Document Type : Research Paper

Authors

1 Department of Biology, College of Science ,University of Anbar , Ramadi - Iraq

2 Department of Biology ,College of Education ,University of Sulaimani , Sulaimaniya-Iraq

Abstract

Unculturable and non sporulating fungi represent a great challenge in studying biotrophic ,endotrophic and mycorrhizal fungal groups. In this study a novel culture dependent technique complemented with PCR was used to detect and identify of unculturable fungi in soil . To develop techniques for cultivation of unculturable fungi for the purpose of expanding studies on fungal biodiversity in soil , Soil Infusion Agar (SIA) was developed . By this technique, from higher dilutions of soil five tiny colonies (less than 1mm in diameter) had grown on SIA after incubation for 1-3 months at 280C , but had not shown growth when replicated on traditional mycological media ,were selected , purified studied culturally and microscopically and identified by molecular methods . Growth of the five clones on PDA, but not Sabouraud Dextrose Agar and Czpak Dox Agar of incubation when a loopful of a colony grown after several successive subculturing on SIA was transferred to PDA. The growth on PDA has been empirically proven due to the inoculums size effect and the period of incubation at 280C. Two fungal specific primer sets (EF4F/ITS4r and EF60F/ITS4r) were used to amplify partial sequences of fungal r RNA gene included ITS sequences .The five partial sequences of the five clones were aligned through the BLASTN phylogenetic analysis against NCBI database which revealed higher identities. The blast tree showed that all clones are neighbor joined to Aspergillus ssp and Pichia sp. These results led us to consider the clones as viable but non culturable fungi (VBNC fungi) like the common phenomenon found in some bacterial species.

