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Compendium of Potato Diseases - (PDF, 101 mb) - USAID

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invaders through the IFusarium lesions and rapidly rot the reinainder<br />

<strong>of</strong> the tuber. Suspended bacteria and juices exuded<br />

from the s<strong>of</strong>t rot endanger surrounding tubers.<br />

Whole-tuber seed becomes infected through wounds during<br />

storage or preparation for planting. The cut surfaces <strong>of</strong> large<br />

seed tubers are major infection courts. In stored seed tubers,<br />

brown to black flecks appear on the cut surface in about one<br />

week and depressions or pits form in two weeks (Fig. 65A and B).<br />

Mycelia <strong>of</strong>ten grow on the depressed surfaces, and undet humid<br />

conditions, depressions may become slimy and black from<br />

bacterial growth. S<strong>of</strong>t rotting bacteria may also invade through<br />

the IFttsarium lesions and accelerate decay. With numerous<br />

cut-surfacc infections, lesions coalesce: the seed piece rots from<br />

the surface inward: and buds (eyes) are destroved as decay<br />

progresses.<br />

In the field, the shriveling <strong>of</strong> infected seed tubeis and pitting<br />

<strong>of</strong> infected pieces may not he evident. The surface over the<br />

lesions is brown, and the underlying necrotic tissues have fewer<br />

cavities. Necrotic tissue may attract soil insects and larvae such<br />

as the seed-corn maggot, which is avector <strong>of</strong> Erwiniaspecies. In<br />

wet soils, these species <strong>of</strong>ten enter as secondary pathogens.<br />

Fusarin spp. alone or in conjunction with Erwinia spp.<br />

partially or completely destroy the seed piece, resulting in<br />

extreme variability in plant size and manl, missing plants (Fig.<br />

651) and E). Often single ;prots emerge: these are small, grow<br />

slowly, produce few marketable tubers, and have a high<br />

incidence <strong>of</strong> blackleg.<br />

Causal Organisms<br />

1usariun solani (Mart.) App. & Wr. emend Snyd. & Hans.<br />

'Coeruleum and 1.ro'seum (l.k.) Snyd. & Hans. 'Sa<strong>mb</strong>ucinum'<br />

are most frequently implicated in seed piece decay. In sonic<br />

regions one species is dominant over the other, nut both are<br />

<strong>of</strong>ten associated with a seed stock. I. solani is most frequently<br />

encountered and is the more aggressive pathogen. Both grow<br />

and are maintained ott potato-dextrose agar, and the acidified<br />

medium facilitates their isolation when bacteria are present. F<br />

roseu'um grows more rapidly, forming athin, white mycelial mat<br />

and abundant pink to salmon spores. The slower growing .<br />

soani forms a denser, white mycelial mat that exhibits a purple<br />

pigment with age (Plate 48). F.slthnisporulates in culture more<br />

sparsely than does I-'. rosetun (Fig. 66). The optimum temperature<br />

for growth in culture is 20-25°C and for infection,<br />

10-20" .<br />

1:.roseum 'Avenaceum' also causes adry rot <strong>of</strong> potatoes, but<br />

less frequently than the other species do.<br />

Histopathology<br />

Fusariumn spp. cannot infect intact tuber periderni or<br />

lenticels. Cuts and periderm-breaking wounds incident to harvesting,<br />

storage, grading, and transport are the major infection<br />

courts. Wounds from insect and rodent feeding and frost are<br />

sometimes infected. The Fusaria can also invade surface lesions<br />

<strong>of</strong> powdery scab, late blight, mop top virus, and possibly other<br />

