# Whole-genome characterization and molecular epidemiology of Feline coronavirus (FeCoV) circulating in domestic cats in Thailand: First report of FeCoV-II whole genomes

**Authors:** Yu Nandi Thaw, Kamonpan Charoenkul, Chanakarn Nasamran, Ekkapat Chamsai, Waleemas Jairak, Eaint Min Phyu, Hnin Wai Phyu, Supassama Chaiyawong, Somsak Pakpinyo, Alongkorn Amonsin

PMC · DOI: 10.14202/vetworld.2025.3888-3901 · Veterinary World · 2025-12-14

## TL;DR

This study reports the first complete genome sequences of FeCoV-II in Thailand and finds that FeCoV-I is the dominant strain among domestic cats.

## Contribution

The study provides the first whole-genome sequences of FeCoV-II in Thailand and highlights the predominance of FeCoV-I.

## Key findings

- FeCoV positivity was 21.87% in domestic cats, with genotype I being overwhelmingly predominant (99.03%).
- Thai FeCoV-I strains clustered closely with Chinese and Dutch strains, while FeCoV-II grouped with Chinese FeCoV-II.
- No mutations were detected in the S1/S2 cleavage sites of FeCoV-I, and FeCoV-II showed characteristic deletion and insertion patterns.

## Abstract

Feline coronavirus (FeCoV) is a widely circulating Alphacoronavirus that causes mild enteric infections and, in some cases, progresses to Feline infectious peritonitis, a fatal systemic disease. FeCoV consists of two genotypes (I and II) and two biotypes (FeCoV and feline infectious peritonitis virus [FIPV]). Despite its importance, whole-genome data, particularly for FeCoV genotype II, remain limited in Thailand. This study aimed to determine the prevalence of FeCoV in domestic cats and to genetically characterize circulating strains using whole-genome and S gene sequencing.

A total of 471 rectal swabs were collected from domestic cats presented to private small animal hospitals in Bangkok and neighboring provinces from October 2022 to October 2023. FeCoV detection and genotyping were performed using one-step reverse transcription polymerase chain reaction targeting the 3′UTR and S gene, respectively. Selected FeCoV-positive samples were subjected to whole-genome sequencing (WGS) (n = 4) and complete S gene sequencing (n = 6) using Oxford Nanopore technology with Minimap2, Racon, and Medaka pipelines. Phylogenetic and genetic analyses were conducted using MEGA program.

FeCoV positivity was 21.87% (103/471), with higher detection in young cats (<6 months; 28.46%), though age, clinical status, and season showed no significant association (p > 0.05). Genotype I was overwhelmingly predominant (99.03%), whereas genotype II was rare (0.97%). Phylogenetic analysis revealed that Thai FeCoV-I strains clustered closely with Chinese and Dutch FeCoV-I strains, while the FeCoV-II strain grouped with Chinese FeCoV-II. Whole-genome pairwise comparisons showed high nucleotide and amino acid identities with their respective genotype references. No mutations were detected in the S1/S2 or S2 cleavage sites of Thai FeCoV-I, indicating conserved spike characteristics typical of FECoV biotypes. FeCoV-II exhibited the characteristic deletion and insertion patterns known for this genotype. No evidence of recombination with other coronaviruses was observed.

This study provides updated molecular epidemiology of FeCoV in Thailand and reports the first complete FeCoV-II genome sequences from the country. The predominance of FeCoV-I and the detection of conserved spike regions highlight the need for genotype-specific surveillance and the reconsideration of vaccine strategies that currently target FeCoV-II. Expanded nationwide monitoring and detailed recombination analyses are warranted to better understand FeCoV evolution and transmission in feline populations.

## Linked entities

- **Diseases:** Feline infectious peritonitis (MONDO:0025491)
- **Species:** Feline coronavirus (taxon 12663)

## Full-text entities

- **Diseases:** gastroenteritis (MESH:D005759), FeCoV (MESH:D018352), pain (MESH:D010146), pleuritis (MESH:D010998), disease (MESH:D004194), peritonitis (MESH:D010538), infection (MESH:D007239), diarrhea (MESH:D003967), FIP (MESH:D016766), granulomatous lesions (MESH:D006105), enteric infections (MESH:D004751), Infectious Diseases (MESH:D003141), distress (MESH:D012128)
- **Chemicals:** Eagle's Minimum Essential (-), Agarose (MESH:D012685)
- **Species:** Alphacoronavirus (genus) [taxon 693996], Feline coronavirus (no rank) [taxon 12663], Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685], Canis lupus familiaris (dog, subspecies) [taxon 9615], Canine coronavirus (no rank) [taxon 11153], Deltacoronavirus (genus) [taxon 1159901], Alphacoronavirus 1 (no rank) [taxon 693997], Betacoronavirus (genus) [taxon 694002], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Gammacoronavirus (genus) [taxon 694013], Feline infectious peritonitis virus (no rank) [taxon 11135], Coronaviridae (family) [taxon 11118]
- **Mutations:** C for 5-10, C-48 C, M1058L, C for 1-4
- **Cell lines:** ZJU1617 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_ZZ52), CU31327 — Gallus gallus (Chicken), Marek disease, Cancer cell line (CVCL_T546), SMU — Mus musculus (Mouse), Conditionally immortalized cell line (CVCL_IN93)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913905/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913905/full.md

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Source: https://tomesphere.com/paper/PMC12913905