Rev 01/05/2026
Scutellonema brachyurus (Steiner, 1938) Andrassy, 1958
Synonyms: Rotylenchus brachyurus Steiner, 1938 Rotylenchus coheni Goodey, 1952 Scutellonema coheni (Goodey, 1952) Andrassy, 1958
Scutellonema brachyurum Andrassy, 1958 Scutellonema boocki Lordello, 1957
Nomenclature Note: According to the International Code of Zoological Nomenclature (ICZN, Art. 31.2), the genus name and species name must be in gender agreement. Since the name ending of Scutellonema is gender neuter (ICNZ, Art. 30.1.2), the correct name for the species should be brachyurum as used by Andrassy (1958). However, Maosa et al (2025) present a convincing argument in support of the name ending brachyurus and herein that form is accepted in the interest of consistency.
Scutellonema brachyurus Clades
Through an integrative taxonomy approach, Van den Berg et al. (2013, 2017) distinguished Type A and B of S. brachyurus, based on D2-D3 of 28S rRNA, ITS rRNA and COI mtDNA gene sequences. Type A is predominantly found in the USA, Europe and Asia, while Type B is mainly observed in Africa. Some putative morphological differences between Type A and B include the number of lip annuli (4-6 vs mainly three annuli), variation in the number of regular and irregular blocks on the basal lip annulus (4-12 vs 8-20 blocks) and the position of the secretrory-excretory pore in relation to the pharyngeal lobe (mostly opposite the anterior part to about the middle of the lobe vs rarely opposite the middle to mostly the posterior part of the lobe). Additional differences in c′ ratio, tail length and male stylet length, c and o ratios, further differentiate the two types. Accordingly, Maosa et al (2025) redescribed S. brachyurus Type B as Scutellonema afribrachyurus.
Characteristics of Scutellonema brachyurus (=S. brachyuurus Type A)
Length, female: 0.82 mm av.; length, male: 0.63-0.85 mm.
Female:
Body forming a single spiral (occasionally arcuate); annulations distinct, average annule width 1.4 µm near midbody.
Lateral fields about one fourth as wide as body, areolated from the anterior to the excretory pore and at phasmids, marked by 4 incisures.
Lip region hemispherical, slightly set off by a constriction, with 3 to 4 (sometimes 5) annules of irregular width and a terminal flat labial disc; basal annule marked by 6 longitudinal striae; framework strongly sclerotized, its outer margins inwardly concave, extending posteriorly one body annule.
Stylet well developed, 26-30 µm long, in two almost equal parts; basal knobs prominent, rounded with slightly flattened anterior surfaces, 4.5 um across.
Dorsal esophageal gland opening rather obscure, about 5 µm behind spear knobs.
Cephalids, hemizonid, and hemizonion indistinct.
Esophagus typical of the genus, slightly contracted at base of isthmus.
Median esophageal bulb ovoid, extending over 8 body annules.
Nerve ring encircling isthmus a little behind median bulb, well anterior to excretory pore which lies at approximately 88 body annules behind the lip region and about one body-width behind the esophageal glands.
Esophageal glands overlap intestine dorsally.
Gonads amphidelphic, symmetrical, on left side of intestine. Ovaries outstretched with oocytes in a row except for 4 or 5 in multiplication zone near tip. Single egg in posterior uterus. No spermatheca or sperms in uterus. Epiptygma double, indistinct, not projecting out through vulva.
Intestine extending slightly over rectum.
Tail broadly rounded, about half anal body-width long, annulations following tail contour; annules slightly irregular and coarser than adjacent body annules; 8 annules between anus and tail tip.
Phasmids enlarged, 3-4 um in diameter, just pre-anal. Term "scutellum" refers to Latin "shield" for shape and size of phasmids - hence Scutellonema.
Male:
Rare, absent from most populations. Similar to female in most details.
Spicules arcuate, slightly cephalated, 25-27 um long.
Gubernaculum large, protrusible.
Bursa crenate, terminal.
