Research article
Open Access

Prevalence and antimicrobial susceptibility pattern of anorectal and vaginal group B Streptococci isolates among pregnant women in Jimma, Ethiopia

BMC Research Notes20169:351

https://doi.org/10.1186/s13104-016-2158-4

©  The Author(s) 2016

Received: 25 December 2015

Accepted: 13 July 2016

Published: 19 July 2016

Abstract

Background

Streptococcus agalactiae (group B Streptococcus, GBS) is the most frequent pathogen isolated from neonates with invasive bacterial disease and responsible for serious infections in newborns such as pneumonia, septicemia and meningitis. Infection is primarily acquired vertically from mothers colonized with GBS. However, the prevalence and antimicrobial susceptibility pattern of GBS among pregnant women in Ethiopia are less studied.

Methods

This cross-sectional study involved 126 pregnant women at 35–37 weeks of gestation attending the antenatal clinic at Jimma University Hospital. Anorectal and vaginal swabs were cultured on to Todd-Hewitt broth medium supplemented with Gentamicin and Nalidixic acid and subsequently sub-cultured on 5 % sheep blood agar followed by identification of isolates based on colonial morphology, Gram stain, catalase reaction, hippurate hydrolysis and Christie, Atkins, Munch-Petersen (CAMP) test, and testing for their susceptibility to antimicrobial agents using the Kirby–Bauer method.

Results

The overall carriage rate of GBS was 19.0 % (24/126), and the rectal and vaginal carrier rates were 14.3 % (18/126) and 10.4 % (13/126), respectively. Concomitant vaginal and anorectal colonization was recorded in 29.2 % (7/24) of the women who were culture positive. All GBS isolates were susceptible to penicillin G, ampicillin, and vancomycin, but a considerable proportion was resistant to clindamycin (3.2 %), erythromycin (6.5 %), ciprofloxacin (9.7 %), ceftriaxone (9.7 %), norfloxacin (12.9 %), cotrimoxazole (29 %), and tetracycline (45.2 %).

Conclusion

This study reveals high carriage rate of GBS among pregnant women compared to some previous studies in Ethiopia. However, further epidemiological investigations should be done in different parts of the country in order to know the actual GBS colonization rate of pregnant women and to consider the possibility of implementing prophylactic treatment to prevent potential adverse maternal and neonatal outcomes. Future studies should be conducted to reveal serotype distributions of GBS in this community.

Keywords

Group B Streptococcus (GBS) Pregnant women Antimicrobial susceptibility Ethiopia

Background

Streptococcus agalactiae (group B Streptococcus, GBS) is the most frequent pathogen isolated from neonates with invasive bacterial disease and responsible for serious infections in newborns such as pneumonia, septicemia and meningitis [1–3]. GBS is also associated with significant maternal peripartal disease, including bacteremia, endocarditis, chorioamnionitis, endometritis, urinary tract infections, arthritis, and responsible for serious bacterial illness and deaths in nonpregnant women with underlying diseases and in elderly adults [4–7]. GBS can also pass through the cervix without causing serious cervicitis, and cross-intact amniotic membrane causing amnionitis thereby infecting the foetus within the uterus [4].

The lower gastrointestinal tract is considered as the most likely human reservoir of GBS) with a secondary spread to the genitourinary tract. Pregnant women who are GBS carriers have the potential to transmit the organism to their newborns [8]. Because vaginal colonization is believed to be responsible for the intrapartum exposure of neonates to GBS, it is important clinically to identify these women before delivery. In the absence of maternal chemoprophylaxis, up to 50 % of neonates born to colonized women acquire GBS colonization and 1–2 % of these neonates acquire invasive disease [9]. The rate of GBS colonization during pregnancy varies among different countries [10]. A review that has specifically looked at the prevalence of maternal colonization with GBS indicated the estimated mean prevalence of GBS colonization was 17.9 % overall and was the highest in Africa (22.4 %) followed by the Americas (19.7 %) and Europe (19.0 %). However, Studies from Southeast Asia had the lowest estimated mean prevalence (11.1 %) [10]. In this review, significant heterogeneity was noted across and within regions. Differences in the timing of specimen collection in pregnancy, selective culture methods, and study sample size did not explain the heterogeneity [10]. In Ethiopia, the study by Muhammed et al. showed that GBS colonization rates (20.6 %) were higher than reported by Lakew et al. (7.2 %) [11, 12].

