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1 November 2013 New Records of Digenean Parasites of Clarias gariepinus (Pisces: Clariidae) from the Okavango Delta, Botswana, with Description of Thaparotrema botswanensis sp. n. (Plathelminthes: Trematoda)
Candice Jansen van Rensburg, Jo G. van As, Pieter H. King
Author Affiliations +
Abstract

Forty-two specimens of African sharptooth catfish Clarias gariepinus (Clariidae) were collected from a number of localities in the Okavango Delta in Botswana and examined for digenean parasites. The morphology of these parasites was studied using light and scanning electron microscopy. Six digenean species, four represented by adults and two by metacercariae, belonging to five different genera were collected from various organs within the fish. Clinostomoides brieni is described from the branchial chamber; a Neodiplostomum type metacercariae from the musculature; Phyllodistomimi bavuri and Phyllodistomum vanderwaali from the urinary bladder; Glossidium pedatum from the intestine and one new species, Thaparotrema botswanensis sp. n. from the gall bladder. These are all new geographical records for southern Africa.

INTRODUCTION

Digeneans were collected from a number of fish hosts, including the African sharptooth catfish, Clarias gariepinus (Burchell, 1822), during fish parasitological studies carried out in the Okavango Delta, Botswana. According to Safriel and Bruton (1984) and Skelton (2001), C. gariepinus is a widely distributed food fish in Africa and is a popular species being targeted for aquaculture and biological research. When compared to other African fish, C. gariepinus is known to possess one of the richest parasite fauna, which can be attributed to its diet and the number of predator species feeding on them. According to Khalil (2003), Zhokhov (2010) and Zhokhov et al. (2010), 19 species of monogeneans, nine digeneans and one species of acanthocephalan, together with 16 various larval forms have been found infecting this catfish; although the number of named species will undoubtedly grow in the future (Chibwana et al. 2013).

Information concerning digenean parasites of freshwater fish in southern Africa and parts of Africa is scant and far from complete. The life history of trematodes, which (at the adult stage) infect African fish, has so far not been studied in detail and their first molluscan and other intermediate hosts remain unknown as yet. When consulting literature, most of the studies carried out in South Africa have been surveys on helminth parasites in general, not concentrating on a specific group as such.

Khalil and Polling (1997) provided a checklist of helminth parasites of African freshwater fish, while Canaris and Gardner (2003) compiled a guide to helminth species described from African vertebrates. In both publications no information is given on digenean parasites from the Okavango Delta.

This paper provides additional information on the morphology, distribution and host records for known and new digenean species from C. gariepinus.

MATERIAL AND METHODS

Forty-two specimens of African sharptooth catfish Clarias gariepinus were collected from a number of localities in the Okavango Delta by gill nets, rod and line. Fish were taken to the field laboratory and kept in aerated aquariums until examination. Fish species were identified using Skelton' (2001) guide. The fish were anesthetized using MS222 and killed, the internal organs were removed, dissected and examined under a Nikon SMZ 800 dissection microscope for the presence of digenetic trematodes.

All digeneans were removed and fixed in warm 70% ethanol. Whole-mounts were stained using Van Cleave's haematoxylin with additional drops of Ehrlich's haematoxylin. The stain was then made alkaline at 70 % ethanol with lithium carbonate and butylamine. Specimens were then dehydrated in increasing percentages of ethanol and cleared using cedarwood oil and mounted in Canada Balsam. These were then drawn with the aid of a microscope drawing tube.

Some specimens were prepared for scanning electron microscopy (SEM) using standard techniques for digenetic trematodes, then examined at different accelerating voltages (5–10kV) and working distances, using a Leica Stereoscan 420 SEM. Reference material is kept in the Department of Zoology and Entomology Parasite Collection, University of the Free State, Bloemfontein. Type material is stored in the parasite collection of the National Museum, Bloemfontein (NMBP), South Africa and a voucher specimen is deposited in the Natural History Museum (BMNH), London, United Kingdom. Measurements are reported in millimetres as the range, followed by the arithmetic mean and standard deviation in parentheses.

TAXONOMY

Family Clinostomidae Lühe, 1901
Genus Clinostomoides Dollfus, 1950
Clinostomoides brieni Dollfus, 1950
Figs 1A, 2A–E; Table 1

  • Clinostomoides brieni. Dollfus 1950: 77, fig. 54; Manter & Pritchard 1969: 54–56, figs 1–4; Fischthal & Thomas 1970: 74–76, fig. 1.

  • Clinostomoides ophicephali (Tubangui & Masilungan, 1944): Agarwal 1959: 17; Manter & Pritchard 1969: 56.

  • Clinostomoides dollfusi Agarwal, 1959: 13–16, fig. 1; Manter & Pritchard 1969: 56.

  • Redescription:

  • Metacerearia.

