Hostname: page-component-6898cfcb55-kwdml Total loading time: 0 Render date: 2026-11-11T23:56:53.737Z Has data issue: false hasContentIssue false
  • English
  • Français

New evidence of a lateral transfer of monogenean parasite between distant fish hosts in Lake Ossa, South Cameroon: the case of Quadriacanthus euzeti n. sp.

Published online by Cambridge University Press:  17 August 2015

J. Nack,
A.R. Bitja Nyom,
A. Pariselle and
C.F. Bilong Bilong
J. Nack
Affiliation:
University of Douala, Faculty of Science, PO Box 24157 Douala, Cameroon
A.R. Bitja Nyom
Affiliation:
University of Ngaoundéré, Faculty of Science, PO Box 454 Ngaoundéré, Cameroon
A. Pariselle*
Affiliation:
Institut des Sciences de l'Évolution de Montpellier, IRD, BP 1857, Yaoundé, Cameroon
C.F. Bilong Bilong
Affiliation:
University of Yaoundé 1, Faculty of Science PO Box 812 Yaoundé, Cameroon
*
* E-mail: antoine.pariselle@ird.fr
Rights & Permissions [Opens in a new window]

Abstract

Species of the monogenean genus Quadriacanthus mainly infect fish belonging to the Siluriformes, especially the genera Clarias, Heterobranchus or Bagrus, and their host specificity is strict (oioxenous) or narrow (stenoxenous). An examination of the gills of 19 Papyrocranus afer from Lake Ossa, South Cameroon, revealed for the first time the presence of a species of Quadriacanthus from a fish host belonging to the Notopteridae. The morphology and the size of sclerotized parts of haptor and the male and female copulatory complexes suggest that this monogenean is a new species named Quadriacanthus euzeti n. sp. The fish genus Papyrocranus differs taxonomically from the usual fish hosts of Quadriacanthus and hence the presence of a species belonging to this genus on the gills of this host suggests the occurrence of a lateral transfer of Quadriacanthus from species belonging to Clarias or Bagrus which live sympatrically with P. afer in Lake Ossa.

Information

Type
Research Papers
Information
Journal of Helminthology , Volume 90 , Issue 4 , July 2016, pp. 455 - 459
Copyright
Copyright © Cambridge University Press 2015 

Introduction

Fish belonging to the Notopteridae are represented in lower Guinea by two species, Papyrocranus afer (Günther, 1868) and Xenomystus nigri Günther, 1868 (Roberts, Reference Roberts1992; Paugy et al., Reference Paugy, Lévêque and Teugels2003; Lavoué & Sullivan, Reference Lavoué and Sullivan2004; Stiassny et al., Reference Stiassny, Teugels and Hopkins2007). In Cameroon, P. afer is reported in the basins of Sanaga, Cross, Meme and Wouri rivers while X. nigri is only known from the latter (Stiassny et al., Reference Stiassny, Teugels and Hopkins2007). Up until now, both species were declared free of monogenean parasites (Birgi, Reference Birgi1987). In a recent parasitological survey on monogenean fish parasites from Cameroon, the gills of P. afer, which were sampled in Lake Ossa (Sanaga River basin), unexpectedly revealed the presence of a new Quadriacanthus Paperna, Reference Paperna1961 species. In the present study we describe this monogenean species for the first time and its probable origin is discussed.

Materials and methods

Collection and examination of fish hosts and monogeneans

Lake Ossa (3°45′–3°53′N; 9°58′–10°04′E, and 8 m above sea level) is located 20 km to the west of the city of Edéa and 30 km from the Atlantic Ocean (Kossoni, Reference Kossoni2003). According to Wirrmann (Reference Wirrmann1992), Wirrmann et al. (Reference Wirrmann, Bertaux and Kossoni2001) and Kossoni (Reference Kossoni2003), Lake Ossa is in fact composed of several lakes, reaching a total surface of about 3800 ha. This system presents three main lakes: Mevia, which is located in the north, Ossa in the middle and Mwembe in the south. Ossa and Mevia, which are the two largest lakes, communicate through a short channel, while Mwembe is isolated. In the south-eastern part, Lake Ossa and Lake Mwembe communicate with the Sanaga River by a sinuous outlet (fig. 1).

