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Genetics and Molecular Biology

Print version ISSN 1415-4757

Genet. Mol. Biol. vol.35 no.4 supl.1 São Paulo  2012

http://dx.doi.org/10.1590/S1415-47572012000600020 

REVIEW ARTICLE

 

Plant growth-promoting rhizobacteria (PGPR): their potential as antagonists and biocontrol agents

 

 

Anelise Beneduzi; Adriana Ambrosini; Luciane M.P. Passaglia

Universidade Federal do Rio Grande do Sul, Instituto de Biociências, Departamento de Genética, Porto Alegre, RS, Brazil

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ABSTRACT

Bacteria that colonize plant roots and promote plant growth are referred to as plant growth-promoting rhizobacteria (PGPR). PGPR are highly diverse and in this review we focus on rhizobacteria as biocontrol agents. Their effects can occur via local antagonism to soil-borne pathogens or by induction of systemic resistance against pathogens throughout the entire plant. Several substances produced by antagonistic rhizobacteria have been related to pathogen control and indirect promotion of growth in many plants, such as siderophores and antibiotics. Induced systemic resistance (ISR) in plants resembles pathogen-induced systemic acquired resistance (SAR) under conditions where the inducing bacteria and the challenging pathogen remain spatially separated. Both types of induced resistance render uninfected plant parts more resistant to pathogens in several plant species. Rhizobacteria induce resistance through the salicylic acid-dependent SAR pathway, or require jasmonic acid and ethylene perception from the plant for ISR. Rhizobacteria belonging to the genera Pseudomonas and Bacillus are well known for their antagonistic effects and their ability to trigger ISR. Resistance-inducing and antagonistic rhizobacteria might be useful in formulating new inoculants with combinations of different mechanisms of action, leading to a more efficient use for biocontrol strategies to improve cropping systems.

Keywords: antagonism, siderophore, antibiotic, SAR, ISR.


 

 

Plant-Associated Bacteria - A General Introduction

The rhizosphere is the narrow zone of soil specifically influenced by the root system (Dobbelaere et al., 2003). This zone is rich in nutrients when compared with the bulk soil due to the accumulation of a variety of plant exudates, such as amino acids and sugars, providing a rich source of energy and nutrients for bacteria (Gray and Smith, 2005). This situation is reflected by the number of bacteria that are found around the roots of plants, generally 10 to 100 times higher than that in the bulk soil (Weller and Thomashow, 1994). The rhizosphere is populated by a diverse range of microorganisms and the bacteria colonizing this habitat are called rhizobacteria (Schroth and Hancock, 1982).

Plant-associated bacteria can be classified into beneficial, deleterious and neutral groups on the basis of their effects on plant growth (Dobbelaere et al., 2003). Beneficial free-living soil bacteria are usually referred to as plant growth-promoting rhizobacteria (PGPR, Kloepper et al., 1989). Independent of the mechanisms of vegetal growth promotion, PGPRs colonize the rhizosphere, the rhizo-plane (root surface), or the root itself (within radicular tissues) (Gray and Smith, 2005). It is well established that only 1 to 2% of bacteria promote plant growth in the rhizosphere (Antoun and Kloepper, 2001). Bacteria of diverse genera have been identified as PGPR, of which Bacillus and Pseudomonas spp. are predominant (Podile and Kishore, 2006).

PGPR affect plant growth in two different ways, indirectly or directly. The direct promotion of plant growth by PGPR entails either providing the plant with a compound that is synthesized by the bacterium, for example phyto-hormones, or facilitating the uptake of certain nutrients from the environment (Glick, 1995). The indirect promotion of plant growth occurs when PGPR lessen or prevent the deleterious effects of one or more phytopathogenic organisms. This can happen by producing antagonistic substances or by inducing resistance to pathogens (Glick, 1995). A particular PGPR may affect plant growth and development by using any one, or more, of these mechanisms. PGPR, as bio-control agents, can act through various mechanisms, regardless of their role in direct growth promotion, such as by known production of auxin phytohormone (Patten and Glick, 2002), decrease of plant ethylene levels (Glick et al., 2007) or nitrogen fixing associated with roots (Döbereiner, 1992).