  • Excysted metacercariae from gill chamber or branchial region move around freely (Fig. 2A). Body elongate, narrow, parallel lateral margins, extremities round with maximum width at acetabulum level or just pre-acetabular (Figs 1A, 2B). Cuticular spines fingerlike projections, pointed, occurring from level of posterior part of oral sucker or prepharynx to posterior extremity, unspined anteriorly (Fig. 2C). Oral sucker small. Acetabulum larger than oral sucker. Prepharynx short; pharynx muscular, 0.18 in diameter; no apparent oesophagus. Caecal bifurcation pre-acetabular closer to oral sucker than to acetabulum, forming caecal shoulders before beginning descent from acetabular level; posteriorly caeca thick-walled, with short diverticula on median and lateral sides terminating just above excretory bladder (Fig. 1A). Testes transversely elongated, in posterior fi01_431.gif body length; anterior testis crescent shaped extending across intercaecal space; posterior testis crescent to Y-shaped sometimes less wide, mostly dextral (Fig. 2D). Cirrus sac thick-walled, comma-shaped, inter-testicular, dextral (Fig. 1A). Genital pore just submedian to right, immediately anterior to posterior testis. Ovary small, intercaecal, longitudinally elongate. Uterus extending anteriorly on left side; uterine sac median, without lateral sacculations in posterior half of body, well separated from acetabulum, receiving uterus near middle;vitellarium undeveloped; no eggs (Fig. 2D). Excretory pore dorso-terminal (Fig. 2E); vesicle small, Y to V-shaped, entirely postcaecal, thick-walled, arms extending anteriorly on each side of body in extra-caecal position, uniting at anterior margin of oral sucker (Fig. 1A).

  • Material examined: BOTSWANA: 24 metaeereariae, Okavango Delta, 5 Shakawe mainstream (18°26′05.0″S 21°54′23.0″E); 9 Kalatog channel (18°25′08.2″S 21°54′05.0″E); 5 Nxamasen backwaters (18°37′34.9″S 22°06′24.4″E); 3 Mokoro lagoon (18°29′10.1″S 21°55′10.1″E); 2 Samochima lagoon (18°25′44.0″S 21°54′01.0″E).

  • Site of infection: Gill chamber/branchial region.

  • Prevalence of infection: 26.1%.

  • Remarks: Clinostomoides brieni was described by Dollfus (1950) from the Goliath heron, Ardea goliath Cretzschmar, 1827 from the Congo. Agarwal (1959) described C. dollfusi occurring in siluroid fishes from India; however, this species was later synonymised with C. brieni by Manter and Pritchard (1969). They briefly redescribed the metacercaria from Clarias sp. from Rwanda and synonymised C. ophiocephali with C. dollfusi. They also suggested that C. brieni is the only species in the genus with its synonyms being C. dollfusi and C. ophicephali.

  • The material from the current survey is similar to C. brieni in having the testes, ovary and uteroduct in the same position, the uterine sac being removed far from the acetabulum and the latter being larger than the oral sucker. Specimens from this study differ from C. brieni described by Fischthal and Thomas (1970) in that the metacercariae are larger, oral and ventral suckers are slightly larger and the testes differ in shape. Considering the above mentioned morphological differences and similarities, specimens of the present material are assigned to C. brieni. This is the first record of C. brieni in the Okavango Delta, and the first documented record from Botswana.

  • Fig. 1.

    Light microscope projection drawings of digeneans from Clarias gariepinus in the Okavango Delta: (A) Clinostomoides brieni Dollfus, 1950; (B) Neodiplostomum Railliet, 1919 type 1 metacercaria; (C) Phyllodistomum bavuri Boomker, 1984; (D) Phyllodistomum vanderwaali Prudhoe & Hussey, 1977; (E) Glossidium pedaturn Looss, 1899; (F) Thaparotrema botswanensis sp. n. Scale bars: A, C - 1 mm; D - 0.3 mm; B, E - 0.1 mm; F - 0.2 mm.

    f01_431.jpg

    Family Diplostomidae Poirier, 1886 Genus
    Neodiplostomum Railliet, 1919
    Neodiplostomum type 1 metacercaria
    Figs 1B, 2F–H; Table 1

  • Neodiplostomum type metacercaria: Prudhoe & Hussey 1977: 136–139, fig. 12.

  • Description:

  • Metacercaria.

  • Cysts white. Body divided into a relatively large, dorsoventrally flattened forebody, much smaller hindbody with maximum width occurring pre-acetabular (Fig. 1B). Oral sucker subterminal, longitudinally oval (Fig. 2G). Acetabulum round to transversely oval. Prepharynx absent. Pharynx longitudinally elongate, opens into oesophagus (Fig. 2G). Caecal bifurcation pre-acetabular, extending to level of gonads. Caeca only visible in live specimens. Holdfast organ elliptical, longitudinally elongate, situated post-acetabular (Fig. 2H). Single reproductive anlagen round to longitudinally elongate, lying posterior to holdfast organ in forebody (Fig. 1B).