Keywords

Main Subjects

[1] Tsui C.K.M., James woodall, wenchen, Levesque C.A., Ama Lau, corD.Schoen, Christiane Baschian, Najafzodeh M.J., and Hoog G.S. 2011. Molecular Techniques for pathogen identification and fungus detection in the environment. IMA fungus .Vol.2. No2: 177-18 .
[2] Zengler K . 2009. Culturing the uncultured proc. Natl .Aead. Sci. USA 99.p.15681-15686.
[3] Giovannoni S.J., .foster RA.Rappe Ms. Epstein S 2007. New Cultivation strategies bring more microbial plankton strategies bring more microbial planjton species into the labrotary Oceanography 20:62-69
[4] Hideyuki Tamaki, Yuji Sekiguchi ,Satoshi Hanada , Kazunori Nakomura ,Nakao Nomura , Masatoshi Matsumura,andYoichiKamagata . 2005. Comparative analysis of bacterial diversity in fresh water Sedimmt of a shallow Eutrophic lake by molecular and Improved cultivation- based techniques Appl Environ Microb.,vol. 71,No.4,p:2162-2169..
[5]Kim Lewis, Slava Epstein, Anthony Donfrio, and LossLLing.2012.Unculturedmicroorganisms as a source of secondary metabolites. The Journal of Antibiotics, 1-9.
[6] Hughes,D.P., S. AndersonN.L.HywelJones, w. Himaman, J.Billen, and J.J Bomsma. 2011. Behavioral Mechanisms and morphological symptoms of zombie ants dying from fungal infction. BMc Ecol. 11:13 Dol:10 .1168/1472-6785-11-13.
[7]Omprakash,YogeshShouche,KamleshJangid,kotka,J.,E.2013.microbial cultivation and the role of microbial resource centers in the omicsera. Appl microbial Biotechnol 97:51-62
[8] DarineTrabels,andRidhaMhamdi , .2013. Microbial incoulants and their impact on soil microbial communities: Areview BiomedRes.Int.863240,
[9] Han I.,Lee T.K.,Han J., Doan T.V., Kim S.B., Park J. 2012. Improved detection of microbial risk of releasing genetically modified bacteria in soil by using massive.sequenceing and antibiotic resistance selection. J Hazard Mat.227-228,172-178
[10] Yang L., LubeckM,andLubeck P.S.2014. Deletion of glucose oxidase changes the pattern of organic acid production in u AMB Express, 4:54.
[11] Singh, Raghukumar .c.,verma p., shouche. Y.2011a .fungal community analysis in the deep-sea sediments of the central Indian Basin by culture- independent approach. Microbial Ecology 61:507-517.
[12] Waksman S.A.1922. A method for counting the number of fungi in the soil.J. Bacteriol. 7: 339- 341.
[13] Nagamani A., Kunwar J.K., and C. Monotrarachary .2006.Hand book of soil fungi.I.K, International pyt. Ltd.
[14] Watanabe T.2012. Quantile forecasts of financial returns using realized garch models. Jap. Economic Rev. 63 (1).
[15] Choi Y.W., Hyde K.D., and W. H. Ho .1999.Single spore isolation of fungi. Fungal Diversity, 3: 29-38.
[16] E. Smit, P. Leeflang, B. Glandorf, J. D. Van Elsas and K. Wernars .1999. Analysis of fungal diversity in the wheat rhizosphere by sequencing of cloned PCR-amplified genes encoding 18S rRNA and temperature gradient gel Electrophoresis. Appl. Environ. Microbiol. 65: 2614–2621, 1999.
[17] White T.J., T. Bruns, S. Lee and Taylor J.W. .1990.Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR Protocols: A Guide to Methods and Applications” In: M. A. Nis, D. H. Gelfand, J. Sninsky and T. J. White, Eds. Academic Press Inc., New York. pp. 315–322.
[18] Weber S,D., N. Hofmann, A. Pilhofer, E. Wanner, E. Agerer, O. Ludwig, A-H. Schleifer, O. Fried .2009. Thediversity of fungi in aerobic sewage granules assessed by 18S rRNA gene and ITS sequence analyses. FEMS Microbiol. Ecol. 68 (2), 246–254.
[19] Bell T.H., Joly S., Pitre F.E., Yergeau E. 2014. Increasing phytoremediation efficiency and reliability using novel omics approaches Trends in Biotechnology 32:271-280.
[20] Ashley Shade , Hogan C.S., Klimowicz A.K., Matthew Linske , McManus P.S., and HandelsmanjJ.O.2012.culturing captures members of the soil rare biosphere. Environ microbial 14:2247-2252.
[21] Pitkaranta M., Meklin T., Hyvarinen A., PaulinL., Auvinen P. , Nevalainen A, et al. 2008. Analysis of fungal Flora indoor dust by ribosomal DNA Sequence analysis, quantitative PCR nd culture. Appl Environ Microb 74:233-244.
[22] Stewart E.J.2012. Growing unculturable bacteria, journal Bacterial 194 (16):415-4160.
[23] Mahatma M.K., Mahatma L.2015 . Soil Suppressive Microorganisms and The Impact on Fungal Wilt Pathogens .p.249- 273
[24] Christel Leyronas, MagaliDuffaud and philippe C. Nicot. 2012. Compared efficiency of the isolation methods for Botrytis cinerra. Mycology. Vol.3, No.4, 221-225.
[25] Nour E.H., Hamza M.A.,Mohamed Fayez, Mohamed Monib, Silke Ruppel and Hegazi N.A. 2012. The crude plant juices of desert plants as appropriate culture media for the cultivation of rhizospheric microorganisms- Journal of Advance Research , 3, 35-43.
[26] Davis K.R., Joseph S.J., and Janssen P.H. 2005. Effects of growth medium, inoculums size, and Incubation time on culturability and isolation of soil bacteria. Applied and environmental microbiology, Vol.71, No.2,p. 826-834
[27] Thomas C., Hill D.M. 2002 . Mabey Culturability, injury and morphological dynamics of thermophilic Campylobacter spp. within a laboratory-based aquatic model system. J. Appl. Microbiol. 92, 433– 442.
[28] Geiser D.M., C. Gueidan, J. Miadlikowska, F. Lutzoni, F. Kauff, V. Hofstetter, E. Fraker, C.L. Schoch, L.Tibell, W.A. Untereiner, and A. Aptroot.2006. Eurotiomycetes: Eurotiomycetidae and Chaetothyriomycetidae. Mycologia, 98, 1053-1064.
 [29] Chenuil A. 2006. Choosing the right molecular genetic markers for studying biodiversity: From molecular evolutionto practical aspects.Genetica, 1, 101-120.
 [30] Y. Al-Doory, M. K. Tolba and H. Al-Ani.1959. On the fungal flora of Iraqi soils. II. Central Iraq .Mycologia. 51 (3),429-439.