$\require{mediawiki-texvc}$

연합인증

연합인증 가입 기관의 연구자들은 소속기관의 인증정보(ID와 암호)를 이용해 다른 대학, 연구기관, 서비스 공급자의 다양한 온라인 자원과 연구 데이터를 이용할 수 있습니다.

이는 여행자가 자국에서 발행 받은 여권으로 세계 각국을 자유롭게 여행할 수 있는 것과 같습니다.

연합인증으로 이용이 가능한 서비스는 NTIS, DataON, Edison, Kafe, Webinar 등이 있습니다.

한번의 인증절차만으로 연합인증 가입 서비스에 추가 로그인 없이 이용이 가능합니다.

다만, 연합인증을 위해서는 최초 1회만 인증 절차가 필요합니다. (회원이 아닐 경우 회원 가입이 필요합니다.)

연합인증 절차는 다음과 같습니다.

최초이용시에는
ScienceON에 로그인 → 연합인증 서비스 접속 → 로그인 (본인 확인 또는 회원가입) → 서비스 이용

그 이후에는
ScienceON 로그인 → 연합인증 서비스 접속 → 서비스 이용

연합인증을 활용하시면 KISTI가 제공하는 다양한 서비스를 편리하게 이용하실 수 있습니다.

프리온 질환과 어류의 관련성에 관한 연구 동향
Fish and Prion Diseases 원문보기

한국수산과학회지 = Korean journal of fisheries and aquatic sciences, v.47 no.4, 2014년, pp.341 - 346  

김재일 (부경대학교 식품영양학과)

Abstract AI-Helper 아이콘AI-Helper

Transmissible spongiform encephalopathies (TSEs), also termed prion diseases, are a threat to food safety and to human and animal health. Variant Creutzfeldt-Jakob disease (vCJD) in humans is caused by the consumption of meat contaminated with bovine spongiform encephalopathy (BSE, mad cow disease)....

주제어

AI 본문요약
AI-Helper 아이콘 AI-Helper

* AI 자동 식별 결과로 적합하지 않은 문장이 있을 수 있으니, 이용에 유의하시기 바랍니다.

문제 정의

  • 이상과 같이 어류양식은 사람과 동물의 주요 단백질 자원을 제공해주는 경제적으로 주요한 사업이므로 프리온 병원체에 의한 양식어류의 오염가능성, 또는 양식어류의 프리온 질환 발병가능성에 대한 기초연구는 중요하다고 할 수 있다. 따라서, 본 논문에서는 프리온질환의 특성과 최근까지 발표된 어류 프리온 단백질(prion protein, PrP)의 동정 및 질병발병 가능성에 대한 국제적인 연구동향을 고찰함으로써 향후 연구방향에 대한 자료를 제시하고자 한다.
본문요약 정보가 도움이 되었나요?

질의응답

핵심어 질문 논문에서 추출한 답변
프리온 질환이란? 전염성 해면상 뇌증(transmissible spongiform encephalopathies; TSEs)이라고도 하는 프리온 질환(prion diseases)은 사람 및 동물의 중추신경계에 영향을 미치는 치명적인 신경퇴행성 질환이다(Kim YS, 1990). 질병에 걸린 뇌의 신경병리학적인 병변으로는 전반적인 신경세포의 소실에 의한 해면모양(spongiform)의 퇴화와 함께 별아교세포비대증(astrocytosis)을 나타내고, 일부의 경우 비정상적인 프리온단백질(PrPSc)로 이루어진 아밀로이드 플라크(amyloid plaque)가 뇌조직에 침착하는 것이 그 특징이다(Prusiner SB, 1998).
프리온 질환에 걸린 뇌의 신경병리학적인 병변은? 전염성 해면상 뇌증(transmissible spongiform encephalopathies; TSEs)이라고도 하는 프리온 질환(prion diseases)은 사람 및 동물의 중추신경계에 영향을 미치는 치명적인 신경퇴행성 질환이다(Kim YS, 1990). 질병에 걸린 뇌의 신경병리학적인 병변으로는 전반적인 신경세포의 소실에 의한 해면모양(spongiform)의 퇴화와 함께 별아교세포비대증(astrocytosis)을 나타내고, 일부의 경우 비정상적인 프리온단백질(PrPSc)로 이루어진 아밀로이드 플라크(amyloid plaque)가 뇌조직에 침착하는 것이 그 특징이다(Prusiner SB, 1998).
동물에서 유발되는 질환에는 어떤 것들이 있는가? 동물에서 유발되는 질환으로는 양의 스크래피(scrapie), 소의 우해면상뇌병증(bovine spongiform encephalopathy, BSE 또는 일명 광우병, mad cow disease), 그리고 사슴과 고라니에서 발생하는 만성소모성질환(chronic wasting disease, CWD) 등이 있다. 사람에서는 산발성(sporadic), 가족성(familial), 그리고 감염성(infectious)의 세 가지의 형태로 발생한다.
질의응답 정보가 도움이 되었나요?

