Mycorrhizal fungi isolated from native terrestrial orchids of pristine regions in Córdoba (Argentina)
Hongos micorrízicos aislados de orquídeas terrestres nativas de regiones pristinas en Córdoba (Argentina)
Agustina Fernández Di Pardo1*,2*, Viviana M. Chiocchio2, Viviana Barrera3*, Roxana P. Colombo1, Alicia E. Martinez1, Laura Gasoni3 & Alicia M. Godeas1
Abstract
Orchidaceae is a highly dependent group on the Rhizoctonia complex that includes Ceratorhiza, Moniliopsis, Epulorhiza and Rhizoctonia, for seed germination and the development of new orchid plants. Thus, the isolation and identification of orchid mycorrhizal fungi are important to understand the orchid-fungus relationship, which can lead to the development of efficient conservation strategies by in vivo germination of seeds from endangered orchid plants. The aim of our work was to isolate and characterize the different mycorrhizal fungi found in roots of terrestrial orchids from Córdoba (Argentina), and, to learn about the natural habit and fungal associations in the Chaco Serrano woodland pristine region. In this study, bloomed orchid root and rhizosphere soil samples were obtained in two times from Valle de Punilla during spring of 2007; samples were kept in plastic bags until processed within 48 hours, and mycorrhizal condition confirmed assessing peloton presence. A total of 23 isolates of the orchideous mycorrhizal Rhizoctonia complex were obtained. The isolates were studied based on morphological characters and ITS-rDNA sequences. Morphological characteristics as color of colonies, texture, growth rate, hyphal diameter and length and presence of sclerotia were observed on culture media. To define the number of nuclei per cell, the isolates were grown in Petri dishes containing water-agar (WA) for three days at 25°C and stained with Safranine-O solution. The mycorrhizal fungi were grouped into binucleate (MSGib, 10 isolates) and multinucleate (MSGim, 13 isolates) based on morphological characteristics of the colonies. We obtained the ITS1-5.8s-ITS4 region that was amplified using primers ITS1 and ITS4. Based on DNA sequencing, isolates Q23 and Q29 were found to be related to species of Ceratobasidium. Isolates Q24 and Q4 were related to the binucleated anastomosis group AG-C of Rhizoctonia sp. The rest of the isolates grouped in the Ceratobasidium clade without grouping. From our knowledge this is the first report of the association of the AG-C testers with terrestrial orchids. A high specificity was observed in the symbiotic relationship. As the mycorrhizal fungal isolates were obtained from native orchids, they could be incorporated in conservation programes of endangered orchids in Argentina.
La Familia Orchidaceae se encuentra estrechamente relacionada con hongos micorrízicos que pertenecen al complejo Rhizoctonia, e incluyen los géneros Ceratorhiza, Moniliopsis, Epulorhiza y Rhizoctonia. Esta asociación ]]>
Rhizoctonia. Estos aislamientos fueron caracterizados con base en caracteres morfológicos y ]]>
Ceratobasidium, aisladas de raíces de orquídeas. Los aislamientos Q24 y Q4 se asocian con el grupo de anastomosis de Rhizoctonia AG-C. Finalmente, se observó una alta ]]>
Terrestrial orchids have mutualistic associations with mycorrhizal fungi that are considered necessary for seed germination and growth of orchid plants (Batty, ]]>
Habenaria hexaptera Lindl. 1835 and Pelexia bonariensis (Lindl.) Schltr. 1920. They have been previously studied for fungal colonization in roots (Richardson, Currah, & Hambleton,1993; Girlanda et al., 2011). The habitat of ]]>
A. achalensis is an endemic species which has been recently included in the red list of the International Union for Conservation of Nature (Vischi, Natale, & Villamil, 2004).
Mycorrhizal fungi of orchids form septate hyphae and coiled structures in the roots known as pelotons within cortical cells (Urcelay, Pasquín, Canovas, & Liébana, 2005). The fungal species mycorrhizal associations have been classified as Rhizoctonia (Vilgalys, & Cubeta, ]]>
Ceratorhiza, Moniliopsis and Epulorhiza (Ma, Tan, & Wong, 2003). This last genus, Epulorhiza, is one of the most common genera forming mycorrhizas with terrestrial orchids (Zelmer, & Currah, 1997).
