Chromosomal Locus That Affects Pathogenicity of Rhodococcus fascians

ABSTRACT The gram-positive plant pathogen Rhodococcus fascians provokes leafy gall formation on a wide range of plants through secretion of signal molecules that interfere with the hormone balance of the host. Crucial virulence genes are located on a linear plasmid, and their expression is tightly controlled. A mutant with a mutation in a chromosomal locus that affected virulence was isolated. The mutation was located in gene vicA, which encodes a malate synthase and is functional in the glyoxylate shunt of the Krebs cycle. VicA is required for efficient in planta growth in symptomatic, but not in normal, plant tissue, indicating that the metabolic requirement of the bacteria or the nutritional environment in plants or both change during the interaction. We propose that induced hyperplasia on plants represents specific niches for the causative organisms as a result of physiological alterations in the symptomatic tissue. Hence, such interaction could be referred to as metabolic habitat modification.

[1]  M. Van Montagu,et al.  The att locus of Rhodococcus fascians strain D188 is essential for full virulence on tobacco through the production of an autoregulatory compound , 2001, Molecular microbiology.

[2]  T. Ritsema,et al.  The plant pathogen Rhodococcus fascians colonizes the exterior and interior of the aerial parts of plants. , 2001, Molecular plant-microbe interactions : MPMI.

[3]  D. Inzé,et al.  The fas locus of the phytopathogen Rhodococcus fascians affects mitosis of tobacco BY‐2 cells , 2001, FEBS letters.

[4]  M. Van Montagu,et al.  Leafy Gall Formation Is Controlled byfasR, an AraC-Type Regulatory Gene inRhodococcus fascians , 2000, Journal of bacteriology.

[5]  James C. Sacchettini,et al.  Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase , 2000, Nature.

[6]  D. Inzé,et al.  The Rhodococcus fascians-plant interaction: morphological traits and biotechnological applications , 2000, Planta.

[7]  David G. Russell,et al.  Characterization of Activity and Expression of Isocitrate Lyase in Mycobacterium avium andMycobacterium tuberculosis , 1999, Journal of bacteriology.

[8]  Y. Dessaux,et al.  The cryptic plasmid of Agrobacterium tumefaciens cointegrates with the Ti plasmid and cooperates for opine degradation , 1998 .

[9]  B. Barrell,et al.  Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.

[10]  D. Emerich,et al.  Isocitrate dehydrogenase and glyoxylate cycle enzyme activities in Bradyrhizobium japonicum under various growth conditions , 1998, Archives of Microbiology.

[11]  R. Huber,et al.  The complete genome of the hyperthermophilic bacterium Aquifex aeolicus , 1998, Nature.

[12]  P. Murphy,et al.  Opines and Opine-Like Molecules Involved in Plant-Rhizobiaceae Interactions , 1998 .

[13]  H. Spaink,et al.  The rhizobiaceae : molecular biology of model plant-associated bacteria , 1998 .

[14]  S. Salzberg,et al.  Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi , 1997, Nature.

[15]  H. Sahm,et al.  Regulation of acetate metabolism in Corynebacterium glutamicum: transcriptional control of the isocitrate lyase and malate synthase genes , 1997, Archives of Microbiology.

[16]  N. W. Davis,et al.  The complete genome sequence of Escherichia coli K-12. , 1997, Science.

[17]  V. Citovsky,et al.  Agrobacterium-plant cell DNA transport: have virulence proteins, will travel. , 1996, The Plant cell.

[18]  H. Kinashi,et al.  A set of ordered cosmids and a detailed genetic and physical map for the 8 Mb Streptomyces coelicolor A3(2) chromosome , 1996, Molecular microbiology.

[19]  L. Valinsky,et al.  The genes involved in cytokinin biosynthesis in Erwinia herbicola pv. gypsophilae: characterization and role in gall formation , 1995, Journal of bacteriology.

[20]  X. Nesme,et al.  Novel Ti plasmids in Agrobacterium strains isolated from fig tree and chrysanthemum tumors and their opinelike molecules. , 1995, Molecular plant-microbe interactions : MPMI.

[21]  H. Sahm,et al.  Malate synthase from Corynebacterium glutamicum: sequence analysis of the gene and biochemical characterization of the enzyme. , 1994, Microbiology.

[22]  F. Barras,et al.  EXTRACELLULAR ENZYMES AND PATHOGENESIS OF SOFT-ROT ERWINIA , 1994 .

[23]  J. Badia,et al.  Molecular characterization of Escherichia coli malate synthase G. Differentiation with the malate synthase A isoenzyme. , 1994, European journal of biochemistry.

[24]  M. Van Montagu,et al.  Cloning and sequence analysis of the gene encoding isocitrate lyase from Rhodococcus fascians. , 1994, Gene.

