4.8 Article

Structure of the phage TP901-1 1.8 MDa baseplate suggests an alternative host adhesion mechanism

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1200966109

Keywords

bacteriophage; crystal structure; Lactococcus lactis; siphoviridae; viral infection

Funding

  1. Agence Nationale de la Recherche [ANR BLAN07-1_191968, ANR-11-BSV8-004-01]
  2. Ministere Francais de l'Enseignement Superieur et de la Recherche [22976-2006]
  3. Science Foundation Ireland [08/IN.1/B1909]
  4. Science Foundation Ireland (SFI) [08/IN.1/B1909] Funding Source: Science Foundation Ireland (SFI)

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Phages of the Caudovirales order possess a tail that recognizes the host and ensures genome delivery upon infection. The X-ray structure of the approximately 1.8 MDa host adsorption device (baseplate) from the lactococcal phage TP901-1 shows that the receptor-binding proteins are pointing in the direction of the host, suggesting that this organelle is in a conformation ready for host adhesion. This result is in marked contrast with the lactococcal phage p2 situation, whose baseplate is known to undergo huge conformational changes in the presence of Ca2+ to reach its active state. In vivo infection experiments confirmed these structural observations by demonstrating that Ca2+ ions are required for host adhesion among p2-like phages (936-species) but have no influence on TP901-1-like phages (P335-species). These data suggest that these two families rely on diverse adhesion strategies which may lead to different signaling for genome release.

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