INTRODUCTION
Several facultative and obligatory parasitic members of the order Isopoda are deleterious parasites on fishes and are capable of exhibiting tremendous destructive activity Isopods are conspicuous parasites, on the body surface, in the branchial chamber, or inside the buccal cavity. Menzibes et al. (1955) noted erosion of gill filaments by isopod parasite Lironeca conveka whose males often crowded the branchial chamber. Rockicki (1982) observed partial or complete disappearance of gill filaments of Selar crumenophthalmus.
The infestation of isopod parasites in fishes is scanty (Williams and Williams, 1994; Ravichandran et al., 1999, 2000, 2001, 2007a,b; Grutter, 2003; Cuyas et al., 2004) and no such studies have been made on the infestation of Lironeca puhi in Strongylura leiura. Hence the present attempt was made to study the influence of isopod infestation on host fishes along with reduction of the respiratory surface area, extensiveness of parasite damage like lesions due to reproduction, feedings, pressure and developmental stages of the parasites.
MATERIALS AND METHODS
In the routine observation of S. leiura fishery in Parangipettai, an
interesting incidence of isopod parasitization in several specimens was observed.
Fishes were collected from three major landing centres viz., Mudasaodai, Annankovil;
Pudupettai and subsequently preserved in 10% neutral buffered formalin for further
studies (Fig. 1). The total median dorsal surface of the isopod
from the anterior region between the eyes to the posterior extremity of the
telson. Egg and larvae were removed from female isopods, counted and random
samples of 10 were measured for total length and maximum width to the nearest
0.01 mm.
|
| Fig. 1: |
The sampling stations along Parangipettai coast |
Respiratory Surface Area
The influence of infestation of respiratory surface area of gill arch was
studied. The gill arches of infested and uninfested fishes were carefully dissected
out and blotted to remove the moisture. The imprint drawing of each gill arch
on millimetre graph paper was used to calculate the surface area of gill arch.
Surface area of each tracing was determined by counting then number of small
squares and the total area was obtained. The value was taken 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, third and fourth gill arches of S.
leuira was made. The data collected were tabulated and variation in the
gill raker count as a function of infestation was recorded. They were then analysed
statistically using students t-test.
RESULTS
Frequency of Infestation
Infestation frequencies ranged between 12 and 23% in S. leiura from
the 3 stations (Table 1). The infested fishes were in poorer
condition with hemorrhages from the eyes, opaque lenses in snouts and fins and
body scars. Fish in the uninfested appeared healthy.
During transitional stage the parasite facing posteriorly in the host and attached to the gills. It caused considerably damage to gill filaments, arches rakers and opercles. After the transition was complete the parasite faced anteriorly in the buccal cavity.
Isopods of different developmental stages were separated into two groups according to their positions in the fish (Table 1). The largest isopods, all of which faced anteriorly, are called mature females. Those facing posteriorly and attached to the gills were called transitional.
The amount of gill damage caused by the presence of isopods in the transitional stage varied among the fish. The severe damage would suggest that the host tissue were eaten. Gill damage was subjectively determined as minor when a small section of filaments was destroyed, as major when large section of filaments was destroyed and as massive when a gill arch was broken (Fig. 2).
Brood Pouch Reproduction
The number and sizes of eggs and embryos in broods were not known for the
proteanderous hermaphrodites and gravid females when the young were held until
they were juvenile (Manca larvae) with eyes, antenae and six pereopods formed
(Table 2 and Fig. 3).
Respiratory Surface Area
The reduction of surface area of gill arch of S. leiura due to infestation
of L. puhi is represented in Table 3. Considerable
variation in the respiratory area was observed owing to the attachment of the
L. puhi. The percentage reduction of respiratory surface area was maximum
(30.2) in the III gill arch and minimum (9.4) in the I gill arch. The percentage
reduction of respiratory surface area in the II and IV gill arches was 18.3
and 29.7, respectively. A significant (p<0.01) reduction in the gill surface
area was observed due to infestation.
| Table 1: |
Infestation frequency and estimated damage by different stages
of Lironeca puhi in Strongylura leiura |
 |
| Table 2: |
Description of embryos and larvae in the brood pouches of
Lironeca puhi |
 |
| Table 3: |
Gill surface area of Strongyluva leiura due to the
infestation of Lironeca puhi |
 |
| *Significant (p<0.01) |
|
| Fig. 2: |
Lironeca puhi attached to the branchial chamber of
Strongylura leiura |
|
| Fig. 3: |
Brood pouch of Lironeca puhi in different stages |
| Table 4: |
Gill raker count of Strongylura leiura due to the
infestation of Lironeca puhi |
 |
| * Significant (p<0.01) |
Effects on Gill Raker Count
Reduction in the number of gill rakers was noticed due to the attachment
of L. puhi in the branchial chamber (Table 4). In infested
male fish, the percentage of gill raker count was 43.0 and that of uninfested
it was 58.2. In infested female fish, the percentage gill raker count was 44.8
and in uninfested it was 53.9. The percentage reduction of gill raker count
was more pronounced in male fish (15.2) than in female fish (9.1). The reduction
in gill raker count observed as a function of infestation was found to be statistically
significant (p<0.01).
