Genomic Diversity, Host Associations, and Tissue Tropism of Hydrangea Ringspot Virus: A Global and Regional Perspective

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This study investigated the genomic diversity, host associations, and tissue tropism of hydrangea ringspot virus by screening 210 publicly available Hydrangea spp. transcriptomes from diverse tissues and generating four additional H. macrophylla transcriptomes from Colombia, followed by viral genome assembly and phylogenetic analysis. Two well-supported viral lineages (HdRSV-L1 and HdRSV-L2) were recovered from full-genome and replicase coding sequence analyses, and HdRSV was detected in all tissues examined with the highest median viral loads in roots, then stems and leaves. H. macrophylla contained both lineages whereas H. serrata was infected only with HdRSV-L1, and cultivar-level analysis showed differences in viral abundance with distinct tissue preferences; co-infection was not generally observed except in the ‘Bailer’ cultivar. The authors identified a lineage-defining nonsynonymous replicase mutation (C1578T; Thr→Ile) fixed in most HdRSV-L2 genomes, and the paper does not explicitly discuss limitations beyond the reliance on transcriptome-derived data and publicly available samples. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ABSTRACT Hydrangea ringspot virus (HdRSV) is an emerging plant virus infecting ornamental hydrangea species worldwide, yet its genomic diversity and host associations remain poorly understood. To expand the available genomic resources and assess HdRSV variability, we screened 210 publicly available Hydrangea spp. transcriptomes from diverse tissues, complemented with four newly generated H. macrophylla transcriptomes from Colombia. Viral genomes were assembled from infected samples and analyzed to infer phylogenetic relationships, lineage distribution, and relative viral RNA abundance. Two well-supported phylogenetic lineages (HdRSV-L1 and HdRSV-L2) were recovered from both full-genome and replicase coding sequence (CDS) analyses. HdRSV was detected across all host tissues examined, with the highest median viral loads in roots, followed by stems and leaves. H. macrophylla harbored both viral lineages, while H. serrata was exclusively infected by HdRSV-L1. Cultivar-level analysis revealed marked differences in viral abundance, with lineages showing distinct tissue preferences but no co-infection patterns, except in the ‘Bailer’ cultivar. Comparative analysis of the replicase CDS identified a single lineage-defining nonsynonymous mutation (C1578T; Thr→Ile), fixed in 90% of HdRSV-L2 genomes, corresponding to a polar-to-nonpolar amino acid change potentially associated with structural adaptation. Together, these findings provide the most comprehensive overview to date of HdRSV genomic diversity, host and tissue distribution, and molecular variation, offering new insights into the evolution and epidemiology of this understudied plant virus.
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ABSTRACT Hydrangea ringspot virus (HdRSV) is an emerging plant virus infecting ornamental hydrangea species worldwide, yet its genomic diversity and host associations remain poorly understood. To expand the available genomic resources and assess HdRSV variability, we screened 210 publicly available Hydrangea spp. transcriptomes from diverse tissues, complemented with four newly generated H. macrophylla transcriptomes from Colombia. Viral genomes were assembled from infected samples and analyzed to infer phylogenetic relationships, lineage distribution, and relative viral RNA abundance. Two well-supported phylogenetic lineages (HdRSV-L1 and HdRSV-L2) were recovered from both full-genome and replicase coding sequence (CDS) analyses. HdRSV was detected across all host tissues examined, with the highest median viral loads in roots, followed by stems and leaves. H. macrophylla harbored both viral lineages, while H. serrata was exclusively infected by HdRSV-L1. Cultivar-level analysis revealed marked differences in viral abundance, with lineages showing distinct tissue preferences but no co-infection patterns, except in the ‘Bailer’ cultivar. Comparative analysis of the replicase CDS identified a single lineage-defining nonsynonymous mutation (C1578T; Thr→Ile), fixed in 90% of HdRSV-L2 genomes, corresponding to a polar-to-nonpolar amino acid change potentially associated with structural adaptation. Together, these findings provide the most comprehensive overview to date of HdRSV genomic diversity, host and tissue distribution, and molecular variation, offering new insights into the evolution and epidemiology of this understudied plant virus. Competing Interest Statement The authors have declared no competing interest.

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