Genetic Characterization of Lumpy Skin Disease Viruses Circulating in Lesotho Cattle

Author:

Makalo Mabusetsa Joseph Raporoto12ORCID,Settypalli Tirumala Bharani Kumar3ORCID,Meki Irene Kasindi3ORCID,Bakhoum Mame Thierno4ORCID,Ahmed Hatem Ouled3,Phalatsi Moeketsi Solomon5,Ramatla Tsepo1,Onyiche ThankGod Emmanuel16ORCID,Nionzima-Bohloa Lineo2,Metlin Artem7ORCID,Dhingra Madhur7,Cattoli Giovanni3,Lamien Charles Euloge3ORCID,Thekisoe Oriel Matlhahane Molifi1ORCID

Affiliation:

1. Unit for Environmental Sciences and Management, North-West University, Potchefstroom 2531, South Africa

2. Department of Livestock Services, Ministry of Agriculture, Food Security, and Nutrition, Private A82, Maseru, Lesotho

3. Animal Production and Health Laboratory, Animal Production and Health Section, Joint FAO/IAEA Division, Department of Nuclear Sciences and Applications, International Atomic Energy Agency, P.O. Box 100, 1400 Vienna, Austria

4. Laboratoire National de l’Elevage et de Recherches Vétérinaires ISRA/LNERV(LNERV), BP 2057, Dakar, Senegal

5. Department of Animal Science, National University of Lesotho, P.O. Roma 180, Lesotho

6. Department of Veterinary Parasitology and Entomology, University of Maiduguri, P. M. B. 1069, Maiduguri 600230, Nigeria

7. Food and Agriculture Organization of the United Nations, Viale delle Terme di Caracalla, 00153 Rome, Italy

Abstract

Lumpy skin disease is one of the fast-spreading viral diseases of cattle and buffalo that can potentially cause severe economic impact. Lesotho experienced LSD for the first time in 1947 and episodes of outbreaks occurred throughout the decades. In this study, eighteen specimens were collected from LSD-clinically diseased cattle between 2020 and 2022 from Mafeteng, Leribe, Maseru, Berea, and Mohales’ Hoek districts of Lesotho. A total of 11 DNA samples were analyzed by PCR and sequencing of the extracellular enveloped virus (EEV) glycoprotein, G-protein-coupled chemokine receptor (GPCR), 30 kDa RNA polymerase subunit (RPO30), and B22R genes. All nucleotide sequences of the above-mentioned genes confirmed that the PCR amplicons of clinical samples are truly LSDV, as they were identical to respective LSDV isolates on the NCBI GenBank. Two of the elevem samples were further characterized by whole-genome sequencing. The analysis, based on both CaPV marker genes and complete genome sequences, revealed that the LSDV isolates from Lesotho cluster with the NW-like LSDVs, which includes the commonly circulating LSDV field isolates from Africa, the Middle East, the Balkans, Turkey, and Eastern Europe.

Funder

Peaceful Uses Initiatives

IAEA

Publisher

MDPI AG

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