  • Material examined: BOTSWANA: 36 metaeereariae, Okavango Delta, 18 Shakawe mainstream (18°26′05.0″S 21°54′23.0″E); 18 Xaro mainstream (18°25′19.7″S 21°56′19.9″E).

  • Site of infection: Cysts distributed throughout musculature (Fig. 2F).

  • Prevalence of infection: 4.7%.

  • Remarks: Prudhoe and Hussey (1977) described three diplostomid metacercariae from Clarias gariepinus in South Africa. The first Diplostomum type I was found in the eyes and does not conform to the species in the present study. The second was Diplostomum type II found in the mesenteries. The species from the current survey is similar to it in having the body divided into a fore- and hindbody and possessing a pharynx just posterior to the oral sucker. It differs from Diplostomum type II in that the fore and hind bodies are not as well developed, the gonads are a small mass and not horseshoe-shaped, and the pseudosuckers are not prominent.

  • The third type was identified as a Neodiplostomum type. The species on hand is similar to it in possessing a fore- and hindbody and has a transversely oval acetabulum. It differs, however, in that the gonads are not situated in the hindbody and the holdfast organ is not situated immediately posterior to the end of the forebody. Bisseru (1956) described three Neodiplostomum species from birds of prey from Africa as well as from the Nile crocodile (Bisseru 1957), but these were all adult specimens and could not be compared to the larval forms. According to Niewiadomska (2002), Neodiplostomum type metacercaria cannot be assigned to adult genera with certainty without knowing their complete life cycle; metacercariae are then referred to as types. This metacercaria is thus assigned to Neodiplostomum type 1. This is the first record of a Neodiplostomum metacercaria in the Okavango Delta, and the first documented record from Botswana.

  • Fig. 2.

    Light and scanning electron micrographs of Clinostomoides brieni Dollfus, 1950 (A–E) and Neodiplostomum type 1 metacercaria (F–H) from Clarias gariepinus in the Okavango Delta: (A) excysted metacercariae; (B) whole mount; (C) spines on body surface; (D) reproductive system; (E) excretory pore; (F) metacercariae encysted in muscle; (G) oral sucker and pharynx; (H) holdfast organ. Scale bars: A, B - 1 mm; C - 2 µm, D, F - 0.1 mm; E -20 µm; G - 0.05 mm; H - 0.01 mm.

    f02_431.jpg

    Family Gorgoderidae Looss, 1901 Genus
    Phyllodistomum Braun, 1899

  • Eight species of Phyllodistomum have been recorded from African fishes (Khalil & Polling 1997; Zhokhov 2010): Ph. linguale Odhner, 1902 from Gymnarchus niloticus Cuvier, 1829, Ph. spatula (Odhner, 1902) from Bagrus bajad (Forskål, 1775) and Bagrus docmak (Forskål, 1775), and Ph. spatulaeforme (Odhner, 1902) from Malapterurus electricus (Gmelin, 1789) from the Sudan; Ph. tana Zhokhov, 2010 from C. gariepinus from Ethiopia; Ph. ghanense Thomas, 1958 from Ctenopoma kingsleyae Günther, 1896 and Caecomastacembelus nigromarginatus (Boulenger, 1898), and Ph. symmetrorchis Thomas, 1958 from Auchenoglanis occidentalis (Valenciennes, 1840) from Ghana; and Ph. vanderwaali Prudhoe & Hussey, 1977 and Ph. bavuri Boomker, 1984 from C. gariepinus from South Africa. The genus has also been recorded from several fish species in the Nile River in Egypt (Mansour et al. 2003).

  • Phyllodistomum bavuri Boomker, 1984
    Figs 1C, 3A–C; Table 1

  • Phyllodistomum bavuri Boomker 1984: 129–130, fig. 1.

  • Redescription:

  • Body aspinose, ampullate in shape (Fig. 1C). Anterior part subcylindrical, amounts to fi02_431.gif total body length. Posterior part of body thin, flattened dorsoventally, various internal structures microscopically visible without staining (Fig. 3A). Oral sucker round, situated subventrally. Acetabulum circular, larger than oral sucker, situated just posterior to junction of anterior end of hind body (Fig. 1C). Pharynx absent. Oesophagus short. Caecal bifurcation nearer to oral sucker than to acetabulum. Intestinal caeca terminate almost at end of posterior body margin. Excretory vesicle, excretory pore indistinct. Genital pore lies in midline of body halfway between oral and ventral suckers beneath gut bifurcation, in some specimens slightly more towards oral sucker (Fig. 3B). Cirrus sac absent. Two fairly large testes, deeply and irregularly lobed lying in middle of body on either side of midline between intestinal caeca. In some specimens testes slightly displaced one in front of other but mostly opposed (Fig. 3C). Ovary trilobed, sometimes round; situated to right of body midline in three specimens, to left in five specimens, between vitellarium and testes. Vitellarium compact, roughly round to lobed, opposed, lies just posterior to rim of acetabulum, anterior to ovary. Uterus consists of numerous loops, runs between testes and vitellarium to reach genital pore, loops rarely extend laterally beyond caeca (Fig. 3C). Uterine loops full of eggs. Eggs rounded to oval.

