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本文引用的文献

1
Clinical validation of a new real-time PCR assay for detection of enteroviruses and parechoviruses, and implications for diagnostic procedures.一种用于检测肠道病毒和帕里病毒的新型实时聚合酶链反应检测方法的临床验证及其对诊断程序的影响
J Clin Virol. 2008 Feb;41(2):75-80. doi: 10.1016/j.jcv.2007.09.011.
2
Rapid detection of human parechoviruses in clinical samples by real-time PCR.通过实时聚合酶链反应快速检测临床样本中的人细小病毒
J Clin Virol. 2008 Feb;41(2):69-74. doi: 10.1016/j.jcv.2007.10.004.
3
Prevalence, types, and RNA concentrations of human parechoviruses, including a sixth parechovirus type, in stool samples from patients with acute enteritis.急性肠炎患者粪便样本中人类细小病毒(包括第六种细小病毒型)的患病率、类型及RNA浓度
J Clin Microbiol. 2008 Jan;46(1):242-8. doi: 10.1128/JCM.01468-07. Epub 2007 Dec 5.
4
Cultivation of the Lansing Strain of Poliomyelitis Virus in Cultures of Various Human Embryonic Tissues.脊髓灰质炎病毒兰辛株在各种人胚胎组织培养物中的培养
Science. 1949 Jan 28;109(2822):85-7. doi: 10.1126/science.109.2822.85.
5
Isolation and characterization of novel human parechovirus from clinical samples.从临床样本中分离和鉴定新型人细小病毒
Emerg Infect Dis. 2007 Jun;13(6):889-95. doi: 10.3201/eid1306.060896.
6
Association of zoonotic Ljungan virus with intrauterine fetal deaths.人畜共患的吕永病毒与宫内胎儿死亡的关联。
Birth Defects Res A Clin Mol Teratol. 2007 Jun;79(6):488-93. doi: 10.1002/bdra.20359.
7
A new quantitative real-time reverse transcriptase PCR assay and melting curve analysis for detection and genotyping of Ljungan virus strains.一种用于检测和基因分型吕宋病毒株的新型定量实时逆转录聚合酶链反应检测方法及熔解曲线分析
J Virol Methods. 2007 Apr;141(1):71-7. doi: 10.1016/j.jviromet.2006.11.029. Epub 2006 Dec 28.
8
Fourth human parechovirus serotype.人细小病毒第四血清型。
Emerg Infect Dis. 2006 Oct;12(10):1572-5. doi: 10.3201/eid1210.051647.
9
Analysis of a new human parechovirus allows the definition of parechovirus types and the identification of RNA structural domains.对一种新型人细小病毒的分析有助于确定细小病毒的类型并识别RNA结构域。
J Virol. 2007 Jan;81(2):1013-21. doi: 10.1128/JVI.00584-06. Epub 2006 Sep 27.
10
Sensitive, seminested PCR amplification of VP1 sequences for direct identification of all enterovirus serotypes from original clinical specimens.用于直接从原始临床标本中鉴定所有肠道病毒血清型的VP1序列的灵敏半巢式PCR扩增。
J Clin Microbiol. 2006 Aug;44(8):2698-704. doi: 10.1128/JCM.00542-06.

通过实时聚合酶链反应检测所有已知的细小病毒。

Detection of all known parechoviruses by real-time PCR.

作者信息

Nix W Allan, Maher Kaija, Johansson E Susanne, Niklasson Bo, Lindberg A Michael, Pallansch Mark A, Oberste M Steven

机构信息

Polio and Picornavirus Laboratory Branch, Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, N.E., Atlanta, GA 30333, USA.

出版信息

J Clin Microbiol. 2008 Aug;46(8):2519-24. doi: 10.1128/JCM.00277-08. Epub 2008 Jun 4.

DOI:10.1128/JCM.00277-08
PMID:18524969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2519456/
Abstract

The Parechovirus genus of the Picornaviridae family contains two species, Human parechovirus (HPeV) and Ljungan virus (LV). The HPeVs (including the former echoviruses 22 and 23, now HPeV type 1 (HPeV1) and HPeV2, respectively) cause a wide spectrum of disease, including aseptic meningitis, gastroenteritis, encephalitis, acute respiratory illness, and neonatal sepsis-like disease. The LVs were isolated from bank voles in Sweden during a search for an infectious agent linked to fatal myocarditis cases in humans. Because of the decline in use of cell culture and neutralization to investigate enterovirus-like disease, very few laboratories currently have the capability to test for parechoviruses. We have developed a real-time reverse transcription-PCR (RT-PCR) assay for detection of all known members of the genus Parechovirus. The assay targets the conserved regions in the 5' nontranslated region (5'NTR) of the parechovirus genome and can detect both HPeVs and LVs, unlike other published parechovirus 5' NTR assays, which only detect known HPeVs or only LVs. HPeV and LV can be differentiated by sequencing the 5'NTR real-time RT-PCR amplicon, when needed. The assay is approximately 100 times more sensitive than cell culture and may be used to test original clinical specimens. The availability of a broad-specificity PCR method should facilitate the detection of new human parechoviruses, as well as new parechoviruses in other mammalian species, and provide an opportunity to investigate the role of these viruses in human and animal disease.

摘要

小RNA病毒科的帕里病毒属包含两个种,即人帕里病毒(HPeV)和吕宋病毒(LV)。人帕里病毒(包括以前的埃可病毒22型和23型,现在分别为1型人帕里病毒(HPeV1)和2型人帕里病毒(HPeV2))可引发多种疾病,包括无菌性脑膜炎、肠胃炎、脑炎、急性呼吸道疾病以及新生儿败血症样疾病。吕宋病毒是在瑞典从银行田鼠中分离出来的,当时正在寻找一种与人类致命心肌炎病例相关的感染因子。由于用于研究肠道病毒样疾病的细胞培养和中和技术的使用减少,目前很少有实验室具备检测帕里病毒的能力。我们开发了一种实时逆转录聚合酶链反应(RT-PCR)检测方法,用于检测帕里病毒属的所有已知成员。该检测方法针对帕里病毒基因组5'非翻译区(5'NTR)的保守区域,与其他已发表的仅检测已知人帕里病毒或仅检测吕宋病毒的帕里病毒5'NTR检测方法不同,它可以同时检测人帕里病毒和吕宋病毒。如有需要,可通过对5'NTR实时RT-PCR扩增子进行测序来区分人帕里病毒和吕宋病毒。该检测方法的灵敏度比细胞培养高约100倍,可用于检测原始临床标本。一种具有广泛特异性的PCR方法的出现,应有助于检测新的人帕里病毒以及其他哺乳动物物种中的新帕里病毒,并为研究这些病毒在人类和动物疾病中的作用提供机会。