Transformation of Acinetobacter sp BD413 with DNA from commercially available genetically modified potato and papaya

被引:7
作者
Iwaki, M. [1 ]
Arakawa, Y. [1 ]
机构
[1] Natl Inst Infect Dis, Dept Bacterial Pathogenesis & Infect Control, Musashino, Tokyo 2080011, Japan
关键词
antibiotic resistance; genetically modified plant; GMO (genetically modified organisms);
D O I
10.1111/j.1472-765X.2006.01924.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To estimate the likelihood of transfer of kanamycin-resistance gene (nptII) from commercially available genetically modified (GM) plants. Methods and Results: Acinetobacter sp. BD413 carrying a plasmid containing an inactivated nptII gene was treated with DNA derived from GM potato and GM papaya. Kanamycin-resistant transformants were obtained at a frequency of 10-30 mu g(-1) DNA. Calculation of the results suggested that 6-9 x 10(4) molecules of genomic DNA from GM plants were needed to obtain one transformant. However, such transformation events were not detectable in the absence of the plasmid in the host strain. Conclusions: Acinetobacter sp. BD413 was transformed with DNA derived from GM potato and GM papaya, in the presence of an inactivated nptII gene on a plasmid. However, the frequency of such events in the natural environment on wild-type strains, while evidently low, remains unknown. Significance and Impact of the Study: Our results may help to evaluate potential risks associated with the use of antibiotic-resistance determinants as genetic markers in GM plants. Complete risk assessment must consider factors other than transformation frequency alone, including the natural background of antibiotic resistance present in bacterial populations, and the spectrum and clinical use of the antimicrobial agents in question.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 32 条
[1]  
Ausubel F.M., 1992, SHORT PROTOCOLS MOL, V2nd
[2]   SPECIFIC-PURPOSE PLASMID CLONING VECTORS .2. BROAD HOST RANGE, HIGH COPY NUMBER, RSF1010-DERIVED VECTORS, AND A HOST-VECTOR SYSTEM FOR GENE CLONING IN PSEUDOMONAS [J].
BAGDASARIAN, M ;
LURZ, R ;
RUCKERT, B ;
FRANKLIN, FCH ;
BAGDASARIAN, MM ;
FREY, J ;
TIMMIS, KN .
GENE, 1981, 16 (1-3) :237-247
[3]   PLASMID DETECTION AND SIZING IN SINGLE COLONY LYSATES [J].
BARNES, WM .
SCIENCE, 1977, 195 (4276) :393-394
[4]   Facing fear of biotechnology [J].
Beachy, RN .
SCIENCE, 1999, 285 (5426) :335-335
[5]   NUCLEOTIDE-SEQUENCE AND EXACT LOCALIZATION OF THE NEOMYCIN PHOSPHOTRANSFERASE GENE FROM TRANSPOSON TN5 [J].
BECK, E ;
LUDWIG, G ;
AUERSWALD, EA ;
REISS, B ;
SCHALLER, H .
GENE, 1982, 19 (03) :327-336
[6]  
BRYAN G, 2002, APPL POTAT UHD GENET, P143
[7]   The fate of antibiotic resistance marker genes in transgenic plant feed material fed to chickens [J].
Chambers, PA ;
Duggan, PS ;
Heritage, J ;
Forbes, JM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (01) :161-164
[8]   Detection of nptII (kanamycin resistance) genes in genomes of transgenic plants by marker-rescue transformation [J].
de Vries, J ;
Wackernagel, W .
MOLECULAR AND GENERAL GENETICS, 1998, 257 (06) :606-613
[9]  
de Vries J, 2001, FEMS MICROBIOL LETT, V195, P211, DOI 10.1111/j.1574-6968.2001.tb10523.x
[10]   Horizontal gene transfer as a biosafety issue:: A natural phenomenon of public concern [J].
Dröge, M ;
Pühler, A ;
Selbitschka, W .
JOURNAL OF BIOTECHNOLOGY, 1998, 64 (01) :75-90