ArticlePDF Available

Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata

Authors:

Abstract

Net blotch caused by Pyrenophora teres is an important pathogen of barley plants worldwide. There are two biotypes of the fungus. Pyrenophora teres f. teres (Ptt) causes the net form of the disease and Pyrenophora teres f. maculata (Ptm) causes the spot form of the disease. Barley landraces are good sources of disease resistance. In this study, seedling response of 25 barley landraces obtained from different regions of northwest Iran to 3 single spore isolates of Ptt and 3 single spore isolates of Ptm were determined under greenhouse conditions. Differences in virulence among the isolates were evident. Some landraces showed different responses to different isolates. Landraces # 9 and # 16 showed moderately resistant reactions to one isolate of Ptt and showed moderately resistant-moderately susceptible reactions to 2 isolates of Ptt. Landraces # 7, # 11, # 15, # 17, # 21, # 22, # 23 and # 25 showed moderately resistant-moderately susceptible reactions to all 3 isolates of Ptt. Landrace # 23 showed resistant-moderately resistant reaction to one isolate of Ptm and showed moderately resistant reactions to 2 isolates of Ptm. Landrace # 16 showed moderately resistant reactions to all isolates of Ptm. Landraces # 11, # 15, # 21 and # 25 showed moderately resistant reaction to one isolate of Ptm and showed moderately resistant-moderately susceptible reactions to 2 isolates of Ptm. Landraces that exhibited reactions between resistant and moderately resistant-moderately susceptible range could be used as a direct seeding material to the field or could be used as breeding materials.
Tarım Bilimleri Dergisi
Tar. Bil. Der.
Dergi web sayfası:
www.agri.ankara.edu.tr/dergi
Journal of Agricultural Sciences
Journal homepage:
www.agri.ankara.edu.tr/journal
TARIM BİLİMLERİ DERGİSİ JOURNAL OF AGRICULTURAL SCIENCES 25 (2019) 86-92
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f.
teres and Pyrenophora teres f. maculata
Arzu ÇELİK OĞUZa, Amir RAHİMİb, Aziz KARAKAYAa
a
b
ARTICLE INFO
Research Article
Corresponding Author: Aziz KARAKAYA, E-mail: karakaya@agri.ankara.edu.tr, Tel: +90 (312) 596 12 58
Received: 05 December 2017, Received in Revised Form: 21 March 2018, Accepted: 01 April 2018
ABSTRACT
Net blotch caused by Pyrenophora teres is an important pathogen of barley plants worldwide. There are two biotypes
of the fungus. Pyrenophora teres f. teres (Ptt) causes the net form of the disease and Pyrenophora teres f. maculata
(Ptm) causes the spot form of the disease. Barley landraces are good sources of disease resistance. In this study, seedling
                  Ptt
and 3 single spore isolates of Ptm  

moderately resistant reactions to one isolate of Ptt and showed moderately resistant-moderately susceptible reactions
to 2 isolates of Ptt
susceptible reactions to all 3 isolates of Ptt
of Ptm and showed moderately resistant reactions to 2 isolates of Ptm   
reactions to all isolates of Ptm
of Ptm and showed moderately resistant-moderately susceptible reactions to 2 isolates of Ptm
reactions between resistant and moderately resistant-moderately susceptible range could be used as a direct seeding

Keywords: Drechslera teres
© Ankara Üniversitesi Ziraat Fakültesi
1. Introduction
Barley (Hordeum vulgare    
(FAO 2015). It is the most planted cereal after wheat in Turkey (TUIK 2016; Geçit 2016).

(Zohary & Hopf 1993). Parts of Turkey and Iran are located in the Fertile Crescent region. Hordeum
spontaneum, progenitor of cultivated barley, is also common in this region (Harlan & Zohary 1966; Nevo
1992). Eight main regions including China, India, Near East, Central Asia, Ethiopia, Mediterranean, Central

Turkey and Iran are very important phytogeographical regions due to presence of Mediterranean as well
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
87Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92

landraces are still planted in these areas.
Barley plant is resistant to adverse conditions
and has high adaptation capability. It can grow in
various soil and climatic conditions (Mathre 1982;
Geçit 2016). Wild barleys and barley landraces are

stress tolerances. They are regarded as a ‘gold mine’
because of their potential power to develop new
genotypes against various biotic and abiotic stress
factors (Yitbarek et al 1998; Ceccarelli & Grando
2000; Ellis et al 2000). Barley landraces show
optimum adaptability to changing environmental
     

properties can be used to develop varieties with
better quality traits (Newton et al 2010). Iranian
barley landraces can be considered as important
gene sources for modern cultivar improvement
(Khodayari et al 2012).
Net blotch is an important barley foliar disease

      
symptoms. Pyrenophora teres f. maculata (Ptm)
incites spot type of net blotch and P. teres. f. teres
(Ptt) incites net type of net blotch (Shipton et al

et al 2011). The prevalence of net blotch disease is
related to the susceptibility of cultivated varieties.

