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. 2010 Nov 26;1(2):197–205. doi: 10.5598/imafungus.2010.01.02.13

Aspergillus sect. Aeni sect. nov., a new section of the genus for A. karnatakaensis sp. nov. and some allied fungi

János Varga 1,2,*, Jens C Frisvad 3, Robert A Samson 1
PMCID: PMC3348773  PMID: 22679580

Abstract

The new species Aspergillus karnatakaensis sp. nov. is described and illustrated. All three isolates of this species were isolated from Indian soil; two from soil under a coconut palm in a coffee plantation in Karnataka, and one from soil in the Machrar river bed in Bansa district. This species is closely related to, but clearly distinct, from A. aeneus based on β-tubulin or calmodulin sequence data. Sequences of the ITS region of these two species are identical. Aspergillus karnatakaensis produced terrein, gregatins, asteltoxin, karnatakafurans A and B and the unknown metabolite, provisionally named NIDU. Aspergillus karnatakaensis belongs to a well-defined clade within Aspergillus subgenus Nidulantes together with eight other species including A. aeneus, A. crustosus, A. eburneocremeus, A. heyangensis, and the teleomorph producing-species Emericella bicolor, E. discophora, E. spectabilis, and E. foeniculicola. This clade is placed in a new section, Aspergillus sect. Aenei sect. nov. All teleomorph species assigned to this section are able to produce sterigmatocystin.

Keywords: Aspergillus subgen. Nidulantes, β-tubulin, calmodulin, Eurotiales, extrolites, ITS, polyphasic taxonomy

INTRODUCTION

Aspergillus subgenus Nidulantes is one of the largest subgenera of the genus Aspergillus, including about 80 species (Peterson 2008, Peterson et al. 2008). Several species of this subgenus have a teleomorph assigned to Emericella (Pitt et al. 2000, Samson 2000, Frisvad & Samson 2004). Species of subgenus Nidulantes are important as opportunistic human pathogens (Verweij et al. 2008, Varga et al. 2008), as producers of various secondary metabolites which are useful for the pharmaceutical industry (e.g. penicillin, echinocandins, ophiobolins), and mycotoxins which are harmful to animals and humans (e.g. aflatoxins, sterigmatocystin; Frisvad et al. 2004, 2005, Frisvad & Samson 2004, Zalar et al. 2008).

During surveys of Aspergillus isolates from soil samples from subtropical regions, two interesting isolates were recovered which did not match any known species of the genus. We used the polyphasic approach, including sequence analysis of parts of the β-tubulin and calmodulin genes and the ITS nrDNA region, macro- and micromorphological analyses, and examination of the extrolite profiles of the isolates to differentiate the new species Aspergillus karnatakaensis sp. nov. We also analysed strains of species which appeared to be closely related to the new species for the production of extrolites and found sterigmatocystin in all species with a teleomorphic state studied and also in Aspergillus ebureocremeus.

MATERIALS AND METHODS

Isolates

The strains used in this study are listed in Table 1.

Table 1. Isolates of Aspergillus and Emericella spp. examined in this study.

