Charity Julia A, Klimaszewska Krystyna
Cellwall Biotechnology Centre, Scion Group (formerly Forest Research), Private Bag 3020, Rotorua, New Zealand.
Environ Biosafety Res. 2005 Jul-Sep;4(3):167-77. doi: 10.1051/ebr:2006001.
Previous studies have shown that the widely used plant transformation vector Agrobacterium tumefaciens can persist in genetically engineered plants in vitro and in transgenic greenhouse-grown plants, despite the use of counter-selective antibiotics. However, little is known regarding Agrobacterium persistence in tree species. To understand the kinetics of A. tumefaciens decline and persistence in transformation experiments, we assayed for the presence of A. tumefaciens in spruce and pine embryogenic tissue for up to 10 weeks post-transformation. The A. tumefaciens populations declined rapidly in the first five days post-cocultivation but generally declined more slowly in pine, relative to spruce. No bacteria were detected in spruce embryogenic tissue beyond four weeks after cocultivation, however in pine there were -100 colony forming units per g tissue at 10 weeks post-cocultivation. We present evidence that the detection limit for PCR using virD2 primers to detect A. tumefaciens in a background of pine needle DNA was approximately 10(9)-10(10) A. tumefaciens cells per g of tissue. We also assayed for A. tumefaciens in transgenic pine and spruce embryogenic tissue and from needles, branches, stems and roots of transformed plants, up to four years post-inoculation. Occasionally A. tumefaciens was detected in embryogenic tissue up to 12 months post-inoculation. A. tumefaciens was never detected in cultured embryogenic tissue more than twelve months after inoculation, nor in developing somatic embryos or germinating plantlets, nor any of the parts of greenhouse-grown plants. From these data we conclude that if A. tumefaciens persists in transgenic conifers, it does so beneath our ability to detect it.
先前的研究表明,尽管使用了反选择抗生素,但广泛使用的植物转化载体根癌农杆菌能够在体外的基因工程植物以及转基因温室种植植物中存活。然而,关于根癌农杆菌在树种中的存活情况却知之甚少。为了了解根癌农杆菌在转化实验中的减少和存活动力学,我们在转化后长达10周的时间里,检测了云杉和松树胚性组织中根癌农杆菌的存在情况。共培养后的头五天,根癌农杆菌数量迅速下降,但相对于云杉,松树中的根癌农杆菌数量通常下降得更慢。共培养四周后,在云杉胚性组织中未检测到细菌,但在共培养10周后,松树每克组织中有-100个菌落形成单位。我们提供的证据表明,在松针DNA背景下,使用virD2引物通过PCR检测根癌农杆菌的检测限约为每克组织10(9)-10(10)个根癌农杆菌细胞。我们还检测了转基因松树和云杉胚性组织以及接种后长达四年的转化植物的针叶、枝条、茎和根中的根癌农杆菌。接种后长达12个月,偶尔在胚性组织中检测到根癌农杆菌。接种超过12个月后,在培养的胚性组织、发育中的体细胞胚或发芽的幼苗中从未检测到根癌农杆菌,在温室种植植物的任何部位也未检测到。从这些数据我们得出结论,如果根癌农杆菌在转基因针叶树中存活,那么其存活水平低于我们的检测能力。