Effects of Nod Factors on Alfalfa Root Hair Ca++ and H+ Currents and on Cytoskeletal Behavior

Author(s):  
Nina S. Allen ◽  
Marty N. Bennett ◽  
Daniel N. Cox ◽  
Alan Shipley ◽  
David W. Ehrhardt ◽  
...  
Keyword(s):  
Science ◽  
1992 ◽  
Vol 256 (5059) ◽  
pp. 998-1000 ◽  
Author(s):  
D. Ehrhardt ◽  
E. Atkinson ◽  
Long

2001 ◽  
Vol 47 (6) ◽  
pp. 475-487
Author(s):  
Pedro F Mateos ◽  
David L Baker ◽  
Maureen Petersen ◽  
Encarna Velázquez ◽  
José I Jiménez-Zurdo ◽  
...  

A central event of the infection process in the Rhizobium–legume symbiosis is the modification of the host cell wall barrier to form a portal of entry large enough for bacterial penetration. Transmission electron microscopy (TEM) indicates that rhizobia enter the legume root hair through a completely eroded hole that is slightly larger than the bacterial cell and is presumably created by localized enzymatic hydrolysis of the host cell wall. In this study, we have used microscopy and enzymology to further clarify how rhizobia modify root epidermal cell walls to shed new light on the mechanism of primary host infection in the Rhizobium–legume symbiosis. Quantitative scanning electron microscopy indicated that the incidence of highly localized, partially eroded pits on legume root epidermal walls that follow the contour of the rhizobial cell was higher in host than in nonhost legume combinations, was inhibited by high nitrate supply, and was not induced by immobilized wild-type chitolipooligosaccharide Nod factors reversibly adsorbed to latex beads. TEM examination of these partially eroded, epidermal pits indicated that the amorphous, noncrystalline portions of the wall were disrupted, whereas the crystalline portions remained ultrastructurally intact. Further studies using phase-contrast and polarized light microscopy indicated that (i) the structural integrity of clover root hair walls is dependent on wall polymers that are valid substrates for cell-bound polysaccharide-degrading enzymes from rhizobia, (ii) the major site where these rhizobial enzymes can completely erode the root hair wall is highly localized at the isotropic, noncrystalline apex of the root hair tip, and (iii) the degradability of clover root hair walls by rhizobial polysaccharide-degrading enzymes is enhanced by modifications induced during growth in the presence of chitolipooligosaccharide Nod factors from wild-type clover rhizobia. The results suggest a complementary role of rhizobial cell-bound glycanases and chitolipooligosaccharides in creating the localized portals of entry for successful primary host infection.Key words: Rhizobium leguminosarum, cellulase, cell wall, chitolipooligosaccharide, clover, root hair.


2000 ◽  
Vol 21 (1) ◽  
pp. 109-119 ◽  
Author(s):  
Joachim Goedhart ◽  
Mark A. Hink ◽  
Antonie J. W. G. Visser ◽  
Ton Bisseling ◽  
Theodorus W. J. Gadella

2008 ◽  
Vol 56 (5) ◽  
pp. 802-813 ◽  
Author(s):  
Luis Cárdenas ◽  
Adán Martínez ◽  
Federico Sánchez ◽  
Carmen Quinto

2003 ◽  
Vol 16 (10) ◽  
pp. 884-892 ◽  
Author(s):  
Joachim Goedhart ◽  
Jean-Jacques Bono ◽  
Ton Bisseling ◽  
Theodorus W. J. Gadella

Nod factors are signaling molecules secreted by Rhizobium bacteria. These lipo-chitooligosaccharides (LCOs) are required for symbiosis with legumes and can elicit specific responses at subnanomolar concentrations on a compatible host. How plants perceive LCOs is unclear. In this study, using fluorescent Nod factor analogs, we investigated whether sulfated and nonsulfated Nod factors were bound and perceived differently by Medicago truncatula and Vicia sativa root hairs. The bioactivity of three novel sulfated fluorescent LCOs was tested in a root hair deformation assay on M. truncatula, showing bioactivity down to 0.1 to 1 nM. Fluorescence microscopy of plasmolyzed M. truncatula root hairs shows that sulfated fluorescent Nod factors accumulate in the cell wall of root hairs, whereas they are absent from the plasma membrane when applied at 10 nM. When the fluorescent Nod factor distribution in medium surrounding a root was studied, a sharp decrease in fluorescence close to the root hairs was observed, visualizing the remarkable capacity of root hairs to absorb Nod factors from the medium. Fluorescence correlation microscopy was used to study in detail the mobilities of sulfated and nonsulfated fluorescent Nod factors which are biologically active on M. truncatula and V. sativa, respectively. Remarkably, no difference between sulfated and nonsulfated Nod factors was observed: both hardly diffuse and strongly accumulate in root hair cell walls of both M. truncatula and V. sativa. The implications for the mode of Nod factor perception are discussed.


2000 ◽  
Vol 124 (3) ◽  
pp. 1373-1380 ◽  
Author(s):  
Hubert H. Felle ◽  
Éva Kondorosi ◽  
Ádam Kondorosi ◽  
Michael Schultze
Keyword(s):  

2016 ◽  
Vol 108 ◽  
pp. 488-498 ◽  
Author(s):  
Danxia Ke ◽  
Xiangyong Li ◽  
Yapeng Han ◽  
Lin Cheng ◽  
Hongyu Yuan ◽  
...  

2014 ◽  
Vol 55 (3) ◽  
pp. 580-592 ◽  
Author(s):  
Isaac Zepeda ◽  
Rosana Sánchez-López ◽  
Joseph G. Kunkel ◽  
Luis A. Bañuelos ◽  
Alejandra Hernández-Barrera ◽  
...  

1997 ◽  
Vol 10 (7) ◽  
pp. 791-802 ◽  
Author(s):  
Christoph A. Gehring ◽  
Helen R. Irving ◽  
Akram A. Kabbara ◽  
Roger W. Parish ◽  
Nawal M. Boukli ◽  
...  

Rhizobia excrete variously substituted lipo-oligosaccha-ride Nod factors into the legume rhizosphere. Homologous legumes respond to these signals through deformation of the root hairs and the development of nodulation foci in the root cortex. Cellular events in root hairs from the susceptible zone of nearly mature root hairs were studied in root segments loaded with the calcium indicators Fura-2 or Fluo-3. Application of 10-9 M Nod factors of the broad-host-range Rhizobium sp. NGR234 to the homologous legume Vigna unguiculata resulted, within seconds, in plateau-like increases in intracellular free calcium ([Ca2+]i) in the root hairs and root epidermal cells. Nod factors of R. meliloti at 10-9 M caused equally rapid increases in [Ca2+]i in the root hairs and epidermal cells of the nonhost V. unguiculata, and also induced root-hair deformation. The chitin tetramer, N-N′-N″-N′″-tetracetylchitotetraose, which represents the backbone of Nod factors, induced neither root-hair deformation nor changes in [Ca2+]i in V. unguiculata. Root hairs and epidermal cells of the nonlegume non-host Arabidopsis thaliana showed neither [Ca2+]i increases nor root-hair deformation in response to both factors.


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