Monitoring of chronic wasting disease using real-time quaking-induced conversion assay in Japan
There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of...
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Published in | Journal of Veterinary Medical Science Vol. 83; no. 11; pp. 1735 - 1739 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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JAPANESE SOCIETY OF VETERINARY SCIENCE
2021
The Japanese Society of Veterinary Science |
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ISSN | 0916-7250 1347-7439 1347-7439 |
DOI | 10.1292/jvms.21-0368 |
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Abstract | There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of CWD prions. A total of 690 obex samples collected from sika deer and Reeves’s muntjac in Hokkaido and Honshu was tested for CWD prions. No CWD-positive cases were found, suggesting that CWD is nonexistent in Japan. Our results also indicate that RT-QuIC assay is useful for continuous monitoring of CWD. Furthermore, nucleotide sequence analysis of the PrP gene revealed sika deer in Japan harbor CWD susceptible allele. |
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AbstractList | There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of CWD prions. A total of 690 obex samples collected from sika deer and Reeves’s muntjac in Hokkaido and Honshu was tested for CWD prions. No CWD-positive cases were found, suggesting that CWD is nonexistent in Japan. Our results also indicate that RT-QuIC assay is useful for continuous monitoring of CWD. Furthermore, nucleotide sequence analysis of the PrP gene revealed sika deer in Japan harbor CWD susceptible allele. There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of CWD prions. A total of 690 obex samples collected from sika deer and Reeves's muntjac in Hokkaido and Honshu was tested for CWD prions. No CWD-positive cases were found, suggesting that CWD is nonexistent in Japan. Our results also indicate that RT-QuIC assay is useful for continuous monitoring of CWD. Furthermore, nucleotide sequence analysis of the PrP gene revealed sika deer in Japan harbor CWD susceptible allele.There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of CWD prions. A total of 690 obex samples collected from sika deer and Reeves's muntjac in Hokkaido and Honshu was tested for CWD prions. No CWD-positive cases were found, suggesting that CWD is nonexistent in Japan. Our results also indicate that RT-QuIC assay is useful for continuous monitoring of CWD. Furthermore, nucleotide sequence analysis of the PrP gene revealed sika deer in Japan harbor CWD susceptible allele. There has been no report on Chronic wasting disease (CWD) cases in Japan to date; however, there is concern about the geographic spread of CWD. To clarify the CWD status in Japan, we conducted CWD monitoring using real-time quaking-induced conversion (RT-QuIC) assay which can detect the low level of CWD prions. A total of 690 obex samples collected from sika deer and Reeves’s muntjac in Hokkaido and Honshu was tested for CWD prions. No CWD-positive cases were found, suggesting that CWD is nonexistent in Japan. Our results also indicate that RT-QuIC assay is useful for continuous monitoring of CWD. Furthermore, nucleotide sequence analysis of the PrP gene revealed sika deer in Japan harbor CWD susceptible allele. |
ArticleNumber | 21-0368 |
Author | SUGA, Kinuyo SUZUKI, Akio HORIUCHI, Motohiro SAWADA, Kazuhei TOBIUME, Minoru YAMASAKI, Takeshi ERDENEBAT, Temuulen |