where highly susceptible cultivars are planted.
However, general losses range between 10-40%
(Mathre 1982). The use of fungicides, cultural
practices and planting resistant barley genotypes


method to control of net blotch is through using
resistant barley cultivars.
In this study, we evaluated the seedling
responses of 25 Iranian barley landraces obtained

of Ptt and 3 single spore isolates of Ptm collected
  
this study has been published previously (Çelik

2. Materials and Methods
2.1. Plant materials
Barley landraces were collected from Oshnaviye,
Piranshahr, Bukan and Naghadeh regions of
northwest Iran. From these, healthy looking
individial seeds were selected and planted into 24 cm

pots were placed outside and watered as needed.
Both light colored and dark colored seeds were
selected. Seeds of these landraces were harvested

2.2. Making single spore isolates
The infected barley leaves with net and/or spot form

   

surface sterilized with 1% sodium hypochloride.
These pieces were incubated for 3 days on moist

taken under a stereomicroscope and then transferred

(PDA).
2.3. Inoculation and incubation
No sporulation was observed in PDA, therefore,
hyphal parts were used as inoculum. Previous studies
showed that inoculation with hyphae was successful
(Douiyssi et al 1998; Karakaya & Akyol 2006; Çelik
       
10 days old Ptt and Ptm cultures grown on PDA
       
     4 per
        

1995; Douiyssi et al 1998; Karakaya & Akyol

sprayed onto barley leaves using a hand sprayer at
the growth stages 12-13 (Zadoks et al 1974). The
         
greenhouse conditions. After this period, ventilation
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
88 Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92

hours. The temperature of the greenhouse was 17±2
oC night and 22±2 oC day with a 14h/10h light/dark
regime. Three replications were employed.
2.4. Disease assessment
Disease evaluations were made 7 days after
inoculation using Tekauz (1985) scales which are
based on lesion morphology of net blotch biotypes.
3. Results and Discussion
    
Ptt and 3 Ptm isolates (Table
1). Pathogenic variation was observed between P.
teres isolates and Iranian barley landraces. Response
of landraces to Ptt and Ptm isolates ranged between
moderately resistant and moderately susceptible-
susceptible. The most virulent isolates of Ptt and
Ptm were Ptt 1 Sivas and Ptm 1 Ankara isolates,
respectively.
Table 1- Seedling reactions of 25 Iranian barley landraces to 3 Pyrenophora teres f. teres and 3 Pyrenophora
teres f. maculata isolates. For disease evaluation scales developed for net form of net bloth and spot form of
net blotch by Tekauz (1985) were used
Landrace
no  
type

color
Pyrenophora teres f. teres Pyrenophora teres f. maculata
Ptt 1

Ptt 2

Ptt 3

Mean Ptm 1
Ankara
Ptm 2

Ptm 3

Mean
1 Naghadeh 2  7 7 5 6.3 7 7 7 7
2 Naghadeh 2  8 7 3 6 5 7 7 6.3
3 Bukan 2  6 8 5 6.3 7 5 5 5.6
4 Naghadeh 2 Dark 8 6 5 6.3 8 7 5 6.6
5 2 8 4 3 5 8 5 7 6.6
6 Naghadeh 2 Dark 7 4 6 5.6 7 7 7 7
7 Bukan 2  5 5 5 5 5 7 5 5.6
8 2 7 6 3 5.3 5 7 3 5
9 Bukan 2  4 4 3 3.6 7 2 5 4.6
10  2 6 6 7 6.3 7 3 5 5
11  6 5 4 5 4.6 5 3 5 4.3
12 Naghadeh 2  8 4 6 6 7 7 5 6.3
13 Naghadeh 2 Dark 8 6 6 6.6 7 7 5 6.3
14 Naghadeh 2 Dark 7 4 6 5.6 7 7 7 7
15 Naghadeh 2  5 5 5 5 5 3 5 4.3
16 Bukan 2  6 6 3 5 3 3 3 3
17  6 6 6 4 5.3 7 5 3 5
18  2 6 4 7 5.6 5 5 7 5.6
19  2 7 5 7 6.3 7 3 7 5.6
20 Naghadeh 2 Dark 7 4 5 5.3 7 7 5 6.3
21 Naghadeh 2  5 5 4 4.6 5 3 5 4.3
22  2 5 4 4 4.3 7 7 3 5.6
23 Naghadeh 2  4 6 4 4.6 3 3 2 2.6
24 Naghadeh 2 Dark 5 7 4 5.3 7 5 3 5
25 Bukan 2  4 4 4 4 5 5 3 4.3
Mean 6.16 5.24 4.76 6.12 5.2 4.96
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
89Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92

