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

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Virus diseases, although seldom lethal. reduce plant vigorand<br />

yield potential <strong>of</strong> seed tubers. Identification is complicated by<br />

wide symptom variation attributable to virus strain differences,<br />

plant response in relation to maturity and duration <strong>of</strong> infection,<br />

potato cultivar. and environmental influences. l)ifferentiation<br />

<strong>of</strong> viruses may involve purification, electron microscopy,<br />

comparison <strong>of</strong> physical properties, clectrophoresis. serology,<br />

and possibly other techniques. Recent developments in serology<br />

using the ELISA (eniyme-linked immunosorbent assay)<br />

,echnique provide an extremely sensitive test for virus presence<br />

and identity and have for the first time permitted serology with<br />

certain viruses difficult to detect in potato.<br />

General References<br />

BODE. 0. 1958, Die Virosen der Kart<strong>of</strong>fel und des'Tahaks. Pages 1-30<br />

in: M. Klinkowski, ed. i'lianliche Virologie. Vol. II. Akademie-<br />

Verlag. Berlin. 393 pp.<br />

CI.ARK. M. F., and A. N. ADAMS. 1977. Characteristics <strong>of</strong> the<br />

microplate method <strong>of</strong> eniime-linked immunosorbent assay for the<br />

detection <strong>of</strong> plant viruses. .1.Gen. Virol. 34:475-483.<br />

de BOKX, J. A.. ed. 1972. Viruses <strong>of</strong> <strong>Potato</strong>es and Seed-<strong>Potato</strong><br />

Production. Pudoc, Wageningen, The Netherlands. 233 pp.<br />

FERNANDEZ VAI.IEI.A, M. V. 1969. Introducci6n a la<br />

Fitopatologiii. Vol. I. Virus, 3rd ed. Pages 764-845. Inst. Nac. de<br />

lecnol. Agropecuaria. Buenos Aires. 1,011 pp.<br />

GIBBS. A.. and B. HARRISON. 1976. Plant Virology: The Principles.<br />

.Joh n Wiley and S o ns, New Y o rk. 292 pp .<br />

KI.INKOWSKI. M.. and 1H.KEGI.ER. 1962. Viruskrankheiten der<br />

Kart<strong>of</strong>fel. pages 1025-1138 in: R. Schick and M. Klinkowski. eds.<br />

Die Kart<strong>of</strong>fel, Vol. II.2.112 pp.<br />

MATItEWVS, R. E. F. 1970. Plant Vir,',,gy. Academic Press, New<br />

York. 778 pp.<br />

SMITH. K. M. 1972. A texlbook <strong>of</strong> .< virus diseases, 3rd ed.<br />

Longman, Iondon. 684 pp.<br />

<strong>Potato</strong> Leafroll Virus<br />

<strong>Potato</strong> leafroll, an aphid-transmitted disease is one <strong>of</strong> the<br />

most serious in potato and is responsible for high yield losses<br />

throughout the world wherever potatoes are grown. In<br />

Colo<strong>mb</strong>ia and the Andes, the potato leafroll virus (PLVR)<br />

occurs in Solanum andigena potatoes: the disease has been<br />

known as "enanismo amarillo" for many years.<br />

Symptoms<br />

Primary symptoms (Plate 55) follow transmission by aphids<br />

Symptoms appear mainly in the young leaves, which usually<br />

stand uprigh:, roll, and turn slightly pale. In some cultivars,<br />

young leaves are pink to reddish starting at tile margins. Rolling<br />

sometimes affects only the base <strong>of</strong> the leaflet rather than the<br />

whole leaflet. These symptoms may spread later to the lower<br />

leaves. Primary symptoms may be lacking with late season<br />

infection, making diagnosis in seed stocks a major problem.<br />

Secondary symptoms (Plate 56) become evident when an<br />

infected tuber produces a plant. Lower leaflets are rolled and<br />

higher leaves are slightly pale. l.eaves are stiff,dry, and leathery<br />

and make a crisp, somewhat paperlike sound when touched.<br />

Older leaves <strong>of</strong> some cultivars are i..ak and or severely necrotic,<br />

especially at the margins. Plants are <strong>of</strong>ten noticeably stunted<br />

and rigid. Symptoms are less pronounced in the top <strong>of</strong> a plant<br />

with secondary infection than in one with primary irfection, and<br />

secondary infection is more damaging to the plant. Severity <strong>of</strong><br />

symptoms depends on the isolate <strong>of</strong> the virus, the potato<br />

cultivar, and the growing conditions.<br />

In S. tuherosumssp. antdigena cultivars. secondary symptoms<br />

(enanismo amarillo) tend to be somewhat different from those<br />

in S. tuherosum ssp. tuherosutm, consisting <strong>of</strong> a marked upright<br />

