Key result
The rotavirus NSP4 viroporin domain forms a cation-selective ion channel capable of conducting calcium, establishing the mechanism by which it disrupts host cell calcium homeostasis.
The rotavirus NSP4 viroporin domain forms an ion channel capable of conducting calcium, establishing the mechanism by which it disrupts host cell calcium homeostasis.
NSP4 may disrupt calcium homeostasis in infection; leaves open cardiac relevance and need for in vivo validation.
Viroporins are small virus-encoded ion channel proteins. Most viroporins are monovalent selective cation channels, with few showing the ability to conduct divalent cations, like calcium (Ca 2+ ). Nevertheless, some viroporins are known to disrupt host cell Ca 2+ homeostasis, which is critical for virus replication and pathogenesis. Rotavirus nonstructural protein 4 (NSP4) is an endoplasmic reticulum transmembrane glycoprotein that has a viroporin domain (VPD), and NSP4 viroporin activity elevates cytosolic Ca 2+ in mammalian cells. The goal of this study was to demonstrate that the NSP4 VPD forms an ion channel and determine whether the channel can conduct Ca 2+ . Using planar lipid bilayer and liposome patch clamp electrophysiology, we show that a synthetic peptide of the NSP4 VPD has ion channel activity. The NSP4 VPD was selective for cations over anions and channel activity was observed to have both well-defined “square top” openings as well as fast current fluctuations, similar to other viroporins. Importantly, the NSP4 VPD showed similar conductance of divalent cations (Ca 2+ and Ba 2+ ) as monovalent cations (K + ), but a viroporin defective mutant lacked Ca 2+ conductivity. These data demonstrate that the NSP4 VPD is a Ca 2+ -conducting viroporin and establish the mechanism by which NSP4 disturbs host cell Ca 2+ homeostasis.
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Pham et al. (2017) studied Rotavirus infection. Rotavirus NSP4 Viroporin Domain (VPD) vs. Viroporin defective mutant (VPD-Mut) or vehicle was evaluated on Ion channel activity and calcium conductivity. The rotavirus NSP4 viroporin domain forms a cation-selective ion channel capable of conducting calcium, establishing the mechanism by which it disrupts host cell calcium homeostasis.