Aittamaa M, Somervuo P, Pirhonen M, Mattinen L, Nissinen R, Auvinen P, Valkonen J P T
Department of Applied Biology, PO Box 27, FIN-00014 University of Helsinki, Finland.
Mol Plant Pathol. 2008 Sep;9(5):705-17. doi: 10.1111/j.1364-3703.2008.00482.x.
A set of 9676 probes was designed for the most harmful bacterial pathogens of potato and tested in a microarray format. Gene-specific probes could be designed for all genes of Pectobacterium atrosepticum, c. 50% of the genes of Streptomyces scabies and c. 30% of the genes of Clavibacter michiganensis ssp. sepedonicus utilizing the whole-genome sequence information available. For Streptomyces turgidiscabies, 226 probes were designed according to the sequences of a pathogenicity island containing important virulence genes. In addition, probes were designed for the virulence-associated nip (necrosis-inducing protein) genes of P. atrosepticum, P. carotovorum and Dickeya dadantii and for the intergenic spacer (IGS) sequences of the 16S-23S rRNA gene region. Ralstonia solanacearum was not included in the study, because it is a quarantine organism and is not presently found in Finland, but a few probes were also designed for this species. The probes contained on average 40 target-specific nucleotides and were synthesized on the array in situ, organized as eight sub-arrays with an identical set of probes which could be used for hybridization with different samples. All bacteria were readily distinguished using a single channel system for signal detection. Nearly all of the c. 1000 probes designed for C. michiganensis ssp. sepedonicus, c. 50% and 40% of the c. 4000 probes designed for the genes of S. scabies and P. atrosepticum, respectively, and over 100 probes for S. turgidiscabies showed significant signals only with the respective species. P. atrosepticum, P. carotovorum and Dickeya strains were all detected with 110 common probes. By contrast, the strains of these species were found to differ in their signal profiles. Probes targeting the IGS region and nip genes could be used to place strains of Dickeya to two groups, which correlated with differences in virulence. Taken together, the approach of using a custom-designed, genome-wide microarray provided a robust means for distinguishing the bacterial pathogens of potato.
针对马铃薯最具危害性的细菌病原体设计了一组9676个探针,并以微阵列形式进行测试。利用现有的全基因组序列信息,可为黑胫果胶杆菌的所有基因、约50%的疮痂链霉菌基因和约30%的密执安棒杆菌马铃薯环腐亚种基因设计基因特异性探针。对于肿胀链霉菌,根据一个含有重要毒力基因的致病岛序列设计了226个探针。此外,还针对黑胫果胶杆菌、胡萝卜软腐果胶杆菌和达氏果胶杆菌的毒力相关nip(坏死诱导蛋白)基因以及16S - 23S rRNA基因区域的基因间隔序列(IGS)设计了探针。青枯雷尔氏菌未纳入本研究,因为它是一种检疫性生物,目前在芬兰未发现,但也为该物种设计了一些探针。这些探针平均含有40个靶标特异性核苷酸,并在阵列上原位合成,组织成八个子阵列,每个子阵列具有相同的探针集,可用于与不同样本杂交。使用单通道系统进行信号检测可以轻松区分所有细菌。为密执安棒杆菌马铃薯环腐亚种设计的近1000个探针、为疮痂链霉菌基因设计的约4000个探针中的50%和40%以及为肿胀链霉菌设计的100多个探针,分别仅在各自的物种中显示出显著信号。黑胫果胶杆菌、胡萝卜软腐果胶杆菌和果胶杆菌属菌株均用110个通用探针检测到。相比之下,发现这些物种的菌株在信号图谱上存在差异。靶向IGS区域和nip基因的探针可用于将果胶杆菌属菌株分为两组,这与毒力差异相关。总体而言,使用定制设计的全基因组微阵列方法为区分马铃薯细菌病原体提供了一种可靠的手段。