Since it is difficult to ]]>
The area of Chaco Serrano Woodland in Central Argentina has been dramatically reduced during the past 30 years. Fragmentation of the woodland has reached a dramatic scale, affecting plant reproduction and impairing the regeneration of various ]]>
Material and Methods
Area of study and plant source: The study sites were located at approximately 30°50′ S - 64°30′ W (site A) and 30°51′ S - 64°33′ W (site B) at the Valle de Punilla in Córdoba Province. Overall, the region is classified as subtropical with annual average air temperature of 16°C (10°C in winter and 22°C during summer) and total annual ]]>
Mycorrhizal colonization: In order to confirm mycorrhization, presence of peloton structure was assessed. Orchid roots were washed with tap water and cleared using 10% (w/v) KOH solution. Roots with fungal structures were subsequently stained with 0.05% (w/v) trypan blue in lactoglycerol (1:1:1 lactic acid, glycerol, and water) following procedures described by Phyllips and Hayman (1970). Finally, transversal sections of roots were prepared and observed under a Nikon (Optiphot-2) light binocular microscope at a 100X magnification.
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Fungal isolation: Mycorrhizal fungi were isolated from roots of 23 different orchid plants. The roots were rinsed with tap water to remove debris, and were cut into 1cm length segments. The surfaces of these root segments were sterilized in 10% sodium hypochlorite solution for 3min; then segments were rinsed three times with sterile distilled water. The segments were placed on potato dextrose agar (PDA) in Petri dish plates. The plates were incubated in the dark at 25°C, and microscopic observations were made daily during seven days (Fracchia, Silvani, Flachsland, Terada, & Sede, ]]>
The pure cultures were kept, for further use, on PDA and malt extract-agar (MEA) in tubes containing soil: oat bran (1:2) at 4°C, and in eppendorf tubes with wheat seeds at -20°C. All isolates were included in the collection of the Instituto de Microbiología y Zoología Agrícola ]]>
Morphological and cytological observations: Morphological characteristics determined in the cultures were: the color of colonies, texture, growth rate, number of nuclei per cell, hyphal diameter and length and presence of sclerotia on PDA and MEA. In order to observe the number of nuclei per cell, the isolates were grown in Petri dishes containing water-agar (WA) for three days at ]]>
Growth rates were determined on PDA by measuring the colony diameter in two perpendicular directions every 24h for eight days. The colony diameter includes the diameter of the initial inoculum (5mm). The measurements were carried out in triplicate. Growth data were analyzed with ANOVA and means of different subgroups were compared by Tukey´s test on days four and six. All ]]>
The potential relationship between the mycorrhizal fungal isolates and orchid species was compared by Fisher`s Exact Test, according to data shown in Table 1. ]]>
Molecular analysis: Mycelia grown in potato broth (2mL) was placed in a -80ºC freezer for two minutes, then transfered to a water bath at 95ºC for one minute and macerated with glass beads three times to homogenization. DNA was precipitated with 100% chloroform solution (Harju, Fedosyuk, & Peterson, 2004). The genomic DNA was quantified with a spectrophotometer at 260nm and at 280nm to check interfering substances. ]]>
The ITS1-5.8s-ITS4 region was amplified using primers ITS1 and ITS4 (White, Bruns, Lee, & Taylor, 1990). In a 50μL total volume, 10-100ng genomic DNA was used as template, using 20mM Tris-HCl (pH 8.4), 50mM KCl, 0.2mM dNTPs, 0.2μM primer, 3mM MgCl2, and 0.2U/μL High Fidelity Platinum taq polymerase (Invitrogen). The amplification program was as follows: 1min at 94ºC, 1 cycle; 15s at 94ºC, 15s at 58ºC, 15s at ]]>
