Abstract
The present emphasis on increased food and fibre production has underscored the need for new methods to control plant diseases and to fertilize crops in ways that are less energy-intensive than those in current practice. Although many approaches to these problems are possible, one area that offers much promise for the future is the study of plant-bacterial interactions. There are several arguments in support of this statement. First, bacteria cause numerous, devastating diseases of plants in the field and of plant products in storage, for which no adequate controls have been devised. Chemical treatments are either too expensive or are ineffective, and breeding for disease resistance is often constrained by the highly variable nature of plant pathogenic bacteria. Thus, alternative means for control must be devised. Second, bacteria take part in associative and symbiotic relationships with plants that are extremely important because they allow better plant growth and endow certain plants with the capacity to fix atmospheric nitrogen. Yet it is clear that the host range of these bacteria and their efficiency under a wide range of environmental conditions are limited, but could be improved substantially if we knew more about the details of their interactions with plants. Thus, this review will attempt to: (a) assess the present status of the field of bacterial plant relationships, with particular emphasis on the nature of the host and parasite/symbiont surface components that come in contact at the initial stages of the interaction, and (b) to point out how this knowledge may lead to new methods for disease control and for increased productivity.
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References
Aronson M, Medalia O, Schori L, Mirelman D, Sharon N, Ofek I (1979) Prevention of colonization of the urinary tract of mice with Escherichia coli by blocking adherence with methyl-D-mannopyranoside. J Infect Dis 139: 329–332
Atkinson MM, Huang JS (1982) Hypersensitive-like reaction in tobacco suspension cultures to Pseudomonas pisi. (Abstr) Phytopathology 72: 354
Atkinson MM, Huang J-S, Van Dyke CG (1981) Adsorption of pseudomonads to tobacco cell walls and its significance to bacterium-host interactions. Physiol Plant Pathol 18: 1–5
Ayers AR, Ayers SB, Goodman RN (1979) Extracellular polysaccharide of Erwinia amylovora: a correlation with virulence. Appl Env Microbiol 38: 659–666
Baker CJ, Sequeira L (1981) Further characterization of the lipopolysaccharide ( LPS) produced by Pseudomonas solanacearum. ( Abstr) Phytopathology 71: 201
Bal AK, Shantharam S, Ratnam S (1978) Ultrastructure of Rhizobium japonicum in relation to its attachment to root hairs. J Bact 133: 1393–1400
Banerjee D, Basu M, Choudhury I, Chatterjee GC (1981) Cell surface carbohydrates of Agrobacterium tumefaciens involved in adherence during crown gall tumor initiation. Biochem Biophys Res Commun 100: 1384–1388
Bauer WD (1981) Infection of legumes by rhizobia. Annu Rev Plant Physiol 32: 407–449
Bauer WD, Bhuvaneswari TV, Mort AJ, Turgeon BG (1979) The initiation of infections in soybean by Rhizobium. 3. R. japonicum polysaccharide pretreatment induces root hair infectibility. Plant Physiol 63 (Suppl): 135
Beachey EH (1981) Bacterial adherence: adhesin-receptor interactions mediating the attachment of bacteria to mucosal surfaces. J Infect Dis 143: 325–345
Bhuvaneswari TV, Bauer WD (1978) Role of lectins in plant-microorganism interactions 3. Influence of rhizosphere-rhizoplane culture conditions on soybean lectin-binding properties of rhizobia. Plant Physiol 62: 71–74
Bhuvaneswari TV, Pueppke SG, Bauer WD (1977) Role of lectins in plant-microorganism interactions. 1. Binding of soybean lectin to rhizobia. Plant Physiol 60: 486–491
Bhuvaneswari TV, Turgeon BG, Bauer WD (1980) Early events in the infection of soybean (iGlycine max Merr.) by Rhizobium japonicum. 1. Localization of infectible root cells. Plant Physiol 66: 1027–1031
Bhuvaneswari TV, Bhagwat A A, Bauer WD (1981) Transient susceptibility of root cells in four common legumes to nodulation by rhizobia. Plant Physiol 68: 1144–1149
