Diazotrophic bacteria isolated from wild rice Oryza glumaepatula (Poaceae) in the Brazilian Amazon Bacterias diazotróficas aisladas de arroz silvestre Oryza glumaepatula (Poaceae) en la Amazonia brasileña
Paulo Ivan Fernandes Júnior1*, Gilmara Maria Duarte Pereira2*, Liamara Perin3*, Luana Mesquita da Silva4*, Alexandre Cardoso Baraúna2, Francilene Muniz Alves5*, Samuel Ribeiro Passos6* & Jerri Édson Zilli7*
The association of wild grasses with diazotrophic bacteria in Brazilian biomes is poorly understood. The isolation and characterization of bacteria associated with wild grasses can contribute to understand the diazotrophic ecology as well as to identify bacteria with biotechnological applications. In this study, we isolated and characterized diazotrophic bacterial isolates from Oryza glumaepatula collected in Cerrado and Forest areas of the Amazon ]]>
O. glumepatula plants were collected at five sampling sites at Forest and seven at Cerrado, respectively. The plants were collected at the Cerrado areas in September 2008 while the Forest plants were collected in June/2008 and April/2009. The plants and the soil adhering to the roots were transferred to pots and grown for 35 days in greenhouse conditions. During the harvest, the shoots and the roots were crushed separately in a saline solution; the suspension was diluted serially and inoculated in Petri dishes ]]>
nifH gene. The diversity of nifH+ bacteria was analyzed by Box-PCR fingerprinting. For selected strains, the growth promoting capacity of O. sativa as a model plant was also evaluated. A ]]>
nifH gene fragment. Among the 38 nifH+ isolates, 24 were obtained from the shoots, while 14 originated from the roots. The Box-PCR profiles showed that the bacterial isolates obtained in this study presented a low similarity with the reference strains belonging to the Herbaspirillum, Azospirillum and Burkholderia ]]>
genus. The growth- promoting ability was confirmed for at least five isolates. For these bacteria, the root and shoot growing results showed higher increases when compared to those observed in plants inoculated with the evaluated reference strains. These results indicate that O. glumaepatula is colonized by a high diverse diazotrophic community in the Brazilian Amazon. Further investigations are now being carried out to determine the taxonomic positions of these isolates and their growth ]]>
Resumen ]]>
La asociación de gramíneas silvestres con bacterias diazotróficas en los biomas brasileños es poco conocida. El aislamiento y caracterización de las bacterias asociadas con gramíneas silvestres puede contribuir a entender la ecología de las diazotróficas y bacterias con aplicaciones biotecnológicas. En este estudio, caracterizamos aislamientos bacterianos de diazotróficas de
Oryza glumaepatula recolectadas en Cerrado y zonas boscosas de la Amazonía en el estado de Roraima, Brasil. Plantas sanas de O. glumepatula fueron recolectadas en cinco zonas boscosas y siete en Cerrado. Las plantas de Cerrado fueron recolectadas en septiembre 2008, mientras que las del bosque en Junio 2008 y Abril 2009. Las plantas y el suelo adherido a las raíces se transfirieron a macetas y se cultivaron durante 35 días en condiciones de invernadero. ]]>
nifH. ]]>
nifH+ se analizó por Huella Genética utilizando la Reacción en Cadena de la Polimerasa. Para las cepas seleccionadas, la capacidad de promover el crecimiento de O. sativa como modelo de planta también se evaluó. Se obtuvo un total de 992 cepas bacterianas. Cincuenta y un bacterias fueron capaces de formar películas en el medio semisólido y 38 amplificaron positivamente el fragmento 360bp del gen nifH. De los 38 ]]>
nifH+, 24 fueron obtenidos de los brotes, mientras que 14 se originaron a partir de las raíces. Los perfiles de PCR-Box mostraron que los aislamientos bacterianos obtenidos en este estudio presentaron una baja similitud con las cepas de referencia pertenecientes a Herbaspirillum, Azospirillum y el género Burkholderia. La capacidad promotora ]]>
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Palabras clave: fijación biológica de nitrógeno, bacterias promotoras de crecimiento de plantas, asociaciones no- simbióticas, ecología microbiana, inoculante. Interaction among diazotrophic bacteria and non-legume plants is widely described in scientific ]]>
In Brazil four species of wild rice have been identified and among them Oryza ]]>
Steud (Poaceae) is now indicated as a potential gene source to transfer to rice cultivars by crop breeding, due their similarity in genomic structure (Rangel et al. 2006, Rosa et al. 2006, Veasey et al. 2011). Although the potential of O. glumaepatula as a genetic resource was shown, the interaction of this species with soil microorganisms remains largely unknown and must be investigated. Recent studies have shown that the Amazonian wild rice O. glumaepatula is able to associate with dark septate endophytic (DSE) fungi that are able to colonize the roots of O. ]]>
and O. sativa (Pereira et al. 2011, Ribeiro et al. 2011).