[25]  M. Van Montagu,et al.  The fas operon of Rhodococcus fascians encodes new genes required for efficient fasciation of host plants , 1994, Journal of bacteriology.

[26]  P. Hooykaas,et al.  The Virulence System of Agrobacterium Tumefaciens , 1994 .

[27]  M. Malumbres,et al.  Codon preference in corynebacteria. , 1993, Gene.

[28]  Y. Dessaux,et al.  Chemistry and biochemistry of opines, chemical mediators of parasitism , 1993 .

[29]  R. Rodicio,et al.  Two structural genes are encoding malate synthase isoenzymes in Saccharomyces cerevisiae , 1993, FEBS letters.

[30]  T. Yamada The role of auxin in plant-disease development. , 1993, Annual review of phytopathology.

[31]  T. Cooper,et al.  Differentially regulated malate synthase genes participate in carbon and nitrogen metabolism of S. cerevisiae. , 1992, Nucleic acids research.

[32]  M. Montagu,et al.  The plasmid‐encoded chloramphenicol‐resistance protein of Rhodococcus fascians is homologous to the transmembrane tetracycline efflux proteins , 1992, Molecular microbiology.

[33]  F Wright,et al.  Codon usage in the G+C-rich Streptomyces genome. , 1992, Gene.

[34]  M. Montagu,et al.  Fasciation induction by the phytopathogen Rhodococcus fascians depends upon a linear plasmid encoding a cytokinin synthase gene. , 1992, The EMBO journal.

[35]  J. Leigh,et al.  Exopolysaccharides in plant-bacterial interactions. , 1992, Annual review of microbiology.

[36]  M. Ueda,et al.  Presence of two transcribed malate synthase genes in an n-alkane-utilizing yeast, Candida tropicalis. , 1991, Journal of biochemistry.

[37]  M. Montagu,et al.  IIIegitimate integration of non‐replicative vectors in the genome of Rhodococcus fascians upon electro‐transformation as an insertional mutagenesis system , 1991, Molecular microbiology.

[38]  A. Hayward Biology and epidemiology of bacterial wilt caused by pseudomonas solanacearum. , 1991, Annual review of phytopathology.

[39]  M. Montagu,et al.  Transformation of Rhodococcus fascians by High-Voltage Electroporation and Development of R. fascians Cloning Vectors , 1990, Applied and environmental microbiology.

[40]  T. McDermott,et al.  Carbon metabolism in Bradyrhizobium japonicum bacteroids , 1989 .

[41]  D. Inzé,et al.  Strong cellular preference in the expression of a housekeeping gene of Arabidopsis thaliana encoding S-adenosylmethionine synthetase. , 1989, The Plant cell.

[42]  M. Van Montagu,et al.  Conjugative transfer of cadmium resistance plasmids in Rhodococcus fascians strains , 1988, Journal of bacteriology.

[43]  D. Lipman,et al.  Improved tools for biological sequence comparison. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[44]  S. Maloy,et al.  Isolation and characterization of Salmonella typhimurium glyoxylate shunt mutants , 1987, Journal of bacteriology.

[45]  Michael J. Davis PLANT-PATHOGENIC CORYNEFORM BACTERIA , 1986 .

[46]  J. Bradbury Guide to plant pathogenic bacteria. , 1986 .

[47]  M. Goodfellow Reclassification of Corynebacterium fascians (Tilford) Dowson in the Genus Rhodococcus, as Rhodococcus fascians comb. nov. , 1984 .

[48]  J. Messing,et al.  Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis. , 1983, Gene.

[49]  J. Lecocq,et al.  Chromogenic identification of genetic regulatory signals in Bacillus subtilis based on expression of a cloned Pseudomonas gene. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[50]  C. C. Smith,et al.  Seed transmission and pathology of Corynebacterium flaccumfaciens in beans (Phaseolus vulgaris). , 1983 .

[51]  S. Maloy,et al.  Genetic regulation of the glyoxylate shunt in Escherichia coli K-12 , 1982, Journal of bacteriology.

[52]  S. Cohen,et al.  Analysis of gene control signals by DNA fusion and cloning in Escherichia coli. , 1980, Journal of molecular biology.

[53]  M. Montagu,et al.  Interactions and DNA transfer between Agrobacterium tumefaciens, the Ti-plasmid and the plant host , 1979, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[54]  H. Kornberg The role and control of the glyoxylate cycle in Escherichia coli. , 1966, The Biochemical journal.

[55]  F. Skoog,et al.  A revised medium for rapid growth and bio assays with tobacco tissue cultures , 1962 .

[56]  B. McFadden,et al.  The determination of glyoxylic acid in biological systems , 1960 .