scholarly journals Role of Crop Debris and Weeds in the Epidemiology of Bacterial Leaf Spot of Lettuce in California

Plant Disease ◽  
2001 ◽  
Vol 85 (2) ◽  
pp. 169-178 ◽  
Author(s):  
Jeri D. Barak ◽  
Steven T. Koike ◽  
Robert L. Gilbertson

Bacterial leaf spot of lettuce (BLS), caused by Xanthomonas campestris pv. vitians, has increased in importance in California over the past 5 years. The pathogen can be seedborne, but it was not recovered from selected commercial lettuce seed lots planted during this time. Survival of X. campestris pv. vitians in association with plant debris was investigated in a 3-year field experiment in Salinas, CA. The initial lettuce spring crop was spray inoculated with X. campestris pv. vitians, which resulted in 100% disease incidence. Spring crops were followed by a 1-month summer fallow period, whereas fall crops were followed by a 5-month winter fallow period. High populations of X. campestris pv. vitians (up to 106 CFU/g) were recovered from lettuce plant debris after the 1-month summer fallow and BLS developed on all subsequent fall lettuce crops. During the winter fallow period, X. campestris pv. vitians populations associated with plant debris declined and, by 2 months after harvest, only small populations were detected. Spring crops also developed BLS, but at reduced levels. X. campestris pv. vitians was recovered from leaves of several symptomless weed species collected around commercial infested fields, but not from weeds collected around previously infested fields during fallow periods. During the course of this study, an X. campestris pv. vitians-specific polymerase chain reaction primer pair was developed.

Plant Disease ◽  
2005 ◽  
Vol 89 (6) ◽  
pp. 683-683 ◽  
Author(s):  
S. Gaetán ◽  
N. López

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 (107 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.


2005 ◽  
Vol 6 (1) ◽  
pp. 3 ◽  
Author(s):  
Carolee T. Bull ◽  
Steve T. Koike

The efficacy of Serenade, Maneb, Cuprofix, and mixtures of these products were evaluated for efficacy in reducing disease incidence and severity of bacterial leaf spot of lettuce caused by Xanthomonas campestris pv. vitians in six trials at two locations between 2001 and 2003. Additionally, Messenger, elemental copper, Quadris, and Actigard were evaluated in at least two of these trials. Mixtures of Serenade and Cuprofix reduced disease incidence in three of six experiments and reduced disease severity in a fourth experiment. Treatment with the Maneb and Cuprofix mixture was less effective but resulted in significantly less disease and lower severity in single experiments. These results indicate that a mixture of Serenade and Cuprofix may be a useful addition to an integrated bacterial leaf spot disease management strategy but this treatment may be too variable to justify it as a stand-alone treatment. Accepted for publication 21 October 2005. Published 21 November 2005.


HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1098A-1098 ◽  
Author(s):  
Ryan J. Hayes ◽  
Carolee T. Bull ◽  
Polly H. Goldman ◽  
Edward J. Ryder

Bacterial leaf spot of lettuce caused by Xanthomonas campestris pv. vitians (Xcv) is an important lettuce disease in California. No adequate control measures have been found, although resistance exists in several heirloom cultivars. Deployment of cultivars resistant to bacterial leaf spot will reduce these periodic and costly disease events. The objectives of this research were to 1) identify new sources of resistance within modern crisphead cultivars and 2) select for resistance in `Salad Crisp' × `Iceberg' progeny. Field plots were established and grown with overhead irrigation, and a three-strain mixture of Xcv was applied until runoff 1 week after thinning at 1 × 109 CFU/mL. Twenty-six crisphead cultivars were tested in unreplicated field trials and rated on a 1 (susceptible) to 4 (resistant) scale. Selection was carried out between and within families from the F2 to F4 generation. Sixteen F3 families were evaluated in unreplicated plots, and 12 F5 families were tested in replicated plots for disease incidence and severity. No usable levels of resistance were identified in the modern crisphead cultivars tested to date. All F3 families had resistance greater than `Iceberg', and 19 plants from eight families were selected for further breeding. Subsequently, 12 plants from two F4 families were selected. Replicated trials of 12 F5 families indicated that all lines have disease severity comparable to both parents. Breeding lines from crosses to `Salinas 88' are currently being developed.


Plant Disease ◽  
2013 ◽  
Vol 97 (8) ◽  
pp. 1109-1109
Author(s):  
C. Biswas ◽  
P. Dey ◽  
A. Bera ◽  
S. Satpathy ◽  
B. S. Mahapatra

