Plasmids are extrachromosomal DNA molecules that can be transferred vertically as well as horizontally between bacteria. They have been shown to code for numerous bacterial phenotypes, the most concerning of which is resistance to commonly used antibiotics. Plasmid-mediated transfer of drug resistance genes has notably led to the rapid spread of resistant strains, which now presents a human health crisis. While this rapid evolution of bacteria due to horizontal plasmid transfer has historically dominated this research field, increasing attention is being paid to the (co-)evolutionary interactions that shape the long-term population dynamics of bacteria and plasmids.
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Linking plasmid-based beta-lactamases to their bacterial hosts using single-cell fusion PCR
The horizonal transfer of plasmid-encoded genes allows bacteria to adapt to constantly shifting environmental pressures, bestowing functional advantages to their bacterial hosts such as antibiotic resistance, metal resistance, virulence factors, and polysaccharide utilization. However, common molecular methods such as short- and long-read sequencing of microbiomes cannot associate extrachromosomal plasmids with the genome of the host bacterium. Alternative methods to link plasmids to host bacteria are either laborious, expensive, or prone to contamination. Here we present the One-step Isolation and Lysis PCR (OIL-PCR) method, which molecularly links plasmid-encoded genes with the bacterial 16S rRNA gene via fusion PCR performed within an emulsion. After validating this method, we apply it to identify the bacterial hosts of three clinically relevant beta-lactamases within the gut microbiomes of neutropenic patients, as they are particularly vulnerable multidrug-resistant infections. We successfully detect the known association of a multi-drug resistant plasmid with Klebsiella pneumoniae , as well as the novel associations of two low-abundance genera, Romboutsia and Agathobacter . Further investigation with OIL-PCR confirmed that our detection of Romboutsia is due to its physical association with Klebsiella as opposed to directly harboring the beta-lactamase genes. Here we put forth a robust, accessible, and high-throughput platform for sensitively surveying the bacterial hosts of mobile genes, as well as detecting physical bacterial associations such as those occurring within biofilms and complex microbial communities.
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- Award ID(s):
- 1661338
- PAR ID:
- 10279661
- Date Published:
- Journal Name:
- eLife
- Volume:
- 10
- ISSN:
- 2050-084X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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