Gross Lesions
Infested fishes had extremely pale gills indicating severe anemia. Gill
rakers were seriously lost, apical edges were damaged and gill lamellae were
cut off and heavily destroyed. Some secondary gill lamallae were fused or thickened.
Between the gill lamellae calus-like thickenings were observed. Gill lamellae
of the first and second gill arches were eroded due to L. puhi and the
damage was concentrated towards the posterior position. A wide depression was
found due to the lodging of parasites at the gill clefts and the gill arches
showed torsion (Fig. 2 and 3).
DISCUSSION
Cymothoid isopod causes serious problems to host fishes either directly or indirectly affecting the physiological functions of the host (Brusca, 1981; Segal, 1989; Maxwell, 1982; Williams and Williams, 1994; Ravichandran et al., 1999, 2001). According to Kabata (1985), no serious attempt has so for been made to estimate quantitatively the variation of the branchial region, exuberant production of epithelial tissue and significant reduction of the respiratory area of the gills. In the present study, a marked increase in the size of the parasite with the development of a marsupium full of juvenile isopods (Fig. 3) and this significantly increases the pressure atrophy caused by the presence of the parasites.
The percentage reduction of respiratory surface area varies depending upon the nature of attachment of the parasites. The maximum reduction observed in the III gill arch (30.2%) is mainly due to the heavy pressure exerted by L. puhi and second maximum reduction in the IV gill arch (29.7%). The difference in the percentage reduction among different gill arches can be attributed to the location of attachment of L. puhi on gill arches. Significant reduction of respiratory surface area may depend largely on the longevity of infestation. Similar observation has been made by Williams and Williams (1985) in the serious erosion of gill filaments in the III and IV gill arches of Akudefdut saxatilis due to the adult female isopod Kuna insularis.
The gill filaments of Hawain morey cell Gmnothorax eurostus are lost
in the anterior or posterior region of gill arches owing to the attachment of
L. puhi (Bowman, 1960). The smaller males and juveniles for isopod Oleneira
praegustator parasitic on gulf of menhaden cause change on the gill filaments
through seeding (Overstreet, 1978) A similar nature of damage due to seeding
has been noticed in the case of L. puhi which ensures firm grip through
its ventral side facing the gill filaments of third gill arch. But Ravichandran
et al. (1999) have found a situation reverse to the above in that the
dorsal surface of the parasite is facing the first gill arch of Ilisha melastoma
infested by Joryma brachysoma. The damage of gill filaments is not only
due to feeding, but also by the pressure exerted by the parasite. The reduction
in the surface area is due to several factors such as mode of contact, size,
movement and duration of stay of the parasites.
Severe gross lesions observed as a consequence of isopod infestation are the pale gills, erosion of gill lamellae and damaged gill rakers. Pale gills of infested fishes indicate anemia, which may be due to loss blood as a result of obstruction of branchial circulation by the attachment of parasite and of the haemophageous nature of the branchial cymothoids (Ramestand, 1979). The calus-like thickenings on the gill filaments and gill arches are mainly due to the heavy pressure exerted by the parasite and also by their feeding nature. Kabata (1985) has also observed destruction of host tissue as a result of the pressure exerted by the parasite body, when present in the gill cavity. Longer stay of parasite within in the gill chamber may also prevent and obstruct the normal growth of the gill arches. This is due to the torsion of gill arch and fusion of gill lamellae. Penetration of pereopods also causes bulging of gill arches at the affected portion.
A lesion associated with reproduction of parasites to the host is related to the direct activity of the parasites. A marked increase in the size of the parasite is associated with the development of marsupium full of juvenile parasite. This can significantly be increased the pressure atrophy caused by the presence of the parasites. The marsupium of Lironeca is swollen with young, fills up most of the gill chamber and must diminish the flow of water through oxygen uptake in the parasitized gill chamber. The fish reaction is increased encapsulation, inflammation of those portions of the parasite that enter the fish. The infestation of parasites is related to attachment feeding and reproductive activity of the parasite. The infestation usually pressure atrophy often accompanies the presence of larger parasites. They may lead to economic losses in commercial species of fish.
Subscribe Today 
