1. Introduction
Camallanidae Railliet and Henry (1915) is a single family from the Spirurida order within the Camallanoidea superfamily. Adult camallanid nematodes are common parasites that infect the digestive tract of marine, freshwater, or estuarine predaceous vertebrates (Bullard and Overstreet, 2002). Six genera of Camallanus, Onchophora, Paracamallanus, Procamallanus, Spirocamallanus, and Spirocotyle form this family. Species of the genus Camallanus are widespread across the globe (Akinsanya and Otubanjo, 2006; Kakar et al., 2013). Numerous species of this nematode group have been described from the stomach or intestine of frogs, tortoises, and most often from numerous species of fish (Kuzmin et al., 2009; Enyidi and Uwanna, 2019). Relatively few details are available on the morphology and systemic evaluation of Camallanus species.
The members of this genus are distinguished by an external circle of cephalic papillae around well-sclerotized buccal capsules consisting of four large and four rudimentary papillae. Six very small papillae form an inner circle (Rigby and Rigby, 2014; Svitin et al., 2019). The structure of the buccal capsule is of great importance for the identification and classification of Camallanidae (Yeh, 1960). Males are usually smaller than females and have a ventrally curved tail with caudal alae and pedunculate papillae, spicules are unequal, and gubernaculum is either present or absent (Moravec, 1994). Females are ovoviviparous with a heteroxenic life cycle, and copepods develop as obligatory intermediate hosts (Sures et al., 1994; Moravec, 1998).
In light of the aforementioned issues, the present study aimed to detect morphological and morphometric characterization for a nematode parasite infecting the African sharptooth catfish Clarias gariepinus using light and scanning electron microscopy.
2. Material and Methods
A total of 80 specimens of the African sharptooth catfish Clarias gariepinus (F: Clariidae) were captured alive from Lake Manzala, Egypt, throughout the whole year of 2019. Fish specimens were transported to Parasitology Research Laboratory, Zoology Department, Faculty of Science, Cairo University, Egypt. All fish were dissected and microscopically examined to detect helminths. The recovered nematodes were fixed in 70% ethanol and subsequently clarified with lactophenol for identification and photographing using a Leica DM 2500 microscope (NIS ELEMENTS software, version 3.8). For scanning electron microscopy (SEM), worms were fixed with 3% buffered glutaraldehyde, post-fixed with aqueous OsO4 for 4h, and dehydrated by ascending ethyl alcohol series. Thereafter, they were dried with liquid CO2 using a critical point dryer "LEICA, EM CPD300", placed on an aluminum stub, covered with gold palladium, and then examined and photographed in a JEOL scanning electron microscope (JSM-6060LV). The measurements were carried out in millimeters presented as a range, followed by the arithmetic mean±SD in parentheses.
3. Results
In each of the six necropsied African sharptooth catfish Clarias gariepinus (F: Clariidae), among 80 specimens, adult specimens of Camallanus polypteri were found to spontaneously parasitize the stomach with an infection rate of 7.5%. The infection was reported to be only 15.0% (6 out of 40) in the winter season, without any records in other seasons.
3.1. Description
(Figures 1 and Figure 2) The recovered nematodes were small-sized and slender with a thin cuticle transversely striated with striations. Lateral valves of the buccal capsule with smooth internal longitudinal ridges ranged from 8-14 in male and 8-9 in female worms. Some ridges were very short, confined to the anterior portion of the valves. The esophagus is divided into muscular and glandular portions, with the muscular esophagus being longer than the glandular one. The excretory pore is at the middle portion of the muscular esophagus. Deirids is very thin and slightly anterior to the nerve ring.
3.2. Body of the Male Worm
It was 2.87-3.1 (2.91±0.1) mm long and 0.090-0.15 (0.098±0.01) mm wide. The length and width of the buccal capsule were 0.041-0.052 (0.48±0.01) and 0.048-0.069 (0.051±0.01) mm, respectively. The muscular esophagus was 0.25-0.39 (0.31±0.1) mm long, and the glandular esophagus was 0.20-0.34 (0.29±0.1) mm long. The posterior part of the body is provided with caudal papillae and two unequal spicules: the left one is 0.07-0.12 (0.09±0.1) mm, while the right spicule is 0.08-0.16 (0.12±0.1) mm long. The tail is bifid and measured as 0.057-0.069 (0.061±0.01) mm long.