PGPR and their interactions with plants are exploited commercially (Podile and Kishore, 2006) and hold great promise for sustainable agriculture. Applications of these associations have been investigated in maize, wheat, oat, barley, peas, canola, soy, potatoes, tomatoes, lentils, radicchio and cucumber (Gray and Smith, 2005).

In this review, we will consider the mechanisms of action of biocontrol agents and describe some successful examples of these rhizobacteria controlling plant diseases.

 

Microbial Antagonism

According to Beattie (2006), bacteria that reduce the incidence or severity of plant diseases are often referred to as biocontrol agents whereas those that exhibit antagonistic activity toward a pathogen are defined as antagonists. The following rhizospheric environment and bacterial antagonistic activities can be highlighted: (1) synthesis of hydro-lytic enzymes, such as chitinases, glucanases, proteases, and lipases, that can lyse pathogenic fungal cells (Neeraja et al. 2010; Maksimov et al. 2011), (2) competition for nutrients and suitable colonization of niches at the root surface (Ste-phens et al., 1993; Kamilova et al. 2005; Validov S, 2007, PhD thesis, Leiden University, The Netherlands), (3) regulation of plant ethylene levels through the ACC-deaminase enzyme, which can act to modulate the level of ethylene in a plant in response to stress imposed by the infection (Glick and Bashan, 1997; Van Loon, 2007), and (4) production of siderophores and antibiotics.

 

Siderophores, bacteriocins, and antibiotics production as antagonistic activities

The ability of rhizobacteria to produce siderophores and metabolites contributing to antibiosis has been the focus of many studies dedicated to investigating PGPR (Maksi-mov et al., 2011). The uptake of ferric ion via side-rophore is largely used by pathogenic and non-pathogenic microorganisms from the soil, human body and marine environments. The importance of siderophore is closely related to iron, which is an essential element for different biological processes (Crosa and Walsh, 2002). On the other hand, bacteria can produce a wide variety of compounds with antimicrobial activity used as defense systems. These include broad-spectrum antibiotics, lactic acid produced by lactobacilli, lytic agents such as lyso-zymes, numerous types of exotoxins and bac-terio-cins, which also have a bactericidal mode of action (Riley and Wertz, 2002). Sidero-phores, bacteriocins and antibiotics are three of the most effective and well known mechanisms that an antagonist can employ to minimize or prevent phytopathogenic proliferation.

 

Siderophores

To satisfy nutritional requirements of iron, microorganisms have evolved highly specific pathways that employ low molecular weight iron chelators termed side-rophores. Siderophores are secreted to solubilize iron from their surrounding environments, forming a complex ferric-siderophore that can move by diffusion and be returned to the cell surface (Andrews et al., 2003). The active transport system through the membrane begins with the recognition of the ferric-siderophore by specific membrane receptors of Gram-negative and Gram-positive bacteria (Bou-khal-fa and Crumbliss, 2002). Siderophores can chelate ferric ion with high affinity, allowing its solubilization and extraction from most mineral or organic complexes (Wandersman and Delepelaire, 2004). In aerobic conditions at physiological pH, the reduced ferrous (Fe2+) form is unstable and is readily oxidized to the oxidized ferric (Fe3+) form, which normally occurs as a poorly soluble iron hydroxide basically unavailable to biological systems (Krewu-lak and Vogel, 2008; Osorio et al., 2008).

Siderophores can be defined as small peptidic molecules containing side chains and functional groups that can provide a high-affinity set of ligands to coordinate ferric ions (Crosa and Walsh, 2002). Based on their iron-coordi-nating functional groups, structural features and types of ligands, bacterial siderophores have been classified into four main classes (carboxylate, hydroxamates, phenol cate-cholates and pyoverdines) (Crowley, 2006). Hundreds of siderophores have been identified and reported for cultivable microorganisms, some of which are widely recognized and used by different microorganisms, while others are species-specific (Crowley, 2006; Sandy and Butler, 2009).

