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Cited by 39Escherichia coli research studiesAntibiotic Resistance in BacteriaSalmonella and Campylobacter epidemiology

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Pathotyping and Antibiotic Resistance Profiling of Escherichia coli Isolates from Children with Acute Diarrhea in Amatole District Municipality of Eastern Cape, South Africa

Open access
Omolajaiye, S. A., Afolabi, K. O., Iweriebor, B. C.·2020·BioMed Research International

Abstract

Background. Diarrhea has been reported as the leading cause of childhood mortality and morbidity globally but with disproportionate impacts in developing nations. Among bacterial etiologic agents of diarrhea, diarrheagenic Escherichia coli is the main cause of the disease among children under the age of 5 years. This study is aimed at determining the prevalence and antibiogram pattern of diarrheagenic Escherichia coli (DEC) pathotypes associated with diarrhea cases in the study area. Methods. A total of 120 presumptive isolates of E. coli were obtained from diarrheal stool samples from male and female patients below 12 years of age using chromogenic agar. Confirmation of the isolates and screening for virulence genes were determined by polymerase chain reaction (PCR) while antimicrobial susceptibility testing was performed using the disk diffusion method. The presence of antibiotic resistance genes to chloramphenicol and tetracycline among the confirmed isolates was also profiled by PCR based on the observed phenotypic resistance pattern. Results. Of the 120 presumptive isolates, 88.3% (106/120) were confirmed as E. coli through PCR. The molecular pathotyping of the confirmed isolates showed their distribution as 41% (43/106) of diffusely adhering E. coli (DAEC), 17% (18/106) of enterohemorrhagic E. coli (EHEC), 17% (18/106) of enteropathogenic E. coli (EPEC), and 10% (11/106) of enteroinvasive E. coli (EIEC), while enteroaggregative E. coli (EAEC) and enterotoxigenic E. coli (ETEC) were not detected, and the remaining 15% did not belong to any pathotype. Notably, high resistance of the isolates to commonly used antimicrobials was observed as follows: ampicillin (98%), chloramphenicol (94%), trimethoprim‐sulfamethoxazole (96%), and tetracycline (90.6%), while a relatively low number of the confirmed isolates were resistant to ciprofloxacin (45%) and imipenem (36%). In addition, 94% of the isolates that exhibited phenotypic resistance against chloramphenicol harbored the cat A1 resistance gene while 89% that showed resistance to tetracycline had tet A genes. Conclusions. These findings showed that DEC could be considered as the leading etiologic bacterial agent responsible for diarrhea in the study community, and the observable high degree of resistance of the isolates to antimicrobial agents is of huge significance, calling for stakeholders to adopt and consolidate the existing antimicrobial stewardship scheme of the government, in order to ensure an uncompromised public health.

