Journal of Veterinary Medicine
Volume 2014 (2014), Article ID 245878, 4 pages
http://dx.doi.org/10.1155/2014/245878

Research Article

High Infestation by Dawestrema cycloancistrioides in Arapaima gigas Cultured in the Amazon Region, Peru

Patrick D. Mathews,¹ Antonio F. Malheiros,² Narda D. Vasquez,³ and Milton D. Chavez⁴

¹Department of Parasitology, Institute of Animal Biology, University of Campinas, 13083-862 Campinas, Brazil
²Department of Biological Science, University of State of Mato Grosso, 78200-000 Cáceres, Brazil
³Department of Tropical Aquaculture, Institute of Biology, National University of the Peruvian Amazon, 765 Iquitos, Peru
⁴Department of Health, Safety and Environment, Enersul Limited Partnership, Calgary, Canada T2H 1M5

Received 12 June 2014; Accepted 28 July 2014; Published 30 November 2014

Academic Editor: Antonio Ortega-Pacheco

Copyright © 2014 Patrick D. Mathews et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The aim of this study was to evaluate the presence of Dawestrema cycloancistrioides in semi-intensive fish farming of fingerlings of Arapaima gigas. Between September and November 2013, 60 individuals of A. gigas born in captivity, were collected in three concrete ponds, from a semi-intensive fish farm in the Peruvian Amazon. For the study of sclerotized structures, parasites were fixed in a solution of ammonium picrate glycerine and mounted in Canada balsam. To visualize internal structures, parasites were fixed in hot formaldehyde solution (4%) for staining with Gomori’s trichrome. The parasitic indexes calculated were prevalence, mean intensity, and mean abundance. This study identified a high infestation of a monogenean D. cycloancistrioides in gills of A. gigas. The prevalence was 100%. The mean intensity and mean abundance of the parasite were 144.9 of parasites per individual. This study confirms the necessity of constant monitoring of fish in order to reduce fish mortality.

1. Introduction

The Arapaima gigas is an endemic species of the Basin Amazon and is considered one of the largest freshwater fish in the world. The A. gigas can reach up to three meters in length and 200 kg of total weight [1] and is a much appreciated species with great acceptance in the Amazonian market being regarded as a protein source of the highest quality. However, due to its high nutritional demand for the population of the Amazon region, in recent years the natural stocks of this fish have suffered drastic reduction [2]. Farming paiche is thus a possible solution to the overexploitation of this species in many rivers of the Amazon. However, to allow the breeding, it turns out that the necessity to solve the problems regarding diseases and parasites upsurge, which are affecting this species in controlled environments as a consequence of intensive farming under inadequate management.

The dactylogyrid monogeneans are ectoparasites usually attached to the gills of fish. Like other monogeneans, dactylogyrids have a direct life cycle and can easily multiply and disperse under fish culture conditions, reaching very high intensities. These monogeneans have been linked to major losses in fish culture [3, 4]. Recently, studies in several species of farmed fishes in the Amazon region of Peru showed a high infestation by monogeneans species, indicated as the probable cause of high mortality [5–8].

Therefore, with the gradual increase of intensive and semi-intensive fish farming in the Peruvian Amazon, there is a need for constant monitoring of the fish for the diagnosis and timely control of infestations by monogeneans. In this sense, the present study aims to evaluate the monogenean infestation in A. gigas bred in a fish farm in the Peruvian Amazon.

2. Materials and Methods

2.1. Study Site and Animals

Between September and November 2013, the period which corresponds to the relative dry season, 60 individuals of the species A. gigas ( cm of length and weight of  g), born in captivity (Figure 1), were collected in three concrete ponds, from a semi-intensive fish farm, belonging to the fish culture station Quistococha Research Center, located between the cities Iquitos and Nauta, northeast of Department of Loreto, Peru (3°48′48.9′′ N and 073°19′18.2′′ W). The relative humidity in this region varies between 80% and 100%. Annual rainfall ranged between 1500 and 3000 mm at 328 mean sea level.

Figure 1: Specimen of Arapaima gigas collected from cultured ponds.

2.2. Physicochemical Parameters of the Water

The parameters were measured three times daily (at 7 AM and noon and at 5 PM) with daily checks of dissolved oxygen, pH, temperature, and conductivity by means of an YSI multiparameter meter (Model MPS 556). Ammonium values, hardness, carbon dioxide, and total alkalinity were monitored weekly in the morning at 8 AM, using a complete package for analysis of freshwater (LaMotte AQ-2).

2.3. Parasitological Analysis

Following that, the fish were sacrificed by cerebral puncture and placed in individual containers. For examination of the gills, the samples were separated and placed in glass containers with a 1 : 4.000 formalin solution. After one hour, the gills were stirred in the same solution and then removed from the containers. Helminthes were allowed to settle on the bottom of the glass containers in the remaining formalin solution and subsequently collected with the aid of a small probe and a dissecting microscope (Nikon SM-30). For the study of sclerotized structures, parasites were fixed in a solution of ammonium picrate glycerine (GAP) and mounted in Canada balsam according to Thatcher [9]. Some specimens were mounted unstained in Gray and Wess’ medium. To visualize internal structures, parasites were fixed in hot formaldehyde solution (4%) for staining with Gomori’s trichrome. The identification of the parasites was based on the methodology of Thatcher [9] and Kritsky et al. [10].

