4.7 Article

A New Family of Bacteriolytic Proteins in Dictyostelium discoideum

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FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2020.617310

关键词

Dictyostelium discoideum; protein purification; bacteriolytic proteins; Klebsiella pneumoniae; intracellular killing; Bacteriolytic D; discoideum A (BadA)

资金

  1. Swiss National Science Foundation [31003A_172951]
  2. Swiss National Science Foundation (SNF) [31003A_172951] Funding Source: Swiss National Science Foundation (SNF)

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Phagocytic cells efficiently consume and destroy bacteria to defend against infections. In D. discoideum, a bacteriolytic activity targeting Klebsiella pneumoniae was discovered, with BadA protein identified as essential for bactericidal activity in cells. This study provides a new strategy for identifying and characterizing bactericidal proteins in D. discoideum.
Phagocytic cells ingest and destroy bacteria efficiently and in doing so ensure the defense of the human body against infections. Phagocytic Dictyostelium discoideum amoebae represent a powerful model system to study the intracellular mechanisms ensuring destruction of ingested bacteria in phagosomes. Here, we discovered the presence of a bacteriolytic activity against Klebsiella pneumoniae in cellular extracts from D. discoideum. The bacteriolytic activity was detected only at a very acidic pH mimicking the conditions found in D. discoideum phagosomes. It was also strongly decreased in extracts of kil1 KO cells that were previously described to kill inefficiently internalized bacteria, suggesting that the activity observed in vitro is involved in killing of bacteria in phagosomes. We purified a fraction enriched in bacteriolytic activity where only 16 proteins were detected and focused on four proteins selectively enriched in this fraction. Three of them belong to a poorly characterized family of D. discoideum proteins exhibiting a DUF3430 domain of unknown function and were named BadA (Bacteriolytic D. discoideum A), BadB, and BadC. We overexpressed the BadA protein in cells, and the bacteriolytic activity increased concomitantly in cell extracts. Conversely, depletion of BadA from cell extracts decreased significantly their bacteriolytic activity. Finally, in cells overexpressing BadA, bacterial killing was faster than in parental cells. Together these results identify BadA as a D. discoideum protein required for cellular bactericidal activity. They also define a new strategy to identify and characterize bactericidal proteins in D. discoideum cells.

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