The PCR products were purified using the Geneclean Spin kit (Qbiogene), eluted in 30μL ultrapure water. Sequencing was conducted under BigDyeTM Terminator v 3.1 (Applied Biosystems) based on Sanger´s method. The reacted ]]>
For the phylogenetic analysis the multiple alignments were performed with ClustalW in MEGA version 4.0 (Tamura, Dudley, Nei, & Kumar, 2007) among 11 rDNA-ITS sequences from our isolates and the following sequences retrieved from GenBank: ]]>
Waitea circinata (EF429315); Rhizoctonia zeae (AB213595); Epulorhiza albertensis (AF345563); Epulorhiza anaticula (EU218891);
Tulasnella calospora (DQ388045); Rhizoctonia solani AG6-HG-I (AF354102); AG-8 (AF153795); AG-3 (AF153771); AG-10 (AF153800); Ceratobasidiumalbasitensis (HQ680963); Ceratobasidium sp. (JF912482); AG-B(0) (DQ102430); AG-H (AF354089); AG-C (AB290021); AG-12 (AF153805); AG-4 (DQ102449); AG-F (DQ102440); AG-Fb (AB219145.1); AG-L (AF354093); AG-O (AF354094); AG-G (AB196646); AG-A (DQ102417). Cladogram construction was done with NONA (Goloboff, 1999) in Winclada (Nixon, 2002). Heuristic search strategy was performed using Multiple TBR + TBR with 10 000 hold and 1 000 replicates in a matrix of 35 taxa with 397 informative characters. Bootstrap values were calculated from 1 000 ]]>
Results
Isolation of mycorrhizal fungi from orchid roots: All the orchid roots were of characteristic coarse ]]>
Fig. 1A, example of Sacoila australis). All roots were colonized by mycorrhizal fungi, evidenced by the presence of mycorrhizal structures (Fig 1B) and of peloton structures in cells (Fig. 1C). A total of 23 strains were obtained with characteristic morphology resembling the Rhizoctonia group. Ten isolates showed two nuclei per cell, whereas 13 showed multinucleate cells (Table 1).
Morphological identification: The isolated fungi were grouped into morphological subgroup binucleate ]]>
ib) and multinucleate (MSGim) isolates. Further grouping was by colour of the colonies (Table 1). One-factor ANOVA and Tukey contrasts showed that there were no significant differences were found in the length and width of hyphae among all the isolates of mycorrhizal fungi Sclerotia formation on PDA was observed in the isolates: Q23, Q9, Q8, Q28, Q21, Q10, Q13, Q6 and Q29. ]]>
Growth rate was analysis with one-factor ANOVA and Tukey contrasts showed significant different among binucleate morphological subgroups on days four and six (F 4,1=13.94, p<0.01). Also, in the multinucleate subgroups the one-factor ANOVA and Tukey contrasts showed significant differences among subgroups on days four (F4,1= 8.19, p<0.01) and six (F 4,1= 6.39, p<0.05) (Table 2).
Molecular data analysis: Amplification products 600 to 800bp size from ITS1-5.8s-ITS4 region were obtained from one isolate of each subgroup. The sequences of the fungi obtained during this study were deposited at GenBank (Table 1).
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The Parsimony Analysis gave six most likely parsimonious trees, length 1 218 steps with Consistency Index = 60 and Retention Index = 68; 108 suboptimal trees were generated. The strict consensus analysis (Fig. 2) generated 12 clades. The topology shows two main clades: one corresponds to fungal isolates of Epulorhiza/Waitea (65%bv) and the other to isolates of the Rhizoctonia / Ceratobasidium group (100% bv).
The native isolates ]]>
C. albasitensis with 100%bv. The isolate Q23 grouped (77%bv) with Ceratobasidium sp. EE-2011 isolate OP7. The isolates Q24 and Q4 grouped with high bootstrap value (100%) with Ceratobasidium sp. AG-C reference sequence. The rest of the isolates grouped in the Ceratobasidium clade without grouping.
