- Open Access
Fecal carriage and factors associated with extended-spectrum β-lactamase-producing Enterobacteriaceae among pregnant women at the tertiary referral hospital, Tanzania
Tropical Medicine and Health volume 48, Article number: 84 (2020)
Infections due to extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) are increasing worldwide. Evidence indicates that fecal carriage of ESBL-E in pregnancy predisposes women to potential life-threatening urinary tract infections and subsequently increasing the risk of neonatal infections. There is limited data regarding fecal carriage of ESBL-E and associated factors among pregnant women in Tanzania. We aimed to address the gap by determining the proportion of pregnant women with ESBL-E fecal carriage and identify the related factors.
A hospital-based cross-sectional study was conducted at Muhimbili National Hospital in Dar es Salaam, Tanzania. A total of 182 pregnant women at the gestational age of 37 weeks and above were enrolled. Participants’ socio-demographic, clinical, and hygienic information were collected by using a well-structured questionnaire. Rectal swabs were collected and processed for isolation of ESBL-E. The extended-spectrum β-lactamase production and antibiotic susceptibility test (AST) were performed using a double-disc synergy test and Kirby-Bauer disc diffusion method, respectively.
A total of 117 (64.3%) pregnant women were found to carry ESBL-E. Factors such as self-prescription of antibiotic medication during pregnancy, low education level, and toilet sharing were independently associated with ESBL-E fecal carriage. Five ESBL-E species that were isolated include Escherichia coli (84.6%), Klebsiella pneumoniae (8.9%), Klebsiella oxytoca (3.3%), Citrobacter spp. (1.6%), and Enterobacter spp. (1.6%). ESBL-E isolates demonstrated high resistance to aztreonam and sulphamethoxazole-trimethoprim.
This study has revealed a relatively high fecal carriage of ESBL-E among pregnant women, suggesting that there is a need for routine screening among that population. We recommend further studies to explore comprehensively the factors associated with high fecal carriage of ESBL-E in pregnancy and the potential transmission kinetics to their newborn babies.
Antimicrobial resistance (AMR) is an emerging challenge in humans worldwide . Extensive use of antibiotics in humans, animals, and plants may induce continuous and dynamic mutations to the bacteria . Mutations can result in the production of resistant genes such as those encoding for extended-spectrum β-lactamase (ESBL) enzymes, which confer multidrug resistance . Previous studies have reported the fecal carriage of ESBL-producing Enterobacteriaceae (ESBL-E) to range from 3.2 to 67.9% [4,5,6,7,8]. Around 110 million individuals in Africa are estimated to be ESBL-E carriers, which is attributed to high population density, disadvantaged access to drinking water, and poverty . A study conducted in Tanzania reported ESBL-E fecal carriage of 11.6% among healthy children that resulted from extensive use of antibiotics .
Globally, the fecal carriage rate of ESBL-E among pregnant women is reported to range from 7.3 to 15.4%, which is comparable to the healthy population in different regions [11,12,13]. In Africa, ESBL-E fecal carriage average is 17% among pregnant women  and 15% in post-delivery women . The main concern of ESBL-E fecal carriage in pregnancy is the increased risk of transmission of these resistant strains to newborn babies that subsequently may contribute to neonatal sepsis [13, 16]. Also, ESBL-E carriage increases the risk of transmission to health care providers and other hospitalized patients.
Furthermore, pregnant women are among the immunocompromised group, who are prone to different bacterial infections. The colonization of ESBL-E in the urinary tract of pregnant women due to fecal-vaginal transmission often results in urinary tract infection (UTI) [17, 18]. Globally, the proportion of pregnant women colonized by ESBL-E in the urinary tract ranges from 2.0 to 75%, the highest percentage found in developing countries [19, 20]. In Africa, a high proportion above 70% is seen in sub-Saharan countries due to extensive antibiotic use in agriculture, veterinary, and human health centers [14, 21]. In Tanzania, the proportion of ESBL-E to urinary isolates in pregnant women ranges between 18.8 and 45.2% .
