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Molecular diversity of rhizobia-nodulating native Mimosa of Brazilian protected areas

https://doi.org/10.1007/s00203-021-02537-7

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Phylogeny, Diversity, Geographical Distribution, and Host Range of Legume‐Nodulating Betaproteobacteria: What Is the Role of Plant Taxonomy?

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Paraburkholderia guartelaensis sp. nov., a nitrogen-fixing species isolated from nodules of Mimosa gymnas in an ecotone considered as a hotspot of biodiversity in Brazil

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Paraburkholderia atlantica sp. nov. and Paraburkholderia franconis sp. nov., two new nitrogen-fixing nodulating species isolated from Atlantic forest soils in Brazil

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Burkholderia sp. Induces Functional Nodules on the South African Invasive Legume Dipogon lignosus (Phaseoleae) in New Zealand Soils

inferredcites →https://doi.org/10.1007/s11033-018-4506-zopenalex-snapshot

Phylogenetic diversity of rhizobia nodulating native Mimosa gymnas grown in a South Brazilian ecotone

inferredcites →https://doi.org/10.1007/s11104-015-2470-0openalex-snapshot

Woody Mimosa species are nodulated by Burkholderia in ombrophylous forest soils and their symbioses are enhanced by arbuscular mycorrhizal fungi (AMF)

inferredcites →https://doi.org/10.1007/s11104-017-3521-5openalex-snapshot

Soil characteristics determine the rhizobia in association with different species of Mimosa in central Brazil

inferredcites →https://doi.org/10.1007/s11274-013-1400-7openalex-snapshot

Diversity and symbiotic effectiveness of beta-rhizobia isolated from sub-tropical legumes of a Brazilian Araucaria Forest

inferredcites →https://doi.org/10.1016/j.agee.2017.06.017openalex-snapshot

Isolation, characterization and selection of indigenous Bradyrhizobium strains with outstanding symbiotic performance to increase soybean yields in Mozambique

inferredcites →https://doi.org/10.1016/j.sajb.2013.06.005openalex-snapshot

A 2013 linear sequence of legume genera set in a phylogenetic context — A tool for collections management and taxon sampling

inferredcites →https://doi.org/10.1016/j.soilbio.2008.10.011openalex-snapshot

Novel strains of nodulating Burkholderia have a role in nitrogen fixation with papilionoid herbaceous legumes adapted to acid, infertile soils

inferredcites →https://doi.org/10.1016/j.soilbio.2020.107854openalex-snapshot

Native legumes of the Farrapos protected area in Uruguay establish selective associations with rhizobia in their natural habitat

inferredcites →https://doi.org/10.1016/j.syapm.2015.09.003openalex-snapshot

Burkholderia kirstenboschensis sp. nov. nodulates papilionoid legumes indigenous to South Africa

inferredcites →https://doi.org/10.1016/j.syapm.2017.04.005openalex-snapshot

Phylogenies of symbiotic genes of Bradyrhizobium symbionts of legumes of economic and environmental importance in Brazil support the definition of the new symbiovars pachyrhizi and sojae

inferredcites →https://doi.org/10.1016/j.syapm.2017.12.003openalex-snapshot

Brazilian species of Calliandra Benth. (tribe Ingeae) are nodulated by diverse strains of Paraburkholderia

inferredcites →https://doi.org/10.1016/j.syapm.2020.126053openalex-snapshot

Characterization of Bradyrhizobium strains indigenous to Western Australia and South Africa indicates remarkable genetic diversity and reveals putative new species

inferredcites →https://doi.org/10.1016/j.syapm.2020.126151openalex-snapshot

Phylogeny of symbiotic genes reveals symbiovars within legume-nodulating Paraburkholderia species

inferredcites →https://doi.org/10.1016/j.syapm.2020.126152openalex-snapshot

Paraburkholderia youngii sp. nov. and ‘Paraburkholderia atlantica’ – Brazilian and Mexican Mimosa-associated rhizobia that were previously known as Paraburkholderia tuberum sv. mimosae

