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1.
Int J Mol Sci ; 20(5)2019 Mar 03.
Article in English | MEDLINE | ID: mdl-30832430

ABSTRACT

Pigeon pea (Cajanus cajan (L.) Millspaugh) is cultivated widely in semiarid agricultural regions in over 90 countries around the world. This important legume can enter into symbiotic associations with a wide range of rhizobia including Bradyrhizobium and fast-growing rhizobia. In comparison with other major legumes such as soybean and common bean, only limited information is available on the symbiotic interaction of pigeon pea with rhizobia. In this study, we investigated the ability of two classical soybean symbionts-S. fredii USDA191 and B. diazoefficiens USDA110-and their type 3 secretion system (T3SS) mutants, to nodulate pigeon pea. Both S. fredii USDA191 and a T3SS mutant S. fredii RCB26 formed nitrogen-fixing nodules on pigeon pea. Inoculation of pigeon pea roots with B. diazoefficiens USDA110 and B. diazoefficiens Δ136 (a T3SS mutant) resulted in the formation of Fix- and Fix+ nodules, respectively. Light and transmission electron microscopy of Fix- nodules initiated by B. diazoefficiens USDA110 revealed the complete absence of rhizobia within these nodules. In contrast, Fix+ nodules formed by B. diazoefficiens Δ136 revealed a central region that was completely filled with rhizobia. Ultrastructural investigation revealed the presence of numerous bacteroids surrounded by peribacteroid membranes in the infected cells. Analysis of nodule proteins by one- and two-dimensional gel electrophoresis revealed that leghemoglobin was absent in B. diazoefficiens USDA110 nodules, while it was abundantly present in B. diazoefficiens Δ136 nodules. Results of competitive nodulation assays indicated that B. diazoefficiens Δ136 had greater competitiveness for nodulation on pigeon pea than did the wild type strain. Our results suggest that this T3SS mutant of B. diazoefficiens, due to its greater competitiveness and ability to form Fix+ nodules, could be exploited as a potential inoculant to boost pigeon pea productivity.


Subject(s)
Bradyrhizobium/pathogenicity , Cajanus/microbiology , Phenotype , Sinorhizobium fredii/pathogenicity , Symbiosis , Bradyrhizobium/genetics , Bradyrhizobium/metabolism , Cajanus/metabolism , Host Specificity , Nitrogen Fixation , Root Nodules, Plant/metabolism , Root Nodules, Plant/microbiology , Root Nodules, Plant/ultrastructure , Sinorhizobium fredii/genetics , Sinorhizobium fredii/metabolism , Glycine max/microbiology , Type III Secretion Systems/genetics
2.
Mol Plant Microbe Interact ; 28(7): 790-9, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25775271

ABSTRACT

Plants that interact with pathogenic bacteria in their natural environments have developed barriers to block or contain the infection. Phytopathogenic bacteria have evolved mechanisms to subvert these defenses and promote infection. Thus, the type 3 secretion system (T3SS) delivers bacterial effectors directly into the plant cells to alter host signaling and suppress defenses, providing an appropriate environment for bacterial multiplication. Some rhizobial strains possess a symbiotic T3SS that seems to be involved in the suppression of host defenses to promote nodulation and determine the host range. In this work, we show that the inactivation of the Sinorhizobium (Ensifer) fredii HH103 T3SS negatively affects soybean nodulation in the early stages of the symbiotic process, which is associated with a reduction of the expression of early nodulation genes. This symbiotic phenotype could be the consequence of the bacterial triggering of soybean defense responses associated with the production of salicylic acid (SA) and the impairment of the T3SS mutant to suppress these responses. Interestingly, the early induction of the transcription of GmMPK4, which negatively regulates SA accumulation and defense responses in soybean via WRKY33, could be associated with the differential defense responses induced by the parental and the T3SS mutant strain.


