Skip to main content
Saudi Journal of Biological Sciences logoLink to Saudi Journal of Biological Sciences
. 2014 Jan 28;21(6):520–523. doi: 10.1016/j.sjbs.2014.01.002

First records of Ambiphrya and Vorticella spp. (Protozoa, Ciliophora) in cultured Nile tilapia (Oreochromis niloticus) in the central region of Saudi Arabia

Abdel-Azeem S Abdel-Baki a,b,, Mohamed M Gewik a, Saleh Al-Quraishy a
PMCID: PMC4250488  PMID: 25473359

Abstract

The present study was carried out as part of an ongoing general survey seeking to uncover protozoan parasites infecting cultured tilapia in the central region of Saudi Arabia. In the sample of 400 specimens of tilapia (Oreochromis niloticus) 30 were infested with Ambiphrya ameiuri simultaneously with Vorticella sp. Morphometric criteria were used to describe and identify these species and this study presents the first records of these species among cultured fish in Saudi Arabia.

Keywords: Ciliate, Cultured fish, Ambiphrya, Vorticella, Saudi Arabia, Tilapia

1. Introduction

Aquaculture is now the fastest growing food-producing sector worldwide but suffers significant economic losses due to the effects of parasitic infections of fish (Munoz et al., 2000). Saudi Arabian aquaculture has intensified on tilapia development, and the fish has been enthusiastically acknowledged by Saudis and expatriates living in the nation (FAO, 2012). Protozoan parasites undoubtedly comprise one of the most important groups of pathogens negatively influencing the wellbeing of both cultured and feral fish. They have not received much attention, because of the technical difficulties inherent in their study in comparison to the much larger helminthic parasites (Lom and Dykova, 1992). Enhanced knowledge of protozoans that parasitise fish would, therefore, fill a long neglected gap in scholarship whilst also being a prerequisite for the rapid and correct diagnosis of the infection agency of epizootics. Parasitic ciliates are among the most pathogenic protozoa that infect fishes (Van As and Basson, 1988). Whilst usually not considered to be a problem in the wild, many species cause extensive losses under conditions of intensive aquaculture (Dickerson and Clark, 1996). Infections by sessile peritrichs such as Ambiphrya and Vorticella are common in many cultured fishes (Basson and Van As, 2006) but, thus far, have not been reported from cultured tilapia in Saudi Arabia. The aim of this study, therefore, was to survey the presence of Ambiphrya and Vorticella in cultured tilapia in the central region of Saudi Arabia.

2. Materials and methods

Specimens of the Nile tilapia (Oreochromis niloticus) were collected randomly from a number of different farms in Riyadh, Saudi Arabia (24° 38′ 26″ N/46° 46′ 22″ E). The fish were transported immediately, alive, to our laboratory in the Zoology Department, College of Science, King Saud University, where they were maintained alive in well aerated glass aquaria.

Wet smears were taken from the skin, fins and gills and carefully examined for any ciliated ectoparasitic protozoan. Positive smears were air dried, fixed in methanol for 10 min, and then stained with 5% Giemsa’s solution in phosphate buffer (pH 7.3) for 30 min. Smears were then examined, measured and photographed using an Olympus microscope fitted with an oil immersion lens. All measurements are in micrometres (μm) and data is expressed as mean (range).

3. Results

Of the 400 examined fish, only 30 (7.5%) were discovered infested with Ambiphrya simultaneously with Vorticella. The noted parasites are identified as follows:

