- Open Access
Kombocles bakaiana gen. sp. nov. (Boletaceae), a new sequestrate fungus from Cameroon
IMA Fungus volume 7, pages239–245(2016)
Kombocles bakaiana gen. sp. nov. is described as new to science. This sequestrate, partially hypogeous fungus was collected around and within the stilt root system of an ectomycorrhizal (ECM) tree of the genus Uapaca (Phyllanthaceae) in a Guineo-Congolian mixed tropical rainforest in Cameroon. Molecular data place this fungus in Boletaceae (Boletales, Agaricomycetes, Basidiomycota) with no clear relationship to previously described taxa within the family. Macro- and micromorphological characters, habitat, and DNA sequence data are provided. Unique morphological features and a molecular phylogenetic analysis of 304 sequences across the Boletales justify the recognition of the new taxa. Kombocles bakaiana is the fourth sequestrate Boletaceae described from the greater African tropics, and the first to be described from Cameroon.
Numerous genera of sequestrate fungi within Boletaceae (Boletales) have been recognized from various regions of the world, including the widely distributed north temperate Chamonixia, Gastroboletus, and Octaviania, Australasian Rossbeevera, South-East Asian Durianella, Spongiforma, and Rhodactina, Australian Solioccasus and Royoungia, and tropical South American Castellanea, Costatisporus, and Jimtrappea (Binder & Bresinski 2002, Desjardin et al. 2008, 2009, Hailing et al. 2012, Lebel et al. 2012, Orihara et al. 2012a, b, Moreau et al. 2013, Trappe et al. 2013, Smith et al. 2015). For the African tropics, despite a high diversity of non-sequestrate, epigeous Boletaceae known from some areas (e.g. Heinemann & Goossens-Fontana 1954), known sequestrate Boletaceae are currently limited to a single species each of Mackintoshia, Mycoamaranthus, and Octaviania (Dissing & Lange 1962, Castellano et al. 2000, Mueller et al. 2007, Pacioni & Sharp 2000, Tedersoo & Smith 2013). Of late, the sequestrate Lactarius megalopterus (Russulaceae) was described from lowland rainforests of Cameroon (Beenken et al. 2016). Our recent collecting in the Dja Biosphere Reserve of southern Cameroon discovered a number of sequestrate fungi, including the first continental African records for Elaphomyces ascomata from native plant communities (Castellano et al. 2016). Included in the Dja Biosphere Reserve collections is a morphologically distinctive fungus that produces basidiomata gregariously in soil in lowland, mixed tropical rainforests in close proximity to ectomycorrhizal (ECM) trees of the genus Uapaca (Phyllanthaceae). Molecular and morphological data indicate that this Cameroonian sequestrate fungus is a member of Boletaceae but is evolutionarily distinct from all other described epigeous and sequestrate genera and species within the family.
Materials and Methods
Basidiomata were collected during the August—September early rainy season of 2014 from Cameroon’s Dja Biosphere Reserve, Northwest Sector near the village of Somalomo, Upper Dja River Basin, ∼1.4 km west of a base camp located at 3°21′29.8″ N 12°43′46.9″ W, 650 m a.s.l., in mixed forest containing Uapaca species (Peh et al. 2014).
Descriptions of macromorphological features are from fresh material in the field. Colour terms follow Kornerup & Wanscher (1978) and are cited in parentheses (e.g. 5A4). Collections were dried with silica gel. Preserved specimens were later examined in 3 % KOH, Melzer’s reagent, and Cotton blue. Microscopic descriptions are based on 3 % KOH mounts unless specified otherwise. Twenty basidiospores were measured from the type collection. Dried basidiospores were mounted on aluminum pegs with double-sided tape and coated with gold for scanning electron microscopy (SEM) with an AmRay 3300 FE field emission scanning electron microscope using 5 kV. Type specimens are deposited in the following herbaria: YA (Cameroon National Herbarium, Yaoundé); HSC (Humboldt State University, Arcata, CA); OSC (Oregon State University, Corvallis); K(M) (Fungarium, Royal Botanic Gardens, Kew).
