Molecular characterization of Fusarium sp. from maize seeds
DOI:
https://doi.org/10.5958/2582-2683.2023.00033.3Keywords:
Internal transcribed spacer, polymerase chain reaction, NCBI, seed mycoflora, maize, cultivarAbstract
The investigation was undertaken at the Department of Plant Pathology, B. A. College of Agriculture, Anand Agricultural University, Anand, India during 2021-22. Genetic identification was done to identify the fungal pathogen and Internal Transcribed Spacer (ITS) rDNA was employed to identify the fungal pathogen at the species level. The molecular identification of the dominant seed mycoflora of maize i.e. Fusarium oxysporum was performed via, PCR amplification and sequencing of the ITS region of fungal DNA (rDNA) with universal primer pairs ITS1 and ITS4. The ITS primers produced an amplicon of 547 bp which was purified and sequenced. The sequences of rDNA region (Accession No. ON637065.1) were aligned and analyzed in the NCBI nucleotide BLAST. It showed 99.16% similarity with the already reported F. oxysporum (MN272279.1, MK751702.1, MF063025.1, KF534741.1, and JN585764.1) sequences.
Downloads
References
Ehlam, S., Modhi, D. and Elshamry, K. 2015. Mycoflora of maize (Zea mays) at different locations in hail Are-Saudi Arabia. International Journal of Scientific & Technology Research, 4: 227- 230.
alignment editor and analysis program for Windows95/ 98/NT. Nucleic Acids Symposium Series, 41: 95-98. Tamura, K., Dudley, J., Nei, M. and Kumar, S. 2007. MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0. Molecular Biology and Evolution, 24: 1596-1599. Tulin, J.M. and Askun, D.I. 2006. Investigation of fungal species diversity of maize kernels. Journal of Biological Sciences, 6: 275-288.
USDA. 1960. Index of Plant Disease in the United States. Agriculture Hand Book No. 165, Agricultural Research Service, A. Research Service, & Crops Research Division, C. Research Division, United States Department of Agriculture, pp. 165- 531.