The AG-Bo, AG-A, and AG-12 were found in separate clades and none of them were related with our ]]>
Relationship among different isolates and their corresponding hosts: Fisher’s test showed significant differences (p<0.0001) for the MSGib and MSGim associated to different species of orchids. The specificity among the orchid species collected at the Valle de Punilla and the strains isolated showed the following distribution: H. hexaptera and
C. elatus were colonized by only one group, AG-C (AB290021) and C. albasitensis (HQ680963), respectively. On the other hand, A. achalensis roots were colonized by AG-C and Ceratobasidium sp. (JF912482).
Discussion
Based on the morphological description of the colonies and the growth rate in PDA, it was possible to classify the isolates in ten subgroups. Both binucleate and ]]>
The phylogenetic analysis of the ITS sequences showed that the native isolates were grouped within the Ceratobasidium/Rhizoctonia Clade, independently of the nuclear number. The isolate Q29 is highly similar to C. albasitensis showing that it could belong to that species. Eisold and Grosch (2010) obtained
C. albasitensis, identified as isolate 26/5, from root tips of Dactylorhiza purpurella, so this species is related to orchid’s species (http://dpg.phytomedizin.org/fileadmin/daten/04_Verlag/03_JB/Jahresbericht_2010.pdf).
The isolate Q23 is similar to the Ceratobasidium strain EE-2011 OP7 ]]>
Orchis purpurea (Girlanda et al., 2011). Only isolates Q24 and Q4 were related to known binucleate AG, corresponding to AG-C (AB290021). Although one of them (Q4) is a multinucleate strain, they both present similar morphological characteristics.
It is important to highlight that ]]>
On the other hand, ]]>
Rhizoctonia sp. This result indicates that our isolates may represent a polyphyletic group. However, most AGs have been reported as representing monophyletic units (Vilgalys, & Cubeta, 1994; Shan et al., 2002). ]]>
In agreement with the results reported by Bonnardeaux et al. (2007), we observed different behavior (Bonnardeaux et al., 2007). While some orchid species, such as C. elatus and P. bonariensis, established associations with only one subgroup, others such as S. australis were colonized by more than one ]]>
Rhizoctonia indicate a preference for the colonization of some orchid species. S. australis is the species that mainly contributed to this difference. Although in other species this behavior cannot be ruled out, these results must be confirmed with a larger number of isolates. ]]>
McCormick, Whigham, and O’Neill, (2004), Otero et al. (2005), McCormick Whigham, Sloan, O´Malley, and Hodkinson (2006) and Dearnaley (2007) have established that there is a considerable variation in the colonization of terrestrial orchid roots (Dearnaley, 2007; McCormick et al., 2004; Otero et al., 2005, McCormick et al., 2006). Some species are associated with different fungi along their life cycles. McCormick et al. (2006) reported that Goodyera pubescens is able to ]]>
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The results of this study will contribute to the understanding of the orchid-fungus relationship and consequently to the development and improvement of conservation strategies for endangered orchid species in pristine regions, currently degraded after the high human impact level.
Acknowledgments
The authors wish to thank to University of Buenos Aires (UBA) and the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) for their financial support.
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1. Facultad de Ciencias Exactas y Naturales – Universidad de Buenos Aires (UBA). Avenida Intendente Güiraldes S/N. Ciudad Universitaria. 4to. Piso Laboratorio 12. Ciudad Autónoma de Buenos Aires (CABA), Argentina; afernandez@agro.uba.ar, roxanacolombo@hotmail.com, martae@bg.fcen.uba.ar, godeas@bg.fcen.uba.ar
2. Cát. Microbiología Agrícola y Ambiental. Facultad de Agronomía (FA-UBA) - Instituto en Biociencias Agrícolas y Ambientales (INBA) - CONICET. Avenida San Martín 4453- (1417) Ciudad Autónoma de Buenos Aires (CABA), Argentina; chiocchi@agro.uba.ar
3. Instituto de Microbiología y Zoología Agrícola (IMYZA) - Institución Nacional de Tecnología Agropecuaria (INTA-Castelar). Nicolás Repetto y De Los Reseros s/n - Hurlingham - Buenos Aires, Argentina; barrera.viviana@inta.gob.ar, gasoni.amelia@inta.gob.ar
Received 21-IV-2014. Corrected 01-IX-2014. Accepted 03-X-2014.