Clavijo A, Nagy E
Department of Veterinary Microbiology and Immunology, University of Guelph, Ontario, Canada.
Avian Dis. 1997 Jan-Mar;41(1):241-6.
Oligonucleotide primers derived from infectious laryngotracheitis virus (ILTV) DNA clones of vaccine and virulent strains were used to develop a polymerase chain reaction (PCR) for the identification and differentiation of ILTV strains. The PCR followed by restriction endonuclease analysis was used to group four strains of ILTV. A 458-bp sequence that for the LT-IVAX ILTV strain contains a unique BamHI site was amplified by PCR and digested with BamHI restriction endonuclease. From the sizes of the resultant DNA fragments the virulent strain was distinguished from the three low virulence strains.
源自传染性喉气管炎病毒(ILTV)疫苗株和强毒株DNA克隆的寡核苷酸引物被用于开发一种聚合酶链反应(PCR),以鉴定和区分ILTV毒株。通过PCR及限制性内切酶分析对四株ILTV进行分类。通过PCR扩增出一段458碱基对的序列,该序列对于LT-IVAX ILTV毒株含有一个独特的BamHI位点,并用BamHI限制性内切酶进行消化。根据所得DNA片段的大小,将强毒株与三株低毒力毒株区分开来。