In soil, siderophore production activity plays a central role in determining the ability of different microorganisms to improve plant development. Microbial siderophores enhance iron uptake by plants that are able to recognize the bacterial ferric-siderophore complex (Masalha et al. 2000; Katiyar and Goel, 2004; Dimkpa et al., 2009) and are also important in the iron uptake by plants in the presence of other metals such as nickel and cadmium (Burd et al., 1998; Dimkpa et al., 2008). However, it is still unclear if bacterial siderophore complexes can significantly contribute to the iron requirements of the plant.

Siderophore production confers competitive advantages to PGPR that can colonize roots and exclude other microorganisms from this ecological niche (Haas and Défago, 2005). Under highly competitive conditions, the ability to acquire iron via siderophores may determine the outcome of competition for different carbon sources that are available as a result of root exudation or rhizodeposition (Crowley, 2006). Among most of the bacterial sidero-pho-res studied, those produced by pseudomonads are known for their high affinity to the ferric ion. The potent side-rophore, pyoverdin, for example, can inhibit the growth of bacteria and fungi that present less potent siderophores in iron-depleted media in vitro (Kloepper et al. 1980a). A pseudobactin siderophore produced by P. putida B10 strain was also able to suppress Fusarium oxysporum in soil deficient in iron; this suppression was lost when the soil was replenished with iron, a condition that represses the production of iron chelators by microorganisms (Kloepper et al., 1980b). Recent studies have demonstrated the suppression of soil-borne fungal pathogens through the release of iron-chelating siderophores by fluorescent pseudomonads, rendering it unavailable to other organisms (Loper, 1988; Paulitz and Loper, 1991; Dwivedi and Johri, 2003).

 

Antibiotics

Besides siderophore production, the biocontrol abilities of pseudomonad strains essentially depend on aggressive root colonization, induction of systemic resistance in the plant, and production of antifungal antibiotics (Haas and Keel, 2003). The production of one or more antibiotics is the mechanism most commonly associated with the ability of plant growth-promoting bacteria to act as antagonistic agents against phytopathogens (Glick et al., 2007). The basis of antibiosis, activity of biocontrol based on secretion of molecules that kill or reduce the growth of the target pathogen, has become better understood over the past two decades (Dowling and O'Gara, 1994; Whipps, 2001; Lugtenberg and Kamilova, 2009). Antibiotics encompass a heterogeneous group of organic, low-mole-cu-lar-weight compounds that are deleterious to the growth or metabolic activities of other microorganisms (Duffy, 2003).

According to Haas and Défago (2005), six classes of antibiotic compounds (for which their modes of action are partly understood) are better related to the biocontrol of root diseases: phenazines, phloroglucinols, pyoluteorin, pyrrol-nitrin, cyclic lipopeptides (all of which are diffusible) and hydrogen cyanide (HCN; which is volatile). More recently, lipopeptide biosurfactants produced by Pseudomonas and Bacillus species have been implied in biocontrol due to their potential positive effect on competitive interactions with organisms including bacteria, fungi, oomycetes, protozoa, nematodes and plants (de Bruijn et al., 2007; Raaijmakers et al., 2010).

Numerous types of antibiotics have been isolated from fungal and bacterial strains and this diversity includes mechanisms of action that inhibit synthesis of pathogen cell walls, influence membrane structures of cells and inhibit the formation of initiation complexes on the small subunit of the ribosome (Maksimov et al., 2011). Pyrrolnitrin, the antibiotic produced by the P. fluorescens BL915 strain, is able to prevent the damage of Rhizoctonia solani during damping-off of cotton plants (Hill et al., 1994). The 2,4-dia-cetylphloroglucinol (DAPG) produced by pseudo-monads, an effective and extensively studied antibiotic, causes membrane damage to Pythium spp. and is particularly inhibitory to zoospores of this oomycete (de Souza et al., 2003). Phenazine, also produced by pseudomonads, possesses redox activity and can suppress pathogens of plants such as F. oxysporum and Gaeuman-no-myces grami-nis (Chin-A-Woeng et al., 2003). The P. chlororaphis PCL1391 strain, isolated from roots of tomato plants, synthesizes phena-zine-1-carboxamide, which is able to release soluble iron from insoluble ferric oxides at neutral pH, raising the possibility that phenazines might contribute to iron mobilization in soils (Hernandez et al., 2004; Haas and Défago, 2005).