3.1. Ambiphrya ameiuri Thompson, Kirkegaard and Jahn, 1974

Solitary sessilian peritrichs with a barrel-shaped body are shown in Figs. 1 and 2. The body measurements were 68 (60–80) μm in length and 43 (40–48) μm in width. The body was divided into oral and basal regions by an equatorial ciliary girdle (Fig. 2), with the oral region measuring 40 (35–45) μm and the basal region measuring 24 (20–32) μm. The peristomial disc was mostly convex and was surrounded by a conspicuous peristomial lip (Figs. 1 and 2). Infundibulum was conspicuous, slightly oblique and never exceeded the equatorial girdle (Figs. 1 and 2). The macronucleus measured approximately 40 μm and was typically ribbon-shaped, folding back on itself throughout the body cell and extended beyond the equatorial girdle (Figs. 1 and 2). A large number of different sized food vacuoles as well as one contractile vacuole were observed in the oral region (Fig. 1). The scopula, whilst it never exceeded the overall breadth of the body (Figs. 1 and 2), was in the form of a very wide (about 37–42 μm) undulated disc located at the base, with adhesive fibres for attachment.

Figure 1.

Figure 1

Photomicrographs of Giemsa stained Ambiphrya ameiuri showing: (CV) Contractile vacuole; (FV) Food vacuole; (In) Infundibulum; (Ma) Macronucleus; (PD) Peristomial disc; (PL) Peristomial lip; (SC) Scapula. Scale-bar = 50 μm.

Figure 2.

Figure 2

Photomicrographs of Giemsa stained Ambiphrya ameiuri showing: (EG) Equatorial ciliary girdle; (In) Infundibulum; (Ma) Macronucleus; (PD) Peristomial disc; (PL) Peristomial lip; (SC) Scapula. Scale-bar = 50 μm.

3.2. Vorticella sp.

This sessile peritrich was characterised by its inverted bell-shaped body which was composed of two parts; zooid and scopula (Figs. 3 and 4). The zooid was a spherical shape, about 55 (50–65) μm in diameter and occurred solitarily on a retractile stalk (Figs. 3 and 4). The peristomial disc was flat convex with a circular ring of feeding cilia on the upper margin (Fig. 4). The peristomial disc and feeding cilia were surrounded by the peristomial lip (Fig. 4). The macronucleus was ribbon-shaped and extended throughout the zooid (Fig. 3). A large number of different sized food vacuoles were observed in the central part of the zooid (Fig. 3). The scopula, meanwhile, secreted a contractile stalk with an inner element, called the spasmoneme, which can contract very rapidly (Figs. 3 and 4). The stalk measured 65 μm in length and 4 μm in width.

Figure 3.

Figure 3

Photomicrographs of Giemsa stained Vorticella sp. showing: (Ma) Macronucleus; (SC) Scapula; (St) Stalk; (Zo) Zooid. Scale-bar = 50 μm.

Figure 4.

Figure 4

Photomicrographs of Giemsa stained Vorticella sp. showing: (FV) Food vacuole; (PD) Peristomial disc; (PL) Peristomial lip; (C) Cilia; (SC) Scapula; (St) Stalk; (Zo) Zooid. Scale-bar = 50 μm.

4. Discussion

Parasitic ciliates are the most common parasites encountered in fish in both aquaria and ponds but have not thus far been investigated in cultured tilapia in Saudi Arabia. Since it is impossible to control parasitic infections effectively unless their cause is correctly identified (Tonguthai, 1997), there is a clear need for intensive research in the presence of parasitic ciliates in fish stocks of all kinds in Saudi Arabia. The present study confirmed the presence of Ambiphrya and Vorticella among cultured tilapia in a number of farms in Riyadh. Members of the genus Ambiphrya were characterised by the macronucleus, which is in the form of a long winding ribbon in this species and, furthermore, by the presence of a wide scopula with an equatorial ciliary girdle (Lom and Dykova, 1992). Based on these morphometric characteristics, the recorded species could be identified as Ambiphrya ameiuri, described by Thompson et al. (1947) and which is also similar to those reported by Basson and Van As, 2006; Romero and Tanzola, 2009; Reda, 2011. Ambiphrya ameiuri is here reported for the first time in Saudi Arabia. Members of the genus Vorticella are characterised by having a single zooid with a retractile stalk and ribbon-shaped macronucleus (Viljoeni and Van As, 1987). The present reported species conforms well to the genus characters. Vorticella, however, is a mostly free-living ciliophoran but, when fish are stressed by adverse environmental conditions, this free-living ciliophoran becomes a facultative ectoparasite (Basson and Van As, 2006; El-Tantawy and El-Sherbiny, 2010). This presents considerable difficulties in species identification within this genus (Reda, 2011). Therefore, the present parasite is tentatively identified as Vorticella sp., which is the first such record in cultured tilapia in Saudi Arabia.

