4.8 Article

Prophage-triggered membrane vesicle formation through peptidoglycan damage in Bacillus subtilis

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-00492-w

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) [25701012, 16K14795, 16H06189]
  2. Japanese Society for the Promotion of Science (JSPS)
  3. Japan Science and Technology Agency, ERATO [JPMJER1502]
  4. MEXT [60292520]
  5. Swiss National Science Foundation (SNSF) [3100A0-104215]
  6. SNSF [Sinergia CRSII3_154430, 31003A_152878, 316030_164092]
  7. European Research Council [STG 679209]
  8. Grants-in-Aid for Scientific Research [16H06189, 16K14795, 25701012] Funding Source: KAKEN
  9. Swiss National Science Foundation (SNF) [31003A_152878, 316030_164092] Funding Source: Swiss National Science Foundation (SNF)

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Bacteria release membrane vesicles (MVs) that play important roles in various biological processes. However, the mechanisms of MV formation in Gram-positive bacteria are unclear, as these cells possess a single cytoplasmic membrane that is surrounded by a thick cell wall. Here we use live cell imaging and electron cryo-tomography to describe a mechanism for MV formation in Bacillus subtilis. We show that the expression of a prophage-encoded endolysin in a sub-population of cells generates holes in the peptidoglycan cell wall. Through these openings, cytoplasmic membrane material protrudes into the extracellular space and is released as MVs. Due to the loss of membrane integrity, the induced cells eventually die. The vesicle-producing cells induce MV formation in neighboring cells by the enzymatic action of the released endolysin. Our results support the idea that endolysins may be important for MV formation in bacteria, and this mechanism may potentially be useful for the production of MVs for applications in biomedicine and nanotechnology.

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