Author_xml | – sequence: 1 fullname: SAWADA, Kazuhei organization: Laboratory of Veterinary Hygiene, Faculty of Veterinary Medicine, Graduate School of Infectious Diseases, Hokkaido University, Kita 18, Nishi 9, Kita-ku, Sapporo, Hokkaido 060-0818, Japan – sequence: 1 fullname: YAMASAKI, Takeshi organization: Biomedical Animal Research Laboratory, Institute for Genetic Medicine, Hokkaido University, Kita 15, Nishi 9, Kita-ku, Sapporo, Hokkaido 060-0815, Japan – sequence: 1 fullname: SUGA, Kinuyo organization: Hyogo Prefecture Nishiharima Meat Hygiene Inspection Office, Shingu-cho, Tatsuno, Hyogo 679-4322, Japan – sequence: 1 fullname: ERDENEBAT, Temuulen organization: Laboratory of Veterinary Hygiene, Faculty of Veterinary Medicine, Graduate School of Infectious Diseases, Hokkaido University, Kita 18, Nishi 9, Kita-ku, Sapporo, Hokkaido 060-0818, Japan – sequence: 1 fullname: HORIUCHI, Motohiro organization: Global Station for Zoonosis Control, Global Institute for Collaborative Research and Education, Hokkaido University, Kita 20, Nishi 10, Kita-ku, Sapporo, Hokkaido 001-0020, Japan – sequence: 1 fullname: SUZUKI, Akio organization: Laboratory of Veterinary Hygiene, Faculty of Veterinary Medicine, Graduate School of Infectious Diseases, Hokkaido University, Kita 18, Nishi 9, Kita-ku, Sapporo, Hokkaido 060-0818, Japan – sequence: 1 fullname: TOBIUME, Minoru organization: Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan |
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Cites_doi | 10.1099/vir.0.069906-0 10.1099/vir.0.81077-0 10.1038/35081095 10.1523/JNEUROSCI.2467-05.2005 10.1111/brv.12568 10.1111/j.1365-2052.2005.01276.x 10.7589/2018-10-262 10.1080/19336896.2020.1858694 10.1038/nm.2294 10.2903/j.efsa.2019.5863 10.3201/eid1509.090253 10.1111/j.1348-0421.2007.tb03988.x 10.1126/science.1132661 10.1146/annurev-animal-022114-111001 10.1016/j.celrep.2015.04.036 10.1128/JCM.01258-14 10.1111/bpa.12696 10.1292/jvms.67.349 10.3390/ijms22052271 |
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References | 15. Meng, L. P., Zhao, D. M., Liu, H. X., Yang, J. M., Ning, Z. Y., Wu, C. D. and Han, C. X. 2005. Polymorphisms of the prion protein gene (PRNP) in Chinese domestic sika deer (Cervus nippon hortulorum). Anim. Genet. 36: 266–267. 17. Pritzkow, S., Morales, R., Moda, F., Khan, U., Telling, G. C., Hoover, E. and Soto, C. 2015. Grass plants bind, retain, uptake, and transport infectious prions. Cell Rep. 11: 1168–1175. 4. Escobar, L. E., Pritzkow, S., Winter, S. N., Grear, D. A., Kirchgessner, M. S., Dominguez-Villegas, E., Machado, G., Townsend Peterson, A. and Soto, C. 2020. The ecology of chronic wasting disease in wildlife. Biol. Rev. Camb. Philos. Soc. 95: 393–408. 12. Koutsoumanis, K., Allende, A., Alvarez-Ordoňez, A., Bolton, D., Bover-Cid, S., Chemaly, M., Davies, R., De Cesare, A., Herman, L., Hilbert, F., Lindqvist, R., Nauta, M., Peixe, L., Ru, G., Skandamis, P., Suffredini, E., Andreoletti, O., Benestad, S. L., Comoy, E., Nonno, R., da Silva Felicio, T., Ortiz-Pelaez, A., Simmons, M. M., EFSA Panel on Biological Hazards (BIOHAZ). 2019. Update on chronic wasting disease (CWD) III. EFSA J. 17: e05863. 18. Race, B., Meade-White, K. D., Miller, M. W., Barbian, K. D., Rubenstein, R., LaFauci, G., Cervenakova, L., Favara, C., Gardner, D., Long, D., Parnell, M., Striebel, J., Priola, S. A., Ward, A., Williams, E. S., Race, R. and Chesebro, B. 2009. Susceptibilities of nonhuman primates to chronic wasting disease. Emerg. Infect. Dis. 15: 1366–1376. 3. Atarashi, R., Satoh, K., Sano, K., Fuse, T., Yamaguchi, N., Ishibashi, D., Matsubara, T., Nakagaki, T., Yamanaka, H., Shirabe, S., Yamada, M., Mizusawa, H., Kitamoto, T., Klug, G., McGlade, A., Collins, S. J. and Nishida, N. 2011. Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. Nat. Med. 17: 175–178. 8. Houston, F. and Andréoletti, O. 2019. Animal prion diseases: the risks to human health. Brain Pathol. 29: 248–262. 2. Arifin, M. I., Hannaoui, S., Chang, S. C., Thapa, S., Schatzl, H. M. and Gilch, S. 2021. Cervid prion protein polymorphisms: role in chronic wasting disease pathogenesis. Int. J. Mol. Sci. 22: 2271. 21. Vikøren, T., Våge, J., Madslien, K. I., Røed, K. H., Rolandsen, C. M., Tran, L., Hopp, P., Veiberg, V., Heum, M., Moldal, T., Neves, C. G. D., Handeland, K., Ytrehus, B., Kolbjørnsen, Ø., Wisløff, H., Terland, R., Saure, B., Dessen, K. M., Svendsen, S. G., Nordvik, B. S. and Benestad, S. L. 2019. First detection of chronic wasting disease in a wild red deer (Cervus elaphus) in Europe. J. Wildl. Dis. 55: 970–972. 5. Haley, N. J. and Hoover, E. A. 2015. Chronic wasting disease of cervids: current knowledge and future perspectives. Annu. Rev. Anim. Biosci. 3: 305–325. 11. Kong, Q., Huang, S., Zou, W., Vanegas, D., Wang, M., Wu, D., Yuan, J., Zheng, M., Bai, H., Deng, H., Chen, K., Jenny, A. L., O’Rourke, K., Belay, E. D., Schonberger, L. B., Petersen, R. B., Sy, M. S., Chen, S. G. and Gambetti, P. 2005. Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. J. Neurosci. 25: 7944–7949. 1. Agriculture & Livestock Industries Corporation (ALIC). 2021. Statistical Data, Livestock and Livestock Products. https://www.alic.go.jp/joho-c/joho05_000073.html [accessed on May 31, 2021]. 6. Haley, N. J., Carver, S., Hoon-Hanks, L. L., Henderson, D. M., Davenport, K. A., Bunting, E., Gray, S., Trindle, B., Galeota, J., LeVan, I., Dubovos, T., Shelton, P. and Hoover, E. A. 2014. Detection of chronic wasting disease in the lymph nodes of free-ranging cervids by real-time quaking-induced conversion. J. Clin. Microbiol. 52: 3237–3243. 7. Henderson, D. M., Davenport, K. A., Haley, N. J., Denkers, N. D., Mathiason, C. K. and Hoover, E. A. 2015. Quantitative assessment of prion infectivity in tissues and body fluids by real-time quaking-induced conversion. J. Gen. Virol. 96: 210–219. 10. Kataoka, N., Nishimura, M., Horiuchi, M. and Ishiguro, N. 2005. Surveillance of chronic wasting disease in sika deer, Cervus nippon, from Tokachi district in Hokkaido. J. Vet. Med. Sci. 67: 349–351. 20. Suzuki, A., Sawada, K., Yamasaki, T., Denkers, N. D., Mathiason, C. K., Hoover, E. A. and Horiuchi, M. 2020. Involvement of N- and C-terminal region of recombinant cervid prion protein in its reactivity to CWD and atypical BSE prions in real-time quaking-induced conversion reaction in the presence of high concentrations of tissue homogenates. Prion 14: 283–295. 13. Masujin, K., Shimada, K., Kimura, K. M., Imamura, M., Yoshida, A., Iwamaru, Y., Mohri, S. and Yokoyama, T. 2007. Applicability of current bovine spongiform encephalopathy (BSE) diagnostic procedures for chronic wasting disease (CWD). Microbiol. Immunol. 51: 1039–1043. 14. Mathiason, C. K., Powers, J. G., Dahmes, S. J., Osborn, D. A., Miller, K. V., Warren, R. J., Mason, G. L., Hays, S. A., Hayes-Klug, J., Seelig, D. M., Wild, M. A., Wolfe, L. L., Spraker, T. R., Miller, M. W., Sigurdson, C. J., Telling, G. C. and Hoover, E. A. 2006. Infectious prions in the saliva and blood of deer with chronic wasting disease. Science 314: 133–136. 19. Saborio, G. P., Permanne, B. and Soto, C. 2001. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 411: 810–813. 9. Jewell, J. E., Conner, M. M., Wolfe, L. L., Miller, M. W. and Williams, E. S. 2005. Low frequency of PrP genotype 225SF among free-ranging mule deer (Odocoileus hemionus) with chronic wasting disease. J. Gen. Virol. 86: 2127–2134. 16. Ministry of Agriculture Forestry and Fisheries (MAFF). 2020. Statistical Data, Survey on Wildlife Resource Utilization. https://www.maff.go.jp/j/tokei/kouhyou/jibie/index.html [accessed on June 14, 2021]. 11 12 13 14 15 16 17 18 19 1 2 3 4 5 6 7 8 9 20 10 21 |