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Figures

Figure 1 Confirmation of the presumptive E. coli isolates through the amplification of uidA genes (147 bp). Lane M: molecular weight marker (50 bp); lanes 1 to 3: positive control (E. coli ATCC 25922); lane 4: nuclease free water as negative control; lanes 5 to 15: representative positive isolates.
Figure 1 Confirmation of the presumptive E. coli isolates through the amplification of uidA genes (147 bp). Lane M: molecular weight marker (50 bp); lanes 1 to 3: positive control (E. coli ATCC 25922); lane 4: nuclease free water as negative control; lanes 5 to 15: representative positive isolates.CC BY · PubMed Central
Figure 2 Gel electrophoresis of PCR products amplified with the eaeA primers for the detection of enterohemorrhagic E. coli. Lane 1: DNA ladder 100 bp; lane 2: nuclease-free water as negative control; lanes 3-11: enterohemorrhagic E. coli.
Figure 2 Gel electrophoresis of PCR products amplified with the eaeA primers for the detection of enterohemorrhagic E. coli. Lane 1: DNA ladder 100 bp; lane 2: nuclease-free water as negative control; lanes 3-11: enterohemorrhagic E. coli.CC BY · PubMed Central
Figure 3 A gel electrophoresis of PCR products amplified with vir primers for the detection of enteroinvasive E. coli (EIEC). Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water as negative control; lanes 3 to 13: E. coli isolates.
Figure 3 A gel electrophoresis of PCR products amplified with vir primers for the detection of enteroinvasive E. coli (EIEC). Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water as negative control; lanes 3 to 13: E. coli isolates.CC BY · PubMed Central
Figure 4 Gel electrophoresis of PCR products amplified with thye daaE gene for the detection of diffusely adherent E. coli. Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water as negative control; lanes 3-12: diffusely adherent E. coli.
Figure 4 Gel electrophoresis of PCR products amplified with thye daaE gene for the detection of diffusely adherent E. coli. Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water as negative control; lanes 3-12: diffusely adherent E. coli.CC BY · PubMed Central
Figure 5 Gel electrophoresis of PCR products amplified with eae (intimin) primers for the detection of enteropathogenic E. coli. Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water negative control; lanes 3-13: enteropathogenic E. coli.
Figure 5 Gel electrophoresis of PCR products amplified with eae (intimin) primers for the detection of enteropathogenic E. coli. Lane 1: 100 bp DNA ladder; lane 2: nuclease-free water negative control; lanes 3-13: enteropathogenic E. coli.CC BY · PubMed Central

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Research works printed but not linked: 1

  1. Halawani E. M., 2010, Beta-lactam antibiotic resistance in Escherichia coli commensal fecal flora of healthy population in Taif, Saudi Arabia, African Journal of Microbiology Research, 5, 73

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Metadata

Authors
Omolajaiye, S. A., Afolabi, K. O., & Iweriebor, B. C.
Affiliations
  • Anchor University Lagos (NG)
  • Sefako Makgatho Health Sciences University (ZA)
Corresponding author
Iweriebor, B. C.
Venue
BioMed Research International
Publisher
Wiley
Published
2020-01
Volume
2020
Issue
1
Pages
4250165-4250165
ISSN
  • 1110-7243 (ISSN-L)
  • 2314-6133
  • 2314-6141
OpenAlex
W3102002835
Cited by
39
References
57
Citations by year
2026: 5 · 2025: 2 · 2024: 8 · 2023: 8 · 2022: 13 · 2021: 3
FWCI
3.71
Type
journal article
Language
en
Open access
Locations
  • BioMed Research International (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Funders
SAMRC
Topics
  • Life Sciences › Immunology and Microbiology › Microbiology › Escherichia coli research studies
  • Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Salmonella and Campylobacter epidemiology
Keywords
diarrheagenic Escherichia coli, childhood diarrhea, antibiotic resistance, virulence genes, diffuse adherence, enterohemorrhagic Escherichia coli, enteropathogenic Escherichia coli, enteroinvasive Escherichia coli, enteroaggregative Escherichia coli, enterotoxigenic Escherichia coli, antimicrobial susceptibility, chloramphenicol resistance, tetracycline resistance, Eastern Cape, children under five
MeSH terms
Child, Child, Preschool, Diarrhea, Drug Resistance, Microbial, Escherichia coli, Female, Humans, Infant, Male, South Africa, Gene Expression Regulation, Bacterial

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CoChat. (2026). Citation check: Pathotyping and Antibiotic Resistance Profiling of Escherichia coli Isolates from Children with Acute Diarrhea in Amatole District Municipality of Eastern Cape, South Africa. https://app.cochat.ai/papers/10.1155/2020/4250165
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Omolajaiye, S. A., Afolabi, K. O., & Iweriebor, B. C. (2020). Pathotyping and Antibiotic Resistance Profiling of Escherichia coli Isolates from Children with Acute Diarrhea in Amatole District Municipality of Eastern Cape, South Africa. BioMed Research International. https://doi.org/10.1155/2020/4250165

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