참고문헌 (62)

  1. Atarashi R, Moore RA, Sim VL, Hughson AG, Dorward DW, Onwubiko HA, Priola SA and Caughey B. 2007. Ultrasensitive detection of scrapie prion protein using seeded conversion of recombinant prion protein. Nat Methods 4, 645-650. 

  2. 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 SJ and Nishida N. 2011. Ultrasensitive human prion detection in cerebrospinal fluid by real-time quakinginduced conversion. Nat Med 17, 175-178. http://dx.doi.org/10.1038/nm.2294. 

  3. Baboli MJ, Dawodi M and Gorjipor A. 2013. Effect of replacement fish meal by poultry meal on growth, survival and body composition of rainbow trout (Oncorhynchos mykiss). Int Res J Appl Basic Sci 4, 4197-4201. 

  4. Billeter M, Riek R, Wider G, Hornemann S, Glockshuber R and Wuthrich K. 1997. Prion protein NMR structure and species barrier for prion diseases. Proc Natl Acad Sci USA 94, 7281-7285. 

  5. Bolton DC, McKinley MP and Prusiner SB. 1982. Identification of a protein that purifies with the scrapie prion. Science 218, 1309 -1311. 

  6. Brown DR, Qin K, Herms JW, Madlung A, Manson J, Strome R, Fraser PE, Kruck T, von Bohlen A, Schulz-Schaeffer W, Giese A,Westaway D and Kretzschmar H. 1997a. The cellular prion protein binds copper in vivo. Nature 390, 684-687. 

  7. Brown DR, Schulz-Schaeffer WJ, Schmidt B and Kretzschmar HA. 1997b. Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity. Exp Neurol 146, 104-112. 

  8. Brown P. 2004. Mad-cow disease in cattle and human beings. American Scientist 92, 334. http://dx.doi.org/10.1511/2004.4.334 

  9. Bruce ME, Will RG, Ironside JW, McConnell I, Drummond D, Suttie A, McCardle L, Chree A, Hope J, Birkett C, Cousens S, Fraser H and Bostock CJ. 1997. Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent. Nature 389, 498-501. 

  10. Bueler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M and Weissmann C. 1993. Mice devoid of PrP are resistant to scrapie. Cell 73, 1339-1347. 

  11. Bueler H, Fischer M, Lang Y, Bluethmann H, Lipp HP, DeArmond SJ, Prusiner SB, Aguet M and Weissmann C. 1992. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356, 577-582. 

  12. Cashman NR, Loertscher R, Nalbantoglu J, Shaw I, Kascsak RJ, Bolton DC and Bendheim PE. 1990. Cellular isoform of the scrapie agent protein participates in lymphocyte activation. Cell 61, 185-192. 

  13. Castilla J, Saa P, Hetz C and Soto C. 2005. In vitro generation of infectious scrapie prions. Cell 121, 195-206. 

  14. Caughey B, Raymond GJ, Callahan MA, Wong C, Baron GS and Xiong LW. 2001. Interactions and conversions of prion protein isoforms. Adv Protein Chem 57, 139-169. 