Subject(s)
Glycine max/microbiology , Host-Pathogen Interactions , Plant Roots/microbiology , Sinorhizobium fredii/physiology , Sinorhizobium fredii/pathogenicity , Gene Expression Regulation, Plant , Isoleucine/metabolism , Mutation , Plant Roots/metabolism , Salicylic Acid/metabolism , Glycine max/genetics , Symbiosis/genetics
3.
PLoS Pathog ; 9(2): e1003204, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23468637

ABSTRACT

Two diametric paradigms have been proposed to model the molecular co-evolution of microbial mutualists and their eukaryotic hosts. In one, mutualist and host exhibit an antagonistic arms race and each partner evolves rapidly to maximize their own fitness from the interaction at potential expense of the other. In the opposing model, conflicts between mutualist and host are largely resolved and the interaction is characterized by evolutionary stasis. We tested these opposing frameworks in two lineages of mutualistic rhizobia, Sinorhizobium fredii and Bradyrhizobium japonicum. To examine genes demonstrably important for host-interactions we coupled the mining of genome sequences to a comprehensive functional screen for type III effector genes, which are necessary for many Gram-negative pathogens to infect their hosts. We demonstrate that the rhizobial type III effector genes exhibit a surprisingly high degree of conservation in content and sequence that is in contrast to those of a well characterized plant pathogenic species. This type III effector gene conservation is particularly striking in the context of the relatively high genome-wide diversity of rhizobia. The evolution of rhizobial type III effectors is inconsistent with the molecular arms race paradigm. Instead, our results reveal that these loci are relatively static in rhizobial lineages and suggest that fitness conflicts between rhizobia mutualists and their host plants have been largely resolved.


Subject(s)
Bradyrhizobium/genetics , Evolution, Molecular , Genes, Bacterial , Sinorhizobium fredii/genetics , Arabidopsis/microbiology , Bradyrhizobium/pathogenicity , Conserved Sequence , DNA, Bacterial/analysis , Genome , Host-Pathogen Interactions , Polymorphism, Single Nucleotide , Sinorhizobium fredii/pathogenicity , Species Specificity
4.
Appl Environ Microbiol ; 76(11): 3758-61, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20382805

ABSTRACT

Sinorhizobium fredii is a nitrogen-fixing legume symbiont that stimulates the formation of root nodules. S. fredii nodulation of roots is influenced by Nop proteins, which are secreted through a type III secretion system (T3SS). We demonstrate that S. fredii injects NopP into Vigna unguiculata nodules in a T3SS-dependent manner.


Subject(s)
Bacterial Proteins/metabolism , Fabaceae/microbiology , Plant Roots/microbiology , Sinorhizobium fredii/pathogenicity , Virulence Factors/metabolism , Protein Transport
5.
Mol Plant Microbe Interact ; 19(6): 635-43, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16776297

ABSTRACT

Sinorhizobium fredii USDA257, a soybean symbiont, exports several nodulation outer proteins (Nops) into the rhizosphere. These proteins, which are exported by a type III secretion system (TTSS), have a pivotal role in host-specific nodulation. The entire TTSS of S. fredii lies within a 31-kb region that includes conserved genes that code for secretion machinery proteins, Nops, and several open reading frames (ORF) of unknown function. Identifying the functions of these ORF is essential to understand fully the role of TTSS in nodulation. Here, we report the characterization of y4xP, an ORF of previously unknown function. Southern blot analysis revealed that USDA257 contains two copies of y4xP, while a sibling, USDA191, contains a single copy. The amino acid sequence of Y4XP is homologous to both eukaryotic and prokaryotic cysteine synthase, a key enzyme in sulfur assimilation. The coding region of USDA257 y4xP under control of T7 promoter was expressed in Escherichia coli, and the recombinant protein was purified by nickel-affinity chromatography. Antibodies generated against soybean cysteine synthase cross-reacted with the recombinant protein. A nonpolar mutant of y4xP of USDA191 showed a marked reduction in cysteine synthase activity. Enzyme activity was completely restored when the mutant was complemented with a plasmid containing the y4xP sequence. Cysteine synthase activity was confined to the cell cytosol. Extracellular protein fraction from genistein-induced USDA191 showed no cysteine synthase activity. This observation indicates that cysteine synthase, which is located in the TTSS locus, is not a type III secreted protein. A nonpolar cysteine synthase mutant was able to export all the Nops to the rhizosphere, albeit in reduced amounts compared with the wild-type USDA191. Interestingly, USDA191 cysteine synthase mutant was able to initiate nodules on 'McCall' soybean more efficiently than the wild-type. Our results demonstrate that y4xP encodes a cysteine synthase and inactivation of this gene enhances the ability of USDA191 to form nodules on 'McCall' soybean by regulating Nops production.


