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. 2024 Apr 3;16(4):557.
doi: 10.3390/v16040557.

Sequencing and Analysis of Lumpy Skin Disease Virus Whole Genomes Reveals a New Viral Subgroup in West and Central Africa

Affiliations

Sequencing and Analysis of Lumpy Skin Disease Virus Whole Genomes Reveals a New Viral Subgroup in West and Central Africa

Ismar R Haga et al. Viruses. .

Abstract

Lumpy skin disease virus (LSDV) is a member of the capripoxvirus (CPPV) genus of the Poxviridae family. LSDV is a rapidly emerging, high-consequence pathogen of cattle, recently spreading from Africa and the Middle East into Europe and Asia. We have sequenced the whole genome of historical LSDV isolates from the Pirbright Institute virus archive, and field isolates from recent disease outbreaks in Sri Lanka, Mongolia, Nigeria and Ethiopia. These genome sequences were compared to published genomes and classified into different subgroups. Two subgroups contained vaccine or vaccine-like samples ("Neethling-like" clade 1.1 and "Kenya-like" subgroup, clade 1.2.2). One subgroup was associated with outbreaks of LSD in the Middle East/Europe (clade 1.2.1) and a previously unreported subgroup originated from cases of LSD in west and central Africa (clade 1.2.3). Isolates were also identified that contained a mix of genes from both wildtype and vaccine samples (vaccine-like recombinants, grouped in clade 2). Whole genome sequencing and analysis of LSDV strains isolated from different regions of Africa, Europe and Asia have provided new knowledge of the drivers of LSDV emergence, and will inform future disease control strategies.

Keywords: cattle; lumpy skin disease virus; poxvirus.

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Conflict of interest statement

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Figures

Figure 1
Figure 1
Core genome phylogenies for (A) all 22 LSDV samples and (B) clade 1.2 only (18 samples). (A) The clade 1.1 Neethling strain was distinct from the clade 2 Hong Kong/Mongolia isolates. (B) Clade 1.2 was divided into three groups: clade 1.2.2 related to Kenyan sheep and goat pox (KSGP) vaccines (blue, n = 6), clade 1.2.3 linked to west and central Africa (green, n = 5) and clade 1.2.1 with samples from the Middle East and east Africa (red, n = 7). Bootstraps with values > 90 are shown.
Figure 2
Figure 2
Phylogenies of the (A) central (67,250 to 99,575 bp) and (B) adjacent core genome regions (13,851–66,966 and 99,608–106,910 bp, concatenated). (A) At the central core genome, clade 2’s Hong Kong and the Mongolia pair (grey) had ancestry more like clade 1.2.2 (clade 1.2.2 in blue, clade 1.2.3 in green, clade 1.2.1 in red). (B) At the adjacent core genome regions, clade 2 was more like Neethling (clade 1.1).
Figure 3
Figure 3
Geographic distribution of the LSDV strains. Colour designations: clade 1.2.1 red, clade 1.2.2 blue, clade 1.2.3 green, and clade 2 yellow.

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