  • Material examined: BOTSWANA: 8 adult specimens, Okavango Delta, Shakawe mainstream (18°26′05.0″S 21°54′23.0″E).

  • Site of infection: Urinary bladder.

  • Prevalence of infection: 2.3 %.

  • Remarks: According to Boomker (1984) and Brooks and MacDonald (1986), species in the genus can mainly be distinguished from each other by the position of the ovary relative to the vitellarium, i.e. lying anterior, opposite or posterior to the vitellarium.

  • The species from the present study resembles Ph. linguale occurring in the urinary bladder of G. niloticus from Sudan, in having similar body size, the ovary being irregularly lobed, uterine coils that seldom cross the intestinal caeca laterally and the ovary lies posterior to the vitellarium. It differs in that the caeca does not terminate a distance from the posterior margin and the intestinal bifurcation being closer to the oral sucker in this species. The genital pore in Ph. linguale lies between the gut bifurcation and rim of the ventral sucker, while in our specimens it is halfway between the bifurcation and the ventral sucker.

  • The studied material also resembles Ph. bavuri described by Boomker (1984) from the urinary bladder of C. gariepinus from the Bangu River, Transvaal (presently Gauteng), in having the same body size and shape, the ovary being round to weakly trilobed and the vitellarium also being weakly lobed. It differs in that the gut bifurcation occurs near to the oral sucker and not halfway between the oral and ventral suckers. It also differs in that the intestinal caeca terminate close to the posterior margin of the body. The general morphology and measurements of specimens from the present material correspond to a certain degree with those in Ph. bavuri as described by Boomker (1984). However, in contrast to data by Boomker (1984), the present specimens show more variation in ovary shape, and vitellarium being slightly more lobed and irregularly shaped.

  • The above mentioned morphological differences are, however, considered to be within the intraspecific variability of Ph. bavuri and therefore the specimens of the present material are assigned to this species. This is the first record of Ph. bavuri in the Okavango Delta, and the first documented record from Botswana.

  • Fig. 3.

    Light and scanning electron micrographs of Phyllodistomum bavuri Boomker, 1984 (A–C), Phyllodistomum vanderwaali Prudhoe & Hussey, 1977 (D–I) and Glossidium pedatum Looss, 1899 (J–L) collected from Clarias gariepinus in the Okavango Delta: (A) whole mount; (B) genital pore; (C) vitellaria, ovary and testes; (D) adults attached to urinary bladder; (E) whole mount; (F) body surface with papillae; (G) genital pore; (H) genital pore and pars prostatica; (I) vitellaria, ovary, uterus and testes; (J) whole mount; (K) anterior and posterior testes; (L) acetabulum and cirrus sac. Scale bars: A - 1 mm; B–D, H - 0.1 mm; E, I, K, L - 0.05 mm; J - 0.5 mm; F - 2 µm; G - 20 µm.

    f03_431.jpg

    Phyllodistomum vanderwaali Prudhoe & Hussey, 1977
    Figs 1D, 3D–I; Table 1

  • Phyllodistomum vanderwaali. Prudhoe & Hussey 1977: 116–119, fig. 2; Boomker 1984: 131, fig. 7.

  • Redescription:

  • Body ampullaceous with subcylindrical forebody and leaf-like dorsoventrally flattened hindbody (Figs 1D, 3E). Forebody constitutes fi03_431.gifA of total length, hindbody almost circular. Body surface unspined, papillae present on the lateral sides of body (Fig. 3F). Oral sucker terminal, almost round. Acetabulum circular, larger than oral sucker, situated at anterior level of hindbody (Figs 1D, 3F). Pharynx absent. Oesophagus short. Caecal bifurcation immediately posterior to oral sucker, terminating near posterior body margin. Excretory pore opens dorsally near posterior extremity of body. Genital pore opens halfway between gut bifurcation and acetabulum (Fig. 3G, H). No cirrus sac, terminal organs of male and female complexes lie free in parenchyma. Ejaculatory duct short, runs from genital pore to open into small pars prostatica, which is endowed with a large number of deeply staining gland-cells (Fig. 3H). Two indented, irregularly lobed testes situated on either side of median line of mid region of body in between intestinal caeca, may lie opposite each other or one slightly in front of other (Fig. 31). Ovary lies to right of median line in six specimens; to left in other six specimens, but always in front of testes and posterior to vitellarium. Ovary irregularly round or lobed mass (Fig. 31). Vitellarium compact diagonally opposed bodies, lie posterior to rim of acetabulum, anterior to ovary between intestinal caeca (Fig. 31). Uterus consists of numerous loops that pass anteriorly along the median line between testes and vitelline bodies to reach genital pore, may extend beyond ends of caeca occasionally crossing caeca laterally (Fig. ID). Uterus contains thin-shelled oval eggs. Eggs larger towards the distal end.

