Detection of Plant-Pathogenic Bacteria in Seed and Other Planting Material, Second Edition 2017
DOI: 10.1094/9780890545416.017
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CHAPTER 17: Detection of Clavibacter michiganensis subsp. michiganensis in Tomato Seeds

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Cited by 11 publications
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“…; Table ). In order to characterize bacterial colonies, the strains were grown on nonselective media YPGA, and two semiselective media used routinely to identify Cmm, CMM1 (10 g L −1 sucrose, 3.32 g L −1 Tris base, 11.44 g L −1 Tris.HCl, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 5 g L −1 LiCl, 2 g L −1 yeast extract, 1 g L −1 NH 4 Cl, 4 g L −1 casein hydrolysate, 15 g L −1 agar, 10 mg L −1 polymyxin B sulphate, 28 mg L −1 nalidixic acid, 100 mg L −1 nystatin) and SCM (10 g L −1 sucrose, 2 g L −1 K 2 HPO 4 , 0.5 g L −1 KH 2 PO 4 , 1.5 g L −1 H 3 BO 3 , 0.1 g L −1 yeast extract, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 1.5 g L −1 boric acid, 18 g L −1 agar, 100 mg L −1 nicotinic acid, 30 mg L −1 nalidixic acid, 10 mg L −1 potassium tellurite, 200 mg L −1 cycloheximide) (Fatmi & Schaad, ) media at 28 °C for 3, 5 and 7 days, respectively. Cultures of each strain were grown in YPGB (5 g L −1 yeast extract, 5 g L −1 bactopeptone, 10 g L −1 glucose) medium to keep as stocks using 20% glycerol at −20 and −80 °C.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…; Table ). In order to characterize bacterial colonies, the strains were grown on nonselective media YPGA, and two semiselective media used routinely to identify Cmm, CMM1 (10 g L −1 sucrose, 3.32 g L −1 Tris base, 11.44 g L −1 Tris.HCl, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 5 g L −1 LiCl, 2 g L −1 yeast extract, 1 g L −1 NH 4 Cl, 4 g L −1 casein hydrolysate, 15 g L −1 agar, 10 mg L −1 polymyxin B sulphate, 28 mg L −1 nalidixic acid, 100 mg L −1 nystatin) and SCM (10 g L −1 sucrose, 2 g L −1 K 2 HPO 4 , 0.5 g L −1 KH 2 PO 4 , 1.5 g L −1 H 3 BO 3 , 0.1 g L −1 yeast extract, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 1.5 g L −1 boric acid, 18 g L −1 agar, 100 mg L −1 nicotinic acid, 30 mg L −1 nalidixic acid, 10 mg L −1 potassium tellurite, 200 mg L −1 cycloheximide) (Fatmi & Schaad, ) media at 28 °C for 3, 5 and 7 days, respectively. Cultures of each strain were grown in YPGB (5 g L −1 yeast extract, 5 g L −1 bactopeptone, 10 g L −1 glucose) medium to keep as stocks using 20% glycerol at −20 and −80 °C.…”
Section: Methodsmentioning
confidence: 99%
“…After infection is established, Cmm invades xylem vessels, moving systemically throughout the plant (Wallis, ). Symptoms include wilting and chlorosis (Fatmi & Schaad, ), first in one side of the plant or leaves, and then throughout the whole plant. Stem canker and vascular necrosis can also be observed.…”
Section: Introductionmentioning
confidence: 99%
“…michiganensis in tomato transplants: The method used in this study for the detection of Clavibacter michiganensis subsp. michiganensis in symptomless tomato seedlings was elaborated according to the protocols of the International Seed Federation 13 and the European and Mediterranean Plant Protection Organisation 4 which are normally adopted for the detection of Cmm on tomato seed. The principles of this method involve the isolation of Cmm from tomato seedlings tissue on non-selective and semi-selective media, followed by the identification of presumptive Cmm-isolates by PCR and pathogenicity test.…”
Section: Detection Ofmentioning
confidence: 99%
“…Hot water disinfection has been proposed for the control of bacterial plant pathogens, for example Erwinia carotovora in potato tubers and Erwinia chrysanthemi (Mackay & Shipton 1983;Robinson & Foster 1987), Agrobacterium tumefaciens in grapevine cuttings (Burr et al 1989;Bazzi et al (1991), Clavibacter michiganensis pv. michiganensis in tomato seeds (Fatmi et al 1991), and Xanthomonas campestris pv. malvacearum in cotton seeds (Honervogt & Lehmann-Danzinger 1992).…”
Section: Introductionmentioning
confidence: 99%