Abstract
Two PCR primer pairs, based on the virD2 and ipt genes, detected a wide variety of pathogenic Agrobacterium strains. The endonuclease domain of VirD2 protein, which cleaves transferred DNA (T-DNA) border sequences, is highly conserved; primer oligonucleotides specific for the endonuclease portion of virD2 detected all pathogenic strains of Agrobacterium tested. PCR primers corresponding to conserved sequences in ipt, the T-DNA-borne cytokinin synthesis gene, detected only Agrobacterium tumefaciens and distinguished it from Agrobacterium rhizogenes. The virD2 and ipt primer pairs did not interfere with each other when included in the same PCR amplification, and this permitted simultaneous detection of both genes in a single reaction. One nonpathogenic Agrobacterium radiobacter strain contained virD2 but not ipt; we speculate that this strain arose from a pathogenic progenitor through a deletion in the T-DNA. The virD2 primer pair appears to be universal for all pathogenic Agrobacterium species; used together, the primer sets reported here should allow unambiguous identification of Ti plasmid DNA in bacteria isolated from soil and plants.
Full Text
The Full Text of this article is available as a PDF (365.0 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Akiyoshi D. E., Klee H., Amasino R. M., Nester E. W., Gordon M. P. T-DNA of Agrobacterium tumefaciens encodes an enzyme of cytokinin biosynthesis. Proc Natl Acad Sci U S A. 1984 Oct;81(19):5994–5998. doi: 10.1073/pnas.81.19.5994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barry G. F., Rogers S. G., Fraley R. T., Brand L. Identification of a cloned cytokinin biosynthetic gene. Proc Natl Acad Sci U S A. 1984 Aug;81(15):4776–4780. doi: 10.1073/pnas.81.15.4776. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bereswill S., Pahl A., Bellemann P., Zeller W., Geider K. Sensitive and species-specific detection of Erwinia amylovora by polymerase chain reaction analysis. Appl Environ Microbiol. 1992 Nov;58(11):3522–3526. doi: 10.1128/aem.58.11.3522-3526.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bouzar H., Moore L. W. Isolation of different agrobacterium biovars from a natural oak savanna and tallgrass prairie. Appl Environ Microbiol. 1987 Apr;53(4):717–721. doi: 10.1128/aem.53.4.717-721.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Buchmann I., Marner F. J., Schröder G., Waffenschmidt S., Schröder J. Tumour genes in plants: T-DNA encoded cytokinin biosynthesis. EMBO J. 1985 Apr;4(4):853–859. doi: 10.1002/j.1460-2075.1985.tb03710.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chilton M. D., Drummond M. H., Merio D. J., Sciaky D., Montoya A. L., Gordon M. P., Nester E. W. Stable incorporation of plasmid DNA into higher plant cells: the molecular basis of crown gall tumorigenesis. Cell. 1977 Jun;11(2):263–271. doi: 10.1016/0092-8674(77)90043-5. [DOI] [PubMed] [Google Scholar]
- Chilton M. D., Saiki R. K., Yadav N., Gordon M. P., Quetier F. T-DNA from Agrobacterium Ti plasmid is in the nuclear DNA fraction of crown gall tumor cells. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4060–4064. doi: 10.1073/pnas.77.7.4060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fortin C., Marquis C., Nester E. W., Dion P. Dynamic structure of Agrobacterium tumefaciens Ti plasmids. J Bacteriol. 1993 Aug;175(15):4790–4799. doi: 10.1128/jb.175.15.4790-4799.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fortin C., Nester E. W., Dion P. Growth inhibition and loss of virulence in cultures of Agrobacterium tumefaciens treated with acetosyringone. J Bacteriol. 1992 Sep;174(17):5676–5685. doi: 10.1128/jb.174.17.5676-5685.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Garfinkel D. J., Simpson R. B., Ream L. W., White F. F., Gordon M. P., Nester E. W. Genetic analysis of crown gall: fine structure map of the T-DNA by site-directed mutagenesis. Cell. 1981 Nov;27(1 Pt 2):143–153. doi: 10.1016/0092-8674(81)90368-8. [DOI] [PubMed] [Google Scholar]