Prevention guidelines for perinatal GBS disease were issued by Centers for Disease Control and Prevention (CDC) in 1996 [13]. The recommendations were revised in 2002, when guidelines for prevention of vertical transmission, through routine screening (culture of vaginal and anorectal secretions between the 35th and 37th gestational week) and intrapartum antibiotic prophylaxis of the colonized women was definitely established. Positivity for GBS colonization found during this period of gestation is highly predictive of the presence of GBS at a time of childbirth [14].

In Ethiopia, few studies have been conducted on GBS [11, 12, 15–17] although infant mortality is high in this population. Until today, there are no public health policies or strategies in Ethiopia aimed at the reduction of GBS neonatal infection. This study, therefore, aimed at determining the proportion of pregnant women colonized with GBS and antimicrobial susceptibility pattern of the isolates at Jimma University Hospital.

Methods

Study area and participants

The present cross-sectional study included 126 pregnant women (from 35 to 37 weeks of gestation) who were attending the antenatal clinic at Jimma University Hospital, Jimma, Ethiopia for routine antenatal visits, during the period from July 2012 and December 2012. Jimma is located 355 km southwest of Addis Ababa. At this institution, it is not a common practice to determine colonization status, and hence, not common practice either, to offer prophylaxis.

Data collection

Data was collected by the attending midwifery nurse using a well-structured questionnaire designed to obtain socio-demographic data and other relevant information such as age, occupation, educational level and gravidity from participants following their written informed consent and the ethical approval of the study from Jimma University ethics reviewed board. All consenting mothers with gestation age 35–37 weeks were included. Participants with a history of using antibiotic(s) 2 weeks prior to the study were excluded from the study.

Sample collection and laboratory procedure

Samples were collected by the attending midwifery nurse from the lower third of the vagina and rectum of all participants at 35–37 weeks of gestation using a sterile cotton swab and transported in Amies transport media with charcoal (Oxoid, UK) to the microbiology laboratory. Thereafter, specimens were inoculated in Todd-Hewitt broth (Oxoid, UK), an enrichment medium for GBS, supplemented with 8 µg/ml gentamicin and 15 µg/ml nalidixic acid (Biomerieux, France) to prevent the growth of contaminants. The broth cultures were incubated at 37 °C aerobically. After 18–24 h of incubation, specimens were sub cultured onto 5 % sheep blood agar plates (Oxoid, UK) and re-incubated at the recommended incubation conditions. Observation of cultures was conducted at 24 h and all negative culture plates were re-incubated for an additional 18–24 h and then re-examined. Suspicious GBS colonies were identified by colony morphology, gram stain and biochemical tests such as catalase, sodium hippurate hydrolysis and Christie, Atkins, Munch-Petersen (CAMP) factor positivity’s. Finally, antimicrobial susceptibility of all GBS isolates was determined by Kirby–Bauer disk diffusion method on Mueller–Hinton agar supplemented with 5 % sheep blood according to the guideline recommendations of the Clinical and Laboratory Standards Institute [18]. The following antimicrobial discs and concentrations (in brackets) were used: penicillin G (10 IU), ampicillin (10 μg), clindamycin (2 μg), erythromycin (15 μg), vancomycin (30 μg), ciprofloxacin (5 μg), ceftriaxone (30 μg), cotrimoxazole (25 μg), tetracycline (30 µg), and norfloxacin (10 µg). The plates were incubated at 37 °C for 20–24 h. The results were interpreted according to Clinical and Laboratory Standards Institute guidelines [18].

Statistical analysis

All statistical calculations were done using SPSS for windows version 16. Descriptive statistics were computed to determine the rate of GBS and other variables. The relationships between GBS colonization and various risk factors were tested using the Chi square test. A p value of ≤0.05 was considered indicative of a statistically significant.