habit <strong>of</strong> growth. stunting, and a marginal and interveinal<br />

68<br />

Viruses<br />

chlorosis <strong>of</strong> leaflets (Plate 57), especially <strong>of</strong>' dwarfed upper<br />

leaves. Rolling <strong>of</strong> lower leaves is <strong>of</strong>ten lacking. Secondary<br />

symptoms in hybrids <strong>of</strong> S. tuherosum ssp. andigena X S.<br />

tuherosum ssp. tuherosum consist <strong>of</strong> the rolling <strong>of</strong> lower leaves<br />

typical <strong>of</strong> S. tuherosuim ssp. tuherostni cultivars. In some<br />

cultivars, however, distinct interveinal and marginal chlorosis<br />

occurs as in S. tuherosumn ssp. antdigena cultivars.<br />

Internal net necrosis (Figs. 28B and 73A), visible to the<br />

unaided eye when the tuber is cut, is particularly marked in<br />

certain American cultivars such as Russet Burbank, Green<br />

Mountain, and Norgold Russet. This net necrosis is found in<br />

tubers from plants with primary, secondary, or tertiary<br />

infection. The color may vary from light translucent to dark. A<br />

definite trend toward a less severe type <strong>of</strong> infection from<br />

primary to tertiary has been found in tubers <strong>of</strong> Russet Burbank.<br />

Causal Agent<br />

PI.VR has icosahedral particles 24 nm in diameter(Figs. 73D<br />

and E).<br />

'ransmission is successful only by aphids and grafting;<br />

artificial inoculation by mechanical means has never been<br />

accomplished. The virus is transmitted by aphids in a persistent<br />

(circulative) manner (i.e.. after an aphid has fed on an infected<br />

plant it normally transmits the virus for the rest <strong>of</strong> its life).<br />

Isolates have not been differentiated by serological, physical,<br />

or chemical properties nor by vector specificity or transmission<br />

e mical No per ti ano r no All tra ns i ssi on<br />

efficiency. No differential plants are known. All strains give the<br />

same type <strong>of</strong> symptoms. Isolates vary in severity <strong>of</strong> symptoms<br />

on potato cultivars and on Ph'salisfloridana, but existence <strong>of</strong><br />

strains has not been well defined. Some workers refer to three<br />

strains called severe, moderate, and mild; others refer to<br />

four strains called No. 1,2, 3, and 4. A fifth isolate, differing in<br />

symptom severity from No. I on P.floridana but not on other<br />

hosts, has been isolated.<br />

Histopathology<br />

From the moment <strong>of</strong> symptom appearance, infections are<br />

always accompanied by phloem necrosis, which consists <strong>of</strong><br />

thickening <strong>of</strong> the walls <strong>of</strong> the primary phloem cells in the stem<br />

and petioles (Fig. 73B). Accumulation <strong>of</strong> callose is <strong>of</strong>ten<br />

pronounced around the sieve plates in the phloem <strong>of</strong>tubersand<br />

stems (Fig. 73C). Stiffness <strong>of</strong> leaves in primary and secondary<br />

infections isaconsequence <strong>of</strong> starch accumulation in leaf cells.<br />

Epidemiology<br />

SThe virus istuberborne and isalso efficiently<br />

persistent<br />

transmitted<br />

manner<br />

in<br />

by<br />

a<br />

aphids that colonize potatoes, My'zus<br />

persicae being the most efficient. Infection efficiency increases<br />

with the length <strong>of</strong> feeding. The virus is spread over long<br />

distances by windborne winged aphids and over short distances<br />

by nonwinged aphids moving from plant to plant. Aphid<br />

transmission occurs from tuber t(. tuber during seed storage,<br />

especially in tropical countries. Plants from infected tubers and<br />

diseased volunteer potato plants also serve as virus sources.<br />

Moderate temperatures and dry weather favor spread. Plants<br />

become resistant to infection with age, and occasionally some<br />

tubers <strong>of</strong> plants infected late in the season escape infection.<br />

Other Hists<br />

Several plant species, mostly in the Solanaceac, are known as<br />

hosts.<br />

P.floridana is asuitable indicator, test, and propagation host<br />

that reacts with interveinal chlorosis, darkening <strong>of</strong> the veinal<br />

areas, and a slight cupping at the first two or three true leaves.<br />

Infections at a later stage cause plants to become somewhat<br />

pale.<br />

Datura siraionium is favored by some workers, especially in<br />

the more tropical regions, as a test and propagation host in<br />

which chlorosis develops. In Brazil, alternative hosts to PI.VR

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