Abstract

Lumpy skin disease virus (LSDV) is the causative agent of lumpy skin disease (LSD) that has been recently reported in the South-East and North Asian parts of the Russian Federation. During 2017–2019, there were more than 30 LSD outbreaks in Saratov Region despite active inoculation of cattle with heterologous vaccine. Importantly, the first case of the novel recombinant LSDV strain was reported here in 2017. This study aimed to determine the main clonal lineage(s) of LSDV strains circulated within Saratov Region and other regions of Russia since the first introduction of LSDV. The molecular typing and subtyping based on the coding regions of the G-protein-coupled chemokine receptor (GPCR) gene resulted in a discrimination of all outbreak-related LSDV strains into two main types, such as Type I and Type II, and subtypes Ia-d and IIa-g. Phylogenetically, eleven LSDV lineages were revealed in Russia including the five ones in Saratov Region. They were the following: (i) the Neethling wild Type Ia/2017; (ii) the recombinant Saratov IIc/2017/2019; (iii) the specific Dergachevskyi IId/2017; (iv) the Khvalynsky IIg/2018, and (v) the Haden-Type IIa lineage for the six LSDV strains detected in cattle immunized with heterologous vaccine during the last LSD outbreak in the Saratov Region, Nesterovo Village, in 2019 (Nesterovo-2019 strains). A single LSDV strain detected in Saratov Region in 2017 had the same Type Ia that was identified in 2016 in the bordered Republic of Kazakhstan. Phylogeographic analysis demonstrated three nominal clusters of LSDV types in the following Russian Federation territories: (I) the Central European part; (II) the South-East of the European part; (III) the North Asian part. Cluster I was represented by mainly Type I strains, while both Clusters 2 and 3 contained predominantly Type II strains. The Clusters I and II partially overlapped, while Cluster 3 was separate. Multiple introductions of LSDV into Saratov Region in 2017–2019 using GPCR-based molecular typing and subtyping were revealed. This scheme is a promising tool for molecular discrimination of LSDV strains derived from both vaccinated and unvaccinated against LSD cattle as well as for molecular epidemiology.

Highlights

  • Lumpy skin disease virus (LSDV), the causative agent of lumpy skin disease (LSD)is known as one of the three species, namely LSDV, sheeppox virus (SPPV) and goatpox virus (GTPV) in the genus Capripoxvirus (CapPVs) within the Poxviridae family [1,2,3,4,5,6,7,8,9,10]

  • The aim of this study was: (i) to conduct molecular typing of the LSDV strains detected in cattle immunized with SPPV vaccine during the last LSD outbreak in Saratov Region in September–October, 2019; and (ii) to determine the main clonal lineage(s) of LSDV

  • Molecular typing of the LSDV strains detected in cattle immunized with SPPV vaccine during the last LSD outbreak in Saratov Region, the Nesterovo Village, in September–October, 2019, was successfully performed

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Summary

Introduction

Lumpy skin disease virus (LSDV), the causative agent of lumpy skin disease (LSD). Is known as one of the three species, namely LSDV, sheeppox virus (SPPV) and goatpox virus (GTPV) in the genus Capripoxvirus (CapPVs) within the Poxviridae family [1,2,3,4,5,6,7,8,9,10]. The LSDV is a relatively large, double-stranded DNA enveloped virus with a genome of 151-kbp that contains 156 putative genes sharing 97% nucleotide identity with the genomes of two other CapPVs, SPPV and GTPV [7,11]. All SPPV and GTPV genes have been found in LSDV [12] providing the marked serologic cross-reactivity between these three CapPVs [2].

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