resistant-moderately susceptible reactions to Ptt 1
Sivas, Ptt    Ptt 3 Kilis isolates,

16) showed moderately resistant reactions to Ptt 3

      
moderately susceptible reactions to all 3 isolates
of Ptt        
resistant-moderately susceptible to two isolates of
Ptt and were moderately resistant to one isolate of
Ptt. Eight, 6 and 11 landraces showed moderately
resistant-moderately susceptible reactions to Ptm 1
Ankara, Ptm 2 Konya and Ptm  

were moderately resistant to Ptm 1 Ankara isolate.
In addition, 7 landraces were moderately resistant
      
resistant to Ptm
       
resistant-moderately resistant to Ptm  

resistant reaction to one isolate of Ptm and showed
moderately resistant reactions to 2 isolates of
Ptm   
reactions to all isolates of Ptm 

isolate of Ptm    
moderately susceptible reactions to 2 isolates of
Ptm
to one isolate of Ptm 

resistant to one isolate of Ptm.
Fertile Crescent is the most likely geographical
area where the wild barley is domesticated and wild
barley populations located in the Fertile Crescent
have contributed genetic material to the cultured
barley (Zohary & Hoph 1993; Badr et al 2000;
Morrell & Clegg 2007). This creates a large variaton
    
reported the presence of resistant genotypes among
barley genotypes in the Middle East.
Barley has been grown in Fertile Crescent
region a long period of time and a rich genetic
       
2000; Khodayari et al 2012). Ebrahimi et al (2013)
investigated the genetic diversity of 115 barley
landraces and wild barleys from 5 Hordeum species
     
the landraces. Khodayari et al (2012), using
microsatellite markers, investigated the genetic
diversity among the Iranian barley landraces and
Khazaei et al (2012) characterized the agronomic
traits of winter barley landraces and 4 advanced
varieties collected from Iran. Both studies reported
high levels of polymorphism and genetic diversity
among the Iranian barley genotypes.
There are limited studies on the resistance of
Iranian barley landraces to P. teres. Ghazvini &
Tekauz (2007) tested 160 barley accessions from
Iran for their reactions to Fusarium graminearum,
Bipolaris sorokiniana and Dreschlera teres f. teres
(teleomorph: Pyrenophora teres f. teres) in order to

found to be resistant to Dreschlera teres f. teres. No
resistance to Fusarium graminearum and Bipolaris
sorokiniana isolates was found. It is concluded
that disease resistant landraces were important in
achieving sustainability and they were valuable
sources in germplasm collections. In the current

        
blotch. In current study, 5 Iranian barley landraces
showed moderately resistant reactions to Ptt 3 Kilis
   
resistant reactions to all Ptm isolates and landrace
number 23 showed moderately resistant reactions to
2 isolates of Ptm and showed resistant-moderately
resistant reaction to one isolate of Ptm.
     
genotypes were found in the gene centers of barley
(Afanasenko et al 2000). Numerous studies reported
the resistance of barley landraces to P. teres from
        
and Yitbarek et al (1998) assessed the reactions of
Ethiopian barley landraces to P. teres and observed

tested the resistance status of 176 Turkish barley
lines to P. teres. More lines showed resistance to spot
form of net blotch than net form of net blotch. In our
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
90 Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92

levels of resistance to P. teres isolates and more
Iranian landraces showed resistance to spot form of
net blotch. In a study conducted by Semeane (1995)
in Ethiopia only 4 of 900 barley landraces were
found to be resistant to net blotch. Silvar et al (2010)
tested 159 barley landraces and 16 barley cultivars
from Spanish Barley Core Collection to 3 P. teres
f. teres     
and only one landrace showed resistant reaction to
all isolates used. Endresen et al (2011) evaluated
  