- Hartung J. S., Daniel J. F., Pruvost O. P. Detection of Xanthomonas campestris pv. citri by the polymerase chain reaction method. Appl Environ Microbiol. 1993 Apr;59(4):1143–1148. doi: 10.1128/aem.59.4.1143-1148.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirayama T., Muranaka T., Ohkawa H., Oka A. Organization and characterization of the virCD genes from Agrobacterium rhizogenes. Mol Gen Genet. 1988 Aug;213(2-3):229–237. doi: 10.1007/BF00339586. [DOI] [PubMed] [Google Scholar]
- Huffman G. A., White F. F., Gordon M. P., Nester E. W. Hairy-root-inducing plasmid: physical map and homology to tumor-inducing plasmids. J Bacteriol. 1984 Jan;157(1):269–276. doi: 10.1128/jb.157.1.269-276.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jayaswal R. K., Veluthambi K., Gelvin S. B., Slightom J. L. Double-stranded cleavage of T-DNA and generation of single-stranded T-DNA molecules in Escherichia coli by a virD-encoded border-specific endonuclease from Agrobacterium tumefaciens. J Bacteriol. 1987 Nov;169(11):5035–5045. doi: 10.1128/jb.169.11.5035-5045.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jouanin L. Restriction map of an agropine-type Ri plasmid and its homologies with Ti plasmids. Plasmid. 1984 Sep;12(2):91–102. doi: 10.1016/0147-619x(84)90055-6. [DOI] [PubMed] [Google Scholar]
- Picard C., Ponsonnet C., Paget E., Nesme X., Simonet P. Detection and enumeration of bacteria in soil by direct DNA extraction and polymerase chain reaction. Appl Environ Microbiol. 1992 Sep;58(9):2717–2722. doi: 10.1128/aem.58.9.2717-2722.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Porter S. G., Yanofsky M. F., Nester E. W. Molecular characterization of the virD operon from Agrobacterium tumefaciens. Nucleic Acids Res. 1987 Sep 25;15(18):7503–7517. doi: 10.1093/nar/15.18.7503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Powell G. K., Morris R. O. Nucleotide sequence and expression of a Pseudomonas savastanoi cytokinin biosynthetic gene: homology with Agrobacterium tumefaciens tmr and tzs loci. Nucleic Acids Res. 1986 Mar 25;14(6):2555–2565. doi: 10.1093/nar/14.6.2555. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sawada H., Ieki H., Matsuda I. PCR detection of Ti and Ri plasmids from phytopathogenic Agrobacterium strains. Appl Environ Microbiol. 1995 Feb;61(2):828–831. doi: 10.1128/aem.61.2.828-831.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schmülling T., Schell J., Spena A. Single genes from Agrobacterium rhizogenes influence plant development. EMBO J. 1988 Sep;7(9):2621–2629. doi: 10.1002/j.1460-2075.1988.tb03114.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schröder G., Waffenschmidt S., Weiler E. W., Schröder J. The T-region of Ti plasmids codes for an enzyme synthesizing indole-3-acetic acid. Eur J Biochem. 1984 Jan 16;138(2):387–391. doi: 10.1111/j.1432-1033.1984.tb07927.x. [DOI] [PubMed] [Google Scholar]
- Seal S. E., Jackson L. A., Daniels M. J. Isolation of a Pseudomonas solanacearum-specific DNA probe by subtraction hybridization and construction of species-specific oligonucleotide primers for sensitive detection by the polymerase chain reaction. Appl Environ Microbiol. 1992 Nov;58(11):3751–3758. doi: 10.1128/aem.58.11.3751-3758.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shen W. H., Petit A., Guern J., Tempé J. Hairy roots are more sensitive to auxin than normal roots. Proc Natl Acad Sci U S A. 1988 May;85(10):3417–3421. doi: 10.1073/pnas.85.10.3417. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Slightom J. L., Durand-Tardif M., Jouanin L., Tepfer D. Nucleotide sequence analysis of TL-DNA of Agrobacterium rhizogenes agropine type plasmid. Identification of open reading frames. J Biol Chem. 1986 Jan 5;261(1):108–121. [PubMed] [Google Scholar]