  • Material examined: BOTSWANA: 12 adult specimens, Okavango Delta, 7 Xaro mainstream (18°25′19.7″S 21°56′19.9″E); 5 Xaro lagoon (18°25′19.7″S 21°56′19.9″E).

  • Site of infection: Numerous worms observed in urinary bladder (Fig. 3D).

  • Prevalence of infection: 4.7%.

  • Remarks: This species differs from Ph. spatula, Ph. symmetrorchis and Ph. ghanense in having the ovary not anterior or slightly posterior to the vitellarium. It also differs from Ph. ghanense in having the uterine coils not filling the entire posterior two-thirds of the body. In Ph. spatula the ovary is completely round, while in Ph. spatulaeforme the ovary is kidney-shaped and the testes are small in relation to the body size.

  • Ph. vanderwaali differs from Ph. linguale and Ph. bavuri in being much smaller and in having the vitellarium immediately posterior of the acetabulum and the intestine bifurcating almost immediately posterior of the oral sucker. It also differs from Ph. bavuri, as redescribed in this paper, in that the testes, ovary and vitellarium are different in shape and size, the ovary lies more adjacent to the vitellarium and the body size is far smaller. The general morphology and measurements of specimens of the present material also correspond to a certain degree with Ph. vanderwaali as described by Prudhoe and Hussey (1977) and redescribed by Boomker (1984). However, in contrast to data by Prudhoe and Hussey (1977) and Boomker (1984), the present specimens show more variation in the shape, size and position of the testes, which in different specimens may be directly diagonal or nearly at the same level and dissimilar in size. Generally, the testes are larger than the ovary but in some specimens they are smaller.

  • All the above mentioned morphological differences are considered to be within the intraspecific variability of Ph. vanderwaali and therefore the specimens of the present material are assigned to this species. This is the first record of Ph. vanderwaali in the Okavango Delta, and the first documented record from Botswana.

  • TABLE 1

    Morphological measurements of the digenean species collected from Clarias gariepinus (Burchell, 1822) in the Okavango River and Delta, Botswana. Abbreviations: L – length, W – width.

    t01_431.gif

    Family Macroderoididae McMullen, 1937
    Genus Glossidium Looss, 1899
    Glossidium pedatum Looss, 1899
    Figs 1E, 3J–L; Table 1

  • Glossidium pedatum. Looss 1899: 705–706, fig. 27; Fischthal 1973: 166–167.

  • Afromacroderoides lazerae Khalil, 1972: 341–344, fig. 1; Mashego & Saayman 1989: 19.

  • Redescription:

  • Elongate trematodes with truncated posterior end (Figs 1E, 3J). Body with maximum width at acetabulum level. Cuticle covered with tiny spines which are dense on anterior end of body, gradually diminishing posteriorly. Both suckers well developed, almost equal in size. Oral sucker slightly oval to spherical in shape (Fig. 1E). Acetabulum spherical. Prepharynx short. Pharynx fairly large, opens into oesophagus which may sometimes be indistinct. Intestinal caeca extend posteriorly, ending near posterior extremity of body. Testes tandem, oval-shaped, smooth (Figs. 1E, 3K). Testes separated from each other by number of eggs. Cirrus sac large, elongate, curves to right of acetabulum, contains bipartite seminal vesicle with posterior half being larger than anterior part (Fig. 3L). Common genital pore median or submedian, immediately anterior to acetabulum. Ovary round to oval situated posterior to, or next to cirrus sac. Uterus forming upward and downward loops reaching to posterior end of body, where it fills in almost whole post testicular space (Fig. 1E). Numerous yellow to brown operculate eggs present. Vitellarium irregularly shaped, extends laterally on either side of body from ovarian level to posterior margin of posterior testis.

  • Material examined: BOTSWANA: 21 adult specimens, Okavango Delta, Shakawe mainstream (18°26′05.0″S 21°54′23.0″E).

  • Site of infection: Posterior third of intestine.

  • Prevalence of infection: 11.9%.

  • Remarks: Glossidium pedatum was first reported by Looss (1899) from Bagrus bajad (Forskål, 1775) and Bagrus docmak (Forskål, 1775) from the lower reaches of the Nile River. Fischthal (1973) collected and redescribed specimens of Glossidium pedatum from the intestine of C. gariepinus in Ethiopia, and noted that there were similarities between his material and Afromacroderoides lazerae Khalil, 1972 (also from C. gariepinus). It was found that Khalil's (1972) description corresponded to those of G. pedatum, and Mashego and Saayman (1989) thus synonymised A. lazerae with G. pedatum. Although Tkach (2008) treated Afromacroderoides as a synonym of Glossidium; however, he did not consider G. pedatum and G. lazerae to be synonyms and thus made the new combination Glossidium lazerae on the basis of the length of the oesophagus.

