First Report of Lumpy Skin Disease in Myanmar and Molecular Analysis of the Field Virus Isolates

• Published in: Microorganisms (Basel) Vol. 10; no. 5; p. 897
• Main Authors: Maw, Min Thein, Khin, Myint Myint, Hadrill, David, Meki, Irene Kasindi, Settypalli, Tirumala Bharani Kumar, Kyin, Maung Maung, Myint, Win Win, Thein, Wai Zin, Aye, Ohnmar, Palamara, Elisa, Win, Ye Tun, Cattoli, Giovanni, Lamien, Charles Euloge
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 25.04.2022; MDPI AG
• Subjects: LSDV; lumpy skin disease; molecular analysis; Myanmar; outbreak; Myanmar; lumpy skin disease; outbreak; LSDV; molecular analysis
• ISSN: 2076-2607; 2076-2607
• DOI: 10.3390/microorganisms10050897

Lumpy skin disease virus (LSDV) causes lumpy skin disease in cattle and buffaloes, which is associated with significant animal production and economic losses. Since the 2000s, LSDV has spread from Africa to several countries in the Middle East; Europe; and Asia; including, more recently, several south-east Asian countries. In November 2020, Myanmar reported its first LSD outbreak. This study reports on the first incursion of LSD in Myanmar and the molecular analysis of the LSDV detected. Staff from the Livestock Breeding and Veterinary Department (LBVD) of the Ministry of Agriculture, Livestock, and Irrigation collected samples from cattle with suspected LSD infection. The Food and Agriculture Organization (FAO) of the United Nations' Emergency Centre for Transboundary Animal Diseases (ECTAD) and the Joint International Atomic Energy Agency (IAEA)/FAO program's Animal Health and Production laboratory provided LSDV diagnostic support to two regional veterinary diagnostic laboratories in Myanmar. Samples from 13 cattle tested positive by real-time PCR. Selected samples underwent sequence analysis in IAEA laboratories. The results show that the Myanmar LSDV sequences clustered with LSDV isolates from Bangladesh and India, LSDV Kenya, and LSDV NI-2490. Further characterization showed that the Myanmar LSDV is 100% identical to isolates from Bangladesh and India, implying a common source of introduction. These findings inform diagnosis and development of control strategies.