of net blotch. Neupane et al (2015) evaluated 2062
barley accessions obtained from World Barley Core
Collection to four P. teres f. teres isolates obtained
from Australia, United States, Denmark and New
Zealand. Fifteen accessions were found to be
resistant to all isolates. In our study, a high number
of Iranian barley landraces showed reactions in the
range of resistant-moderately resistant to moderately
resistant- moderately susceptible to both forms of
the pathogen. Chakrabarti (1968) and Khan & Boyd
(1969) tested barley varieties from World Barley
Core Collection for their reactions to net blotch.
In their studies, thirty of 6246 barley varieties and
6 of 8756 barley varieties were found to be very
resistant, respectively. Turkey, which is located in
the Fertile Crescent region, is one of the important
gene centers of barley and has important barley
genetic resources. Wild barley and cultivated barley
landraces obtained from Turkey and Jordan were
evaluated for their resistance status to Cochliobolus
sativus, P. teres f. maculata and P. teres f. teres
collected from Canada. Wild barley genotypes were
found to be more resistant to C. sativus and P. teres f.
teres. Equal amounts of wild barleys and cultivated
landraces of barley were found to be resistant to P.
teres f. maculata 
et al (2017b) tested 198 Turkish barley landraces
to 6 virulent isolates of net form of net blotch and
spot form of net blotch. 13 barley landraces showed
resistant reactions to all P. teres f. maculata isolates
and 7 barley landraces showed resistant reactions to
all P. teres f. teres isolates. In addition, numerous

isolate. Similarly, in our current study, more Iranian
barley landraces showed resistant group reactions
to Ptm isolates than Ptt isolates. Several Iranian
landraces were found to be resistant-moderately
resistant or moderately resistant to both forms of the
pathogen.
New gene resources resistant to diseases, pests
and changing climatic conditions are needed for
    
agronomical traits and are sources of wide variation
(Ceccarelli & Grando 2000; Ergün et al 2017).
Useful agronomical traits could be transferred to
advanced varieties successfully (Newton et al 2010).
These genetic resources should be collected from
natural habitats and should be protected (Frankel &
Hawkes 1975).
4. Conclusions
Barley landraces are valuable sources of disease
resistance. In this study, 25 barley landraces
     
Iran were tested to both forms of P. teres with the

landraces showed moderately resistant or resistant-
moderately resistant reactions to 1 or more isolates.
A wide variation was observed among the Iranian
barley landraces to pathogen isolates.

fungi and resistant genotypes may show susceptible
reactions to emerging virulent pathogens (Burdon &
    
pathotypes, resistance studies should be continuous
and the establishment of a broad genetic base is
necessary for durable and sustainable resistance.
Iranian barley landraces determined in this study
could be used as gene sources in future breeding
studies in order to obtain net blotch resistant barley
genotypes.
References
Afanasenko O S, Makarova I G & Zubkovich A A (2000).
     Pyrenophora
teres Dreschs. strains in barley accession CI 5791.
    Proceedings of 8th International
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
91Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92
Barley Genetics Symposium, 22-27 October, Adelaide,
Australia, 2: 73-75
       
barley varieties and lines to the virulent strain T4 of
Pyrenophora teres.  14: 9-13
Allard R W & Bradshaw A D (1964). Implications of
genotype-environment interaction in applied plant
breeding. Crop Science 4: 503-508

Ibrahim H H, Pozzi C, Rohde W & Salamini F (2000).
On the origin and domestication history of barley
(Hordeum vulgare). 
17(4): 499-510
Burdon J J & Silk J (1997). Sources and patterns of
diversity in plant-pathogenic fungi. Phytopathology
87: 664-669
Ceccarelli S & Grando S (2000). Barley landraces from
the Fertile Crescent. A lesson for plant breeders.
In: S B Brush (Ed.),     
conservation of crop diversity. Int. Plant Gen. Res.
Institute, International Developmet Research Center,
      
Washington, D.C. pp. 51-76
       
radiation on resistance of barley to net blotch and spot
blotch. Phytopathology 58(4): 467-471

response of Iranian barley landraces to Pyrenophora
teres f. teres and Pyrenophora teres f. maculata.
   
