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Sorghum Diseases in India

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leaf-disease resistance (polygenic) perhaps coupled,<br />

where needed, with pathogen-specific<br />

(monogenic or oligogenic) resistance has been<br />

successful <strong>in</strong> other crops and might be a valuable<br />

approach with sorghum (Hooker and Perk<strong>in</strong>s<br />

1980). <strong>Sorghum</strong>s with the "stay-green" or<br />

nonsenescent characters (Duncan 1984; Rosenow<br />

1984) may be valuable sources for general<br />

leaf-disease resistance.<br />

<strong>Sorghum</strong> breeders often treat sorghum as a<br />

self-poll<strong>in</strong>at<strong>in</strong>g crop which is most amenable to<br />

identification of monogenic resistance, while<br />

population breed<strong>in</strong>g—be<strong>in</strong>g dependent on both<br />

self- and cross-poll<strong>in</strong>ation—is useful <strong>in</strong> identify<strong>in</strong>g<br />

monogenic and polygenic sources of resistance.<br />

Frederiksen and Rosenow (1986) suggest<br />

that resistance traits should be present at levels<br />

that can be readily evaluated and they must be<br />

heritable and stable across environments- They<br />

state that progress <strong>in</strong> disease-resistance breed<strong>in</strong>g<br />

can be made us<strong>in</strong>g several methods, <strong>in</strong>clud<strong>in</strong>g<br />

pedigree l<strong>in</strong>e breed<strong>in</strong>g, backcross breed<strong>in</strong>g,<br />

and population breed<strong>in</strong>g.<br />

Resistance (monogenic or polygenic) that reduces<br />

the rate of disease development aga<strong>in</strong>st all<br />

races of a pathogen effectively is especially<br />

needed for pathogens with known races (Frederiksen<br />

and Rosenow 1986). This type of resistance<br />

may also reduce selection pressure for<br />

variants of other foliar pathogens. General or<br />

durable resistance conferred by many genes can<br />

have several additive and synergistic effects <strong>in</strong><br />

host response to pathogens but their collective<br />

response under disease-conducive environments<br />

is the important factor and more easily<br />

measured.<br />

The world collections of landrace and other<br />

sorghums represent a vast and diverse resource<br />

conta<strong>in</strong><strong>in</strong>g all types of resistances to many foliar<br />

and other pathogens. Scientists have already<br />

identified a large number of elite disease-resistant<br />

materials and they are be<strong>in</strong>g used and evaluated<br />

<strong>in</strong> sorghum programs around the world.<br />

Yet, this represents only a small proportion of<br />

what is available.<br />

There are a multitude of germplasm-screen<strong>in</strong>g<br />

techniques that range from fully natural disease<br />

development <strong>in</strong> the field to strictly<br />

controlled pathogen and environment conditions<br />

<strong>in</strong> the greenhouse and laboratory (Sharma<br />

1980; Williams et al. 1980; Frederiksen and<br />

Frankl<strong>in</strong> 1980). Mughogho (1982) stated that no<br />

screen<strong>in</strong>g techniques were available for sooty<br />

stripe and gray leaf spot. This was due largely to<br />

the lack of laboratory techniques to mass produce<br />

conidia for greenhouse or field <strong>in</strong>oculation.<br />

Odvody (1981) developed a sporulation technique<br />

for Cercospora sorghi that was successfully<br />

utilized <strong>in</strong> germplasm screen<strong>in</strong>g by Wall (1983).<br />

Ramulispora sorghi sporulates <strong>in</strong> almost a yeastlike<br />

fashion on potato dextrose agar if <strong>in</strong>cubated<br />

under a cont<strong>in</strong>uous source of longwave UV light<br />

(Odvody, unpublished). The conidia can be serially<br />

transferred and streaked, as with bacteria,<br />

onto media for mass production.<br />

Other Disease Controls<br />

Destruction of <strong>in</strong>fested host debris<br />

The ecology of foliar pathogens is of considerable<br />

<strong>in</strong>fluence on how cultural practices and<br />

farm<strong>in</strong>g systems affect the <strong>in</strong>cidence of specific<br />

diseases. Most foliar pathogens of sorghum are<br />

favored by tillage that permits pathogen survival<br />

<strong>in</strong> surface host-residue lesions. Control by<br />

m<strong>in</strong>imalization of host residues is more effective<br />

with some pathogens than others. Pathogens<br />

dissem<strong>in</strong>ated primarily by w<strong>in</strong>d, like E. turcicum,<br />

can more easily overcome distance limitations<br />

imposed by such practices (Frederiksen<br />

1986). Those pathogens surviv<strong>in</strong>g as sclerotia <strong>in</strong><br />

soil, e.g., R. sorghi, may be long-lived <strong>in</strong> the soil<br />

but the more rapid destruction of lesion debris<br />

<strong>in</strong>creases the exposure of sclerotia to the deleterious<br />

soil microenvironment. Colletotrichum<br />

gram<strong>in</strong>icola survives only <strong>in</strong> host debris, but its<br />

ability to attack more than one plant organ compensates<br />

somewhat for that dependency.<br />

Destruction of collateral hosts<br />

Pucc<strong>in</strong>ia purpurea, a w<strong>in</strong>d-dissem<strong>in</strong>ated pathogen,<br />

must survive on a liv<strong>in</strong>g host. Destruction<br />

of collateral hosts may at times be an effective<br />

control for P. purpurea and several other pathogens,<br />

but this practice is often impractical except<br />

<strong>in</strong> the proximity of field areas.<br />

Crop rotation and disease escape<br />

Crop rotations are especially effective where<br />

pathogen survival is dependent on debris, but<br />

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