DNA extraction, PCR amplification, and sequencing
All DNA work was carried out in the Jodrell Laboratory, Royal Botanic Gardens, Kew. DNA extractions were performed on dried basidioma tissue using the Extract-N-Amp Plant PCR kit (SIGMA-ALDRICH, Saint Louis, MO), followed or not by plate filtration (Dentinger et al. 2010), or using a Plant DNeasy mini kit (QIAGEN, Valencia, CA). Full ITS 1 and 2 regions, along with the 5.8S rDNA (ITS), were PCR-amplified with primers ITS1F and ITS4 (White et al. 1990, Gardes & Bruns 1993), and the nuclear 28S rDNA D1–D2 domains (28S) were PCR-amplified with LR0R/LR5 (Vilgalys & Hester 1990) following the cycling conditions in Dentinger et al. (2010). PCR products were visualized by UV-fluorescence after running out 2 µL PCR products in a 1 % agarose gel containing 0.005 % ethidium bromide. Prior to sequencing, amplicons were cleaned of unincorporated dNTPs and excess primers by adding 1 µL ExoSAP-IT (USB, Cleveland, OH) to 5 µL PCR reaction mix and incubating for 15 min at 37 °C followed by 15 min at 80 °C. Unidirectional dye-terminator sequencing used BigDye3.1 (Applied Biosystems, Foster City, CA) by adding 2 µL of cleaned PCR template to 3 µL of solution containing 0.2 µL BigDye, 1 µL sequencing buffer, 0.15 µL 50mM MgCl2, 0.15 µL of 10 µM primer, and 1.5 µL of Milli-Q (Merck Millipore, Darmstadt, Germany) purified water. Sequencing was performed with 60 cycles of 95 °C denaturation for 10 sec, 50 °C annealing for 10 sec, and 60 °C extension for 2 min. Sequencing reactions were cleaned using ethanol precipitation and resuspended in purified water before loading into an ABI 3730 DNA Analyzer (Applied Biosystems, Foster City, CA). Complementary unidirectional sequence reads were aligned and edited in Sequencher v. 4.2 (Gene Codes, Ann Arbor, MI) and deposited in GenBank (ITS: KX827004; 28S: KX827003).
Taxa used, sequence alignment, and phylogenetic analysis
The ITS ribosomal DNA sequence from the new taxon was initially subjected to a BLASTn query against GenBank in order to explore its putative phylogenetic relationships. To further assess phylogenetic affinities of the new fungus, we used Maximum Likelihood (ML) analysis of an ultra-large alignment of all ITS sequences from the UNITE general release v. 7 (release date 31 Jan. 2016) (Nilsson et al. 2015) classified as Boletaceae and identified as full-length by ITSx (Bengtsson-Palme et al. 2013), excluding two misclassified sequences. The final ITS dataset consisted of 717 sequences. We also used ML analysis of a large dataset based on 28S sequences of diverse Boletaceae with additional Boletales taxa as outgroups. The 28S analysis included our original sequence data, 288 sequences used in Wu et al. (2014), seven sequences from sequestrate genera used in Smith et al. (2015), and eight sequences from the Heimioporus species used in Hailing et al. (2015). The final dataset consisted of 304 sequences representing species from infrafamilial clades across the Boletaceae based on recent studies (e.g. Nuhn et al. 2013, Wu et al. 2014, 2015, Smith et al. 2015, Henkel et al. 2016) and outgroup taxa. Representatives from all available sequestrate Boletaceae genera were included: Castellanea, Chamonixia, Costatisporus, Durianella, Gymnogaster, Heliogaster, Jimtrappea, Mackintoshia, Mycoamaranthus, Neoboletus, Octaviania, Rossbeevera, Royoungia, Solioccasus, and Spongiforma.
Each dataset was aligned separately using default settings in PASTA (Mirarab et al. 2015). For both datasets, phylogenetic analysis under the ML criterion was performed using the Pthreads parallelised version of RAxML v. 8.2.4 (ITS) or v8.2.9 (28S) (Stamatakis 2006, Ott et al. 2007) with a GTRGAMMA model, allowing model parameters to be estimated for each gene partition separately. Branch support was assessed using nonparametric bootstrapping with the autoMRE option. The alignments and trees have been deposited in TreeBASE and are available at https://doi.org/purl.org/phylo/treebase/phylows/study/TB2:S19818.
