Scientific Reports (Feb 2021)

Click-correlative light and electron microscopy (click-AT-CLEM) for imaging and tracking azido-functionalized sphingolipids in bacteria

  • Simon Peters,
  • Lena Kaiser,
  • Julian Fink,
  • Fabian Schumacher,
  • Veronika Perschin,
  • Jan Schlegel,
  • Markus Sauer,
  • Christian Stigloher,
  • Burkhard Kleuser,
  • Jürgen Seibel,
  • Alexandra Schubert-Unkmeir

DOI
https://doi.org/10.1038/s41598-021-83813-w
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 12

Abstract

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Abstract Sphingolipids, including ceramides, are a diverse group of structurally related lipids composed of a sphingoid base backbone coupled to a fatty acid side chain and modified terminal hydroxyl group. Recently, it has been shown that sphingolipids show antimicrobial activity against a broad range of pathogenic microorganisms. The antimicrobial mechanism, however, remains so far elusive. Here, we introduce ‘click-AT-CLEM’, a labeling technique for correlated light and electron microscopy (CLEM) based on the super-resolution array tomography (srAT) approach and bio-orthogonal click chemistry for imaging of azido-tagged sphingolipids to directly visualize their interaction with the model Gram-negative bacterium Neisseria meningitidis at subcellular level. We observed ultrastructural damage of bacteria and disruption of the bacterial outer membrane induced by two azido-modified sphingolipids by scanning electron microscopy and transmission electron microscopy. Click-AT-CLEM imaging and mass spectrometry clearly revealed efficient incorporation of azido-tagged sphingolipids into the outer membrane of Gram-negative bacteria as underlying cause of their antimicrobial activity.