Xueqing Han, Xiangmei Lin, Yihong Hou, Shaoqiang Wu, Jian Liu, Lin Mei, Guangle Jia, Zexiao Yang
The Institute of Animal and Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing 100029, China.
Wei Sheng Wu Xue Bao. 2008 Sep;48(9):1241-9.
Avian influenza viruses are important human and animal respiratory pathogens and rapid diagnosis of novel emerging avian influenza viruses is vital for effective global influenza surveillance. We developed an oligonucleotide microarray-based method for subtyping all avian influenza virus (16 HA and 9 NA subtypes).
In total 25 pairs of primers specific for different subtypes and 1 pair of universal primers were carefully designed based on the genomic sequences of influenza A viruses retrieved from GenBank database. Several multiplex RT-PCR methods were then developed, and the target cDNAs of 25 subtype viruses were amplified by RT-PCR or overlapping PCR for evaluating the microarray. Further 52 oligonucleotide probes specific for all 25 subtype viruses were designed according to published gene sequences of avian influenza viruses in amplified target cDNAs domains, and a microarray for subtyping influenza A virus was developed. Then its specificity and sensitivity were validated by using different subtype strains and 2653 samples from 49 different areas.
The results showed that all the subtypes of influenza virus could be identified simultaneously on this microarray with high sensitivity, which could reach to 2.47 pfu/mL virus or 2.5 ng target DNA. Furthermore, there was no cross reaction with other avian respiratory virus.
An oligonucleotide microarray-based strategy for detection of avian influenza viruses has been developed. Such a diagnostic microarray will be useful in discovering and identifying all subtypes of avian influenza virus.
禽流感病毒是重要的人类和动物呼吸道病原体,快速诊断新型禽流感病毒对于全球有效的流感监测至关重要。我们开发了一种基于寡核苷酸微阵列的方法,用于对所有禽流感病毒(16种血凝素亚型和9种神经氨酸酶亚型)进行亚型鉴定。
根据从GenBank数据库检索到的甲型流感病毒基因组序列,精心设计了总共25对针对不同亚型的引物和1对通用引物。然后开发了几种多重逆转录聚合酶链反应(RT-PCR)方法,通过RT-PCR或重叠PCR扩增25种亚型病毒的目标互补DNA(cDNA),以评估微阵列。根据扩增的目标cDNA区域中已发表的禽流感病毒基因序列,进一步设计了针对所有25种亚型病毒的52个寡核苷酸探针,并开发了一种用于甲型流感病毒亚型鉴定的微阵列。然后使用不同亚型毒株和来自49个不同地区的2653份样本对其特异性和敏感性进行验证。
结果表明,利用该微阵列能够同时高灵敏度地鉴定出所有流感病毒亚型,灵敏度可达2.47个空斑形成单位/毫升病毒或2.5纳克目标DNA。此外,与其他禽呼吸道病毒无交叉反应。
已开发出一种基于寡核苷酸微阵列的禽流感病毒检测策略。这种诊断性微阵列将有助于发现和鉴定所有亚型的禽流感病毒。