Abstract

The transmission of “lumpy skin disease virus” (LSDV) has prompted intensive research efforts due to the rapid spread and high impact of the disease in recent years, especially in Eastern Europe and Balkan countries. In this study, we experimentally evaluate the vaccine-derived virulent recombinant LSDV strain (Saratov/2017) and provide solid evidence on the capacity of the virus for transmission in a vector-proof environment. In the 60-day long experiment, we used inoculated bulls (IN group) and two groups of in-contact animals (C1 and C2), with the former (C1) being in contact with the inoculated animals at the onset of the trial and the latter (C2) being introduced at day 33 of the experiment. The infection in both groups of contact animals was confirmed clinically, serologically and virologically, and viremia was demonstrated in blood, nasal and ocular excretions, using molecular tools. Further studies into LSDV biology are a priority to gain insights into whether the hypothesized indirect contact mode evidenced in this study is a de novo-created feature, absent from both parental stains of the novel (recombinant) LSDV isolate used, or whether it was dormant, but then unlocked by the process of genetic recombination. Author summary: In global terms, LSD has been termed a “neglected disease” due to its historic natural occurrence of being restricted to Africa and, occasionally, Israel. However, after its slow spread throughout the Middle East, the disease is now experiencing a resurgence of research interest following a recent and rapid spread into more northern latitudes. Given the dearth of solid findings on potential transmission mechanisms, no efficient or reliable control program currently exists, which does not involve the use of live attenuated vaccines or stamping out policies – both of which are controversial for implementation in non-endemic regions or countries. The vector-borne mode is the only working concept currently available, but with scarce evidence to support the aggressive spread northwards – except for human-assisted spread, including legal or illegal animal transportation. The emergence of outbreaks is not consistently linked to weather conditions, with the potential for new outbreaks to occur and spread rapidly. Here, for the first time, we provide evidence for indirect contact-mode transmission for a naturally-occurring recombinant LSDV isolated from the field. In an insect-proof facility, we obtained solid evidence that the novel LSDV strain can pass to in-contact animals. Given the recombinant nature of the virus utilised, its genetic background relating to the observed transmission pattern within the study needs to be delineated.

Highlights

  • The transmission of “lumpy skin disease virus” (LSDV) has prompted intensive research efforts due to the rapid spread and high impact of the disease in recent years, especially in Eastern Europe and Balkan countries

  • Transmission studies conducted to date using arthropod species which may be involved in transmission are mostly species which are restricted to the Southern hemisphere (e.g. Rhipicephalus appendiculatus ticks), which complicates analysis of transmission potential of local species in climatically new geographic areas in the Northern hemisphere

  • All animals infected with LSD virus (LSDV) at the outset of the trial had fevers up to 40.7 °C on p.i. day 3, indicating virus replication and circulation

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Summary

Introduction

The transmission of “lumpy skin disease virus” (LSDV) has prompted intensive research efforts due to the rapid spread and high impact of the disease in recent years, especially in Eastern Europe and Balkan countries. For the first time, we provide evidence for indirect contact-mode transmission for a naturally-occurring recombinant LSDV isolated from the field. Lumpy skin disease (LSD) virus belongs to the genus Capripoxvirus within the family Poxviridae (Buller et al, 2005) It contains a double-stranded, covalently-linked linear DNA genome enveloped by a lipid bilayer. Based on full-genome sequences deposited in GenBank, LSDV exists as two genetic lineages: field isolates and live attenuated vaccine strains, evidence for a naturally occurring recombinant between a vaccine strain and field strain has been reported[4]. Initial evidence and studies suggested that direct or indirect contact (without vectors) are ineffective routes for LSDV transmission[12], whereas the predominant transmission pathway for sheep pox and goat pox viruses is via aerosols. Field evidence suggests that successful transmission can be achieved when naïve animals are allowed to share a drinking trough with severely infected animals[17,18]

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