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从血浆RNA检测不到的感染SHIV的食蟹猴外周血单核细胞中检测环状病毒DNA并分析连接序列。

Circular viral DNA detection and junction sequence analysis from PBMC of SHIV-infected cynomolgus monkeys with undetectable virus plasma RNA.

作者信息

Cara Andrea, Maggiorella Maria Teresa, Bona Roberta, Sernicola Leonardo, Baroncelli Silvia, Negri Donatella R M, Leone Pasqualina, Fagrouch Zahra, Heeney Jonathan, Titti Fausto, Cafaro Aurelio, Ensoli Barbara

机构信息

Laboratory of Virology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.

出版信息

Virology. 2004 Jul 1;324(2):531-9. doi: 10.1016/j.virol.2004.04.006.

Abstract

Extrachromosomal forms of human immunodeficiency virus (HIV)-1 can be detected in peripheral blood mononuclear cell (PBMC) from HIV-infected patients in the absence of detectable viral replication and are thought to be a sign of active but cryptic virus replication. No information, however, are available on whether these forms are also present in animal models for acquired immunodeficiency syndrome (AIDS) and on their relation with other methods of detection of virus replication. To this aim, a polymerase chain reaction (PCR) approach was used to detect and analyze unintegrated circular 2-LTR-containing forms in PBMC of simian human immunodeficiency virus (SHIV)89.6P infected cynomolgus monkeys with RNA levels ranging between 1.8 x 10(6) and less than 50 copies/ml of plasma. 2-LTR forms were detected in 96.5% of monkeys' samples above 50 copies/ml of plasma, whereas they were present in 75.8% of monkeys' samples below 50 copies/ml of plasma. Persistence of unintegrated viral DNA in monkeys with undetectable plasma RNA could indicate either stability in non-dividing cells or ongoing low levels of viral replication in dividing cells.

摘要

在未检测到病毒复制的情况下,可在感染人类免疫缺陷病毒(HIV)-1患者的外周血单核细胞(PBMC)中检测到HIV-1的染色体外形式,并且认为这是活跃但隐匿的病毒复制的标志。然而,关于这些形式是否也存在于获得性免疫缺陷综合征(AIDS)动物模型中以及它们与其他病毒复制检测方法的关系,尚无相关信息。为了实现这一目标,采用聚合酶链反应(PCR)方法检测和分析感染猿猴人类免疫缺陷病毒(SHIV)89.6P的食蟹猴PBMC中未整合的含2-LTR环状形式,这些食蟹猴血浆中的RNA水平在1.8×10⁶至低于每毫升50拷贝之间。在血浆RNA高于每毫升50拷贝的猴子样本中,96.5%检测到2-LTR形式,而在血浆RNA低于每毫升50拷贝的猴子样本中,75.8%存在2-LTR形式。血浆RNA检测不到的猴子中未整合病毒DNA的持续存在可能表明其在非分裂细胞中的稳定性或在分裂细胞中持续存在低水平的病毒复制。

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