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Статті в журналах з теми "Avian influenza virus M2e protein"
Mezhenskaya, Daria, Irina Isakova-Sivak, Victoria Matyushenko, Svetlana Donina, Andrey Rekstin, Konstantin Sivak, Kirill Yakovlev, et al. "Universal Live-Attenuated Influenza Vaccine Candidates Expressing Multiple M2e Epitopes Protect Ferrets against a High-Dose Heterologous Virus Challenge." Viruses 13, no. 7 (June 30, 2021): 1280. http://dx.doi.org/10.3390/v13071280.
Повний текст джерелаShuklina, M. A., L. A. Stepanova, A. A. Kovaleva, A. V. Korotkov, A. A. Shaldzhyan, M. V. Zaitceva, E. I. Eletskaya, and L. M. Tsybalova. "Intranasal immunization with a recombinant protein based on the M2e peptide and second subunit of influenza A viral hemagglutinin fragment induces a cross-protective humoral and Tcell response in mice." Medical Immunology (Russia) 22, no. 2 (April 16, 2020): 357–70. http://dx.doi.org/10.15789/1563-0625-iiw-1584.
Повний текст джерелаKim, Min-Chul, Jun-Gu Choi, Ji-Sun Kwon, Hyun-Mi Kang, Mi-Ra Paek, Ok-Mi Jeong, Jun-Hun Kwon, and Youn-Jeong Lee. "Field Application of the H9M2e Enzyme-Linked Immunosorbent Assay for Differentiation of H9N2 Avian Influenza Virus-Infected Chickens from Vaccinated Chickens." Clinical and Vaccine Immunology 17, no. 12 (October 27, 2010): 1977–84. http://dx.doi.org/10.1128/cvi.00191-10.
Повний текст джерелаZhang, Sixin, Xinming Tang, Si Wang, Fangyun Shi, Chunhui Duan, Feifei Bi, Jingxia Suo, et al. "Establishment of Recombinant Eimeria acervulina Expressing Multi-Copies M2e Derived from Avian Influenza Virus H9N2." Vaccines 9, no. 7 (July 16, 2021): 791. http://dx.doi.org/10.3390/vaccines9070791.
Повний текст джерелаNemchinov, Lev G., and Angela Natilla. "Transient expression of the ectodomain of matrix protein 2 (M2e) of avian influenza A virus in plants." Protein Expression and Purification 56, no. 2 (December 2007): 153–59. http://dx.doi.org/10.1016/j.pep.2007.05.015.
Повний текст джерелаPark, Ki Seok, Yong Bok Seo, Ji Yeung Lee, Se Jin Im, Sang Hwan Seo, Min Suk Song, Young Ki Choi, and Young Chul Sung. "Complete protection against a H5N2 avian influenza virus by a DNA vaccine expressing a fusion protein of H1N1 HA and M2e." Vaccine 29, no. 33 (July 2011): 5481–87. http://dx.doi.org/10.1016/j.vaccine.2011.05.062.
Повний текст джерелаSwinkels, Willem J. C., Jeroen Hoeboer, Reina Sikkema, Lonneke Vervelde, and Ad P. Koets. "Vaccination induced antibodies to recombinant avian influenza A virus M2 protein or synthetic M2e peptide do not bind to the M2 protein on the virus or virus infected cells." Virology Journal 10, no. 1 (2013): 206. http://dx.doi.org/10.1186/1743-422x-10-206.
Повний текст джерелаTang, Yinghua, Yuzhen Gong, Yongwei Wang, Peipei Wu, Yamei Liu, Jihu Lu, Feng Gao, Tao Chen, Fengxiang Hou, and Jibo Hou. "Chimaeric VP2 proteins from infectious bursal disease virus containing the N-terminal M2e of H9 subtype avian influenza virus induce neutralizing antibody responses to both viruses." Avian Pathology 42, no. 3 (June 2013): 260–67. http://dx.doi.org/10.1080/03079457.2013.782096.
Повний текст джерелаReese, Kaleb A., Christopher Lupfer, Rudd C. Johnson, Georgi M. Mitev, Valerie M. Mullen, Bruce L. Geller, and Manoj Pastey. "A Novel Lactococcal Vaccine Expressing a Peptide from the M2 Antigen of H5N2 Highly Pathogenic Avian Influenza A Virus Prolongs Survival of Vaccinated Chickens." Veterinary Medicine International 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/316926.