BLASTn queries and phylogenetic analysis
Using GenBank BLASTn queries of the new taxon’s ITS sequence, the top 100 best hits all belonged to Boletaceae but were uninformative at the generic level. The sequence from the new taxon was, however, nearly identical (99 % over 606 nucleotides) to a sequence (FR731937) from an ECM root tip of Uapaca guineensis from Gabon sampled by Tedersoo et al. (2011). The BLASTn matches to remaining sequences in GenBank covered only a maximum of 79 % of the query sequence with 86 % identity. Final alignments for phylogenetic analysis consisted of 717 sequences and 4009 aligned positions for the ITS (1476 parsimony informative, 2119 constant, 414 autapomorphic), and of 304 sequences and 1293 positions for the 28S (441 parsimony informative, 634 constant, 140 autapomorphic). All characters were included in the analysis of both datasets. For the ITS dataset, RAxML rapid bootstrapping terminated after 350 replicates (WRF average of 100 random splits = 2.603297) and the best ML tree had a likelihood score of −60202.046042. For the 28S dataset, RAxML rapid bootstrapping terminated after 300 replicates (WRF average of 100 random splits = 2.696777) and the best ML tree had a likelihood score of −31601.477718 (Fig. 1). Asecond analysis of the 28S dataset after removing ambiguously aligned regions in GBLOCKS (Castresana 2000) with the option to allow gap positions in the final blocks (468 positions retained) failed to recover a monophyletic Boletaceae, evidence that phylogenetically informative regions were lost (data not shown). In both the ITS and 28S datasets, the new Cameroonian taxon was placed within Boletaceae, but was not nested within, or supported as related to, any previously described epigeous or sequestrate genera. Although the 28S analysis recovered the new taxon in a clade with the epigeous bolete genus Heimioporus, this putative relationship had very low bootstrap support (22 %; Fig. 1), as did other nodes deeper than the terminal clades in the tree.
Kombocles Castellano, T.W. Henkel & Dentinger, gen. nov.
Etymology: Komba and —cles (Gk. suffix m), “Komba the renowned”, referring to the spiritual protector and provider of the forest as recognized by the Baka indigenous people of the type locality of the Dja Biosphere Reserve.
Diagnosis: Distinguished from other Boletaceae by a combination of the following characters: Basidiomata emergent, sequestrate, globose to subglobose. Peridium various shades of brown, unchanging. Gleba brown with irregular off-white veins, unchanging, loculate. Columella absent. Basidiospores asymmetrical, variously shaped from fusoid to allantoid to unevenly ellipsoid, rugulose, yellow-brown, dextrinoid when young, with a distinct hilar appendage. Cystidia and clamp connections absent.
Type species: Kombocles bakaiana Castellano et al. 2016.
Kombocles bakaiana Castellano, T.W. Henkel & Dentinger, sp. nov.
Etymology: Baka and —iana (L. suffix adj.), i.e. “of the Baka” referring to the Baka indigenous people inhabiting the type locality.
Diagnosis: Differs from other known sequestrate taxa by the combination of the pale cream to light yellowish brown peridium, gleba with brown locules unevenly surrounded by bright white to off-white tramai tissue, lack of a columella, yellow-brown basidiospores that appear smooth under light microscopy but rugulose under SEM, are dextrinoid when young with a distinct hilar appendage, uniquely long sterigmata, and absence of cystidia.
Type: Cameroon: East Province: Dja Biosphere Reserve, Northwest Sector near the village of Somalomo, Upper Dja River Basin, ∼1.4 km west of Dja base camp located at 3°21′29.8″ N 12°43′46.9″ W, in mixed forest, around and in between the stilt roots of Uapaca sp., near Gilbertiodendron dewevrei monodominant plot 3, 25 Sept. 2014, Henkel THDJA 136 (YA 66911 —holotype; HSC G1203, OSC 150017, K(M) 205361 — isotypes.) GenBank accession numbers ITS: KX827004; 28S: KX827003.