Results

Socio-demographic and isolation rate

A total of 126 pregnant women were included within this study. The age of the women ranged from 16 to 40 years with mean age of 26.5 years (SD ±4.9). The majority (37.3 %) of the participants were between the ages of 25–29 years. Among the 126 pregnant women screened, 24 (19 %) were colonized with GBS (Table 1). The rectal and vaginal carrier rates were 18 (14.3 %) and 13 (10.3 %), respectively. Of the 24 carriers, GBS was isolated only from the rectum in 11 (45.8 %), from the vagina in 6 (25 %), and concomitant vaginal and anorectal colonization was recorded in 7 (29.2 %) of the women.
Table 1

Isolation sites and number of GBS carriers (n = 24)

Isolation site

N (%)

Only rectum

11 (8.7)

Only vagina

6 (4.8)

Both vagina and rectum

7 (5.6)

Total

24 (19)

Sociodemographic and obstetric characteristics of the pregnant women are described in Table 2. No associations were detected between risk factors and GBS colonization of the study subjects but the study was not powered to assess these.
Table 2

Association between socio-demographic, obstetric factors and GBS colonization among pregnant women (n = 126)

Variables

Total, n (%)

GBS colonization

P value*

Colonized, n (%)

Non-colonized, n (%)

Age in years

 15–19

7 (5.6)

3 (12.5)

4 (3.9)

0.43

 20–24

36 (28.6)

9 (37.5)

27 (26.5)

 25–29

47 (37.3)

7 (29.2)

40 (39.2)

 30–34

25 (19.8)

4 (16.7)

21 (20.6)

 35–39

9 (7.1)

1 (4.2)

8 (7.8)

 40–44

2 (1.6)

0 (0)

2 (2.0)

Educational level

 Illiterate

17 (13.5)

6 (25)

11 (10.8)

0.32

 Primary

27 (21.4)

5 (20.8)

22 (21.6)

 Secondary

58 (46)

9 (37.5)

49 (48.0)

 Post-secondary

24 (19)

4 (16.7)

20 (19.6)

Occupation

 House wife

81 (64.3)

20 (83.3)

61 (59.8)

0.18

 Employed

34 (27)

3 (12.5)

31 (30.4)

 Merchant

3 (2.4)

0 (0)

3 (2.9)

 Student

8 (6.3)

1 (4.2)

7 (6.9)

Gravidity

 Primigravida

38 (30.2)

5 (20.8)

33 (32.4)

0.27

 Multigravida

88 (69.8)

19 (79.2)

69 (67.6)

Total

126 (100)

24 (19)

102 (81)

* p value: chi squared test comparing colonized and non-colonized pregnant women

Antimicrobial susceptibility pattern of GBS isolates

The susceptibility patterns of GBS (n = 31) isolated from pregnant women against ten antimicrobial agents are presented in Table 3. All GBS isolates were uniformly susceptible to penicillin G, ampicillin, and vancomycin. Relatively, GBS showed low resistance to clindamycin (3.2 %) and erythromycin (6.5 %), and high resistance to cotrimoxazole and tetracycline with 29 and 45.2 %, respectively. Excluding penicillin G, ampicillin, and vancomycin, antibiogram of GBS isolates revealed that only 9 (29 %) isolates were susceptible to all antibiotics tested and 22 (71 %) were resistant to one or more antibiotics tested (data not presented).
Table 3

Antimicrobial susceptibility pattern of GBS (n = 31) isolated from pregnant women

Antibiotics

Susceptible (%)

Intermediate (%)

Resistant (%)

Penicillin G

100

–

0

Ampicillin

100

–

0

Vancomycin

100

–

0

Erythromycin

90.3

3.2

6.5

Ceftriaxone

90.3

–

9.7

Ciprofloxacin

90.3

–

9.7

Clindamycin

87.1

9.7

3.2

Norfloxacin

87.1

–

12.9

Cotrimoxazole

71

–

29

Tetracycline

45.2

9.7

45.2

Discussion

GBS is an important cause of infection in pregnant women and their newborns; however, there have been limited studies available in Ethiopia. Approximately one in five (19 %) pregnant women were colonized with GBS in the present study. In 11 (45.8 %) pregnant women GBS was isolated solely from rectal swabs. These rates of GBS would have been missed if only vaginal swabs were obtained, suggesting the importance of obtaining combined vaginal and anorectal swabs. This is consistent with the findings of other investigators who recommended combined vaginal and rectal swabs to maximize culture yield and increase detection rates [2, 19–21].

