Conservation Potentials of Mycorrhizal Fungi Root Cultures of 23 North American Orchids from Herbarium Specimens | Open Access Journals

ISSN: 2320-0189

Conservation Potentials of Mycorrhizal Fungi Root Cultures of 23 North American Orchids from Herbarium Specimens

Jay A Yoder1, Mallory P Dameron1, Savannah M Sullivan1, Lawrence W Zettler2 and Matthew H Collier1*

1Department of Biology, Wittenberg University, Ward Street at North Wittenberg Ave., Springfield, OH, USA

2Department of Biology, Illinois College, Jacksonville, IL, USA

*Corresponding Author:
Matthew H. Collier
Department of Biology, Wittenberg University
Ward Street at North Wittenberg Ave.
Springfield, OH, USA
Tel: 222 (937) 327-6475
E-mail: mcollier@wittenberg.edu

Received Date: 14/12/2017 Accepted Date: 18/12/2017 Published Date: 22/12/2017

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Abstract

Root samples from 23 species of preserved orchid specimens dating back to 1884, and housed in the Jacobs Herbarium at Wittenberg University (Ohio, USA), were sampled for culturable mycorrhizal fungi to determine if herbarium specimens could be enlisted as a source of fungi for conservation purposes (e.g., symbiotic seed germination). Root segments were detached from the specimens, soaked one hour in water, macerated, and immersed in three different types of standard culture media. To verify that this sampling technique was effective, a positive control was established that involved living roots of a greenhouse specimen. After >one week incubation at ambient temperature, seven of 33 orchid herbarium specimens yielded fungal colonies. None of the 800+ Petri plates prepared in this manner yielded living fungus cultures assignable to typical orchid mycorrhizal genera. We conclude that herbarium specimens are generally void of living Rhizoctonia-like fungi, thereby placing a heavier burden on fresh material as a source of these fungi for orchid conservation.

Keywords

Herbarium specimens, Orchid conservation, Pure cultures.

Introduction

Most orchids form a symbiotic relationship with Rhizoctonia-like fungi that include those assignable to Ceratobasidium and Tulasnella [1-6]. Tulasnelloid fungi have been isolated with regularity in North America [7]. These strains are typically extracted from masses of fungal hyphae (pelotons) present in the cortical region of lateral (branch) roots in living specimens. Pure cultures acquired from pelotons are used as a tool for generating large numbers of seedlings in vitro [8].

According to Rasmussen, orchid mycorrhizal fungi are not guaranteed that they are associated with an orchid unless isolated from pelotons [6]. As orchid populations continue to decline, securing material (roots) will become increasingly difficult [6], raising concerns that potentially useful fungi will be lost before they are recovered and safeguarded for use in conservation. This study determines if orchid mycorrhizal fungi could be cultured from herbarium specimens. We are testing the hypothesis that these specimens may represent an untapped resource of orchid mycorrhizal fungi. The Jacobs Herbarium at Wittenberg University (Springfield, OH) was chosen for this study. Methods for preservation and storage used in this herbarium are common for small liberal arts colleges throughout North America. The Jacobs herbarium is a model facility because it contains a mixture of newer (1986) and older (1884) orchid specimens (Figures 1A and 1B). Specimens were preserved and stored on acid-free paper without high heat or drying treatments. To verify the effectiveness of our fungus isolation technique, roots of a live orchid (Phalaenopsis sp.) maintained in the Wittenberg University greenhouse for many years (Figure 1C), was examined to serve as a control.

botanical-sciences-herbarium-specimen

Figure 1: (A) Herbarium specimen of an orchid (Cypripedium calceolus; 1957) showing intact root system taken from the Jacobs Herbarium, (B) magnified view of root system from a century old orchid herbarium pecimen (Goodyera repens; 1898), and (C) live Phalaenopsis sp. from the University greenhouse showing living root system. Photo credit: M. P. Dameron, Department of Biology, Wittenberg University, Springfield, OH (Canon EOS 20D Digital SLR camera; Melville, NY).