inferredcites →https://doi.org/10.1038/35002501openalex-snapshot

Biodiversity hotspots for conservation priorities

inferredcites →https://doi.org/10.1038/35082070openalex-snapshot

Nodulation of legumes by members of the β-subclass of Proteobacteria

inferredcites →https://doi.org/10.1078/07232020260517634openalex-snapshot

Burkholderia tuberum sp. nov. and Burkholderia phymatum sp. nov., Nodulate the Roots of Tropical Legumes

inferredcites →https://doi.org/10.1089/dna.2009.0863openalex-snapshot

Coevolution in Rhizobium -Legume Symbiosis?

inferredcites →https://doi.org/10.1093/aob/mcm227openalex-snapshot

Nodulation of Cyclopia spp. (Leguminosae, Papilionoideae) by Burkholderia tuberum

inferredcites →https://doi.org/10.1093/aob/mct112openalex-snapshot

An invasive Mimosa in India does not adopt the symbionts of its native relatives

inferredcites →https://doi.org/10.1093/femsec/fiu024openalex-snapshot

Symbiotic diversity, specificity and distribution of rhizobia in native legumes of the Core Cape Subregion (South Africa)

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Diversity of species and antimicrobial resistance determinants of staphylococci in superficial waters in Spain

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Genetic diversity of symbiotic Paraburkholderia species isolated from nodules of Mimosa pudica (L.) and Phaseolus vulgaris (L.) grown in soils of the Brazilian Atlantic Forest (Mata Atlântica)

inferredcites →https://doi.org/10.1093/femsec/fiz109openalex-snapshot

Mimosa caesalpiniifolia Benth. adapts to rhizobia populations with differential taxonomy and symbiotic effectiveness outside of its location of origin

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/oso/9780195135848.001.0001openalex-snapshot

Molecular Evolution and Phylogenetics

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040023openalex-snapshot

Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees.

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The number of replications needed for accurate estimation of the bootstrap P value in phylogenetic studies.

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040752openalex-snapshot

Estimation of the number of nucleotide substitutions when there are strong transition-transversion and G+C-content biases.

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040763openalex-snapshot

The rate and pattern of nucleotide substitution in Drosophila mitochondrial DNA.

inferredcites →https://doi.org/10.1094/mpmi-05-16-0091-ropenalex-snapshot

Symbiotic Burkholderia Species Show Diverse Arrangements of nif/fix and nod Genes and Lack Typical High-Affinity Cytochrome cbb3 Oxidase Genes

inferredcites →https://doi.org/10.1099/00207713-51-5-1729openalex-snapshot

Ralstonia taiwanensis sp. nov., isolated from root nodules of Mimosa species and sputum of a cystic fibrosis patient.

inferredcites →https://doi.org/10.1099/ijs.0.028803-0openalex-snapshot

Phylogeny of nodulation and nitrogen-fixation genes in Bradyrhizobium: supporting evidence for the theory of monophyletic origin, and spread and maintenance by both horizontal and vertical transfer

inferredcites →https://doi.org/10.1099/ijs.0.037408-0openalex-snapshot

Burkholderia symbiotica sp. nov., isolated from root nodules of Mimosa spp. native to north-east Brazil

inferredcites →https://doi.org/10.1099/ijs.0.048777-0openalex-snapshot

Burkholderia sprentiae sp. nov., isolated from Lebeckia ambigua root nodules

inferredcites →https://doi.org/10.1099/ijs.0.63247-0openalex-snapshot

Taxonomy of the genus Cupriavidus: a tale of lost and found

inferredcites →https://doi.org/10.1099/ijs.0.64325-0openalex-snapshot

Burkholderia mimosarum sp. nov., isolated from root nodules of Mimosa spp. from Taiwan and South America

inferredcites →https://doi.org/10.1099/ijs.0.64873-0openalex-snapshot

Burkholderia nodosa sp. nov., isolated from root nodules of the woody Brazilian legumes Mimosa bimucronata and Mimosa scabrella

