Molecular Characterization of Mycosphaerella berkeleyiCausing Late Leaf Spot of Groundnut in Nghe An

Received: 05-09-2016

Accepted: 30-10-2016

DOI:

Views

0

Downloads

0

Section:

NÔNG HỌC

How to Cite:

Vi, N., Giang, H., Hoa, T., & Vien, N. (2024). Molecular Characterization of Mycosphaerella berkeleyiCausing Late Leaf Spot of Groundnut in Nghe An. Vietnam Journal of Agricultural Sciences, 14(9), 1312–1322. http://testtapchi.vnua.edu.vn/index.php/vjasvn/article/view/1462

Molecular Characterization of Mycosphaerella berkeleyiCausing Late Leaf Spot of Groundnut in Nghe An

Ngo Thi Mai Vi (*) 1 , Ha Giang 2 , Tran Thi Nhu Hoa 2 , Nguyen Van Vien 3

  • 1 Khoa Nông lâm ngư, Trường đại học Vinh
  • 2 Trung tâm Nghiên cứu Bệnh cây Nhiệt đới, Học viện Nông nghiệp Việt Nam
  • 3 Khoa Nông học, Học viện Nông nghiệp Việt Nam
  • Keywords

    Mycosphaerella berkeleyi, late leaf spot, groundnut, Nghe An, Vietnam, Rep-PCR, ITS

    Abstract


    This study identified the ITS (Internal Transcribed Spacer) sequence of 11 groundnut late leaf spot fungal isolates collected from Vietnam, mainly from Nghe An province in 2013. The ITS sequences of the 11 isolates were identical among them and highly identical (99.7 and 100%) with two available isolates of Mycosphaerella berkeleyi onthe GenBank. Rep-PCR technique (Repetitive sequence primed PCR) with 3 sets of primers designed on the repetitive sequences of bacterial genome including the repetitive extragenic palindromic (REP) sequence, enterobacterial repetitive intergenic consensus (ERIC) and BOX element, was used to investigate the genetic diversity of 33 M. berkeleyi isolates.PCR using BOX primers (BOX-PCR) produced polymorphic bands from tested fungal isolates. Rep-PCR analysis proved that fungal populations in Nghe An were of low genetic diversity. There was no correlation between Rep-PCR defined fugal groups with the origin of the isolates (location of sampling, groundnut cultivars) and morphological characteristics of the isolates (color and size of cultures)

    References

    Abdollahzadeh, J., and Zolfaghari, S. (2014). Efficiency of rep-PCR fingerprinting as a useful technique for molecular typing of plant pathogenic fungal species: Botryosphaeriaceae species as a case study. FEMS microbiology letters, 361: 144 - 157.

    Adiver, K. (2008). Studies on molecular variation in Phaeoisariopsis personata (Berk and M.A. Curtis) van Arx. causinglate leaf spot of groundnut (Arachis hypogaea L.). Master Thesis University of Agricultural Sciences, Dharwad (India).

    Adiver, S., Benagi, V., Byadgi, A., and Nadaf, H. (2009). Molecular variation in Phaeoisariopsis personata (Berk. and MA Curtis) van Arx causing late leaf spot of groundnut (Arachis hypogea L.). Karnataka Journal of Agricultural Sciences, 22: 336 - 339.

    Doyle, J. J., and Doyle, J. L. (1987). A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochemical Bulletin, 19: 11 - 15.

    Ebadi, M., Riahi, H., and Zare, R. (2014). Genetic diversity of Fusarium semitectum isolates from rice, using RAPD and REP - PCR markers. Mycologia Iranica, 1: 19 - 26.

    Ferrater, J. (2003). Analysis of genetic variation in strains of Cercospora canescens Ellis and Martin, the cause of leaf spot of mungbean (Vigna radiata (L.) Wilczek) using Rep - PCR.

    Gillings, M., and Holley, M. (1997). Repetitive element PCR fingerprinting (rep‐PCR) using enterobacterial repetitive intergenic consensus (ERIC) primers is not necessarily directed at ERIC elements. Letters in Applied Microbiology, 25: 17 - 21.

    Goodwin, S. B., Dunkle, L. D., and Zismann, V. L. (2001). Phylogenetic analysis of Cercospora and Mycosphaerella based on the internal transcribed spacer region of ribosomal DNA. Phytopathology, 91: 648 - 658.

    Grichar, W., Besler, B., and Jaks, A. (1998). Peanut (Arachis hypogaea L.) Cultivar Response to Leaf Spot Disease Development UnderFour Disease Management Programs 1. Peanut Science, 25: 35 - 39.