Regarding the diazotrophic community, other studies have also shown that screening of diazotrophic bacteria isolated from wild rice species O. alta Swallen and
O. rufipogon Griff revealed a diverse and efficient diazotrophic community in Asia (Peng et al. 2008, Zhang et al. 2008, Tan et al. 2009). These results indicate the wild rice species as sources of several microorganisms with biotechnological potential. The search for efficient diazotrophic bacteria associated with wild grasses may also result in the obtainment of bacterial strains adapted to harsh conditions and applicable to the inoculation of crop plants. ]]>
In spite of the diazotrophic ability of the microbial community associated with Amazonian O. glumaepatula (Prast & Esteves 1998), there is no information regarding its bacteria isolation and characterization. The aim of this study was to evaluate the diversity and the growth promotion ability of ]]>
O. glumaepatula obtained in Forest and Cerrado areas in the Amazon forest, in Roraima State, Brazil.
Materials and methods
Sample sites, plant cultivation and bacteria isolation: Healthy plants of Oryza glumaepatula were collected at the Cerrado and Forest areas in Roraima State, Brazil. At the Cerrado, seven sites (02°59’6.8” N - 60°21’7.4” W; 02°59’17.5” N; 60°23’26.9” W; 02°58’51.0” N - 60°23’20.8” W; 02°57’58.7” N - 60°21’39.9” W; 02°57’39.1” N; 60°21’20.8” W; ]]>
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The plants were transplanted to pots with the soil adhering to the roots and were maintained in a greenhouse for 35 days. During this period, the plants received weekly 200mL of nitrogen free Hoagland solution (Hoagland & Arnon 1950) and aiming to increase the vegetative growth of these plants, 20mM ammonium sulfate was applied on the 7th and 21st day after the ]]>
th day after transplanting, the plants were collected and cut into shoots and roots. The roots and shoots were then washed separately with tap water and finally washed with sterile distilled water.
Ten grams of each sample (root or shoot) per pot were crushed in a common blender containing 90mL of ]]>
-6 and aliquots of 100μL were, in duplicate, were spread on Petri dishes containing Dyg’s medium (Rodrigues Neto et al. 1986). The Petri dishes were incubated in the dark at 28°C for ten days and, after this period, the colonies, which presented distinct phenotypical characteristics on the same plate, were considered as a single isolate and purified also in the Dyg’s medium.