Species Strain No.a Substratum, country, location GenBank No.
β-tubulin calmodulin ITS
A. aeneus CBS 128.54T = NRRL 4769 Forest soil, Modilen, Somalia EF652298 EF652386 EF652474
A. crustosus CBS 478.65T = NRRL 4988 Skin scrapings, man, Kankakee, Illinois, USA EF652313 EF652401 EF652489
A. eburneocremeus CBS 130.54T = NRRL 4773 Forest soil, Modien Forest, Somalia EF652300 EF652388 EF652476
A. heyangensis CBS 101751T Placentae of Gossypium sp., Heyang, Shaanxi Province, China FJ491520 FJ491521 FJ491522
A. karnatakaensis CBS 102800T = IBT 22153 Soil under coconut palm in coffee plantation, India, Karnataka EU482438 EU482431 EU482441
A. karnatakaensis CBS 102799 = IBT 22154 Soil under coconut palm in coffee plantation, India, Karnataka EU482436 EU482430 EU482443
A. karnatakaensis NRRL 4649 Soil in the Machrar river bed located in district Bansa, state Madhya Pradesh, India EF652292 EF652380 EF652468
E. bicolor CBS 425.77T Soil from Artemisia grassland, USA, Wyoming, Teton Basin EF652335 EF652423 EF652511
E. discophora CBS 469.88T = IBT 21910 Soil, Spain AY339999 EU443970 EU448272
E. discophora CBS 470.88 = IBT 21911 Forest soil, Spain AY340000 EU443969 EU448266
E. foeniculicola CBS 156.80T Foeniculum vulgare seed, China EU443990 EU443968 EU448274
E. heterothallica CBS 489.65T Soil, Costa Rica EU076369 EU076361 AB248987
E. spectabilis CBS 429.77T Coal mine spoil material, Wyoming, USA, Seminole no. 1 mine EU482437 EU482429 EU482442
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aCultures are deposited in/were obtained from the following collections: CBS, CBS-KNAW Fungal Biodiversity Centre, Utrecht, the Netherlands; IBT, Culture Collection of Fungi, Mycology Group, BioCentrum-DTU, Technical University of Denmark, Lyngby, Denmark; NRRL, Agricultural Research Service Culture Collection, Peoria, IL, USA.

Morphological analysis

For macromorphological observations, Czapek yeast autolysate (CYA), malt extract autolysate (MEA) agar, Yeast Extract Sucrose agar (YES), creatine sucrose agar (CREA), and oatmeal agar (OA) were used (Samson et al. 2010). The isolates were inoculated at three points on each plate of each medium and incubated at 25 °C and 37 °C in the dark for 7 d. For micromorphological observations, microscopic mounts were made in lactic acid from MEA and OA colonies and a drop of alcohol was added to remove air bubbles and excess conidia.

Extrolite analysis

The isolates were grown on CYA and YES at 25 °C for 7 d. Extrolites were extracted after incubation. Five 6 mm plugs of each agar medium were taken and pooled together into the same vial for extraction with 0.75 mL of a mixture of ethyl acetate/dichloromethane/methanol (3:2:1) (v/v/v) with 1 % (v/v) formic acid. The extracts were filtered and analyzed by HPLC using alkylphenone retention indices and diode array UV-VIS detection as described by Frisvad & Thrane (1987, 1993), with minor modifications as described by Smedsgaard (1997). The column used was a 50 × 2 mm Luna C-18 (II) reversed phase column (Phenomenex, CA, USA) fitted with a 2 × 2 mm guard column.

Genotypic analysis

The cultures used for the molecular studies were grown on malt peptone (MP) broth using 1 % (w/v) of malt extract (Brix 10) and 0.1 % (w/v) bacto peptone (Difco), 2 mL of medium in 15 mL tubes. The cultures were incubated at 25 °C for 7 d. DNA was extracted from the cells using the Masterpure™ yeast DNA purification kit (Epicentre Biotechnology.) according to the instructions of the manufacturer. The ITS region and parts of the β-tubulin and calmodulin genes were amplified and sequenced as described previously (Varga et al. 2007a–c).

Data analysis

The sequence data was optimised using the software package Seqman from DNAStar Inc. Sequence alignments were performed by MEGA v. 4.0 (Tamura et al. 2007) and improved manually. For parsimony analysis, PAUP v. 4.0b10 software was used (Swofford 2003). Alignment gaps were treated as a fifth character state and all characters were unordered and of equal weight. Maximum parsimony analysis was performed for all data sets individually using the heuristic search option with 100 random taxa additions and tree bisection and reconstruction (TBR) as the branch-swapping algorithm. Branches of zero length were collapsed and all multiple, equally parsimonious trees were saved. The robustness of the trees obtained was evaluated by 1000 bootstrap replications (Hillis & Bull 1993). Eurotium heterothallica was used as outgroup in these analyses (Houbraken et al. 2007). The alignments were deposited in TreeBASE (<treebase.org/treebase-web/home.html>) under accession number S11027.

