Araştırma Makalesi
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Production of polyclonal antibodies against Turkey FMDV strains

Yıl 2021, Cilt: 32 Sayı: 1, 14 - 19, 30.06.2021
https://doi.org/10.35864/evmd.843095

Öz

Antibodies(Abs) have been always a major place in diagnostic laboratories. Many diagnostic techniques like Enzyme-Linked Immuno Sorbent Assays (ELISA), immunofluorescence, Ab-microarray platforms, immunoblots, X-ray crystallography require the Abs. ELISA is the main test that used Abs for Foot and Mouth Disease (FMDV) serology. It needs polyclonal or monoclonal Abs to detect FMDV antigen or Abs. For this purpose, solid-phase competitive ELISA (SPCE) or liquid phase blocking ELISA (LPBE) and non-structural protein (NSP) ELISA are used. SPCE and LPBE have mainly used FMDV structural protein (SP)-Ab detection.
In this study, it was aimed to produce a polyclonal Ab against FMDV ANep84 (Genotype VII) and OTUR07 (OPanAsia II), ATUR11 (A Iran05) strains for LPBE, FMDV SP-antibody detection. For this purpose, 4 guinea pigs and 6 rabbits were used for each serotype of FMDV. After producing Abs, checkerboard ELISA titration was performed to determine the optimal test dilution of Abs. Backgrounds, cross-reactions against three strains of FMDV were also checked. In conclusion, polyclonal Abs were produced against FMDV ANep84 (Genotype VII) and O Tur07 (O Pan Asia II), ATUR11 (A Iran05) strains, and standardized for LPBE test.

Teşekkür

Author are grateful to Dr. Bern Haas for his kind support for blocking procedure of ELISA, and thanks to Yavuz Yıldırım and Yusuf Demir for their laboratory effort. Banu Bayri, for their technical help in 146S test. This study was supported by Foot-and-Mouth Disease Institute, SAP, Ankara.

