Table 1.
Summary of proteomic studies focused on the legume-Rhizobium symbiosis.
Legume sp. | Rhizobium sp. | References | Main outcome |
---|---|---|---|
I. STUDIES FOCUSED ON THE PLANT PARTNER | |||
G. max roots (wt and SS2-2 mutant) | B. japonicum USDA110 | Lim et al., 2010 | Protein-mediated suppression of defense-related responses in root cells upon inoculation with symbiotic bacteria. |
G. max root hairs | B. japonicum USDA110 | Wan et al., 2005 | Induction of phospholipases, phosphoglucomutases, lectins, and an actin isoform in soybean roots upon B. japonicum inoculation. |
G. max nodules (cytosol fraction) | B. japonicum USDA110 | Oehrle et al., 2008 | Proteins related to carbon and nitrogen metabolism, oxygen supply and protection are predominantly found in the cytosol of nodule cells. |
G. max En-b0-1 roots (supernodulating) | B. japonicum MAFF 211342 | Salavati et al., 2012 | Identification of a correlation between the levels of a peroxidase isoform and nodulation at the protein but not transcript level in soybean nodules. |
L. japonicus roots and nodules | M. loti MAFF30309 | Dam et al., 2014 | Establishment of 2D-PAGE reference maps of L. japonicum roots and nodules. |
M. alba nodules | S. meliloti 1021 | Natera et al., 2000 | Identification of nearly 100 plant and bacterial proteins in white sweetclover nodules. |
M. truncatula roots | S. meliloti 2011 | Bestel-Corre et al., 2002 | Two leghemoglobin isoforms and one enolase protein were accumulated in roots upon inoculation with symbiotic bacteria. |
M. truncatula nodules | S. meliloti 2011 | Larrainzar et al., 2007 | Identification of 377 plant proteins in nodules, mostly related to amino acid metabolism and protein synthesis and degradation. |
M. truncatula nodules | S. meliloti 2011 | Larrainzar et al., 2009 | Integrative proteomic and metabolomic analysis of the effects of drought stress in the plant and bacteroid fractions of M. truncatula nodules. |
M. truncatula roots and nodules | S. meliloti 2011 | Larrainzar et al., 2014 | Absolute quantification proteomics and gene expression analyses show that sulfur metabolism and ethylene biosynthesis have key roles in the response of nodules and roots subjected to drought stress. |
M. truncatula shoots and roots | S. meliloti 1021 | Molesini et al., 2014 | Analysis of local and systemic responses of M. truncatula roots and shoots upon inoculation. |
M. truncatula roots (wt and skl mutant) | S. meliloti 1021 | Prayitno et al., 2006 | Increased abundance of one ACC oxidase isoform in wild-type roots but not in roots of the supernodulating skl mutant upon inoculation. |
M. truncatula roots and shoots | S. meliloti 2011 | Staudinger et al., 2012 | Detection of salt and drought stress markers and identification of an improved plant response to stress of plants grown under symbiotic conditions when compared to nitrate-fed plants. |
M. truncatula shoots | S. medicae WSM419 and S. meliloti 2011 | Staudinger et al., 2016 | Plants grown under symbiotic conditions present reduced levels of leaf senescence during drought stress independently of the efficiency of the symbiotic Rhizobium strain used. |
P. sativum shoots | R. leguminosarum bv. viciae | Irar et al., 2014 | Identification of variations in protein abundance as part as the local responses of pea nodules grown under split-root conditions and subjected to water stress. |
P. sativum shoots (soluble and plasma membrane fractions) | R. leguminosarum bv. viciae | Desalegn et al., 2016 | Indications of a positive influence of the symbiotic interaction on the activation of the plant defense responses upon pathogen attack. |
P. sativum shoots | R. leguminosarum bv. viciae | Turetschek et al., 2016 | Proteomic and metabolomic analyses of two pea cultivars with varying pathogen resistance levels associate tolerance to ethylene biosynthesis and suppression of cell death responses. |
V. unguiculata roots | Rhizobium sp. NGR234 | Krause and Broughton, 1992 | One of the first proteomic studies analyzing symbiosis-specific proteins potentially involved in root-hair deformation in cowpea. |
II. STUDIES FOCUSED ON THE Rhizobium PARTNER | |||
B. japonicum USDA110 | Bacteroids | Sarma and Emerich, 2005 | Abundance of proteins related to nitrogen and carbon metabolism, and transport in soybean nodule bacteroids. |
B. japonicum USDA110 | Free-living cells vs. bacteroids | Sarma and Emerich, 2006 | Compared to bacteria under free-living conditions, nodule bacteroids present unusually low levels in proteins related to fatty acid and nucleic acid metabolism. |
B. japonicum USDA110 | Bacteroids | Delmotte et al., 2010 | In contrast to previous reports, application of more sensitive LC-MS/MS-based approaches identifies a complete set of proteins related to de novo nucleoside and nucleotide biosynthesis in bacteroids. |
Bradyrhizobium sp. ORS278 | Bacteroids (Aeschynomene indica root and stem nodules) | Delmotte et al., 2014 | Root and stem nodule bacteroids show expression of similar sets of proteins, mostly related to central metabolism. As exceptions, proteins involved in photosynthesis were exclusive found in stem nodules. |
M. loti MAFF30309 | Free-living cells vs. bacteroids | Tatsukami et al., 2013 | Differentiated bacteroids do not longer express proteins either involved in peptidoglycan biosynthesis or proteins related to the flagellum. |
M. loti MAFF30309 | Bacteroids | Nambu et al., 2015 | Time-course analysis of nodulation suggests that bacteroids experience nitrogen-deficiency at early stages of nodule development. |
S. meliloti 1021 | Free-living cells vs. bacteroids | Djordjevic et al., 2003 | Compared to free-living bacteria, nodule bacteroids appear not to require the expression of sugar transporters or enzymes involved in the early steps of glycolysis. |
S. meliloti 1021 | Bacteroids | Djordjevic, 2004 | Bacteroids express a specific set of ABC-type transporters involved in the transport of amino acids and inorganic ions. |