    Gurel, F., Albayrak, G., Diken, O., Cepni, E., and Tunali, B. (2010). Use of Rep‐PCR for Genetic Diversity Analyses in Fusarium culmorum. Journal of phytopathology, 158: 387 - 389.

    Komatsu, T., Sumino, A., and Kageyama, K. (2001). Characterization of Verticillium dahliae isolates from potato on Hokkaido by random amplified polymorphic DNA (RAPD) and REP-PCR analyses. Journal of General Plant Pathology, 67: 23 - 27.

    Kurose, D., Evans, H. C., Djeddour, D. H., Cannon, P. F., Furuya, N., and Tsuchiya, K. (2009). Systematics of Mycosphaerella species associated with the invasive weed Fallopia japonica, including the potential biological control agent M. polygoni - cuspidati. Mycoscience, 50: 179 - 189.

    Larkin, M. A., Blackshields, G., Brown, N., Chenna, R., McGettigan, P. A., McWilliam, H., Valentin, F., Wallace, I. M., Wilm, A., and Lopez, R. (2007). Clustal W and Clustal X version 2.0. Bioinformatics, 23: 2947 - 2948.

    Matsumoto, M. (2014). Distribution analysis of population structures for Rhizoctonia solani AG - 1 IA in Japanese paddy field, using rep - PCR assay. Archives of Phytopathology and Plant Protection, 47: 1082 - 1088.

    Matsumoto, M., and Cuong, H. (2014). Genetic characterization of the rice sheath blight pathogen Rhizoctonia solani AG1 - IA in North Vietnam by rep - PCR and sequence analysis. Journal of Plant Pathology, 96: 377 - 380.

    McDonald, D., Subrahmanyam, P., Gibbons, R., and Smith, D. (1985). Early and Late Leaf Spots of Groundnut. Information Bulletin No. 21.

    Miller, I., Norden, A., Knauft, D., and Gorbet, D. (1990). Influence of Maturity and Fruit Yield on Susceptibility of Peanut to Cercosporidium personatum (Late Leafspot Pathogen) 1. Peanut Science, 17: 52 - 58.

    Muiru, W., Koopmann, B., Tiedemann, A., Mutitu, E., and Kimenju, J. (2010). Use of repetitive extragenic palindromic (REP), enterobacterial repetitive intergenic consensus (ERIC) and BOX sequences to fingerprint Exserohilum turcicum isolates. Journal of Applied Biosciences, 30: 1828 - 1838.

    Palencia, E. R., Klich, M. A., Glenn, A. E., and Bacon, C. W. (2009). Use of a rep - PCR system to predict species in the Aspergillus section Nigri. Journal of microbiological methods, 79: 1 - 7.

    Rademaker, J., Louws, F., Versalovic, J., De Bruijn, F., Kowalchuk, G., Head, I., Akkermans, A., and van Elsas, J. (2004). Characterization of the diversity of ecologically important microbes by rep - PCR genomic fingerprinting. Molecular microbial ecology manual, (1 + 2): 611 - 643.

    Schoch, C. L., Seifert, K. A., Huhndorf, S., Robert, V., Spouge, J. L., Levesque, C. A., Chen, W., Bolchacova, E., Voigt, K., and Crous, P. W. (2012). Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi. Proceedings of the National Academy of Sciences, 109: 6241 - 6246.

    Stewart, E. L., Liu, Z., Crous, P. W., and Szabo, L. J. (1999). Phylogenetic relationships among some cercosporoid anamorphs of Mycosphaerella based on rDNA sequence analysis. Mycological Research, 103: 1491 - 1499.

    Tamura, K., Stecher, G., Peterson, D., Filipski, A., and Kumar, S. (2013). MEGA6: molecular evolutionary genetics analysis version 6.0. Molecular biology and evolution, 30: 2725 - 2729.

    Toda, T., Hyakumachi, M., and Arora, D. K. (1999). Genetic relatedness among and within different Rhizoctonia solani anastomosis groups as assessed by RAPD, ERIC and REP - PCR. Microbiological research, 154: 247 - 258.

    Versalovic, J., Koeuth, T., and Lupski, R. (1991). Distribution of repetitive DNA sequences in eubacteria and application to finerpriting of bacterial enomes. Nucleic acids research, 19: 6823 - 6831.

    Versalovic, J., Schneider, M., De Bruijn, F. J., and Lupski, J. R. (1994). Genomic fingerprinting of bacteria using repetitive sequence - based polymerase chain reaction. Methods in molecular and cellular biology, 5: 25 - 40.