Kaynakça

  • Anonymus.https://www.oie.int/fileadmin/Home/eng/Health_standards/tahm/3.01.08_FMD.pdf (Accessed: 10.08.2019)
  • Ascoli AG and Aggeler B. (2018) Overlooked benefits of using polyclonal antibodies. Biotechniques. 65, 127- 136.
  • Barteling SJ and Meloen RH. (1974)A simple method for the quantification of 140S particles of foot and mouth disease virus. Arch Ges Virusforsch 45, 362-364
  • Crowther JR. (2001). ELISA guidebook, second edition Humana Press, UK, p:79
  • Diaz-San Segundo F, Medina GN, Stenfeldt C, Arzt J, de Los Santos T. (2017) Foot-and-mouth disease vaccines. Vet Microbiol. 206, 102–112.
  • Ferris NP, Donaldson AJ. (1984) Serological response of guinea pigs to inactivated 146S antigens of FMDV after single or repeated inoculations. Rev Sci Tech OIE. 3, 563-574.
  • Fry EE, Stuart DI, Rowlands DJ. (2005) The structure of FMDV. Current Topics Microbiol Immunol. 288, 71-101.
  • Hamblin C, Barnett ITR, Hedger RS. (1986) A new enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies against foot-and-mouth disease virus I. Development and method of ELISA. J Immunol Methods. 93, 11–121.
  • Harlow E and Lane D. (1988) Antibodies, A laboratory manual. Second edition, CSHL Press, USA, p: 60
  • Have P, Lei JC, Thiesen K. (1984) An enzyme linked immune absorbent assay for the primary diagnosis of FMD. Characterization and comparison with complement fixation. Acta Vet Scand. 25, 280-296.
  • Jamal SM, Belsham, GJ. (2013) Foot-and-mouth disease: past, present and future. Vet Res. 44, 116.
  • Lavoria MÁ, Di-Giacomo S, Bucofusco D, Franco-Mahecha OL, Perez-Filgueira DM, Capozzo AV. (2012) Avidity and subtyping of specific antibodies applied to the indirect assessment of heterologous protection against Foot-and-Mouth Disease Virus in cattle. Vaccine. 30(48), 6845-50.
  • Leenaars M and Hendriksen CF. (2005) Critical steps in the production of polyclonal and monoclonal antibodies: Evaluation and recommendations. ILAR Journal. 46, 269-79.
  • Leenaars PPA, Hendriksen CFM, Leeuw WA, Carat F, Delehaut P, Fischer F, Halder M, Hanly WC, Hartinger J, Hau J, Lindblad EB, Nicklas B, Outschoorn M, Stewart-Tall DE. (1999) The production of polyclonal antibodies in laboratory animals. ATLA. 27, 79-102. doi: 10.1177/ATLA.1999.
  • Lipman NS, Jackson LR, Trudel LJ, Weis-Garcia F. (2005) Monoclonal versus polyclonal antibodies: distinguish characteristics, applications, and information resources. ILAR Journal. 46, 258-268.
  • Low D, O’Leary R, Pujar NS. (2006) Future of antibody purification. J Chrom 848, 48-63.
  • Parida S. (2009) Vaccination against FMDV strategies and effectiveness. Expert Rev Vaccines. 8(3), 347-365.
  • Sala JM, Trotta MV, Mansilla FC, Filgueira MP, Gaston S, Capozzo A. (2018) Alternatives for the serological assessment of foot-and-mouth disease vaccine immunity in buffaloes (Bubalus bubalis) J App Anim Res. 46, 451–458.
  • Sorensen KJ, Madsen KG, Madsen ES, Salt JS, Nqindi J, Mackay DKJ. (1998) Differentiation of infection from vaccination in foot-and-mouth disease by the detection of antibodies to the non- structural proteins 3D, 3AB and 3ABC in ELISA using antigens expressed in baculovirus. Arch Virol. 143, 1461-1476.
  • Voskuil JLA. (2014) Commercial antibodies and their validation. F1000 Research 3, 232.
  • Zumdahl SS and De Coste DJ. (2009). Introduction Chemistry. Nineth edition Cengage Learning, USA, p: 34.
  • Salem R, El-Kholy A, Omar AO, Abu-el Naga EI, Osman G. (2019) Construction, expression and evolution of recombinant VP2 protein for serotype independent detection of FMDV seropositive animals in Egypt. Sci Report. 9, 10135.
  • Bari FD, Parida S, Tekleghiorghis T, Dekker A, Sangula A, Reeve R, Haydon DT, Paton DJ, Mahapatra M (2014) Genetic and antigenic characterization of serotype A FMD viruses from East Africa to select new vaccine strains. Vaccine. 32, 5794-5800.
  • Russell and Burch’s, 3Rs concept (Refine–Reduce–Replace, Russell W. (1959). The principles of humane experimental technique. London.
  • Brocchi E. (2012). New ELISAs for FMD Diagnosis, EUFMD Open Session, October 29-31-Jerez, Spain.
  • Ko YJ, Jeoung HY, Lee HS, Chang BS, Hong S-M, Heo E-J, Lee K-N, Joo H-D, Kim SM, Park J-H, Kweon C-H. (2009) A recombinant protein based ELISA for detecting antibodies to foot-and-mouth disease virus serotype Asia J Virol Methods 159, 112-118.
  • Cao Y, Zhou W, Xing X, Zang J, Fu Y, Li K, Sun P, Li P, Bai X, Ma X, Bao H, Li D, Chen Y, Lu Z, Liu Z. (2018) Indirect ELISA using a multi-epitope recombinant protein to detect antibodies against foot-and-mouth disease virus serotype O in pigs. J Virol Methods. 262, 26-31.
  • Ran X, Yang Z, Bai M, Zhang Y, Wen X, Guo H, Sun Ş. (2019) Development and validation of a competitive ELISA based on bacterium-original virus-like particles of serotype O foot-and-mouth disease virus for detecting serum antibodies. Appl Microbiol Biotech. 103, 3015-3024.
  • Yang M, Xu W, Bitner H, Jacquelyn H, Vosloo W, Goolia M, Lusansky D, Nfon C. (2017) Generation of MAbs to foot–and–mouth disease virus serotype A and application in a competitive ELISA for serodiagnosis. Virol J. 195(13), 195.

