Unknown

Dataset Information

0

The Mesorhizobium huakuii transcriptional regulator AbiEi plays a critical role in nodulation and is important for bacterial stress response.


ABSTRACT:

Background

Bacterial abortive infection (Abi) systems are type IV toxin-antitoxin (TA) system, which could elicit programmed cell death and constitute a native survival strategy of pathogenic bacteria under various stress conditions. However, no rhizobial AbiE family TA system has been reported so far. Here, a M. huakuii AbiE TA system was identified and characterized.

Results

A mutation in M. huakuii abiEi gene, encoding an adjacent GntR-type transcriptional regulator, was generated by homologous recombination. The abiEi mutant strain grew less well in rich TY medium, and displayed increased antioxidative capacity and enhanced gentamicin resistance, indicating the abiEi operon was negatively regulated by the antitoxin AbiEi in response to the oxidative stress and a particular antibiotic. The mRNA expression of abiEi gene was significantly up-regulated during Astragalus sinicus nodule development. The abiEi mutant was severely impaired in its competitive ability in rhizosphere colonization, and was defective in nodulation with 97% reduction in nitrogen-fixing capacity. The mutant infected nodule cells contained vacuolation and a small number of abnormal bacteroids with senescence character. RNA-seq experiment revealed it had 5 up-regulated and 111 down-regulated genes relative to wild type. Of these down-regulated genes, 21 are related to symbiosis nitrogen fixation and nitrogen mechanism, 16 are involved in the electron transport chain and antioxidant responses, and 12 belong to type VI secretion system (T6SS).

Conclusions

M. huakuii AbiEi behaves as a key transcriptional regulator mediating root nodule symbiosis.

SUBMITTER: Chen X 

PROVIDER: S-EPMC8436566 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC3147426 | biostudies-literature
| S-EPMC3147681 | biostudies-literature
| PRJNA578841 | ENA
| PRJNA719262 | ENA
| PRJDB10341 | ENA
| PRJNA48449 | ENA
2012-01-23 | E-BUGS-119 | biostudies-arrayexpress
| S-EPMC6933692 | biostudies-literature
| S-EPMC2869319 | biostudies-literature
| S-EPMC7509050 | biostudies-literature