In our setting, there is limited data on ESBL-E carriage among pregnant women. Therefore, this study determined the fecal carriage of ESBL-E among pregnant women, associated factors, and antimicrobial resistance patterns of ESBL-E bacteria isolates.
Materials and methods
Study design and settings
The study was a hospital-based cross-sectional design conducted from February to May 2019 at Muhimbili National Hospital (MNH) in Dar es Salaam, Tanzania. The MNH is the largest tertiary health care facility in Tanzania with 25 departments, 106 service units, and a 1500-bed capacity. The hospital serves as a research center, university teaching hospital, and a referral hospital. Around 1000 to 1200 outpatients attend different clinics per day with about 1000 to 1200 admissions per week. A total of 2700 employees, including 300 doctors, 900 nurses, and 1500 supporting staffs, are available at the facility. In this hospital, pregnant women attend at least four visits at an interval of 4 weeks, starting at 12-week gestational age. The clinic provides antenatal services to an average of 700 pregnant women per month, with approximately 25 pregnant women per clinic visit. On average, nearly a quarter of pregnant women attending per month have a gestational age equal to or greater than 37 weeks. The total number of deliveries at MNH from January to December 2019 was approximately 2126.
Study population, sample size, and sampling procedure
The study enrolled pregnant women who were at the gestational age of 37 weeks and above attending the antenatal clinic and consented to participate. Pregnant women with known increased risks for bacterial colonization, such as gestational diabetes, history of prolonged hospital stay during pregnancy, malignancy, and renal and liver diseases, were not eligible for inclusion in the study.
The study used the Kish Leslie formula, n = z2 p(1 − p)/e2, to calculate the sample size. In the formula, “n” stands for the required minimum sample size and “z” is the value for the level of confidence (1.96) at a 95% confidence interval. The expected proportion (p) of ESBL-E among pregnant women was estimated at 18.5% from a study conducted in Madagascar , and the margin of error “e” was 6%. The minimum required sample size was estimated to be 161 pregnant women. Convenient sampling was used to recruit pregnant women in the study. New eligible pregnant women were consecutively enrolled during their clinic visit until the representative sample size was attained.
A well-structured questionnaire was used to collect socio-demographic information (age and level of education), history of self-prescription of antibiotic, and hygienic practices (the type of toilet, toilet sharing, handwashing, and use of treated drinking water). The antenatal card was the source of clinical information that included gestational age, number of parity, HIV status, and comorbidities.
Education level was classified as a low level for primary education and below and as a high level for secondary education and above. The self-prescription of antibiotic medication in pregnancy was defined as the use of any antibiotic without a clinician’s prescription during pregnancy at least once in the last 4 weeks. The type of toilet used was the one available at home in the previous 3 months. Toilet sharing in pregnancy meant the use of a common/public toilet at home used by more than one individual in the last 3 months. Handwashing with soap before eating was counted when hands were washed with soap every day during the main meals in the previous week. Handwashing with soap after defecation was defined when soap was used to wash hands after defecation every day in the last week. The use of treated drinking water was considered when treated water was used for drinking at least once a day in the previous week.
Sample collection and laboratory procedures
Rectal swabs were collected from pregnant women by trained medical personnel. Briefly, the medical personnel inserted a sterile cotton wool swab in the rectum for about 10 s. Then, the collected specimen was kept into the Cary-Blair medium and then transported to the Central Pathology Laboratory (CPL) within 2 h after collection .
The rectal swab specimen was inoculated onto MacConkey agar (MCA), supplemented with 2.0 μg/ml ceftazidime and incubated aerobically at 37 °C overnight . Preliminary identification of isolates was based on colonial morphology and Gram staining properties. All isolates were sub-cultured on nutrient agar (NA) and incubated aerobically at 37 °C overnight. Isolates from NA were identified using conventional biochemical tests. The identification tests included the oxidase test, Kligler Iron Agar, Sulfur-Indole-Motility test, Simmons’ citrate test, and urease test, as previously described . Isolates were confirmed as ESBL-E by a double-disc synergy test .