Şap virüsü şuşlarına karşı poliklonal antikor üretimi

Yıl 2021, Cilt: 32 Sayı: 1, 14 - 19, 30.06.2021
https://doi.org/10.35864/evmd.843095

Öz

Antikorlar tanı laboratuvarlarında daima önemli bir yer tutmaktadır. Enzim işaretli bağışıklık testleri (ELISA), immunofloresan, antikor-mikroarray platformları, immunoblotlar, X-ışını kristalografisi gibi birçok tanı tekniği kullanımı antikorların varlığını gerektirir. Şap hastalığı serolojisinde antikorların kullanıldığı temel test ELISA’dır. ELISA testleri Şap virusu antijenini veya şap virusuna karşı organizmada oluşan antikorları tespit etmek için poliklonal veya monoklonal antikorlara ihtiyaç duyar. Bu amaçla, solid faz kompetetif ELISA (SPCE) ve likit faz bloking ELISA (LPBE) ve NSP ELISAlar kullanılır. Şap virusunun yapısal proteinlerine (SP) karşı oluşan antikorları tespit etmek için ise SPCE ve LPBE testleri kullanılır.
Bu çalışma, ANep84 (genotip VII), O TUR07 (O Pan Asia II), ATUR11 (A Iran05) şap virusu suşlarına karşı (LPBE) testinde kullanılmak üzere poliklonal antikor üretmek amaçlandı. Bu amaçla, her bir FMDV serotipi için 4 kobay ve 6 tavşan kullanıldı. Antikorlar üretildikten sonra, dama tahtası (checkerboard ELISA titration) testi ile üretimi yapılan poliklonal antikorlar için optimal dilusyonlar belirlendi. Şap virusu suşlarına karşı oluşabilecek çapraz reaksiyonlar ve background reaksiyonları kontrol edildi. Sonuç olarak, bu çalışmada şap virusu ANep84 (genotip VII) ve O Tur07 (O Pan Asia II), ATUR11 (AIran05) suşlarına karşı poliklonal antikorlar üretildi ve LPBE testi için standardizasyonları yapıldı.