Antibiotics, such as polymyxin, circulin and colistin, produced by the majority of Bacillus ssp. are active against Gram-positive and Gram-negative bacteria, as well as many pathogenic fungi (Maksimov et al., 2011). The B. cereus UW85 strain, which suppresses oomycete pathogens and produces the antibiotics zwittermicin A (aminopolyol) and kanosamine (aminoglycoside), contributes to the bio-control of alfalfa damping off (Silo-Suh et al., 1994; He et al., 1994). Regarding bacteria as biocontrol agents to act as a biological solution, some researchers have highlighted the use of sporulating Gram-positive species such as Bacillus and Paenibacillus spp., which can confer higher population stability during formulation and storage of inoculant products (Emmert and Handelsman, 1999; Kokalis-Burelle et al., 2005).

 

Bacteriocins

Other molecules used in microbial defense systems are bacteriocins. According to a review by Riley and Wertz (2002), bacteriocins differ from traditional antibiotics in one critical way: they commonly have a relatively narrow killing spectrum and are only toxic to bacteria closely related to the producing strain. Almost all bacteria may make at least one bacteriocin, and many bacteriocins isolated from Gram-negative bacteria appear to have been created by recombination between existing bacteriocins (Riley, 1993). The colicins, proteins produced by some strains of Escherichia coli that are lethal for related strains, are the most representative bacteriocins produced by Gram-nega-tive bacteria. Like colicin, a name derived from E. coli, other bacteriocins have been thus defined and named, such as pyocins from P. pyogenes strains, cloacins from Enterobacter cloacae, marcescins from Serratia marcescens and megacins from B. megaterium (Cas-cales et al., 2007). Interestingly, bacteriocins from Bacillus spp. are increasingly becoming more important due to their sometimes broader spectra of inhibition (as compared with most lactic bacterial bacteriocins), which may include Gram-negative bacteria, yeasts or fungi, in addition to Gram-positive species, some of which are known to be pathogenic to humans and/or animals (Abriouel et al., 2011).

 

Biocontrol Agents - Induced Resistance (ISR and SAR)

Non-pathogenic rhizobacteria have been shown to suppress disease by inducing a resistance mechanism in the plant called "Induced Systemic Resistance" (ISR) (Van Loon et al., 1998). Induced resistance is the state of an enhanced defensive ability developed by plants when appropriately stimulated (Van Loon et al., 1998). ISR was formerly described by Van Peer et al. (1991) in carnation plants that was systemically protected by the P. fluorescens strain WCS417r against F. oxysporum f. sp. dianthi and by Wei et al. (1991) in cucumber plants, where rhizobacterial strains protected the leaves against anthracnose caused by Colletotrichum orbiculare. The inducing rhizobacteria and the pathogens were inoculated and remained confined and spatially separated on the same plant so that microbial antagonism was excluded and the protective effect was plant-mediated.

Rhizobacteria-mediated ISR resembles pathogen-in-duced systemic acquired resistance (SAR) in that both types of induced resistance render uninfected plant parts more resistant to plant pathogens (Van Wees et al., 1997; Van Loon et al., 1998), including fungal, bacterial and viral pathogens, as well as nematodes and insects (Zehnder et al., 1997; Van Loon et al., 1998; Bent, 2006; Pozo and Azcon-Aguilar, 2007). The same strain induces resistance against several pathogens in the same plant (Somers et al. 2004). Specifically, Pseudomonas and Bacillus spp. are the rhizo-bacteria most studied that trigger ISR (Kloepper et al., 2004; Van Wees et al., 2008). Vleesschauwer and Höfte (2009) proposed the terminology ISR to depict induced systemic resistance promoted by non-pathogenic rhizo-bac-teria or PGPR, irrespective of the signaling pathway involved in this process, while the term SAR is used to describe salicylic acid-dependent induced resistance triggered by a localized infection.

ISR and SAR act through different signaling pathways. Induction of SAR is through salicylic acid (SA) and ISR requires jasmonic acid (JA) and ethylene (ET) signaling pathways (Van Loon et al., 1998). These accumulating signaling molecules coordinate the defense responses and when applied exogenously, are sufficient to induce resistance (Ryals et al., 1996). The protection mediated by ISR is significantly less than that obtained by SAR (Van Loon , 2000) and a degree of dependence on plant genotype is observed in the generation of ISR (Bloemberg and Lugten-berg, 2001). However, ISR and SAR together provide a better protection than each of them alone, indicating that they can act additively in inducing resistance to pathogens (Van Wees et al., 2000).

