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用聚合酶链反应法测定单纯疱疹病毒1型低反应性毒株HSZP的DNA靶序列

Determination of the DNA target sequence of poorly reactivable strain HSZP of herpes simplex virus type 1 by polymerase chain reaction.

作者信息

Kúdelová M, Dragún M, Kosovský J, Matis J, Rajcáni J

机构信息

Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic.

出版信息

Acta Virol. 1996 Feb;40(1):15-21.

PMID:8886093
Abstract

HSZP strain of herpes simplex virus type 1 (HSV-1)-unlike strains KOS, SC16 and ANGpath-established latency in the homolateral trigeminal ganglion of mice at a limited rate (21%) when tested by reactivation of latent virus in culture. If a nested polymerase chain reaction (PCR) for virus DNA detection was used, the positivity rate was 63-100%. The detection rate of HSZP DNA in acutely infected gangla did not differ from that of SC16 DNA provided that the sensitivity of PCR was below 20 pg of HSZP DNA per 0.5 microgram of total ganglionic DNA. The nested PCR assessed at least 200 fg of HSZP DNA per 0.5 microgram of ganglionic DNA.

摘要

1型单纯疱疹病毒(HSV-1)的HSZP毒株——与KOS、SC16和ANG毒株不同——通过培养中潜伏病毒的再激活进行检测时,在小鼠同侧三叉神经节中以有限的速率(21%)建立潜伏感染。如果使用巢式聚合酶链反应(PCR)检测病毒DNA,阳性率为63%-100%。只要PCR的灵敏度低于每0.5微克总神经节DNA中20皮克HSZP DNA,急性感染神经节中HSZP DNA的检测率与SC16 DNA的检测率没有差异。巢式PCR每0.5微克神经节DNA可检测至少200飞克的HSZP DNA。

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