di:,eases.<br />

Hlyphae are at first intercellular becoming intracellular in<br />

dead cells. In spreading lesions, hyphae may be sparse in intercellular<br />

spaces, with host cells :',owing little reaction to the<br />

fungus. Toward the center <strong>of</strong> the lesion, less<br />

intercelluar<br />

starch<br />

spaces<br />

is<br />

by<br />

present,<br />

suberin audnt deposited abe inhostcellwalsaandnt<br />

nfetoh<br />

and the myceliuni. usually abundant, may be confined to the<br />

intercellular spaces. In susceptible tissue, starch hydrolysis and<br />

suberin deposition are lacking. Small lesions restricted near the<br />

site <strong>of</strong> infection may be underlaid by a continuous layer <strong>of</strong><br />

wound meristem cells with suberin deposition. With other<br />

isolates, hyphae kill and penetrate cells within two cells <strong>of</strong><br />

normal-appearing tissue. Details <strong>of</strong> the reaction depend on the<br />

pathogen, the resistance <strong>of</strong> the tuber, and the part <strong>of</strong> the lesion<br />

examined.<br />

Disease Cycle<br />

Fusariumspp. can survive for several years in field soil, but<br />

the primary inoculum is generally borne on seed tuber surfaces.<br />

Surfaceborne propagules contaminate containers and equipment<br />

used in handling or storing potatoes and enter wounds<br />

incident to handling seed tubers. Infected seed tubersand pieces<br />

decayand infest the soil that adheres to the surfaces <strong>of</strong> harvested<br />

tubers.<br />

Epidemiology<br />

Tubers <strong>of</strong> potato cultivars differ in susceptibility to F. solani<br />

and F roseum, but none tested was immune to either pathogen.<br />

Certain cultivars are tolerant to both.<br />

Tubers are tolerant to infection when harvested.<br />

Susceptibility increases during storage and ,:aches its maximumin<br />

early spring about planting time.<br />

Wound healing can reduce infection. Deposition <strong>of</strong>suberin in<br />

the cell walls does not prevent infection, but wound periderm<br />

does. Wound periderm forms in three to four days at approximately<br />

21°C with adequate aeration and humidity but more<br />

slowly at lower temperatures. At 15'C, near optimum for<br />

infection, a period <strong>of</strong> approximately eight days is required to<br />

form periderm; wound healing is not effective at this cr lower<br />

temperatures.<br />

Dry rot develops most rapidlyin high relative humidityand at<br />

15-20' C. Relative humidities about 70% do not alter rot development,<br />

but lower iiumidities retard infection and disease<br />

development. Disease development continues at the coldest<br />

temperatures safe for potatoes.<br />

If the soil temperature and moisture are suitable for rapid<br />

sprout growth and emergence, seed tuber or piece decay after<br />

planting maybe<strong>of</strong>little consequence. Conditioning seed tubers<br />

from cold storage at 20-25' C for one week before cutting pieces<br />

reduces decay and accelerates sprout growth. Holding contaminated<br />

cut seed several days or weeks before planting or planting<br />

in soils too cold or dry for prompt sprout emergence and plant<br />

growth will accentuate losses. Excessively wet soils after<br />

planting increase secondary infection by Erwinia spp.<br />

Other Hosts<br />

F. solani isolates from Colocasia corms can infect potato<br />

tubers. Generally, tuber-rotting Fusaria do not infect other<br />

plants or plant organs.<br />

Resistance<br />

Differences in resistance exist among potato cultivars. Relative<br />

ranking <strong>of</strong> resistance isinfluenced by the Fusarium sp. used<br />

for inoculation. Seed lots infected with potato virus X are<br />

relatively more resistant than those free from the virus when<br />

harvested within three weeks <strong>of</strong> top kill.<br />

Control<br />

1ontrm<br />

I) For storage and seed purposes, harvest tubers from dead<br />

vine<br />

2) Use all precautions with machinery and equipment to<br />

171V' I,<br />

. __<br />

V..<br />

"<br />

,,00 ,<br />

.)'. .<br />

-<br />

Fig. 66. Fusarium solani from culture with many macroconidia<br />

and a single microconidium in center. (x950) (Courtesy P. E.<br />

Nelson)<br />

59

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