Unreported Fungal Species of Didymosphaeriaceae from Soil in Korea Mahesh Adhikari, Sang Woo Kim, Dil Raj Yadav, Hyun Seung Kim, Yong Hyun Um, Youn Su.

Slides:



Advertisements
Similar presentations
Lesson Overview 1.3 Studying Life.
Advertisements

Soil Microbial Diversity by DNA Analysis By: Jonjala Jackson Mentors: Dr. Elica M. Moss, Dr.Shengzuo Fang, and Prof. Ye Tian.
Yaron Fireizen, Vinay Rao, Lacy Loos, Nathan Butler, Dr. Julie Anderson, Dr. Evan Weiher ▪ Biology Department ▪ University of Wisconsin-Eau Claire From.
Phylogenetic Trees Understand the history and diversity of life. Systematics. –Study of biological diversity in evolutionary context. –Phylogeny is evolutionary.
Characterization of microbial communities in a fluidized-pellet-bed bioreactor by DGGE analysis As an extension of the fluidized pellet bed operation used.
Reliability of ITS in Species Identification by Surachit Waengsothorn.
Bioinformatics and Phylogenetic Analysis
Geomicrobiology.
Microbial Diversity.
Brock Biology of Microorganisms
Isolating Unique Bacteria from Terra Preta Systems: Using Culturing and Molecular Techniques as Tools for Characterizing Microbial Life in Amazonian Dark.
We are developing a web database for plant comparative genomics, named Phytome, that, when complete, will integrate organismal phylogenies, genetic maps.
Methods in Microbial Ecology
The Sorcerer II Global ocean sampling expedition Katrine Lekang Global Ocean Sampling project (GOS) Global Ocean Sampling project (GOS) CAMERA CAMERA METAREP.
A Decade of Altered Temperature Affects Soil Fungal Communities Matt Belus Dr. Bruce Hungate, Dr. George Koch, Rebecca Mau Northern Arizona Department.
DNA BARCODING CHILLIES BIO-NERDS : Say Wah Yugraj Singh Tanja Obradovic Jenny Pham Lovita Bharossa Buai Chuol Diana Corzo.
Unit 1: The Language of Science  communicate and apply scientific information extracted from various sources (3.B)  evaluate models according to their.
Drivers of Soybean Rhizobia Diversity in Un-inoculated Soils of Smallholder Farms in Malawi. Parr M 1, Shumba L 2, Snapp S 3, and Grossman J Department.
Compare and contrast prokaryotic and eukaryotic cells.[BIO.4A] October 2014Secondary Science - Biology.
Library screening Heterologous and homologous gene probes Differential screening Expression library screening.
SEMIARID GRASSLAND: Soil and root-associated fungal communities Dominant root-associated fungi Methodology Bouteloua gracilis, B. eriopoda, Sporobolus.
Roadmap for Soil Community Metagenomics of DOE’s FACE & OTC Sites
2. Objective To develop early, sensitive and specific detection methods for P. horiana 3. Materials and methods Two different strategies were explored:
FISH SPECIES IDENTIFICATION AND BIODIVERSIFICATION IN ENUGU METROPOLIS RIVER BY DNA BACODING PRESENTED BY Chioma Nwakanma (PhD) Michael Okpara University.
An Introduction to the Inquiry Page and the Biology Workbench An Introduction to the Inquiry Page and the Biology Workbench Anu Murphy Department of Molecular.
Studying Life Vodcast 1.3 Unit 1: Introduction to Biology.
Comparison of the Bacterial Community Naturally Occurring on Spinach Seeds and Seedlings Phyllis Carder 1,2, Gabriela Lopez-Velasco 1, Monica Ponder 1.
Comparing DNA Sequences to Understand Evolutionary Relationships with BLAST INVESTIGATION 3 BIG IDEA 1.
Supplementary Fig. S1. 16S RNA Neighbor-joining (NJ) tree of Brevibacterium metallicus sp. nov. NM2E3 T (in bold) and related species of genus Brevibacterium.
الدكتورة أسماء الصالح رقم المكتب 5T201 الموقع : إيميل
Biogeochemical Cycling and Introductory Microbial Ecology
Phylogeography of Leucetta chagosensis (Porifera, Calcarea) Christoph Flucke, Jens Kurz, Rasmus Liedigk, Zdenka Valenzova Fig.4: RAxML Phylogram Fig.5:
ABSTRACT Isolation and phylogeny of endogenous retroviral elements belonging to the HERV-K LTR in cDNA library of human fetal brain and X q 21.3 region.
Northern Star Coral (Astrangia poculata) Populations from the New Jersey Coast. Abstract- This project investigated the distribution and molecular evolution.
Figure S1 Figure S1. Effect of SA on spore germination of M. oryae. The data presented were the means (± standard error) of spore germination from three.