Salicylic acid accumulation occurs both locally and, at lower levels, systemically, in line with the development of SAR. Application of exogenous SA also induces SAR in many plant species (Van Loon et al., 1998). Development of tissue necrosis used to be considered a common and necessary feature for SAR activation (Vleesschauwer and Höfte, 2009), but in many cases, SAR can also be triggered without tissue necrosis as demonstrated in Arabidopsis thaliana (Mishina and Zeier, 2007). In SAR, the first infection predisposes the plant to resist further attacks. SA -activates specific sets of defense-related genes called patho-genesis-related proteins (PRs). Generally, ISR is not accompanied by the activation of PR genes. The enhanced defensive capacity characteristic of SAR is always associated with the accumulation of PRs (Van Loon, 2007). Treatment of tobacco roots with P. fluorescens CHA0 triggers accumulation of SA-inducible PR proteins in the leaves (Maurhofer et al., 1994). These PRs serve as hallmarks of SAR in several plant species and are thought to contribute to the state of resistance attained (Vlees-schau-wer and Höfte, 2009). Some of these PRs are 1,3-glu-canases and chitinases capable of hydrolyzing fungal cell walls, while other PRs are poorly characterized. SAR-associated PRs suggest an important contribution of these proteins to the increased defensive capacity of induced tissues (Van Loon et al., 1998).

The PR-1 gene or protein expression appears to be inducible by SA and it is usually taken as a molecular marker to indicate that SAR has been induced (Van Loon and Bakker, 2006). Arabidopsis plants inoculated with the pa-thogen P. syringae pv. tomato or sprayed with SA developed SAR and accumulated PR-1, -2 and -5 mRNAs (Pieterse et al., 1996) and inoculated with P. fluorescens WCS417r or P. putida WCS358 developed ISR, but PR-gene expression or accumulation of PRs was not detected (Van Wees et al., 1997). ISR can be triggered in plants that are unable to accumulate SA (NahG mutant plants). Based on this, one can conclude that PRs are induced concomitantly with SAR, whereas SA and the activation of PR genes is not part of the pathway leading to ISR in Arabidopsis (Pieterse et al., 1996).

Transduction of the SA signal requires the regulatory (activator) protein NPR1 (or NIM1) that functions in the terminal part of the signaling pathway of SAR (Van Loon et al., 1998). In non-induced plants, NPR1 is present as a multimer and during SAR induction, SA triggers the conversion of NPR1 into a monomeric form (Verhagen et al. 2006). These monomers are translocated to the nucleus (Kinkema et al. 2000), where they interact with members of the TGA/OBF subclass of basic-leucine-zipper (bZIP) transcription factors that are involved in SA-dependent activation of PR genes (Fan and Dong, 2002; Zhang et al., 2003). A direct interaction between NPR1 and a specific TGA transcription factor is required for the binding of the complex to elements within the promoter of the PR genes (Després et al., 2000; Fan and Dong, 2002). Overexpres-sion of the NPR1 gene leads to enhanced resistance to pathogen attack (Cao et al., 1998; Friedrich et al., 2001).

The Arabidopsis mutant npr1 does not express PR genes and does not exhibit SAR. Since rhizo-bacteria-mediated ISR is independent of SA and not associated with PRs, it is expected that ISR would still be expressed in this mutant. However, the npr1 mutant of Arabidopsis does not display P. fluorescens WCS417r-mediated ISR. This -implies that NPR1 regulates defense responses mediated by different signaling pathways that function beyond the expression of PR genes, indicating that SAR and ISR converge at the last part of the signaling pathway (Van Loon et al., 1998). Reports of Pieterse et al. (1996, 1998, 2000) with the reference rhizobacterial strain P. fluorescens WCS417r demonstrated that, at least in Arabidopsis, WCS417r-mediated ISR functioned independently of SA, depended on NPR1, but required components of the JA and ethylene (ET) response pathways.

