October 30, 2003
From:
American Phytopathological Soc., Plant Dis. Notes 87:1399, 2003
[edited]
First report of Zucchini yellow mosaic virus in cucumber in
Poland
H. Pospieszny and M. Cajza, Institute of Plant Protection,
Department of Virology and Bacteriology, Miczurina 20, 60-318
Poznan, Poland; and R. Plewa, Adam Mickiewicz University in
Poznan, Department of Experimental Biology, Animal Physiology,
Fredry 10, 61-701 Poznan, Poland. Plant Dis. 87:1399, 2003;
published on-line as D-2003-0912-01N, 2003. Accepted for
publication 27 Aug 2003.
In June
2002, mosaic and interveinal chlorosis were observed on 2
cucumber plants (_Cucumis sativus_) grown in one commercial
greenhouse in the western region of Poland. Electron microscopic
examination of leaf-dip preparations from infected plants showed
flexuous filamentous virus particles typical of potyviruses (720
to 750 nm long).
_Chenopodium amaranticolor_, _Chenopodium quinoa_, _Citrullus
lanatus_, _C. melo_, _C. sativus_, _Cucurbita maxima_,
_Cucurbita pepo_, _Cucurbita pepo_ cv. Giromontiina, _Cucurbita
pepo_ cv. Patissoniana, _Nicotiana benthamiana_, and _N.
tabacum_ were mechanically inoculated with sap from symptomatic
cucumber leaves. The virus caused local chlorotic lesions on
_Chenopodium amaranticolor_ and _Chenopodium quinoa_ and
systemic infection in all tested cucurbits, but it did not
infect tobacco plants.
Reverse
transcription-polymerase chain reaction (RT-PCR) amplification
of the 3' end of the genomic RNA was done by using P9502 as a
downstream primer and degenerate CPUP as an upstream primer to
amplify a highly conserved region of the potyviral coat protein
(1).
The PCR
products were directly sequenced with the CEQ DTCS dye
terminator cycle sequencing kit (Beckman Coulter, Inc.,
Fullerton, CA), and the analysis of dideoxy terminated fragments
was conducted by capillary electrophoresis using a CEQ 2000 DNA
Analysis System (Beckman Coulter, Inc.).
The
obtained 684 nt sequence (GenBank Accession No. AY347476) was
almost identical with sequences of Zucchini yellow mosaic virus
(ZYMV) isolates from Austria (GenBank Accession Nos.
AJ420012-AJ420019 and AJ420027) and Hungary (GenBank Accession
Nos. AJ459954 and AJ459955). The above suggested that the Polish
isolate of ZYMV belonged to the Central European branch of the
phylogenetic tree (2).
To our
knowledge, this is the first report of ZYMV in Poland.
References:
(1) R. A. A. van der Vlugt et al. Phytopathology 89:148, 1999.
(2) I. Tobias and L. Palkovics. Pest Manage. Sci. 59:493, 2003.
[ZYMV, a potyvirus, first observed in 1981 in France and Italy,
has since spread worldwide, affecting crops in at least 22
countries, especially in Mediterranean countries, Central Europe
and USA. _Cucurbita pepo_ (pumpkin), _Cucumis melo_ (melon) and
_Citrullus lanatus_ (watermelon) are the predominant susceptible
hosts. ZYMV is often associated with papaya ringspot virus
(PRSV-watermelon) or with Watermelon mosaic virus (WMV) in
tropical countries. The virus is transmitted by several aphids
including (_Aphis citricola_, _A. gossypii_, and _Myzus
persicae_). Evidence of seed transmission is equivocal. Disease
management utilizes reflective mulches, judicious application of
insecticides, and resistant cultivars. Some wild cucurbits are
sources of ZYMV resistance genes, which may have application for
developing resistant cultivars.
Additional references: <http://www3.res.bbsrc.ac.uk/webdpv/web/adpv.asp?dpvnum=282>
<http://www.apsnet.org/online/feature/pumpkin/zuccyell.html>
- Mod.DH]