The rates of GBS colonization vary widely throughout the world. In Ethiopia, the study by Muhammed et al. (20.6 %) [11] showed GBS colonization rate that was higher than that reported by Schmidt et al. (9 %) [15]. The overall vaginal and anorectal colonization rate of 19 % in our pregnant population is high compared with the study conducted about 27 years ago among postpartum women in Gondar, Ethiopia, which was 9 % [15]. The differences in colonization rate might be due to geographic, as well as differences in the study participant (pregnant versus postpartum).

The prevalence of GBS colonization among pregnant women population has been documented in several countries, including Africa, Americas, Europe and Southeast Asia with the estimated mean prevalence rates ranging from 11.1 to 22.4 %. The lower prevalence of GBS colonization among pregnant women in Southeast Asia (11.1 %) compared to the present study may be related to regional differences in race and geographic area [10, 11, 22, 23]. The effect of race and geographical area on the prevalence of GBS colonization may be related to the differences in nutrition, socioeconomic status, sexually transmitted diseases, host immunity or sexual behavior [24, 25].

Knowledge about risk factors contributing for GBS colonization in pregnant women is relevant to minimize the morbidity, mortality associated with maternal and neonatal GBS infections [11]. In this study, no significant differences on the GBS colonization rate were detected when the socio-demographic and obstetric variables were considered. Unlike to our result, other studies showed that maternal age, education, gravidity and occupation have been observed as risk factors for GBS colonization among pregnant women [25–28]. However, there have been marked inconsistencies in studies that report the relationship between these factors and GBS colonization. For example, some studies showed that the prevalence of GBS increased with age [29], while others found it more with a younger age group [30, 31]. The findings from this study might be due to the small number of study subjects underpowered to find the possible risk factors, and these indicate the need for future large- scale study.

The universal prenatal screening and the risk-based approach are commonly used strategies proposed by the CDC in order to decrease the incidence of early-onset GBS neonatal infection [13, 14]. Before deciding which of these two strategies is to follow, a prevalence of GBS in the population has to be investigated (i.e., does the proportion of colonized pregnant women) with the identification of maternal risk factors.

In this study, all GBS isolates were uniformly sensitive to penicillin, ampicillin and vancomycin, which is consistent with previous reports recommending these antibiotics as the agent of choice for GBS prophylaxis [2, 11, 18, 29]. The proportion of isolates with in vitro resistance to clindamycin and erythromycin, which are considered first-line prophylaxis for those with an allergy to penicillin, has progressively increased since 1996 [14]. The prevalence of resistance among GBS isolates ranged from 7 to 40 % for erythromycin and from 3 to 26.4 % for clindamycin and might be associated with certain serotypes [19, 32, 33]. A relatively high level of resistance to tetracycline and cotrimoxazole in this study might be attributed to the wide and indiscriminate use of antimicrobial drugs. Since in Ethiopia, members from the public easily move into pharmacy shops to buy antibiotics without prescription (personal communication with drug vendors). This use of antibiotics is indiscriminate and might account for the high resistance rates observed.

Conclusions and recommendations

This study reveals that one-fifth of pregnant women harbored GBS, which may pose a risk for the newborns. Therefore, further large-scale studies and data on the prevalence of GBS neonatal disease, preventative measures, and outcome of infected infants are imperative in this community to allow the preventive strategy. The study also indicates uniform susceptibility of GBS isolates from pregnant women to penicillin G, ampicillin and vancomycin. Even though no standard-of–care practices for GBS prevention in this setting, tetracycline and cotrimoxazole should not be used for GBS prevention. Future studies should be conducted to reveal serotype distributions of GBS in this community since monitoring of regional variations in serotype distribution is required to develop and implement effective vaccine for prevention of GBS disease.

Abbreviations

GBS: 

group B Streptococcus

CDC: 

Centers for Disease Control and Prevention

N: 

number

SD: 

standard deviation

Declarations

Authors’ contributions

KH participated in conception and design of the study, acquisition of data, analysis and interpretation of data. AA participated in conception and design of the study, acquisition of data, analysis and interpretation of data; he also participated in drafting and revision of the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors acknowledge the financial support by the Jimma university college of public health and medical sciences, Southern nation nationalities and people’s regional health bureau and Yirgalem hospital.

