https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkad498/7191423
https://english.cas.cn/newsroom/research_news/life/202306/t20230626_332439.shtml
Human gut hosts a complex ecosystem comprising an intricate plasmidome with abundant undiscovered plasmids, driving horizontal gene transfer events.
Broad host range (BHR) plasmids carrying fitness genes transfer between bacteria across distantly phylogenetic taxa, facilitating the adaptation of their hosts to varying environments. However, accurate identification of BHR plasmids in the gut is still difficult, and their host range and prevalence remain unclear.
A research team led by Prof. MA Yingfei from the CAS Shenzhen Institute of Advanced Technology (SIAT) has identified and characterized plasmids harbored by human gut bacterial isolates from culturomics-based studies. The researchers have revealed their accurate host range, persistence in human gut, accessory genes, prevalence across various environments, and transmission and evolutionary trajectories in detail.
The researchers assembled 820 plasmid-like clusters (PLCs) with high-completeness genomes (comPLCs). The majority of PLCs (81.1%) were classified to known replicon types, which suggested gut plasmids were highly diverse and novel. They found that 175 comPLCs had a broad host range across distinct bacterial genera, of which, 71 were detected in at least two human populations from four distant countries, and 13 were highly prevalent (>10%) in at least one human population. They observed that the broadest PLC (Clstr-417) could spread among the isolates collected from Chinese donors and American donors of 24 genera across five phyla. And some PLCs are so ubiquitous that can even be detected in different species and environmental sewage.
The evolutionary trajectory showed that the BHR plasmid spread between the phyla and the environment was extremely rapid, with all transmission times occurring 0-10 years ago and colonizing the individual gut multiple times.
BHR plasmids may also have great potential to edit the genome of commensal gut microbes and bacteriophages that suffer from lacking editing tools.