Bohlool BB, Schmidt EL (1974) Lectins: a possible basis for specificity in the Rhizobium- legume root nodule symbiosis. Science 185: 269–271
Bohlool BB, Schmidt EL (1976) Immunofluorescent polar tips of Rhizobium japonicum: possible site of attachment or lectin binding. J Bacteriol 125: 1188–1194
Calvert HE, Lalonde M, Bhuvaneswari TV, Bauer WD (1978) Role of lectins in plant- microorganism interactions. 4. Ultrastructural localizations of soybean lectin binding sites on Rhizobium japonicum. Can J Microbiol 24: 785–793
Carlson RW, Sanders RE, Napoli C, Albersheim P (1978) Host-pathogen interactions 13. Purification and partial characterization of Rhizobium lipopolysaccharides. Plant Physiol 62: 912–917
Cason ET, Richardson PE, Essenberg MK, Brinkerhoff LA, Johnson WM, Venere RJ (1978) Ultrastructural cell wall alterations in immune cotton leaves inoculated with Xanthomonas malvacearum. Phytopathology 68: 1015–1021
Chen AP, Philips DA (1976) Attachment of Rhizobium to legume roots as the basis for specific interactions. Physiol Plant 38: 83–88
Chrispeels M (1976) Biosynthesis, intercellular transport and secretion of extracellular macro-molecules. Annu Rev Plant Physiol 27: 19–38
Cook AA (1973) Characterization of hypersensitivity in Capsicum annuum induced by the tomato strain oà Xanthomonas vesicatoria. Phytopathology 63: 915–918
Cook A A, Stall RE (1971) Calcium suppression of electrolyte loss from pepper leaves inoculated with Xanthomonas vesicatoria. Phytopathology 61: 484–487
Cook A A, Stall RE (1977) Influence of watersoaking on development of the hypersensitive response in pepper leaves caused by Xanthomonas vesicatoria. Phytopathology 67: 1101–1103
Crosthwaite LM, Patil SS (1978) Isolation of an endotoxin from Pseudomonas phaseolicola which induces cell collapse in bell pepper. Phytopathol Z 91: 80–90
Daub M, Hagedorn D (1980) Growth kinetics and interactions of Pseudomonas syringae with susceptible and resistant bean cultivars. Phytopathology 70: 429–436
Dazzo FB (1980) Adsorption of microorganisms to roots and other plant surfaces. In: Bitton G, Marshall KC (eds) Adsorption of microorganisms to surfaces. Wiley and Sons, New York, pp 253–316
Dazzo FB, Brill WJ (1979) Bacterial polysaccharide which binds Rhizobium trifolii to clover root hairs. J Bacteriol 137: 1362–1373
Dazzo FB, Hrabak EM (1981) Presence of trifoliin A, a Rhizobium-binding lectin, in clover root exudate. J Supramol Struct Cell Biochem 16: 133–138
Dazzo FB, Hubbell DH (1975) Cross-reactive antigens and lectins as determinants of symbiotic specificity in the Rhizobium-clover association. Appl Microbiol 30: 1017–1033
Dazzo FB, Yanke WE, Brill WJ (1978) Trifoliin - a Rhizobium recognition protein from white clover. Biochim Biophys Acta 539: 276–286
Durbin RD, Klement Z (1977) High-temperature repression of plant hypersensitivity to bacteria: a proposed explanation. In: Kiraly E (ed) Current topics in plant pathology. Akademiai Kiado, Budapest pp 239–242
Duvick J, Sequeira L (1981) Binding of Pseudomonas solanacearum to tobacco and potato suspension culture cells ( Abstr ). Phytopathology 71: 872
Duvick J, Sequeira L, Graham TL (1979) Binding of Pseudomonas solanacearum surface polysaccharides to plant lectins in vitro. (Abstr) Plant Physiol 63: 134
Dye WW (1958) Host specificity in Xanthomonas. Nature 182: 1813–1814
El-Banoby FE, Rudolph K (1979) A polysaccharide from liquid cultures of Pseudomonas phaseolicola which specifically induces water soaking in bean leaves (Phaseolus vulgaris L.) Phytopathol Z 95: 38–50
Esquerre-Tugaye M-T, Lamport DTA (1979) Cell surfaces of plant-microorganism interactions. I. A structural investigation of cell wall hydroxyproline-rich glycoproteins which accumulate in fungus-infected plants. Plant Physiol 64: 314–319
Fett WF, Sequeira L (1980) A new bacterial agglutinin from soybean. II. Evidence against a role in determining pathogen specificity. Plant Physiol 66: 853–858