inferredcites →https://doi.org/10.1099/ijsem.0.001065openalex-snapshot

Transfer of eleven species of the genus Burkholderia to the genus Paraburkholderia and proposal of Caballeronia gen. nov. to accommodate twelve species of the genera Burkholderia and Paraburkholderia

inferredcites →https://doi.org/10.1099/ijsem.0.001648openalex-snapshot

Paraburkholderia piptadeniae sp. nov. and Paraburkholderia ribeironis sp. nov., two root-nodulating symbiotic species of Piptadenia gonoacantha in Brazil

inferredcites →https://doi.org/10.1099/ijsem.0.003640openalex-snapshot

Bradyrhizobium niftali sp. nov., an effective nitrogen-fixing symbiont of partridge pea [Chamaecrista fasciculata (Michx.) Greene], a native caesalpinioid legume broadly distributed in the USA

inferredcites →https://doi.org/10.1111/1462-2920.12211openalex-snapshot

Genus‐wide acid tolerance accounts for the biogeographical distribution of soil Burkholderia populations

inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04458.xopenalex-snapshot

Burkholderia species are ancient symbionts of legumes

inferredcites →https://doi.org/10.1111/j.1469-8137.1912.tb05611.xopenalex-snapshot

THE DISTRIBUTION OF THE FLORA IN THE ALPINE ZONE. 1

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03267.xopenalex-snapshot

Nodulation and nitrogen fixation by Mimosa spp. in the Cerrado and Caatinga biomes of Brazil

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot

CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://doi.org/10.1111/j.1574-6941.2011.01235.xopenalex-snapshot

Genetic diversity of Mimosa pudica rhizobial symbionts in soils of French Guiana: investigating the origin and diversity of Burkholderia phymatum and other beta-rhizobia

inferredcites →https://doi.org/10.1111/j.1574-6941.2012.01393.xopenalex-snapshot

Biodiversity of Mimosa pudica rhizobial symbionts (Cupriavidus taiwanensis, Rhizobium mesoamericanum) in New Caledonia and their adaptation to heavy metal-rich soils

inferredcites →https://doi.org/10.1111/nph.13573openalex-snapshot

Endemic M imosa species from M exico prefer alphaproteobacterial rhizobial symbionts

inferredcites →https://doi.org/10.1126/science.aaf5080openalex-snapshot

Plant diversity patterns in neotropical dry forests and their conservation implications

inferredcites →https://doi.org/10.1128/aem.00591-16openalex-snapshot

Biogeographical Patterns of Legume-Nodulating Burkholderia spp.: from African Fynbos to Continental Scales

inferredcites →https://doi.org/10.1128/aem.04142-15openalex-snapshot

Novel Cupriavidus Strains Isolated from Root Nodules of Native Uruguayan Mimosa Species

inferredcites →https://doi.org/10.1128/jb.183.1.214-220.2001openalex-snapshot

Methylotrophic Methylobacterium Bacteria Nodulate and Fix Nitrogen in Symbiosis with Legumes

inferredcites →https://doi.org/10.1128/jcm.43.1.199-207.2005openalex-snapshot

Microbial DNA Typing by Automated Repetitive-Sequence-Based PCR

inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092839openalex-snapshot

Coordinating Nodule Morphogenesis with Rhizobial Infection in Legumes

inferredcites →https://doi.org/10.12705/622.12openalex-snapshot

Global legume diversity assessment: Concepts, key indicators, and strategies

inferredcites →https://doi.org/10.12705/661.3openalex-snapshot

A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny: The Legume Phylogeny Working Group (LPWG)

inferredcites →https://doi.org/10.1371/journal.pone.0063478openalex-snapshot

Burkholderia Species Are the Most Common and Preferred Nodulating Symbionts of the Piptadenia Group (Tribe Mimoseae)

inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot

BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT

inferredcites →https://doi.org/10.15560/10.3.574openalex-snapshot

Anurans from a Cerrado-Atlantic Forest ecotone in Campos Gerais region, southern Brazil

