Literature DB >> 16535005

Early Interactions of Rhizobium leguminosarum bv. phaseoli and Bean Roots: Specificity in the Process of Adsorption and Its Requirement of Ca(sup2+) and Mg(sup2+) Ions.

A R Lodeiro, A Lagares, E N Martinez, G Favelukes.   

Abstract

Roots of Phaseolus vulgaris L. were incubated with dilute suspensions (1 x 10(sup3) to 3 x 10(sup3) bacteria ml(sup-1)) of an antibiotic-resistant indicator strain of Rhizobium leguminosarum bv. phaseoli in mineral medium and washed four times by a standardized procedure prior to quantitation of adsorption (G. Caetano-Anolles and G. Favelukes, Appl. Environ. Microbiol. 52:371-376, 1986). The population of rhizobia remaining adsorbed on roots after washing was homogeneous, as indicated by the first-order course of its desorption by hydrodynamic shear. Rhizobia were maximally active for adsorption in the early stationary phase of growth. The process leading to adsorption was rapid, without an initial lag, and slowed down after 1 h. Adsorption of the indicator strain at 10(sup3) bacteria ml(sup-1) was inhibited to different extents in the presence of 10(sup3) to 10(sup8) antibiotic-sensitive competitor rhizobia ml(sup-1). After a steep rise above 10(sup4) bacteria ml(sup-1), inhibition by heterologous competitors in the concentration range of 10(sup5) to 10(sup7) bacteria ml(sup-1) was markedly less than by homologous strains, while at 10(sup8) bacteria ml(sup-1) it approached the high level of inhibition by the latter. At 10(sup7) bacteria ml(sup-1), all of the heterologous strains tested were consistently less inhibitory than homologous competitors (P < 0.001). These differences in competitive behavior indicate that in the process of adsorption of R. leguminosarum bv. phaseoli to its host bean roots, different modes of adsorption occur and that some of these modes are specific for the microsymbiont (as previously reported for the alfalfa system [G. Caetano-Anolles and G. Favelukes, Appl. Environ. Microbiol. 52:377-381, 1986]). Moreover, whereas the nonspecific process occurred either in the absence or in the presence of Ca(sup2+) and Mg(sup2+) ions, expression of specificity was totally dependent on the presence of those cations. R. leguminosarum bv. phaseoli bacteria adsorbed in the presence of Ca(sup2+) and Mg(sup2+) were more resistant to desorption by shear forces than were rhizobia adsorbed in their absence. These results indicate that (i) symbiotic specificity in the P. vulgaris-R. leguminosarum bv. phaseoli system is expressed already during the early process of rhizobial adsorption to roots, (ii) Ca(sup2+) and Mg(sup2+) ions are required by R. leguminosarum bv. phaseoli for that specificity, and (iii) those cations cause tighter binding of rhizobia to roots.

Entities:  

Year:  1995        PMID: 16535005      PMCID: PMC1388423          DOI: 10.1128/aem.61.4.1571-1579.1995

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  22 in total

Review 1.  Signaling and host range variation in nodulation.

Authors:  J Dénarié; F Debellé; C Rosenberg
Journal:  Annu Rev Microbiol       Date:  1992       Impact factor: 15.500

2.  The infection of clover root hairs by nodule bacteria studied by a simple glass slide technique.

Authors:  G FAHRAEUS
Journal:  J Gen Microbiol       Date:  1957-04

3.  Association of Rhizobium Strains with Roots of Trifolium repens.

Authors:  J Badenoch-Jones; D J Flanders; B G Rolfe
Journal:  Appl Environ Microbiol       Date:  1985-06       Impact factor: 4.792

4.  Host-Symbiont Specificity Expressed during Early Adsorption of Rhizobium meliloti to the Root Surface of Alfalfa.

Authors:  G Caetano Anollés; G Favelukes
Journal:  Appl Environ Microbiol       Date:  1986-08       Impact factor: 4.792

5.  Quantitation of adsorption of rhizobia in low numbers to small legume roots.

Authors:  G Caetano Anollés; G Favelukes
Journal:  Appl Environ Microbiol       Date:  1986-08       Impact factor: 4.792

Review 6.  Prokaryotic plant parasites.

Authors:  S R Long; B J Staskawicz
Journal:  Cell       Date:  1993-06-04       Impact factor: 41.582

7.  Rhizobium tropici, a novel species nodulating Phaseolus vulgaris L. beans and Leucaena sp. trees.

Authors:  E Martínez-Romero; L Segovia; F M Mercante; A A Franco; P Graham; M A Pardo
Journal:  Int J Syst Bacteriol       Date:  1991-07

8.  Host recognition in the Rhizobium-soybean symbiosis.

Authors:  G Stacey; A S Paau; W J Brill
Journal:  Plant Physiol       Date:  1980-10       Impact factor: 8.340

9.  Reclassification of American Rhizobium leguminosarum biovar phaseoli type I strains as Rhizobium etli sp. nov.

Authors:  L Segovia; J P Young; E Martínez-Romero
Journal:  Int J Syst Bacteriol       Date:  1993-04

10.  Cross-reactive antigens and lectin as determinants of symbiotic specificity in the Rhizobium-clover association.

Authors:  F B Dazzo; D H Hubbell
Journal:  Appl Microbiol       Date:  1975-12
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  3 in total

1.  Surface Properties and Motility of Rhizobium and Azospirillum in Relation to Plant Root Attachment

Authors: 
Journal:  Microb Ecol       Date:  1996-07       Impact factor: 4.552

2.  Influence of Bovine Slurry Deposition on the Structure of Nodulating Rhizobium leguminosarum bv. viciae Soil Populations in a Natural Habitat.

Authors:  G Labes; A Ulrich; P Lentzsch
Journal:  Appl Environ Microbiol       Date:  1996-05       Impact factor: 4.792

3.  Soybean Lectin Enhances Biofilm Formation by Bradyrhizobium japonicum in the Absence of Plants.

Authors:  Julieta Pérez-Giménez; Elías J Mongiardini; M Julia Althabegoiti; Julieta Covelli; J Ignacio Quelas; Silvina L López-García; Aníbal R Lodeiro
Journal:  Int J Microbiol       Date:  2009-05-26
  3 in total

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