. 15-17 May,
Cappadocia, Turkey, pp. 394

Turkish barley landraces resistant to net and spot forms
of Pyrenophora teres. Phytopathologia Mediterranea
56(2): 217-223
Douiyssi A, Rasmusson D C & Roelfs A P (1998).
Responses of barley cultivars and lines to isolates of
Pyrenophora teres. Plant Disease 82: 316-321
Ebrahimi A, Naghavi M R, Sabokdast M, Sarabshelli
A M & Ghaderdan K (2013). Evaluation of genetic
diversity of Iranian wild barley (Hordeum sp.) and
landraces using morphological characters. Iranian
      
 21(1): 56-67

D C, Russell J R & Powell W (2000). Wild barley:
a source of genes for crop improvement in the 21st
century?     51(342):
9-17
Endresen D T F, Street K, Mackay M, Bari A & Pauw D
E (2011). Predictive association between biotic stress
traits and eco-geographic data for wheat and barley
landraces. Crop Science 51: 2036-2055

A (2017). Arpa (Hordeum vulgare

     
26(2): 180-189
FAO (2015). http://www.fao.org/faostat/en/ (Access date:
15.12.2016)
Frankel O H & Hawkes J G (1975). Crop Genetic
Resources for Today and Tomorrow. Cambridge
University Press, Cambridge
     
Yulaf, Triticale). Ankara Üniversitesi Ziraat Fakültesi

Ghazvini H & Tekauz A (2007). Reactions of Iranian
barley accessions to three predominant pathogens in
Manitoba. Canadian Journal of Plant Pathology 29:
69-78
Harlan J R & Zohary D (1966). Distribution of wild
wheats and barley. Science 153: 1074-1080
          
cultivated barley from West Asia to net blotch and
spot blotch. Crop Science 35: 242-246
Karakaya A & Akyol A (2006). Determination of the
seedling reactions of some Turkish barley cultivars to
the net blotch. Plant Pathology Journal 5(1): 113-114
Khan T N & Boyd W J R (1969). Physiologic specialization
in Drechslera teres. Australian Journal of Biological
Sciences 22: 1229-1235
Khazaei A, Moghaddam M & Noormohammadi S (2012).
Genetic diversity among winter barley landraces
collected from west of Iran. Iranian Journal of Crop
Sciences 13(4): 671-683. (In Persian)

Pourkheirandish M & Komatsuda T (2012). Genetic
diversity of cultivated barley landraces in Iran
measured using microsatellites. International Journal
of Bioscience, Biochemistry and Bioinformatics 2(4):
287-290

of Ethiopian barley landraces for disease and
agronomic characters.  14: 21-25
Seedling Response of Iranian Barley Landraces to Pyrenophora teres f. teres and Pyrenophora teres f. maculata, Çelik Oğuz et al
92 Tarım Bilimleri Dergisi – Journal of Agricultural Sciences 25 (2019) 86-92
          
& Tekauz A (1996). Reaction of Turkish barley
accessions to Canadian barley pathogens. Canadian
Journal of Plant Science 76: 927-931
   
Pyrenophora teres    
damaging barley pathogen. Molecular Plant
Pathology 12(1): 1-19
Mathre D E (1982). Compendium of Barley Diseases.
APS Press. Minnesota,78 pp
          
Epidemiology and control of spot form of net blotch
(Pyrenophora teres f. maculata) of barley: a review.
Crop & Pasture Science 60: 303-315
       
& Hollaway G J (2012). Spot form of net blotch
resistance in a diverse set of barley lines in Australia
and Canada. Plant Disease 96: 569-576
   
a second domestication of barley (Hordeum vulgare)
east of the Fertile Crescent. Proceedings of the

 104(9): 3289-3294
  
(2015). Evaluation of a barley core collection for spot
form of net blotch reaction reveals distinct genotype-
     
Phytopathology 105: 509-517
Nevo E (1992). Origin, evolution, population genetics
and resources for breeding of wild barley, Hordeum
spontaneum, in the Fertile Crescent. In: P R Shewry
(Ed.), Barley: genetics, biochemistry, molecular
biology and biotechnology, C.A.B. International, pp.
19-43
Newton A C, Akar T, Baresel J P, Bebeli P J, Bettencourt
    
Katsiotis A, Koutis K, Koutsika-Sotiriou M, Kovacs

     
(2010). Cereal landraces for sustainable agriculture.
A review. Agronomy for Sustainable Development
30(2): 237-269
Semeane Y (1995). Importance and control of barley leaf
blights in Ethiopia.  14: 83-89
Shipton W A, Khan T N & Boyd W J R (1973). Net blotch
of barley 52: 269-290
Silvar C, Casas A M, Kopahnke D, Habekus A, Schweizer