[Ref: CIH Descriptions of Plant-parasitic Nematodes, Set 4, No. 54 (1974)]
Reported median body size for this species (Length mm; width micrometers; weight micrograms) - Click:
Cosmopolitan; may be native to Africa where it is common in uncultivated soil.
Occurs on 85 plant species in California (Siddiqui et al.).
Ectoparasite of roots, but may invade the deeper cortical layers and become endoparasitic.
In African Violets, the nematode was found both within and between cells; several eggs were seen within a single cell, where the juveniles may hatch and develop to fill the cell completely before migrating through the wall to the adjacent cells (Golden, 1956).
Soybean, tobacco, sweet potato, alfalfa, barley, rice, tea, sugarcane, and ornamentals
Ecophysiological Parameters:
On suitable hosts, S. brachyurus quickly builds up to large populations.
Different initial populations when inoculated on red clover reached a very high ceiling level after 325 days, and there was no apparent injury to the host.
On hairy vetch, greatest population increases occured at 28 C, while at 18 C, reproduction was considerably retarded (Malek & Jenkins, 1964).
In the greenhouse, in 7 months, S. brachyurus increased 3.8-fold on tulip tree and 17-fold on sycamore (Ruehle, 1971).
Goodey (1952) observed that parasitized roots of Hippeastrum sp. showed reddish lesions which later turned brown. The internal root cavities produced by the nematodes became isolated by a new tissue - the wound periderm.
Graham (1955) demonstrated that S. brachyurus is pathogenic to, and produces lesions on the roots of, tobacco grown under greenhouse and field conditions. Affected plants of Golden Cure Tobacco showed reduced root weight, top weight, and reduced height compared to non-inoculated plants.
Luc (1959) found this nematode associated with poor growth of sugarcane in Malagasy.
There is no record of associations of this species with other pathogens.
Grass rotations between tobacco crops in Zimbabwe can be effective (Shepherd, 1968).
Fumigation with DBCP eliminated Scutellonema populations in cotton grown in Tanzania.
Heat treatment and use of nematicides on amaryllis bulbs grown in the greenhouse have been employed (Johansson & Niedieck, 1964).
Resistance
Host Plant Resistance, Non-hosts and Crop Rotation alternatives:
Andrássy, I. 1958. Hoplolaimus tylenchiformis Daday, 1905 (syn. H. coronatus Cobb, 1923) und die Gattungen der Unterfamilie Hoplolaiminae Filipjev, 1936. Nematologica 3:44-56.
CIH Descriptions of Plant-parasitic Nematodes, Set 4, No. 54 (1974)
Maosa, J., Sirengo, D.K., Singh, P.R., Couvreur, M., De Waele, D. and Bert, W. 2025. Description of African Scutellonema brachyurus Type B populations as Scutellonema afribrachyurus n. sp. (Tylenchida: Hoplolaimidae) based on integrative taxonomy. Nematology 27: 1055-1080.
Sher, S.A. 1963. Revision of the Hoplolaiminae (Nematoda) III. Scutellonema Andrassy, 1958. Nematologica 9:421-443.
Van den Berg, E., Tiedt, L.R., Coyne, D.L., Ploeg, A.T., Navas-Cortés, J.A., Roberts, P.A., Yeates, G.W. and Subbotin, S.A. 2013. Morphological and molecular characterisation and diagnostics of some species of Scutellonema Andrássy, 1958 (Tylenchida: Hoplolaimidae) with a molecular phylogeny of the genus. Nematology 15: 719-745. DOI: 10.1163/ 15685411-00002714
Van den Berg, E., Tiedt, L.R., Stanley, J.D., Inserra, R.N. & Subbotin, S.A. 2017) Characterisation of some Scutellonema species (Tylenchida: Hoplolaimidae) occurring in Botswana, South Africa, Costa Rica and the USA, with description of S. clavicaudatum sp. n. and a molecular phylogeny of the genus. Nematology 19: 131-173. DOI: 10.1163/15685411-0000303