Forghani u.a.
Sydowia Vol. 73 E-Book/S 217-238
Genomic structure of novel Iranian Rhizoctonia solani ...
Artikel Nr 2915
erschienen 10.02.2021
Preis 32,50
In: Sydowia 73, (2021): 217-238; ISSN 0082-0598, DOI 10.12905/0380.sydowia73-2021-0217, Published online on February 10, 2021

Genomic structure of novel Iranian Rhizoctonia solani AG-3PT isolates on potato, Solanum tuberosum

Dorna Forghani, Eidi Bazgir, Mehdi Nasr Esfahani & Mostafa Darvishnia

Plant Pathology Department, Faculty of Agriculture, Lorestan University, Lorestan, Iran.
Plant Protection Research Department, Isfahan Agricultural and Natural Resources Research and Education Center
(AREEO), Isfahan, Iran.

* e-mails:;

Forghani D., Bazgir E., Nasr Esfahani M. & Darvishnia M. (2021) Genomic structure of novel Iranian Rhizoctonia solani
AG-3PT isolates on potato, Solanum tuberosum. – Sydowia 73: 217–232.

Rhizoctonia solani AG-3PT is relatively specific to potato, Solanum tuberosum, causing considerable yield losses around the
globe, including Iran. A total of 210 R. solani isolates were collected from stem cankers and black scurf of infected potato plant
parts in various potato-growing provinces of Iran, of which morphogenetic diversity of 110 R. solani isolates were characterized.
High morphological and cultural variation was observed on radial colony growth and colour, hyphae diameter and number of
nuclei, and sclerotia initiation, formation and diameter. The fastest mycelium growth rate was in non-pathogenic R. solani isolates.
The pathogenicity and virulence characteristics of 70 R. solani isolates varied ranging from 0–100 % based on disease severity.
There was no correlation between morphological factors, pathogenicity and geographic origin of the isolates. ITS-rDNA region
barcoding of R. solani confirmed the isolates as R. solani AG-3PT. Nineteen polymorphic Inter Simple Sequence Repeat
(ISSR) primers were used to reveal the genetic structure and relationships among 110 R. solani isolates, which 258 bands were
detected. The average number of bands per primer was 21.5 and the size of the amplified DNA bands ranged from 100–5000 bp,
with a high degree of polymorphism (100 %). The majority of the isolates showed nearby associations within the population.
UPGMA classified the R. solani isolates into 16 main groups according to geographical origin, indicating that the ISSR marker
is a reliable tool in characterizing genetic diversity in R. solani isolates. There was no correlation between ISSR analysis and
virulence variability.

Keywords: ISSR, ITS-rDNA, PCR, polymorphism, primer, UPGMA.