3.3. Body of the Female Worm
It is measured as 4.99-6.1 (5.2±0.1) mm long and 0.097-0.14 (0.12±0.01) mm wide. Buccal capsule is 0.060-0.069 (0.062±0.01) mm long and 0.068-0.079 (0.071±0.01) mm wide. Muscular esophagus is 0.32-0.69 (0.39±0.1) mm long, and glandular esophagus is 0.30-0.39 (0.34±0.1) mm long. The vulva is equatorial or slightly post-equatorial, with a prominent anterior lip. The tail is long and measured as 0.01-0.09 (0.03±0.1) mm long. Table (1) displays the maximum and minimum values, as well as the mean values of the different body parts of this species, compared to previously described Camallanus species.
Parameters | Host fish | Dimensions | ||||||||
---|---|---|---|---|---|---|---|---|---|---|
Body | Buccal capsule | Esophagus | Spicules length | Tail Length | ||||||
Related species | Length | Width | Length | Width | Muscular | Glandular | Right | Left | ||
Camallanus cotti | Poecilia reticulata | M: 3.901 (3.44-4.24) | M: 0.195 (0.171-0.220) | M: 0.093 (0.083-0.100) | M: 0.091 (0.076-0.102) | M: 0.356 (0.332-0.377) | M: 0.470 (0.441-0.490) | 0.143 (0.132-0.152) | 0.106 (0.100-0.110) | M: 0.114 (0.108-0.127) |
F: 8.44 (7.42-9.23) | F: 0.332 (0.293-0.366) | F: 0.167 (0.132-0.147) | F: 0.141 (0.122-0.157) | F: 0.535 (0.519-0.588) | F: 0.672 (0.588-0.752) | F: 1.33 (1.08-1.53) | ||||
Camallanus polypteri | Clarias gariepinus | M: 2.98 (2.20-3.75) | M: 0.087 (0.080-1.00) | M: 0.049 (0.045-0.052) | M: 0.053 (0.050-0.060) | M: 0.340 (0.30-0.37) | M: 0.278 (0.25-0.30) | 0.074 (0.065-0.080) | 0.043 (0.032-0.048) | M: 0.067 (0.050-0.090) |
F: 5.92 (5.10-6.87) | F: 0.37 (0.10-0.16) | F: 0.064 (0.062-0.068) | F: 0.075 (0.070-0.080) | F: 0.452 (0.44-0.78) | F: 0.385 (0.31-0.44) | F: 0.0132 (0.011-0.014) | ||||
Camallanus maculatus | Xiphophorus maculatus | M: 3.5±0.3 (2.7-4.1) | M: 0.16±0.03 (0.080-0.20) | M: 0.079±0.004 (0.070-0.084) | M: 0.08±0.009 (0.07-0.09) | M: 0.34±0.049 (0.25-0.40) | M: 0.45±0.05 (0.39-0.56) | 0.148±0.023 (0.107-0.204) | 0.099±0.011 (0.08-0.124) | M: 0.115±0.008 (0.092-0.120) |
F: 7.1±0.1 (4.4-9.02) | F: 0.29±0.073 (0.16-0.45) | F: 0.13±0.043 (0.11-0.32) | F: 0.137±0.043 (0.116-0.324) | F: 0.52±0.06 (0.44-0.65) | F: 0.61±0.054 (0.49-0.68) | F: 0.90±0.180 (0.70-1.3) | ||||
Camallanus boomker | Channa orientalis | M: 2.1 (1.74-1.95) | M: 0.1 (0.07-0.09) | M: 0.042 (0.032-0.039) | M: 0.065 (0.061-0.063) | M: 0.28 (0.23-0.26) | M: 0.33 (0.25-0.29) | 0.32 (0.26-0.29) | 0.016 (0.013-0.015) | M: 0.13 (0.09-0.11) |
F: 2.23 (1.95-2.1) | F: 0.14 (0.1-0.13) | F: 0.06 (0.03-0.05) | F: 0.0554 (0.05-0.053) | F: 0.22 (0.19-0.22) | F: 0.28 (0.21-0.25) | F: 0.11 (0.05-0.09) | ||||
Camallanus polypteri (The present study) | C. gariepinus | M: 2.91±0.1 (2.87-3.1) | M: 0.098±0.01 (0.090-0.15) | M: 0.48±0.01 (0.041-0.052) | M: 0.051±0.01 (0.048-0.069) | M: 0.31±0.1 (0.25-0.39) | M: 0.29±0.1 (0.20-0.34) | 0.12±0.1 (0.08-0.16) | 0.09±0.1 (0.07-0.12) | M: 0.061±0.01 (0.057-0.069) |
F: 5.2±0.1 (4.99-6.1) | F: 0.12±0.01 (0.097-0.14) | F: 0.062±0.01 (0.060-0.069) | F: 0.071±0.01 (0.068-0.079) | F: 0.39±0.1 (0.32-0.69) | F: 0.34±0.1 (0.30-0.39) | F: 0.03±0.1 (0.01-0.09) |
