Molecular characterization of recombinant LSDV isolates from 2022 outbreak in Indonesia through phylogenetic networks and whole-genome SNP-based analysis

Sendow, Indrawati and Meki, Irene Kasindi and Dharmayanti, Ni Luh Putu Indi and Hoerudin, Heri and Ratnawati, Atik and Settypalli, Tirumala Bharani K. and Ahmed, Hatem Ouled and Nuradji, Harimurti and Saepulloh, Muharam and Adji, Rahmat Setya and Fairusya, Nuha and Sari, Faralinda and Anindita, Katamtama and Cattoli, Giovanni and Lamien, Charles Euloge (2024) Molecular characterization of recombinant LSDV isolates from 2022 outbreak in Indonesia through phylogenetic networks and whole-genome SNP-based analysis. BMC Genomics, 25 (1). ISSN 1471-2164

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Abstract

Lumpy skin disease (LSD) is a transboundary viral disease of cattle and water buffaloes caused by the LSD virus, leading to high morbidity, low mortality, and a significant economic impact. Initially endemic to Africa only, LSD has spread to the Middle East, Europe, and Asia in the past decade. The most effective control strategy for LSD is the vaccination of cattle with live-attenuated LSDV vaccines. Consequently, the emergence of two groups of LSDV strains in Asian countries, one closely related to the ancient Kenyan LSDV isolates and the second made of recombinant viruses with a backbone of Neethling-vaccine and field isolates, emphasized the need for constant molecular surveillance. This current study investigated the first outbreak of LSD in Indonesia in 2022. Molecular characterization of the isolate circulating in the country based on selected LSDV-marker genes: RPO30, GPCR, EEV glycoprotein gene, and B22R, as well as whole genome analysis using several analytical tools, indicated the Indonesia LSDV isolate as a recombinant of LSDV_Neethling_vaccine_LW_1959 and LSDV_NI-2490. The analysis clustered the Indonesia_LSDV with the previously reported LSDV recombinants circulating in East and Southeast Asia, but different from the recombinant viruses in Russia and the field isolates in South-Asian countries. Additionally, this study has demonstrated alternative accurate ways of LSDV whole genome analysis and clustering of isolates, including the recombinants, instead of whole-genome phylogenetic tree analysis. These data will strengthen our understanding of the pathogens’ origin, the extent of their spread, and determination of suitable control measures required.

Item Type: Article
Uncontrolled Keywords: LSDV, Whole genome sequencing, Recombinant, Phylogenetic network, SNP
Subjects: Health Resources > Health Care Measurement Methodology
Medicine & Biology > Cytology, Genetics, & Molecular Biology
Depositing User: Saepul Mulyana
Date Deposited: 04 Dec 2025 05:29
Last Modified: 04 Dec 2025 05:29
URI: https://karya.brin.go.id/id/eprint/55592

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