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  1. 学位論文
  2. 獣医学専攻
  3. 博士論文(甲)

鶏アデノウイルス病原性の遺伝子解析および診断用抗原と抗体の開発

https://az.repo.nii.ac.jp/records/5345
https://az.repo.nii.ac.jp/records/5345
5814d9c7-e197-465d-9a87-9efcff9a4f55
名前 / ファイル ライセンス アクション
diss_dv_kou0155.pdf diss_dv_kou0155 (1.8 MB)
diss_dv_kou0155_jab&rev.pdf diss_dv_kou0155_jab&rev.pdf (192.5 kB)
Item type 学位論文 / Thesis or Dissertation(1)
公開日 2019-04-23
タイトル
タイトル 鶏アデノウイルス病原性の遺伝子解析および診断用抗原と抗体の開発
タイトル
タイトル Genetic analysis of the virulence factors and development of a novel diagnostic antigen and antibody test for Fowl Aviadenovirus
言語 en
言語
言語 eng
資源タイプ
資源タイプ doctoral thesis
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
著者 Thanasut, Khompakorn

× Thanasut, Khompakorn

Thanasut, Khompakorn

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Thanasut, Khompakorn

× Thanasut, Khompakorn

en Thanasut, Khompakorn

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Abstract
内容記述タイプ Other
内容記述 Fowl Aviadenovirus (FAdV) belong to the family Adenoviridae and the genus Aviadenovirus. FAdV is a non-enveloped icosahedral viros which has a linear, double- stranded DNA. It has been grouped into five species and 12 serotypes. FAdVs infections often cause Hydropericardium syndrome (HPS), inclusion body hepatitis (IBH), egg drop syndrome (EDS), gizzard erosion (GE), and respiratory tract disease. The disease occurs worldwide leading to great economic losses in the poultry industry.
 To elucidate factors associated with the virulence of Fowl Aviadenovirus, whole genome sequencing using Next Geneneration Sequencing (NGS) of FAdV A strain JM1/1 was carried out. Developing the non-structural protein based Fluorescent antibody virus neutralization (FAVN) and Western Blotting assay (WB) coupled with Immunofluorescence assay (IFA) were studied. The results shown as following
 1) The complete genome of FAdV A strain JM1/1 is 43,809 nucleotide length. It’s revealed 99% nucleotide sequence identical to FAdV A strain CELO (chicken embryo lethal orphan), which is an European apathogenic reference strain. The nucleotide sequence differences were analyzed, interestingly showing multiple sites insertions and deletions. The results will provide information on the evolution and may help elucidate viral pathogenesis on molecular biology especially on genetic roles.
 2) The recombinant DBP was constructed and subjected as the primary antibody in the developed FAVN test. A DNA Binding Protein (DBP), a non-structural protein, which is detectable early and responsible for initiating DNA replication. DBP was found to be a more conserved domain region within the FAdV serotype 1. The developed FAVN test was compared with a conventional VN test by examining the antibody titer in field chicken sera. The results showed the measured neutralizing antibody titers were high correlated with the VN as the correlation coefficient was 0.8. This FAVN test is simple, achieved quickly, easily and could be an alternative test for FAdV infection.
 3) Likewise, the recombinant 52K was constructed and subjected to use as primary antibody in the developed test based on WB and IFA. 52K, non-structural protein, involve in capsid assembly and/or genome packaging. It is especially expressed in late stages of viral life cycle. The C terminal region of 52K was found to be a more conserved domain within all serotypes. WB and IFA analyze revealed that anti-52K antibody can detect FAdVs infection including homologous and heterologous serotypes. Therefore, this antibody possesses a property which could play a role in an alternative method for FAdVs infection diagnosis.
 In conclusion, this research study provided some knowledge, which will be useful in investigation, surveillance, and elimination of FAdV diseases.
学位名
学位名 博士(獣医学)
学位授与機関
学位授与機関識別子Scheme kakenhi
学位授与機関識別子 32701
学位授与機関名 麻布大学
学位授与年月日
学位授与年月日 2019-03-15
学位授与番号
学位授与番号 甲第155号
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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