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Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Acquired antibiotic resistance: are we born with it?
Lu Zhang1, Daniel Kinkelaar, Ying Huang
1Department of Food Science and Technology, The Ohio State University, Columbus, OH 43210-1007, USA.
Applied and Environmental Microbiology
|August 9, 2011
Summary
Antibiotic resistance (AR) emerges early in infant guts, even without antibiotic exposure. Maternal and environmental microbes likely drive this AR development, independent of diet or direct antibiotic use.
Area of Science:
- Microbiology
- Public Health
- Genetics
Background:
- Antibiotic resistance (AR) is a growing global health threat.
- Foodborne antibiotic-resistant (ART) bacteria may spread to humans through diet.
- Understanding the baseline AR in the human gut is crucial for assessing risks.
Purpose of the Study:
- To investigate the early development of antibiotic-resistant bacteria in infant gut microbiota.
- To determine the baseline prevalence of AR in infants without prior antibiotic exposure.
- To identify potential sources and drivers of early AR in the human gut.
Main Methods:
- Analysis of gut microbiota in 16 infants from birth to 1 year.
- Subjects were fed breast milk and/or infant formula, with no antibiotic exposure.
- Detection of antibiotic resistance genes and identification of bacterial species carrying them.
Main Results:
- Predominant antibiotic-resistant bacteria and multiple resistance genes were found in infant guts within the first week of life.
- ART populations shifted without antibiotic or dietary changes.
- Specific AR genes (tet(M), ermB, sul2, bla(TEM)) and carriers (Enterococcus, Staphylococcus, Klebsiella, Streptococcus, E. coli/Shigella) were identified.
- ART bacteria were not found in infant foods, but some breast milk samples contained skin-associated ART bacteria.
Conclusions:
- Early development of AR in the infant gut is independent of direct antibiotic exposure.
- Maternal and environmental microbial exposure appears to significantly impact early AR.
- ART populations can amplify within the host gut even without antibiotic selective pressure.
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