Morphological and comparative genomic analyses of pathogenic and non-pathogenic Fusarium solani isolated from Dalbergia sissoo

• Published in: Molecular biology reports 2015-06, Vol.42 (6), p.1107-1122
• Main Authors: Arif, M., Zaidi, N. W., Haq, Q. M. R., Singh, Y. P., Taj, G., Kar, C. S., Singh, U. S.
• Format: Article
• Language: English
• Subjects: Animal Anatomy; Animal Biochemistry; Benzimidazoles - pharmacology; Biomedical and Life Sciences; Carbamates - pharmacology; Cluster Analysis; Dalbergia - microbiology; Dalbergia sissoo; DNA Primers - genetics; DNA, Fungal - analysis; DNA, Fungal - genetics; Fungicides, Industrial - pharmacology; Fusarium - classification; Fusarium - genetics; Fusarium - pathogenicity; Fusarium solani; Genetic Variation; Genomes; Genomics - methods; Histology; Life Sciences; Microbial Sensitivity Tests; Microsatellite Repeats - genetics; Morphology; Pathogens; Phylogeny; Plant diseases; Random Amplified Polymorphic DNA Technique - methods; Species Specificity; Trees; Virulence - genetics
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-014-3849-3

Sissoo or shisham ( Dalbergia sissoo Roxb.) is one of the finest wood of South Asia. Fusarium solani is a causal organism of sissoo wilt, decline, or dieback. It is also a potential causal organism associated with other valuable tree species. Thirty-eight Fusarium isolates including 24 F. solani and 14 Fusarium sp., were obtained in 2005 from different geographical locations in India. All 38 (18 pathogenic and 20 non-pathogenic) isolates were characterized for genomic analysis, growth behaviour, pigmentation and sensitivity to carbendazim. Based on growth pattern, growth rate, pigmentation and sensitivity to carbendazim, all 38 isolates showed a wide range of variability, but no correlation with pathogenicity or geographical distribution. Three techniques were used for comparative genomic analysis: random amplified polymorphic DNA (RAPD); inter simple sequence repeats (ISSR); and simple sequence repeats (SSR). A total of 90 primers targeting different genome regions resulted a total of 1159 loci with an average of 12.88 loci per primer. These primers showed high genomic variability among the isolates. The maximum loci (14.64) per primer were obtained with RAPD. The total variation of the first five principal components for RAPD, ISSR, SSR and combined analysis were estimated as 47.42, 48.21, 46.30 and 46.78 %, respectively. Among the molecular markers, highest Pearson correlation value (r = 0.957) was recorded with combination of RAPD and SSR followed by RAPD and ISSR (r = 0.952), and SSR and ISSR (r = 0.942). The combination of these markers would be similarly effective as single marker system i.e. RAPD, ISSR and SSR. Based on polymorphic information content (PIC = 0.619) and highest coefficient (r = 0.995), RAPD was found to be the most efficient marker system compared to ISSR and SSR. This study will assist in understanding the population biology of wilt causing phytopathogen, F. solani , and in assisting with integrated disease management measures.