Description: Basidiomata irregularly globose to subglobose, 10–20 mm tall, 15–25 mm broad, firm throughout development; surface pale cream to light yellow brown (4A2–5C4), inherently smooth but with numerous adherent soil particles, occasionally with irregularly spaced cracks revealing the underlying gleba, unchanging with handling but drying rugose to ruminate with numerous shades of brown and darker, humic-stained patches. Peridium two-layered in cross-section; outer layer < 0.5 mm thick, concolorous with the surface but somewhat mottled due to uneven distribution of humic stains, underlain by an inner, pale yellowish (1A2–1A3) layer up to 1 mm thick that becomes cottony near the gleba. Gleba initially marbled, then with increasingly well-defined locules separated by off-white to bright white veins, with clear exudate centrally when cut in mature specimens; locules initially off-white to yellowish orange (4B7) to brown (7E8–7F8) at maturity; locules nearly filled with hymenial elements and basidiospores, irregularly spherical, up to ±1 mm broad. Dried gleba distinctly loculate; locules circular to irregularly polygonal, variably-sized up to 1.1 mm broad, with a dark, thin (± 20 µm) outline, inner portion mottled yellow-brown to medium brown, often with a paler central core, contiguous to irregularly-spaced. Odour mild, pleasant, somewhat sweet. Taste mild, indistinct.
Peridium 220–320 µm thick, two-layered; outer layer ± 20 µm thick but non-uniform in thickness and sometimes absent in small portions of section, of pale yellow-brown tissues that are distinctly and heavily encrusted with minute particles of unknown origin, otherwise of similar structure as underlying inner layer; inner layer 200–300 µm thick, structurally a mix of textura globosa and textura intricata appearing as interwoven tissue with abundant hyaline, elongate, clavate cells, these 26−31 × 13−16(−24) µm, smaller towards peridial surface and larger where the layer adjoins the gleba; walls up to 2 µm thick. Glebal trama similar in structure to the inner peridium but with less elongate hyphae and more clavate or irregularly-shaped cells, variable in thickness to nearly absent, with no apparent color differentiation near the outer locule edge. Basidia elongate, 40−45 × 6−7 µm, hyaline, not rehydrating well; sterigmata four, prominent, 4−8.5 × ± 1µm, hyaline. Basidiospores variably-shaped, fusoid, allantoid to unevenly ellipsoid, asymmetrical in side view, with slight suprahilar depression, smooth under bright field microscopy or faintly roughened with Nomarski imaging, but distinctly rugulose under SEM, in KOH yellow-brown singly and in mass, many distinctly and instantly dextrinoid, particularly those towards the center of some locules, (12.5−)13.5−16.5 × (5−)5.5−6.0 µm (mean 14.3 × 5.7 µm), Q mean = 2.50, range = 1.86−2.67(−3.17) excluding the hilar appendage; hilar appendage prominent, up to 1.5 µm long, hyaline; walls 1.0−1.5 µm thick.
Habit, habitat, and distribution: Scattered and subhypogeous in leaf litter within and around the stilt-root system of an ectomycorrhizal (ECM) Uapaca sp. in mixed forest; known only from the type locality in the Dja River Basin of southern Cameroon. A nearly identical ITS sequence originating from an ECM root tip of U. guineensis from Gabon suggests that the fungus may have a wider distribution in the Guineo-Congolian rainforest.
Commentary: Kombocles bakaiana is recognized in the field by its subglobose basidiomata that remain firm to maturity, pale cream to light yellowish brown peridium, gleba with well-defined locules that are initially white, maturing to yellowish orange and eventually to brown, lack of a columella, and mild odour and taste. Currently basidiomata of K bakaiana are only known in close spatial association with Uapaca trees in forest stands lacking ECM Gilbertiodendron dewevrei trees, and a conspecific ITS sequence has been recovered from a Uapaca root tip from Gabon (Tedersoo et al. 2011), so it may be presumed that Uapaca is the ECM host. Micromorphologically, K bakaiana is distinguished by the variably shaped, asymmetrical, yellow-brown, dextrinoid, smooth basidiospores with a distinct hilar appendage. In the phylogenetic analysis, K bakaiana was putatively sister to the Australasian epigeous bolete genus Heimioporus albeit with very low bootstrap support (Fig. 1). While obviously different macromorphologically (epigeous and non-sequestrate in Heimioporus; hypogeous and fully sequestrate in Kombocles), the basidiospores of H. cooloolae have a somewhat similar shape to those of K bakaiana and are also dextrinoid (though rarely), but differ in having a pitted surface ornamentation compared to the non-pitted basidiospore surface of K bakaiana (Hailing & Fechner 2011, Hailing et al. 2015).
