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Lonsdalea Brady et al. 2012

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Lonsdalea Brady et al. 2012

The description is based on the data of Hildebrand & Schroth (1967), Hauben et al. (2005) and this study. Cells are Gram-negative-staining short rods (0.5–1.0×1.0–2.0 µm) occurring singly, in pairs or in groups. Motile by peritrichous flagella. Facultatively anaerobic, oxidase negative but catalase positive. Optimum temperature for growth is 28–30 °C. Colonies are white to cream on tryptone soya agar, round, convex and smooth with entire margins. Negative in tests for β-galactosidase, arginine dihydrolase, lysine decarboxylase, ornithine decarboxylase and tryptophan deaminase activities. Citrate is utilized but no production of H2S, urease, indole or gelatinase. Nitrates are not reduced to nitrites. Acid is produced from N-acetylglucosamine, arbutin, d-fructose, d-glucose, d-mannose, methyl α-d-glucopyranoside, d-ribose, salicin, sucrose and turanose. Major fatty acids are C14:0, C16:0, C18:1ω7c, C17:0 cyclo and summed features 2 (iso-C16:1 and/or C14:0 3-OH) and 3 (C16:1ω7c and/or iso-C15:0 2-OH). Members of the genus Lonsdalea form a phylogenetic clade as determined by both 16S rRNA gene sequence analysis and MLSA based on four housekeeping genes. Members of the genus may cause disease on oak trees including drippy nut disease and bark canker and may be associated with Acute Oak Decline. The DNA G+C contents range from 54.5 to 55.1 mol%.
The type species is Lonsdalea quercina.

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Lonsdalea Brady et al. 2012
Lonsdalea Brady et al.
Lonsdalea Brady et al. 2012

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Etymology
Lons.da’le.a. N.L. fem. n. Lonsdalea, named for David Lonsdale in honour of his contributions to British forest pathology

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8cc6e52b-ccf8-42da-979d-e611348070bc
scientific name
Names_Fungi
28 November 2012
14 August 2022
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