In conclusion, according to Klinger and Floyd (2009), most fish health problems occur due to environmental problems such as poor water quality, crowding and dietary deficiencies, as well as stress. The best way to avoid any fish health problem is prevention. This means that good water quality management and proper fish husbandry techniques will eliminate the parasites described in this study.

Acknowledgement

The authors extend their appreciation to the Deanship of Scientific Research at King Saud University for funding the work through the research group project number RGP-VPP-004.

Footnotes

Peer review under responsibility of King Saud University.

References

  1. Romero A.M., Tanzola R.D. Ambiphrya ameiuri (Ciliophora, Peritrichia) from the gills of Jenynsia multidentata (Pisces) in the southwest of Buenos Aires province (Argentina). A nearctic invader in our ponds. BioScriba. 2009;2:101–105. [Google Scholar]
  2. Basson L., Van As J. Trichodinidae and other ciliophorans (phylum Ciliophora) In: Woo P.T.K., editor. vol. 1. 2006. pp. 154–182. (Fish diseases and disorders. Protozoan and Metazoan infections. CABI). [Google Scholar]
  3. Dickerson H.W., Clark T.G. Immune response of fishes to ciliates. Ann. Rev. Fish Dis. 1996;6:107–120. [Google Scholar]
  4. El-Tantawy S.A.M., El-Sherbiny H.A.E. Protozoan parasites infecting catfish Clarias gariepinus inhabiting Nile Delta water of the River Nile, Dakahlia province, Egypt. J. Am. Sci. 2010;6:676–696. [Google Scholar]
  5. FAO, 2012. The state of world fisheries and aquaculture. Viale delle Terme di Caracalla, Rome, p. 230.
  6. Klinger R.E., Floyd R.F. Introduction to freshwater fish parasites. Institute of Food and Agricultural Sciences (IFAS) University of Florida, Florida, Fla, USA. CIR. 2009;716:1–13. [Google Scholar]
  7. Lom J., Dykova I. Elsevier Science Publishers; Amsterdam: 1992. Protozoan Parasites of Fishes. [Google Scholar]
  8. Munoz P., Sitja-Bobadilla A., Alvarez-Pellitero P. Ultrastructure localization of carbohydrates in four myxosporean parasites. Parasite. 2000;7:185–191. doi: 10.1051/parasite/2000073185. [DOI] [PubMed] [Google Scholar]
  9. Reda E.S.A. A review of some ecto and endo protozoan parasites Infecting Sarotherodon Galilaeus and Tilapia Zillii from Damietta branch of River Nile, Egypt. J. Am. Sci. 2011;7:362–373. [Google Scholar]
  10. Thompson S., Kirkegaard D., Jahn T.L. Scyphidia ameiuri n. sp., a peritrichous ciliate from the gills of the bullhead, Ameiurus melas melas. Trans. Amer. Microsc. Soc. 1947;66:315–317. [Google Scholar]
  11. Tonguthai K. Control of freshwater fish parasites: a Southeast Asian perspective. Int. J. Parasitol. 1997;27:1185–1191. doi: 10.1016/s0020-7519(97)00116-1. [DOI] [PubMed] [Google Scholar]
  12. Van As, J.G., Basson, L., 1988. The incidence and control of fish ectoparasitic protozoa in South Africa. Technical communication no. 211. Republic of South Africa.
  13. Viljoeni S., Van As J.G. Notes on the morphology and asexual reproductive processes of sessile Peritrichs. Hydrobiologia. 1987;154:75–86. [Google Scholar]

Articles from Saudi Journal of Biological Sciences are provided here courtesy of Elsevier

RESOURCES