HOME JOURNALS CONTACT

Research Journal of Parasitology

Year: 2007 | Volume: 2 | Issue: 1 | Page No.: 45-50
DOI: 10.17311/jp.2007.45.50
Incidence of Parasitic Isopods on the Fish Sphyraena obtusata
S. Ravichandran, T. Balasubramanin and T. Kannupandi

Abstract: The incidence of parasitic isopods in the fish Sphyraena obtusata was studied. The reduction in gill raker count and gill surface area was observed as a function of infestation was found to be statistically significant. Maximum reduction in respiratory surface area was observed in Ist gill arch (10.7%) and minimum (9.2%) in the IIIrd gill arch. The percentage reduction of surface area in the IInd and IVth gill arches was 10.2 and 9.7, respectively. The infestations such as, hemorrhagic lesions, anemia; encapsulation; inflammation and penetration of dactylus usually pressure atrophy often accompanied by the presence of larger parasites. This may lead to huge economic losses in commercial species of fish.

Fulltext PDF Fulltext HTML

How to cite this article
S. Ravichandran, T. Balasubramanin and T. Kannupandi, 2007. Incidence of Parasitic Isopods on the Fish Sphyraena obtusata. Research Journal of Parasitology, 2: 45-50.

Keywords: Infestation, isopod parasites, gill arch, anemia, lesions and inflammation

INTRODUCTION

Fish parasites and diseases constitute one of the most important problems confronting the fishery biologist today. Cymothoids are all obligatory parasites, infesting mostly commercially important fishes. They are protandric hermaphrodites and are blood suckers, living on the skin, in the gill chambers, or in the mouth of the fishes. The parasitic effects include growth retardation, emaciation and frequently death of those fish affected. Mortality losses are increased by weight losses resulting from the lowered conditions of the parasitised fish. Pathological conditions resulting from parasites and diseases assume high magnitude of epidemics under crowded and other unnatural conditions.

The incidence and intensity of isopod parasite exhibited considerable variation (Ravichandran et al., 1999; Ravichandran et al., 2001; Grutter, 2003; Cuyas et al., 2004). The incidence of infection of Lironecea puhi on Hawaian Moray eel Gymnothorax eurostus ranged from 15 to 70% (Bowman, 1960). Histological changes in Mugil cephalus caused by Stellantchasmus falcatus were reported by Lee and Cheng (1979). Kabata (1985) and Ravichandran et al. (2000) described the pathogenecity of isopods and stated that the effect of the destruction of host tissue was mainly due to the pressure exerted by the Parasite’s body.

Although considerable information is available on the pathological effects of different groups of parasites, no serious attempt has so far been made to study on the same due to isopod parasites. Hence the present attempt was made to study the infestation of isopod parasite Cymothoa indica in the fish Sphyraena obtusata.

MATERIALS AND METHODS

In the routine observation of S. obtusata fishery in Parangipettai (Southeast coast of India), an interesting incidence of isopod parasitization was observed in several fishes. Fishes were collected from three major landing centers viz (Fig. 1) Mudasalodai, Annankovil and Pudupettai.

Fig. 1: The study area

Respiratory Surface Area
To find out the influence of infestation over the respiratory surface area, the changes in the gill arch was studied. The gill arches of infested and uninfested fishes were carefully dissected out and blotted to remove the moisture. The surface area of gill arch was calculated by the imprint drawings of each gill arch on a millimeter graph paper. Surface area of each tracing was determined by counting the number of small squares and the total area was obtained by addition. The value was than doubled to consider the total functioning of the gill arch. The total (functional) surface area of gill arch of both infested and uninfested fish was compared and the difference in area was considered as the reduction of respiratory area due to infestation. Students t-test was employed to signify the influence of infestation.

Gill Raker Count
The average gill raker count of first, second, third and fourth gill arches of infested and uninfested S. obtusata were made. The data collected were tabulated and variation in the gill raker count as a function of infestation was recorded. They were then analyzed statistically using students t-test.

RESULTS

Infested fishes, gill rakers were seriously lost, apical edges damaged and gill lamellae heavily destroyed. Gill lamellae of the first and second gill arches were eroded due to Cymothoa indica. A wide depression was found due to the lodging of parasites at the gill debts and the gill arches showed torsion.