Assessment of diazotrophic capacity: To assess qualitatively the biological nitrogen fixation (BNF) capacity of the bacteria in micro- aerophilic conditions (Döbereiner et al. 1995, Mantilla-Paredes et al. 2009, Sgroy et al. 2009, Silva & Melloni 2011), the purified isolates were inoculated, in duplicate, in assay tubes containing 5mL of BMGM ]]>
Molecular fingerprinting of the bacterial isolates: The pellicle-forming isolates where grown in liquid Dyg’s medium with constant shaking of 100 revolutions per minute (rpm) during 24 hours. The culture broth was used for the DNA extraction using the DNA extraction kit “RTP Bacteria DNA” (Invitek, Berlin, Germany) according to the manufacturer’s instructions. To amplify the nifH gene the primers PolF (TGCGAYCCSAARGCBGACTC) and PolR (ATSGCCATCATYTCRCCGGA) were used, and PCR conditions described by Poly ]]>
nifH was carried out for all 51 pellicule-forming isolates at three different annealing temperatures as described above. The PCR products were submitted to electrophoresis in agarose gel (12g/L; 120V by 30min) followed by ethidium bromide (0.5g/L) staining and observation in a UV chamber. The amplifications were considered positive to the nifH gene (nifH+) when it was ]]>
The nifH+ isolates were again evaluated according to their capacity to fix nitrogen in micro-aerophilic conditions now in three semi-selective semisolid media: NFb; LGI and ]]>
The nifH+ isolates were also analyzed by Box-PCR profiles. For PCR amplification, the A1 primer (CTACGGCAAGGCGACGCT- GACG) ]]>
Plant growth assay: To evaluate the ability of selected bacterial isolates to promote the plant growth, an assay was performed using the rice (O. sativa) as a model plant. The growth promotion ability of seven selected bacte¬rial isolates, obtained from O. glumaepatula (ERR 1019, ERR 1021, ERR 1028, ERR 1029, ERR 1030, ERR 1038 and ERR 1042), one Herbaspirillum seropedicae (BR 11175) and an A. brasilense (BR 11001), were evaluated. ]]>
The rice seeds (cv. BRS Roraima) were superficially disinfected with ethanol, hydro¬gen peroxide followed by ten washings with sterile distilled water and germinated previ¬ously in Petri dishes containing agar-water medium. The ]]>
Thirty days after inoculation, the ]]>
Results
Bacterial isolation and BNF assessment: In order to assess the higher bacterial diversity inhabiting the tissues of Oryza glumaepatula, we previously isolated the bacteria in the solid medium. This approach allowed to obtain a large number of different bacterial phenotypes reaching a total of 992 isolates (Table 1) of which fifty one were pellicle-forming bacteria, i.e., possessed the capacity to fix nitrogen in micro-aerophilic conditions assessed in semi¬solid BMGM medium. This amount, there¬fore, indicated that around 5% of the bacteria obtained are pellicle-forming. The percentage (5%) of diazotrophic bacteria found in this study agrees with other studies that have shown similar ranges from wild or cultivated rice genotypes with low breeding improvement, applying the same strategy adopted in this study (the isolation and purification of bacteria previously in the solid medium) (Barraquio et al. 1997, Stoltzfus et al. 1997).
Molecular fingerprinting: The PCR reac¬tion showed that 38 bacteria presented positive amplification to the fragment of around 360bp, the size expected for the nifH gene (Fig. 1). The bacterial isolates that did not present positive amplification of nifH gene were considered nifH- while the isolates with positive amplifi¬cation to the 360bp fragment were considered nifH positive (nifH+).
The analysis of the capacity of the bacte¬rial isolates to grow and fix nitrogen on three different media showed that, in the NFb and LGI media, only one bacterial isolate was not able to grow and fix nitrogen in microaerophil¬ic conditions, while in the JMV medium, three of the 38 isolates were not able to grow and presented positive nitrogen fixation. The ability of the bacterial strains to grow and fix N in dif¬ferent media indicates the metabolic versatility of these bacteria that were able to grow with positive N fixation in media with different pH and carbon sources (Mantilla-Paredes et al. 2009, Silva & Melloni 2011).
The Box-PCR fingerprinting obtained from nifH+ isolates showed that most of the bacteria and also the reference strains present different profiles (Fig. 2), indicating a large genetic diversity of these bacteria. It was possible to observe 13 clusters with 60% of similarity. Some of these clusters were formed exclusively with isolates from Cerrado (clusters IV and XII), either from the roots and shoots, while groups I, III and VIII covered only isolates from the shoots. Other peculiarities observed referred to the four groups with a single isolate (from Cerrado) with a high discrepancy to others (Fig. 2). All of the iso¬lates obtained from the O. glumaepatula also showed low similarity to the reference strains indicating the genetic distance between the reference strains and the new bacteria.
Growth promoting assay: The ability of the bacterial strains to promote plant growth was evaluated and we observed that among the eight bacterial strains evaluated, four of them were able to increase the root dry mass compared to the absolute control and the positive controls inoculated with the BR 11001 (A. brasilense) and BR 11175 (H. seropedicae) (Table 2). Three of the isolates were also able to increase the root dry mass of O. sativa more than BR 11001 and BR 11175. It must be pointed out that the isolate ERR 1028 was the only one able to increase both root and shoot biomass of the O. sativa plants, compared to the absolute and the inoculated controls. None of the evaluated reference strains achieved this capacity, which indicates the biotechnological potential of these bacteria.
