet.
  • 28.Salah A., Al-Subol I., Hudna A., et al. Neonatal sepsis in Sana’a city, Yemen: a predominance of Burkholderia cepacia. BMC Infectious Diseases . 2021;21(1):p. 1108. doi: 10.1186/s12879-021-06808-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Saha S. K., Ahmed Z. B., Modak J. K., et al. Group B streptococcus among pregnant women and newborns in Mirzapur, Bangladesh: colonization, vertical transmission, and serotype distribution. Journal of Clinical Microbiology . 2017;55(8):2406–2412. doi: 10.1128/JCM.00380-17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Mengist A., Kannan H., Abdissa A. Prevalence and antimicrobial susceptibility pattern of anorectal and vaginal group B streptococci isolates among pregnant women in Jimma, Ethiopia. BMC Research Notes . 2016;9(1):1–5. doi: 10.1186/s13104-016-2158-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Nkembe N. M., Kamga H. G., Baiye W. A., Chafa A. B., Njotang P. N. Streptococcus agalactiae prevalence and antimicrobial susceptibility pattern in vaginal and anorectal swabs of pregnant women at a tertiary hospital in Cameroon. BMC Research Notes . 2018;11(1):1–6. doi: 10.1186/s13104-018-3589-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Ji W., Zhang L., Guo Z., et al. Colonization prevalence and antibiotic susceptibility of group B Streptococcus in pregnant women over a 6-year period in Dongguan, China. PLoS One . 2017;12(8, article e0183083) doi: 10.1371/journal.pone.0183083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Hussain T. Z. Epidemiology of Group B Streptococcus in Saudi Parturient Women in a Private Hospital. Obstetrics Gynecology: An International Journal . 2015;2015:1–7. doi: 10.5171/2015.376062. [DOI] [Google Scholar]
  • 34.Khatoon F., Nigam A., Sharma N. R., Srivastava R., Sangal R., Malik N. Prevalence and risk factors for group B streptococcal colonization in pregnant women in Northern India. International Journal of Reproduction, Contraception, Obstetrics and Gynecology. . 2016;5(12):4361–4364. doi: 10.18203/2320-1770.ijrcog20164343. [DOI] [Google Scholar]
  • 35.Wollheim C., Sperhacke R. D., Fontana S. K. R., et al. Group B Streptococcus detection in pregnant women via culture and PCR methods. Revista da Sociedade Brasileira de Medicina Tropical . 2017;50(2):179–183. doi: 10.1590/0037-8682-0454-2016. [DOI] [PubMed] [Google Scholar]
  • 36.Monyama M., Bolukaoto J. Y., Chukwu M. O., et al. Group B streptococcus colonisation in pregnant women at Dr. George Mukhari Hospital, South Africa. Southern African Journal of Infectious Diseases . 2016;31(3):74–78. doi: 10.1080/23120053.2016.1156308. [DOI] [Google Scholar]
  • 37.de Melo S. C. C. S., Costa A. B., Silva F. T. R., et al. Prevalence of Streptococcus agalactiae colonization in pregnant women from the 18th health region of Paraná state. Revista do Instituto de Medicina Tropical de São Paulo . 2018;60 doi: 10.1590/s1678-9946201860002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Assefa S., Desta K., Lema T. Group B streptococci vaginal colonization and drug susceptibility pattern among pregnant women attending in selected public antenatal care centers in Addis Ababa, Ethiopia. BMC Pregnancy and Childbirth . 2018;18(1):1–9. doi: 10.1186/s12884-018-1791-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Atalay A., Ölçü M., Perçin D. Antibiotic susceptibilities and serotyping of clinical Streptococcus agalactiae isolates. Balkan Medical Journal . 2011;2011(4):362–365. doi: 10.5174/tutfd.2010.03979.2. [DOI] [Google Scholar]
  • 40.Andrews J. I., Diekema D. J., Hunter S. K., et al. Group B streptococci causing neonatal bloodstream infection: antimicrobial susceptibility and serotyping results from SENTRY centers in the Western Hemisphere. American Journal of Obstetrics and Gynecology . 2000;183(4):859–862. doi: 10.1067/mob.2000.108839. [DOI] [PubMed] [Google Scholar]
  • 41.Ezeonu I., Agbo M. Incidence and anti-microbial resistance profile of group B Streptococcus (GBS) infection in pregnant women in Nsukka, Enugu State, Nigeria. African Journal of Microbiology Research . 2014;8(1):91–95. doi: 10.5897/AJMR12.2307. [DOI] [Google Scholar]
  • 42.Khan M. A., Faiz A., Ashshi A. M. Maternal colonization of group B Streptococcus: prevalence, associated factors and antimicrobial resistance. Annals of Saudi Medicine . 2015;35(6):423–427. doi: 10.5144/0256-4947.2015.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Wang P., Tong J.-j., Ma X.-h., et al. Serotypes, antibiotic susceptibilities, and multi-locus sequence type profiles of Streptococcus agalactiae isolates circulating in Beijing, China. PLoS One . 2015;10(3, article e0120035) doi: 10.1371/journal.pone.0120035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Mengist H. M., Zewdie O., Belew A., Dabsu R. Prevalence and drug susceptibility pattern of group B Streptococci (GBS) among pregnant women attending antenatal care (ANC) in Nekemte Referral Hospital (NRH), Nekemte, Ethiopia. BMC Research Notes . 2017;10(1):1–6. doi: 10.1186/s13104-017-2725-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Nakamura P. A., Schuab R. B. B., Neves F. P., Pereira C. F., de Paula G. R., Barros R. R. Antimicrobial resistance profiles and genetic characterisation of macrolide resistant isolates of Streptococcus agalactiae. Memórias do Instituto Oswaldo Cruz. . 2011;106(2):119–122. doi: 10.1590/S0074-02762011000200001. [DOI] [PubMed] [Google Scholar]
  • 46.Ferjani A., Gozzi C., Boukadida J. Vaginal colonization of the Streptococcus agalactiae in pregnant woman in Tunisia: risk factors and susceptibility of isolates to antibiotics. Bulletin de la Societe de Pathologie Exotique (1990) . 2006;99(2):99–102. [PubMed] [Google Scholar]
  • 47.Boswihi S. S., Udo E. E., Al-Sweih N. Serotypes and antibiotic resistance in group B streptococcus isolated from patients at the Maternity Hospital, Kuwait. Journal of Medical Microbiology . 2012;61(1):126–131. doi: 10.1099/jmm.0.035477-0. [DOI] [PubMed] [Google Scholar]
  • 48.AL-Subol I. H., Abdul-Aziz M., Almikhlafy A. A., Alqahtani T. Y. An initial survey on the prevalence of group B streptococcus (GBS) among Yemeni pregnant women. 2021. [DOI] [PMC free article] [PubMed]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.


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