Enhancement of clover growth by inoculation of P-solubilizing fungi and arbuscular mycorrhizal fungi

AGRARIAN SCIENCES

Enhancement of clover growth by inoculation of P-solubilizing fungi and arbuscular mycorrhizal fungi

Edson L. Souchie^I; Rosario Azcón^II; Jose M. Barea^II; Eliane M.R. Silva^III; Orivaldo J. Saggin-Júnior^III

^IInstituto Federal de Educação, Ciência e Tecnologia Goiano - Campus Rio Verde Caixa Postal 66, 75901-970 Rio Verde, GO, Brasil

^IIEstación Experimental del Zaidín, Dep. de Microbiología y Sistemas Simbióticos Calle Prof. Albareda 1, 18008 Granada, España

^IIIEmbrapa Agrobiologia, Caixa Postal 101, 23890-970 Seropédica, RJ, Brasil

^{Correspondence to}

ABSTRACT

This study evaluated the synergism between several P-solubilizing fungi isolates and arbuscular mycorrhizal fungi to improve clover ( Trifolium pratense) growth in the presence of Araxá apatite. Clover was sown directly in plastic pots with 300g of sterilized washed sand, vermiculite and sepiolite 1:1:1 (v:v:v) as substrate, and grown in a controlled environment chamber. The substrate was fertilized with 3 g L^-1 of Araxá apatite. A completely randomized design, in 8×2 factorial scheme (eight P-solubilizing fungi treatments with or without arbuscular mycorrhizal fungi)and four replicates were used. The P-solubilizing fungi treatments consisted of five Brazilian P-solubilizing fungi isolates (PSF 7, 9, 20, 21 and 22), two Spanish isolates ( Aspergillus niger and the yeast Yarowia lipolytica) and control (non-inoculated treatment). The greatest clover growth rate was recorded when Aspergillus niger and PSF 21 were co-inoculated with arbuscular mycorrhizal fungi. Aspergillus niger, PSF 7 and PSF 21 were the most effective isolates on increasing clover growth in the presence of arbuscular mycorrhizal fungi. Greater mycorrhizal colonization resulted in greater clover growth rate in most PSF treatments. PSF 7 was the best isolate to improve the establishment of mycorrhizal and rhizobia symbiosis.

Key words: Araxá apatite, phosphate solubilization, co-inoculation, plant growth promotion, rhizosphere.

RESUMO

Este estudo avaliou o sinergismo entre diversos isolados defungos solubilizadores de fosfato e micorrízicos arbusculares para beneficiar o crescimento de trevo ( Trifolium pratense) na presença de apatita de Araxá. A cultura foi semeada diretamente em potes plásticos com 300 g de substrato esterilizado formado por areia lavada, vermiculita e sepiolita 1:1:1 (v:v:v) e cultivada em câmara climática. O substrato foi fertilizado com 3 g L^-1 de apatita de Araxá. O experimento foi instalado em delineamento completamente casualizado, esquema fatorial 8×2 (oito tratamentos de inoculação de fungos solubilizadores de fosfato com ou sem fungos micorrízicos arbusculares) e quatro repetições. Os tratamentos de fungos solubilizadores de fosfato consistiram em cinco isolados brasileiros de fungos solubilizadores de fosfato (FSF 7, 9, 20, 21 e 22), dois isolados procedentes da Espanha ( Aspergillus niger e a levedura Yarowia lipolytica) e o controle (tratamento não inoculado). A maior taxa de crescimento da cultura foi obtida quando Aspergillus niger e FSF 21 foram co-inoculados com fungos micorrízicos arbusculares. Aspergillus niger, FSF 7 e o FSF 21 foram os isolados mais efetivos para incrementar o crescimento de trevo na presença de fungos micorrízicosarbusculares. A maior taxa de colonização micorrízica resultou em alta taxa de crescimento de trevo na maioria dos tratamentos com fungos solubilizadores de fosfato. O isolado FSF 7 foi o melhor para favorecer o estabelecimento das simbioses com fungos micorrízicos e com rizóbio.

Palavras-chave: apatita de Araxá, solubilização de fosfato, co-inoculação, promoção do crescimento vegetal, rizosfera.

INTRODUCTION

Soil microorganisms play an important role in supplying nutrients to plants. Phosphorus (P) is the least mobile and available to plants in most soil conditions, in comparison to other major nutrients (El-Azouni 2008). Nevertheless, some microorganisms are able of mineralizing and solubilizing P from the organic and inorganic soil pools (Richardson 2001). Souchie et al. (2006) stated that P is the most limiting nutrient in tropicalsoils; in contrast, P-solubilizing microorganisms (PSM) and the arbuscular mycorrhizal fungi (AMF) are among the most relevant soil microorganisms.