Discussion
Although only around 5% of the bacterial isolates are able to fix nitrogen in micro-aero¬philic conditions, some of these bacteria may not be isolated if the generally used strategy was applied to obtain the diazotrophic bacte¬rial strains from crop species, during the first isolation step in semisolid medium (Stoltzfus et al. 1997); because the semisolid culture media normally used during these isolations is indicated to obtain the most studied and characterized diazotrophic bacteria such as Azospirillum (Baldani & Döbereiner 1980); Herbaspirillum (Brasil et al. 2005); Burkholdria (Guimarães et al., 2007) and Sphingomonas (Videira et al. 2009).
Among all nifH+ isolates, only 10 bacteria originated from the Forest area (ERR1001; ERR1002; ERR1013; ERR1014; ERR1015; ERR1021; ERR1003; ERR1020; ERR1050 and ERR1019), while 28 were obtained from Cerrado areas (ERR1005; ERR1040; ERR1004; ERR1012; ERR1022; ERR1023; ERR1033; ERR1037; ERR1045; ERR1049; ERR1007; ERR1009; ERR1011; ERR1027; ERR1032; ERR1046; ERR1047; ERR1034; ERR1036; ERR1025; ERR1038; ERR1048; ERR1029; ERR1028; ERR1042 and ERR1030). In addition, most of the bacteria, 24 isolates, were obtained from plant shoots, whereas only 14 from roots. This higher abundance of nifH+ bacteria in Cerrado areas compared to the Forest samples, indicates an ecological adaptation of the wild rice to the environmental conditions. In Cerrado areas, the O. glumaepatula normally presents an annual cycle and the plants originate from seeds that are spread in the soil at the end of the rainy season. The plant growth during this period follows the water availability, and when the water level decreas¬es, the plants reach physiological maturity and disperse the seeds into the environment, which will germinate at the beginning of the next rainy season (Rosa et al. 2006). Instead, in Forest areas, during the larger part of the year, the plants are still in the water because of the drought and flood, which are less prominent. ]]>
It is likely that in these conditions, the well- established Forest plants are less dependent on the associative bacteria then the younger Cerrado plants.
Normally, the studies that evaluate the isolation and characterization of nifH+ bacteria from non-legume plants indicate that the majority of the isolates are obtained from root tissues (Videira et al. 2009, Vendan et al. 2010, Venieraki et al. 2011). However, there is evidence that during the vegetative development of grasses in plots where the water availability ranges from flood to drought, as in the Amazon, more diazotrophs must be isolated from shoots rather than from plant roots (Brasil et al. 2005, Koomnok et al. 2007).
Oryza species are widely colonized by bacteria belonging to the Herbaspirillum, Burkholderia, Azospirillum and other species (Baldani et al. 2009). Genetic evaluations have shown that wild rice species are colonized by a higher diazotrophic community compared to O. sativa (Hurek & Reinhold-Hurek 2005). As we observed in this study, previous evaluations have also shown the low similarity among the strains from wild Oryza, and the reference strains belonging to Herbaspirillum, Burkholderia and Azospirillum (Tan et al. 2009) indicating the presence of new bacteria. The characterization of bacteria from wild Oryza species has also been performed over the last few years and new species (Cheng-Hui & Yokota 2005, Peng et al. 2008) and genera (Zhang et al. 2008) have been described.
DSE fungi were already isolated from Amazonian O. glumaepatula, which are able to colonize and promote the growth of O. sativa (Pereira et al. 2011, Ribeiro et al. 2011). In this study, we found that this species of wild rice is also colonized by diazotrophic plant growth-promoting bacteria with biotechnological potential. The O. glumaepatula has already been indicated as a source of genes for rice breeding programs (Rangel et al. 2006). The recently published studies evaluated the diversity of DSE fungi and the results found in the present study also indicate this species as a source of beneficial microorganisms that must be applied to produce inoculants for rice crops. Further studies are now being carried out to investigate the growth-promoting mechanisms of those bacteria and to evaluate their taxonomic position.