References_xml | – reference: 18. Race, B., Meade-White, K. D., Miller, M. W., Barbian, K. D., Rubenstein, R., LaFauci, G., Cervenakova, L., Favara, C., Gardner, D., Long, D., Parnell, M., Striebel, J., Priola, S. A., Ward, A., Williams, E. S., Race, R. and Chesebro, B. 2009. Susceptibilities of nonhuman primates to chronic wasting disease. Emerg. Infect. Dis. 15: 1366–1376. – reference: 19. Saborio, G. P., Permanne, B. and Soto, C. 2001. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 411: 810–813. – reference: 10. Kataoka, N., Nishimura, M., Horiuchi, M. and Ishiguro, N. 2005. Surveillance of chronic wasting disease in sika deer, Cervus nippon, from Tokachi district in Hokkaido. J. Vet. Med. Sci. 67: 349–351. – reference: 14. Mathiason, C. K., Powers, J. G., Dahmes, S. J., Osborn, D. A., Miller, K. V., Warren, R. J., Mason, G. L., Hays, S. A., Hayes-Klug, J., Seelig, D. M., Wild, M. A., Wolfe, L. L., Spraker, T. R., Miller, M. W., Sigurdson, C. J., Telling, G. C. and Hoover, E. A. 2006. Infectious prions in the saliva and blood of deer with chronic wasting disease. Science 314: 133–136. – reference: 16. Ministry of Agriculture Forestry and Fisheries (MAFF). 2020. Statistical Data, Survey on Wildlife Resource Utilization. https://www.maff.go.jp/j/tokei/kouhyou/jibie/index.html [accessed on June 14, 2021]. – reference: 1. Agriculture & Livestock Industries Corporation (ALIC). 2021. Statistical Data, Livestock and Livestock Products. https://www.alic.go.jp/joho-c/joho05_000073.html [accessed on May 31, 2021]. – reference: 12. Koutsoumanis, K., Allende, A., Alvarez-Ordoňez, A., Bolton, D., Bover-Cid, S., Chemaly, M., Davies, R., De Cesare, A., Herman, L., Hilbert, F., Lindqvist, R., Nauta, M., Peixe, L., Ru, G., Skandamis, P., Suffredini, E., Andreoletti, O., Benestad, S. L., Comoy, E., Nonno, R., da Silva Felicio, T., Ortiz-Pelaez, A., Simmons, M. M., EFSA Panel on Biological Hazards (BIOHAZ). 2019. Update on chronic wasting disease (CWD) III. EFSA J. 17: e05863. – reference: 9. Jewell, J. E., Conner, M. M., Wolfe, L. L., Miller, M. W. and Williams, E. S. 2005. Low frequency of PrP genotype 225SF among free-ranging mule deer (Odocoileus hemionus) with chronic wasting disease. J. Gen. Virol. 86: 2127–2134. – reference: 7. Henderson, D. M., Davenport, K. A., Haley, N. J., Denkers, N. D., Mathiason, C. K. and Hoover, E. A. 2015. Quantitative assessment of prion infectivity in tissues and body fluids by real-time quaking-induced conversion. J. Gen. Virol. 96: 210–219. – reference: 20. Suzuki, A., Sawada, K., Yamasaki, T., Denkers, N. D., Mathiason, C. K., Hoover, E. A. and Horiuchi, M. 2020. Involvement of N- and C-terminal region of recombinant cervid prion protein in its reactivity to CWD and atypical BSE prions in real-time quaking-induced conversion reaction in the presence of high concentrations of tissue homogenates. Prion 14: 283–295. – reference: 6. Haley, N. J., Carver, S., Hoon-Hanks, L. L., Henderson, D. M., Davenport, K. A., Bunting, E., Gray, S., Trindle, B., Galeota, J., LeVan, I., Dubovos, T., Shelton, P. and Hoover, E. A. 2014. Detection of chronic wasting disease in the lymph nodes of free-ranging cervids by real-time quaking-induced conversion. J. Clin. Microbiol. 