Macromorphologically, K bakaiana is reminiscent of species of Melanogaster and Alpova (Paxillaceae), but the dextrinoid, large, yellow-brown basidiospores allow easy separation from these two genera (Moreau et al. 2011). Microscopically K. bakaiana basidiospores are similar to the smooth, subfusiform basidiospores of Castellanea and Jimtrappea (Boletaceae) from tropical forests in Guyana, but these two genera have symmetrical, pedicellate basidiospores compared to those of K bakaiana that have a distinct hilar appendage and are variably-shaped and asymmetrical (Smith et al. 2015). In addition, Jimtrappea has dextrinoid hymenial cystidia, which are absent in K. bakaiana. Solioccasus (Boletaceae) from Queensland, Australia, has variably shaped, pale yellow basidiospores that are nondextrinoid (Trappe et al. 2008).
Among the few sequestrate putatively ECM fungi known from the African tropics, Mackintoshia persica from Zimbabwe is characterized by smooth, dextrinoid, thick-walled basidiospores that are very similar to those of K. bakaiana (Castellano et al. 2000, Pacioni & Sharp 2000). Mackintoshia persica was initially assigned to Cortinariaceae (Pacioni & Sharp 2000) but recent analyses have revealed that it is a member of Boletaceae (Smith et al. 2015). In contrast to K bakaiana, basidia of M. persica lack distinct sterigmata, hymenial cystidia are present, and the basidiospores are uniformly ellipsoid to broadly ellipsoid. Mycoamaranthus congolensis, known from the Congo, Malawi, and Zimbabwe, while confirmed recently as belonging to Boletaceae (Smith et al. 2015), differs from K bakaiana primarily in the spinose basidiospore ornamentation (Castellano et al. 2000). Octaviania ivoryana, while widespread in Africa, being known from Guinea, Kenya, Senegal, and Zimbabwe, differs fundamentally from K bakaiana in the cone-like ornamentation of its basidiospores (Castellano et al. 2000). While the phylogenetic position of O. ivoryana is currently unknown, other members of the genus are members of Boletaceae (Smith et al. 2015, Orihara et al. 2012a). The sequestrate Corditubera staudtii was originally described from Cameroon, but differs from K bakaiana in the reddish (vs. brown loculate in K bakaiana) gleba and basidiospores that are globose with spinose ornamentation (Hennings 1897).
Beenken L, Sainge MN, Kocyan A (2016) Lactarius megalopterus, a new angiocarpous species from a tropical rainforest in Central Africa, shows adaptations to endozoochorous spore dispersal. Mycological Progress 15: 1–10.
Bengtsson-Palme J, Ryberg M, Hartmann M, Branco S, Wang Z, et al. (2013) Improved software detection and extraction of ITS1 and ITS2 from ribosomal ITS sequences of fungi and other eukaryotes for analysis of environmental sequencing data. Methods in Ecology and Evolution 4: 914–919.
Binder M, Bresinsky A (2002) Derivation of a polymorphic lineage of gasteromycetes from boletoid ancestors. Mycologia 94: 85–98.
Castellano MA, Verbeken A, Walleyn R, Thoen D (2000) Some new and interesting sequestrate Basidiomycota from African woodlands. Karstenia 40: 11–21.
Castellano MA, Dentinger BTM, S’en’e O, Elliott TF, Truong C, Henkel TW (2016) New Elaphomyces species (Elaphomycetaceae, Eurotiales, Ascomycota) from tropical rainforests of Cameroon and Guyana. IMA Fungus 7: 59–73.
Castresana J (2000) Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Molecular Biology and Evolution 17: 540–552.