Fig. 1

Map to show the geographical location and hydrography of Lake Ossa.

Specimens of P. afer (n= 19) were caught using hook-lines or gill-nets during the long dry season (December to February 2011). They were dissected immediately on the shore after fishing. The gill arches were isolated by two incisions, one ventral and another dorsal, then preserved in a 25-ml scintillation vial, and maintained at − 15°C in a portable Engel fridge–freezer until examination. Each fish carcass was marked and kept in 10% formaldehyde. In the laboratory, monogenean parasites that were tenaciously attached to the gill filaments were first dislodged using an entomology needle mounted on a mandrel (Bilong Bilong, Reference Bilong Bilong1995), then transferred individually into a drop of ammonium picrate–glycerin (a mixture described by Malmberg, Reference Malmberg1957) on a microscope slide. The preparations were covered with a cover slip and after 24 h they were sealed with Glyceel (made after Bates, Reference Bates1997).

Morphometrics

The drawings of the sclerotized pieces of the haptor and of the copulatory complex were carried out using the camera lucida of a microscope Wild M.20 (Wild, Heerbrugg, Switzerland) and Corel Draw X4 software (ver 14.0.0.701; Corel Corporation, www.corel.com/); their measurements and numbering were carried out following Gussev (Reference Gussev, Bychovskaya–Pavlovskaya, Gussev, Dubinina, Izymova, Smirnova, Sokolovskaya, Shtein, Shul'man and Epsthein1962) modified by N'Douba et al. (Reference N'Douba, Lambert and Euzet1999) (fig. 2). These measurements are given in micrometres (μm) as follows: mean (minimum value–maximum value). Type specimens are deposited in the Royal Museum for Central Africa, Tervuren (RMCA); and the Muséum National d'Histoire Naturelle, Paris (MNHN) as indicated, remaining specimens have been kept in the collection of the Laboratoire de Parasitologie et d'Écologie, University of Yaoundé I, Yaoundé, Cameroon.

Fig. 2

Morphometrics of Quadriacanthus spp. used in this study are based on Gussev (Reference Gussev, Bychovskaya–Pavlovskaya, Gussev, Dubinina, Izymova, Smirnova, Sokolovskaya, Shtein, Shul'man and Epsthein1962) and modified by N'Douba et al. (Reference N'Douba, Lambert and Euzet1999). (An) Anchor: a, length; ba, base width; e, point length; (Cc) copulatory complex: Ap, accessory piece length; Ci, cirrus length; (Cn) cuneus: i, width; j, length; (Db) dorsal bar: Ct, centre length; h, median process length; w, width; x, length; (H) hooklet length; (Vb) ventral bar: w, width; x, length; (Vg) vagina: l, length; d, diameter.

Results

Quadriacanthus euzeti n. sp. Nack, Pariselle & Bilong Bilong

Taxonomic summary

  • Type host. Papyrocranus afer (Günther, 1868).

  • Site. Gills.

  • Type locality. Lake Ossa, Cameroon (03°45′–03°53′N; 9°58′–10°04′E).

  • Type specimens. Holotype no. 37 782 and paratypes no. 37 783 RMCA; paratype no. HEL515 MNHN.

  • Material studied. Sixteen individual adult parasites

  • Parasitic indices. Number of fish infected = 14; prevalence = 73.7%; mean intensity = 8 (1–17).

  • Etymology. Named in honour of our mentor, the late Professor Louis Euzet.