Nature of damage, observed in the gill remained the same, but the degree of damage varies, as the closely opposed gill arch observed a higher damage. Terminal and middle regions of the gill lamellae bulged and the growth was stunted. Secondary gill lamellae uneven clubbed and showed fusion. Middle portion of some of the gill lamellae expanded to have some space or gap. Bifurcation was noticed at the tip of lamellae and the cartilaginous support of the gill arch was twisted (Fig. 2).

Changes in Respiratory Surface Area
Changes in the respiratory surface area of S. obtusata owing to the infestation of C. indica are presented in Table 1. Maximum reduction in respiratory surface area was observed in the I gill arch (10.7%) and minimum (9.2%) in the III gill arch.

Table 1: Infestation of gill surface area of Sphyraena obtusata due to Cymothoa indica

Table 1: Continued
*Significant (p>0.01)

Table 2: Infestation of Cymothoa indica in gill raker count of Sphyraena obtusata
*Significant (p>0.01)

Fig. 2: Cymothoa indica attach to the branchial and buccal region of Sphyraena obtusata.

The percentage reduction of surface area in the II and IV gill arches was 10.2 and 9.7, respectively. A significant (p<0.01) reduction in the gill surface area was observed due to infestation.

Changes in Gill Raker Count
Variation in the gill raker count of S. obtusata due to infestation is presented in Table 2. Reduction in the number of gill rakers was noticed due to the attachment of C. indica in the branchial chamber. The percentage gill raker count in the infested male fish was 47.3 and in uninfested it was 50.4. In the infested female fish, it was 47.0 and in uninfested it was 50.8. The reduction of gill raker count was pronounced (4.2%) in female fish compared to that of the male fish (2.07%). The reduction in gill raker count observed as a function of infestation was found to be statistically significant (p<0.01) (Table 2).

DISCUSSION

Isopods inhabiting the buccal cavity and branchial chamber inflict damage to gills through attachment and feeding and that the extent of damage is directly proportional to the size of the parasite and duration of settlement. Erosion of gill lamellae, damage of gill rakers and pale gills were the severe gross lesions observed as a consequence of isopod infestation. Pale gills of infested fishes indicated anemia, which may be due to loss of blood the obstruction of branchial circulation by the attachment of parasite and of the homophagous nature of the branchial cymothoids (Romestand et al., 1977; Ramestand, 1979). The calus like thickening observed on the gill arch and gill filaments may be due to the constant irritation caused by the body and appendages of the parasite. Stephenson (1976) reported calus-like thickening only between the gill rakers, but in the present study, its occurrence was noticed not only at the gill arches but also at the base of the gill filaments. This extra thickening on the gill arches could be related to constant irritation caused by the body of the parasite.

Thickening and erosion are the two unique morphological changes noticed owing to the infestation. These changes were mainly due to the heavy pressure exerted by the parasite and also by their feeding nature. Kabata (1985) observed destruction of host tissues as a result of the pressure exerted by the parasite’s body. Longer stay of parasite within the gill chamber may also prevail and obstruct the normal growth of the gill arches. This may be the reason for the torsion of gill arch and fusion of gill lamellae.

Kabata (1985) stated that no serious attempt has so far been made to estimate quantitatively the variation of the respiratory surface area in infected fishes. The present study undertaken in this direction, showed significant reduction of respiratory surface area due to infestation of cymothoids in the branchial chamber. The percentage reduction of surface area varied depending up on the nature of attachment of the parasites. The maximum reduction observed in the Ist gill arch was mainly due to the heavy pressure exerted by C.indica. The dorsal surface of the parasite was always in close contact with the Ist gill arch, causing more atrophy of gill filaments. Williams and Williams (1985) reported serious erosion of gill filaments in the IIIrd and IVth gill arches of Abudefeeef sexatilis due to the adult female isopod Kuna insularis. Significant reduction of respiratory surface area to a larger extent may depend on the longevity of infestation. Stephenson (1976) also discussed that the extent of gill damage may reflect the duration of infection, since eroded gill lamellae were noticed more frequently in very young fishes. It was also a fact that, the extent of erosion of gill lamellae was always more towards the posterior half of the gill arch.

Overstreet (1978) reported that the smaller males and juveniles of isopod Olencira praegustator parasitic on Gulf Menhaden caused damage on the gill filaments through feeding. But in case of C. indica a situation reverse to the above was noticed that the dorsal surface of the parasite was facing the first gill arch. The damage of gill filaments thus was not only due to the feeding but also by the pressure exerted by the dorsal side of the parasite. The gross size and shape of parasites can act as physical irritants, which may be responsible for the observed damages of the branchial tissues. The reduction in the surface area was thus due to several factors such as the mode of attachment, movement, size and duration of stay of the parasites.