Five antibiotic discs: gentamicin (10 μg), aztreonam (30 μg), sulphamethoxazole-trimethoprim (1.25/23.75), meropenem (10 μg), and ciprofloxacin (5 μg), were used for the antibiotic susceptibility test by using the Kirby-Bauer disc diffusion method. Except for aztreonam, the remained discs were chosen because they were reported to be susceptible to ESBL-E [15, 27, 28], whereas aztreonam was tested for susceptibility to check if all ESBL-E isolates are either resistant to aztreonam or not. The resistance pattern was defined based on the Clinical and Laboratory Standard Institute (CLSI) guidelines of 2018.
All reference organisms and reagents were clearly and uniquely labeled, dated, and stored at optimal conditions. The operating temperatures of the refrigerator and incubator were monitored and documented daily. All culture media were prepared following the manufacturer’s guidelines and internal standard operating procedures and were tested for performance and sterility. We standardized the turbidity of isolate suspension with a 0.5 McFarland standard. As per CLSI (2018), Klebsiella pneumoniae (ATCC-700603) and Escherichia coli (ATCC-25922) were the positive and negative control bacteria strains, respectively .
STATA version 15.1 software was used for statistical analysis. Continuous variables were summarized as the median and interquartile range (IQR), whereas proportions were used to describe categorical variables. Group differences were examined by using Fisher’s exact test for categorical variables and t test for continuous variables. Binary logistic regression was performed to identify factors associated with ESBL-E fecal carriage among pregnant women depending on the crude odds ratio (COR) with a 95% confidence interval (CI). Multivariable logistic regression was performed to examine the associations between the outcome variable and independent variables after adjustment of all the factors that showed significance in the bivariate analysis, such as education level, self-prescription of antibiotic medication during pregnancy, toilet sharing, and handwashing with soap after defecation. Associations in the multivariable logistic models were presented as adjusted odds ratios (AOR) with 95% CI. A two-sided p value < 0.05 was considered significant.
Characteristics and hygienic practices of the study participants
A total of 182 pregnant women with a median age of 29 years, IQR [25–32], with gestational age, and parity of 39 weeks, IQR [40–38], and 2, IQR [3–1], respectively, were enrolled in the study. Out of 182, 56.0% had a high level of education, and 95.0% were HIV seronegative. Furthermore, 52.2% (95/182) of the participants reported self-prescription of antibiotic medication during pregnancy (Table 1). A total of 154 (84.6%) participants were using flush toilets, whereby 86 (74.7%) reported sharing toilets. Concerning hygiene practices, the majority (87.4%) reported washing hands using soap before eating. Likewise, 85.7% affirmed washing hands using soap after defecation, and 62.1% reported the use of treated drinking water (Table 1).
Fecal carriage of ESBL-E
The fecal carriage of ESBL-E was detected in 117 (64.3%) pregnant women. Participants with a history of self-prescription of antibiotic medication during the current pregnancy were more colonized with ESBL-E than those without a history of self-prescription of antibiotic medication (p < 0.001). Not washing hands with soap after defecation and toilet sharing were associated with higher fecal carriage of ESBL-E (p < 0.05). We observed a trend of decrease in the proportion of ESBL-E fecal carriage with an increase in participants’ education level. The difference between low (77.5%) and high (53.9%) education levels was significant (p = 0.001). The differences of ESBL-E fecal carriage between the categories among age groups, gestational age, parity, HIV status, types of toilet used, handwashing with soap before eating, and use of treated water was not significant (p > 0.05) (Table 2).
Predictors of ESBL-E fecal carriage
By using bivariate analysis, participants with low education level were observed to have three times more odds of ESBL-E fecal carriage than participants with high education level (cOR 2.94, 95% CI 1.53–5.66). The self-prescription of antibiotic medication during pregnancy had an increased probability of ESBL-E fecal carriage (cOR, 2.92, 95% CI 1.56–5.49). Toilet sharing and hand washing after defecation had 2.5 and 3.5 times the odds of ESBL-E fecal carriage, respectively (Table 3).