Description

The anatomy of this ancyrocephalid parasite corresponds to the diagnosis of Quadriacanthus given by Paperna (Reference Paperna1961) and amended by Kritsky & Kulo (Reference Kristky and Kulo1988): body divisible into cephalic region, trunk, peduncle, haptor. Tegument thin, smooth. Two bilateral, terminal cephalic lobes; four pairs of head organs; cephalic glands unicellular, comprising two bilateral groups postero-lateral to pharynx. Ocellae present or absent; granules usually scattered in cephalic area, anterior trunk. Mouth subterminal, midventral; pharynx muscular, glandular; oesophagus short; two intestinal caeca, confluent posterior to gonads. Gonads intercaecal, overlapping; testis dorsal to ovary. Vas deferens looping left intestinal caecum; seminal vesicle a dilation of vas deferens, lying diagonally to left of midline in anterior trunk; two prostatic reservoirs, one C-shaped, wrapping around second. Copulatory complex comprising basally articulated cirrus, accessory piece. Oviduct short; uterus delicate; vagina sinistral; seminal receptacle intercaecal, ventral to anterior end of ovary; vitellaria well developed, dispersed in two bilateral bands coextensive with intestinal caeca; common vitelline duct anterior to seminal receptacle. Haptor armed with dorsal and ventral pairs of anchors, dorsal and ventral bars, posterior muscular pad between bars, 14 pairs of hooklets with ancyrocephaline distribution. Anchors with cuneus; ventral bar comprising two components articulating medially; dorsal bar with bilateral arms, expanded mid-region. Hooklets pair IV with elongate dilated proximal shank; pairs I and III usually with short proximal dilation of shank; pairs II, V, VI and VII lacking dilated shank. Parasites of siluriform fish of Africa and Asia. Type species, host and locality: Quadriacanthus clariadis Paperna, Reference Paperna1961, from Clarias lazera Cuvier and Valenciennes, Lake Galilee, Israel.

Adults of Q. euzeti (figs 3 and 4) measure 630 (560–700) total length, haptor included, and 81.7 (70–90) width at the level of ovary. No ocelles, but many pigmented granules dispersed on the border of the pharynx measuring 37.5 (35–40) in diameter. Haptor wider than the rest of the body, 90 (80–100) in length and 100 (90–110) in width, armed with: four anchors (two dorsal and two ventral) each of them with a triangular cuneus and a thick filament, two transverse bars (one dorsal and one ventral). Dorsal anchors without differentiated guard and shaft, thick curved blade: a, 50.5 (49–53); ba, 14.6 (13–16); e, 9.4 (8–11). Cuneus: i, 8 (7–9); j, 18.2 (17–20). Dorsal transverse bar – a main piece (widely open V) associated with a posterior funnel-shaped sclerite and an anteriorly overlapping trapezoidal piece: Ct, 23 (22–24); x, 32.3 (31–33); w, 15 (14–16); h, 24 (22–27). Ventral anchors smaller than dorsal ones: a, 37.5 (33–40); ba, 12 (10–13); e, 13.7 (11–14). Cuneus: I, 4.5 (4–5); j, 11 (10–12). Ventral transverse bar formed of two articulated equal components: x, 53 (52–54); w, 11.5 (10–13). Fourteen hooklets arranged in seven symmetrical pairs are all similar, except those from the second and the fourth pairs, which are smaller (larval size) and larger, respectively. Hooklet pair I, 16.5 (16–17); II, 13.5 (13–14); III, 16.5 (16–17); IV, 24.5 (23–27); V, 16.5 (16–17); VI, 16.5 (16–17); VII, 16.5 (16–17). Tubular cirrus with flared base: Ci, 38 (36–40). Accessory piece attached to the base of the cirrus, ending with a distal hook: Ap, 27 (25–28). Short and funnel-shaped sclerotized vagina only observed in 10 individuals: l, 17 (16–18); d, 2.5 (2–3).

Fig. 3

Sclerotized parts of Quadriacanthus euzeti n. sp. Nack, Pariselle & Bilong Bilong: Cc, copulatory complex; Da, dorsal anchor; Db, dorsal bar; Dc, dorsal cuneus; I–VII, hooklets; Va, ventral anchor; Vb, ventral bar; Vc, ventral cuneus; Vg, vagina. Scale bar = 20 μm.

