본문 바로가기
KERD
논문KCI 등재

Evaluation of different molecular methods for detection of Senecavirus A and the result of the antigen surveillance in Korea during 2018

1

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류수의학

초록

Senecavirus A (SVA), previously known as Seneca Valley virus, can cause vesicular disease and neonatal losses in pigs that is clinically indistinguishable from foot-and-mouth disease virus (FMDV). After the first case report in Canada in 2007, it had been restrictively identified in North America including United States. But, since 2015, SVA emerged outside North America in Brazil, and also in several the Asian countries including China, Thailand, and Vietnam. Considering the SVA occurrence in neighboring countries, there has been a high risk that Korea can be introduced at any time. In particular, it is very important in terms of differential diagnosis in the suspected case of vesicular diseases in countries where FMD is occurring. So far, several different molecular detection methods for SVV have been published but not validated as the reference method, yet. In this study, seven different molecular methods for detecting SVA were evaluated. Among them, the method by Flowler et al, (2017) targeted to 3D gene region with the highest sensitivity and no cross reaction with other vesicular disease agents including FMDV, VSV and SVD, was selected and applied further to antigen surveillance of SVA. A total of 245 samples of 157 pigs from 61 farms submitted for animal disease diagnose nationwide during 2018 were tested all negative. In 2018, no sign of SVA occurrence have been confirmed in Korea, but the results of the surveillance for SVA needs to be continued and accumulated at a high risk of SVA in neighboring countries.

Abstract

Senecavirus A (SVA), previously known as Seneca Valley virus, can cause vesicular disease and neonatal losses in pigs that is clinically indistinguishable from foot-and-mouth disease virus (FMDV). After the first case report in Canada in 2007, it had been restrictively identified in North America including United States. But, since 2015, SVA emerged outside North America in Brazil, and also in several the Asian countries including China, Thailand, and Vietnam. Considering the SVA occurrence in neighboring countries, there has been a high risk that Korea can be introduced at any time. In particular, it is very important in terms of differential diagnosis in the suspected case of vesicular diseases in countries where FMD is occurring. So far, several different molecular detection methods for SVV have been published but not validated as the reference method, yet. In this study, seven different molecular methods for detecting SVA were evaluated. Among them, the method by Flowler et al, (2017) targeted to 3D gene region with the highest sensitivity and no cross reaction with other vesicular disease agents including FMDV, VSV and SVD, was selected and applied further to antigen surveillance of SVA. A total of 245 samples of 157 pigs from 61 farms submitted for animal disease diagnose nationwide during 2018 were tested all negative. In 2018, no sign of SVA occurrence have been confirmed in Korea, but the results of the surveillance for SVA needs to be continued and accumulated at a high risk of SVA in neighboring countries.

참고문헌 (17)

