Taxonomy and Emended Description of Strains of Erwinia Isolated from Musa paradisiaca Linnaeus

Dickey, R. S.; VICTORIA, J. I.

doi:10.1099/00207713-30-3-604

Cited by 7 publications

(14 citation statements)

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“…However, in present study both strains showed negative result for KCN tolerance. Positive H 2 S production was reported by Dickey and Victoria (1980) and Mandal and Maiti (2005) exactly matches with present result. Production of phosphatase and erythromycin sensitivity recorded by Dicky and Victoria (1980) and Tomlinson and Cox (1987) is exactly similar with the present result.…”

Section: Discussionsupporting

confidence: 92%

“…The blue pigmentation of bacteria matches with report of Hoitink and Daft (1972), Schaad and Brenner (1977). Similarly, the growth at 36-37 0 C were reported by Goto( 1979) Dicky andVictoria( 1980), Bradbury (1986), Tomlinson and Cox ( 1987) and Chellemi et al(1998). No growth at 5% of the isolates exactly matches with results of Dicky and Victoria (1980), Tomlinson and Cox (1987), Janse and Ruissen (1988).…”

Section: Discussionsupporting

confidence: 89%

“…In present study, acid and gas was produced from D (+) glucose, however, acid was produced only from D (-) arabinose, xylose, esculin, mannose, ribose, starch, adonitol and dextrin. Similar results were reported by Hoitink and Daf (1972), Schaad and Brenner (1977), Dickey (1979), Dickey and Victoria (1980) and Mandal and Maiti (2005). Both the soft rot bacteria strains utilized galacturonate, glycerate, D (+) malate, tartrate and malonate as organic compound.…”

Section: Discussionsupporting

confidence: 88%

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Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Nagrale

Borkar

Gawande

et al. 2013

JANS

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A serious collar and rhizome rot disease of banana was observed in the north region of Maharashtra state in post rainy season. The disease was caused by the bacterial strains of Erwinia chrysanthemi pv. paradisiaca identified and characterized by morphological, physiological, biochemical and pathogenicity tests. The infection occurred on new banana plantation of one month old in poorly drained soil. In post rainy season, banana plantations of 8 to 10 weeks were found severely infected. E. chrysanthemi pv. paradisiaca produced soft rot symptom onhealthy banana rhizomes within three weeks. Two strains were isolated from the collar and rhizome rotted diseased samples which were similar in morphological, physiological and biochemical characteristics, however they differed in the virulence aggressiveness to cause the disease in banana. Strain II caused soft rot symptoms within 19 days, however strain I produced it within 23 days of inoculation with suspension of 3×108 CFU ml-1. The result of this study revealed that strain II was more aggressive as compared to strain I of E. chrysanthemi pv. paradisiaca.

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Section: Discussionsupporting

confidence: 92%

Section: Discussionsupporting

confidence: 89%

Section: Discussionsupporting

confidence: 88%

See 1 more Smart Citation

Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Nagrale

Borkar

Gawande

et al. 2013

JANS

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“…Correlation with pathovars. To assess the correlation between patterns of rRNA and the differentiation at the intraspecific level of E. chrysanthemi, the observed RFLP clusters were compared with the pathovar groupings of this organism (11,13,43). The rRNA gene restriction clusters appear to correlate well with the pathovars and botanical classification (Fig.…”

Section: Resultsmentioning

confidence: 99%

Ribotyping of Erwinia chrysanthemi Strains in Relation to Their Pathogenic and Geographic Distribution

Nassar

Bertheau²,

Dervin³

et al. 1994

Appl Environ Microbiol

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16S and 23S rRNAs from Escherichia coli were used to study the relationship among a representative collection of strains of Erwinia chrysanthemi differing in their original host and geographical origin. Phenetic analysis of restriction fragment length polymorphisms allowed the distribution of the studied strains into seven clusters. These clusters were similar to those obtained by cladistic methods and appeared to correlate well with the established pathovars and biovars but to a lesser extent with geographical distribution. Except for two groups of strains defined as tropical and temperate isolates (clusters 3 and 4, respectively), our clustering correlated well with botanical classifications of host plants. However, the rRNA groupings were shown to be more discriminative than biovar analysis. To assess the relationship between rRNA clusters and pathogenicity, 12 representative strains from different clusters were tested for pathogenicity on different plants. The two typical symptoms, maceration and wilting, were observed for these strains. The occurrence of the tobacco

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“…Une caracterisation subspecifique des E. chrysanthemi s'est parallelement developpee sur des criteres physiologiques (Dickey, 1979;Dickey & Victoria, 1980;Hildebrand et al, 1978;Thomson et al, 198 1;Samson & Nassan-Agha, 1978). Elle montre une certaine relation entre les caracteres phhotypiques in vitro des bacteries et l'h6te d'ou elles sont isolkes.…”

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Caractérisation des Erwinia chrysanthemi isolées de Solanum tuberosum et d'autres plantes‐hôtes selon les biovars et sérogroupes¹

Samson¹,

Poutier²,

Sailly

et al. 1987

EPPO Bulletin

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Des pourritures et fletrissements bacteriens dus a Erwiniu chrysanthemi sont inventories aujourd'hui surplus de 25 especes de plantes cultivees (dont la pomme de terre depuis 1971) et dans de nombreux pays temper& ou tropicaux. Cette diversite geographique et de gamme d'h8tes merite des etudes approfondies. L'espece bacterienne E. chrysanthemi est subdiviste dans le Bergey's Manual de 1984 en six pathovars: chrysunthemi, diunthicolu. diefenbachiue, paradisiuca, purtheniiet zeae. Que faire des E. chrysunthemiisoli.es de pomme de terre, tomate, endive, artichaut? Au lieu de classer les isolats en pathovars, il parait souhaitable, car simple et fiable, d'adopter le classement en biovars d'apres des criteres physiologiques de laboratoire mis en evidence ces dernieres annkes, et qui se rtvelent discriminants (croissance a 39°C; hydrolyse de l'arginine selon Moeller, de la lecithine et de la gtlatine; utilisation des sources de carbone suivantes: cis-aconitate, D(-)arabinose, 5-cttogluconate, inuline, mannitol, melibiose, raffinose, D(-)tartrate). I1 est egalement important, avant d'entreprendre une detection par serologie, de connaitre l'appartenance des isolats aux serogroupes connus (antigtnes de paroi) et leur type flagellaire.

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Taxonomy and Emended Description of Strains of Erwinia Isolated from Musa paradisiaca Linnaeus

Cited by 7 publications

References 0 publications

Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Ribotyping of Erwinia chrysanthemi Strains in Relation to Their Pathogenic and Geographic Distribution

Caractérisation des Erwinia chrysanthemi isolées de Solanum tuberosum et d'autres plantes‐hôtes selon les biovars et sérogroupes¹

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Taxonomy and Emended Description of Strains of Erwinia Isolated from Musa paradisiaca Linnaeus

Cited by 7 publications

References 0 publications

Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Characterization of a bacterial collar and rhizome rot of banana (Musa paradisiaca) caused by strains of Erwinia chrysanthemi pv. paradisiaca

Ribotyping of Erwinia chrysanthemi Strains in Relation to Their Pathogenic and Geographic Distribution

Caractérisation des Erwinia chrysanthemi isolées de Solanum tuberosum et d'autres plantes‐hôtes selon les biovars et sérogroupes1

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Caractérisation des Erwinia chrysanthemi isolées de Solanum tuberosum et d'autres plantes‐hôtes selon les biovars et sérogroupes¹