Competing interests

The authors declare that they have no competing interests.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Medical Laboratory Science, College of Health Science and Medical Sciences, Debre Markos University
(2)
Department of Medical Laboratory Science and Pathology, College of Public Health and Medical Sciences, Jimma University

References

  1. Artz LA, Kempf VAJ, Autenrieth IB. Rapid screening for Streptococcus agalactiae in vaginal specimens of pregnant women by fluorescent in situ hybridization. J Clin Microbiol. 2003;41:2170–3.View ArticlePubMedPubMed CentralGoogle Scholar
  2. Motlova J, Strakova L, Urbaskova P, et al. Vaginal and rectal carriage of Streptococcus agalactiae in the Czech Republic: incidence, serotypes distribution and susceptibility to antibiotics. Indian J Med Res. 2004;119:4–87.Google Scholar
  3. Tor-Udom S, Tor-Udom P, Hiriote W. The prevalence of GBS colonization in pregnant women at Thammasat Hospital. J Med Assoc Thai. 2006;89:411–4.PubMedGoogle Scholar
  4. Dzowela T, Komolafe OO, Igbigbi A. Prevalence of group B Streptococcus colonization in antenatal women at the Queen Elizabeth Central Hospital, Blantyre—a preliminary Study. Malawi Med J. 2005;17:97–9.Google Scholar
  5. Tazi A, Gueudet T, Varon E, Gilly L, Trieu-Cout P, Poyart C. Fluoroquinolone-resistant group B Streptococci in acute exacerbation of chronic bronchitis [letter]. Emerg Infect Dis. 2008;14:349–50.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Phares CR, Lynfield R, Farley MM, et al. Group B streptococcal disease in the United States, 1999–2005. JAMA. 2008;299:2056–65.View ArticlePubMedGoogle Scholar
  7. Sendi P, Johnasson L, Dahesh S, et al. Bacterial phenotype variants in group B streptococcal toxic shock syndrome. Emerg Infect Dis. 2009;15:223–32.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Cunningham FG, Leveno KJ, Bloom SL, Hauth JC, Gilstrap L, Wenstrom KD. Williams obstetrics. 22nd ed. New York: McGraw-Hill; 2005. p. 1284–99.Google Scholar
  9. Easmon CS, Hastings MJ, Neill J, et al. Is group B streptococcal screening during pregnancy justified? Br J Obstet Gynaecol. 1985;92:197–201.View ArticlePubMedGoogle Scholar
  10. Kwatra G, Cunnington MC, Merrall E, et al. Prevalence of maternal colonisation with group B streptococcus: a systematic review and meta-analysis. Lancet Infect Dis. 2016. doi:https://doi.org/10.1016/S1473-3099(16)30055-X.PubMedGoogle Scholar
  11. Mohammed M, Asrat D, Woldeamanuel Y, Demissie A. Prevalence of group B Streptococcus colonization among pregnant women attending antenatal clinic of Hawassa Health Center, Hawassa, Ethiopia. Ethiop J Health Dev. 2012;26:36–42.Google Scholar
  12. Lakew Zw, Gebreegziabher TT, Teklu SM, Yigeremu MG. The prevalence of Group B Streptococus recto-vaginal colonization and antimicrobial susceptibility pattern in pregnant mothers at two hospitals of Addis Ababa, Ethiopia. Rep Health. 2014;11:80.View ArticleGoogle Scholar
  13. Centers for Disease Control and Prevention (CDC). Prevention of perinatal group B streptococcal disease: a public health perspective. MMWR Recomm Rep. 1996;45:1–24.Google Scholar
  14. Schrag S, Gorwitz R, Fultz-Butts K, Schuchat A. Prevention of perinatal group B streptococcal disease. Revised guidelines from CDC. MMWR Recomm Rep. 2002;51:1–22.PubMedGoogle Scholar
  15. Schmidt J, Halle H, Mohammed T, Gunther E. Colonization of pregnant women and their newborn infants with group B streptococci in the Gondar College of Medical Sciences. Ethiop Med J. 1989;27:115–9.PubMedGoogle Scholar
  16. Kahsay TG, Abebe TZ, Mihret A, Desta MT. Prevalence and antibiotic susceptibility pattern of Streptococcus agalactiae among pregnant women at Adigrat Zonal Hospital and Adigrat Health Center, Tigray, Ethiopia. J Gynecol Obstet. 2015;3:29–35.View ArticleGoogle Scholar
