4.8 Article

Endocytosis-like DNA uptake by cell wall-deficient bacteria

Journal

NATURE COMMUNICATIONS
Volume 13, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-022-33054-w

Keywords

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Funding

  1. TARGETBIO program of the Netherlands Organization for Scientific Research (NWO) [15812]
  2. Netherlands Organization for Scientific Research (NWO) [VI.C.192.002]
  3. European Union [847675]
  4. ERC Advanced Investigator grant [H2020-ERC-2017-ADV-788982-COLMIN]
  5. NWO [VI.Veni.192.094]

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A new endocytosis-like process has been discovered in cell wall-deficient bacteria, allowing them to engulf DNA and other extracellular materials. This process differs from the traditional mechanisms of horizontal gene transfer and requires energy. The findings suggest a possible mechanism for early life forms to acquire essential resources before the development of the bacterial cell wall.
Horizontal gene transfer in bacteria can occur through mechanisms such as conjugation, transduction and transformation, which facilitate the passage of DNA across the cell wall. Here, Kapteijn et al. show that cell wall-deficient bacteria can take up DNA and other extracellular materials via an endocytosis-like process. Horizontal gene transfer in bacteria is widely believed to occur via conjugation, transduction and transformation. These mechanisms facilitate the passage of DNA across the protective cell wall using sophisticated machinery. Here, we report that cell wall-deficient bacteria can engulf DNA and other extracellular material via an endocytosis-like process. Specifically, we show that L-forms of the filamentous actinomycete Kitasatospora viridifaciens can take up plasmid DNA, polysaccharides (dextran) and 150-nm lipid nanoparticles. The process involves invagination of the cytoplasmic membrane, leading to formation of intracellular vesicles that encapsulate extracellular material. DNA uptake is not affected by deletion of genes homologous to comEC and comEA, which are required for natural transformation in other species. However, uptake is inhibited by sodium azide or incubation at 4 degrees C, suggesting the process is energy-dependent. The encapsulated materials are released into the cytoplasm upon degradation of the vesicle membrane. Given that cell wall-deficient bacteria are considered a model for early life forms, our work reveals a possible mechanism for primordial cells to acquire food or genetic material before invention of the bacterial cell wall.

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