Taxonomy
Morphology
Cultural characteristics
Biochemical characters
Ecology
Pathogenicity
References
Phylum Bacteroidota, Class Gammaproteobacteria, Order Enterobacterales, Family Yersiniaceae, Genus Serratia, Serratia
nematodiphila Zhang et al. 2009.
Species description is based on a single isolate.
Gram-negative, short rods, 0.8-1.3 x 0.6-0.7 μm. Motile by a single flagellum.
Colonies on nutrient agar are red-pigmented, circular and smooth with entire
margins. Grows at 4-42 ºC (optimum, 30-37 ºC), pH 5-11 (optimum, pH 6.0–10.0) and
2-7% NaCl. Growth occurs on trypticase soy agar, nutrient agar, cetrimide agar,
Simmons’ citrate agar and MacConkey agar.
Isolated from the intestine of Heterorhabditidoides chongmingensis. Symbiotic organism.
Undetermined.
- Zhang CX, Yang SY, Xu MX, Sun J, Liu H, Liu JR, Liu H, Kan F, Sun J, Lai R, et al. Serratia nematodiphila sp. nov., associated
symbiotically with the entomopathogenic nematode Heterorhabditidoides chongmingensis (Rhabditida: Rhabditidae). Int J Syst
Evol Microbiol 2009; 59:1603-1608.
- J. G. Holt et al., 1994. Facultatively Anaerobic Gram-Negative Rods. Subgroup 1. Family Enterobacteriaceae. In: Begey’s Manual of
Determinative Bacteriology, 9th-edition, Williams & Wilkins, pp 175-189.
- Don J. Brenner and J.J. Farmer III, 2001. Family I. Enterobacteriaceae. In: Bergey’s Manual of Systematic Bacteriology, Second
edition, Vol two, part B, George M. Garrity (Editor-in-Chief), pp 587-897.
(c) Costin Stoica
Legend: + positive 90-100%, - negative 90-100%, [+] positive 75-89%, [-] negative 75-89%, d positive 25-74% of strains, nd - not determined,
ADH - arginine dihydrolase, LDC -lysine decarboxylase, ODC - ornithine decarboxylase, * S glossinae is not included in ABIS database
Differential characters:
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S. grimesii
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S. liquefaciens
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S. marcescens
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S. nematodiphila
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S. odorifera 1
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S. odorifera 2
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S. plymuthica
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S. proteamaculans
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S. rubidaea
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Positive results for arginine dihydrolase, amylase, catalase, caseinase, beta-galactosidase, aesculin hydrolysis, gelatin, lipase
(Tween 80), lysine decarboxylase, Voges–Proskauer reaction, ornithine decarboxylase, Simmons’ citrate, nitrate reduction, acid
production from D-fructose, L-fucose, D-galactose, D-glucose, inositol, D-mannose, D-mannitol, D-ribose, sucrose, salicin, D-
sorbitol, and xylitol.
Can utilize acetate, lactate, oxalate, succinate, L-arginine, L-histidine, DL-serine, L-ornithine, DL-alanine, L-proline, DL-threonine, DL-
phenylalanine, L-tryptophan and L-hydroxyproline, adonitol, D-xylose, maltose, D-arabinose, D-fructose, D-glucose, D-lactose,
sucrose, D-erythrose, starch, diarabinose, salicin, L-fucose, raffinose, L-arabitol, cellobiose, D-ribose, D-sorbitol, xylitol, D-mannose,
inositol, adonitol, melezitose, melibiose, D-mannitol, D-galactose, amygdalin, erythritol, dextrin, inulin and citrate.
Negative results for cellulose hydrolysis, H2S production, indole production, methyl red test, oxidase, urease, acid production from D-
arabinose, L-arabitol, adonitol, amygdalin, cellobiose, D-erythrose, D-lactose, melezitose, melibiose, D-rhamnose, raffinose, L-
sorbose, starch, and D-xylose.
No utilization of acetate, malonate, tartrate, sodium pyruvate, phenylalanine, oxalate and threonine.