» Articles » PMID: 20331875

Symbiotic Functioning and Bradyrhizobial Biodiversity of Cowpea (Vigna Unguiculata L. Walp.) in Africa

Overview
Journal BMC Microbiol
Publisher Biomed Central
Specialty Microbiology
Date 2010 Mar 25
PMID 20331875
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Cowpea is the most important food grain legume in Sub-Saharan Africa. However, no study has so far assessed rhizobial biodiversity and/or nodule functioning in relation to strain IGS types at the continent level. In this study, 9 cowpea genotypes were planted in field experiments in Botswana, South Africa and Ghana with the aim of i) trapping indigenous cowpea root-nodule bacteria (cowpea "rhizobia") in the 3 countries for isolation, molecular characterisation using PCR-RFLP analysis, and sequencing of the 16S - 23S rDNA IGS gene, ii) quantifying N-fixed in the cowpea genotypes using the 15N natural abundance technique, and iii) relating the levels of nodule functioning (i.e. N-fixed) to the IGS types found inside nodules.

Results: Field measurements of N2 fixation revealed significant differences in plant growth, delta15N values, %Ndfa and amounts of N-fixed between and among the 9 cowpea genotypes in Ghana and South Africa. Following DNA analysis of 270 nodules from the 9 genotypes, 18 strain IGS types were found. Relating nodule function to the 18 IGS types revealed significant differences in IGS type N2-fixing efficiencies. Sequencing the 16S - 23S rDNA gene also revealed 4 clusters, with cluster 2 forming a distinct group that may be a new Bradyrhizobium species. Taken together, our data indicated greater biodiversity of cowpea bradyrhizobia in South Africa relative to Botswana and Ghana.

Conclusions: We have shown that cowpea is strongly dependant on N2 fixation for its N nutrition in both South Africa and Ghana. Strain IGS type symbiotic efficiency was assessed for the first time in this study, and a positive correlation was discernible where there was sole nodule occupancy. The differences in IGS type diversity and symbiotic efficiency probably accounts for the genotype x environment interaction that makes it difficult to select superior genotypes for use across Africa. The root-nodule bacteria nodulating cowpea in this study all belonged to the genus Bradyrhizobium. Some strains from Southern Africa were phylogenetically very distinct, suggesting a new Bradyrhizobium species.

Citing Articles

Unveiling remarkable bacterial diversity trapped by cowpea (Vigna unguiculata) nodules inoculated with soils from indigenous lands in Central-Western Brazil.

Moura F, Delai C, Klepa M, Ribeiro R, Nogueira M, Hungria M Braz J Microbiol. 2025; 56(1):545-562.

PMID: 39847210 PMC: 11885751. DOI: 10.1007/s42770-025-01622-z.


Seed-Coat Pigmentation Plays a Crucial Role in Partner Selection and N Fixation in Legume-Root-Microbe Associations in African Soils.

Jaiswal S, Dakora F Plants (Basel). 2024; 13(11).

PMID: 38891273 PMC: 11175086. DOI: 10.3390/plants13111464.


Genetic control of earliness in cowpea ( (L) Walp).

Owusu E, Kusi F, Kena A, Akromah R, Attamah P, Awuku F Heliyon. 2022; 8(7):e09852.

PMID: 35847611 PMC: 9283894. DOI: 10.1016/j.heliyon.2022.e09852.


Distribution, Characterization and the Commercialization of Elite Rhizobia Strains in Africa.

Wekesa C, Jalloh A, Muoma J, Korir H, Omenge K, Maingi J Int J Mol Sci. 2022; 23(12).

PMID: 35743041 PMC: 9223902. DOI: 10.3390/ijms23126599.


Leaf growth, gas exchange and assimilation performance of cowpea varieties in response to inoculation.

Ayalew T, Yoseph T, Hogy P, Cadisch G Heliyon. 2022; 8(1):e08746.

PMID: 35106387 PMC: 8789522. DOI: 10.1016/j.heliyon.2022.e08746.


References
1.
Steenkamp E, Stepkowski T, Przymusiak A, Botha W, Law I . Cowpea and peanut in southern Africa are nodulated by diverse Bradyrhizobium strains harboring nodulation genes that belong to the large pantropical clade common in Africa. Mol Phylogenet Evol. 2008; 48(3):1131-44. DOI: 10.1016/j.ympev.2008.04.032. View

2.
Robinson D, Handley L, Scrimgeour C, Gordon D, Forster B, Ellis R . Using stable isotope natural abundances (delta 15N and delta 13C) to integrate the stress responses of wild barley (Hordeum spontaneum C. Koch.) genotypes. J Exp Bot. 2000; 51(342):41-50. View

3.
Willems A, Coopman R, Gillis M . Comparison of sequence analysis of 16S-23S rDNA spacer regions, AFLP analysis and DNA-DNA hybridizations in Bradyrhizobium. Int J Syst Evol Microbiol. 2001; 51(Pt 2):623-632. DOI: 10.1099/00207713-51-2-623. View

4.
Laguerre G, Mavingui P, Allard M, Charnay M, Louvrier P, Mazurier S . Typing of rhizobia by PCR DNA fingerprinting and PCR-restriction fragment length polymorphism analysis of chromosomal and symbiotic gene regions: application to Rhizobium leguminosarum and its different biovars. Appl Environ Microbiol. 1996; 62(6):2029-36. PMC: 167981. DOI: 10.1128/aem.62.6.2029-2036.1996. View

5.
Lafay , Burdon . Molecular diversity of rhizobia occurring on native shrubby legumes in southeastern australia . Appl Environ Microbiol. 1998; 64(10):3989-97. PMC: 106590. DOI: 10.1128/AEM.64.10.3989-3997.1998. View