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口蹄疫病毒RNA载量在达到峰值水平后,其在食管-咽部分泌液中的减少程度可能是病毒在感染牛体内持续存在的关键决定因素。

Extent of reduction of foot-and-mouth disease virus RNA load in oesophageal-pharyngeal fluid after peak levels may be a critical determinant of virus persistence in infected cattle.

作者信息

Zhang Zhidong, Murphy Ciara, Quan Melvyn, Knight Jeanette, Alexandersen Soren

机构信息

Institute for Animal Health, Ash Road, Pirbright, Woking, Surrey GU24 0NF, UK.

出版信息

J Gen Virol. 2004 Feb;85(Pt 2):415-421. doi: 10.1099/vir.0.19538-0.

Abstract

To investigate whether foot-and-mouth disease virus (FMDV) RNA loads in oesophageal-pharyngeal fluid (OP-fluid) in the early course of infection is related to the outcome of virus persistence, viral RNA in OP-fluid samples from cattle experimentally infected with FMDV type O was quantitatively analysed by using a quantitative real-time RT-PCR. Viral RNA was detected within 24 h post-infection (p.i.) in all infected animals. Rapid virus replication led to peak levels of viral RNA load by 30-53 h p.i., and then the load declined at various rates. In some animals (n=12, so-called non-carriers) viral RNA became undetectable between 7 and 18 days p.i. In contrast, in persistently infected animals (n=12, so-called carriers) viral RNA persisted in OP-fluid samples at detectable levels beyond 28 days p.i. Analysis of early viral decay/clearance and virus clearance half-life in OP-fluid samples showed that the extent of reduction of viral RNA in OP-fluid samples immediately following peak levels is a critical determinant of the outcome of FMDV persistence.

摘要

为研究感染早期牛的食管-咽部分泌液(OP液)中口蹄疫病毒(FMDV)RNA载量是否与病毒持续感染的结果相关,运用实时定量逆转录PCR对实验感染O型FMDV的牛的OP液样本中的病毒RNA进行了定量分析。所有感染动物在感染后24小时内均检测到病毒RNA。病毒快速复制导致感染后30-53小时病毒RNA载量达到峰值水平,随后载量以不同速率下降。在一些动物(n=12,即所谓的非携带者)中,感染后7至18天病毒RNA变得无法检测到。相反,在持续感染的动物(n=12,即所谓的携带者)中,感染后28天以上OP液样本中的病毒RNA仍以可检测水平持续存在。对OP液样本中早期病毒衰减/清除及病毒清除半衰期的分析表明,病毒RNA载量在达到峰值水平后立即下降的程度是FMDV持续感染结果的关键决定因素。

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