Abstract:Gene chip is a new biological technology based on the principle of nucleic acid hybridization, which shows important applications in the field of life science research. A method of simultaneously detecting Infectious laryngotracheitis virus (ILTV), Newcastle disease virus(NDV) and Infectious bronchitis virus (IBV) using DNA microarray and asymmetric PCR methods was developed. Primers based on specific conservative DNA fragments of the recombinant plasmid containing thymidine kinase (TK) and glycoproteins B (gB) genes of ILTV, fusion (F) and haemagglutinin-neuraminidase (HN) genes of NDV, membrane (M) and nucleocapsid (N) gene of IBV were designed and probe genes were amplified. Probes were purified using ethanol precipitation method and spotted on the amido-coating-glass slides to form a DNA microarray. Target genes were synthesized using fluorescent cy3-labeled primer by asymmetric PCR method and hybridized to microarray. Result of asymmetric PCR showed that single stranded of ILTV-TK, NDV-HN and IBV-N increased the most of all when concentration ratio of the restrictive and non-restrictive primer at 1∶10, and single product of ILTV-gB, NDV-F and IBV-M increased the most of all when the concentration ratio at 1∶20. The hybridization results showed the microarrays specific to the 3 poultry viruses could specifically hybridize with the corresponding sample, while any fluorescent signals could not be seen in negative controls. The sensitivity test showed that the concentration of DNA with 1.8×104 copies was still positive. Compared with the previous chip, hybridization efficiency and the hybridization signals increased significantly. Detection of 12 clinical samples, the results showed that the detection rate of DNA microarray and PCR method was consistent. This study showed that the developed microarray can simultaneously diagnosis 3 poultry disease of NDV-IBV-ILTV with fast, accurately and high-throughput, which can be applied to the detection a variety disease virus of chicken at intensive farming.
曹三杰, 文心田, 肖驰,等.2007.应用基因芯片技术检测禽4种主要疫病的研究 Ⅱ.检测基因芯片的构建及制备[J].中国兽医学报,27(3): 311-314.(Cao S J,Wen X T,Xiao C et al.2007. Detection of four avian infectious diseases using microarray technologyⅡ. Construction and preparation of detection microarray [J]. Chinese Journal of Veterinary Science 27(3): 311-314.)曹三杰, 文心田, 肖驰,等.2006.几种主要禽疫病诊断基因芯片的制备及初步应用[J]. 畜牧兽医学报,37(4):356-360.( Cao S J,Wen X T,Xiao C et al.2006. Preparation and Preliminary Application of Diagnostic GeneChip of Several Avian Infectious Diseases[J]. Acta Veterinaria et Zootechinca Sinica, 37(4):356-360.)陶启蒙, 王秀荣, 武嘉男,等.2009.不对称 RT-PCR 结合芯片技术鉴别 4 种禽病的初步研究 [J].中国预防兽医学报,30(12):954-958.(Tao Q M, Wang X R,Wu J N,et al.2009.Development of DNA microarray for detecting four poultry disease with dissymmetry PCR method[J]. ?Chinese Journal of Preventive Veterinary Medicine, 30(12): 954-958.?)Citartan1, M., Tang1, T.-H., Tan, S.-C, et al. 2012. Asymmetric PCR for good quality ssDNA generation towards DNA aptamer production [J]. Sonklanakarin Journal of Science and Technology , 34(2): 125.Ho, H.A, Doré, K, Boissinot, M, et al. 2005. Direct molecular detection of nucleic acids by fluorescence signal amplification [J]. Journal of the American Chemical Society, 127(36): 12673-12676.Hu, B., Huang, Y, He, Y, et al. 2010. Avian influenza virus and Newcastle disease virus (NDV) surveillance in commercial breeding farm in China and the characterization of Class I NDV isolates [J]. Veterinary Microbiology, 144(12): 82-86.Kaltenboeck, B, Spatafora, J, Zhang, X et al.1992. Efficient production of single-stranded DNA as long as 2 kb for sequencing of PCR-amplified DNA [J]. BioTechniques, 12(2): 16468-16471.Kanabagatte Basavarajappa, M, Kumar, S, Khattar, S.K, et al. 2014. A recombinant Newcastle disease virus (NDV) expressing infectious laryngotracheitis virus (ILTV) surface glycoprotein D protects against highly virulent ILTV and NDV challenges in chickens [J]. Vaccine, 32(28): 3555-3563.Luo, Y, Du, J, Zhan, Z, et al. 2013. A diagnostic gene chip for hereditary spastic paraplegias [J]. Brain Research Bulletin, 97: 112-118.Oldoni, I, Rodríguez-Avila, A, Riblet, S, et al. 2008. Characterization of infectious laryngotracheitis virus (ILTV) isolates from commercial poultry by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) [J]. Avian diseases, 52(1): 59-63.Schena, M, Shalon, D, Davis, R.W, et al.1995. Quantitative monitoring of gene expression patterns with a complementary DNA microarray [J]. Science, 270(5235): 467-470.Thissen, J.B, McLoughlin, K, Gardner, S, et al. 2014. Analysis of sensitivity and rapid hybridization of a multiplexed Microbial Detection Microarray [J]. Journal of Virological Methods, 201(0): 73-78.Tian, L, Wang, H.-n, Lu, D, et al.2008. The immunoreactivity of a chimeric multi-epitope DNA vaccine against IBV in chickens [J]. Biochemical and biophysical research communications, 377(1): 221-225.Townsend, M.B, Dawson, E.D, Mehlmann, M, et al. 2006. Experimental evaluation of the FluChip diagnostic microarray for influenza virus surveillance [J]. Journal of clinical microbiology, 44(8): 2863-2871.Wang, D, Coscoy, L, Zylberberg, M, et al.2002. Microarray-based detection and genotyping of viral pathogens [J]. Proceedings of the National Academy of Sciences of the United States of America, 99(24): 15687-15692.Wang, Z, Orlandi, P.A, Stenger, D.A, 2005. Simultaneous detection of four human pathogenic microsporidian species from clinical samples by oligonucleotide microarray[J]. Journal of clinical microbiology, 43(8): 4121-4128.Xie, Z, Luo, S, Xie, L, et al. 2014. Simultaneous typing of nine avian respiratory pathogens using a novel GeXP analyzer-based multiplex PCR assay [J]. Journal of Virological Methods, 207(0): 188-195.