RESULTS AND DISCUSSION

Phylogeny

Of the aligned β-tubulin sequences, a portion with 438 positions, including 107 parsimony informative characters, was selected for the analysis; MP analysis of the sequence data resulted in two similar, equally most parsimonious trees (tree length = 289 steps, consistency index = 0.7855, retention index = 0.7919), one of which is shown in Fig. 1. The calmodulin data set consisted of 492 characters, including 188 parsimony informative sites; MP analysis resulted in a single most parsimonious tree (length = 485, consistency index = 0.7402, retention index = 0.8040), which is presented in Fig. 2. The ITS data set consisted of 451 characters, including 43 parsimony informative sites; MP analysis resulted in four equally most parsimonious trees (length = 105, consistency index = 0.8190, retention index = 0.8541), one of which is presented in Fig. 3.

Fig. 1.

Fig. 1.

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One of the two equally MP trees obtained based on phylogenetic analysis of β-tubulin sequence data of Aspergillus sect. Aenei. Numbers above branches are bootstrap support values. Only values above 70 % are indicated.

Fig. 2.

Fig. 2.

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The single MP tree obtained based on phylogenetic analysis of calmodulin sequence data of Aspergillus sect. Aenei. Numbers above branches are bootstrap support values. Only values above 70 % are indicated.

Fig. 3.

Fig. 3.

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One of four equally MP trees obtained based on phylogenetic analysis of ITS sequence data of Aspergillus sect. Aenei. Numbers above branches are bootstrap support values. Only values above 70 % are indicated.

The two isolates from Karnataka, India were found to be closely related to Aspergillus aeneus based on phylogenetic analysis of protein coding sequences (Fig. 1, 2), and had identical ITS sequences to A. aeneus (Fig. 3). One additional isolate also from India, “A. aeneus” NRRL 4649 (= IMI 086833) was found to be conspecific with these two isolates. This isolate was obtained from soil of the Machrar river bed in the district of Bansa, Madhya Pradesh (Rai et al. 1964), and is morphologically similar to the other two Indian isolates. The three isolates are described here as a new taxon, A. karnatakaensis sp. nov. A typical characteristic is the formation of a crust of Hülle cells. The strains were incubated on various media for ascoma production, but in none of the strains were ascomata or ascospores found. Also, a mating experiment with the three strains did not induce ascoma production.

Aspergillus karnatakaensis formed a well-supported clade together with four Emericella species, E. foeniculicola, E. bicolor, E. spectabilis and E. discophora, and four species known to reproduce only asexually, including A. aeneus, A. eburneocremeus, A. crustosus and A. heyangensis on the trees based on calmodulin (Fig. 4), β-tubulin, and ITS sequence data (data not shown). Based on these observations, we describe Aspergillus sect. Aenei sect. nov. to accommodate these species within subgenus Nidulantes. This group of species was originally assigned to section Nidulantes (Raper & Fennell 1965, Christensen et al. 1978, Samson 1979, Udagawa & Muroi 1979, Sun & Qi 1994).

Fig. 4.

Fig. 4.

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Phylogenetic affinities of Aspergillus section Aenei to section Nidulantes based on neighbor-joining analysis of calmodulin sequence data of selected species assigned to these sections. Numbers above branches are bootstrap values. Only values above 70 % are indicated.

Extrolites

Aspergillus karnatakaensis isolates were found to produce karnatakafurans A and B (Manniche et al. 2004), terrein, gregatins, asteltoxin (until now only detected in CBS 102799) and the partially characterised metabolite NIDU. Both gregatins and NIDU are also produced by A. granulosus, while karnatakafurans are produced in common with A. aeneus and A. multicolor. However, phylogenetic analysis of sequence data of A. multicolor (Peterson 2008) and A. granulosus (Houbraken et al. 2007) indicated that they are not closely related to A. karnatakaensis, while A. aeneus is.

