High-resolution comparative atomic structures of two Giardiavirus prototypes infecting G. duodenalis parasite.
Han WangGianluca MarucciAnna MunkeMohammad Maruf HassanMarco LalleKenta OkamotoPublished in: PLoS pathogens (2024)
The Giardia lamblia virus (GLV) is a non-enveloped icosahedral dsRNA and endosymbiont virus that infects the zoonotic protozoan parasite Giardia duodenalis (syn. G. lamblia, G. intestinalis), which is a pathogen of mammals, including humans. Elucidating the transmission mechanism of GLV is crucial for gaining an in-depth understanding of the virulence of the virus in G. duodenalis. GLV belongs to the family Totiviridae, which infects yeast and protozoa intracellularly; however, it also transmits extracellularly, similar to the phylogenetically, distantly related toti-like viruses that infect multicellular hosts. The GLV capsid structure is extensively involved in the longstanding discussion concerning extracellular transmission in Totiviridae and toti-like viruses. Hence, this study constructed the first high-resolution comparative atomic models of two GLV strains, namely GLV-HP and GLV-CAT, which showed different intracellular localization and virulence phenotypes, using cryogenic electron microscopy single-particle analysis. The atomic models of the GLV capsids presented swapped C-terminal extensions, extra surface loops, and a lack of cap-snatching pockets, similar to those of toti-like viruses. However, their open pores and absence of the extra crown protein resemble those of other yeast and protozoan Totiviridae viruses, demonstrating the essential structures for extracellular cell-to-cell transmission. The structural comparison between GLV-HP and GLV-CAT indicates the first evidence of critical structural motifs for the transmission and virulence of GLV in G. duodenalis.
Keyphrases
- electron microscopy
- high resolution
- escherichia coli
- pseudomonas aeruginosa
- staphylococcus aureus
- biofilm formation
- antimicrobial resistance
- single cell
- cell therapy
- mass spectrometry
- genetic diversity
- candida albicans
- saccharomyces cerevisiae
- stem cells
- minimally invasive
- multidrug resistant
- optical coherence tomography
- bone marrow
- tandem mass spectrometry
- protein protein
- amino acid
- drug induced