Повний текст джерелаBabapoor, Sankhiros, Tobias Neef, Christian Mittelholzer, Theodore Girshick, Antonio Garmendia, Hongwei Shang, Mazhar I. Khan, and Peter Burkhard. "A Novel Vaccine Using Nanoparticle Platform to Present Immunogenic M2e against Avian Influenza Infection." Influenza Research and Treatment 2011 (January 12, 2011): 1–12. http://dx.doi.org/10.1155/2011/126794.
Повний текст джерелаДисертації з теми "Avian influenza virus M2e protein"
Tam, Ho-man Alex. "Mechanisms underlying the hyper-induction of tumour necrosis factor alpha (TNF-? by avian influenza virus in human macrophages." Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B41508300.
Повний текст джерелаTam, Ho-man Alex, та 譚浩文. "Mechanisms underlying the hyper-induction of tumour necrosis factor alpha (TNF-α) by avian influenza virus in human macrophages". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B41508300.
Повний текст джерелаHasan, Noor Haliza. "Avian Influenza virus M2e protein: Epitope mapping, competitive ELISA and phage displayed scFv for DIVA in H5N1 serosurveillance." Thesis, 2017. http://hdl.handle.net/2440/119643.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Animal and Veterinary Sciences, 2017
陳羽鴻. "Development of the M2 protein of H1N1 avian influenza virus subunit vaccine." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/bm6f8f.
Повний текст джерела國立嘉義大學
生物農業科技學系研究所
106
Avian influenza(Avian Influenza;AI)is commonly known as avian flu. It is one kind of animal infectious diseases caused by flu viruses. AI viruses can be grouped into highly pathogenic avian influenza (HPAI) and low pathogenic avian influenza (LPAI). The mortality of the poultry infected by HPAI can be higher than 80%. In this study, H1N1 viral M2 gene segment was constructed into the E. coli protein expression vector for expressing the M2 gene 's fusion protein with 8X-Histidine tag. The serum samples of vaccinated mice were assayed by dot blotting and ELISA. The specific antibody against the overexpressed M2 gene's protein produced in the vaccinated mice was determined by dot blotting assay. The M2 gene's fusion protein was also shown to have better immune response in association with the commercial adjuvant. These studies have laid a strong foundation for developing an effective AI subunit vaccine.
Vuong, Christine. "Evaluation of Sindbis-M2e Virus Vector as a Universal Influenza A Vaccine." Thesis, 2012. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11706.
Повний текст джерелаChen, Chien-Hao, and 陳建豪. "Expression and application of avian influenza virus hemagglutinin protein." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/24673044416928532096.
Повний текст джерела國立臺灣大學
獸醫學研究所
94
From 1986 to 2003, the avian influenza viruses (AIV) isolated in Taiwan were all low pathogenic. Some low pathogenic H5N2 AIVs were isolated in Taiwan in 2004, resulting in stamping 380 thousands chickens out from 22 poultry flocks. To test if the virus titers increased during passaging, H5N2 and H6N1 isolates were passaged in specific-pathogen-free embryonated eggs. After 45 passages, the virus titer of H5N2 increased 100 times, and two amino acid residues in HA1 of H5N2 virus were changed. The partial fragments of HA1 relating to neutralizing epitopes of the H5N2 and the H6N1 isolates were cloned in pGEX-5X-1 vector (prokaryotic expression) and pcDNA3.1 vector (eukaryotic expression) for expression. The purified recombinant proteins were intramuscualarly injected in 4-week-old SPF chickens for two times. Two weeks after the second immunization, the serum from H6-immunized chickens showed hemagglutination inhibition (HI) titers of 24 to 26, but no antibody was detected in H5-immunized chickens. To test the increase efficiency of liposome compounds on vaccine, Newcastle disease vaccines coated with liposome and with liposome/chitosan were used to immunize chickens. The results showed that Newcastle disease vaccine coated with liposome/chitosan increased HI titers in vaccinated chickens but not vaccine coated with lipsome alone.
Luo, Yu-Li, and 羅昱立. "Studies of avian influenza virus-induced apoptosis and HA protein expression." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/28070314762861980293.
