Tobler K, Ackermann M
Institut für Virologie, Veterinãr-medizinische Fakultät, Universität Zürich.
Schweiz Arch Tierheilkd. 1996;138(2):80-6.
A modified method of the reverse transcription followed by polymerase chain reaction (RT-PCR) was developed in order to examine the genome of a recently discovered virus, the porcine epidemic diarrhoea virus (PEDV), which resembled morphologically the coronaviruses. The published sequences of the genomes of various coronaviruses were compared. On the level of the amino acid sequence, conserved regions, common to all coronaviruses, were found in the gene encoding the nonstructural protein 1b as well as in the genes coding for the major structural proteins (S, M, and N). Due to the degeneration of the genetic code, some amino acids may be encoded by different nucleotide triplets. In order to compensate for this degeneration, mixtures of primers were synthesized, containing a variety of nucleotide sequences which together represented all possible codons for the conserved amino acid sequences. This method allowed to amplify and clone approximately 4000 base pairs of the genome of PEDV. An analysis of the genomic sequences revealed that PEDV holds an interesting intermediate position between human coronavirus 229E and Transmissible Gastroenteritis virus. We postulate that the method presented in this contribution may be useful to study and characterize other unknown viruses, especially viruses for which no cell cultures for propagation are available.
为检测一种最近发现的病毒——猪流行性腹泻病毒(PEDV)的基因组,开发了一种改进的逆转录聚合酶链反应(RT-PCR)方法。该病毒在形态上类似于冠状病毒。比较了各种冠状病毒基因组的已发表序列。在氨基酸序列水平上,在编码非结构蛋白1b的基因以及编码主要结构蛋白(S、M和N)的基因中发现了所有冠状病毒共有的保守区域。由于遗传密码的简并性,一些氨基酸可能由不同的核苷酸三联体编码。为了弥补这种简并性,合成了引物混合物,其中包含多种核苷酸序列,这些序列共同代表了保守氨基酸序列的所有可能密码子。该方法能够扩增和克隆PEDV基因组中约4000个碱基对。对基因组序列的分析表明,PEDV在人冠状病毒229E和传染性胃肠炎病毒之间处于一个有趣的中间位置。我们推测,本文介绍的方法可能有助于研究和鉴定其他未知病毒,特别是那些没有用于增殖的细胞培养物的病毒。