  15. CDC. 2014. vCJD (Variant Creutzfeldt-Jakob Disease). Retrieved from http://www.cdc.gov/ncidod/dvrd/vcjd/epidemiology.htm on June 4. 

  16. Chang B, Gray P, Piltch M, Bulgin MS, Sorensen-Melson S, Miller MW, Davies P, Brown DR, Coughlin DR and Rubenstein R. 2009. Surround optical fiber immunoassay (SOFIA): an ultra-sensitive assay for prion protein detection. J Virol Methods 159, 15-22. http://dx.doi.org/10.1016/j.jviromet.2009.02.019. 

  17. Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR and Jefferys JG. 1994. Prion protein is necessary for normal synaptic function. Nature 370, 295-297. 

  18. Collinge J. 2001. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 24, 519-550. 

  19. Cotto E, Andre M, Forgue J, Fleury HJ and Babin PJ. 2005. Molecular characterization, phylogenetic relationships, and developmental expression patterns of prion genes in zebrafish (Danio rerio). FEBS J 272, 500-513. 

  20. Dalla Valle AZ, Iriti M, Faoro F, Berti C and Ciappellano S. 2008. In vivo prion protein intestinal uptake in fish. APMIS 116, 173-180. http://dx.doi.org/10.1111/j.1600-0463.2008.00863.x. 

  21. European Food Safety Authority. 2007. Health risks of feeding of ruminants with fishmeal in relation to the risk of TSE. The EFSA Journal 443, 1-26. 

  22. Favre-Krey L, Theodoridou M, Boukouvala E, Panagiotidis CH, Papadopoulos AI, Sklaviadis T and Krey G. 2007. Molecular characterization of a cDNA from the gilthead sea bream (Sparus aurata) encoding a fish prion protein. Comp Biochem Physiol B Biochem Mol Biol 147, 566-573. 

  23. Ford MJ, Burton LJ, Morris RJ and Hall SM. 2002. Selective expression of prion protein in peripheral tissues of the adult mouse. Neuroscience 113, 177-192. 

  24. Friedland RP, Petersen RB and Rubenstein R. 2009. Bovine spongiform encephalopathy and aquaculture. J Alzheimers Dis 17, 277-279. http://dx.doi.org/10.3233/JAD-2009-1060. 

  25. Harris DA. 2003. Trafficking, turnover and membrane topology of PrP. Br Med Bull 66, 71-85. 

  26. Harris DA, Falls DL, Johnson FA and Fishbach GD. 1991. A prion-like protein from chicken brain copurifies with an acetylcholine receptor inducing activity. Proc Natl Acad Sci USA 88, 7664-7668. 

  27. Hill AF, Desbruslais M, Joiner S, Sidle KC, Gowland I, Collinge J, Doey LJ and Lantos P. 1997. The same prion strain causes vCJD and BSE. Nature 389, 448-450. 

  28. Ingrosso L, Novoa B, Valle AZ, Cardone F, Aranguren R, Sbriccoli M, Bevivino S, Iriti M, Liu Q, Vetrugno V, Lu M, Faoro F, Ciappellano S, Figueras A and Pocchiari M. 2006. Scrapie infectivity is quickly cleared in tissues of orallyinfected farmed fish. BMC Vet Res 2, 21. http://dx.doi.org/10.1186/1746-6148-2-21 

  29. Jeong BH, Ju WK, Huh K, Lee EA, Choi IS, Im JH, Choi EK and Kim YS. 1998. Molecular analysis of prion protein gene (PRNP) in Korean patients with Creutzfeldt-Jakob disease. J Korean Med Sci 13, 234-240. 

  30. Kim JI and Lee HG. 2008. Increases in the proteins modified by malondialdehyde and hydroxynonenal in the hippocampus of prion-infected mice. J Bacteriol Virol 38, 47-52. 

  31. Kim JI, Cali I, Surewicz K, Kong Q, Raymond GJ, Atarashi R, Race B, Qing L, Gambetti P, Caughey B and Surewicz WK. 2010. Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors. J Biol Chem 285, 14083-14087. http://dx.doi.org/10.1074/jbc.C110.113464. 

