Related Experiment Video
Updated: Aug 22, 2026

Antibiotic Efficacy Testing in an Ex vivo Model of Pseudomonas aeruginosa and Staphylococcus aureus Biofilms in the Cystic Fibrosis Lung
Published on: January 22, 2021
Antibiotic resistance in Staphylococcus aureus colonising the intestines of Swedish infants
E Lindberg1, I Adlerberth, A E Wold
1Department of Clinical Bacteriology, Göteborg University, Göteborg, Sweden. erika.lindberg@microbio.gu.se
Insights
Antibiotic-resistant Staphylococcus aureus strains colonize infant intestines. These resistant strains persist and thrive as well as susceptible ones, potentially worsening antibiotic resistance issues.
Area of Science:
- Microbiology
- Pediatric Health
- Infectious Diseases
Background:
- Staphylococcus aureus frequently colonizes the infant intestinal tract, but health implications remain unclear.
- Understanding the behavior of antibiotic-resistant strains in this commensal microflora is crucial.
Purpose of the Study:
- To determine the antibiotic resistance patterns of Staphylococcus aureus strains colonizing the infant gut.
- To assess the relationship between antibiotic resistance, infant antibiotic consumption, and strain persistence.
- To evaluate the fitness of antibiotic-resistant S. aureus in the infant intestinal microflora.
Main Methods:
- Analysis of 116 S. aureus strains from fecal samples of 81 Swedish infants.
- Determination of antibiotic resistance patterns (methicillin, penicillin G, erythromycin A, tetracycline, clindamycin, fusidic acid).
- Correlation of resistance with infant antibiotic usage, strain fecal population levels, and persistence.
Main Results:
- Prevalence of resistance was modest: Penicillin G (78%), Erythromycin A (3%), Tetracycline (2%), Clindamycin (0.9%), Fusidic Acid (0.9%). Methicillin resistance was 0%.
- Antibiotic resistance was not linked to infant antibiotic consumption.
- Resistant S. aureus strains demonstrated similar persistence and high fecal population levels as susceptible strains.
- No resistance loss or acquisition was observed during colonization.
Conclusions:
- Antibiotic-resistant S. aureus strains are as ecologically fit as susceptible strains in the infant gut microflora, even without antibiotic selective pressure.
- The persistence of these resistant strains may exacerbate the broader ecological consequences of antibiotic resistance development.
- Findings highlight the need to monitor S. aureus colonization in infants and its implications for antibiotic resistance.
Abstract:
Staphylococcus aureus has become a frequent coloniser of the intestinal tract of infants, but the health effects of such colonisation are not clear. In this study, the antibiotic resistance patterns of 116 S. aureus strains from the commensal intestinal microflora were determined. The strains were obtained from 81 Swedish infants who had been followed with regular stool samples and registration of antibiotic usage during their first year of life. The faecal population levels of the individual strains and the duration of their persistence in the microflora had been determined previously. The prevalence of antibiotic resistance among the 116 strains was modest: methicillin, 0%; penicillin G, 78%; erythromycin A, 3%; tetracycline, 2%; clindamycin, 0.9%; and fusidic acid, 0.9%. Colonisation by antibiotic-resistant strains was unrelated to antibiotic consumption by individual infants. Antibiotic-resistant strains were as capable of persisting in the intestinal microflora and reaching high faecal population levels as fully susceptible strains. No strain lost or acquired resistance during the colonisation period. Thus, antibiotic-resistant strains of S. aureus seem to be as fit for competition in the large bowel microflora as susceptible strains, even in the absence of selective pressure from antibiotics. This may aggravate the ecological consequences of antibiotic resistance development.
Related Concept Videos
Clinical Significance of Antibiotic Resistance
Mechanism of Antibiotic Resistance in MRSA
Development of Antibiotic Resistance
Microbiota Modulation by Antibiotics
Staphylococcal Skin Infections
Development of Human Microbiota