Subject(s)
Bacterial Proteins/genetics , Cysteine Synthase/genetics , Open Reading Frames , Sinorhizobium fredii/genetics , Amino Acid Sequence , Bacterial Proteins/metabolism , Cysteine Synthase/metabolism , Escherichia coli/genetics , Gene Dosage , Gene Expression Regulation, Bacterial , Genetic Complementation Test , Genistein/pharmacology , Molecular Sequence Data , Mutation , Recombinant Fusion Proteins/analysis , Sequence Alignment , Sinorhizobium fredii/enzymology , Sinorhizobium fredii/pathogenicity , Glycine max/microbiology , Symbiosis/genetics
6.
Int. microbiol ; 9(2): 125-133, jun. 2006. tab, graf
Article in En | IBECS | ID: ibc-048323

ABSTRACT

It has been postulated that nodulation outer proteins (Nops) avoid effective nodulation of Sinorhizobium fredii USDA257 to nodulate with American soybeans. S. fredii HH103 naturally nodulates with both Asiatic (non-commercial) and American (commercial) soybeans. Inactivation of the S. fredii HH103 gene rhcJ, which belongs to the tts (type III secretion) cluster, abolished Nop secretion and decreased its symbiotic capacity with the two varieties of soybeans. S. fredii strains HH103 and USDA257, that only nodulates with Asian soybeans, showed different SDS-PAGE Nop profiles, indicating that these strains secrete different sets of Nops. In coinoculation experiments, the presence of strain USDA257 provoked a clear reduction of the nodulation ability of strain HH103 with the American soybean cultivar Williams. These results suggest that S. fredii Nops can act as either detrimental or beneficial symbiotic factors in a strain-cultivar-dependent manner. Differences in the flavonoid-mediated expression of rhcJ with respect to nodA were also detected. In addition, one of the Nops secreted by strain HH103 was identified as NopA (AU)


Se ha propuesto que las proteínas externas de nodulación (Nops) impiden la nodulación efectiva de Sinorhizobium fredii USDA257 con las sojas americanas. S. fredii HH103 nodula de forma natural tanto con las sojas asiáticas (no comercializadas) como con las americanas (comercializadas). La inactivación del gen rhcJ de HH103, que pertenece a la agrupación génica tts (secreción de tipo III), anuló la secreción de Nops y redujo la capacidad simbiótica de esta bacteria con las dos variedades de soja. Las cepas HH103 y USDA257 de S. fredii, que sólo nodula sojas asiáticas, mostraron perfiles SDS-PAGE diferentes de Nop, lo cual sugiere que estas cepas podrían secretar distintos conjuntos de Nops. Cuando las cepas USDA257 y HH103 fueron inoculadas conjuntamente, la capacidad de nodulación de esta última cepa con el cultivar americano Williams de soja se redujo significativamente. Estos resultados indican que las Nops secretadas por S. fredii pueden actuar como factores simbióticos tanto positivos como negativos dependiendo de la cepa-cultivar rizobiana. Se detectaron también diferencias entre la expresión mediada por flavonoides del gen rhcJ y del nodA. Además, una de las Nops secretadas por la cepa HH103 fue identificada como NopA (AU)


Subject(s)
Bacterial Proteins , Sinorhizobium fredii/pathogenicity , Symbiosis , Gene Silencing , Genes, Bacterial , Molecular Sequence Data , Mutation , /genetics , Sinorhizobium fredii/genetics , Sinorhizobium fredii/metabolism
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