The parasitic indexes calculated for assessing the level of infestation of parasites in the fish, prevalence (number of hosts infected divided by the total number of hosts in a sample), mean intensity (total number of parasites divided by number of hosts infected), and mean abundance (number of parasites divided by the total number of hosts in a sample) are the same as those described in Bush et al. [11]. The research was authorized by the Research Institute of the Peruvian Amazon.

3. Results

The moribund fishes collected for analysis were in emaciated condition. Due to the accumulation of mucus, the gills were pale and viscous. The necropsy of fingerlings from A. gigas evidenced the infestation by Dawestrema cycloancistrioides in the gill filaments of the fish (Figure 2). Indeed, the totality of the examined fish (60) showed a high parasitic infestation (Table 1).

Table 1: Parasitic indexes of Dawestrema cycloancistrioides in juveniles of paiche (Arapaima gigas) cultured in the Peruvian Amazon.

Parasitic indexes
Dawestrema cycloancistrioides

Prevalence (%)
100

Abundance
8695

Mean abundance
144.9

Mean intensity
144.9

(a)

(b)

Figure 2: Dawestrema cycloancistrioides (a) total. (b) Posterior region, 1—ventral bar, 2—ventral anchor, 3—dorsal anchor. Scale bars = 10 μm.

In the present study, the values of the physicochemical parameters of the water from the culture ponds were dissolved oxygen ( mg L⁻¹), pH (), temperature (24 to 30°C) and conductivity ( μs cm⁻¹), ammonium values ( mg L⁻¹), hardness ( mg L⁻¹), carbon dioxide ( mg L⁻¹), and total alkalinity ( mg L⁻¹).

4. Discussion

In intensive fish farming, diseases outbreaks are a major concern to the farmers because in such systems fish are exposed to a high number of stressors (poor water quality, crowding, manipulation, breeding, and transport) which may negatively affect their immune system and disease resistance [12, 13]. Water temperature of the fish ponds presented a strong variation during the present study, reaching its lowest values (24°C) during the first hours of the day and the highest values (30°C) between noon and three hours later. In the same sense, in our study the concentration of ammonia, found in the ponds of cultivated A. gigas, was not within the expected range of values for tropical species. In this context, the fish are subjected to stress thus becoming more susceptible to infestation by parasites and reduced disease resistance [14, 15]. We suspect that the high parasitism by monogeneans was due to the imbalance in the homeostasis of fish.

Parasites that have a direct life cycle, such as monogeneans, are more frequently found in lentic environments and this type of environment favors the transmission of these parasites [3]. In regions with tropical and semitropical climates, the life cycle of monogenean can be completed in less than one day and the monogeneans proliferate rapidly [3, 9]. The climate in the region of this study is tropical humid with annual average temperature of 28.3°C and relative humidity of 85%, favoring the speed of life cycle. In the earthen ponds where fish were collected, the water circulation is almost negligible or nonexistent and the same have a high density of fish population. These drawbacks favor the contact with the monogeneans [3] and may justify the fact that the fishes have shown elevated prevalence of monogenean.

In A. gigas three species of monogeneans assigned to Dawestrema genus (D. cycloancistrium, D. cycloancistrioides, and D. punctatum) have been reported from natural environments and two in specimens from fish farming (D. cycloancistrium and D. cycloancistrioides) [9, 10, 16, 17], evidencing a high specificity of Dawestrema species parasitizing A. gigas. However, this specificity may be related to the fact that many of monogeneans which parasitize fish are host-specific, because they have co-evolved with their hosts [18].

In the present study, D. cycloancistrioides showed high parasitism along with prevalence rates of 100%. Our results agree with Hargreaves and Tucker [15], who reported similar prevalence, with mean intensity and mean abundance of 280 for specimens of A. gigas collected from fish farming in Brazil. In addition, Gross et al. [14] reported a prevalence of 100% from an aquarium in the United States, confirming the occurrence of this parasite in cultivated A. gigas.

5. Conclusion

The results of this study and studies addressing various aspects of parasites in other cultivated species confirm the necessity of constant monitoring of fish, seeking the diagnosis and timely control of infestations by monogeneans, in order to reduce fish mortality.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors thank Conselho Nacional de Desenvolvimento Cientifico e Tecnológico (CNPq) for a postdoctoral fellowship to Antonio F. Malheiros and Narda D. Vasquez is in receipt of a fellowship from CONCYTEC.

References

E. A. Ono, R. Roubach, and M. F. Pereira, “Pirarucu production-advances in central Amazon, Brazil,” Global Aquaculture Advocate, vol. 6, pp. 44–46, 2003.