Materials and Methods

Sections of roots (1 cm portions) were excised from the orchid, and they were soaked in 20 ml of sterile deionized double-distilled water (DI water) in Syracuse dishes for one hour (fresh water, twice for 30 min). The root portion was then surface sterilized following the method outlined in Zettler [9]. The root portions were then cut into smaller pieces in a 100 × 15 mm sterile Petri dish and covered with 20 ml molten agar: modified Melin-Norkrans agar (MMN), potato dextrose agar (PDA), and modified potato dextrose agar (MPDA, pH lowered to 5.5. with lactic acid) (Fisher Scientific, Pittsburgh, PA). Three different agar media were used in order to obtain as many different fungi as possible. Petri plates were incubated at 20 ± 1°C and total darkness once the agar solidified.

Plates were examined daily by light microscopy (40/100x) for emerging fungal hyphae (each one was an isolate). Hyphae that could not be traced back to the internal content of the root portion were not used. Subcultures for fungal identification were conducted by plating excised hyphal tips as a 1 cm3 block that was placed on to fresh solidified agar media. Fungal identification was based on macroscopic (colony) and microscopic (conidia) characteristics at 1000x under oil. Fungi were identified according to Currah and Barnett and Hunter and by pure culture comparison once spore characteristics appeared [10,11].

Each experiment was replicated three times. Nine 1 cm root portions (main and lateral roots) from each orchid specimen were cut into thirds and plated on each type of agar media. Root samples from a live orchid (Phalaenopsis sp.; n=5 plants in different pots) acted as a control. The numbers of Tulasnelloid isolates from the herbarium specimens to the number of isolates in the control were compared using an analysis of covariance (ANCOVA, P=0.05; SPSS 14.0 for Windows; IBM, Armonk, NY) [12].

Results and Discussion

Seven of the 33 herbarium specimens spanning 23 orchid taxa (n>800 plates) yielded fungi: Corrallorhiza maculata (Rafinesque) Rafinesque (1927, PDA only), Cypripedium acaule Aiton (1965, 1970, PDA only), Cypripedium passerinum Richardson (1973, MPDA only), Goodyera pubescens (Willdenow) R. Brown (1936, MMN only), Liparis liliifolia (L.) Richard ex Lindley (1982, PDA only) Listera cordata (L.) R. Brown (1969, PDA only), Platanthera hyperborean (L.) Lindley (1973, MMN only), and Spiranthes ovalis Lindley (MPDA only) (Table 1). These fungi were identified as common saprophytic molds verified by microscopic examination of asexual propagules and cultural morphology on PDA, consisting of: Mucor (two isolates), Cunninghamella (one isolate), Aspergillus (one isolate), Penicillium (one isolate), Trichoderma (two isolates), and Mycelia sterilia (four isolates). Fungal isolates from Cypripedium passerinum and Spiranthes ovalis appear to require a lower pH, because these isolates are restricted to growth on MPDA that contained lactic acid, pH 5.5. The majority (5/8) of the isolates were acquired from thinner lateral root sections immersed and cultured on MMN (Table 1). Common saprophytic molds were also evident in roots of the live orchid, and these were identified as: Aspergillus niger (one isolate), Penicillium glabrum (two isolates), and Cladosporium cladosporioides (one isolate). In addition, more fungal isolates were acquired from the live orchid than any of the herbarium specimens (P<0.05 in each pairwise comparison), the majority of which were obtained using MMN (Table 1). In contrast, most of the fungi from the herbarium specimens were cultured on PDA (Table 1).

Orchid species (from collection label) Year collected No. fungal isolates on agar media Total
MMN PDA MPDA
Live specimen 2012 5 0 2 7
Phalaenopsis sp. 2008 3 1 1 5
Herbarium specimens 1894 0 0 0 0
Aplectrum hyemale
Corallorhiza maculata 1927 0 2 0 2
Corallorhiza multiflora 1884 0 0 0 0
Corallorhiza odontorhiza 1937 0 0 0 0
Cypripedium acaule 1979 0 0 0 0
1970 0 1 0 1
1968 0 0 0 0
1965 0 1 0 1
1899 0 0 0 0
Cypripedium calceolus 1957 0 0 0 0
Cypripedium passerinum 1973 0 0 1 1
Goodyera oblongifolia 1927 0 0 0 0
Goodyera pubescens 1979 0 0 0 0
1974 0 0 0 0
1973 0 0 0 0
1936 1 0 0 1
Goodyera repens 1898 0 0 0 0
Habenaria clavellata 1912 0 0 0 0
Habenaria hyperborea 1969 0 0 0 0
Habenaria obtusata 1969 0 0 0 0
Habenaria orbiculata 1885 0 0 0 0
Habenaria repens 1968 0 0 0 0
Liparis liliifolia 1982 0 2 0 2
1912 0 0 0 0
1899 0 0 0 0
Listera cordata 1969 0 1 0 1
Orchis spectabilis 1974 0 0 0 0
1894 0 0 0 0
Platanthera hyperborea 1973 1 0 0 1
Spiranthes cernua 1960 0 0 0 0
Spiranthes gracilis 1968 0 0 0 0
Spiranthes ovalis 1966 0 0 1 1
Spiranthes romanzoffiana 1951 0 0 0 0