Barley Core Collection for disease resistance. Plant
Breeding 129: 45-52
Tekauz A (1985). A numerical scale to classify reactions
of barley to Pyrenophora teres. Canadian Journal of
Plant Pathology 7: 181-183

üretimi https://biruni.tuik.gov.tr/bitkiselapp/bitkisel.
zul. (Access date: 29.12.2016)
  
breeding of cultivated plants, (translated from the
Russian by K. S. Chester). Chronica Botanica 13(1-
6): 1-364
      
preferences in the genus Hordeum in Iran and Turkey
     
98B Supplement: pp. 107-116


landrace populations for resistance to barley leaf scald
and net blotch. Plant Breeding 117: 419-423
Zadoks J C, Chang T T & Konzak C F (1974). A decimal
code for the growth stages of cereals. 
14: 415-421
Zohary D & Hopf M (1993). Domestication of plants in
the Old World. The origin and spread of cultivated
        

... due to net blotch infection, resulting in the projected losses of 192 USD × 10 6 for the spot and 117 USD × 10 6 for the net form of the pathogen. According to Martin et al. (2021), yield losses in favourable conditions for an epidemic on the sensitive Maritime variety in South Australia can reach up to 70%, while other authors are of the view that, in areas where very sensitive barley varieties are grown, and the crop is heavily affected by the disease, 100% yield losses can occur (Oğuz et al. 2019;Abebe 2021). Yield losses are often accompanied by significant reductions in 1 000 grain weight, number of spikes per m 2 , number of kernels per spike, grain size and malt quality (Sutton & Steele 1983;Khan 1987 Tini et al. 2022). ...
... vulgare) is commercially cultivated (Williams et al. 2001;Frisen et al. 2006;Tuohy et al. 2006;Liu et al. 2012;Adawy et al. 2013;Novakazi et al. 2019;Backes et al. 2021). The disease is present in many European countries, including Serbia (Tančić-Živanov et al. 2017) and other countries that previously formed Yugoslavia such as Bosnia and Herzegovina (Stojčić & Trkulja 2001;Tomić unpublished data), Russia (Afanasenko et al. 2007;Mikhailova et al. 2010;Volkova et al. 2020), Italy (Aragona et al. 2000;Rau et al. 2003), France (Arabi et al. 1992;Youcef-Benkada et al. 1994;Toubia-Rahme et al. 1995), Hungary (Tóth et al. 2008), Poland (Baturo-Ciesniewska et al. 2012, Finland (Peltonen et al. 1996;Robinson & Jalli 1996;Serenius et al. 2005;Tuohy et al. 2006), Slovakia (Tuohy et al. 2006), Ukraine (Retman et al. 2022), Lithuania (Statkeviciute et al. 2010(Statkeviciute et al. , 2012, Estonia (Sooväli & Koppel 2010), Norway (Tuohy et al. 2006;Wonneberger et al. 2017), Sweden (Jonsson et al. 1997;Tuohy et al. 2006), Denmark (Smedegård-Petersen 1971Tuohy et al. 2006), Germany (Vatter et al. 2017), Czech Republic (Minarikova & Polisenska 1999;Tuohy et al. 2006), Bulgaria (Vasileva et al. 2022), Great Britain (Abebe 2021), Turkey (Oğuz et al. 2019), Austria, Baltic States, Cyprus, Faroe Islands, Greece, Ireland, Malta, Moldova, Netherlands, and Romania. In the USA, its presence was recorded in North Dakota and Montana (Liu et al. 2012;Lartey et al. 2013), California and Minnesota (Steffenson & Webster 1992), and Pennsylvania (Delserone & Cole 1987), while in Canada, net blotch was found in Alberta, Saskatchewan and Manitoba (Tekauz & Mills 1974;Tekauz 1990;Van den Berg & Rossnagel 1990;Akhavan et al. 2015Akhavan et al. , 2016. ...
... Economically, it is a very important pathogen that can significantly reduce the yield, as well as the quality of production, which directly affects the economic profit and justification of production. Yield losses can vary depending on the sensitivity of the variety, climatic conditions, the presence and amount of inoculum, the time of infection, the stage of crop growth, the method of testing, and ranged from 10-40% average, and even up to an incredible 100% in conditions where sensitive varieties are grown and where the crop is heavily affected by disease attack (Oğuz et al., 2019). In addition to yield reduction, the disease can affect root size, percentage of dry matter, size of healthy leaves, number of spikes, number of grains per spike, etc. ...
Article
Full-text available
