OpenLegislation

Division 7.1 Biovar determinationF1

United Kingdom

Original text. Later amendments are not shown.

R. solanacearum is separated into biovars on the basis of the ability to utilise and/or oxidise three disaccharides and three hexose alcohols (Hayward, 1964 and Hayward et al. , 1990). Growth media for the biovar test is described in Appendix 2. The test can be successfully performed by stab inoculating the media with pure cultures of R. solanacearum isolates and incubating at 28 °C. If the media are dispensed into sterile 96 well cell culture plates (200 µl per well) colour change from olive green to yellow can be observed within 72 hours, indicating a positive test result.

Biovar
1 2 3 4 5
Utilisation of:
Maltose – + + – +
Lactose – + + – +
D (+) Cellobiose – + + – +
Mannitol – – + + +
Sorbitol – – + + –
Dulcitol – – + + –

Additional tests differentiate biovar 2 sub-phenotypes

See Lelliott and Stead (1987)

Biovar 2A (Worldwide distribution) Biovar 2A (Found in Chile and Colombia) Biovar 2T (Found in tropical areas)
Utilisation of trehalose – + +
Utilisation of meso -inositol + – +
Utilisation of D ribose – – +
Pectolytic activity f1 low low high

Annotations

Textual amendments

F1

Substituted by Commission Directive 2006/63/CE of 14 July 2006 amending Annexes II to VII to Council Directive 98/57/EC on the control of Ralstonia solanacearum (Smith) Yabuuchi et al..

Footnotes

f1

See Lelliott and Stead (1987)