  1. Agnol AMD, "A TaqMan-based qRT-PCR assay for Senecavirus A detection in tissue samples of neonatal piglets", Molecular and Cellular Probes, 33, pp.28~31 (2017)
  2. Arzt J, "First detection and genome sequence of Senecavirus A in Vietnam", Microbiology Resource Announcements, 8(3) (2019)
  3. Bracht AJ, "Real-time reverse transcription PCR assay for detection of Senecavirus A in swine vesicular diagnostic specimens", PLoS One, 11(1), pp.e0146211~ (2016)
  4. Feronato C, "Development and evaluation of a nested-PCR assay for Senecavirus A diagnosis", Tropical Animal Health and Production, 50(2), pp.337~344 (2018)
  5. Fowler VL, "Development of a novel real-time RT-PCR assay to detect Seneca Valley virus-1associated with emerging cases of vesicular disease in pigs", Journal of Virological Methods, 239, pp.34~37 (2017)
  6. Joshi LR, "Detection of the emerging picornavirus Senecavirus A in pigs, mice, and houseflies", Journal of Clinical Microbiology, 54(6), pp.1536~1545 (2016)
  7. Knowles NJ, "Epidemiology of Seneca Valley virus: identification and characterization of isolates from pigs in the United States", Northern Lights EUROPIC, ~ (2006)
  8. Leme RA, "Update on Senecavirus infection in pigs", Viruses, 9(7), pp.170~ (2017)
  9. Leme RA, "Clinical manifestations of Senecavirus A infection in neonatal pigs, Brazil, 2015", Emerging Infectious Diseases, 22(7), pp.1238~ (2016)
  10. Leme RA, "Senecavirus A : an emerging vesicular infection in Brazilian pig herds", Transboundary and Emerging Diseases, 62(6), pp.603~611 (2015)
  11. Liu F, "A 5-year Review of Senecavirus A in China since Its Emergence in 2015", Frontiers in Veterinary Science, 7 (2015)[DOI]
  12. Maggioli MF, "Adaptive immune responses following Senecavirus A infection in pigs", Journal of Virology, 92(3) (2018)
  13. Pasma T, "Idiopathic vesicular disease in swine in Manitoba", The Canadian Veterinary Journal, 49(1), pp.84~ (2008)
  14. Rudin CM, "Phase I clinical study of Seneca Valley Virus (SVV-001), a replicationcompetent picornavirus, in advanced solid tumors with neuroendocrine features", Clinical Cancer Research, 17(4), pp.888~895 (2011)
  15. Saeng-Chuto K, "The first detection of Senecavirus A in pigs in Thailand, 2016", Transboundary and Emerging Diseases, 65(1), pp.285~288 (2018)
  16. Wu Q, "Complete genome sequence of Seneca Valley virus CH-01-2015identified in China", Genome Announcements, 4(1) (2016)
  17. Zhang X, "Identification and genomic characterization of the emerging Senecavirus A in southeast China, 2017", Transboundary and Emerging Diseases, 65(2), pp.297~302 (2018)

관련 논문AI추천

구제역바이러스 혈청형 A 검출을 위한 peptide nucleic acid (PNA)기반 multiplex real-time RT-PCR 개발구복경, 김태성, 나진주, 박혜진, 신문균, 위성환, 유소윤, 이수미, 이정원, 이진우, 이현지, 정세민, 하병석한국동물위생학회 · 한국동물위생학회지2019 · 제42권 제1호구제역바이러스 신속진단을 위한 pan-serotype reverse transcription loop-mediated isothermal amplification (RT-LAMP) 진단법구복경, 김지정, 김혜령, 나진주, 박민지, 박선영, 박유리, 박최규, 위성환, 유소윤, 이형우, 임다래, 전보영, 전효성한국동물위생학회 · 한국동물위생학회지2018 · 제41권 제1호Comparative evaluation of commercial multiplex real-time RT-PCR kits for differential detection of PRRSV-1, PRRSV-2, and PCV2 currently circulating in Korean pig farmsChoi-Kyu Park, Da-Young Kim, Dong-Kyu Lee, Ho-Seok Do, Hwan-Ju Kim, Hye-Ryung Kim, Ji-Hyeon Baek, Jonghyun Park, Jung-Hoon Kwon, Ki Beom Park, Nam-Yeon Kim, Seung-Chai Kim, Won-Il Kim한국동물위생학회 · 한국동물위생학회지2025 · 제48권 제2호포유자돈 선천성 진전증 증례에서 atypical porcine pestivirus (APPV) 검출강석진, 김범석, 김승채, 김원일, 양면식, 윤승민, 이기호, 이승윤, 정창기한국동물위생학회 · 한국동물위생학회지2017 · 제40권 제3호Prevalence and co-infection status of three pathogenic porcine circoviruses (PCV2, PCV3, and PCV4) by a newly established triplex real-time polymerase chain reaction assay박최규, Hye-Ryung Kim, Jonghyun Park, Won-Il Kim, Young S. Lyoo한국동물위생학회 · 한국동물위생학회지2022 · 제45권 제2호Whole genome sequencing of foot-and-mouth disease virus using benchtop next generation sequencing (NGS) system오연수, 조호성, Dongseob Tark, Sung-Hyun Moon한국동물위생학회 · 한국동물위생학회지2019 · 제42권 제4호

이 간행물의 다른 논문 (7건)