Jute (Corchorus olitorius L.) is the second most important fiber crop after cotton in terms of global production (3). In November 2011, symptoms suggestive of bacterial infection were observed on a seed crop of jute at the CRIJAF research farm, Barrackpore, West Bengal, India. The disease appeared as small, brown, circular spots, usually less than 5 mm in diameter on the leaves and some of the spots were surrounded by a yellow halo. The lesions on the stems were elongated and in some cases were found to girdle the stem. In the later stages of disease, brown sunken spots were found on the green capsules. Disease incidence varied from about 20% to 90% of the total plants in different affected fields at the CRIJAF research farm. Bacterial leaf spot of jute with similar symptoms was reported in 1957 from Sudan (4). Five symptomatic and three asymptomatic leaf samples were collected from different jute fields. Bacterial colonies isolated on nutrient agar medium from infected young leaves were Xanthomonas-like and pale yellow cream in color. Total DNA was extracted from symptomatic as well as asymptomatic leaf samples by using an improved salt concentration and simple sodium acetate CTAB method (2). Single bacterial colonies were transferred to nutrient agar (NA) medium plates and incubated at 28°C for 48 h. Pure colonies from plates were used directly for DNA extraction using the QIAGEN DNeasy Blood and Tissue kit. PCR was carried out with Xanthomonas campestris specific primers NZ8F3/NZ85R3 (1), which generated an amplicon of 530 bp from all the symptomatic leaf samples as well as pure cultures of the isolated bacteria. No amplification was obtained from asymptomatic leaves. The amplicons from the five symptomatic samples collected from the field were sequenced and showed 100% identity with one another, and one sequence (strain JB-CO-13) was deposited in GenBank (Accession No. KC342185). The BLASTn analysis revealed that bacterial strain JB-CO-13 had 100% identity with X. campestris pv. olitorii (EU285213). Nucleotide span and ORF finder (NCBI) analysis indicated the 530-bp PCR amplicon coded part of a gyrase B gene that had 100% identity with a translated gene product (Protein ID: ABX84334). Three leaves of five 1-month-old jute plants (cv. JRO 204) in pot culture were infiltrated each with a separate bacterial strain using suspensions (1 × 105 CFU/ml) in distilled water. The negative control consisted of leaves infiltrated with sterile distilled water. The plants were kept in a greenhouse with mean maximum and minimum temperatures of 28.96 and 21.8°C, respectively. The plants were covered with plastic bags to maintain high relative humidity (>80%). Typical bacterial lesions were recorded on all the inoculated plants after 1 week. No lesions were seen on the negative control. To the best of our knowledge, this is the first report of bacterial leaf spot on C. olitorius caused by X. campestris pv. olitorii from India. References: (1) J. Adriko et al. Plant Pathol. 61:489, 2012. (2) C. Biswas, et al. Lett. Appl. Microbiol. 56:105, 2013. (3) Food and Agriculture Organization of the United Nations. Agricultural Commodities: Profiles and Relevant WTO Negotiating Issues. Online: http://www.fao.org/docrep/006/Y4343E/y4343e03.htm , 2003. (4) K. A. Sabet. Ann. Appl. Biol. 45:516, 1957.


2007 ◽  
Vol 8 (1) ◽  
pp. 11 ◽  
Author(s):  
Carolee T. Bull ◽  
Polly H. Goldman ◽  
Ryan Hayes ◽  
Laurence V. Madden ◽  
Steven T. Koike ◽  
...  

Lettuce plants were artificially inoculated with three isolates of Xanthomonas campestris pv. vitians in field and greenhouse evaluations for genetic variation in resistance to bacterial leaf spot. The cultivar Little Gem had the least amount of disease, whether evaluated for disease severity or disease incidence. Disease severity levels for cultivar Batavia Reine des Glaces were not significantly different from those of Little Gem. Several cultivars including Vista Verde, Pybas 251, Pacific, Clemente, Salinas 88, and Sniper were highly susceptible. There was a strong correlation between results obtained in the greenhouse and those obtained in the field (r = 0.77, P = 0.009) indicating that greenhouse assays may be used to increase the number of cultivars evaluated and to speed breeding efforts. Accepted for publication 17 May 2007. Published 17 September 2007.


Plant Disease ◽  
1997 ◽  
Vol 81 (12) ◽  
pp. 1443-1446 ◽  
Author(s):  
F. Sahin ◽  
S. A. Miller

In 1995, a bacterial leaf spot disease was observed on lettuce plants grown on muck soils in north central Ohio. Characteristic symptoms were water-soaked circular, dark brown- or olivecolored spots, approximately 1 to 2 mm in diameter, along the margin of leaves; V-shaped lesions beginning at the leaf margins and advancing along the veins; and individual black spots scattered on the leaf surface. Five bacterial strains were isolated from infected leaves of two lettuce cultivars, Darkland and Go Go Green. These strains were identified as Xanthomonas campestris pv. vitians based on morphological, physiological, biochemical, and pathogenicity tests, as well as fatty acid methyl ester (FAME) analyses. One of the five strains tested was resistant to streptomycin sulfate (100 μg/ml), and none were resistant to copper sulfate. Eight commercial lettuce cultivars were evaluated for resistance to X. campestris pv. vitians. Of these cultivars, Redine was highly resistant; Focus and Crisp and Green were partially resistant; Slobolt, Tiara, and Carmona were susceptible; and Darkland and Go Go Green were highly susceptible to the pathogen. Surface disinfection with 0.52% sodium hypochlorite for 5 min nearly eliminated the bacterium from lettuce seed without affecting seed viability.