Gade W, Jack MA, Dahl JB, Schmidt EL, Wold F (1981) The isolation and characterization of a root lectin from soybean [Glycine max ( L.) cultivar Chippewa]. J Biol Chem 256: 12905–12910
Giddix LR, Lukezic FL, Pell EJ (1981) Effect of light on bacteria-induced hypersensitivity in soybean. Phytopathology 71: 111–115
Goodman RN (1968) The hypersensitive reaction in tobacco: a reflection of changes in host permeability. Phytopathology 58: 872–873
Goodman RN, Plurad SR (1971) Ultrastructural changes in tobacco undergoing the hypersensitive reaction caused by plant pathogenic bacteria. Physiol Plant Pathol 1: 11–16
Goodman RN, Huang PY, White J A (1976) Ultrastructural evidence for immobilization of an incompatible bacterium, Pseudomonas pisi, in tobacco leaf tissue. Phytopathology 66: 754–764
Graham TL (1981) Recognition in the RhizobiumAzgume symbiosis. Int Rev Cytol (Suppl) 13: 127–148
Graham TL, Sequeira L, Huang TR (1977) Bacterial lipopolysaccharides as inducers of disease resistance in tobacco. Appl Environ Microbiol 34: 424–432
Gulyas A, Barnes B, Klement Z, Farkas GL (1979) Effect of plasmolytica on the hypersensitive reaction induced by bacteria in tobacco: a comparison with the virus-induced hypersensitive reaction. Phytopathology 69: 121–124
Gurlitz RHG, Matthysee AG (1982) Receptors for Agrobacterium tumefaciens on the surface of carrot tissue culture cells. Proc Ann Meeting Am Soc Microbiol p 22
Hahn MG, Darvill AG, Albersheim P (1981) Host-pathogen interactions XIX. The endogenous elicitor, a fragment of a plant cell wall polysaccharide that elicits phytoalexin accumulation in soybeans. Plant Physiol 68: 1161–1169
Hendrick CA, Sequeira L (1981) Lipopolysaccharide-defective mutants of Pseudomonas solanacearum. (Abstr) Phytopathology 71: 880
Heslop-Harrison J (1978) Cellular recognition systems in plants. Arnold, London
Hildebrand DC, Alosi MC, Schroth MN (1980) Physical entrapment of Pseudomonads in bean leaves by films formed in air-water interfaces. Phytopathology 70: 98–109
Hrabak E, Urbano MR, Dazzo FB (1981) Growth-phase-dependent immunodetermin- ants of Rhizobium trifolii lipopolysaccharide which bind trifoliin A, a white clover lectin. J Bacteriol 148: 697–711
Huang JS, Van Dyke CG (1978) Interaction of tobacco callus tissue with Pseudomonas tabaci, P. pisi, and P. fluorescens. Physiol Plant Path 13: 65–72
Kato G, Maruyama Y, Nakamura M (1979) Role of lectins and lipopolysaccharides in the recognition process of specific legum-Rhizobium symbiosis. Agric Biol Chem 43: 1085–1092
Kato G, Maruyama Y, Nakamura M (1981) Involvement of lectins in Rhizobium-pea recognition. Plant Cell Physiol 22: 759–771
Keen NT, Ersek T, Long M, Bruegger B, Holliday M (1981) Inhibition of the hypersensitive reaction of soybean leaves to incompatible Pseudomonas spp. by blasticidin S, streptomycin or elevated temperature. Physiol Plant Pathol 18: 325–337
Klement Z (1963) Method for the rapid detection of the pathogenicity of phytopathogenic Pseudomonads. Nature 199: 299–300
Klement Z, Goodman RN (1968) The hypersensitive reaction to infection by bacterial plant pathogens. Ann Rev Phytopathol 5: 17–44
Lamport DTA (1980) Structure and function of plant glycoproteins. In: Preiss J (ed) Biochemistry of plants. Vol 3. Academic Press, London New York, pp 501–542
Law I J, Strijdom BW (1977) Some observations on plant lectins and Rhizobium specificity. Soil Biol Biochem 9: 79–84
Law I J, Yamamoto Y, Mort AJ, Bauer WD (1982) Nodulation of soybean by Rhizobium japonicum mutants with altered capsule synthesis. Planta 154: 100–109
Leach J (1981) Localization, characterization, and quantification of a bacterial agglutinin from potatoes. Ph D Thesis, Univ Wisconsin, Madison
Lippincott BB, Lippincott J A (1969) Bacterial attachment to a specific wound site as an essential stage in tumor initiation by Agrobacterium tumefaciens. J Bacterial 97: 620–628
Lippincott JA, Lippincott BB (1978) Cell walls of crown-gall tumors and embryonic plant tissues lack Agrobacterium adherence sites. Science 199: 1075–1077
Lippincott J A, Lippincott BB (1980) Microbial adherence in plants. In: Beachey EH (ed) Bacterial adherence. Chapman and Hall, London, pp 377–397