Barley is one of the most economically important cereals grown in our country, and it is used as a basis for making nutrients for domestic animals, as well as for the production of beer malt. It is of particular importance to know the spectrum of the most significant barleys’ diseases that can significantly disturb the quality and quantity of barley yield. Based on visits to plots under barley on a large number of production plots, the presence of symptoms manifested in the form of various types of spotting, necrosis and drying of the diseased tissue of barley leaves, which indicate the potential presence of species of the genus Pyrenophora, was determined. The significance of this occurrence is all the greater because the symptoms caused by certain species of the genus Pyrenophora on diseased barley leaves are difficult to distinguish visually in most cases, so correct diagnosis is the basis for their successful control. Through the laboratory analysis of the collected samples, we determined that the mentioned changes on the diseased barley leaves were caused by two species from the genus Pyrenophora: P. teres and P. graminea. In addition to these species, in the paper we have given an overview of potential species whose occurrence could be expected, among which the most significant are P. triticirepentis, P. semeniperda, P. erythrospila, P. trichostoma and P. wirreganensis. In the future, continuous surveillance of barley plots across the state is needed to adequately respond to future challenges with the emergence of new species of barley pathogens.
... Barley landraces can be planted either directly in the field or utilized in breeding programs for developing new resistant varieties. In Turkey, limited work exists on the net type resistance status of barley genotypes (Yazıcı et al., 2015;Çelik Oğuz et al., 2016;, 2019b. ...
Article
Full-text available
Seedling stage reactions of thirty-eight 2-rowed barley landraces representing different areas of Turkey obtained from Osman Tosun Gene Bank to two Pyrenophora teres f. teres isolates were evaluated. In addition, barley cultivars Bülbül 89 and Avcı 2002 were included. Landraces exhibited different reactions to the disease and their reactions ranged from resistant- moderately resistant to susceptible. Landrace number 33 obtained from Diyarbakır was found the most resistant to the disease compared to all other landraces whereas landrace number 10 obtained from Bilecik-Söğüt, and cultivar Bülbül 89 were the most susceptible. The majority of the landraces were classified between the Moderately Resistant-Moderately Susceptible to Moderately Susceptible-Susceptible. Landrace number 33 exhibited Resistant-Moderately Resistant reactions to both isolates. This landrace from Diyarbakır could be used as the seed source and in the breeding studies for obtaining barley cultivars resistant to the net form of net blotch disease.
Article
Full-text available
Unimproved landraces and wild relatives of crops are sources of genetic diversity that were lost post domestication in modern breeding programs. To tap into this rich resource, genome-wide association studies in large plant genomes have enabled the rapid genetic characterization of desired traits from natural landrace and wild populations. Wild barley (Hordeum spontaneum), the progenitor of domesticated barley (Hordeum vulgare), is dispersed across Asia and North Africa, and has co-evolved with the ascomycetous fungal pathogens Pyrenophora teres f. teres and P. teres f. maculata, the causal agents of the diseases net form of net blotch and spot form of net blotch, respectively. Thus, these wild and local adapted barley landraces from the region of origin of both the host and pathogen represent a diverse gene pool to identify new sources of resistance, due to millions of years of co-evolution. The barley—P. teres pathosystem is governed by complex genetic interactions with dominant, recessive, and incomplete resistances and susceptibilities, with many isolate-specific interactions. Here, we provide the first genome-wide association study of wild and landrace barley from the Fertile Crescent for resistance to both forms of P. teres. A total of 14 loci, four against P. teres f. maculata and 10 against P. teres f. teres, were identified in both wild and landrace populations, showing that both are genetic reservoirs for novel sources of resistance. We also highlight the importance of using multiple algorithms to both identify and validate additional loci.
Article
Full-text available
Pyrenophora teres is an important pathogen of barley. The pathogen has two biotypes: Pyrenophora teres f. teres, which causes the net type of net blotch, and P. teres f. maculata causing the spot type of net blotch. Turkey is an important gene centre of barley and has a rich barley landrace population. Finding disease resistant barley germplasm has potential for world agriculture. Three virulent Pyrenophora teres f. maculata (Ptm) isolates and three virulent Pyrenophora teres f. teres (Ptt) isolates were tested for their pathogenicity to 198 barley landraces, and landraces resistant to both forms of the pathogen were identified. Thirteen landraces (numbered 17, 40, 71, 98, 101, 103, 104, 143, 162, 167, 171, 183 and 185) were resistant to the Ptm isolates and seven (numbered 18, 21, 22, 24, 40, 71 and 153) were resistant to the Ptt isolates. Two landraces (40 and 71) were resistant to all six P. teres isolates. In addition, several of the landraces exhibited reactions to one or two isolates of Ptt or Ptm, in the resistant to moderately resistant range. Using disease resistant host genotypes will help to reduce the use of disease control chemicals, and with development of efficient host resistance strategies to combat net blotch diseases. These landraces could be used as sources of resistance for barley breeding.
