# Profiling of the microRNA transcriptome in feline whole blood

**Authors:** Åsa Ohlsson, Sofia Hanås, Bodil S. Holst, Julie Lorent, Göran Andersson, Katja Höglund, Anna Tidholm, Ingrid Ljungvall, Jens Häggström

PMC · DOI: 10.1038/s41598-025-09478-x · Scientific Reports · 2025-07-31

## TL;DR

This study identifies hundreds of microRNAs in cat blood, highlighting breed differences and potential biomarkers for heart disease.

## Contribution

The study provides the first comprehensive profiling of the feline whole blood miRNA transcriptome using high-throughput sequencing.

## Key findings

- A total of 459 mature miRNAs were identified in feline whole blood, including 40 potential novel miRNAs.
- Most miRNAs showed sequence similarity with human miRNAs, and breed differences were observed in miRNA abundance.
- One miRNA, miR-204-5p, was potentially associated with preclinical hypertrophic cardiomyopathy in Norwegian Forest cats.

## Abstract

Circulating microRNAs (miRNAs) are potential biomarkers for numerous diseases. Characterization of the whole blood (WB) miRNA-transcriptome (miRNome) in cats is lacking, which limits the potential use of miRNAs as biomarkers for diseases such as feline cardiovascular disease. The aims of the present study were to profile and evaluate circulating miRNAs in feline WB by high-throughput sequencing of the total miRNome in WB from twelve domestic mixed breed (DOM) and Norwegian Forest (NFO) cats stringently diagnosed with or without preclinical hypertrophic cardiomyopathy (HCM). A total of 459 mature miRNAs were identified in feline WB, of which 40 were potential novel feline miRNAs. A majority, 85.3%, of the miRNAs showed sequence similarity with human miRNAs. An effect of breed was found, with up to thirteen WB miRNAs being differentially abundant between breeds. The majority of the significant breed-specific miRNAs in feline WB could be associated with regulation of haematopoietic cells. One miRNA, miR-204-5p, was potentially associated with preclinical HCM in NFO cats, but the results need to be confirmed in a larger and sex-unbiased cohort. In conclusion, here we used miRNome-sequencing to identify hundreds of circulating miRNAs in feline WB. Breed should be considered when evaluating the miRNome in feline WB.

The online version contains supplementary material available at 10.1038/s41598-025-09478-x.

## Linked entities

- **Diseases:** hypertrophic cardiomyopathy (MONDO:0005045)

## Full-text entities

- **Genes:** apelin-receptor [NCBI Gene 101088782], ABO [NCBI Gene 101087791], AGO2 (argonaute RISC catalytic component 2) [NCBI Gene 27161] {aka CASC7, EIF2C2, LESKRES, LINC00980, PPD, Q10}, PRKG1 (protein kinase cGMP-dependent 1) [NCBI Gene 5592] {aka AAT8, PKG, PKG1, PRKG1B, PRKGR1B, cGK}, MIR26B (microRNA 26b) [NCBI Gene 407017] {aka MIRN26B, hsa-mir-26b, miR-26b}, MIR29A (microRNA 29a) [NCBI Gene 407021] {aka MIRN29, MIRN29A, hsa-mir-29, hsa-mir-29a, miRNA29A, mir-29a}, MIR27A (microRNA 27a) [NCBI Gene 407018] {aka MIR27, MIRN27A, mir-27a}, DICER1 (dicer 1, ribonuclease III) [NCBI Gene 23405] {aka DCR1, Dicer, Dicer1e, GLOW, HERNA, K12H4.8-LIKE}, MIR21 (microRNA 21) [NCBI Gene 406991] {aka MIRN21, hsa-mir-21, miR-21, miRNA21}
- **Diseases:** hypertrophy (MESH:D006984), pyruvate kinase deficiency (MESH:C564858), cardiovascular disease (MESH:D002318), NFO (MESH:C537312), erythrocyte disease (MESH:D012010), anaemia (MESH:D000743), cancer (MESH:D009369), systolic arterial hypertension (MESH:D000092244), CHF (MESH:D006333), sickle cell disease (MESH:D000755), neurodegenerative (MESH:D019636), fibrosis (MESH:D005355), WB (MESH:C531766), dental disease (MESH:D009057), HCM (MESH:D002312), arrhythmia (MESH:D001145), sudden cardiac death (MESH:D016757), haemolysis (MESH:D006461), Cardiomyopathy (MESH:D009202), DOM (MESH:D060085), hypertrophy of the left ventricle (MESH:D017379), arterial thromboembolism (MESH:D013923), cardiac dysfunction (MESH:D006331)
- **Chemicals:** BH (-), cGMP (MESH:D006152), thyroxine (MESH:D013974), EDTA (MESH:D004492), ATP (MESH:D000255)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Rattus norvegicus (brown rat, species) [taxon 10116], Equus caballus (domestic horse, species) [taxon 9796], Mus musculus (house mouse, species) [taxon 10090], Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615]
- **Mutations:** p.V878L, serine/threonine

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12313912