- Spanò L., Mariotti D., Cardarelli M., Branca C., Costantino P. Morphogenesis and Auxin Sensitivity of Transgenic Tobacco with Different Complements of Ri T-DNA. Plant Physiol. 1988 Jun;87(2):479–483. doi: 10.1104/pp.87.2.479. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Spena A., Schmülling T., Koncz C., Schell J. S. Independent and synergistic activity of rol A, B and C loci in stimulating abnormal growth in plants. EMBO J. 1987 Dec 20;6(13):3891–3899. doi: 10.1002/j.1460-2075.1987.tb02729.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steffan R. J., Atlas R. M. Polymerase chain reaction: applications in environmental microbiology. Annu Rev Microbiol. 1991;45:137–161. doi: 10.1146/annurev.mi.45.100191.001033. [DOI] [PubMed] [Google Scholar]
- Thomashow L. S., Reeves S., Thomashow M. F. Crown gall oncogenesis: evidence that a T-DNA gene from the Agrobacterium Ti plasmid pTiA6 encodes an enzyme that catalyzes synthesis of indoleacetic acid. Proc Natl Acad Sci U S A. 1984 Aug;81(16):5071–5075. doi: 10.1073/pnas.81.16.5071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomashow M. F., Hugly S., Buchholz W. G., Thomashow L. S. Molecular basis for the auxin-independent phenotype of crown gall tumor tissues. Science. 1986 Feb 7;231(4738):616–618. doi: 10.1126/science.3511528. [DOI] [PubMed] [Google Scholar]
- Van Larebeke N., Engler G., Holsters M., Van den Elsacker S., Zaenen I., Schilperoort R. A., Schell J. Large plasmid in Agrobacterium tumefaciens essential for crown gall-inducing ability. Nature. 1974 Nov 8;252(5479):169–170. doi: 10.1038/252169a0. [DOI] [PubMed] [Google Scholar]
- Wang K., Herrera-Estrella A., Van Montagu M. Overexpression of virD1 and virD2 genes in Agrobacterium tumefaciens enhances T-complex formation and plant transformation. J Bacteriol. 1990 Aug;172(8):4432–4440. doi: 10.1128/jb.172.8.4432-4440.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson B., Currier T. C., Gordon M. P., Chilton M. D., Nester E. W. Plasmid required for virulence of Agrobacterium tumefaciens. J Bacteriol. 1975 Jul;123(1):255–264. doi: 10.1128/jb.123.1.255-264.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White F. F., Ghidossi G., Gordon M. P., Nester E. W. Tumor induction by Agrobacterium rhizogenes involves the transfer of plasmid DNA to the plant genome. Proc Natl Acad Sci U S A. 1982 May;79(10):3193–3197. doi: 10.1073/pnas.79.10.3193. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White F. F., Nester E. W. Relationship of plasmids responsible for hairy root and crown gall tumorigenicity. J Bacteriol. 1980 Nov;144(2):710–720. doi: 10.1128/jb.144.2.710-720.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White F. F., Taylor B. H., Huffman G. A., Gordon M. P., Nester E. W. Molecular and genetic analysis of the transferred DNA regions of the root-inducing plasmid of Agrobacterium rhizogenes. J Bacteriol. 1985 Oct;164(1):33–44. doi: 10.1128/jb.164.1.33-44.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Winans S. C. Two-way chemical signaling in Agrobacterium-plant interactions. Microbiol Rev. 1992 Mar;56(1):12–31. doi: 10.1128/mr.56.1.12-31.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yanofsky M. F., Porter S. G., Young C., Albright L. M., Gordon M. P., Nester E. W. The virD operon of Agrobacterium tumefaciens encodes a site-specific endonuclease. Cell. 1986 Nov 7;47(3):471–477. doi: 10.1016/0092-8674(86)90604-5. [DOI] [PubMed] [Google Scholar]