  17. Alemseged G, Niguse S, Hailekiros H, Abdulkadir M, Saravanan M, Asmelash T. Isolation and anti-microbial susceptibility pattern of group B Streptococcus among pregnant women attending antenatal clinics in Ayder Referral Hospital and Mekelle Health Center, Mekelle, Northern Ethiopia. BMC Res Notes. 2015;8:518.View ArticlePubMedPubMed CentralGoogle Scholar
  18. Cockerill FR, Wikler MA, Bush K, et al. Performance standard for antimicrobial susceptibility testing; twentieth information supplement. CLSI. 2011;31:1–153.Google Scholar
  19. Abdelmoaty A, Zaki W, Mohammed K. Prevalence and antibiotic susceptibility of anogenital GBS colonization in pregnant women: a hospital based study. Egypt J Med Lab Sci. 2009;18:105–11.Google Scholar
  20. Badri MS, Zawaneh S, Cruz AC, et al. Rectal colonization with group B streptococcus: Relation to vaginal colonization of pregnant women. J Infect Dis. 1977;135:308–12.View ArticlePubMedGoogle Scholar
  21. El-Kersh TA, Al-Nuaim LA, Kharfy TA, et al. Detection of genital colonization of group B Streptococci during late pregnancy. Saudi Med J. 2002;23:56–61.PubMedGoogle Scholar
  22. Whitney CG, Daly S, Limpongsanurak S, et al. The international infections in pregnancy study: group B streptococcal colonization in pregnant women. J Mat FET Neo Med. 2004;15:267–74.Google Scholar
  23. Colbourn T, Gilbert R. An overview of the natural history of early-onset group B streptococcal disease in the UK. Early Human Dev. 2007;83:149–56.View ArticlePubMedGoogle Scholar
  24. Jahromi BN, Poorarian S, Poorbarfehee S. The prevalence and adverse effects of group B streptococcal colonization during pregnancy. Arch Iranian Med. 2008;11:654–7.Google Scholar
  25. Kim EJ, Young OK, Young KM, et al. Risk factors for group B Streptococcus colonization among pregnant women in Korea. Epidemiol Health. 2011;33:e2011010–6.PubMedPubMed CentralGoogle Scholar
  26. Eren A, Kakercan M, Oguzoglu N, Unal N, Karateke A. The carriage of group B Streptococci in Turkish pregnant women and its transmission rate in newborns and serotype distribution. Turk J Pediatr. 2005;47:28–33.PubMedGoogle Scholar
  27. Tsui HY, Ip M, Ng P, Sahota DS, Leung T, Lau T. Change in prevalence of group B Streptococcus maternal colonization in Hong Kong. Hong Kong Med J. 2009;15:C1–66.Google Scholar
  28. Tsolia M, Psoma M, Gavrili S, et al. Group B Streptococcus colonization of Greek pregnant women and neonates: prevalence, risk factors and serotypes. Clin Microbiol Infect. 2003;9:832–8.View ArticlePubMedGoogle Scholar
  29. Orrett FA. Colonization with group B Streptococci in pregnancy and outcome of infected neonates in Trinidad. Pediatr Int. 2003;45:319–23.View ArticlePubMedGoogle Scholar
  30. Schuchat A, Deaver-Robinson K, Plikaytis BD, Zangwill KM, Mohle-Boetani J, Wenger JD. Multistate case–control study of maternal risk factors for group B streptococcal disease. The Active Surveillance Study Group. Ped Infect Dis J. 1994;13:623–9.View ArticleGoogle Scholar
  31. Kadanali A, Altoparlak U, Kadanali S. Maternal carriage and neonatal colonization of group B Streptococcus in eastern Turkey: prevalence, risk factors and antimicrobial resistance. Int J Clin Pract. 2005;59:437–40.View ArticlePubMedGoogle Scholar
  32. Ulett KB, Benjamin WH, Zhuo JF, et al. Diversity of group B Streptococcus serotypes causing urinary tract infection in adults. J Clin Microbiol. 2009;47:2055–60.View ArticlePubMedPubMed CentralGoogle Scholar
  33. Orji FA, Nwachukwu NC, Iheukwumere I, Emeana U. GBS infections among infants in Port Harcourt city, Nigeria. Aust J Basic Appl Sci. 2011;5:1114–8.Google Scholar

Copyright

© The Author(s) 2016

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