Kaynakça

  • Anonymus.https://www.oie.int/fileadmin/Home/eng/Health_standards/tahm/3.01.08_FMD.pdf (Accessed: 10.08.2019)
  • Ascoli AG and Aggeler B. (2018) Overlooked benefits of using polyclonal antibodies. Biotechniques. 65, 127- 136.
  • Barteling SJ and Meloen RH. (1974)A simple method for the quantification of 140S particles of foot and mouth disease virus. Arch Ges Virusforsch 45, 362-364
  • Crowther JR. (2001). ELISA guidebook, second edition Humana Press, UK, p:79
  • Diaz-San Segundo F, Medina GN, Stenfeldt C, Arzt J, de Los Santos T. (2017) Foot-and-mouth disease vaccines. Vet Microbiol. 206, 102–112.
  • Ferris NP, Donaldson AJ. (1984) Serological response of guinea pigs to inactivated 146S antigens of FMDV after single or repeated inoculations. Rev Sci Tech OIE. 3, 563-574.
  • Fry EE, Stuart DI, Rowlands DJ. (2005) The structure of FMDV. Current Topics Microbiol Immunol. 288, 71-101.
  • Hamblin C, Barnett ITR, Hedger RS. (1986) A new enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies against foot-and-mouth disease virus I. Development and method of ELISA. J Immunol Methods. 93, 11–121.
  • Harlow E and Lane D. (1988) Antibodies, A laboratory manual. Second edition, CSHL Press, USA, p: 60
  • Have P, Lei JC, Thiesen K. (1984) An enzyme linked immune absorbent assay for the primary diagnosis of FMD. Characterization and comparison with complement fixation. Acta Vet Scand. 25, 280-296.
  • Jamal SM, Belsham, GJ. (2013) Foot-and-mouth disease: past, present and future. Vet Res. 44, 116.
  • Lavoria MÁ, Di-Giacomo S, Bucofusco D, Franco-Mahecha OL, Perez-Filgueira DM, Capozzo AV. (2012) Avidity and subtyping of specific antibodies applied to the indirect assessment of heterologous protection against Foot-and-Mouth Disease Virus in cattle. Vaccine. 30(48), 6845-50.
  • Leenaars M and Hendriksen CF. (2005) Critical steps in the production of polyclonal and monoclonal antibodies: Evaluation and recommendations. ILAR Journal. 46, 269-79.
  • Leenaars PPA, Hendriksen CFM, Leeuw WA, Carat F, Delehaut P, Fischer F, Halder M, Hanly WC, Hartinger J, Hau J, Lindblad EB, Nicklas B, Outschoorn M, Stewart-Tall DE. (1999) The production of polyclonal antibodies in laboratory animals. ATLA. 27, 79-102. doi: 10.1177/ATLA.1999.
  • Lipman NS, Jackson LR, Trudel LJ, Weis-Garcia F. (2005) Monoclonal versus polyclonal antibodies: distinguish characteristics, applications, and information resources. ILAR Journal. 46, 258-268.
  • Low D, O’Leary R, Pujar NS. (2006) Future of antibody purification. J Chrom 848, 48-63.
  • Parida S. (2009) Vaccination against FMDV strategies and effectiveness. Expert Rev Vaccines. 8(3), 347-365.
  • Sala JM, Trotta MV, Mansilla FC, Filgueira MP, Gaston S, Capozzo A. (2018) Alternatives for the serological assessment of foot-and-mouth disease vaccine immunity in buffaloes (Bubalus bubalis) J App Anim Res. 46, 451–458.
  • Sorensen KJ, Madsen KG, Madsen ES, Salt JS, Nqindi J, Mackay DKJ. (1998) Differentiation of infection from vaccination in foot-and-mouth disease by the detection of antibodies to the non- structural proteins 3D, 3AB and 3ABC in ELISA using antigens expressed in baculovirus. Arch Virol. 143, 1461-1476.
  • Voskuil JLA. (2014) Commercial antibodies and their validation. F1000 Research 3, 232.
  • Zumdahl SS and De Coste DJ. (2009). Introduction Chemistry. Nineth edition Cengage Learning, USA, p: 34.
  • Salem R, El-Kholy A, Omar AO, Abu-el Naga EI, Osman G. (2019) Construction, expression and evolution of recombinant VP2 protein for serotype independent detection of FMDV seropositive animals in Egypt. Sci Report. 9, 10135.
  • Bari FD, Parida S, Tekleghiorghis T, Dekker A, Sangula A, Reeve R, Haydon DT, Paton DJ, Mahapatra M (2014) Genetic and antigenic characterization of serotype A FMD viruses from East Africa to select new vaccine strains. Vaccine. 32, 5794-5800.
  • Russell and Burch’s, 3Rs concept (Refine–Reduce–Replace, Russell W. (1959). The principles of humane experimental technique. London.
  • Brocchi E. (2012). New ELISAs for FMD Diagnosis, EUFMD Open Session, October 29-31-Jerez, Spain.
  • Ko YJ, Jeoung HY, Lee HS, Chang BS, Hong S-M, Heo E-J, Lee K-N, Joo H-D, Kim SM, Park J-H, Kweon C-H. (2009) A recombinant protein based ELISA for detecting antibodies to foot-and-mouth disease virus serotype Asia J Virol Methods 159, 112-118.
  • Cao Y, Zhou W, Xing X, Zang J, Fu Y, Li K, Sun P, Li P, Bai X, Ma X, Bao H, Li D, Chen Y, Lu Z, Liu Z. (2018) Indirect ELISA using a multi-epitope recombinant protein to detect antibodies against foot-and-mouth disease virus serotype O in pigs. J Virol Methods. 262, 26-31.
  • Ran X, Yang Z, Bai M, Zhang Y, Wen X, Guo H, Sun Ş. (2019) Development and validation of a competitive ELISA based on bacterium-original virus-like particles of serotype O foot-and-mouth disease virus for detecting serum antibodies. Appl Microbiol Biotech. 103, 3015-3024.
  • Yang M, Xu W, Bitner H, Jacquelyn H, Vosloo W, Goolia M, Lusansky D, Nfon C. (2017) Generation of MAbs to foot–and–mouth disease virus serotype A and application in a competitive ELISA for serodiagnosis. Virol J. 195(13), 195.
Toplam 29 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Viroloji
Bölüm Araştırma Makaleleri
Yazarlar

Beyhan Sareyyüpoğlu 0000-0002-0279-1673

Erken Görünüm Tarihi 7 Ocak 2021
Yayımlanma Tarihi 30 Haziran 2021
Gönderilme Tarihi 18 Aralık 2020
Yayımlandığı Sayı Yıl 2021 Cilt: 32 Sayı: 1

Kaynak Göster

APA Sareyyüpoğlu, B. (2021). Production of polyclonal antibodies against Turkey FMDV strains. Etlik Veteriner Mikrobiyoloji Dergisi, 32(1), 14-19. https://doi.org/10.35864/evmd.843095


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