Article
Full-text available
Spot form net blotch (SFNB) caused by Pyrenophora teres f. maculata is a major foliar disease of barley (Hordeum vulgare) worldwide. SFNB epidemics have recently been observed in major barley producing countries, suggesting that the local barley cultivars are not resistant and that virulence of the local pathogen populations may have changed. Here we attempt to identify sources of resistance effective against four diverse isolates of P. teres f. maculata collected from around the world. A total of 2,062 world barley core collection accessions were phenotyped using isolates of the pathogen collected in the United States (FGO), Australia (SG1), New Zealand (NZKF2), and Denmark (DEN 2.6). Isolate-specific susceptibility was identified in several of the barley accessions tested, indicating variability in both pathogen virulence and host resistance/susceptibility. Collectively, only 15 barley accessions were resistant across all isolates tested. These resistant accessions will be used to generate mapping populations and for germplasm development. Future research will involve the characterization of host resistance, pathogen virulence, and the host-pathogen interaction associated with SFNB of barley.
Article
Full-text available
The cultivated barley (Hordeum vulgare subsp. vulgare) is one of the major crops in the world. In this study the genetic diversity of 32 individuals of two-rowed and six-rowed Iranian landraces barley evaluated using 17 microsatellite markers. A high level of polymorphism information content (PIC; average = 0.651) and an average of 8.117 allele per locus were observed. In dendrograms constructed based on the SSR data, the two group of cultivars (var. distichon and var. hexastichon) were separated. Based on the results of this study, it can be concluded that there is a high level of genetic diversity between the barely landraces in Iran and that the barely Iranian gene pool is valuable source to search for new useful alleles for crop improvement.
Article
Recent changes in the virulence patterns of Canadian barley pathogens have necessitated the search for new sources of genetic resistance in barley. Evaluation of 176 Turkish barley accessions for disease reaction to barley pathogens prevalent in Canada indicated that this germplasm is a good source of resistance to Septoria passerinii, Rhynchosporium secalis and the spot- form of Pyrenophora teres, but not to Cochliobolus sativus (spot blotch phase), Puccinia graminis tritici, Ustilago nuda or barley stripe mosaic virus. A small number of accessions with resistance to the net-form of P. teres were identified.
Article
The responses of 95 barley lines and cultivars to spot form of net blotch (SFNB) caused by Pyrenophora teres f. maculata were analyzed as seedlings and adults in Australia and Canada. Cluster analyses revealed complex reaction responses. Only 2 lines (Esperance Orge 289 and TR3189) were resistant to all isolates at the seedling stage, whereas 15 lines and cultivars (81-82/033, Arimont, BYDV-018, CBSS97M00855T-B2-M1-Y1-M2-Y-1M-0Y, C19776, Keel, Sloop, Torrens, TR326, VB0111, Yarra, VB0229, WI-2477, WI2553, and Wisconsin Pedigree) were resistant toward the two Canadian isolates and mixture of Australian isolates at the adult stages. In Australian field experiments, the effectiveness of SFNB resistance in three barley cultivars (Barque. Cowabbie, and Schooner) and one breeding line (VB9104) with a different source of resistance was tested. Barque, which possessed a resistance gene that provided complete resistance to SFNB, was the most effective and showed no effect on grain yield or quality in the presence of inoculum. Generally, cultivars with seedling or adult resistance had less disease and better grain quality than the susceptible control. Dash, but they were not as effective as Barque. A preliminary differential set of 19 barley lines and cultivars for P teres I. maculata is proposed.
Article
The occurrence of physiologic specialization in D. tere8 is reported. Three distinct physiologic races could be differentiated on two barley varieties, Algerian (C.l. 1179) and C.l. 7584. The distribution of these physiologic races in Western Australia is shown.