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The First Report on the Complete Sequence Characterization of Bluetongue Virus Serotype 3 in the Republic of Korea.
Kim, Hyun-Jeong; Choi, Jun-Gu; Seong, Da-Seul; Jeong, Jong-Uk; Kim, Hye-Jung; Park, Sang-Won; Yun, Seung-Pil; Roh, In-Soon.
Affiliation
  • Kim HJ; Division of Foreign Animal Disease, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Republic of Korea.
  • Choi JG; Laboratory Animal Research Center, Central Scientific Instrumentation Facility, Gyeongsang National University, Jinju 52828, Republic of Korea.
  • Seong DS; Division of Foreign Animal Disease, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Republic of Korea.
  • Jeong JU; Division of Foreign Animal Disease, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Republic of Korea.
  • Kim HJ; Division of Foreign Animal Disease, Animal and Plant Quarantine Agency, Gimcheon-si 39660, Republic of Korea.
  • Park SW; Department of Pharmacology, Institute of Medical Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Republic of Korea.
  • Yun SP; Department of Convergence Medical Sciences, Gyeongsang National University Graduate School, Jinju 52727, Republic of Korea.
  • Roh IS; Department of Pharmacology, Institute of Medical Sciences, College of Medicine, Gyeongsang National University, Jinju 52727, Republic of Korea.
Vet Sci ; 11(1)2024 Jan 11.
Article in En | MEDLINE | ID: mdl-38250935
ABSTRACT
The bluetongue virus (BTV) is a significant animal pathogen with economic implications in the ruminant industry. Despite global reports on BTV detection and epidemiologic investigations, limited studies have focused on the virus in the ROK. In this study, BTV epidemiological research was conducted on blood samples from cattle and goat farms across nine regions during 2013-2014. The results showed that 3.33% of bovine blood samples (194/5824) and 0.19% of goat blood samples (2/1075) tested positive for BTV antibodies using ELISA. In Jeju-do, BTV RNA amplification occurred in 51 of 422 samples (12.1%) using real-time reverse transcription (RT-qPCR). The isolation of one sample revealed it as serotype 3, as indicated by the sequence of segments 2 (Seg-2) and 6 (Seg-6), associated with the eastern BTV topotype. However, based on Seg-1, -3, -4, -5, -7, -8, -9, and -10 analyses, the BTV-3/JJBB35 strain is more closely related to distinct BTV strains. These findings imply BTV circulation and that the Korean-isolated BTV might originate from Asian BTV strains due to multiple reassortment events. This study provides foundational data for ongoing BTV monitoring and disease-control policies in the ROK.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Vet Sci Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Vet Sci Year: 2024 Document type: Article