Tang Kathy F J, Navarro Solangel A, Lightner Donald V
Department of Veterinary Science and Microbiology, University of Arizona, Tucson, Arizona 85721, USA.
Dis Aquat Organ. 2007 Feb 28;74(2):165-70. doi: 10.3354/dao074165.
We developed a PCR assay that can detect infectious hypodermal and hematopoietic necrosis virus (IHHNV) but that does not react with IHHNV-related sequences in the genome of Penaeus monodon from Africa and Australia. IHHNV is a single-stranded DNA virus that has caused severe mortality and stunted growth in penaeid shrimp. Recently, IHHNV-related sequences were found in the genome of some stocks of P. monodon from Africa and Australia. These virus-related sequences have a high degree of similarity (86 and 92% identities in nucleotide sequence) to the viral genome, which has often generated false-positive reactions during PCR screening of these stocks. For this assay, a pair of IHHNV primers (IHHNV309F/R) was selected. The sequences of these primers match (100% of nucleotides) the target sequence in IHHNV, but mismatch 9 or 12 nucleotides of the genomic IHHNV-related sequences. This PCR assay was tested with various IHHNV isolates and with a number of samples of shrimp DNA that contained IHHNV-related sequences. This assay can reliably distinguish IHHNV DNA from shrimp DNA: it only detects IHHNV. Also, this pair of primers was included in a duplex PCR to detect IHHNV and simultaneously determine the presence of an IHHNV-related sequence. Using these primers, the PCR assay has a sensitivity equivalent to a PCR assay commonly used for detecting IHHNV in Litopenaeus vannamei, and can be used for routine detection.
我们开发了一种聚合酶链反应(PCR)检测方法,该方法能够检测传染性皮下和造血组织坏死病毒(IHHNV),但不会与来自非洲和澳大利亚的斑节对虾基因组中的IHHNV相关序列发生反应。IHHNV是一种单链DNA病毒,已导致对虾严重死亡和生长发育迟缓。最近,在来自非洲和澳大利亚的一些斑节对虾种群的基因组中发现了IHHNV相关序列。这些病毒相关序列与病毒基因组具有高度相似性(核苷酸序列同一性分别为86%和92%),这在对这些种群进行PCR筛选时经常产生假阳性反应。对于该检测方法,选择了一对IHHNV引物(IHHNV309F/R)。这些引物的序列与IHHNV中的靶序列完全匹配(100%的核苷酸),但与基因组中IHHNV相关序列的9个或12个核苷酸不匹配。该PCR检测方法用各种IHHNV分离株以及许多含有IHHNV相关序列的对虾DNA样本进行了测试。该检测方法能够可靠地将IHHNV DNA与对虾DNA区分开来:它只检测IHHNV。此外,这对引物被用于双重PCR中,以检测IHHNV并同时确定是否存在IHHNV相关序列。使用这些引物,该PCR检测方法的灵敏度与常用于检测凡纳滨对虾中IHHNV的PCR检测方法相当,可用于常规检测。