ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. H-1. がん進展制御研究所
  2. h-1 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Human cytomegalovirus persistent infection in a human central nervous system cell line: Production of a variant virus with different growth characteristics

http://hdl.handle.net/2297/29184
http://hdl.handle.net/2297/29184
e87f9ce6-48cd-48a2-b3e1-cb1145abb405
名前 / ファイル ライセンス アクション
CA-PR-SATO-H-2605.pdf CA-PR-SATO-H-2605.pdf (5.2 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-05
タイトル
タイトル Human cytomegalovirus persistent infection in a human central nervous system cell line: Production of a variant virus with different growth characteristics
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Ogura, Tsutomu

× Ogura, Tsutomu

WEKO 47691

Ogura, Tsutomu

Search repository
Tanaka, Junji

× Tanaka, Junji

WEKO 47692

Tanaka, Junji

Search repository
Kamiya, Shigeru

× Kamiya, Shigeru

WEKO 47693

Kamiya, Shigeru

Search repository
Sato, Hiroshi

× Sato, Hiroshi

WEKO 23232
e-Rad 00115239
研究者番号 00115239

Sato, Hiroshi

Search repository
Ogura, Hisashi

× Ogura, Hisashi

WEKO 47688
研究者番号 10115222

Ogura, Hisashi

Search repository
Hatano, Motoichi

× Hatano, Motoichi

WEKO 47694

Hatano, Motoichi

Search repository
書誌情報 Journal of General Virology

巻 67, 号 12, p. 2605-2616, 発行日 1986-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0022-1317
NCID
収録物識別子タイプ NCID
収録物識別子 AA00698722
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.1099/0022-1317-67-12-2605
出版者
出版者 Society for General Microbiology
抄録
内容記述タイプ Abstract
内容記述 The susceptibility of human central nervous system cell lines to human cytomegalovirus (HCMV) and the fate of infected cultures were studied. Significant amounts of infectious progeny virus were produced in 118MGC glioma and IMR-32 neuroblastoma, but not in KGC oligodendroglioma cells when the cultures were infected with wild-type virus (HCMVwt) at an m.o.i. of 10 p.f.u. per cell. Further passage of infected 118MGC cells resulted in the establishment of a long-term persistent infection. This infection, designated 118MGC/Towne, continuously produced infectious virus (HCMVpi) with titres ranging from 102 to 105 p.f.u./106 cells up to 360 days post-infection (corresponding to 50 subcultures). Since no temperature-sensitive mutants, defective interfering particles or interferon-like activity were found in the 118MGC/Towne cultures, maintenance of the persistent infection seemed to be due to a balance between the release of infectious virus and the growth of uninfected cells. The HCMVpi produced in long-term persistently infected cultures was shown to be different from the HCMVwt originally used to infect by the following characteristics: (i) HCMVpi replicated slowly and yielded lower amounts of progeny virus than HCMVwt; (ii) HCMVpi induced a 73000 mol. wt. immediate early protein that was not synthesized in HCMVwt-infected cells; (iii) HCMVpi had a different DNA structure from that of HCMVwt. These results suggest that HCMVpi is a slower growing variant of HCMVwt and probably plays an important role in the maintenance of the persistent infection.
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
戻る
0
views
See details
Views

Versions

Ver.1 2023-07-27 11:21:26.686103
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3