Cucurbit Genetics Cooperative Report 4:38-40 (article 21) 1981
Sources of Resistance to Viruses in Lagenaria siceraria
R. Provvidenti
New York State Agricultural Experiment
Station, Cornell University, Geneva, NY 14456
In 1977, we reported (2) that an accession of Lagenaria
siceraria, PI 391602 from China, was resistant to squash
mosaic virus (SqMV), watermelon mosaic virus 1 (WMV-1),
watermelon mosaic virus 2 (WMV-2). and that an occasional
plant was resistant to cucumber mosaic virus (CMV). In 1978,
Greber (1) also reported resistance to WMV-1 and MWV-2 in
an accession of the same species from Queensland, Australia.
Since it is known that some of these viruses are frequently
destructive where L. siceraria is cultivated, additional
germplasm of this species was evaluated with CMV, SqMV,
WMV-1, WMV-2, tobacco ringspot virus (TRSV), and tomato
ringspot virus (TmSV). These last two viruses are transmitted
by nematodes and are found with a certain frequency in New
York State (3).
Plants of 18 lines representing 12 countries were screened
for resistance under greenhouse and field conditions. All
plants received from one to three inoculations and those
which, upon assay, were found free of systemic infection,
were transferred to the field for further evaluation. Plants
were rated resistant if, at maturity, they were still free
of systemic infection.
From the results given in Table 1, it is evident that resistance
was found in one or more lines to five of the six viruses
used. Resistance to CMV was confined to PI 269506, PI 271353,
and a few plants of PI 391602. In these lines, virus infection
was confined to the inoculated leaves. However, further
testing using a large number of CMV isolates revealed the
existence of two strains able to infect systemically these
resistant lines. All lines were resistant to SqMV and the
plants responded with a few, small and often inconspicuous
necrotic local lesions. This hypersensitive reaction greatly
localized viral infection. Resistance to TmRSV was found
in PI 188809 and PI 271353, in which plants reacted only
with localized infection. Resistance to WMV-1 was more common
and was detected in plants of PI 188809, PI 271353, PI 280631,
PI 288499, PI 391602 and the Hawaiian cultivar Hyotan. Resistance
to WMV-2 was found in plants of PI 271353, PI 391602, 'Hyotan',
ad G-24386. All plants resistant to WMV-1 and/or WMV-2 were
free of local and systemic symptoms, but virus infection
occurred in inoculated leaves of some plants.
Three lines, PI 271353, PI 391602, and 'Hyotan', were resistant
to both WMV-1 and susceptible to WMV-2, or vice versa, suggesting
that resistance to these viruses in conferred by different
genetic factors. As a source of multi-resistance, PI 271353,
from India, appears to be the most valuable for a breeding
program. However, no information appears to be available
on the mode of resistance to these or any other virus affecting
L. siceraria.
Viral resistance in L. siceraria can be also useful
in separating viruses which may occur simultaneously in
naturally infecting cucurbit plants. We have used this host
to free CMV, WMV-1, or WMV-2 when found in association with
SqMV, or to separate WMV-1 from WMV-2 or vice versa. Although
most of the lines, when inoculated with SqMV, reacted with
a few and sparse necrotic local lesions, an occasional plant
responded with numerous lesions which remained small and
rather distinct for a long time. Thus, using selected plants,
it may be possible to use L. siceraria as a local
lesion host for qualitative and quantitative assay of SqMV.
In this respect, Lagenaria is potentially more
valuable than Cucumis metuliferus (4).
Table 1. Reaction to cucumber mosaic virus (CMV), squash
mosaic virus (SqMV), tobacco ringspot virus (TRSV) tomato
ringspot virus (TmRSV), watermelon mosaic virus 1 (WMV-1),
and watermelon mosaic virus 2 (WMV-2) of accessions of Lagenaria
siceraria.
Accession |
Origin |
CMV |
SqMV |
TRSV |
TmRSV |
WMV-1 |
WMV-2 |
PI 181913 |
Syria |
S |
R |
S |
S |
S |
S |
PI 188809 |
Philippines |
S |
R |
S |
R |
R |
S |
PI 197437 |
Ethiopia |
S |
R |
S |
S |
S |
S |
PI 269506 |
Pakistan |
R* |
R |
S |
S |
S |
S |
PI 270456 |
Mexico |
S |
R |
S |
S |
S |
S |
PI 271353 |
India |
R* |
R |
S |
R |
R |
R |
PI 273663 |
Ethiopia |
S |
R |
S |
S |
S |
S |
PI 287533 |
Italy |
S |
R |
S |
S |
S |
S |
PI 287534 |
Italy |
S |
R |
S |
S |
S |
S |
PI 280631 |
S. Africa |
S |
R |
S |
S |
R |
S |
PI 280636 |
S. Africa |
S |
R |
S |
S |
S |
S |
PI 288499 |
India |
S |
R |
S |
S |
R |
S |
PI 349591 |
New Guinea |
S |
R |
S |
S |
S |
S |
PI 391602 |
China |
S/R* |
R |
S |
S |
R |
R |
PI 414369 |
India |
S |
R |
S |
S |
S |
S |
Paphos |
Cyprus |
S |
R |
S |
S |
S |
S |
Hyotan |
Hawaii |
S |
R |
S |
S |
R |
R |
G-24386 |
California |
S |
R |
S |
S |
S |
R |
R = Resistant (no systemic infection).
S = susceptible (systemic symptoms).
* = some strains may cause systemic infection
Literature Cited
- Greber, R. S. 1978. Watermelon mosaic virus 1 and 2
in Queensland cucurbit crops. Aust. J. Agr. Res. 29:1235-1245.
- Provvidenti, R. 1977. Evaluation of vegetable introductions
from the People's Republic of China for resistance to
viral diseases. Plant Dis. Reptr. 61:851-855.
- Provvidenti, R., R. W. Robinson, and H. M. Munger. 1978.
Resistance in feral species to six viruses infecting Cucurbita.
Plant Dis. Reptr. 62:326-329.
- Provvidenti, R. and R. W. Robinson. 1974. Resistance
to squash mosaic virus and watermelon mosaic virus 1 in
Cucumis metuliferus. Plant Dis. Reptr. 58:735-738.