Contribution of fungi activity for N 2 O emission in no-tillage with cover crop fields Zhaorigetu 1,2, T.Nishizawa 2, Y.Sato 2, M.Komatsuzaki 1, H.Ohta.
Systematics of Clavicipitaceous Fungi Associated with Morning Glories Based on rpb1 Sequence Data Saroj Simkhada, Alyssa M. Brown, and Richard E. Miller.
A New Record of Pseudeurotium bakeri (KNU14-21) from Crop Field Soil in Korea Mahesh Adhikari, Sang Woo Kim, Hyun Seung Kim, Young Hyum Um and Youn Su.
Introduction Biodiversity is important in an ecosystem because it allows the species living in that ecosystem to adapt to changes made in the environment.
Plant microbiome interactions: Growth of the facultative pathogen Lasiodiplodia theobromae is altered by endophytic bacteria Ivelisse Irizarry, Mónica.
Bacterial Infection in the Dungeness Crab, Cancer magister Sarah Dunn, Hannah Pramuk, David Scholnick and Györgyi Nyerges Pacific University, Department.
Ectomycorrhizas of Cercocarpus ledifolius (rosaceae) Kelly R. McDonald, Jason Pennell, Jonathan L. Frank,and Darlene Southworth 學生 : 生科三甲 葉茱玫.
Entomopathogenic Fungi on Hemiberlesia pitysophila Chengqun Lv*, Baoling Huang, Mengji Qiao, Jiguang Wei, Bo Ding Entomopathogenic Fungi on Hemiberlesia.
Isolation of microorganisms
Soil Microbiome of Native and Invasive Marsh Grasses in Blackbird Creek, Delaware Lathadevi K.Chintapenta 1#, Gulnihal Ozbay 1#, Venu Kalavacharla 1* Figure.
Identification of Drosophila species based on 16S rRNA and CO1 gene sequences Mohammad Shamimul Alam, Khandaker Asif Ahmed, Rowshan Ara Begum, and Reza.
Introduction to Bioinformatics Resources for DNA Barcoding
Introduction Conclusion References Aim of the work
Authors: Danish Farooq, Gregory Kowalczyk, Michael Steffanetta
INVESTIGATION 3 BIG IDEA 1
Jae Seok Yang, Hyun Goo Lee and Youn Su Lee*
Effect of Plant Growth Promoting Rhizobacteria on Growth Attributes of Different Vegetable Crops under Greenhouse Conditions Mahesh Adhikari, Kabir Lamsal,
Warm-Up (2/1) On the piece of white paper from the back, answer the following question. Name Date Period A fossil was newly discovered with three intact.
Identification of nifH and nodC genes from Rhizobium aegyptiacum
RESULTS AND DISCUSSION
New host records for Verticillium tricorpus, Corynespora cassiicola, Aphelenchoides fragariae and Helicotylenchus dihystera, associated with dieback and.
RESULTS AND DISCUSSION
Workshop on the analysis of microbial sequence data using ARB
Operational Taxonomic Units (OTU’s)
Isolation and Identification of Fungi
INVESTIGATION 3 BIG IDEA 1
INVESTIGATION 3 BIG IDEA 1
Overview Bioinformatics: Analyzing biological data using statistics, math modeling, and computer science BLAST = Basic Local Alignment Search Tool Input.
INVESTIGATION 3 BIG IDEA 1
Principles of Microbiology (Part-1)
High-Throughput Identification and Quantification of Candida Species Using High Resolution Derivative Melt Analysis of Panfungal Amplicons  Tasneem Mandviwala,
S. De Grazia, G.M. Giammanco, C. Colomba, A. Cascio, S. Arista 
Claudio H Slamovits, Naomi M Fast, Joyce S Law, Patrick J Keeling 
K. S. Ko, T. Kuwahara, L. Haehwa, Y. -J. Yoon, B. -J. Kim, K. -H
Tree depicting the phylogenetic relationships of all strains included in this study. Tree depicting the phylogenetic relationships of all strains included.