Dentinger BTM, Ammirati JF, Both EE, Desjardin DE, Hailing RE, et al. (2010) Molecular phylogenetics of porcini mushrooms (Boletus section Boletus). Molecular Phylogenetics and Evolution 57: 1276–1292.
Desjardin DE, Wilson AW, Binder M (2008) Durianella, a new gasteroid genus of boletes from Malaysia. Mycologia 100: 956–961.
Desjardin DE, Binder M, Roekring S, Flegel T (2009) Spongiforma, a new genus of gasteroid boletes from Thailand. Fungal Diversity 37: 1–8.
Dissing H, Lange M (1962) Gasteromycetes of Congo. Bulletin de le Jardin Botanique de I’Etat 32: 325–416.
Gardes M, Bruns TD (1993) ITS primers with enhanced specificity for basidiomycetes — application to the identification of mycorrhizae and rusts. Molecular Ecology 2: 113–118.
Hailing RE, Fechner NA (2011) Heimioporus (Boletineae) in Australia. Australasian Mycologist 29: 47–51.
Hailing RE, Nuhn M, Osmundson T, Fechner N, Trappe J, et al. (2012) Affinities of the Boletus chromapes group to Royoungia and the description of two new genera, Harrya and Australopilus. Australian Systematic Botany 25: 418–431.
Hailing RE, Fechner NA, Nuhn M, Osmundson TW, Soytong K, et al. (2015) Evolutionary relationships of Heimioporus and Boletellus (Boletales), with an emphasis on Australian taxa including new species and new combinations in Aureoboletus, Hemileccinum and Xerocomus. Australian Systematic Botany 28: 1–22.
Heinemann P, Goossens-Fontana M (1954) Flore iconographique des champignons du Congo. Fascicle 3. Boletineae. Brussels: Jardin Botanique de I’Etat.
Henkel TW, Obase K, Husbands D, Uehling JK, Bonito G, et al. (2016) New Boletaceae taxa from Guyana I: Binderoboletus segoi gen. et sp. nov, Guyanaporus albipodus gen. et sp. nov., Singerocomus rubriflavus gen. etsp. nov., and a new combination for Xerocomus inundabilis. Mycologia 108: 157–173.
Hennings P (1897) Fungi camerunenses II. Botanische Jahrbücher für Systematik Pflanzengeschichte und Pflanzengeographie 23: 537–558.
Kornerup A, Wanscher JH (1978) Methuen Handbook of Colour. 3rd edn. London: Eyre Methuen.
Lebel T, Orihara T, Maekawa N (2012) The sequestrate genus Rosbeeva T. Lebel & Orihara gen. nov. (Boletaceae) from Australasia and Japan: new species and new combinations. Fungal Diversity 52: 49–71.
Mirarab S, Nguyen N, Guo S, Wang L, Kim J, Warnow T (2015) PASTA: ultra-large multiple sequence alignment for nucleotide and amino-acid sequences. Journal of Computational Biology 22: 377–386.
Moreau PA, Rochet J, Richard F, Chassange F, Manzi S, Gardes M (2011) Taxonomy of Alnus-associated hypogeous species of Alpova and Melanogaster (Basidiomycota, Paxillaceae) in Europe. Cryptogamie, Mycologie 32: 33–62.
Mueller GM, Schmit JP, Leacock PR, Buyck B, Cifuentes J, et al. (2007) Global diversity and distribution of macrofungi. Biodiversity and Conservation 16: 37–48.
Nilsson RH, Tedersoo L, Ryberg M, Kristiansson E, Hartmann M, et al. (2015) A comprehensive, automatically updated fungal ITS sequence dataset for reference-based chimera control in environmental sequencing efforts. Microbes and Environments 30: 145–150.
Nuhn ME, Binder M, Taylor AF, Hailing RE, Hibbett DS (2013) Phylogenetic overview of the Boletineae. Fungal Biology 117: 479–511.
Orihara T, Smith ME, Shimomura N, Iwase K, Maekawa N (2012a) Diversity and systematics of the sequestrate genus Octaviania in Japan: two new subgenera and eleven new species. Persoonia 28: 85–112.