Acknowledgments
To Conselho Nacional para o Desenvolvimento Científico e Tecnológico (CNPq) (MCT/ CNPq/CT-Amazonia 554022/2006-0) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for financial support.
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*Correspondencia: Paulo Ivan Fernandes Júnior: Embrapa Semiárido, BR 428, Km 152, Zona Rural, CEP 56302-970, Petrolina, PE, Brazil. paulo.ivan@embrapa.br Gilmara Maria Duarte Pereira: Universidade Federal de Roraima; Centro de Estudos da Biodiversidade, Avenida Capitão Ene Garcez, 2314, Aeroporto CEP 69304-000, Boa Vista, RR, Brazil. gmdpereira@hotmail.com Liamara Perin: Instituto Federal de Educação, Ciência e Tecnologia de Sergipe, Campus Glória, Rod. Rota do Sertão, s/n°, CEP 49680-000, Nossa Senhora da Glória, SE, Brazil. liaperin@yahoo.com.br Luana Mesquita da Silva: Fundação Nacional de Saúde, Av. Capitão Ene Garcez, 1636, São Francisco, CEP 69304-000, Boa Vista, RR, Brazil. bioluana-rr@hotmail.com Alexandre Cardoso Baraúna: Universidade Federal de Roraima; Centro de Estudos da Biodiversidade, Avenida Capitão Ene Garcez, 2314, Aeroporto CEP 69304-000, Boa Vista, RR, Brazil. alexandre.barauna.bio@gmail.com Francilene Muniz Alves: Faculdade Cathedral de Ensino Superior, Av. Luís Canuto Chaves, 293, Caçari, CEP 69.307-053, Boa Vista, RR, Brazil. francilenemuniz_bio@hotmail.com Samuel Ribeiro Passos: Universidade Federal Rural do Rio de Janeiro, Instituto de Agronomia, Departamento de Solos, Rod. BR 465 km 07, Ecologia, CEP 23890-000, Seropédica, RJ, Brazil. passos.samuel@gmail.com Jerri Édson Zilli: Embrapa Agrobiologia, Rod. BR 465 km 07, Ecologia, CEP 23890-000, Seropédica, RJ, Brazil. jerri.zilli@embrapa.br 1. Embrapa Semiárido, BR 428, Km 152, Zona Rural, CEP 56302-970, Petrolina, PE, Brazil; paulo.ivan@embrapa.br 2. Universidade Federal de Roraima; Centro de Estudos da Biodiversidade, Avenida Capitão Ene Garcez, 2314, Aeroporto CEP 69304-000, Boa Vista, RR, Brazil; gmdpereira@hotmail.com; alexandre.barauna.bio@gmail.com 3. Instituto Federal de Educação, Ciência e Tecnologia de Sergipe, Campus Glória, Rod. Rota do Sertão, s/n°, CEP 49680-000, Nossa Senhora da Glória, SE, Brazil; liaperin@yahoo.com.br 4. Fundação Nacional de Saúde, Av. Capitão Ene Garcez, 1636, São Francisco, CEP 69304-000, Boa Vista, RR, Brazil; bioluana-rr@hotmail.com 5. Faculdade Cathedral de Ensino Superior, Av. Luís Canuto Chaves, 293, Caçari, CEP 69.307-053, Boa Vista, RR, Brazil; francilenemuniz_bio@hotmail.com 6. Universidade Federal Rural do Rio de Janeiro, Instituto de Agronomia, Departamento de Solos, Rod. BR 465 km 07, Ecologia, CEP 23890-000, Seropédica, RJ, Brazil; passos.samuel@gmail.com 7. Embrapa Agrobiologia, Rod. BR 465 km 07, Ecologia, CEP 23890-000, Seropédica, RJ, Brazil; jerri.zilli@embrapa.br ]]>
Received 23-III-2012. Corrected 10-IX-2012. Accepted 18-X-2012. ]]>198012433-43920091203-271199719415-24200529179-1902005551435-1438199519-252001672790-279820112012200742393-39819502010331413-42520082005173-198200733429-435200628423-32200957915-9272008582158-2163201146331-334200115295-1031998189189-19220062011597-105198612162006651-10200985371-3812009441437-1443201135359-371199719425-362009542839-2848201168440-446201048559-565201149525-5341994525-40200929311-192008189431-