Infected plants increased their levels of JA and ET as a sign of active defense (De Laat and Van Loon, 1982; Gundlach et al., 1992; Mauch et al., 1994). These signaling molecules coordinate the activation of a large set of defense responses and when applied exogenously, can induce resistance themselves (Pieterse et al., 1998). The dependency of ISR on JA and ethylene is based on enhanced sensitivity to these hormones rather than on an increase in their production (Pieterse et al., 2000, 2001). The Arabidopsis JA response mutant jar1 and the ET response mutant etr1 were tested in the development of ISR. Both mutants were unable to develop ISR against P. syringae pv. tomato upon colonization of the roots by WCS417r bacteria (Pieterse et al., 1998), illustrating the dependency of ISR signaling on these phytohormones. The signal-transduction pathways leading to pathogen-induced SAR and rhizo-bacteria-mediated ISR in Arabidopsis thaliana are summarized in Figure 1.

 

 

Methyl jasmonate (MeJA) and the ethylene precursor 1-aminocyclopropane-1-carboxylate (ACC) also promote resistance against P. syringae pv. tomato DC3000 in SA-non-accumulating NahG plants. Besides that, MeJA-induced protection is blocked in jar1-1, etr1-1 and npr1-1 plants, whereas ACC-induced protection is affected in etr1-1 and npr1-1 plants, but not in jar1-1 plants. Therefore, WCS417r-mediated ISR follows a signaling path-way in which components from the JA and ethylene -response pathways are successively engaged to trigger a defense reaction that, like SAR, is regulated by NPR1 (Pie-terse et al., 1998).

One or more bacterial determinant must be recognized by specific plant receptors so that resistance is induced. A variety of resistance-inducing molecules have been described: lipopolysaccharides and siderophores, -including SA (Van Loon et al., 1998), flagella, bio-sur-fac-tants, N-acyl-homoserine lactones (AHL), N-alkylated ben-zylamines, antibiotics and exopolysaccharides (EPS) (Vleesschauwer and Höfte, 2009).

The ability to develop ISR in response to certain rhizobacteria has been demonstrated in several species of plants (Van Loon et al., 1998) and appears to depend on the specificity of the interaction between rhizobacteria and plants (Van Loon, 2007). Failure to elicit ISR in certain hosts may be due to the absence of production of inducing components in the rhizosphere or an inability of the particular plant species to perceive such compounds (Van Loon, 2007). The evidence support that it is necessary specific recognition between the plant and the rhizobacteria for induction of resistance. For instance, Pseudomonas putida WCS358r and P. fluorescens WCS374r act in different ways depending on the plant species: in Arabidopsis, WCS358r elicits ISR, but not in radish and carnation plants (Van Peer et al., 1991; Van Peer and Schippers, 1992; Leeman et al., 1995; Van Wees et al., 1997). In contrast, radish plants are responsive to WCS374r, while Arabidopsis is not (Leeman et al., 1995; Van Wees et al., 1997).

 

Conclusion

The ability of bacterial siderophores and antibiotics to suppress phytopathogens could be of significant agronomic importance. Both mechanisms have essential functions in microbial antagonism but also are able to elicit induced resistance. Resistance-inducing and antagonistic rhizo-bac-teria might be useful in formulating new inoculants, offering an attractive alternative of environmentally friendly biological control of plant disease and improving the cropping systems into which it can be most profitably applied. These new PGPR will require a systematic strategy designed to fully utilize all these beneficial factors, applying combinations of different mechanisms of action allowing crop yields to be maintained or even increased while chemical treatments are reduced.

 

Acknowledgments

This work was financed by a grant and fellowships from the Conselho Nacional de Desenvolvimento Cien-tífico e Tecnológico (CNPq/Brazil) and the INCT da Fixa-ção Biológica do Nitrogênio (Brazil).

 

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Luciane M.P. Passaglia
Departamento de Genética
Instituto de Biociências
Universidade Federal do Rio Grande do Sul
Av. Bento Gonçalves 9500
Caixa Postal 15.053
91501-970 Porto Alegre, RS, Brazil
E-mail: lpassaglia@terra.com.br

 

 

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