Fig. 4

Photomicrographs of hard parts of Quadriacanthus euzeti n. sp. (a) Haptor: Da, dorsal anchor; Db, dorsal bar; Va, ventral anchor; Vb, ventral bar; (b) copulatory complex: Ap, accessory piece; Ci, cirrus.

Differential diagnosis

Among the species of Quadriacanthus already described, Quadriacanthus euzeti n. sp. is close to Q. levequei Birgi, Reference Birgi1988 and Q. nyongensis Birgi, Reference Birgi1988, based on the morphology of the male copulatory complex. However, it is distinguished from these two species by the size of the sclerotized pieces of haptor and/or copulatory complex, of the hooklets, of the ventral and dorsal anchors, and of the ventral and dorsal transverse bars, which are all generally smaller than in either of these two species (Birgi, Reference Birgi1988). These observations allow us to assert that the parasite of P. afer is a new species.

Discussion

Before the finding and description of this new monogenean species, all Quadriacanthus species were reported only from Siluriformes and Perciformes hosts. Among Siluriformes, these parasites infect fish belonging to Bagrus Bosc, 1816 (Bagridae) (Paperna, Reference Paperna1979), Clarias and Heterobranchus (Clariidae) (Paperna, Reference Paperna1979; Shotter, Reference Shotter1980; Long, Reference Long1981; El-Naggar & Serag, 1986; Birgi, Reference Birgi1988; Kristky & Kulo, Reference Kristky and Kulo1988; Douëllou & Chishawa, Reference Douëllou and Chishawa1995; N'Douba et al., Reference N'Douba, Lambert and Euzet1999; N'Douba & Lambert, Reference N'Douba and Lambert2001). Among Perciformes, Paperna (Reference Paperna1973, Reference Paperna1979) noticed the presence of Q. tilapiae Paperna, Reference Paperna1973 on Tilapia esculenta (syn. Oreochromis esculenta) (Cichlidae); this could be the result of sample contamination, as this is the only report of a Quadriacanthus specimen on a cichlid host. The description of Q. euzeti n. sp. from P. afer: (1) broadens the host spectrum of Quadriacanthus to a new family (Notopteridae) and a new order (Osteoglossiformes); and (2) leads us to consider this parasitism as the result of a lateral transfer from Clariidae or Bagridae host species, since in Lake Ossa these fish live in sympatry with P. afer (Vivien, Reference Vivien1991; Roberts, Reference Roberts1992; Stiassny et al., Reference Stiassny, Teugels and Hopkins2007). This recent or ancient lateral transfer could have been promoted by ecological and ethological changes (Combes, Reference Combes1990; Bilong Bilong, Reference Bilong Bilong1995). For instance, in the same environment, a species of Scutogyrus Pariselle & Euzet, 1995, another genus of monogenean parasites usually recognized as specific to the mouthbreeder cichlid fish assigned to Oreochromis Günther, 1889 and Sarotherodon Rüppel, 1852, has recently and unexpectedly been described from Tilapia (Coptodon) mariae (Pariselle et al., Reference Pariselle, Bitja Nyom and Bilong Bilong2013). The second species of Notopteridae reported in Cameroon, X. nigri, is rare (Vivien, Reference Vivien1991) and was not captured during our research to reveal whether or not it hosts monogenean parasites.

Acknowledgements

This is publication ISE-M 2015-108 SUD.

Conflict of interest

None.

