Journal of Threatened Taxa | www.threatenedtaxa.org | 26 June 2016 | 8(6): 8919–8922

 

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Rediscovery of Penicillium paradoxum (Ascomycete: Aspergillaceae) from Maharashtra, India

 

Kunhiraman C. Rajeshkumar 1, Sayali D. Marathe 2, Sneha S. Lad 3, Deepak K. Maurya 4, Sanjay K. Singh 5 & Santosh V. Swami 6

 

1,2,3,4,5 National Fungal Culture Collection of India, Agharkar Research Institute, G.G. Agarkar Road, Pune, Maharashtra 411004, India

6 Manshya Enviro-Biotech Pvt Ltd., Vrindavan Park, Gokul Nagar, Pune, Maharashtra 411048, India

1 rajeshfungi@gmail.com (corresponding author), 2 sayalim89@gmail.com, 3 sneha.nfcci@gmail.com, 4 deepak.nbaim@gmail.com, 5 singhsksingh@gmail.com, 6 swamisantosh3@gmail.com

 

 

 

 

doi: http://dx.doi.org/10.11609/jott.2569.8.6.8919-8922

 

Editor: R.K. Verma, Tropical Forest Research Institute, Jabalpur, India. Date of publication: 26 June 2016 (online & print)

 

Manuscript details: Ms # 2569 | Received 22 February 2016 | Final received 10 May 2016 | Finally accepted 13 June 2016

 

Citation: Rajeshkumar, K.C., S.D Marathe, S.S. Lad, D.K. Maurya, S.K. Singh & S.V. Swami (2016). Rediscovery of Penicillium paradoxum (Ascomycete: Aspergillaceae) from Maharashtra, India. Journal of Threatened Taxa 8(6): 8919–8922; http://dx.doi.org/10.11609/jott.2569.8.6.8919-8922

 

Copyright: © Rajeshkumar et al. 2016. Creative Commons Attribution 4.0 International License. JoTT allows unrestricted use of this article in any medium, reproduction and distribution by providing adequate credit to the authors and the source of publication.

 

Funding: Department of Science and Technology (DST), Government of India, New Delhi (under scheme No. SP/SO/PS-55/2005).

 

Conflict of Interest: The authors declare no competing interests.

 

Acknowledgements: We thank the Department of Science and Technology (DST), Government of India, New Delhi for providing financial support. Dr. K.M. Paknikar, Director, ARI Pune for facilities and Dr. S.M. Ghaskhadbi, Coordinator, Biodiversity and Palaebiology for suggestions and advice. RKC also thankful to Dr. Rahul Sharma for backing in molecular studies.

 

 

 

Abstract: Penicillium paradoxum has an enigmatic Aspergillus-like anamorphic state; earlier named as Aspergillus paradoxus with a teleomorph state Hemicarpenteles paradoxus. The present paper describes the rediscovery of this species from India after five decades and includes a phylogenetic study of this strain. This is the first record of this strain from peninsular India including the Western Ghats.

Keywords: Anamorphic ascomycete, phylogeny, taxonomy, Western Ghats

 

 

 

 

Aspergillus paradoxus Raper & Fennell was described on its type strain, NRRL 2162 T, (J.H. Warcup, Isolate No. A-28, January 1948) on opossum dung, Wellington, New Zealand (Raper & Fennell 1955) and WB 4695 (J.N. Rai, IMI 86829, 1962), in flood inundated soil (Gomti River) from Lucknow, India. The species forms clavate vesicles, uniseriate conidiophores and abundant sclerotia and therefore Raper & Fennell (1955) placed this species in the Aspergillus ornatus-group. Afterwards, Sarbhoy & Elphick (1965) recollected A. paradoxus from dog excreta from Knole Park, Kent (IMI 117502) which formed cleistothecia, globose asci and lenticular ascospores having equatorial crusts. The teleomorph state was named as Hemicarpenteles paradoxus A.K. Sarbhoy & Elphick.

The exploration and ex situ conservation of fungal biological resources of the Western Ghats is the leading goal of the National Fungal Culture Collection of India (NFCCI-WDCM 932). During January 2011 a survey was conducted to study the microfungal diversity in the natural forests of Mahabaleshwar and the surrounding forests situated in the northern part of the Western Ghats, India, between 17058’N and 73043’E. The Mahabaleshwar forests consist of unique stunted semi evergreen patches which form suitable microhabitats for many rare and new species of fungi (Rajeshkumar et al. 2011a,b). During the survey, an unusual mycelial growth associated with carnivorous animal excrement (containing feathers and bones) was collected. The morphological characterization of the isolate showed taxonomic affinity with genus Aspergillus. Partial β-tubulin (BenA) gene sequences were generated as a step toward accurate identification and to study the position of the species among other closely related species.

