Abstract

Biological nitrogen fixation by Rhizobium-legume symbioses represents an environmentally friendly and inexpensive alternative to the use of chemical nitrogen fertilizers in legume crops. Rhizobial inoculants, applied frequently as biofertilizers, play an important role in sustainable agriculture. However, inoculants often fail to compete for nodule occupancy against native rhizobia with inferior nitrogen-fixing abilities, resulting in low yields. Strains with excellent performance under controlled conditions are typically selected as inoculants, but the rates of nodule occupancy compared to native strains are rarely investigated. Lack of persistence in the field after agricultural cycles, usually due to the transfer of symbiotic genes from the inoculant strain to naturalized populations, also limits the suitability of commercial inoculants. When rhizobial inoculants are based on native strains with a high nitrogen fixation ability, they often have superior performance in the field due to their genetic adaptations to the local environment. Therefore, knowledge from laboratory studies assessing competition and understanding how diverse strains of rhizobia behave, together with assays done under field conditions, may allow us to exploit the effectiveness of native populations selected as elite strains and to breed specific host cultivar-rhizobial strain combinations. Here, we review current knowledge at the molecular level on competition for nodulation and the advances in molecular tools for assessing competitiveness. We then describe ongoing approaches for inoculant development based on native strains and emphasize future perspectives and applications using a multidisciplinary approach to ensure optimal performance of both symbiotic partners.

Highlights

  • Biological nitrogen fixation (BNF) is an important source of nitrogen, and the various legume crops and pasture species often fix as much as 200 to 300 kg of nitrogen per hectare per year (Peoples et al, 1995)

  • Genetic Components for Rhizosphere Colonization. When it comes to exploitative competition, where bacteria compete for the same common resources without directly interacting, bacterial chemotaxis toward exuded compounds is an important trait for root colonization and plant-driven selection of microorganisms (Bais et al, 2006; Raina et al, 2019)

  • This study identified 38 mutations in genes that were not previously known to be involved in competitiveness or symbiosis in E. meliloti, confirming 23 with attenuated competitiveness phenotypes when they were tested for competition against the wild type

Read more

Summary

INTRODUCTION

Biological nitrogen fixation (BNF) is an important source of nitrogen, and the various legume crops and pasture species often fix as much as 200 to 300 kg of nitrogen per hectare per year (Peoples et al, 1995). Onishchuk et al (2017) identified two types of competition influenced by different factors: exploitative (indirect) competition, involving a more effective use of a common limiting nutrient, or interference (direct) competition, whereby other cells are prevented from growing and surviving in the environment To be both competitive and N2effective, an elite strain should have genetic components that enable it to (i) successfully colonize the rhizosphere and benefit from available nutrients in an effective way, (ii) prevent the growth of other bacterial cells, (iii) establish an efficient symbiosis, and (iv) promote plant growth. The genetic knowledge on the pre-infection, infection and nodulation stages has mainly been gained from experiments with defective mutants When it comes to exploitative competition, where bacteria compete for the same common resources without directly interacting, bacterial chemotaxis toward exuded compounds is an important trait for root colonization and plant-driven selection of microorganisms (Bais et al, 2006; Raina et al, 2019). New methods based on Periodic Acid-Schiff to visualize the three-dimensional structure of infection threads in sufficient detail using novel and traditional cell wall fluorescent labels combined with laser confocal scanning microscopy presents an exciting opportunity for research in this area, including competition (Rae et al, 2021)

METHODS
Findings
Method
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call