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Retrovirus D/New England and its relation to Mason-Pfizer monkey virus.

机译:逆转录病毒D /新英格兰及其与梅森-辉瑞猴病毒的关系。

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摘要

Seventeen isolates of retrovirus D/New England have been obtained from three species of macaques at the New England Regional Primate Research Center. Seven of the isolates were obtained from macaques who subsequently died with the macaque immunodeficiency syndrome; other isolates were obtained from macaques with less severe or other forms of illness. Attempts to isolate type D retrovirus from peripheral lymphocytes of 97 apparently healthy macaques have not been successful. Cloned DNA was prepared from Hirt supernatants of cells infected with one of these isolates (D/New England 398). By restriction endonuclease analysis, cloned pD398 DNA represented full-length viral DNA with one long terminal repeat. A detailed restriction endonuclease map of pD398 was derived and compared with a map of the cloned Mason-Pfizer monkey virus genome. Forty-six percent (13 of 28) of restriction endonuclease sites were found to be conserved when these related viruses were compared. Five of the D/New England isolates, including those from three different macaque species, were examined for strain variability by restriction endonuclease typing. Comparison of over 30 restriction endonuclease sites has not distinguished any of these D/New England isolates. It thus appears that a single strain of type D retrovirus is infecting three different species of macaques in the New England colony. Markedly reduced cross-hybridization was observed between cloned pD398 and Mason-Pfizer monkey virus DNAs at high stringency; this reduced cross-hybridization was localized to the pol-env regions of the genome. Only very weak hybridization of D/New England DNA to cloned squirrel monkey type D retrovirus DNA could be detected even at low-stringency conditions. What role type D retrovirus plays in the immunodeficiency syndrome of macaques remains to be determined.
机译:在新英格兰地区灵长类动物研究中心,从三种猕猴中获得了17种逆转录病毒D /新英格兰分离株。从猕猴中分离出七个分离株,这些猕猴随后死于猕猴免疫缺陷综合症。从病情较轻或其他形式的猕猴中获得了其他分离株。从97个看似健康的猕猴的外周淋巴细胞中分离出D型逆转录病毒的尝试尚未成功。从感染了这些分离株之一的细胞的Hirt上清液中制备克隆的DNA(D / New England 398)。通过限制性核酸内切酶分析,克隆的pD398 DNA代表具有一个长末端重复的全长病毒DNA。推导了pD398的详细限制性核酸内切酶图谱,并将其与克隆的Mason-Pfizer猴病毒基因组的图谱进行了比较。比较这些相关病毒时,发现有46%(28个中的13个)限制性内切酶位点是保守的。通过限制性核酸内切酶分型,检查了五个D / New England分离株,包括来自三个不同猕猴的分离株。超过30个限制性核酸内切酶位点的比较尚未区分出这些D / New England分离株。因此看来,单一的D型逆转录病毒株正在感染新英格兰殖民地的三种猕猴。在严格的条件下,在克隆的pD398和Mason-Pfizer猴病毒DNA之间观察到明显减少的交叉杂交。这种减少的交叉杂交位于基因组的pol-env区。即使在低严格条件下,也只能检测到D /新英格兰DNA与克隆的松鼠D型逆转录病毒DNA的杂交非常弱。 D型逆转录病毒在猕猴的免疫缺陷综合症中起什么作用还有待确定。

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