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First Outbreak of Bacterial Leaf Spot Caused by Xanthomonas campestris
on Canola in Argentina. S. Gaetán, Facultad de Agronomía, Universidad de
Buenos Aires, A. San Martín 4453, 1417, Argentina; and N. López, Facultad de
Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina. Plant Dis.
89:683, 2005; published on-line as DOI: 10.1094/PD-89-0683B. Accepted for
publication 31 March 2005.
Canola (Brassica napus) is an alternative crop to wheat in Argentina and
~16,000 ha are grown commercially in southern Buenos Aires Province. During
2003, experimental field plots of canola plants located at Agronomy Faculty,
University of Buenos Aires, in Buenos Aires were severely damaged by a bacterial
leaf spot. Average disease incidence across 25 2- to 5-month-old canola
cultivars was 58% (range = 27 to 89%). During 2004, identical infection
associated with blackened veins (8 to 12% of plants) were found in two
commercial fields and experimental crops (rosette and flowering stages) in Tres
Arroyos in southern Buenos Aires Province. Symptoms observed on adaxial surfaces
consisted of v-shaped necrotic lesions on leaf margin surrounded by yellow
halos. Yellow bacterial ooze was found on young lesions. The advanced phases of
the disease included lesion enlargement, foliar chlorosis, and death of leaves.
The disease developed from the lower leaves to the apex, resulting in complete
leaf necrosis and defoliation. Ten samples (five plants per sample) with lesions
were arbitrarily collected from 2003 to 2004 from commercial and experimental
canola crops. Diseased leaf tissue was surface sterilized in 0.50% sodium
hypochlorite for 30 s and rinsed in sterile distilled water (SDW). Leaf sections
were macerated in SDW, and the extract was streaked onto nutrient agar. Plates
were incubated at 28°C for 3 days. Resultant colonies were yellow, mucoid, and
convex. Gram-negative, aerobic, and rod-shaped bacteria were obtained. Eight
strains were biochemically characterized using API 20NE (BioMerieux, Marcy l’Etoile,
France) and identified as Xanthomonas campestris (1). Strains hydrolyzed
starch, gelatine, and aesculin and were positive for catalase and negative for
oxidase, nitrate reduction, ureasa, and triptophanase. Strains were capable of
utilizing D-glucose, D-mannose, D-maltose, malic acid, and N-acetyl-glucosamine.
X. campestris. pv. campestris 8004 was used as a reference strain
(2). Pathogenicity and host range for three isolates were completed by injecting
a bacterial suspension (10(^7) CFU/ml) into leaves of 2-week-old canola plants
(cvs. Eclipse, Impulse, Master, and Mistral), cabbage (B. oleracea var. capitata),
and cauliflower (B. oleracea var. botrytis) seedlings
(two-leaf stage). The experiment (four inoculated and two control plants for
each cultivar and each strain) was conducted in a greenhouse at 24°C and 75%
relative humidity. Inoculated and control plants were enclosed in a plastic bag
for 48 h after inoculation. Chlorotic patches on the leaves followed by a dry,
brown necrosis spread beyond the initial injected area were observed in
inoculated plants 8 days after inoculation. Enlarged spots caused death of
leaves. The pathogen was successfully reisolated. Control plants, inoculated
only with SDW, remained symptomless. The results suggest that the bacterium
represents a potential threat to canola production in Argentina and indicate the
need for further study to identify the pathovar involved in canola leaf spots.
To our knowledge, this is the first report of an outbreak of X. campestris
causing leaf spot of canola and in which the bacteria affecting canola
commercial crops was biochemically characterized and host range was carried out
in Argentina.
References: (1) N. W. Schaad et al. Laboratory Guide for Identification of
Plant Pathogenic Bacteria. 3rd ed. The American Phytopathological Society, St.
Paul. MN, 2001. (2) P. Turner et al. Mol. Gen. Genet. 195:101, 1984.
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