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Molecular cloning, expression, and serological evaluation of an 8-kilodalton subunit of antigen B from Echinococcus multilocularis.

https://asahikawa-med.repo.nii.ac.jp/records/691
https://asahikawa-med.repo.nii.ac.jp/records/691
19370f58-2eeb-4755-8a4d-b873fb4e720d
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866.pdf 866.pdf (390.3 kB)
Item type 学術雑誌論文 / Journal Article_02(1)
公開日 2008-02-28
タイトル
タイトル Molecular cloning, expression, and serological evaluation of an 8-kilodalton subunit of antigen B from Echinococcus multilocularis.
言語 en
言語
言語 eng
資源タイプ
資源タイプ journal article
著者 伊藤, 亮

× 伊藤, 亮

伊藤, 亮

ja-Kana イトウ, アキラ

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Mamuti, W

× Mamuti, W

Mamuti, W

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Yamasaki, H

× Yamasaki, H

Yamasaki, H

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Sako, Y

× Sako, Y

Sako, Y

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Nakao, M

× Nakao, M

Nakao, M

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Xiao, N

× Xiao, N

Xiao, N

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Nakaya, K

× Nakaya, K

Nakaya, K

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Sato, N

× Sato, N

Sato, N

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Vuitton, DA

× Vuitton, DA

Vuitton, DA

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Piarroux, R

× Piarroux, R

Piarroux, R

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Lightowlers, MW

× Lightowlers, MW

Lightowlers, MW

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Craig, PS

× Craig, PS

Craig, PS

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著者 ローマ字
Ito, Akira
書誌情報 Journal of Clinical Microbiology.

巻 42, 号 3, p. 1082-1088, 発行日 2004-03-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0095-1137
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1128/JCM.42.3.1082-1088.2004
リンクURL
内容記述タイプ Other
内容記述 http://www.ncbi.nlm.nih.gov/pubmed?term=Molecular%20cloning%2C%20expression%2C%20and%20serological%20evaluation%20of%20an%208-kilodalton%20subunit%20of%20antigen%20B%20from%20Echinococcus%20multilocularis. | http://www.ncbi.nlm.nih.gov/pubmed?term=Molecular%20cloning%2C%20expression%2C%20and%20serological%20evaluation%20of%20an%208-kilodalton%20subunit%20of%20antigen%20B%20from%20Echinococcus%20multilocularis.
抄録
内容記述タイプ Abstract
内容記述 Full-length cDNA and genomic DNA encoding an 8-kDa subunit of antigen B from Echinococcus multilocularis (designated EmAgB8/1) were isolated from an E. multilocularis metacestode cDNA library and a protoscolex genomic DNA library, respectively. The open reading frame of the cDNA clone encodes a polypeptide comprising 85 amino acids with a 20-amino-acid NH(2)-terminal signal sequence, which was confirmed following N-terminal sequencing of the native antigen. Reverse transcription-PCR analysis revealed that the clone encoding EmAgB8/1 is predominantly transcribed in larval E. multilocularis. The gene consists of two exons (encoding the signal sequence and mature protein) separated by a 91-bp intron. The mature form was expressed in Escherichia coli, and its antigenic reactivity was compared with that of a counterpart, an 8-kDa subunit of antigen B from Echinococcus granulosus (EgAgB8/1) by Western blotting and enzyme-linked immunosorbent assay (ELISA) with serum samples from patients confirmed to have cystic echinococcosis (CE) and alveolar echinococcosis (AE). Recombinant EmAgB8/1 showed positive reactions in Western blots with 81.3% (65 of 80) of serum samples from CE patients and 40.6% (26 of 64) of serum samples from AE patients, while recombinant EgAgB8/1 showed positive reactions with 86% (43 of 50) and 42% (19 of 45) of the serum samples from these CE and AE patients, respectively. By the ELISA, both EmAgB8/1 and EgAgB8/1 exhibited similar positive reactions with 88% (44 of 50) of serum samples from CE patients and 37.8% (17 of 45) serum samples from AE patients. Statistical analysis revealed that the sensitivity of EmAgB8/1 was comparable to that of EgAgB8/1 for the serodiagnosis of echinococcal diseases. There was no cross-reaction with sera from patients with cysticercosis, which often cross-react when native antigens are used for serodiagnosis.
注記
内容記述タイプ Other
注記 Copyright © American Society for Microbiology, Journal of Clinical Microbiology, volume 42, 1082-1088, 2004
\npublisher
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資源タイプ text
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出版タイプ VoR
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