  • The specimens from the present study are similar to G. pedatum described by Fischthal (1973) in that it possesses a four-lobed pharynx, the ovary and testes are in the same position; the vitellaria extend from the ovarian level to the posterior margin of the posterior testis; the prepharynx has a sphincter-like structure situated just anterior to the pharynx. On the basis of the above mentioned characteristics, specimens of the present material are thus assigned to G. pedatum. This is the first record of G. pedatum in the Okavango Delta, and the first documented record from Botswana.

  • Family Opisthorchiidae Braun, 1901
    Genus Thaparotrema Gupta, 1955

  • The genus Thaparotrema was erected for Thaparotrema vittalani Gupta, 1955 that was described from the intestine of the bagrid catfish Rita rita (Hamilton, 1822) in India (Gupta 1955). Scholz (2008) transferred species with a small, elongate or fusiform body covered with tegumental spines, having no prepharynx and with sinuous excretory system, which had been previously placed in the genus Opisthorchis Blanchard, 1895, to Thaparotrema. Thaparotrema piscicola (Odhner, 1902) was described by Odhner (1902) from the gall bladder of Gymnarchus niloticus from Sudan.

  • Thaparotrema botswanensis sp. n.
    Figs 1F, 4A–H; Table 1

  • Etymology: This species is named after Botswana, where the material was collected.

  • Description:

  • Body elongate, narrow with round extremities, maximum width at level of acetabulum (Figs 1F, 4A). Tegument spined except for extreme part of post-testicular end of body. Suckers muscular. Oral sucker terminal round to oval in shape. Acetabulum slightly smaller than oral sucker, situated in first quarter of anterior part of body (Fig. 1F). Prepharynx absent. Pharynx round, some instances overlaps oral sucker dorsally (Fig. 4B). Oesophagus long; caecal bifurcation pre-acetabular closer to oral sucker; caeca narrow, extend to almost end of posterior extremity (Fig. 1F). Two testes, slightly oval, tandem to diagonal within inter-caecal space near to posterior extremity of body, separated from each other by excretory bladder (Fig. 4C). Posterior testis slightly bigger than anterior. Cirrus sac absent. Seminal vesicle tubular commencing post-acetabular (Fig. 4D). Genital pore median, just pre-acetabular (Fig. 4E). Ovary smooth, intercaecal (Figs 1F, 4F). Mehlis' gland present. Seminal receptacle situated obliquely anterior to ovary (Fig. 4F). Laurer's canal not observed. Vitelline follicles extending post-acetabular to level of ovary, slightly overlapping caeca (Figs 1F, 4G). Uterus extensively coiled, intercaecal, with ascending limb only, sinistral to seminal vesicle (Fig. 4G). Eggs yellow-brown, operculate. Excretory bladder saccular, passing between testes ending at posterior level of ovary; pore sub terminal (Figs 1F, 4H).

  • Comparison: The new species is similar to Th. piscicola with the body being elongate and spined, having suckers that are almost of equal size and position, the absence of the cirrus sac, as well as the vitellarium beginning post-acetabular and extending to the level of the ovary, but differs in having a prominent seminal receptacle, greater space between the testes, and the testes being also not situated as close to the posterior extremity. The vitelline follicles are also much larger than those in Th. piscicola.

  • The new species is also similar to Th. pedicellatum (Verma, 1927) from the intestine of Rita rita from India in having suckers of almost equal size and a more prominent seminal receptacle. It differs, however, in that the body is not as wide nearer to the posterior extremity, the distance between the oral sucker and acetabulum is shorter and the vitelline follicles begin a distance post-acetabular and extend to the level of the ovary. Thaparotrema botswanensis sp. n. also differs from Th. vitallani in that the vitelline follicles do not begin anterior to the level of the acetabulum, the vitelline follicles are also more compact and the testes are situated close together. Based on the above remarks and the differences between Th. botswanensis sp. n. and the known species, it can be regarded as a new species. This is the first record of Thaparotrema from Clarias gariepinus, as well as the first report of the genus from the Okavango Delta.

  • Holotype: BOTSWANA: Okavango Delta, Shakawe mainstream ( 18°26′05 0″S 21°54′23.0″E), 01/10/25-9c (NMBP355).

  • Paratype: BOTSWANA: Okavango Delta, Kalatog channel (18°25′08.2″S 21°54′05.0″E), 01/10/25-9b (NMBP 356).

  • Other material examined: same as paratype, 01/10/25-9e (BMNH 2013.9.27.1).

  • Site of infection: Gall bladder.

  • Prevalence of infection: 4.7%.

  • Fig. 4.

