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ICRISAT Archival Report 2006 - The seedlings of success in the ...

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studied. Percentage <strong>of</strong> micro-conidia was significantly more than macro-conidia <strong>in</strong> all isolates. Highest percentage<br />

<strong>of</strong> micro conidia (81.4%) <strong>in</strong> FOC 4 and lowest (51.6) <strong>in</strong> R4 was recorded. Largest micro-conidia (10.1x 5.5 μ m)<br />

were observed <strong>in</strong> FOC 38, and smallest (7.7 x 4.8 μ m) <strong>in</strong> FOC 8. Macro-conidia were larger (22.1 x 5.8 μ m) <strong>in</strong> <strong>the</strong><br />

isolate R4, while <strong>the</strong>y were smaller (14.9 x 5.5 μ m) <strong>in</strong> FOC 32. Mean number <strong>of</strong> cells <strong>in</strong> macro-conidia were 3.1<br />

<strong>in</strong> FOC 10 and 4.6 <strong>in</strong> FOC 41.<br />

Characterization <strong>of</strong> variability <strong>of</strong> Ascochyta rabiei : Differential reaction <strong>of</strong> cultivars to AB at different locations<br />

<strong>in</strong> India <strong>in</strong>dicated <strong>the</strong> probable existence <strong>of</strong> races/pathotypes <strong>in</strong> <strong>the</strong> pathogen, A. rabiei. Hence, we <strong>in</strong>itiated a<br />

systematic research to characterize races/pathotypes <strong>in</strong> A. rabiei. <strong>The</strong> A. rabiei <strong>in</strong>fected chickpea plants were<br />

collected from 14 locations <strong>in</strong> different agroclimatic regions <strong>in</strong> India. Isolations were made from <strong>the</strong>se <strong>in</strong>fected<br />

plants and pure cultures <strong>of</strong> s<strong>in</strong>gle spore isolates <strong>of</strong> A. rabie were obta<strong>in</strong>ed.<br />

Morphological and cultural variation: Seven s<strong>in</strong>gle spore isolates represent<strong>in</strong>g different agroclimatic zones were<br />

selected for study<strong>in</strong>g morphological, cultural, and pathogenic characters. Five mm diameter discs from actively<br />

grow<strong>in</strong>g cultures <strong>of</strong> A. rabiei were placed at <strong>the</strong> center <strong>of</strong> 90 mm diameter petri plates conta<strong>in</strong><strong>in</strong>g CDA, and<br />

<strong>in</strong>oculated at 20 0 C. Colony color, <strong>in</strong>tensity <strong>of</strong> <strong>the</strong> mycelium, colony diameter, number <strong>of</strong> conidiomata, and conidia<br />

were recorded. <strong>The</strong> A. rabiei isolates differed <strong>in</strong> morphology, colony color, colony size, pycnidial color (brown to<br />

slate grey), number <strong>of</strong> conidioamata (42.3 to 90.7 cm- 2 ), number <strong>of</strong> conidia (0.55 to 3.01 conidia 10 3 cm- 2 ), and<br />

conidial size (10.7 x 4.6 to 14 x 6.2 μm).<br />

Pathogenic variation: All <strong>the</strong> 14 isolates were used for <strong>in</strong>oculation on 180 germplasm and advanced breed<strong>in</strong>g l<strong>in</strong>es<br />

under controlled environment conditions. All <strong>the</strong> 14 isolates <strong>of</strong> A. rabiei differed <strong>in</strong> <strong>the</strong>ir virulence pattern aga<strong>in</strong>st<br />

180 l<strong>in</strong>es with AB 13 hav<strong>in</strong>g maximum virulence <strong>in</strong>dex <strong>of</strong> 7.9 and AB 6 with a m<strong>in</strong>imum <strong>in</strong>dex <strong>of</strong> 5.4 (Fig. 1). None<br />

<strong>of</strong> <strong>the</strong> l<strong>in</strong>es were asymptomatic to any <strong>of</strong> <strong>the</strong> test isolates. Of <strong>the</strong> 180 l<strong>in</strong>es, 10 l<strong>in</strong>es to AB 6 and seven l<strong>in</strong>es to AB<br />

27 showed a resistant reaction. None <strong>of</strong> <strong>the</strong> entries were resistant to five isolates (AB 4, AB 17, AB 26, AB 1, and<br />

AB 13), whereas only one entry showed resistant reaction to four isolates (AB 8, AB 15, AB 3, and AB 18). Of <strong>the</strong><br />

180 entries, 15 entries (ICC 12, ICC 607, ICC 2165, ICC 3918, ICC 4200, ICC 4475, ICC 5124, ICC 6306, ICC<br />

7002, ICC 13754, ICC 14911, ICCX 810800, ICCX 910028-39ABR-BP-10, ABR-BR, ILC 3870, and FLIP 82-258)<br />

differed significantly <strong>in</strong> <strong>the</strong>ir reaction to different isolates <strong>of</strong> A. rabiei, and hence were selected as differentials.<br />

Characterization <strong>of</strong> variability <strong>of</strong> Botrytis c<strong>in</strong>erea: Thirty-two isolates <strong>of</strong> B. c<strong>in</strong>erea <strong>in</strong>fect<strong>in</strong>g chickpea, lentil, and<br />

marigold were collected from different locations to determ<strong>in</strong>e <strong>the</strong> variability <strong>of</strong> <strong>the</strong> fungus. Of <strong>the</strong> 32 isolates, 23<br />

were collected from chickpea, 5 from lentil, 2 from marigold, 1 from Dahlia and 1 from grasspea. All <strong>the</strong> isolates<br />

were purified us<strong>in</strong>g BGM specific medium conta<strong>in</strong><strong>in</strong>g tannic acid. Prelim<strong>in</strong>ary analysis <strong>of</strong> eight Indian isolates<br />

us<strong>in</strong>g 20 RAPD primers (decamers) categorized <strong>the</strong>m <strong>in</strong>to two dist<strong>in</strong>ct groups. Detailed molecular analysis will be<br />

followed dur<strong>in</strong>g 2007-08 season.<br />

Fig. 1. Dendrogram show<strong>in</strong>g <strong>the</strong> cluster<strong>in</strong>g <strong>of</strong> <strong>the</strong> s<strong>in</strong>gle<br />

spore isolates <strong>of</strong> A. rabiei based on AFLP analysis;<br />

203

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