Plant Disease ◽  
1997 ◽  
Vol 81 (8) ◽  
pp. 892-896 ◽  
Author(s):  
E. L. Little ◽  
S. T. Koike ◽  
R. L. Gilbertson

Pseudomonas syringae pv. apii, causal agent of bacterial leaf spot (BLS) of celery, was first identified in California in 1989. By 1991, BLS was apparent in all celery-growing areas of the state. Greenhouse-produced transplants were affected most severely, and disease incidence approached 100% in some greenhouses. In this study, sources of inoculum and factors contributing to disease development were investigated in three Salinas Valley greenhouse operations during the 1991, 1992, and 1993 celery transplant seasons (January to August). Epiphytic P. syringae pv. apii was not detected on celery transplants until April or May of each year. Increased epiphytic populations preceded BLS outbreaks, and high-pressure, overhead irrigation favored bacterial infiltration and disease development. In seed-wash assays, P. syringae pv. apii was recovered from 5 of 24 commercial celery seed lots. In field tests, epiphytic P. syringae pv. apii was found on umbels of inoculated celery plants, and seeds from these plants were heavily contaminated with P. syringae pv. apii. Contaminated seed produced seedlings with large epiphytic P. syringae pv. apii populations. Hot-water treatment (50°C for 25 min) eliminated >99.9% of seed contamination. Based on these results, disease management techniques are proposed.


Plant Disease ◽  
2012 ◽  
Vol 96 (7) ◽  
pp. 1064-1064 ◽  
Author(s):  
I.-S. Myung ◽  
J. Y. Lee ◽  
H. L. Yoo ◽  
J. M. Wu ◽  
H.-S. Shim

In September 2011, bacterial leaf spot was observed on zinnia plants (Zinnia elegans L.) grown in a garden in Suwon, Korea. Leaf symptoms included angular lesions that were yellow or brown-to-reddish brown in the center. Bacterial isolates (BC3293 to BC3299) were recovered on trypticase soy agar from lesions surface-sterilized in 70% ethyl alcohol for 1 min. Pathogenicity of the isolates was confirmed by spray inoculation with a bacterial suspension (106 CFU/ml) prepared in sterile distilled water and applied to zinnia plants at the four- to five-leaf growth stage (two plants per isolate). Sterile distilled water was used as the negative control. The inoculated plants were incubated in a greenhouse at 26 to 30°C and 95% relative humidity. Characteristic leaf spot symptoms developed on inoculated zinnia plants 5 days after inoculation. No symptoms were observed on the negative control plants. The bacterium reisolated from the inoculated leaves was confirmed through gyrB gene sequence analysis (3). All isolates were gram-negative, aerobic rods, each with a single flagellum. Isolates were positive for catalase and negative for oxidase. The biochemical and physiological tests for differentiation of Xanthomonas were performed using methods described by Shaad et al. (2). The isolates were positive for mucoid growth on yeast extract-dextrose-calcium carbonate agar, growth at 35°C, hydrolysis of starch and esculin, protein digestion, acid production from arabitol, and utilization of glycerol and melibiose. Colonies were negative for ice nucleation, and alkaline in litmus milk. The gyrB gene (870 bp) and the 16S-23S rRNA internal transcribed spacer (ITS) regions (884 bp) were sequenced to aid in identification of the original field isolates using published PCR primer sets Xgyr1BF/Xgyr1BR (3) and A1/B1 (1), respectively. Sequence of the gyrB gene (GenBank Accession Nos. JQ665732 to JQ665738) from the zinnia field isolates shared 100% sequence identity with the reference strain of Xanthomonas campestris pv. zinniae (GenBank Accession No. EU285210), and the ITS sequences (GenBank Accession Nos. JQ665725 to JQ665731) had 99.9% sequence identity with X. campestris pv. zinnia XCZ-1 (GenBank Accession No. EF514223). On the basis of the pathogenicity assays, biochemical and physiological tests, and sequence analyses, the isolates were identified as X. campestris pv. zinniae. To our knowledge, this is the first report of bacterial leaf spot of zinnia caused by X. campestris pv. zinniae in Korea. The disease is expected to result in economic and aesthetic losses to plants in Korean landscapes. Thus, seed treatment with bactericides will be required to control the bacterial leaf spot of zinnia before planting. References: (1) T. Barry et al. The PCR Methods Appl. 1:51, 1991. (2) N. W. Schaad et al. Page 189 in: Laboratory Guide for Identification of Plant Pathogenic Bacteria. 3rd ed. N. W. Schaad et al., eds. The American Phytopathological Society, St. Paul, MN, 2001. (3) J. M. Young et al. Syst. Appl. Microbiol. 31:366, 2008.


1993 ◽  
Vol 21 (1) ◽  
pp. 75-78 ◽  
Author(s):  
A. R. Wasnikar ◽  
S. K. Khatik ◽  
M. L. Nayak ◽  
S. K. Vishwakarma ◽  
L. K. Punekar

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