Table 1. Isolation attempts of endomycorrhizal fungi using three different agar media from orchid herbarium specimens taken from the Jacobs Herbarium (Wittenberg University, Springfield, OH) and live orchid (Phalaenopsis sp.) from the Wittenberg University greenhouse. MMN, modified Melin-Norkrans agar; PDA, potato dextrose agar; MPDA, modified potato dextrose agar (PDA, pH lowered to 5.5 with lactic acid). Data are the number of fungal isolates that were obtained from nine–1 cm portions of roots, three portions on MMN, three portions on PDA and three portions on MPDA.

Fungi recovered from root cortical cells in the live orchid control (Phalaenopsis sp.) matched published descriptions for ubiquitous orchid mycorrhizae, in particular Tulasnelloid fungi (with many examples provided in a review by Currah [13]. Despite inspection of >800 plates, we did not isolate any Rhizoctonia-like fungi from the herbarium specimens in dated (1884) and more recently collected (1986) orchid material. The presence of Tulasnelloid fungi in the live orchid control rules out that our isolation protocol was ineffective. These findings support an earlier report by Zettler et al. [9]. which attempted to isolate mycorrhizal fungi from four orchid specimens housed in the Illinois College Herbarium (Jacksonville, IL) spanning four species: Epidendrum conopseum– syn. E. magnolia Mühlenberg (1995), Goodyera repens (L.) R. Brown (1895), Orchid spectabilis– syn. Galearis spectabilis (L.) Rafinesque (1890), and Platanthera integrilabia (Cornell) Luer (1995). In that study, fungi from cortical pelotons failed to initiate growth on MMN, even in recently preserved specimens collected approximately five years earlier. As to why common molds were successfully cultured whereas orchid mycorrhizal fungi were not remains to be determined, but it is conceivable that mold spores (conidia) might be more resistant to prolonged desiccation on specimens in storage. Although many strains of orchid mycorrhizal fungi do produce spore-like structures they do not typically produce asexual spores common to many of the molds recovered in the present study (conidia, sporangiospores) [13,14].

We emphasize that a living orchid must have a fungal symbiont to allow for proper growth, reproduction and development. Therefore, the orchid specimens we sampled possessed a fungal symbiont, where the specificity of both fungus and host orchid are codependent [15-19]. Although pelotons may be present in the cortical cells of our preserved specimens, they did not produce viable fungal isolates as evidenced by our study. For conservation purposes, targeting herbarium specimens as a source of living orchid mycorrhizal fungi does not appear to be a viable alternative to collecting live material. Thus, conservation programs that enlist mycorrhizal fungi for orchid species recovery projects and symbiotic seed germination will likely require the persistence of extant orchid sites as a source of fresh root material. As natural populations continue to experience environmental degradation accelerated by human activities, securing orchid material for this purpose will become increasingly more difficult in the coming decades [20-22].

Conclusion

We recommend that professional botanists consider sending fresh root samples to specialists (mycologists) from orchid specimens destined for herbaria as one possible mechanism for safeguarding mycorrhizal fungi for conservation purposes [23,24].

Acknowledgments

Special thanks to Dr. Ronald deLanglade, Professor Emeritus, Wittenberg University (Springfield, OH), for his assistance with obtaining orchid voucher specimens from the Jacobs Herbarium. Funded by competitive research grants from Wittenberg University.

References