Lozano JC, Sequeira L (1970) Differentiation of races of Pseudomonas solanacearum by a leaf infiltration technique. Phytopathology 60: 833–838
Lyon F, Wood RKS (1976) The hypersensitive reaction and other responses of bean leaves to bacteria. Ann Bot 40: 489 - 491
Maier R, Brill WJ (1978) Involvement of Rhizobium japonicum O antigen in soybean nodulation. J Bacteriol 133: 1295–1299
Marshall K, Cruikshank R, Bushby H (1975) The orientation of certain root-nodule bacteria at interfaces including legume-root hair surfaces. J Gen Microbiol 91: 198–200
Matthysse AG, Lamb PW (1982) The role of bacterial cellulose fibrils in the interaction of Agrobacterium tumefaciens with plant host cells. Ann Meet Am Soc Microbiol, p22
Matthysse AG, Wyman PM, Holmes KV (1978) Plasmid-dependent attachment of Agrobacterium tumefaciens to plant tissue culture cells. Infect Immun 22: 516–522
Matthysse AG, Holmes KV, Gurlitz RHG (1982) Binding of Agrobacterium tumefaciens to carrot protoplasts. Physiol Plant Pathol 20: 27–33
Meadows ME, Stall RE (1981) Different induction periods for hypersensitivity in pepper to Xanthomonas vesicatoria determined with antimicrobial agents. Phytopathology 71: 1024–1027
Mort AJ, Bauer WD (1980) Composition of the capsular and extracellular polysaccharides of Rhizobium japonicum. Changes with culture age and correlations with binding of soybean seed lectin to the bacteria. Plant Physiol 66: 158–163
Mort AJ, Bauer WD (1982) Application of two new methods for cleavage of polysaccharides into specific oligosaccharide fragments. Structure of the capsular and extracellular polysaccharides of Rhizobium japonicum that bind soybean lectin. J Biol Chem 257: 1870–1875
Napoli C, Dazzo FB, Hubbell D (1975) Production of cellulose microfibrils by Rhizobium. Appl Microbiol 30: 123–132
Nemeth J, Klement Z, Farkas GL (1969) An enzymological study of the hypersensitive reaction induced by Pseudomonas syringae in tobacco leaf tissues. Phytopathol Z 65: 267–278
Nester EW, Kosuge T (1981) Plasmids specifying plant hyperplasias. Ann Rev Microbiol 35: 531–565
Nikaido H, Nakae T (1979) The outer membrane of Gram-negative bacteria. Advances in Microbial Physiology. Vol 20. Academic Press, London New York
Ohyama K, Pelcher LE, Schaeffer A (1979) In vitro binding of Agrobacterium tumefaciens to plant cells from suspension culture. Plant Physiol 63: 382–387
Planqué K, Kijne JW (1977) Binding of pea lectins to a glycan type polysaccharide in the cell walls of Rhizobium leguminosarum. FEBS Lett 73: 64–66
Pueppke SG, Benny UK (1981) Induction of tumors on Solanum tuberosum L. by Agro- bacterium: quantitative analysis, inhibition by carbohydrates, and virulence of selected strains. Physiol Plant Pathol 18: 169–179
Pueppke SG, Bauer WD, Keegstra K, Ferguson AL (1978) Role of lectins in plant microorganism interactions. II. Distribution of soybean lectin in tissues of Glycine max ( L.) Merr. Plant Physiol 61: 779–784
Pueppke SG, Freund TG, Schultz BC, Friedman HP (1980) Interaction of lectins from soybeans and peanut with rhizobia that nodulate soybean, peanut, or both plants. Can J Microbiol 26: 1489–1497
Robertsen BK, Aman P, Darvill AG, McNeil M, Albersheim P (1981) Host-symbiont interactions. V. The structure of acidic extracellular polysaccharides secreted by Rhizobium leguminosarum and Rhizobium trifolii. Plant Physiol 67: 389–400
Rogler CE (1981) Strain-dependent temperature-sensitive phase in crown gall tumorigenesis. Plant Physiol 68: 5–10
Romeiro R, Karr A, Goodman R (1981) Isolation of a factor from apple that agglutinates Erwinia amylovora. Plant Physiol 68: 772–777
Russa R, Urbanik T, Kowalczuk E, Lorkiewicz Z (1982) Correlation between the occurrence of plasmid pUCS202 and lipopolysaccharide alterations in Rhizobium. FEMS Microbiol Lett 13: 161–165
Sanders R, Raleigh E, Signer E (1981) Lack of correlation between extracellular polysaccharide and nodulation ability in Rhizobium. Nature 292: 148–149
Sasser M, Andrews AK, Doganay ZV (1974) Inhibition of photosynthesis diminishes antibacterial action of pepper plants. Phytopathology 64: 770–772