Among the other species found to belong to the same clade as A. karnatakaensis, Emericella bicolor produces sterigmatocystin, versicolorins, some anthraquinones, and a polar extrolite with end-absorption; E. foeniculicola produces sterigmatocystin (and many other sterigmatocystin and versicolorin-related compounds), xanthocillin derivatives, and the partially characterized (but common) metabolite DRI; E. spectabilis produces two members of the shamixanthone biosynthetic family (both more polar than shamixanthone itself) and a member of the sterigmatocystin biosynthetic family; A. heyangensis produces a decaturin in common with A. aeneus and A. karnatakaensis and NIDU, while E. discophora produces sterigmatocystin and versicolorins (Zalar et al. 2008). Decaturins are antiinsectan metabolites which have previously been identified in Penicillium species including P. thiersii and P. decaturense (Zhang et al. 2003, Li et al. 2005). Aspergillus eburneocremeus has both sterigmatocystin and mer NF-8054X in common with E. heterothallica. Aspergillus crustosus is different from all these species in producing only PR-toxin and related mycotoxins, and has no extrolites in common with the other species in sect. Aenei. All Emericella species in sect. Aenei produce sterigmatocystin, while the Aspergillus species without a known teleomorph apparently cannot produce it, with the exception of A. eburneocremeus. However, sterigmatocystin is common throughout the different sections of subgenus Nidulantes, and has even been found in sections Ochraceorosei and Flavi (Frisvad et al. 2005). Other extrolites such as shamixanthones, mer NF-8054X and the related emesterones, and terrein have also been found in other species in section Nidulantes. Aspergillus heyangensis is only known from ex-type cultures and re-examination of the cultures showed that the taxon has great similarities with the species mentioned above, including its inability to grow at 37 °C, and the shape of the conidial heads and vesicles, although this species does not produce Hülle cells (Fig. 5). That species also produces the unknown metabolite NIDU, as do A. karnatakaensis and E. discophora (Table 2).

Fig. 5.

Fig. 5.

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Aspergillus heyangensis (CBS 101751). A–C. Colonies incubated at 25 °C for 7 d; A on CYA, B on MEA, C on CREA. D–I. Conidiophores and conidia. Bars = 10 μm.

Table 2. Extrolites produced by members of Aspergillus section Aenei.

Species Culture collection number Extrolites
A. aeneus IMI 069855ii = CBS 128.54 asteltoxin, fumitremorgin B, karnatakafurans, a decaturin, GUUM*
A. crustosus IMI 135819 = CBS 478.65 PR-toxin
A. eburneocremeus IMI 069856 = CBS 130.54 mer-NF 8054X, sterigmatocystin
A. heyangensis CBS 101751 = IBT 29634 a decaturin, NIDU*
A. karnatakaensis IBT 22154 = CBS 102799 asteltoxin, gregatins, karnatakafuran A and B, quinolactacin, terrein, NIDU*, GUUM*
A. karnatakaensis IBT 22153 = CBS 102800 asteltoxin, gregatins, karnatakafuran A and B, physcion, quinolactacin, terrein, NIDU*, GUUM*
A. karnatakaensis IMI 086833ii = WB 4649 a decaturin, karnatakafuran A and B, terrein, GUUM*
E. bicolor CBS 425.77 = IBT 22833 sterigmatocystin
E. discophora CBS 469.88 = IBT 21910 sterigmatocystin
E. discophora CBS 470.88 = IBT 21911 sterigmatocystin, NIDU*
E. foeniculicola CBS 156.80 = IBT 22831 DRI, sterigmatocystin, xanthocillin FA
E. heterothallica WB 5097 = IBT 22604 DRI, emeheteron, sterigmatocystin, mer-NF 8054X, stellatin
E. heterothallica CBS 489.65 = WB 5096 = IBT 22607 DRI*, NIDU*, versicolorins, mer-NF 8054X
E. heterothallica WB 4981 = IBT 22605 DRI*, sterigmatocystin, mer-NF 8054X
E. heterothallica WB 4983 = IBT 22606 DRI*, sterigmatocystin, mer-NF 8054X
E. spectabilis CBS 429.77 = IBT 22891 extrolites with shamixanthone chromophore, trace of sterigmatocystin
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*NIDU, GUUM, and DRI are common extrolites with a characteristic UV chromophore. Their structure has not been elucidated yet.