  32. Kim JI, Choi SI, Kim NH, Jin JK, Choi EK, Carp RI and Kim YS. 2001. Oxidative stress and neurodegeneration in prion diseases. Ann N Y Acad Sci 928, 182-186. 

  33. Kim TY, Shon HJ, Joo YS, Mun UK, Kang KS and Lee YS. 2005. Additional cases of chronic wasting disease in imported deer in Korea. J Vet Med Sci 67, 753-759. 

  34. Kim YS. 1990. Unconventional slow infectious agents: Virus, prion, or virino? Mol Biol News 2, 11-21. 

  35. Kromhout D. 2001. 'Protective nutrients' and up-to-date dietary recommendations. Eur Heart J Supplement 3, D33-D36. 

  36. Kuwahara C, Takeuchi AM, Nishimura T, Haraguchi K, Kubosaki A, Matsumoto Y, Saeki K, Matsumoto Y, Yokoyama T, Itohara S and Onodera T. 1999. Prions prevent neuronal cell-line death. Nature 400, 225-226. 

  37. Liao M, Zhang Z, Yang G, Sun X, Zou G, Wei Q and Wang D. 2005. Cloning and characterization of prion protein coding genes of Japanese seabass (Lateolabrax japonicus) and Japanese flounder (Paralichthys olivaceus). Aquaculture 249, 47-53. 

  38. Malaga-Trillo E, Salta E, Figueras A, Panagiotidis C, Sklaviadi T. 2011. Fish models in prion biology: Underwater issues. Biochimica Biophysica Acta 1812, 402-414. http://dx.doi.org/10.1016/j.bbadis.2010.09.013. 

  39. Matthews D and Cooke BC. 2003. The potential for transmissible spongiform encephalopathies in non-ruminant livestock and fish. Rev Sci Tech 22, 283-296. 

  40. Miesbauer M, Bamme T, Riemer C, Oidtmann B, Winklhofer KF, Baier M and Tatzelt J. 2006. Prion protein-related proteins from zebrafish are complex glycosylated and contain a glycosylphosphatidylinositol anchor. Biochem Biophys Res Commun 341, 218-224. 

  41. Mouillet-Richard S, Ermonval M, Chebassier C, Laplanche JL, Lehmann S, Launay JM, Kellermann O. 2000. Signal transduction through prion protein. Science 289, 1925-1928. 

  42. Oesch B, Westaway D, Walchli M, McKinley MP, Kent SB, Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE, Prusiner SB and Weissmann C. 1985. A cellular gene encodes scrapie PrP 27-30 protein. Cell 40, 735-746. 

  43. Oh JM, Shin HY, Park SJ, Kim BH, Choi JK, Choi EK, Carp RI and Kim YS. 2008. The involvement of cellular prion protein in the autophagy pathway in neuronal cells. Mol Cell Neurosci 39, 238-247. http://dx.doi.org/10.1016/j.mcn.2008.07.003. 

  44. Oidtmann B, Simon D, Holtkamp N, Hoffmann R and Baier M. 2003. Identification of cDNAs from Japanese pufferfish (Fugu rubripes) and Atlantic salmon (Salmo salar) coding for homologues to tetrapod prion proteins. FEBS Lett 538, 96-100. 

  45. Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, Mehlhorn I, Huang Z, Fletterick RJ, Cohen FE and Prusiner SB. 1993. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. Proc Natl Acad Sci USA 90, 10962-10966. 

  46. Premzl M, Gready JE, Jermlin LS, Simonic T and Marshall Graves JA. 2004. Evolution of vertebrate genes related to prion and shadoo proteins clues from comparative genomic analyses. Mol Biol Evol 21, 2210-2231. 

  47. Prusiner SB. 1998. Prions. Proc Natl Acad Sci USA 95, 13363-13383. 

  48. Prusiner SB, Scott M, Foster D, Pan KM, Groth D, Mirenda C, Torchia M, Yang SL, Serban D, Carlson GA, Hoppe PC, Westaway D and DeArmond SJ. 1990. Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63, 673-686. 