References

Bates, J.W. (1997) The slide-sealing compound ‘Glyceel’. Journal of Nematology 29, 565–566.Google ScholarPubMed
Bilong Bilong, C.F. (1995) Les Monogènes parasites de poissons d'eau douce du Cameroun : biodiversité et spécificité, biologie des populations inféodées à Hemichromis fasciatus . Thèse de Doctorat d'État, University of Yaoundé I, Yaoundé, Cameroon.Google Scholar
Birgi, E. (1987) Monogènes parasites des poissons d'eau douce au Tchad et au Sud-Cameroun. Taxonomie et essaie de biogéographie comparée. Thèse de Doctorat d'État, Université des Sciences et Techniques du Languedoc, Montpellier, France.Google Scholar
Birgi, E. (1988) Monogènes du genre Quadriacanthus Paperna, 1961, parasites branchiaux de deux Siluridae (Teleostei) Clarias pachynema, Boulenger, 1903, et Clarias jaensis Boulenger, 1909 au Sud-Cameroun (description de 4 espèces nouvelles). Annales de la Faculté des Sciences de l'Université de Yaoundé. Biologie, Biochimie III 5, 113–129.Google Scholar
Combes, C. (1990) Rencontre, identification, installation dans le cycle des métazoaires parasites. Bulletin de la Société Zoologique de France 115, 99–105.Google Scholar
Douëllou, L. & Chishawa, A.M. (1995) Monogeneans of three Siluriform fish species in Lake Kariba, Zimbabwe. Journal of African Zoology 109, 99–119.Google Scholar
El-Naggar, M.M. & Serag, H.M. (1986) Quadriacanthus aegypticus n. sp., a monogenean gill parasite from the Egyptian teleost Clarias lazera . Systematic Parasitology 8, 129–140.CrossRefGoogle Scholar
Gussev, A.V. (1962) Order Dactylogyridea. pp. 204–342 in Bychovskaya–Pavlovskaya, I.E., Gussev, A.V., Dubinina, M.N., Izymova, N.A., Smirnova, T.S., Sokolovskaya, I.L., Shtein, G.A., Shul'man, S.S. & Epsthein, V.M. (Eds) Key to the parasites of freshwater fish of the USSR. Jerusalem, Israel Program for Scientific Translations (Russian original: Opredelitel’ parazitov presnovohnyh ryb SSSR. Moscow–Leningrad, Izadtel'stovo Akademii Nauk SSSR).Google Scholar
Kossoni, A. (2003) Processus sédimentaires du Lac Ossa (Dizangué, Sud–ouest Cameroun) et évolution paléoclimatique holocène. Thèse de Doctorat, Université de Perpignan, Perpignan, France.Google Scholar
Kristky, D.C. & Kulo, S.D. (1988) The African species of the genus Quadriacanthus with proposal of Quadriacanthoides gen. n. (Monogenea: Dactylogyridae). Proceeding of the Helminthological Society of Washington 55, 175–187.Google Scholar
Lavoué, S. & Sullivan, J.P. (2004) Simultaneous analysis of five molecular markers provides a well-supported phylogenetic hypothesis for the living bony-tongue fishes (Osteoglossomorpha: Teleostei). Molecular Phylogenetics and Evolution 33, 171–185.CrossRefGoogle ScholarPubMed
Long, S. (1981) A new species of Quadriacanthus Paperna, 1961 a description of Byshowskyella Achmerov, 1952, and the esthablisment of Clarotrema, gen. nov. Acta Zootaxonomica Sinica 6, 347–354.Google Scholar
Malmberg, G. (1957) On the occurrence of Gyrodactylus on Swedish fishes. Skrifter utgivna av Södra Sveriges Fiskeriföreningen 1956, 19–76 (in Swedish with English abstract and species descriptions).Google Scholar
N'Douba, V. & Lambert, A. (2001) Deux monogènes nouveaux parasites branchiaux de Clarias ebriensis Pellegrin, 1920 (Siluriformes, Clariidae) en Côte d'Ivoire. Zoosystema 23, 411–416.Google Scholar
N'Douba, V., Lambert, A. & Euzet, L. (1999) Seven new species of Quadriacanthus Paperna, 1961 (Monogenea) from the gills of Heterobranchus longifilis and H. isopterus from the Ivory Coast, West Africa. Systematic Parasitology 44, 105–118.Google Scholar
Paperna, I. (1961) Studies of the monogenetic trematodes in Israel 3: Monogenetic trematodes of the Cyprinidae and Clariidae of the Lake of Galilée. Bamidgeh, Bulletin of Fish Culture in Israël 13, 14–29.Google Scholar
Paperna, I. (1973) New species of Monogenea (Vermes) from African freshwater fish. A preliminary report. Revue de Zoologie et de Botanique africaine 87, 505–518.Google Scholar
Paperna, I. (1979) Monogenea of the inland-water fish in Africa. Annales du Musée Royal de l'Afrique Centrale, série 8°, Sciences Zoologiques 226, 1–131.Google Scholar
Pariselle, A., Bitja Nyom, A.R. & Bilong Bilong, C.F. (2013) Check-list of the Ancyrocephalidae (Monogenea) parasitizing fish of the genus Tilapia Smith in Cameroon, with the description of four new species. Zootaxa 3599, 78–86.CrossRefGoogle Scholar
Paugy, D., Lévêque, C. & Teugels, G.G. (2003) Poissons d'eaux douces et saumâtres de l'Afrique de l'Ouest. Tome I. 457 pp. Paris, France, MRAC-MNHN-IRD.Google Scholar
Roberts, T.R. (1992) Systematic revision of the old world freshwater fish family Notopteridae. Ichthyological Exploration of Freshwaters 2, 361–383.Google Scholar
Shotter, R.A. (1980) Aspects of the parasitology of the catfish Clarias anguillaris (L.) from a river and lake at Zaria, Kaduna State, Nigeria. Bulletin de l'Institut Fondamental d'Afrique Noire 42, 836–859.Google Scholar
Stiassny, M.L.J., Teugels, G.G. & Hopkins, C.D. (2007) Poissons d'eaux douces et saumâtres de basse Guinée, ouest de l'Afrique Centrale. Vol. 1. 789 pp. Paris, France, MNHN-MRAC-IRD.Google Scholar
Vivien, J. (1991) Faune du Cameroun. Guide des Mammifères et Poissons. 271 pp. Yaoundé, Cameroun, Ed GICAM; and Paris, France, Ministère de la Coopération et du Développement.Google Scholar
Wirrmann, D. (1992) Le Lac Ossa: une monographie préliminaire. Revue Géographique du Cameroun, XI 1, 27–38.Google Scholar
Wirrmann, D., Bertaux, J. & Kossoni, A. (2001) Late Holocene paleoclimatic changes in western Central Africa inferred from mineral abundance in dated sediments from Lake Ossa (southwest Cameroon). Quaternary Research 56, 275–287.Google Scholar
Figure 0

