A Functional K+ Channel from Tetraselmis Virus 1, a Member of the Mimiviridae

Viruses. 2020 Sep 29;12(10):1107. doi: 10.3390/v12101107.

Abstract

Potassium ion (K+) channels have been observed in diverse viruses that infect eukaryotic marine and freshwater algae. However, experimental evidence for functional K+ channels among these alga-infecting viruses has thus far been restricted to members of the family Phycodnaviridae, which are large, double-stranded DNA viruses within the phylum Nucleocytoviricota. Recent sequencing projects revealed that alga-infecting members of Mimiviridae, another family within this phylum, may also contain genes encoding K+ channels. Here we examine the structural features and the functional properties of putative K+ channels from four cultivated members of Mimiviridae. While all four proteins contain variations of the conserved selectivity filter sequence of K+ channels, structural prediction algorithms suggest that only two of them have the required number and position of two transmembrane domains that are present in all K+ channels. After in vitro translation and reconstitution of the four proteins in planar lipid bilayers, we confirmed that one of them, a 79 amino acid protein from the virus Tetraselmis virus 1 (TetV-1), forms a functional ion channel with a distinct selectivity for K+ over Na+ and a sensitivity to Ba2+. Thus, virus-encoded K+ channels are not limited to Phycodnaviridae but also occur in the members of Mimiviridae. The large sequence diversity among the viral K+ channels implies multiple events of lateral gene transfer.

Keywords: K+ channel evolution; Kcv; Mimiviridae; Phycodnaviridae; viral K+ channel.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Evolution, Molecular
  • Genome, Viral
  • Ion Channels
  • Lipid Bilayers
  • Mimiviridae / genetics
  • Mimiviridae / physiology*
  • Phycodnaviridae / genetics
  • Phylogeny
  • Potassium / metabolism*
  • Potassium Channels / classification
  • Potassium Channels / genetics
  • Potassium Channels / physiology*
  • Sequence Alignment
  • Sequence Analysis
  • Sodium / metabolism
  • Sodium Channels
  • Viruses, Unclassified / genetics
  • Viruses, Unclassified / physiology*

Substances

  • Ion Channels
  • Lipid Bilayers
  • Potassium Channels
  • Sodium Channels
  • Sodium
  • Potassium