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Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
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Rapid methicillin resistance diversification in Staphylococcus epidermidis colonizing human neonates
Manoshi S Datta1, Idan Yelin1, Ori Hochwald2
1Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
Nature Communications
|October 19, 2021
Summary
Infant gut bacteria, Staphylococcus epidermidis, rapidly change gene content shortly after birth. This rapid evolution, driven by gene gain/loss, impacts antibiotic resistance, even in genetically identical cells.
Area of Science:
- Microbiology
- Genomics
- Neonatal Health
Background:
- Infants are colonized by diverse bacterial strains with significant health implications.
- Metagenomics shows strain differences, but within-strain gene content evolution is less understood.
Purpose of the Study:
- Investigate the rate, mechanisms, and phenotypic consequences of gene content diversification within Staphylococcus epidermidis strains in newborns.
Main Methods:
- Whole-genome sequencing and phenotyping of over 600 Staphylococcus epidermidis isolates from newborns.
- Long-read Nanopore sequencing to map genomic architecture of structural variants.
Main Results:
- Observed rapid gene gain and loss events within S. epidermidis strains, exceeding point mutation rates.
- Identified variations in the methicillin resistance gene (mecA) and SCCmec island, impacting antibiotic resistance.
- Structural variants evolved rapidly, leading to patient-specific genomic diversity.
Conclusions:
- Gene content diversification, not just single-nucleotide polymorphisms, is a primary driver of S. epidermidis evolution in newborns.
- Rapid structural variant evolution contributes to phenotypic diversity and antibiotic resistance within strains.
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