Symbiotic properties of a chimeric Nod‐independent photosynthetic Bradyrhizobium strain obtained by conjugative transfer of a symbiotic plasmid

2019 ◽  
Vol 21 (9) ◽  
pp. 3442-3454 ◽  
Author(s):  
Pongpan Songwattana ◽  
Panlada Tittabutr ◽  
Jenjira Wongdee ◽  
Kamonluck Teamtisong ◽  
Dyah Wulandari ◽  
...  
2003 ◽  
Vol 185 (5) ◽  
pp. 1681-1692 ◽  
Author(s):  
Cristina Tun-Garrido ◽  
Patricia Bustos ◽  
Víctor González ◽  
Susana Brom

ABSTRACT Rhizobium etli CFN42 contains six plasmids. Only one of them, p42a, is self-conjugative at high frequency. This plasmid is strictly required for mobilization of the symbiotic plasmid (pSym). To study the transfer mechanism of p42a, a self-transmissible cosmid clone containing its transfer region was isolated. Its sequence showed that most of the tra genes are highly similar to genes of Agrobacterium tumefaciens pTiC58 and other related plasmids. Four putative regulatory genes were identified; three of these (traI, traR, and cinR) belong to the LuxR-LuxI family. Mutagenesis of these genes confirmed their requirement for p42a transfer. We found that the conjugative transfer of p42a is dependent on quorum sensing, and consequently pSym transfer also was found to be similarly regulated, establishing a complex link between environmental conditions and pSym transfer. Although R. etli has been shown to produce different N-acyl-homoserine lactones, only one of them, a 3-oxo-C8-homoserine lactone encoded by the traI gene described here, was involved in transfer. Mutagenesis of the fourth regulatory gene, traM, had no effect on transfer. Analysis of transcriptional fusions of the regulatory genes to a reporter gene suggests a complex regulation scheme for p42a conjugative transfer. Conjugal transfer gene expression was found to be directly upregulated by TraR and the 3-oxo-C8-homoserine lactone synthesized by TraI. The traI gene was autoregulated by these elements and positively regulated by CinR, while cinR expression required traI. Finally, we did not detect expression of traM, indicating that in p42a TraM may be expressed so weakly that it cannot inhibit conjugal transfer, leading to the unrepressed transfer of p42a.


Plasmid ◽  
2019 ◽  
Vol 106 ◽  
pp. 102443
Author(s):  
Laura Cervantes ◽  
Fabiola Miranda-Sánchez ◽  
Gonzalo Torres Tejerizo ◽  
David Romero ◽  
Susana Brom

2013 ◽  
Vol 195 (20) ◽  
pp. 4668-4677 ◽  
Author(s):  
R. Hernandez-Tamayo ◽  
C. Sohlenkamp ◽  
J. L. Puente ◽  
S. Brom ◽  
D. Romero

2004 ◽  
Vol 186 (22) ◽  
pp. 7538-7548 ◽  
Author(s):  
Susana Brom ◽  
Lourdes Girard ◽  
Cristina Tun-Garrido ◽  
Alejandro García-de los Santos ◽  
Patricia Bustos ◽  
...  

ABSTRACT Plasmid p42a from Rhizobium etli CFN42 is self-transmissible and indispensable for conjugative transfer of the symbiotic plasmid (pSym). Most pSym transconjugants also inherit p42a. pSym transconjugants that lack p42a always contain recombinant pSyms, which we designated RpSyms*. RpSyms* do not contain some pSym segments and instead have p42a sequences, including the replication and transfer regions. These novel recombinant plasmids are compatible with wild-type pSym, incompatible with p42a, and self-transmissible. The symbiotic features of derivatives simultaneously containing a wild-type pSym and an RpSym* were analyzed. Structural analysis of 10 RpSyms* showed that 7 shared one of the two pSym-p42a junctions. Sequencing of this common junction revealed a 53-bp region that was 90% identical in pSym and p42a, including a 5-bp central region flanked by 9- to 11-bp inverted repeats reminiscent of bacterial and phage attachment sites. A gene encoding an integrase-like protein (intA) was localized downstream of the attachment site on p42a. Mutation or the absence of intA abolished pSym transfer from a recA mutant donor. Complementation with the wild-type intA gene restored transfer of pSym. We propose that pSym-p42a cointegration is required for pSym transfer; cointegration may be achieved either through homologous recombination among large reiterated sequences or through IntA-mediated site-specific recombination between the attachment sites. Cointegrates formed through the site-specific system but resolved through RecA-dependent recombination or vice versa generate RpSyms*. A site-specific recombination system for plasmid cointegration is a novel feature of these large plasmids and implies that there is unique regulation which affects the distribution of pSym in nature due to the role of the cointegrate in conjugative transfer.


Author(s):  
Susmita Mukherjee ◽  
Manjusha Lekshmi ◽  
Parvathi Ammini ◽  
Binaya Bhusan Nayak ◽  
Sanath H. Kumar

Microbiology ◽  
1983 ◽  
Vol 129 (10) ◽  
pp. 2973-2977 ◽  
Author(s):  
N. J. Brewin ◽  
E. A. Wood ◽  
J. P. W. Young

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Pongpan Songwattana ◽  
Clémence Chaintreuil ◽  
Jenjira Wongdee ◽  
Albin Teulet ◽  
Mamadou Mbaye ◽  
...  

AbstractThe Bradyrhizobium vignae strain ORS3257 is an elite strain recommended for cowpea inoculation in Senegal. This strain was recently shown to establish symbioses on some Aeschynomene species using a cocktail of Type III effectors (T3Es) secreted by the T3SS machinery. In this study, using a collection of mutants in different T3Es genes, we sought to identify the effectors that modulate the symbiotic properties of ORS3257 in three Vigna species (V. unguiculata, V. radiata and V. mungo). While the T3SS had a positive impact on the symbiotic efficiency of the strain in V. unguiculata and V. mungo, it blocked symbiosis with V. radiata. The combination of effectors promoting nodulation in V. unguiculata and V. mungo differed, in both cases, NopT and NopAB were involved, suggesting they are key determinants for nodulation, and to a lesser extent, NopM1 and NopP1, which are additionally required for optimal symbiosis with V. mungo. In contrast, only one effector, NopP2, was identified as the cause of the incompatibility between ORS3257 and V. radiata. The identification of key effectors which promote symbiotic efficiency or render the interaction incompatible is important for the development of inoculation strategies to improve the growth of Vigna species cultivated in Africa and Asia.


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