Orihara T, Smith ME, Ge ZW, Maekawa N (2012b) Rossbeevera yunnanensis (Boletaceae, Boletales), a new sequestrate species from southern China. Mycotaxon 120: 139–147.
Ott M, Zola J, Aluru S, Stamatakis A (2007) Large-scale Maximum Likelihood-based Phylogenetic Analysis on the IBM BlueGene/L. In: Proceedings of ACM/IEEE Supercomputing Conference, Article no. 4. New York: Association for Computing Machinery.
Pacioni G, Sharp C (2000) Mackintoshia, a new sequestrate basidiomycete genus from Zimbabwe. Mycotaxon 75: 225–228.
Peh KS, Sonke B, S’en’e O, Djuikouo MN, Nguembou CK, et al. (2014) Mixed-forest species establishment in a monodominant forest in central Africa: implications for tropical forest invasibility. PLoS One 9: e97585.
Smith ME, Amses K, Elliott T, Aime MC, Henkel TW (2015) New sequestrate fungi from Guyana: Jimtrappea guyanensis gen. sp. nov, Castellanea pakaraimophila gen. sp. nov, and Costatisporus cyanescens gen. sp. nov. (Boletaceae, Boletales). IMA Fungus 6: 263–283.
Stamatakis A (2006) RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22: 2688–2690.
Tedersoo L, Bahram M, Jairus T, Bechem E, Chinoya S, et al. (2011) Spatial structure and the effects of host and soil environments on communities of ectomycorrhizal fungi in wooded savannas and rain forests of Continental Africa and Madagascar. Molecular Ecology 20: 3071–3080.
Tedersoo L, Smith ME (2013) Lineages of ectomycorrhizal fungi revisited: foraging strategies and novel lineages revealed by sequences from belowground. Fungal Biology Reviews 27: 83–99.
Trappe JM, Castellano MA, Hailing RE, Osmundson TW, Binder M, et al. (2013) Australasian sequestrate fungi 18: Solioccasus polychromus gen. & sp. nov, a richly colored, tropical to subtropical, hypogeous fungus. Mycologia 105: 888–895.
Vilgalys R, Hester M (1990) Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. Journal of Bacteriology 172: 4238–4246.
White TJ, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: PCR Protocols: a guide to methods and applications (Innis M, Gelfand D, Sninsky J, White T, eds): 315–322. San Diego: Academic Press.
Wu G, Feng B, Zhu XT, Xu J, Li YC, et al. (2014) Molecular phylogenetic analyses redefine seven major clades and reveal 22 new generic clades in the fungal family Boletaceae. Fungal Diversity 63: 93–115.
Wu G, Zhao K, Li YC, Zeng NK, Feng B, etal. (2015) Four new genera of the fungal family Boletaceae. Fungal Diversity. doi:https://doi.org/10.1007/s13225-015-0322-0.
We thank the following funding sources: The National Geographic Society’s Committee for Research and Exploration grant 9235-13 and National Science Foundation (NSF) DEB-1556338 to T.W.H., and a grant to C.T. from the Basler Stiftung für Biologische Forschung. In Cameroon, the Ministry of Research and Scientific Innovation issued research permits. Jean Michel Onana, Head of The National Herbarium of Cameroon (Institute of Agricultural Research for Development, IRAD) provided much logistical assistance. The Conservator of the Dja Biosphere Reserve, Mengamenya Goue Achille, and his staff greatly assisted the fieldwork in the Dja. Field assistance in Cameroon was provided by Alamane Gabriel (a.k.a. Sikiro), Abate Jackson, Mamane Jean-Pierre, and Mei Lin Chin. James Trappe assisted with the etymology. Two anonymous reviewers provided very helpful comments on an earlier version of the manuscript.
This paper was prepared by USA Government employees on official time, and is therefore in the public domain and not subject to copyright.
About this article
Cite this article
Castellano, M.A., Elliott, T.F., Truong, C. et al. Kombocles bakaiana gen. sp. nov. (Boletaceae), a new sequestrate fungus from Cameroon. IMA Fungus 7, 239–245 (2016) doi:10.5598/imafungus.2016.07.02.03
- false truffle
- Guineo-Congolian rainforest
- hypogeous fungi