52: 3237–3243. – reference: 17. Pritzkow, S., Morales, R., Moda, F., Khan, U., Telling, G. C., Hoover, E. and Soto, C. 2015. Grass plants bind, retain, uptake, and transport infectious prions. Cell Rep. 11: 1168–1175. – reference: 13. Masujin, K., Shimada, K., Kimura, K. M., Imamura, M., Yoshida, A., Iwamaru, Y., Mohri, S. and Yokoyama, T. 2007. Applicability of current bovine spongiform encephalopathy (BSE) diagnostic procedures for chronic wasting disease (CWD). Microbiol. Immunol. 51: 1039–1043. – reference: 15. Meng, L. P., Zhao, D. M., Liu, H. X., Yang, J. M., Ning, Z. Y., Wu, C. D. and Han, C. X. 2005. Polymorphisms of the prion protein gene (PRNP) in Chinese domestic sika deer (Cervus nippon hortulorum). Anim. Genet. 36: 266–267. – reference: 5. Haley, N. J. and Hoover, E. A. 2015. Chronic wasting disease of cervids: current knowledge and future perspectives. Annu. Rev. Anim. Biosci. 3: 305–325. – reference: 11. Kong, Q., Huang, S., Zou, W., Vanegas, D., Wang, M., Wu, D., Yuan, J., Zheng, M., Bai, H., Deng, H., Chen, K., Jenny, A. L., O’Rourke, K., Belay, E. D., Schonberger, L. B., Petersen, R. B., Sy, M. S., Chen, S. G. and Gambetti, P. 2005. Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. J. Neurosci. 25: 7944–7949. – reference: 8. Houston, F. and Andréoletti, O. 2019. Animal prion diseases: the risks to human health. Brain Pathol. 29: 248–262. – reference: 3. Atarashi, R., Satoh, K., Sano, K., Fuse, T., Yamaguchi, N., Ishibashi, D., Matsubara, T., Nakagaki, T., Yamanaka, H., Shirabe, S., Yamada, M., Mizusawa, H., Kitamoto, T., Klug, G., McGlade, A., Collins, S. J. and Nishida, N. 2011. Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion. Nat. Med. 17: 175–178. – reference: 2. Arifin, M. I., Hannaoui, S., Chang, S. C., Thapa, S., Schatzl, H. M. and Gilch, S. 2021. Cervid prion protein polymorphisms: role in chronic wasting disease pathogenesis. Int. J. Mol. Sci. 22: 2271. – reference: 4. Escobar, L. E., Pritzkow, S., Winter, S. N., Grear, D. A., Kirchgessner, M. S., Dominguez-Villegas, E., Machado, G., Townsend Peterson, A. and Soto, C. 2020. The ecology of chronic wasting disease in wildlife. Biol. Rev. Camb. Philos. Soc. 95: 393–408. – reference: 21. Vikøren, T., Våge, J., Madslien, K. I., Røed, K. H., Rolandsen, C. M., Tran, L., Hopp, P., Veiberg, V., Heum, M., Moldal, T., Neves, C. G. D., Handeland, K., Ytrehus, B., Kolbjørnsen, Ø., Wisløff, H., Terland, R., Saure, B., Dessen, K. M., Svendsen, S. G., Nordvik, B. S. and Benestad, S. L. 2019. First detection of chronic wasting disease in a wild red deer (Cervus elaphus) in Europe. J. Wildl. Dis. 55: 970–972. – ident: 7 doi: 10.1099/vir.0.069906-0 – ident: 9 doi: 10.1099/vir.0.81077-0 – ident: 19 doi: 10.1038/35081095 – ident: 11 doi: 10.1523/JNEUROSCI.2467-05.2005 – ident: 4 doi: 10.1111/brv.12568 – ident: 1 – ident: 15 doi: 10.1111/j.1365-2052.2005.01276.x – ident: 21 doi: 10.7589/2018-10-262 – ident: 20 doi: 10.1080/19336896.2020.1858694 – ident: 3 doi: 10.1038/nm.2294 – ident: 12 doi: 10.2903/j.efsa.2019.5863 – ident: 18 doi: 10.3201/eid1509.090253 – ident: 13 doi: 10.1111/j.1348-0421.2007.tb03988.x – ident: 16 – ident: 14 doi: 10.1126/science.1132661 – ident: 5 doi: 10.1146/annurev-animal-022114-111001 – ident: 17 doi: 10.1016/j.celrep.2015.04.036 – ident: 6 doi: 10.1128/JCM.01258-14 – ident: 8 doi: 10.1111/bpa.12696 – ident: 10 doi: 10.1292/jvms.67.349 – ident: 2 doi: 10.3390/ijms22052271 |
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Title | Monitoring of chronic wasting disease using real-time quaking-induced conversion assay in Japan |
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ispartofPNX | Journal of Veterinary Medical Science, 2021, Vol.83(11), pp.1735-1739 |
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