Materials & Methods

Isolates and morphology: The highly sporulated fungal mycelia formed in plenty on the animal excrement were directly isolated using a Nikon binocular stereo microscope (Model SMZ 1500 with Digi-CAM, Japan) and plated on 2% MEA and further sub-cultured on CREA, CYA, CZA, G25N, MEA and OMA media (Image 1). For morpho-taxonomic studies and photomicrographs a Carl Zeiss Image Analyzer 2 (Germany) microscope was used. Dimensions of conidiophores, phialides and conidia were measured using the software Axiovision Rel 4.8. The specimens were deposited in Ajrekar Mycological Herbarium (AMH 9426) and an axenic culture was deposited in National Fungal Culture Collection of India (NFCCI 2356), Agharkar Research Institute, Pune, India.

DNA extraction, amplification and phylogeny: Fungal colonies were grown on MEA plates, and genomic DNA was isolated following the rapid salt-extraction method (Aljanabi & Martinez 1997). A fragment of the BenA gene was amplified using primer pairs Bt2a and Bt2b (Glass & Donaldson 1995). The PCR conditions, sequence alignment and subsequent phylogenetic analysis followed the methods of Houbraken & Samson (2011). Analyses were carried out in MEGA6 (Molecular Evolutionary Genetics Analysis version 6.0.) on the BenA data set using the Maximum Parsimony method with 1000 bootstrap replications. Sequence data were deposited in GenBank.

Results

Penicillium paradoxum (Fennell & Raper) Samson, Houbraken, Visagie & Frisvad. MycoBank 547045.

Basionym: Aspergillus paradoxus Fennell & Raper, Mycologia 47: 69. 1955. MB292853

Type description: Colonies at 250C after 10 days to two weeks, 7–8 cm. fast growing, deep flocculent mass in light yellow shades near marguerite yellow to primrose yellow, bearing limited to fairly abundant conidial structures primarily from the submerged mycelium. Conidial heads loosely columnar, up to 150–200 µm, or smaller. Conidiophores 1–2 mm (up to 1cm) × 12–20 µm, thin walled, delicately roughened, several times septate, strongly phototropic; Vesicles subclavate, 15–25 µm in diameter, seldom larger. Sterigmata in a uniseriate, 10–12 × 3.5–5.5 µm, borne on the terminal portion of the vesicular areas, with tips often incurved. Conidia ovoid, delicately echinulate, 5.5–6.5 × 4.0–5.0 µm.

Material examined: AMH 9426, Mahabaleshwar, Maharashtra State, India 17058’N & 73043’E, on carnivorous animal excrement, Ajrekar Mycological Herbarium, coll. K.C. Rajeshkumar and S.V. Swami; axenic culture NFCCI 2356, 30.i.2011. GenBank: KT201347.

AMH 9426 (Image 2): Colonies persistent white to off white in nature, Conidiophores 300µm ˗ 1.2cm. Vesicles larger, clavate, up to 50–63.5 µm wide, Conidiophores in single series, phialides ampulliform, apical pore broad, 15–21 × 4–5.5 µm. Conidia mostly ellipsoid, subglobose or variously shaped, smooth, hyaline, 5.5–9.7 × 3.5–5.7 µm.

Phylogenetic analyses: β-tubulin (KT201347): based on MegaBLAST search of NCBI GenBank nucleotide database, the closest hits using the BenA gene sequences are Hemicarpenteles paradoxus strain IBT 17513 (GenBank FJ530992.1, Identities = 373/373(100%), Gaps 0/373(0%), Aspergillus paradoxus isolate NRRL 2162 (GenBank EF669683.1, Identities = 373/373(100%), Gaps = 0/373(0%) and Hemicarpenteles paradoxus strain IBT 19365 (Genbank = FJ530993.1, Identities = 372/373(99%), Gaps = 0/373(0%). The analyses using BenA gene sequences revealed that the isolate NFCCI 2356 is closely related to Hemicarpenteles paradoxus and Aspergillus paradoxus (current name Penicillium paradoxum) and phylogenetically formed a unique monophyletic lineage in Penicillium sensu stricto (Aspergillaceae) (Fig. 1).