M. Casares, M. A. Arevalo, and E. Fernandez, “Notes on the husbandry of the arapaima Arapaima gigas, at ‘Faunia’, Madrid,” Zoologische Garten, vol. 72, no. 4, pp. 238–244, 2002.

J. Flores-Crespo and C. F. Flores, “Monogenean, parasites in Mexican fish: a recapitulation,” Técnica Pecuaria México, vol. 41, no. 2, pp. 175–192, 2003.

D. C. Kritsky and F. Stephens, “Haliotrema abaddon n. sp. (Monogenoidea: Dactylogyridae) from the gills of wild and maricultured West Australian dhufish Glaucosoma hebraicum (Teleostei: Glaucosomatidae), in Australia,” Journal of Parasitology, vol. 87, no. 4, pp. 749–754, 2001.

D. P. Mathews, J. P. D. Mathews, and O. R. Ismiño, “Massive infestation by Gussevia undulata (Platyhelminthes: Monogenea: Dactylogyridae) in fingerlings of Cichla monoculus cultured in the Peruvian Amazon,” Neotropical Helminthology, vol. 6, no. 2, pp. 231–237, 2012.

D. P. Mathews, J. P. D. Mathews, and O. R. Ismiño, “Parasitic infections in juveniles of Prochilodus nigricans kept in a semi-intensive fish farm in the Peruvian Amazon,” Bulletin of the European Association of Fish Pathologists, vol. 33, no. 1, pp. 28–32, 2013.

P. D. Mathews, O. Mertins, J. P. D. Mathews, and R. I. Orbe, “Massive parasitism by Gussevia tucunarense (Platyhelminthes: Monogenea: Dactylogyridae) in fingerlings of bujurqui-tucunare cultured in the Peruvian Amazon,” Acta Parasitologica, vol. 58, no. 2, pp. 223–225, 2013.

D. P. Mathews, A. F. Malheiros, O. R. Ismiño, and N. D. Vasquez, “Jainus amazonensis (Monogenea : Dactylogyridae) parasites of Brycon cephalus (Günther, 1869) cultured in the lowland of the Peruvian Amazon,” Croatian Journal of Fisheries, vol. 72, no. 2, pp. 83–86, 2014.

V. E. Thatcher, Amazon Fish Parasites, Pensoft Publishers, Moscow, Russia, 2nd edition, 2006.

D. C. Kritsky, A. Boeger, and V. E. Thatcher, “Neotropical monogenea. 7. Parasites of the pirarucu, Arapaima gigas (Cuvier), with descriptions of two new species and redescription of Dawestrema cycloancistrium Price and Nowlin, 1967 (Dactylogyridae: Ancyrocephalinae),” Proceedings of the Biological Society of Washington, vol. 98, no. 2, pp. 321–331, 1985.

A. O. Bush, K. D. Lafferty, J. M. Lotz, and A. W. Shostak, “Parasitology meets ecology on its own terms: margolis et al. revisited,” Journal of Parasitology, vol. 83, no. 4, pp. 575–583, 1997.

R. Y. Sado, Á. J. A. Bicudo, and J. E. P. Cyrino, “Dietary levamisole influenced hematological parameters of juvenile pacu, Piaractus mesopotamicus (Holmberg 1887),” Journal of the World Aquaculture Society, vol. 41, supplement 1, pp. 66–75, 2010.

A. K. Jha, A. K. Pal, N. P. Sahu, S. Kumar, and S. C. Mukherjee, “Haemato-immunological responses to dietary yeast RNA, ω-3 fatty acid and β-carotene in Catla catla juveniles,” Fish and Shellfish Immunology, vol. 23, no. 5, pp. 917–927, 2007.

A. Gross, C. E. Boyd, and C. W. Wood, “Nitrogen transformations and balance in channel catfish ponds,” Aquacultural Engineering, vol. 24, no. 1, pp. 1–14, 2000.

J. A. Hargreaves and C. A. Tucker, Managing Ammonia in Fish Ponds, vol. 4603, Southern Regional Aquaculture Center, 2004.

C. J. Bonar, S. L. Poynton, Y. F. Schulman, R. L. Rietcheck, and M. M. Garner, “Hepatic Calyptospora sp. (Apicomplexa) infection in a wild-born, aquarium-held clutch of juvenile arapaima Arapaima gigas (Osteoglossidae),” Diseases of Aquatic Organisms, vol. 70, no. 1-2, pp. 81–92, 2006.

C. S. O. Araújo, S. M. Andrade, M. Tavares-Dias et al., “Parasitic infections in pirarucu fry, Arapaima gigas Schinz, 1822 (Arapaimidae) ket in a semi-intensive fish farm in Central Amazon, Brazil,” Veterinarski Arhiv, vol. 79, no. 5, pp. 499–507, 2009.

A. Šimková, O. Verneau, M. Gelnar, and S. Morand, “Specificity and specialization of congeneric monogeneans parasitizing cyprinid fish,” Evolution, vol. 60, no. 5, pp. 1023–1037, 2006.