Повний текст джерела國立屏東科技大學
生物科技研究所
94
Avian influenza virus(AIV)belongs to orthomyxoviridae family. Highly pathogenetic avian influenza virus causes flowl plague in chickens and turkeys. The HA protein of AIV 1209 strain was expressed by Pichia pastoris yeast expression system. The results indicated that the tagged fusion protein was present both in medium and pellet. The HA protein could be cleaved into HA1(47 kDa) and HA2(22 kDa). The AIV CE9 could induce apoptosis in MDCK cell. To further study the molecular mechanism of AIV-induced apoptosis, the NA protein of AIV H5N2 CE9 strain was cloned into pcDNA3.1(-), and the recombinant DNA transfected into MDCK cell lines. The results indicated that at the same focus, caspase 3 were not detected in the MDCK cell expressing the GFP-NA fusion protein. Phylogenesis analysis of HA and NA gene of strains Taiwanese 1209 and CE9 was done to sequence with other H5N2 viruses in the world using MEGA 3.1 software. The result indicate the 1209 and CE9 strain belong to the same group as the Italy strain.
Singh, Shailbala. "First Characterization of Avian Memory T Lymphocyte Responses to Avian Influenza Virus Proteins." 2009. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7534.
Повний текст джерелаChien, Pin-Cheng, and 錢品澄. "Characterization of Monoclonal Antibodies against Nonstructural Protein 1 (NS1) of Avian Influenza Virus." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/43455856100074850441.
Повний текст джерела國立臺灣大學
獸醫學研究所
102
NS1 is an indictor Ag of influenza virus (IV) infection and it’s only produced during IV replication in very early stage of infection. It can be used in determining whether the chicken was infected or not, which also can be applied on early diagnosis of IV infection. Therefore, my study aimed to characterize the anti-NS1 MAb (αNS1 MAb) by indirect ELISA (iELISA), indirect immunofluorescence assay (IFA), western blotting (WB), immunohistochemistry stain (IHC) and mapping the antibody binding site by eukaryotic expression system (EES). Subsequently, to develop a rapid, sensitive and specific diagnostic MAbs-based NS1 Ag sandwich ELISA that might be incorporated with NP and M Ag ELISA kit for detecting the IV infection. The parental hybridoma have been prepared by immunizing Balb/c mice with E. coli expressed recombinant nonstructural protein 1 (rNS1) oringinated from IV isolates of A/chicken/Taiwan/2838V/00 (H6N1/2838). 16 αNS1 MAbs have been characterized by WB, IFA and iELISA with NS1 Ag from several IV isolates such as A/chicken/Miaoli/2904/00 (H6N1/2904), A/chicken/Taiwan/1209/03 (H5N2/1209). Meanwhile, the epitope mapping was studied in EES. Expression of full length rNS1 (residues 1-230) were all positive and 4 αNS1 MAb (4M4, 4M6, 4N5, 4R3) were negative in C-terminal deletion (residues 1-207). Accroding to epitope mapping analysis results, which can divide 16 αNS1 MAb into four groups (A, B, C &; D). The predictive epitopes of 16 αNS1 MAb mainly recognize the effector domain (residues 74-230) and group B recognize the C-terminal tail (residues 202-230) of NS1 protein. MAb-based NS1 Ag sandwich ELISA was designed as sixteen MAb individually conjugated with HRP as the tracer Ab paired with each non-conjugated MAb acted as docking Ab respectively to compare the binding ability of those combinations with E. coli expressed rNS1. Current results indicated that MP-5 (4R11 – 4M2/HRP), MP-9 (4R11 – 4J12/HRP) and MP-10 (4M2 – 4M2/HRP) can detect NS1 Ag from 15 subtypes of IV (H1~H15). It is believed the three MP (MP-5, MP-9 &; MP-10) we studied have potential to be applied on detecting the IV NS1 Ag.
陳廷軒. "Immunogenicity of recombinant protein, adenovirus vector and virus-like particles of the avian-origin influenza H7N9 virus hemagglutinin." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/7ed3h7.
Повний текст джерелаКниги з теми "Avian influenza virus M2e protein"
Alexander, D. J., N. Phin, and M. Zuckerman. Influenza. Edited by I. H. Brown. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0037.
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