Skip to main content
Log in

Variability of United States Isolates of Macrophomina phaseolina Based on Simple Sequence Repeats and Cross Genus Transferability to Related Genera Within Botryosphaeriaceae

  • Published:
Mycopathologia Aims and scope Submit manuscript

Abstract

Twelve simple sequence repeat (SSRs) loci were used to evaluate genetic diversity of 109 isolates of Macrophomina phaseolina collected from different geographical regions and host species throughout the United States (US). Genetic diversity was assessed using Nei’s minimum genetic distance, and the usefulness of each locus was determined by calculating the polymorphism information content (PIC). A total of 98 alleles were detected and of these 31 were unique to individual genotypes. Eight of twelve loci were highly informative with PIC values greater than 0.50. The majority of pairwise comparisons of genetic distance were greater than 0.60 indicating moderate to high genetic diversity. Dendrograms based on the genetic dissimilarities were created for the 109 isolates of which 79 were from soybean. Some clustering by host and geography was noted, but, the dendrograms generally grouped isolates independent of host or geography. Additionally, sequencing of the internal transcribed spacer region (ITS) for 10 isolates revealed that all of these isolates were 99% similar. Three SSR loci from M. phaseolina were cross amplified in other genera in the Botryosphaeriaceae. This was the first study of genotyping and assessing genetic diversity of M. phaseolina isolates collected from a widespread host and geographic range across the US with SSRs. With an additional 34 loci publically available for M. phaseolina, the results indicate that previously developed SSRs from one species can be used in future population, ecological, and genetic studies of M. phaseolina and other genera within the Botryosphaeriaceae.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Dhingra OD, Sinclair JB. Biology and pathogenicity of Macrophomina phaseolina. Viscosa, Brazil: Universidade Federal de Viscosa; 1978.

    Google Scholar 

  2. Mihail JD. Macrophomina. In: Singleton LS, Mihail JD, Rush CM, editors. Methods for research on soilborne phytopathogenic fungi. St. Paul, MN: American Phytopathological Society Press; 1992. p. 134–6.

    Google Scholar 

  3. Srivastava AK, Singh T, Jana TK, Arora DK. Microbial colonization of Macrophomina phaseolina and suppression of charcoal rot of chickpea. In: Sinha A, editor. Microbes and plants. New Dehli: Vedams eBooks; 2001. p. 269–319.

    Google Scholar 

  4. Kunwar IK, Singh T, Machado CC, Sinclair JB. Histopathology of soybean seed and seedling infection by Macrophomina phaseolina. Phytopathology. 1986;76:532–5.

    Article  Google Scholar 

  5. Mihail JD, Taylor SJ. Interpreting variability among isolates for Macrophomina phaseolina in pathogenicity, pcynidium production and chlorate utilization. Can J Bot. 1995;10:1596–603.

    Article  Google Scholar 

  6. Srivastava AK, Singh RB. Effects of organic amendment on interaction of Macrophomina phaseolina and Meloidogyne incognita on fresh bean (Phaseolina vulgaris). New Agri. 1990;1:99–100.

    Google Scholar 

  7. Wrather JA, Anderson TR, Arsyad DM, Tan Y, Ploper LD, Porta-Puglia A, et al. Soybean disease loss estimates for the top 10 soybean producing counties in 1998. Can J Plant Pathol. 2001;23:115–21.

    Google Scholar 

  8. Su G, Suh SO, Schneider RW, Russin JS. Host specialization in the charcoal rot fungus, Macrophomina phaseolina. Phytopathology. 2001;91:120–6.

    Article  CAS  PubMed  Google Scholar 

  9. Crous PW, Slippers B, Wingfield MJ, Rheeder J, Marasas WFO, Philips AJL, et al. Phylogenetic lineages in the Botryosphaeriaceae. Stud Mycol. 2006;55:235–53.

    Article  PubMed  Google Scholar 

  10. Mayek-Pérez N, López CC, González-Chavira M, García-Espinosa R, Acosta-Gallegos JA, Martínez-De la Vega O, et al. Variability of Mexican isolates of Macrophomina phaseolina based on pathogenesis and AFLP genotype. Mol Plant Pathol. 2001;59:257–63.

    Article  Google Scholar 

  11. Vandemark G, Martínez O, Pecina V, Alvarado MJ. Assessment of genetic relationships among isolates of Macrophomina phaseolina using a simplified AFLP technique and two different methods of analysis. Mycologia. 2000;92:656–64.

    Article  CAS  Google Scholar 

  12. Jana TK, Sharma TR, Prasad RD, Arora DK. Molecular characterization of Macrophomina phaseolina and Fusarium species by using single primer RAPD technique. Microbiol Res. 2003;158:249–57.

    Article  CAS  PubMed  Google Scholar 

  13. Jana T, Sharma TR, Singh NK. SSR-based detection of genetic variability in the charcoal root rot pathogen Macrophomina phaseolina. Mycol Res. 2005;109:81–6.

    Article  CAS  PubMed  Google Scholar 

  14. Purkayastha BK, Arora P, Bisyer I, Dilbaghi N, Chaudhury A. Molecular genotyping of Macrophomina phaseolina isolates: Comparison of microsatellite primed PCR and repetitive element sequence-based PCR. J Phytopathol. 2008;156:372–81.

