Anses, French Agency for Food, Environmental and Occupational Health Safety, Ploufragan/Plouzané Laboratory, Avian and Rabbit Virology Immunology and Parasitology Unit, VIPAC, BP 53, 22440 Ploufragan, France.
J Virol Methods. 2013 Oct;193(1):121-7. doi: 10.1016/j.jviromet.2013.05.007. Epub 2013 May 23.
Determining the sequence of non-segmented, negative sense RNA viral genomes is far from routine and often requires the application of several techniques. In this study, an existing method used currently just for determination of the genomic 3' extremity was used to determine both the 3' and 5' sequence extremities of a Newcastle disease virus and an avian metapneumovirus. This was achieved with a single 3' nucleotide tailing reaction of both the genomic RNA and the full length, positive sense, antigenomic RNA, followed by a single reverse transcription reaction targeted to the common polynucleotide tails, and then individual PCRs specific for each extremity using PCR primers derived from the sequence of the RT primer or from neighbouring virus sequences known previously. For each virus the method was employed separately. Sequences from both viruses were in agreement with those reported previously for other paramyxoviruses, yet one extra base at the 3' and one extra base at the 5' were identified for the avian metapneumovirus. In this study, importantly, the newly determined extremities maintained the complementarity known to exist between the extremities of these viruses. The method was equally successful with both viruses and can be tailored easily to function with other non-segmented, negative sense viruses through minor modification of only the primer sequences.
确定不分节、负义 RNA 病毒基因组的序列远非常规,通常需要应用几种技术。在这项研究中,我们使用了一种目前仅用于确定基因组 3' 末端的现有方法,来确定新城疫病毒和禽偏肺病毒的 3' 和 5' 序列末端。这是通过对基因组 RNA 和全长、正义、反义基因组 RNA 进行单次 3' 核苷酸加尾反应来实现的,然后针对共同的多核苷酸尾巴进行单次反转录反应,然后使用源自 RT 引物序列或先前已知的相邻病毒序列的针对每个末端的特异性 PCR 引物进行单独的 PCR。对于每种病毒,我们分别使用该方法。两种病毒的序列与其他副粘病毒先前报道的序列一致,但禽偏肺病毒在 3' 末端和 5' 末端分别多了一个碱基。在这项研究中,重要的是,新确定的末端保持了这些病毒末端之间已知的互补性。该方法对两种病毒同样有效,并且可以通过仅对引物序列进行微小修改,轻松适应其他不分节、负义病毒。