Aspergillus karnatakaensis Varga, Frisvad & Samson, sp. nov.

MycoBank MB517549

(Fig. 6)

Fig. 6.

Fig. 6.

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Aspergillus karnatakaensis (CBS 102800). A, B. Colonies incubated at 25 °C for 7 d, A on CYA, B on MEA. C, Crusts of Hülle cells,. D, E, and G–I. Conidiophores and conidia. F. Hülle cells. Bars = 10 μm, except F = 100 μm.

  • Coloniis Emericellae similibus. Conidiophoris cum stipitibus laevibus, conidiis subglobosis vel late ellipsoideis. Aggregationibus insignibus cum tegumento ex cellulis globosis efferentibus.

Typus: India: Karnataka, near Chickmagalur, Netraconda Estate, isolated from soil under coconut palm (Cocos nucifera) in coffee plantation, 20 Dec. 1996, J.C. Frisvad (CBS H-20502 -- holotypus, culture ex-holotype CBS 102800).

Colonies on CYA, at 25 °C: 31–37 mm diam after 7 d, reverse orange; on MEA, at 25 °C: 12–19 mm, reverse yellow; on YES, at 25 °C: 33–45 mm, reverse pink to raspberry-red reverse; on OAT, at 25 °C: 16–23 mm, Hülle cells present; on CYA, at 37 °C: no growth to micro-colony (<1 mm); on CREA: weak to moderate growth, no acid production. Conidial heads reddish brown, yellow exudate droplets on CYA colonies. Conidiophores biseriate, smooth, light brown stipes, 2.5–4 μm wide; vesicles subglobose to subclavate, 5–8 μm diam. Conidiogenous cells (phialides) 2–2.5 × 4–5 μm, metulae, 2–3 × 4–6 μm. Conidia globose or rarely subglobose, smooth to finely roughened, Hülle cells produced in crusts, globose to ellipsoidal, thick-walled, hyaline, 75–200 μm diam.

Diagnostic features: Apart from producing gregatins, terrein, and karnatakafuran A and B, isolates of this species produce a series of fluorescing extrolites (more than 33) with characteristic UV spectra. Also distinguished by producing Hülle cells in crusts.

Aspergillus sect. Aenei Varga & Samson, sect. nov.

MycoBank MB517672

  • Sectionis Nidulantium similis, sed taxis cum conidiophoris brunneolis, vesiculis ampulliformibus et capitulis conidiorum biserialibus; statu anamorphoso cum ascosporis laevibus, convexis, aequatorialiter bicristatis; in cultura ad 40 °C haud crescenti.

Typus: Aspergillus aeneus Sappa. 1954.

Species assigned to Aspergillus sect. Aenei form a well-supported clade, basal to section Nidulantes sensu Peterson (2008) based on ITS, β-tubulin, calmodulin, and RNA polymerase 2 sequences (see Fig. 11 in Peterson 2008). The section includes four species able to reproduce both sexually and asexually (Emericella discophora, E. bicolor, E. spectabilis, E. foeniculicola), and five species for which the teleomorph is unknown (A. aeneus, A. eburneocremeus, A. crustosus, A. heyangensis, and A. karnatakaensis). All species are characterised by brownish conidiophores, flask-shaped vesicles, and biseriate conidial heads. Several species produce Hülle cells abundantly in masses (except for A. heyangensis, which does not produce Hülle cells at all). The teleomorph-producing species assigned to this section all have smooth convex ascospores with two equatorial crests. None of the species assigned to this section are able to grow at or above 40 °C. All teleomorph species, together with A. eburneocremeus, are able to produce sterigmatocystin. The relationship of E. spectabilis to A. crustosus has already been suggested by Christensen et al. (1978), while E. discophora was found to be related to E. foeniculicola (Zalar et al. 2008).

Acknowledgments

We are grateful to Dr R Naidu for permission to sample soil for mycological examinations in the Coffee Research Station and associated estates near Chickmagalur, Karnataka, India. Tineke van Doorn helped with the morphological data and Uwe Braun kindly provided the Latin diagnosis. We are also indebted to our referees.

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