The inoculation of PSM is a promising technique in order to increase P availability in soils fertilized with rock phosphates (Reyes et al. 2002). Several authors reported yield increases on maize (Reyes et al. 2002), sorghum (Kumar et al. 1999), and wheat (Whitelaw et al. 1997, Wahid and Mehana 2000) by inoculation of P-solubilizing fungi (PSF). Rodríguez et al. (1999) reported a greatest alfalfa growth in soil fertilized withrock phosphate and sugar beet waste through inoculation of Aspergillus niger (an isolate with high P solubilization potential) and Glomus deserticola. The synergism between these microorganisms also promoted considerable increases in P absorption and growth in clover ( Trifolium repens) (Vassileva et al. 1998). Similarly, the co-inoculation of Yarowia lipolytica (a P-solubilizingyeast) increased mycorrhizal colonization by Glomusdeserticola in tomato roots (Vassilev et al. 2001). Ravnskov et al. (1999) also observed mycorrhizal colonization increasing forage leguminous roots after the inoculation of Saccharomyces cerevisiae. Nowadays, it is widely accepted that several PSM, besides solubilizing P, also increase mycorrhizal colonization, produce vitamins, amino acids and phytohormones (Barea et al. 1997, Arshad and Frankenberger Jr. 1998). Therefore, more studies to establish the functional compatibility among these microorganisms on improving plant growth of several species are required.

The PSF efficiency changes according to isolateand phosphate type (Souchie et al. 2005). Therefore, studies about P solubilization of rock phosphates in systems involving plants inoculated with PSM and AMF should be done. This study evaluated the synergism between several PSF and AMF isolates in improvingclover growth fertilized with Araxá apatite.

MATERIALS AND METHODS

The experiment was done at Estación Experimental del Zaidín, Granada, Spain, in a controlled environmentchamber. Clover ( Trifolium pratense) was sown in plastic pots containing 300 g of substrate (washed sand, vermiculite and sepiolite, 1:1:1, v:v:v). Each component was autoclaved (C, 20 min) separately. Araxá apatite (12 g of P kg) was mixed to the substrate at3 g L.

A completely randomized design, in factorial scheme (eight inoculation treatments and presenceor absence of AMF) and four replicates were used.The inoculation treatments were: 1) control (non-inoculated); 2) PSF 7; 3) PSF 9; 4) PSF 20; 5) PSF 21; 6) PSF 22; 7) Aspergillus niger and 8) Yarowia lipolytica. The isolates Aspergillus niger and Yarowia lipolytica belong to the Estación Experimental del Zaidín collection and are considered to be isolates with high P-solubilization potential (Vassileva et al. 1998, 2000). PSF 7 and 9 were isolated from the rhizosphere of Mimosa caesalpiniifolia grown in an Argisol collected at an Atlantic Forest area in Paraty, Rio de Janeiro, Brazil. PSF 20, 21 and 22 were obtained from the rhizosphere of Acacia holosericea grown in Planosol collected at Seropédica, Rio de Janeiro, Brazil.

The mycorrhizal inoculum consisted of soil containing spores, mycelia and root fragments colonized by Glomus clarum and Glomus geosporum. Equal proportions were prepared by mixing 300 mL of soil containing 8 and 20 spores per mL of soil of G. clarum and G. geosporum, respectively. Both AMF were multiplied in sorghum and maize trap plants and maintained as a stock culture. Prior to sowing, an amount of 5 mL of inoculum was added to each pot and homogenized with the substrate. In the control, 2 mL of an inoculum filtrate, obtained by mixing 1 mL of both G. clarum and G. geosporum inoculum filtrates without AMF propagules, were added to the plant basis in each pot.

Four days after emergence, seedlings were thinned to one plant per pot. Each plant was inoculated with 1 mL of Rhizobium trifolii (strain 2152). This strain wasincubated in Ty liquid medium (Beringer 1974), to CFU mL. Two days after R. trifolii inoculation, the plants were inoculated with PSF treatments. These PSF isolates were grown in Petri dishes (four days, C, darkness), with GL solid medium (Sylvester-Bradley et al. 1982) covering the Petri dish basis. Spores were suspended in water + tween (1%) solution, quantified following the successive dilution technique till CFU mL and, subsequently, 1 mL of spore suspension was applied to each pot.

The experiment lasted 60 days in a controlled environment chamber with 50% relative humidity, day and night temperature of 27 and C, respectively, and a photoperiod of 14 hours, with photosynthetic photonflux density of 503 m s. Twice a week, 25 mL of a modified nutrient solution (Hewitt 1966) (without N, 10% of P and pH 5.5) were added to each pot.

Forty days after emergence, shoot dry matter was determined. Sixty days after emergence, plants were harvested and shoot dry matter, colonized root length (Tennant 1975, Giovannetti and Mosse 1980), number of nodules, N and P shoot contents were evaluated. Data were submitted to ANOVA and the averages compared by the F and Tukey tests .

RESULTS

AMF and PSF inoculation increased shoot dry matter in most treatments, except for plants inoculated withPSF 7, PSF 22 and Y. lipolytica (Fig. 1). PSF 7 andPSF 21 stimulated the greatest shoot dry matter production in the absence of AMF. Aspergillus niger and PSF 21 with AMF inoculation were the best treatments to increase shoot dry matter. In contrast, plants inoculated with Y. lipolytica showed little shoot dry matter production both in the presence and in the absence of AMF (Fig. 1).