  49. Rivera-Milla E, Oidtmann B, Panagiotidis CH, Baier M, Sklaviadis T, Hoffmann R, Zhou Y, Solis GP, Stuermer CAO and Malaga-Trillo E. 2006. Disparate evolution of prion protein domains and the distinct origin of doppel and prion-related loci revealed by fish-to-mammal comparisons. FASEB J 20, 317-319. 

  50. Rivera-Milla E, Stuermer CAO and Malaga-Trillo E. 2003. An evolutionary basis for scrapie disease: identification of a fish prion mRNA. Trends Genet 19, 72-75. 

  51. Saborio GP, Permanne B and Soto C. 2001. Sensitive detection of pathological prion protein by cyclic amplification of protein misfolding. Nature 411, 810-813. 

  52. Salta E, Panagiotidis C, Teliousis K, Petrakis S, Eleftheriadis E, Arapoglou F, Grigoriadis N, Nicolaou A, Kaldrymidou E, Krey G and Sklaviadis T. 2009. Evaluation of the possible transmission of BSE and scrapie to gilthead sea bream (Sparus aurata). PLoS One 4, e6175. http://dx.doi.org/10.1371/journal.pone.0006175. 

  53. Schmitt-Ulms G, Legname G, Baldwin MA, Ball HL, Bradon N, Bosque PJ, Crossin KL, Edelman GM, DeArmond SJ, Cohen FE and Prusiner SB. 2001. Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein. J Mol Biol 314, 1209-1225. 

  54. Simonic T, Duga S, Strumbo B, Asselta R, Ceciliani F and Ronchi S. 2000. cDNA cloning of turtle prion protein. FEBS Lett 469, 33-38. 

  55. Sohn HJ, Kim JH, Choi KS, Nah JJ, Joo YS, Jean YH, Ahn SW, Kim OK, Kim DY and Balachandran A. 2002. A case of chronic wasting disease in an elk imported to Korea from Canada. J Vet Med Sci 64, 855-858. 

  56. Steele AD, Lindquist S and Aguzzi A. 2007. The prion protein knockout mouse: a phenotype under challenge. Prion 1, 83-93. 

  57. Strumbo B, Ronchi S, Bolis LC and Simonic T. 2001. Molecular cloning of the cDNA coding for Xenopus laevis prion protein. FEBS Lett 508, 170-174. 

  58. Suzuki T, Kurokawa T, Hashimoto H and Sugiyama M. 2002. cDNA sequence and tissue expression of Fugu rubripes prion protein-like: a candidate for the teleost orthologue of tetrapod PrPs. Biochem Biophys Res Comm 294, 912-917. 

  59. The Korean Nutrition Society. 2010. Dietary reference intakes for Koreans, 1st Revision., Hanarum, Seoul, Korea, 73-95 

  60. Watts JC, Giles K, Patel S, Oehler A, DeArmond SJ and Prusiner SB. 2014. Evidence that bank vole PrP is a universal acceptor for prions. PLoS Pathog 10, e1003990. http://dx.doi.org/10.1371/journal.ppat.1003990. 

  61. Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A, Poser S, Pocchiari M, Hofman A and Smith PG. 1996. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 347, 921-925. 

  62. Yang Y, Xie S, Cui Y, Lei W, Zhu X, Yang Y and Yu Y. 2004. Effect of replacement of dietary fish meal by meat and bone meal and poultry by-product meal on growth and feed utilization of gibel carp, Carassius auratus gibelio. Aquaculture Nutr 10, 289-294. http://dx.doi.org/10.1111/j.1365-2095.2004.00301.x 

저자의 다른 논문 :

섹션별 컨텐츠 바로가기

AI-Helper ※ AI-Helper는 오픈소스 모델을 사용합니다.

AI-Helper 아이콘
AI-Helper
안녕하세요, AI-Helper입니다. 좌측 "선택된 텍스트"에서 텍스트를 선택하여 요약, 번역, 용어설명을 실행하세요.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.

선택된 텍스트

맨위로