Shell J (1982) The Ti-plasmids of Agrobacterium tumefaciens In: Parthier B, Boulter D (eds) Encyclopedia of plant physiology, Vol 14 B, Berlin Heidelberg New York, Springer pp 455–474
Sequeira L (1976) Induction and suppression of the hypersensitive reaction induced by phytopathogenic bacteria: specific and nonspecific components. In: Wood RKS, Graniti A (eds) Specificity in Plant Diseases Vol 10, NATO ASI Ser. Plenum, New York London, pp 289–306
Sequeira L (1979) Bacterial hypersensitivity. In: Durbin RD (ed) Nicotiana: procedures for experimental use. USDA Tech Bull 1586, pp 111–120
Sequeira L, Graham TL (1977) Agglutination of avirulent strains of Pseudomonas solanacearum by potato lectin. Physiol Plant Pathol 11: 43–54
Sequeira L, Gaard G, de Zoeten GA (1977) Attachment of bacteria to host cell walls: its relation to mechanisms of induced resistance. Physiol Plant Pathol 10: 43–50
Shantharam S, Wong PP (1982) Recognition of leguminous hosts by a promiscuous Rhizobium strain. Appl Environ Microbiol 43: 677–685
Sing VO, Schroth MN (1977) Bacteria-plant cell surface interactions: active immobilization of saprophytic bacteria in plant leaves. Science 197: 759–761
Smith MA, Kennedy BW (1970) Effect of light on reactions of soybean to Pseudomonas glycinea. Phytopathology 60: 723–725
Stacey T, Paau AS, Brill WJ (1980) Host recognition in the Rhizobium-soybean symbiosis. Plant Physiol 66: 609–614
Stall RE, Cook A A (1979) Evidence that bacterial contact with the plant cell is necessary for the hypersensitive reaction but not the susceptible reaction. Physiol Plant Pathol 14: 77–84
Stemmer W, Sequeira L (1981) Pili of plant pathogenic bacteria ( Abstr ). Phytopathology 71: 906
Stuart DA, Varner JE (1980) Purification and characterization of a salt-extractable hy droxyproline-rich glycoprotein from aerated carrot discs. Plant Physiol 66: 787–792
Su LC, Pueppke SG, Friedman HP (1980) Lectins and the soybean-Rhizobium symbiosis. I. Immunological investigation of soybean lines, the seeds of which have been reported to lack the 120,000 dalton soybean lectin. Biochim Biophys Acta 629: 292–304
Siile S, Klement Z (1971) Effect of high temperature and the age of bacteria on the hypersensitive reaction of tobacco. Acta Phytopathol Ac Sc Hungarica 6: 119–122
Turner JG, Novacky A (1974) The quantitative relation between plant and bacterial cells involved in the hypersensitive reaction. Phytopathology 64: 885–890
Whatley MH, Sequeira L (1981) Bacterial attachment to plant cell walls. In: Loewus F, Ryan C (eds) Recent advances in phytochemistry. Vol 5. Plenum Press, New York London, pp 213–240
Whatley MH, Bodwin JS, Lippincott BV, Lippincott J A (1976) Role for Agrobacterium cell envelope lipopolysaccharide in infection site attachment. Infect Immun 13: 1080–1083
Whatley MH, Margot JB, Schell J, Lippincott BB, Lippincott J A (1978) Plasmid and chromosomal determination of Agrobacterium adherence specificity. J Gen Microbiol 107: 395–398
Whatley MH, Hunter N, Cantrell MA, Hendrick CA, Keegstra K, Sequeira L (1980) Lipopolysaccharide composition of the wilt pathogen, Pseudomonas solanacearum: correlation with the hypersensitive response in tobacco. Plant Physiol 65: 557–559
Wilkinson SG (1977) Composition and structure of bacterial lipopolysaccharides. In: Sutherland I (ed) Surface carbohydrates of the prokaryotic cell I. Academic Press, London New York
Wolpert JS, Albersheim P (1976) Host-symbiont interactions. I. The lectins of legumes interact with the O-antigen containing lipopolysaccharides of their symbiont rhizobia. Biochem Biophys Res Commun 70: 729–737
Wong PP (1980) Interactions between rhizobia and lectins of lentil, pea, broad bean, and jackbean. Plant Physiol 65: 1049–1052
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Sequeira, L. (1984). Plant-Bacterial Interactions. In: Linskens, H.F., Heslop-Harrison, J. (eds) Cellular Interactions. Encyclopedia of Plant Physiology, vol 17. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69299-4_10
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