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Kuwata, R.

Publications and source records attributed to Kuwata, R..

2 recordsLinked to original sources

Systematic analysis of intracellular replication competence of mammalian, avian, and reptilian kolmioviruses.

Kolmioviruses (KoVs) are circular, single-stranded RNA viruses whose evolution may have involved host switching between vertebrate classes. However, the host specificity of their intracellular replication remains poorly understood. Here, we examined six mammalian, one avian, and one reptilian KoVs using cell lines derived from the same three vertebrate classes. We transfected cells with plasmids encoding 1.2x genome-length KoV sequences and assessed persistent replication by monitoring delta antigen-positive cells for up to 18 days. Four mammalian KoVs replicated persistently only in mammalian cell lines, whereas avian and reptilian KoVs replicated persistently only in both avian and reptilian cell lines. By contrast, the remaining two mammalian KoVs, nested within the clade whose deepest lineages are the avian and reptilian KoVs, replicated in cell lines from all three vertebrate classes. The observed patterns of persistent replication are concordant with the phylogenetic grouping of the KoVs. Our findings support a possible evolutionary scenario in which the common ancestor of the two mammalian KoVs in the avian-reptilian clade acquired compatibility with mammalian cells while retaining the capacity to replicate in avian and reptilian cells, contributing to the transition of this lineage to mammalian hosts.

microbiology↗

Optimization of culture and transfection methods for primary snake cells

Snakes serve as important models for understanding how changes in genes and genome sequences drive vertebrate morphological evolution. However, the lack of established primary culture methods and gene delivery techniques for snake cells has hindered functional analyses of evolutionarily modified genes and genomic elements. Here, we optimized primary culture conditions and screened for efficient transfection methods using corn snake embryonic fibroblasts. Our culture optimization experiments revealed that TeSR medium, designed for stem cells, with fetal bovine serum supplementation, and incubation at 28 provided a suitable condition for primary snake fibroblasts. Transcriptome analysis further demonstrated that under this optimized condition, genes associated with cytoskeletal organization, extracellular matrix components, and sterol biosynthetic process were upregulated, likely promoting snake cell proliferation. Additionally, screening of various gene transfection methods identified three efficient approaches, including electroporation. These findings enhance the utility of snake cells and pave the way for functional analyses of genes and genomic elements using snake cell-based systems.

developmental biology↗