On multivariate analysis, the factors that were independently associated with ESBL-E fecal carriage were education level, self-prescription of antibiotic medication during pregnancy, and toilet sharing. The odds of carrying ESBL-E were two times higher among participants having a low education level than high education level (aOR = 2.19, 95% CI = 1.08–4.43). Participants with a history of self-prescription of antibiotic medication had three times higher probability of carrying ESBL-E (aOR = 3.11, 95% CI = 1.59–6.01). The odds of carrying ESBL-E was two times higher among those who shared toilets during their pregnancy (aOR = 2.39, 95% CI = 1.10–5.21) (Table 4).
ESBL-E species and antimicrobial resistance patterns
Five bacterial species were identified among 123 isolates. Escherichia coli was the most predominant with a proportion of 84.6%, followed by Klebsiella pneumoniae (8.9%), Klebsiella oxytoca (3.3%), Citrobacter spp. (1.6%), and Enterobacter spp. (1.6%) (Fig. 1).
The antibiotic susceptibility test was conducted using five drugs. Aztreonam was highly resisted by Citrobacter spp. (100.0%), K. pneumoniae (90.9%), E. coli (85.6%), and K. oxytoca (75.0%). High resistance to sulphamethoxazole-trimethoprim was shown by Enterobacter spp. (100.0%), E. coli (76.0%), K. oxytoca (75.0%), and K. pneumoniae (63.6%). Resistance to ciprofloxacin was the lowest ranging from 0 to 25%. Among ESBL-E isolates, K. oxytoca was found to have the highest resistance to most antibiotics tested, while Citrobacter spp. had the least resistance compared to all other isolates (Table 5).
This study revealed a high fecal carriage of ESBL-E among pregnant women, which coincide with findings by Djuikoue et al. in Cameroon that reported the fecal carriage of 66.3% in a similar population . In contrast, other studies have reported a lower fecal carriage compared to our findings. For example, Fortin et al. in Nigeria reported the fecal carriage of 31.7% , Chereau et al. in Madagascar reported 18.6% , and Nelson et al. in Mwanza, Tanzania reported 15% . Several factors may attribute to the high ESBL-E fecal carriage rate reported in this study, including misuse of antibiotics, low level of education, and poor hygienic practices.
The majority of women with ESBL-E fecal carriage had a low level of education, indicating an increased risk of ESBL-E fecal carriage with a low level of education; which is consistent with results from other previous studies [17, 30]. The low level of education could be accompanied by a lack of knowledge that predisposes these women to misuse of antibiotics and poor hygienic practices. These factors have been previously reported to be associated with ESBL-E carriage [11, 26,27,28].
We observed that the irrational use of antibiotics during pregnancy was significantly associated with ESBL-E carriage. The participants who had self-prescription of antibiotic medication had an increased chance of ESBL-E fecal carriage. This finding is comparable with other studies that have demonstrated an association between prior antibiotic exposure and carriage or infection with ESBL-E [15, 29, 31]. In this study, pregnant women who reported sharing toilets with others had a high risk of carrying ESBL-E. The increased risk might be influenced by poor toilet cleanliness and self-hygienic practices, which create a high chance of transmission of resistant pathogens [32,33,34].
In the present study, we observed that ESBL-E had low and moderate resistance to ciprofloxacin and gentamicin as well as meropenem, respectively. However, ESBL-E demonstrated high resistance to aztreonam and sulphamethoxazole-trimethoprim. These findings concur with other studies [15, 35, 36]. With the current status of an increase in antimicrobial resistance, our findings emphasize the need to perform susceptibility tests for ESBL pathogens to provide guidance on the drug of choice for treatment in our setting.
Our study may have some limitations. First, the findings from hospital-based design cannot be generalized to the community as there might be selection bias. The study recruited pregnant women at the last visit, so there is a possibility that these participants contacted ESBL-E during other antenatal visits rather than from the community. Second, we acknowledge that reliance on self-reported information may have introduced the recall bias; because some questions are required to recall back as far as 3 months. Thirdly, the study was not able to determine the seasonality of ESBL-E prevalence. Lastly, the study was conducted in a tertiary hospital where there is an increase in accessibility of antibiotics in the urban area compared to suburban and rural areas; hence, the present findings cannot be generalized.