Fig. 1Map to show the geographical location and hydrography of Lake Ossa.

Figure 1

Fig. 2Morphometrics of Quadriacanthus spp. used in this study are based on Gussev (1962) and modified by N'Douba et al. (1999). (An) Anchor: a, length; ba, base width; e, point length; (Cc) copulatory complex: Ap, accessory piece length; Ci, cirrus length; (Cn) cuneus: i, width; j, length; (Db) dorsal bar: Ct, centre length; h, median process length; w, width; x, length; (H) hooklet length; (Vb) ventral bar: w, width; x, length; (Vg) vagina: l, length; d, diameter.

Figure 2

Fig. 3Sclerotized parts of Quadriacanthus euzeti n. sp. Nack, Pariselle & Bilong Bilong: Cc, copulatory complex; Da, dorsal anchor; Db, dorsal bar; Dc, dorsal cuneus; I–VII, hooklets; Va, ventral anchor; Vb, ventral bar; Vc, ventral cuneus; Vg, vagina. Scale bar = 20 μm.

Figure 3

Fig. 4Photomicrographs of hard parts of Quadriacanthus euzeti n. sp. (a) Haptor: Da, dorsal anchor; Db, dorsal bar; Va, ventral anchor; Vb, ventral bar; (b) copulatory complex: Ap, accessory piece; Ci, cirrus.