inferredcites →https://doi.org/10.15560/13.6.879openalex-snapshot

Floristic survey of the Furnas Gêmeas region, Campos Gerais National Park, Paraná state, southern Brazil

inferredcites →https://doi.org/10.1590/s1676-06032010000300034openalex-snapshot

Composição florística e fitofisionomia de remanescentes disjuntos de Cerrado nos Campos Gerais, PR, Brasil - limite austral do bioma

inferredcites →https://doi.org/10.2307/2419739openalex-snapshot

Sensitivae Censitae: A Description of the Genus Mimosa Linnaeus (Mimosaceae) in the New World.

inferredcites →https://doi.org/10.2307/3225339openalex-snapshot

Numerical Taxonomy: The Principles and Practice of Numerical Classification

inferredcites →https://doi.org/10.3389/fgene.2014.00001openalex-snapshot

Cytoplasmic 5′-3′ exonuclease Xrn1p is also a genome-wide transcription factor in yeast

inferredcites →https://doi.org/10.3389/fgene.2014.00429openalex-snapshot

Molecular signatures and phylogenomic analysis of the genus Burkholderia: proposal for division of this genus into the emended genus Burkholderia containing pathogenic organisms and a new genus Paraburkholderia gen. nov. harboring environmental species

inferredcites →https://doi.org/10.3390/genes9080389openalex-snapshot

Whole Genome Analyses Suggests that Burkholderia sensu lato Contains Two Additional Novel Genera (Mycetohabitans gen. nov., and Trinickia gen. nov.): Implications for the Evolution of Diazotrophy and Nodulation in the Burkholderiaceae

inferredcites →https://doi.org/10.3732/ajb.1000520openalex-snapshot

The evolutionary history of Mimosa (Leguminosae): Toward a phylogeny of the sensitive plants

inferredcites →https://doi.org/10.5860/choice.30-0290openalex-snapshot

Sensitivae censitae: a description of the genus Mimosa Linnaeus (Mimosaceae) in the New World

inferredcites →https://doi.org/10.5902/198050986618openalex-snapshot

Análise estrutural em relictos de Cerrado no Parque Estadual do Guartelá, município de Tibagi, Estado do Paraná, Brasil

inferredcites →https://doi.org/10.5923/j.ije.20120206.03openalex-snapshot

Grassland Vegetation of Pitangui River Valley, Southern Brazil

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4860743openalex-extracted

Mimosa Species Endemic to Acidic Soils in Central Brazil are Nodulated by a High Diversity of Paraburkholderia Genotypes, But Widespread Species are Nodulated by Paraburkholderia, Cupriavidus or Rhizobium Depending on Soil Characteristics

inferred← citeshttps://doi.org/10.1007/s13199-022-00831-6openalex-snapshot

So many rhizobial partners, so little nitrogen fixed: The intriguing symbiotic promiscuity of common bean (Phaseolus vulgaris L.)

inferred← citeshttps://doi.org/10.1007/s42770-023-01113-zopenalex-snapshot

Pioneering Desmodium spp. are nodulated by natural populations of stress-tolerant alpha- and beta-rhizobia

inferred← citeshttps://doi.org/10.1007/s42770-024-01472-1openalex-snapshot

Phenotypic and genomic characterization of phosphate-solubilizing rhizobia isolated from native Mimosa and Desmodium in Brazil

inferred← citeshttps://doi.org/10.1016/j.apsoil.2024.105741openalex-snapshot

Soil characteristics drive contrasting patterns of association between symbiotic rhizobia of endemic and widespread Mimosa species in Brazil

inferred← citeshttps://doi.org/10.1101/2024.06.11.598400openalex-snapshot

Mimosa species endemic to acidic soils in central Brazil are nodulated by a high diversity of Paraburkholderia genotypes, but widespread species are nodulated by Paraburkholderia , Cupriavidus or Rhizobium depending on soil characteristics

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