The fecal carriage of ESBL-E among pregnant women is relatively high, and most of the isolates are resistant to some antibiotics commonly used in our settings. We observed that prior exposure to antibiotics increases the possibility of ESBL-E carriage. The findings indicate that antimicrobial stewardship is essential for checking the susceptible drugs for treating ESBL-E-associated infections. Our findings suggest a need to undertake comprehensive precaution measures by providing health education to the health care providers and patients on the prevention of nosocomial transmission. In light of these findings, more studies are needed to determine further the risk of transmission to the newborns from mothers who are colonized by ESBL-E and determine the antibiotic profile for ESBL-producing bacteria.
Availability of data and materials
All relevant data generated and analyzed during this study are available from the corresponding author on reasonable request.
Antibiotic susceptibility test
Clinical Laboratory Standard Institute
Double-disc synergy test
Extended-spectrum beta-lactamase-producing Enterobacteriaceae
Human immunodeficiency virus
Muhimbili National Hospital
Muhimbili University of Health and Allied Sciences
Urinary tract infection
World Health Organization
World Health Organization. Antimicrobial resistance: global report on surveillance. World Health Organization; 2014. Section 1: resistance to antibacterial drugs; p. 1-5. https://www.who.int/antimicrobial-resistance/publications/infographic-antimicrobial-resistance-20140430.pdf?ua=1. Accessed 17th August 2020.
Nikaido H. Multidrug resistance in bacteria. Annu Rev Biochem. 2009;78:119–46.
Bradford PA. Extended-spectrum beta-lactamases in the 21st century: characterization, epidemiology, and detection of this important resistance threat. Clin Microbiol Rev. 2001;14(4):933–51.
Kader AA, Kamath KA. Faecal carriage of extended-spectrum beta-lactamase-producing bacteria in the community. East Mediterr Health J. 2009;15(6):1365–70.
Herindrainy P, Randrianirina F, Ratovoson R, Ratsima Hariniana E, Buisson Y, Genel N, Decre D, Arlet G, Talarmin A, Richard V. Rectal carriage of extended-spectrum beta-lactamase-producing gram-negative bacilli in community settings in Madagascar. PLoS One. 2011;6(7):e22738.
Hawkey PM. Prevalence and clonality of extended-spectrum beta-lactamases in Asia. Clin Microbiol Infect. 2008;14(Suppl 1):159–65.
Friedmann R, Raveh D, Zartzer E, Rudensky B, Broide E, Attias D, Yinnon AM. Prospective evaluation of colonization with extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae among patients at hospital admission and of subsequent colonization with ESBL-producing Enterobacteriaceae among patients during hospitalization. Infect Control Hosp Epidemiol. 2009;30(6):534–42.
Rodriguez-Bano J, Lopez-Cerero L, Navarro MD, Diaz de Alba P, Pascual A. Faecal carriage of extended-spectrum beta-lactamase-producing Escherichia coli: prevalence, risk factors and molecular epidemiology. J Antimicrob Chemother. 2008;62(5):1142–9.
Woerther PL, Burdet C, Chachaty E, Andremont A. Trends in human fecal carriage of extended-spectrum β-lactamases in the community: toward the globalization of CTX-M. Clin Microbiol Rev. 2013;26(4):744–58.
Tellevik MG, Blomberg B, Kommedal Ø, Maselle SY, Langeland N, Moyo SJ. High prevalence of faecal carriage of ESBL-producing Enterobacteriaceae among children in Dar es Salaam. Tanzania. 2016;11(12):e0168024.
Sáez-López E, Guiral E, Fernández-Orth D, Villanueva S, Goncé A, López M, et al. (2016) Vaginal versus obstetric infection Escherichia coli isolates among pregnant women: antimicrobial resistance and genetic virulence profile. PLoS One. 2016;11(1):e0146531.
Pathak A, Chandran SP, Mahadik K, Macaden R, Lundborg CS. Frequency and factors associated with carriage of multidrug resistant commensal Escherichia coli among women attending antenatal clinics in Central India. BMC Infect Dis. 2013;13:199.