4. Discussion
In the present study, African sharptooth catfish C. gariepinus was found to be naturally infected with C. polypteri inhabiting the stomach of the examined fish with an infection rate of 7.5%. Moreover, during the winter season, the infection was recorded at only 15.0%. These results coincide with data obtained by Adeyemi and Toluhi (2014) who claimed that Synodontis resupinatus inhabiting Lower Niger River, Kogi State, Nigeria, was infected with Camallanus sp. with an infection rate of 17.7%. Nonetheless, it was lower than the data obtained by Ranibala et al. (2013) who reported high infection rates of Anabas testudineus with C. anabantis in the summer (88.7%), medium in autumn (66.8), and spring (42.5%), and lower in winter (23.2%).
The morphology of the present C. polypteri specimens recovered from C. gariepinus has all the diagnostic generic characteristics of the genus Camallanu. They have tridents attached to the buccal capsule reaching to the level of the nerve ring, caudal alae joining anteriorly, and the larger spicule as the left one (usually the longer spicule is on the right side in camallanids). These results were similar to earlier explanations of C. polypteri infecting the same host as those provided by Moravec, 1973, Gupta and Verma (1978), Kabré and Petter, 1997, and Moravec et al., 2003, with little variation in the measurements of different body parts. Nevertheless, it is different from other species of the genus Camallanus, such as C. longicaudatus Moravec (1973), C. kirandensisAmin (1978), C. ancylodirusBaker (1979), and C. tholukodensis Lakshmi et al. (1990) in the measurements of the total length, buccal capsule length and width, number of longitudinal ridges, length of the muscular and glandular esophagus, number of genital papillae, and spicules length. Furthermore, it differs from C. magathi Sprehn (1932), C. parvus Caballero (1939), C. mazabukaeKung (1948), C. unispiculus Khera (1954), C. johniYeh (1960), and C. unispiculusKhera (1954) in having two unequal spicules instead of one for other species. Therefore, the present study is considered a re-description of C. polypteri from C. gariepinus with a new geographical location in Egyptian freshwater.
Authors' Contribution
Study concept and design: R. A. G.
Acquisition of data: S. M and R. A. G.
Analysis and interpretation of data: S. M and R. A. G.
Drafting of the manuscript: R. A. G.
Critical revision of the manuscript for important intellectual content: R. A. G. and S. M.
Statistical analysis: R. A. G. and S. M.
Administrative, technical, and material support: S. M and R. A. G.
Ethics
We hereby declare all ethical standards have been respected in preparation of the submitted article.
Conflict of Interest
The authors declare that they do not have any conflict of interest regarding the publication of the current article.
Grant Support
The authors confirmed that there is no grant support for this article.
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