Presentation transcript:

Unreported Fungal Species of Didymosphaeriaceae from Soil in Korea Mahesh Adhikari, Sang Woo Kim, Dil Raj Yadav, Hyun Seung Kim, Yong Hyun Um, Youn Su Lee* Division of Biological Resource Sciences, Kangwon National University, Chuncheon , Korea ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION INTRODUCTION  Soil samples were collected from different places of Chuncheongbuk-do province of Korea.  Soil samples were taken approximately from (0~15 cm) depth, air dried and stored in plastic bags at 4ºC until use.  Fungi were isolated through serial dilution technique and purified and differentiated according to their morphological and microscopic characteristics.  The strains were inoculated at one point on 9-cm petri dishes and incubated for 7 days at 25 ℃ in dark place.  DNA of purified fungal isolates was extracted using the QIAGEN Plasmid Mini Kit (Qiagen Sciences, USA) following the manufacturer's instructions.  The PCR product was sequenced with an ABI prism 3730 DNA analyzer (Applied Biosystems, Foster City, CA, USA).  Extracted DNA samples were sent to Macrogen, Korea for sequencing.  The sequences were analyzed using BLAST (Basic Local Alignment Search Tool) on the NCBI website ( to find the sequences with the highest similarity to studied sequences.  The identified sequences were listed and alignment was conducted to construct a phylogenetic tree by neighbour-joining method, with a bootstrap value of 1,000 replicated, using MEGA 6.0. In total five hundred soil samples were collected and isolated through the serial dilution technique. Among the isolated fungal isolates, Paraphaeosphaeria sporulosa from the Didymosphaeriaceae family was encountered new in Korea on the basis of morphological and molecular analysis. Colonies on PDA were growing very fast and attains mm diameter in 7 days at 25 0 C. The colony color was creamy white. Spores are globose to sub-globose and 1.0 to 2.5 µm in diameter. Evolutionary status of the isolate KNU15-2 and previously identified Paraphaeosphaeria sporulosa was evaluated by the phylogenetic analysis. The isolate was most closely related to Paraphaeosphaeria sporulosa and form a monophyletic group with bootstrap value of 99 %. The phylogenetic analysis showed that the study isolate is Paraphaeosphaeria sporulosa. Further studies of this fungal isolate is worthwhile. REFERENCES The Didymosphaeriaceae are a family of fungi in the order pleosporales. Fungi of this family have a worldwide distribution and are saprobic in both woody and herbaceous plants. Some species are parasitic on other fungi. Soil fungi are one of the important components of microbial communities in terrestrial ecosystem and play vital role in decomposition of organic matter and nutrient cycling [1]. In spite of their immense importance in agro-ecosystem, yet they are probably the most poorly studied organisms. The microbial composition of soil is largely affected by edaphic factors and cropping system [2]. Soil fungal diversity study was undertaken to assess the diversity of fungi in the crop field soil of Chuncheongbuk-do, Korea. Out of identified isolates, Paraphaeosphaeria sporulosa was encountered new in Korea. This study presents the comparison of newly recorded species with previously described Paraphaeosphaeria sporulosa with regard to morphological and phylogenetic characteristics. Soil is a diversified micro-habitat for the development of microbial populations. Soil fungi are important integral components in the soil ecosystem and play a crucial role as a source of food for larger organisms, pathogens and maintain beneficial symbiotic relationships with plants or other organisms. Soil fungal diversity study was carried out to check the species diversity in the crop field soil of Chuncheongbuk-do, Korea in In total five hundred soil samples were collected and isolated through the serial dilution technique. Isolated fungi were then purified and differentiated according to their morphological and microscopic characteristics. Genomic DNA of the isolates was extracted by using QIAGEN® Plasmid Mini Kit(QIAGEN Sciences, USA) and the identification of fungi was carried out by sequence analysis of internal transcribed spacer (ITS) region of the 18S ribosomal DNA (18S rDNA). Morphologically 220 isolates were found distinct. Among them species of Didymosphaeriacea family were encountered namely Paraphaeosphaeria sporulosa, new and unreported in Korea. This species was identified based on the molecular and morphological analysis and have not been reported officially in the past from Korea. Fig.1. Procedures illustrating isolation of fungi from soil samples. Fig.2. Morphology of the Paraphaeosphaeria sporulosa (KNU15-2) on potato dextrose agar (PDA); A, Back view B, Front view C and D. spores of the isolate. Gen regionIsolateGenBank accession NoClosest GenBank library strainSimilarity (%) ITS regions KNU15-2 JX496114Paraphaeosphaeria sporulosa100 JX496091Paraphaeosphaeria neglecta97 KM873041Paraphaeosphaeria arecacerum95 JQ676199Paraphaeosphaeria sporulosum97 Fig. 1. Neighbor-joining phylogenetic analysis of the partial 18S-ITS1-5.8S-28Sr DNA sequence of Paraphaeosphaeria sporulosa (KNU15-2) obtained from soil in Korea. The phylogenetic tree was constructed using the MEGA 6 program. The sequence obtained this study is shown in boldface. Numerical values on branches are the percentage of 1,000 bootstrap replicates that support the branch.The scale bar represents the number of substitutions per site. Table.2. Identification of fungal isolates to species level with reference species based on the analyses of internal transcribed spacer gene sequences. Warcup JH. Soil-steaming: A selective method for the isolation of ascomycetes from soil. Br Mycol Soc 1951: Hargreaves SK, Williams RJ, Hofmockel KS. Environmental Filtering of Microbial communities in Agricultural Soil Shifts with Crop Growth. PloS ONE 2015;7:2-14.