Denkel LA, Schwab F, Kola A, Leistner R, Garten L, von Weizsäcker K, Geffers C, Gastmeier P, Piening B. The mother as most important risk factor for colonization of very low birth weight (VLBW) infants with extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E). J Antimicrob Chemother. 2014;69(8):2230–7.
Bulabula AN, Dramowski A, Mehtar S. Maternal colonization or infection with extended-spectrum beta-lactamase-producing Enterobacteriaceae in Africa: a systematic review and meta-analysis. Int J Infect Dis. 2017;64:58–66.
Nelson E, Kayega J, Seni J, Mushi MF, Kidenya BR, Hokororo A, Zuechner A, Kihunrwa A, Mshana SE. Evaluation of existence and transmission of extended spectrum beta lactamase producing bacteria from post-delivery women to neonates at Bugando Medical Center. Mwanza-Tanzania. BMC Res Notes. 2014;7:279.
Rettedal S, Löhr IH, Bernhoff E, Natås OB, Sundsfjord A, Øymar K. Extended-spectrum β-lactamase-producing Enterobacteriaceae among pregnant women in Norway: prevalence and maternal–neonatal transmission. J Perinatol. 2015;35(11):907–12.
Watt S, Lanotte P, Mereghetti L, Moulin-Schouleur M, Picard B, Quentin R. Escherichia coli strains from pregnant women and neonates: intraspecies genetic distribution and prevalence of virulence factors. J Clin Microbiol. 2003;41(5):1929–35.
Obata-Yasuoka M, Ba-Thein W, Tsukamoto T, Yoshikawa H, Hayashi H. Vaginal Escherichia coli share common virulence factor profiles, serotypes and phylogeny with other extraintestinal E. coli. Microbiology. 2002;148(Pt 9):2745–52.
Padmavathy K, Krishnan P, Rajasekaran S. Fluoroquinolone resistance among CTX-M producing uropathogenic Escherichia coli from HIV and non-HIV patients in South India. BMC Infect Dis. 2014;14:P63.
Bouchillon SK, Johnson BM, Hoban DJ, Johnson JL, Dowzicky MJ, Wu DH, Visalli MA, Bradford PA. Determining incidence of extended spectrum β-lactamase producing Enterobacteriaceae, vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus in 38 centres from 17 countries: the PEARLS study 2001–2002. Int J Antimicrob Agents. 2004;24(2):119–24.
Tansarli GS, Poulikakos P, Kapaskelis A, Falagas ME. Proportion of extended-spectrum β-lactamase (ESBL)-producing isolates among Enterobacteriaceae in Africa: evaluation of the evidence—systematic review. J Antimicrob Chemother. 2014;69(5):1177–84.
Moyo SJ, Aboud S, Kasubi M, Lyamuya EF, Maselle SY. Antimicrobial resistance among producers and non-producers of extended spectrum beta-lactamases in urinary isolates at a tertiary Hospital in Tanzania. BMC Res Notes. 2010;3:348.
Chereau F, Herindrainy P, Garin B, Huynh BT, Randrianirina F, Padget M, Piola P, Guillemot D, Delarocque-Astagneau E. Colonization of extended-spectrum-β-lactamase-and NDM-1-producing Enterobacteriaceae among pregnant women in the community in a low-income country: a potential reservoir for transmission of multiresistant Enterobacteriaceae to neonates. Antimicrob Agents Chemother. 2015;59(6):3652–5.
Cheesbrough M. District laboratory practice in tropical countries. 2nd Edi. Cambridge University Press; 2006. Chapter 3: examination of faecal specimen; p. 97-105.
Dr. Rao SP. Extended spectrum beta-lactamases-a comprehensive review. 2015. Chapter 5: laboratory detection of ESBLs; p. 49-51.
Dhara M, Disha P, Sachin P, Manisha J, Seema B, Vegad M. Comparison of various methods for the detection of extended spectrum beta-lactamase in Klebsiella pneumoniae isolated from neonatal intensive care unit. National J Med Res. 2012;2:348–53.