    Light micrographs of Thaparotrema botswanensis sp. n. collected from Clarias gariepinus in the Okavango Delta: (A) whole mount; (B) pharynx; (C) anterior and posterior testes; (D) seminal vesicle; (E) genital opening; (F) ovary and seminal receptacle; (G) vitellaria and uterus filled with eggs; (H) excretory bladder. Scale bars: A - 1 mm; B, C, E, F, H - 0.1 mm; D, G - 0.05 mm.

    f04_431.jpg

    CONCLUDING REMARKS

    Among the digeneans collected during the present investigation only Clinostomoides brieni, Neodiplostomum sp. (both metacercariae), Glossidium pedatum, Phyllodistomum vanderwaali, Phyllodistomum bavuri and Thaparotrema botswanensis sp. n. were found infecting C. gariepinus. A certain degree of site specificity was also observed, with T. botswanensis sp. n. being found only in the gall bladder of C. gariepinus, while both Phyllodistomum species were found only in the urinary bladder and thus seem to occupy a certain niche within their host. At any one time a single C. gariepinus may host four species of digeneans, each occupying its own niche within the host. Not only are these fish infected with adult and larval digeneans, but they also host other ectoand endoparasites, sometimes having a heavy parasite burden (Jansen van Rensburg et al 2001).

    Clarias gariepinus plays a notably important role in the life cycles of digenean parasites in the Okavango Delta, as it acts as a definitive host for adults of four species, and as a second intermediate host to two metacercarial trematodes.

    ACKNOWLEDGEMENTS

    This research was financially facilitated by the National Research Foundation (NRF) of South Africa. Findings, opinions, conclusions or recommendations expressed in this article are solely those of the authors, and do not necessarily reflect views of the NRF. Debswana Diamond Company Ltd is acknowledged for their financial support of the Okavango Fish Parasite Project.

    REFERENCES

    1.

    S.M. Agarwal 1958. Studies on the metacercaria Clinostomoides dollfusi n. sp. (Trematoda: Clinostomatidae) from Siluroid fishes. Indian Journal of Helminthology 10: 13–18. Google Scholar

    2.

    B. Bisseru 1956. Three new species of the genus Neodiplostomum Railliet, 1919, from Central African birds of prey, with a note on Neodiplostomum canaliculatum (Nicoll, 1914) Dubois, 1937. Journal of Helminthology 30: 51–62. Google Scholar

    3.

    B. Bisseru 1957. On two new trematodes (Proterodiplostomatidae) from an African crocodile, and a list of strigeid parasites from Africa. Journal of Helminthology 31 (1–2): 85–102. Google Scholar

    4.

    J. Boomker 1984. Parasites of South African freshwater fish. II. Redescription of the African species of the genus Phyllodistomum Braun, 1899 (Trematoda: Gorgoderinae) and the description of a new species. Onderstepoort Journal of Veterinary Research 51 (2): 129–139. Google Scholar

    5.

    D.R. Brooks & C.A. Macdonald 1986. A new species of Phyllodistomum Braun, 1899 (Digenea: Gorgoderidae) in a Neotropical catfish, with discussion of the generic relationships of the Gorgoderidae. Canadian Journal of Zoology 64: 1326–1330. Google Scholar

    6.

    A.G. Canaris & S.L. Gardner 2003. Bibliography of helminth species described from African vertebrates 1800–1967. Lincoln, NE, USA: The Harold W. Manter Laboratory of Parasitology. Google Scholar

    7.

    F.D. Chibwana , I. Blasco-Costa , S. Georgieva , K.M. Hosea , G. Nkwengulila , T. Scholz & A. Kostadinova 2013. A first insight into the barcodes for African diplostomids (Digenea: Diplostomidae): Brain parasites in Clarias gariepinus (Siluriformes: Clariidae) Infection , Genetics and Evolution 17: 62–70. (  http://dx.doi.org/10.1016/j-meegid.2013.03.037Google Scholar

    8.

    R.P Dollfus 1950. Trématodes récoltés au Congo Belge par le Professeur Paul Brien (mai-août 1937). Annales du Musée Congo Belge, C, Zoologie série 5 1: 1–136. Google Scholar

    9.

    J.H. Fischthal 1973. Three digenetic trematodes of Cliarias mossambicus Peters (Clariidae) from Ethiopia. Proceedings of the Helminthological Society of Washington 40 (1): 166–167. Google Scholar

    10.

    J.H. Fischthal & J.D. Thomas 1970. Some metacercariae of digenetic trematodes in fishes from the Nungua Lake, Ghana. Anales del Instituto de Biologia Universidad Nacional Autónoma de México, Serie Zoologia 41 (1): 73–80. Google Scholar

    11.

    S.P. Gupta 1955. Trematode parasites of fresh-water fishes. Indian Journal of Helminthology 5: 1–80. Google Scholar

    12.