Stephenson (1976) reported that the gill rakers are often widely spaced in parasitized individuals of Trichiurus spp. and Hyporhamphus ihi and that the gill raker counts were not significantly different from that of the gill raker counts of the uninfested fish. In the present study more similar effects were noticed in parasitized individuals of S. obtusata. However, contrary to the observation of Stephenson (1976), a significant reduction of gill raker count was observed in the present study. The reason for the significant reduction in gill raker count could be related to the direct impact of the branchial parasites on the respective gill arches. The present study also reported different types of effects and this could be attributed to the nature and position of attachment of isopods. In the case of S. obtusata the gill raker count was less in the posterior half of first and second gill arches. This is owing to the fact that the isopod parasite C. indica was oriented towards the posterior end and that its ventral side was facing the opercular covering. The antero-lateral margins of the parasite lied over the gill rakers thereby preventing its growth. Further more due to the pressure exerted, the gill rakers become damaged showing more space in between. In the case of C. indica, the damage to gill arch was not as intense as the parasite was facing towards the operculum and not the gill arches. The infestation such as, haemorrhagic lesions, anemia, inflammation and penetration of dactylus usually pressure atrophy which often accompanies the presence of larger parasites. They may lead to severe economic loss in the commercial species of fishes.

REFERENCES

  • Bowman, T.E., 1960. Description and notes on the biology of Lironeca puhi nsp isopoda cymothoidae parasite of the hawaiian moray ee Gymnothorax eurostus Abbott. Crustaceana, I: 82-91.


  • Cuyas, C., J.J. Castro, A.T. Santana Ortega and E. Carbonell, 2004. Insular stock identification of Serranus atricauda pisces serranidae through the presence of Ceratothoa steindachneriisopoda cymothoidae) and Pentacapsula cutaneamyoxoa entacapsulidae) in the canary islands. Scientia Marina, 68: 159-163.


  • Grutter, A.S., 2003. Feeding ecology of the fish ectoparasite Gnathia sp. crustacea isopoda from the great barrier reef and its implications for fish cleaning behavior. Marine Ecol. Programe Series, 259: 295-302.
    Direct Link    


  • Kabata, Z., 2003. Parasites and Diseases of Fish Cultured in the Tropics. Isopoda Tayler and Francis, London, pp: 265- 271


  • Overstreet, R.M., 1978. Marine Maladies Worms Germs and Other Symbionts from the Nortern Gulf of Mexico. Mississippi Alabama Sea Grant consortium, Sea Grant College, pp: 140


  • Ramestand, B., 1979. Ecophysiology of parasitic cymthoidea. Annales de Parasito. Paris, 54: 423-448.


  • Ravichandran, S., A.J.A. Ranjith Singh, N. Veerappan and T. Kannupandi, 1999. Effect of isopod parasite Joryma brachysoma on Illisha melastoma from Parangipettai coastal waters Southeast coast of India. Ecol. Environ. Conserv., 5: 95-101.


  • Ravichandran, S., P. Soundarapandian and T. Kannupandi, 2000. Infestation of isopod parasite Epipenaeon ingens Nobili parasitized on Penaeus monodon from Parangipettai coastal environment. Adv. Biosci., 19: 73-78.


  • Ravichandran, S., A.J.A. Ranjith Singh and N. Veerappan, 2001. Parasite induced vibriosis in Chirocentrus dorab off Parangipettai coastal waters. Current Sci., 80: 101-102.
    Direct Link    


  • Romestand, B., M. Janicot and J.P. Trilles, 1977. Modifications tissulaires et reactions de defence chez quelques teleosteens parasites par les cymothoidae crustaces isopodes hemalophages. Annales de Parasitologie Humaine et Eomparee, 52: 171-180.


  • Stephenson, A.B., 1976. Gill damage in fish produced by buccal parasites. Rec. Auckland Inst. Mus., 13: 167-173.


  • Williams, E.H. Jr. and L.B. Williams, 1985. Cuna insularis from the gill chamber of the sergeant major Abudefduf saxatilis linneaus in the West Indies. J. Parasitol., 71: 209-214.

  • © Science Alert. All Rights Reserved