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绵羊慢病毒产后传播后前病毒清除的证据。

Evidence of proviral clearance following postpartum transmission of an ovine lentivirus.

作者信息

Herrmann-Hoesing Lynn M, Palmer Guy H, Knowles Donald P

机构信息

Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture, Pullman, WA 99164-6630, USA.

出版信息

Virology. 2007 May 25;362(1):226-34. doi: 10.1016/j.virol.2006.12.021. Epub 2007 Jan 30.

Abstract

Lentiviral transmission by transfer of infected colostrum and/or milk is considered to be highly efficient. In this study, postpartum transmission of ovine progressive pneumonia virus (OPPV) from 10 naturally infected ewes to their 23 lambs was followed from the perinatal period throughout a four-year period. The lambs were allowed to suckle from their dam from birth through 32 weeks of age. Virus was tracked by virus isolation, quantitative PCR (qPCR), and anti-OPPV antibody responses as measured by cELISA. Cell-associated OPPV was isolated from colostrum/milk cells in 7 out of 10 ewes and provirus envelope (env) loads ranged 8 to 10(5) copies/mug DNA in colostrum/milk cells from the 10 ewes using qPCR. Provirus env loads were also detected in the peripheral circulation of 21 lambs at 8 weeks and two lambs at 22 weeks. The qPCR product at 8 weeks was confirmed as the transmembrane (tm) gene of OPPV by cloning and sequencing. Both cELISA titers ranging from 325 to 3125 and cross-neutralizing antibody titers ranging from 6 to 162 to seven different OPPV strains were found in the colostrum of the 10 ewes. Furthermore, cELISA titers in serum from lambs remained detectable through 32 weeks following the clearance of provirus at 24 weeks. After 32 weeks, both provirus and anti-OPPV antibody responses have subsequently remained undetectable through 4 years of age. These data suggest the clearance of cell-associated lentiviruses from lamb circulation after passive transfer of antibody via colostrum.

摘要

通过感染的初乳和/或乳汁传播慢病毒被认为效率很高。在本研究中,从围产期开始,对10只自然感染的母羊向其23只羔羊进行绵羊进行性肺炎病毒(OPPV)的产后传播情况进行了为期四年的跟踪。羔羊从出生到32周龄一直由其母羊哺乳。通过病毒分离、定量PCR(qPCR)以及用cELISA检测抗OPPV抗体反应来追踪病毒。从10只母羊中的7只的初乳/乳汁细胞中分离出细胞相关的OPPV,使用qPCR检测,10只母羊的初乳/乳汁细胞中前病毒包膜(env)载量范围为8至10(5)拷贝/μg DNA。在21只羔羊8周龄时和2只羔羊22周龄时的外周循环中也检测到前病毒env载量。通过克隆和测序确认8周龄时的qPCR产物为OPPV的跨膜(tm)基因。在10只母羊的初乳中发现cELISA效价范围为325至3125,以及针对七种不同OPPV毒株的交叉中和抗体效价范围为6至162。此外,在24周前病毒清除后,羔羊血清中的cELISA效价在32周内仍可检测到。32周后,在前病毒和抗OPPV抗体反应在4岁之前均未检测到。这些数据表明,通过初乳被动转移抗体后,羔羊循环中的细胞相关慢病毒被清除。

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