    C. Jansen van Rensburg , J.G. Van As , L. Basson , L.L. Van As & C.C. Reed 2001. Parasites infecting the sharptooth catfish, Clarias gariepinus in the Okavango Delta, Botswana. Microscopy Society of Southern AfricaProceedings 31: 78. Google Scholar

    13.

    L.F. Khalil 1972. Afromacroderoides lazerae gen. et sp. nov. (Allocreadiidae: Walliniinae), a new digenean from the African freshwater fish Clarias lazera. Journal of Helminthology 46 (4): 341–344. Google Scholar

    14.

    L.F. Khalil 2003. The helminth parasites of the most economically important African freshwater fish, Clarias gariepinus, and their relation to the fish biology and zoogeography. Journal of the South African Veterinary Association 74: 91. Google Scholar

    15.

    L.F. Khalil & L. Polling 1997. Checklist of the helminth parasites of African freshwater fishes. Pietersburg, South Africa: Review Printers. Google Scholar

    16.

    A. Looss 1899. Weitere Beiträge zur Kenntnis der Trematoden-Fauna Aegyptens, zugleich Versuch einer natürlichen Gliederung des Genus Distomum Retzius. Zoologische Jahrbücher: Abteilung für Systematik, Geographie und Biologie der Thiere 12: 521–784. Google Scholar

    17.

    M.F.A. Mansour , S.H. Hassan , A.E.-A.A. Khidr & M.A. Ghanem 2003. General survey on certain helminth parasites infecting some Nile fishes at El-Mansoura, Egypt. Egyptian Journal of Aquatic Biology and Fisheries 7 (4): 423–446. Google Scholar

    18.

    H.W. Manter & M.H. Pritchard 1969. Some digenetic trematodes of Central Africa, chiefly from fishes. Revue de Zoologie et de Botanique Africaines 80: 51–61. Google Scholar

    19.

    S.N. Mashego & J. Saayman 1989. Digenetic trematodes and cestodes of Clarias gariepinus (Burchell, 1822) in Lebowa, South Africa, with taxonomic notes. South African Journal of Wildlife Research 19: 17–20. Google Scholar

    20.

    K. Niewiadomska 2002. Family Diplostomidae Poirier, 1886. In : D.I. Gibson , A. Jones & R.A. Bray , eds, Keys to the Trematoda. Vol. 1. Wallingford, Oxfordshire, UK: CABI Publishing and the Natural History Museum, pp. 159–170. Google Scholar

    21.

    T. Odhner 1902. Mitteilungen zur Kenntnis der Distomen II. Drei neue Distomen aus der Gallenblase von Nilfischen. Zentralblatt für Bakteriologie, Parasitenkunde und Infektionskrankheiten 31 (4): 152–162. Google Scholar

    22.

    S. Prudhoe & C.G. Hussey 1977. Some parasitic worms in freshwater fishes and fish predators from the Transvaal, South Africa. Zoologica Africana 12 (1): 113–147. Google Scholar

    23.

    O. Safriel & M.N. Bruton 1984. Aquaculture in South Africa: A cooperative research programme. South African National Scientific Programmes Report No. 89. Pretoria: Council for Scientific and Industrial Research. Google Scholar

    24.

    T. Scholz 2008. Family Opisthorchiidae Looss, 1899. In : R.A. Bray , D.I. Gibson & A. Jones , eds, Keys to the Trematoda. Vol. 3. Wallingford, Oxfordshire, UK: CABI Publishing and the Natural History Museum, pp. 9–49. Google Scholar

    25.

    P. Skelton 2001. A complete guide to the freshwater fishes of southern Africa. Cape Town: Struik. Google Scholar

    26.

    V.V. Tkach 2008. Genera incertae sedis. In: R.A. Bray , Gibson D & A. Jones , eds. Keys to the Trematoda. Vol. 3. Wallingford, Oxfordshire, UK: CABI Publishing and the Natural History Museum, pp. 736–752. Google Scholar

    27.

    A.E. Zhokhov 2010. A new gorgoderid trematode of the genus Phyllodistomum (Digenea: Gorgoderidae) from Clarias gariepinus (Actinopterygii: Clariidae) in Lake Tana, Ethiopia. Zoosystematica rossica 19 (1): 9–12. Google Scholar

    28.

    A.E. Zhokhov , D.A. Morozova & A. Tessema 2010. Trematode metacercariae from the cranial cavity of African catfish Clarias gariepinus (Burchell, 1822) from Lake Tana, Ethiopia. Inland Water Biology 3 (2): 160–164. Google Scholar
    Candice Jansen van Rensburg, Jo G. van As, and Pieter H. King "New Records of Digenean Parasites of Clarias gariepinus (Pisces: Clariidae) from the Okavango Delta, Botswana, with Description of Thaparotrema botswanensis sp. n. (Plathelminthes: Trematoda)," African Invertebrates 54(2), 431-446, (1 November 2013). https://doi.org/10.5733/afin.054.0210
    Published: 1 November 2013
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