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Sorghum Diseases in India

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sclerotia or on leaf lesions are borne <strong>in</strong> a similarly<br />

function<strong>in</strong>g water-soluble matrix (Olive et<br />

al. 1946; Ba<strong>in</strong> and Edgerton 1943). Under dry<br />

conditions, s<strong>in</strong>gle conidial masses of G. sorghi<br />

and R. sorghi are held so tightly together that<br />

their removal from lesions is possible only en<br />

masse, but when the mass is placed <strong>in</strong>to free<br />

water, the conidia immediately disperse as<br />

<strong>in</strong>dividual spores (Odvody, unpublished observation).<br />

The spore-dispersal mechanisms are consistent<br />

with the epidemiology of these pathogens,<br />

especially the latter group that form spores <strong>in</strong><br />

protective structures and matrices. They have<br />

high free water requirements for both <strong>in</strong>oculum<br />

dispersal and <strong>in</strong>itial <strong>in</strong>fection.<br />

The <strong>in</strong>itial <strong>in</strong>oculum of S. rolfsii and Rhizoctonia<br />

spp caus<strong>in</strong>g blights of the leaf sheaths is<br />

primarily mycelial, and derives probably from<br />

sclerotia and other colonized substrate, because<br />

<strong>in</strong>fection usually beg<strong>in</strong>s on basal sheaths near<br />

the soil l<strong>in</strong>e (Odvody and Madden 1984; O'Neill<br />

and Rush 1982). Rhizoctonia spp may also produce<br />

basidiospores as <strong>in</strong>itial and secondary <strong>in</strong>oculum<br />

(O'Neill and Rush 1982).<br />

Host Range and Pathology Variability<br />

Exserohilum turcicum and C. gram<strong>in</strong>icola can be<br />

pathogenic on sorghum, maize (Zea mays), and<br />

other grasses, but naturally occurr<strong>in</strong>g isolates<br />

from host crops are generally genus-specific<br />

(Frederiksen 1980,1984). Gloeocercospora sorghi is<br />

reported to attack sorghum, maize, and some<br />

other grasses, but more <strong>in</strong>formation concern<strong>in</strong>g<br />

host specificity (Tarr 1962) is needed.<br />

Sclerotium rolfsii and the Rhizoctonia spp<br />

(probably R. solani) caus<strong>in</strong>g sheath blights on<br />

sorghum are pathogenic to a wide variety of<br />

hosts, and might be described as facultative<br />

parasites (O'Neill and Rush 1982; Odvody and<br />

Madden 1984).<br />

The other pathogens listed (Table 1) are generally<br />

regarded as occurr<strong>in</strong>g only on <strong>Sorghum</strong><br />

spp. Isolated reports of some of these pathogens<br />

on other hosts could be the result of error <strong>in</strong><br />

identification of the pathogen, saprophytic <strong>in</strong>stead<br />

of parasitic attack, or extremely unusual<br />

conditions allow<strong>in</strong>g <strong>in</strong>fection. The large number<br />

of m<strong>in</strong>or, seldom-reported diseases of sorghum<br />

could be due to similar factors, especially as<br />

senesc<strong>in</strong>g sorghum leaves become vulnerable to<br />

170<br />

weak pathogens and saprophytes (Frederiksen<br />

1986).<br />

Of the pathogens listed <strong>in</strong> Table 1, only<br />

C. gram<strong>in</strong>icola (Frederiksen 1984) and P. purpurea<br />

(Bergquist 1974) currently have pathotypes<br />

(races) described on sorghum.<br />

Geographic Distribution<br />

Frederiksen (1982), S.B. K<strong>in</strong>g, and N.V. Sundaram<br />

classified the major diseases of sorghum<br />

on the basis of prevalence and severity <strong>in</strong> temperate<br />

(outside 34° latitude), subtropical (between<br />

23 °15' and 34° latitude), and tropical (with<strong>in</strong><br />

23°15' latitude) regions. Accord<strong>in</strong>g to their<br />

classification, the foliar pathogens E. turcicum,<br />

C. gram<strong>in</strong>icola, C. sorghi, P. purpurea, G. sorghi,<br />

R. sorghi, and A. sorgh<strong>in</strong>a are all commonly or<br />

generally found on sorghum grown <strong>in</strong> the subtropics<br />

and on sorghum grown <strong>in</strong> the tropical<br />

lowland dur<strong>in</strong>g summer. Occurrence of these<br />

pathogens was less consistent <strong>in</strong> the cooler temperate<br />

and tropical highland or tropical w<strong>in</strong>ter<br />

environments. The pathogens C. sorghi, E. turcicum,<br />

and P. purpurea, easily w<strong>in</strong>d-dissem<strong>in</strong>ated,<br />

are apparently the most consistent <strong>in</strong> their<br />

occurrence and <strong>in</strong>cidence across all these diverse<br />

sorghum-grow<strong>in</strong>g environments. Bipolaris<br />

sorghicola also occurs, but only occasionally, <strong>in</strong><br />

all these environments. The potential misidentification<br />

of B. sorghicola lesions as those of<br />

C. sorghi could partially account for its lower reported<br />

occurrence.<br />

The reported observations of C. sorghi may<br />

also <strong>in</strong>clude occurrences of the newly described<br />

C fusimaculans. Ramulispora sorghicola seems to<br />

be restricted to warmer conditions <strong>in</strong> the subtropics<br />

and tropical lowland summers, and it<br />

usually does not have a high disease <strong>in</strong>cidence.<br />

Phyllachora sacchari is limited to high-ra<strong>in</strong>fall<br />

tropical areas (Dalmacio 1986), possibly due <strong>in</strong><br />

part to requirements for a liv<strong>in</strong>g weed-host reservoir<br />

for significant pathogen survival and the<br />

need for wet conditions for <strong>in</strong>fection, disease development,<br />

and <strong>in</strong>oculum dispersal.<br />

Host: Parasite Interaction<br />

Initial <strong>in</strong>fection of sorghum by foliar pathogens<br />

requires high moisture conditions for specific<br />

periods to allow spore germ<strong>in</strong>ation and penetra-

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