 

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Discussion

The taxonomic characterization and literature review revealed that P. paradoxum (as A. paradoxus) is only recorded from Lucknow (Rai et al. 1964) and has never been isolated and recorded so far from India. The present collection is also evident that P. paradoxus is associated with a unique microhabitat namely animal excrements as this species was found earlier in New Zealand (NRRL 2162) and England (IMI 117502). Peterson (2008) analysed the relationships of Aspergillus using a four gene loci (β-tubulin, calmodulin, ITS and LSU and RNA polymerase II (RPB2) sequences) stated that H. paradoxus is phylognetically associated with members of the Eupenicillium clade. Similarly, Varga et al. (2007), excluded H. paradoxus from the Aspergillus section Clavati and stated its affinity with Penicillium species. Houbraken & Samson (2011) revolutionized the concepts of Penicillium and Aspergillus taxonomy and segregated Trichocomaceae into three separate families Aspergillaceae, Thermoascaceae and Trichocomaceae. Their phylogenetic analysis also positioned the genus Hemicarpenteles under the Penicillium sensu stricto clade. Recently while redefining the genus concept of Penicillium to accommodate in the one-fungus-one-name concept (as per International Code of Nomenclature for algae, fungi and plants) Visagie et al. (2014) combined A. paradoxus with Penicillium paradoxum and positioned this species in the Penicillium section Paradoxa. The present taxonomic study and phylogenetic analysis from the Western Ghats, India also placed P. paradoxum under the Penicillium section Paradoxa in accordance with the current concepts of Aspergillaceae.

 

References

Aljanabi, S.M. & I. Martinez (1997). Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acids Research 25(22): 4692–4693; http://dx.doi.org/10.1093/nar/25.22.4692

Fennell, D.I. & K.B. Raper (1955). New species and varieties of Aspergillus. Mycologia 47: 68–89; http://dx.doi.org/10.2307/3755757

Glass, N.L. & G.C. Donaldson (1995). Development of premier sets designed for use with the PCR to amplify conserved genes from filamentous Ascomycetes. Applied and Environmental Microbiology 61: 1323–1330.

Houbraken, J. & R.A. Samson (2011). Phylogeny of Penicillium and the segregation of Trichocomaceae into three families. Studies in Mycology 70: 1–51; http://dx.doi.org/10.3114/sim.2011.70.01

Peterson, S.W. (2008). Phylogenetic analysis of Aspergillus species using DNA sequences from four loci. Mycologia 100: 205–226; http://dx.doi.org/10.3852/mycologia.100.2.205

Rajeshkumar, K.C., R.P. Hepat, S.B. Gaikwad & S.K. Singh (2011a). Pilidiella crousii sp. nov. from northern Western Ghats, India. Mycotaxon 115: 155–162; http://dx.doi.org/10.5248/115.155

Rajeshkumar, K.C., R. Sharma, R.P. Hepat, S.V. Swami, P.N. Singh & S.K. Singh (2011b). Morphology and molecular studies on Pseudocercospora kamalii sp. nov. a foliar pathogen on Terminalia from India. Mycotaxon 117: 227–237; http://dx.doi.org/10.5248/117.227

Rai, J.N., J.P. Tewari & K.G. Mukerji (1964). Cultural and taxonomic studies on two rare species of Aspergillus - A. paradoxus and A. aeneus, and an interesting strain of A. variecolor from Indian soils. Mycopathologia et Mycologia Applicata 24: 369–376; http://dx.doi.org/10.1007/BF02053650

Sarbhoy, A.K. & J.J. Elphick (1968). Hemicarpenteles paradoxus gen. & sp. nov.: the perfect state of Aspergillus paradoxus. Transactions of the British Mycological Society 51: 155–157; http://dx.doi.org/10.1016/S0007-1536(68)80137-8

Varga, J., M. Due, J.C. Frisvad & R.A. Samson (2007). Taxonomic revision of Aspergillus section Clavati based on molecular, morphological and physiological data. Studies in Mycology 59: 89–106; http://dx.doi.org/10.3114/sim.2007.59.11

Visagie, C.M., J. Houbraken, J.C. Frisvad, S.B. Hong, C.H.W. Klaassen, G. Perrone, K.A. Seifert, J. Varga, T. Yaguchi & R.A. Samson (2014). Identification and nomenclature of the genus Penicillium. Studies in Mycology 78: 343–371; http://dx.doi.org/10.1016/j.simyco.2014.09.001