No interactions were observed between AMF and PSF when N shoot content was evaluated since AMF inoculation did not affect this parameter. The PSF inoculation yielded the greatest shoot N content (3.2 g N kg), which was similar to the control (3.1 g N kg). Similar values of shoot P content were found in plants inoculated or not with AMF in the presence of PSF 7,PSF 21 and A. niger (Fig. 2). AMF inoculation increased the shoot P content on the other treatments. No significant differences were found among plants inoculated with PSF, without AMF inoculation, and the control treatment (Fig. 2).

Although PSF 7 and PSF 21 increased the numberof nodules in plants, AMF inoculation affected neitherthis parameter nor the interaction between PSF andAMF (Fig. 3). However, an enhancement on mycorrhizal colonization was observed in plants inoculated with AMF in the presence of PSF 7 and PSF 20 (Fig. 4). The other treatments were similar to the control.

DISCUSSION

Since plants were grown in an inert substrate where a nutritive solution with low P concentration was periodically amended, PSF contribution on growth promotion was probably due to an effective Araxá apatite solubilization (Souchie et al. 2005) and/or by phytohormone production (Barea et al. 1997), or even to the increase of rhizobia and AMF symbiosis (Omar 1998, Zaidi et al. 2004). In the case of PSF 21, growth promotion can be related to greater nodulation or release of stimulating substances since this isolate did not increase AMF colonization. Similarly, Cabello et al. (2005) reported that mycorrhizal colonization in Mentha piperita was not affected by inoculation with the PSF Penicilliumthomii, despite this isolate increased other analyzed variables. Zaidi et al. (2004) reported some incompatibility when Glomus fasciculatum, Bradyrhizobium sp. and Penicillium sp. were inoculated in mung bean without any improvement on plant growth. Otherwise, Valdenegro et al. (2001) reported that the inoculation of plant growth promoting rhizobacteria was effective only when Glomus mosseae and a native strain of Rhizobium meliloti were also inoculated. The success of the inoculation technique is directly related to the functional compatibility among the chosen microorganisms. Therefore, more research is required to discover the best combinations among them in order to increase nutrition and growth of plant species.

Yarowia lipolytica inoculation yielded similar results to the control treatment for almost all the analyzed variables. However, several authors (Vassileva et al.2000, Vassilev et al. 2001, Medina et al. 2004) reported considerable improvement on plant growth with Y. lipolytica inoculation. Probably, in this study, the main limiting factor was the substrate since no source of organic matter was used. Consequently, the establishment of Y. lipolytica was negatively affected.

PSF 7 increased clover shoot dry matter in the absence of AMF similarly to plants inoculated with AMF (Fig. 1). Since this isolate is capable of solubilizing Araxá apatite in liquid medium, and aluminum phosphate in solid and liquid media (Souchie et al. 2005), it has probably greater solubilization ability in comparison to the other isolates. Moreover, PSF 7 was the one that stimulated the greatest nodulation and mycorrhizal colonization (Figs. 3 and 4). Reyes et al. (2002) alsoreported that all Penicillium rugulosum P-solubilizing strains were able to stimulate maize growth as indicated by 3.6 to 28.6% increases in dry matter yield. Peixet al. (2001) observed a greater number of nodules in common bean plants inoculated with a P-solubilizing Burkholderia cepacia strain. Similarly, Fracchia et al. (2004) reported an increased mycorrhizal colonization in soybean after inoculation with the PSF Aspergillusniger. Since biological nitrogen fixation depends on the available forms of phosphorus, the combined inoculation of nitrogen fixers, P-solubilizing microorganisms and AMF may benefit plant growth more than any organism group alone.

In this study, although all PSF isolates belonged to the Aspergillus genus, it is possible that PSF 7 is a different species, explaining its different effect on clover growth. Also, Nguyen et al. (1992) reported that the P solubilization ability can vary among microorganisms within the same species. Silva Filho et al. (2002) reported that the most efficient P-solubilizing fungi belong to Aspergillus and Penicillium genera. Future research should be done to determine the organic acids released by these PSF, especially by PSF 7. Moreover, evaluation of the ability to improve plant growth and rhizobia and AMF symbiosis under non-sterilized substrate conditions should be done.

CONCLUSIONS

1- Aspergillus niger, PSF 7 and PSF 21 were the best isolates to increase clover growth in the presence of AMF.

2 - High mycorrhizal colonization resulted in greater clover growth rate in most PSF treatments.

3 - The greatest clover growth rate was recorded when Aspergillus niger and PSF 21 were co-inoculated with AMF.

4 - The isolate PSF 7 was the best isolate to increase clover growth and to establish rhizobia and AMF symbiosis.

ACKNOWLEDGMENTS

To Coordenação de Aperfeiçoamento de Pessoal de Nível Superior/ Programa de Doutorado com Estágio no Exterior (CAPES/PDEE) for the scholarship grant.

Manuscript received on May 17, 2009; accepted for publication on February 15, 2010

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Publication Dates

• Publication in this collection
  27 Aug 2010
• Date of issue
  Sept 2010

History

• Accepted
  15 Feb 2010
• Received
  17 May 2009