Marwa KJ, Mushi MF, Konje E, Alele PE, Kidola J, Mirambo MM. Resistance to cotrimoxazole and other antimicrobials among isolates from HIV/AIDS and non-HIV/AIDS patients at Bugando Medical Centre, Mwanza. Tanzania. AIDS Res Treat. 2015;2015:103874.
Seni J, Najjuka CF, Kateete DP, Makobore P, Joloba ML, Kajumbula H, Kapesa A, Bwanga F. Antimicrobial resistance in hospitalized surgical patients: a silently emerging public health concern in Uganda. BMC Res Notes. 2013;6:298.
Institute Cliniacal and Laboratory Standards. M100 Performance Standards for Antimicrobial. 28th ed; 2018.
Djuikoue IC, Woerther PL, Toukam M, Burdet C, Ruppé E, Gonsu KH, Fokunang C, El Mniai A, Larissa K, Pieme AC, Mboupaing MG. Intestinal carriage of extended spectrum beta-lactamase producing E. coli in women with urinary tract infections, Cameroon. J Infect Dev Ctries. 2016;10:1135–9.
Fortini D, Fashae K, Villa L, Feudi C, García-Fernández A, Carattoli A. A novel plasmid carrying blaCTX-M-15 identified in commensal Escherichia coli from healthy pregnant women in Ibadan. Nigeria. J Glob Antimicrob Resist. 2015;3(1):9–12.
Kagia N, Kosgei P, Ooko M, Wafula L, Mturi N, Anampiu K, Mwarumba S, Njuguna P, Seale AC, Berkley JA, Bottomley C. Carriage and acquisition of extended-spectrum β-lactamase–producing Enterobacterales among neonates admitted to hospital in Kilifi. Kenya. Clin Infect Dis. 2019;69(5):751–9.
Mandal DK, Sah SK, Mishra SK, Sharma S, Kattel HP, Pandit S, Yadav PK, Laghu U, Lama R, Sah NP, Sherchand JB, Parajuli K, Bastola A, Pun SB, Rijal BP, Pokharel BM. Carriage of extended-spectrum-β-lactamase- and AmpC-β-lactamase-producing Enterobacteriaceae (ESBL-PE) in healthy community and outpatient department (OPD) patients in Nepal. Can J Infect Dis Med Microbiol. 2020;2020:5154217.
Day MJ, Hopkins KL, Wareham DW, Toleman MA, Elviss N, Randall L, Teale C, Cleary P, Wiuff C, Doumith M, Ellington MJ. Extended-spectrum β-lactamase-producing Escherichia coli in human-derived and foodchain-derived samples from England, Wales, and Scotland: an epidemiological surveillance and typing study. Lancet Infect Dis. 2019;19(12):1325–35.
Bishara J, Livne G, Ashkenazi S, Levy I, Pitlik S, Ofir O, Lev B, Samra Z. Antibacterial susceptibility of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae and Escherichia coli. Isr Med Assoc J. 2005;7(5):298–301.
Falagas ME, Karageorgopoulos DE. Extended-spectrum β-lactamase-producing organisms. J Hosp Infect. 2009;73(4):345–54.
The authors would like to acknowledge all patients who participated in this study. We wish to thank nurses from MNH who assisted in patient recruitment and specimen collection. We also thank all staff from the Microbiology Department, CPL, at MNH for their dedicated cooperation during laboratory works.
No fund was received for this study.
Ethics approval and consent to participate
Ethical clearance was obtained from the Senate of Research and Publications Committee of the Muhimbili University of Health and Allied Sciences (MUHAS). Permission to conduct the study was obtained from the MNH administration. Participants provided written informed consent before enrolment in the study. We ensured the confidentiality of the study participants through the use of codes instead of the participant’s names.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Mwandigha, A.M., Kamori, D., Kibwana, U.O. et al. Fecal carriage and factors associated with extended-spectrum β-lactamase-producing Enterobacteriaceae among pregnant women at the tertiary referral hospital, Tanzania. Trop Med Health 48, 84 (2020). https://doi.org/10.1186/s41182-020-00271-2
- Extended-spectrum beta-lactamase
- Fecal carriage
- Antimicrobial resistance