    Article  CAS  Google Scholar 

  15. Reyes-Franco MC, Hernández-Delgado S, Beas-Fernández R, Medina-Fernández M, Simpson J, Mayek-Pérez N. Pathogenic and genetic variability within Macrophomina phaseolina from Mexico and other countries. J Phytopathol. 2006;154:447–53.

    Article  CAS  Google Scholar 

  16. Baird RE, Wadl PA, Wang X, Johnson DH, Rinehart TA, Abbas HK, et al. Microsatellites from the charcoal rot fungus (Macrophomina phaseolina). Mol Ecol Resour. 2009;9:946–8.

    Article  CAS  Google Scholar 

  17. Groppe K, Sanders I, Wiemken A, Boller T. A microsatellite marker for studying the ecology and diversity of fungal endophytes (Epichloë spp.) in grasses. Appl Environ Microb. 1995;61:3943–9.

    CAS  Google Scholar 

  18. Baird RE, Trigiano RN, Windham G, Williams P, Kelly R, Abbas HK, et al. Comparison of aflatoxigenic and nonaflatoxigenic isolates of Aspergillus flavus using DNA amplification fingerprinting techniques. Mycopathologia. 2006;161:93–9.

    Article  CAS  PubMed  Google Scholar 

  19. White TJ, Brun T, Lee S, Taylor J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR Protocols. A guide to methods and applications. San Diego, USA: Academic Press; 1990. p. 315–20.

    Google Scholar 

  20. Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, et al. Clustal W and Clustal X version 2.0. Bioinformatics. 2007;23:2947–8.

    Article  CAS  PubMed  Google Scholar 

  21. Amos W, Hoffman JI, Frodsham A, Zhang L, Best S, Hill VS. Automated binning of microsatellite alleles: problems and solutions. Mol Ecol Notes. 2007;7:10–4.

    Article  CAS  Google Scholar 

  22. Anderson JA, Churcill GA, Autrique JE, Tanksley SD, Sorrels ME. Optimizing parental selection for genetic linkage maps. Genome. 1992;36:181–6.

    Article  Google Scholar 

  23. Langella O. Populations: population genetic software (individuals or populations distances, phylogentic trees). 2002. www.bioinformatics.org/project/?group_id=84.

  24. Nei M. Genetic distance between populations. Am Nat. 1973;106:283–92.

    Article  Google Scholar 

  25. Rohlf FJ. NTSYS-pc numerical taxonomy and multivariate analysis system, version 1.70. Setauket, NY: Exeter Software; 1992.

    Google Scholar 

  26. Botstein D, White RL, Skolnick M, Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet. 1980;32:314–31.

    CAS  PubMed  Google Scholar 

  27. Karaoglu H, Lee CMY, Meyer W. Survey of simple sequence repeats in completed fungal genomes. Mol Biol Evol. 2005;22:639–49.

    Article  CAS  PubMed  Google Scholar 

  28. Rossetto M. Sourcing of SSR markers from related plant species. In: Henry RJ, editor. Plant genotyping—the DNA fingerprinting of plants. New York, NY: CABI Publishing; 2001. p. 211–24.

    Chapter  Google Scholar 

  29. Peakall R, Gilmore S, Keys W, Morgante M, Rafalski A. Cross species amplification of soybean (Glycine max) simple sequence repeats (SSRs) within the genus and other legume genera: implications for the transferability of SSRs in plants. Mol Biol Evol. 1998;15:1275–87.

    CAS  PubMed  Google Scholar 

  30. Dutech C, Enjalbert J, Fournier E, Delmotte F, Barrès B, Carlier J, et al. Challenges of microsatellite isolation in fungi. Fungal Genet Biol. 2007;44:933–49.

    Article  CAS  PubMed  Google Scholar 

  31. Cristancho M, Escobar C. Transferability of SSR markers from related Uredinales species to the coffee rust Hemileia vastatrix. Genet Mol Res. 2008;7:1186–92.

    Article  CAS  PubMed  Google Scholar 

  32. Das IK, Fakrudin B, Arora DK. RAPD cluster analysis and chlorate sensitivity of some Indian isolates of Macrophomina phaseolina from sorghum and their relationships with pathogenicity. Mycol Res. 2008;163:215–24.

    CAS  Google Scholar 

  33. Rajkumar FB, Kuruvinashetti MS. Genetic variability of sorghum charcoal rot pathogen (Macrophomina phaseolina) assessed by random DNA markers. Plant Pathology J. 2007;23:45–50.

    Google Scholar 

Download references

Acknowledgments

Approved for publication as Journal Article No. J-11724 of the Mississippi Agricultural and Forestry Experiment Station, Mississippi State University. This work was supported by USDA Agreement no. 58-6404-7-213. Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the University of Tennessee or the USDA.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Richard E. Baird.

Additional information

Equal work was done by Richard E. Baird and Phillip A. Wadl.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Baird, R.E., Wadl, P.A., Allen, T. et al. Variability of United States Isolates of Macrophomina phaseolina Based on Simple Sequence Repeats and Cross Genus Transferability to Related Genera Within Botryosphaeriaceae. Mycopathologia 170, 169–180 (2010). https://doi.org/10.1007/s11046-010-9308-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11046-010-9308-3

Keywords

Navigation