Omanicotyle heterospina n. gen. et n. comb. (Monogenea: Microcotylidae) from the gills of Argyrops spinifer (Forsskål) (Teleostei: Sparidae) from the Sea of Oman
© Yoon et al.; licensee BioMed Central Ltd. 2013
Received: 2 May 2013
Accepted: 21 May 2013
Published: 7 June 2013
The Sultanate of Oman’s aquaculture industry is expanding with an on-going assessment of potential new fish species for culture. The king soldier bream, Argyrops spinifer (Forsskål) (Sparidae), is one such species that is under consideration. During a routine health assessment of specimens caught in the Sea of Oman throughout the period November 2009 to March 2011, a number of gill polyopisthocotylean monogeneans were recovered.
A subsequent study of the monogeneans using a range of morphology-based approaches indicated that these were Bivagina heterospina Mamaev et Parukhin, 1974. In the absence of pre-existing molecular data, an expanded description of this species is provided, including a differential diagnosis with other species and genera belonging to the subfamily Microcotylinae Monticelli, 1892 with the subsequent movement of this species to a new genus to accommodate it.
The polyopisthocotyleans collected from the gills of A. spinifer appear to be unique within the family Microcotylidae Taschenberg, 1879 in that, morphologically, they possess a pair of large, muscular vaginae each armed with a full crown of 16–18 robust spines and a unique dorsal region of folded tegument, which permits their discrimination from species of Bivagina Yamaguti, 1963. Sequencing of the SSU rDNA (complete 1968 bp) and LSU rDNA (partial 949 bp) places the specimens collected during this study within the subfamily Microcotylinae, but the LSU rDNA sequence differs from Bivagina and also from other microcotylid genera. Morphological features of B. heterospina sensu Mamaev et Parukhin, 1974 and the specimens collected from the current study are consistent with one another and represent a single species. The vaginal armature of these worms is unique and differs from all other genera within the Microcotylinae, including Bivagina, and its movement to Omanicotyle n. gen. to accommodate this species is proposed.
A new genus, Omanicotyle n. gen., is erected to accommodate Omanicotyle [Bivagina] heterospina n. comb. which represents the first monogenean to be described from Omani marine waters. Given the pathogenic potential of microcotylids on captive held fish stocks, a full assessment of Omanicotyle heterospina n. gen. et n. comb. is now required before large-scale production commences.
In addition to the ~150,000 tonnes of commercially important species of wild marine fish landed through Omani ports, the Omani aquaculture industry, which currently exceeds 500 tonnes p.a. and primarily concerns the production of Dicentrarchus labrax (L.) and Oreochromis niloticus niloticus (L.), is exploring the potential of a number of native species suitable for aquaculture. Of the 990+ fish species known from Omani waters, approximately 50 species are under consideration for use in aquaculture, which will include an assessment of various species of seabream, grouper and snapper. Although global aquaculture production is expected to rise to meet the shortfall in wild catches, there is a parallel requirement to identify potential threats to the health and welfare of wild fisheries and aquaculture stocks so that contingencies to mitigate against their establishment or to minimise their potential impacts can be taken. During a recent assessment of these new aquaculture species by the Ministry of Fisheries Wealth, a sample of king soldier bream, Argyrops spinifer (Forsskål), was found to be infected with a microcotylid polyopisthocotylean monogenean, whose morphology is consistent with Bivagina heterospina Mamaev et Parukhin, 1974, which was previously described from the same host from Mokura Bay, Kuria Muria Islands in the Arabian Sea. The morphological features of B. heterospina, however, appear unique and differ from other species of the genus Bivagina Yamaguti, 1963 and an expanded description of the microcotylid is provided in the current study. A new genus to accommodate this species is proposed.
Collection of host and parasite material
Thirty specimens of Argyrops spinifer, with a standard length of 26–52 cm, were collected by line angling in the Oman Sea off the coastal city of Muscat and landed at Muttrah (23° 37′ 08.65″ N; 58° 35′ 33.76 E) throughout the period November 2009 to June 2010. After landing, the fish were placed on ice and then directly transferred to the Ministry of Fisheries Wealth where the gills were excised. A total of 18 adult monogeneans (mean intensity of infection 0.6 ± 1.0 parasites fish-1; range 0–3) parasitising the gills, were removed using mounted surgical needles. Fifteen of the specimens were transferred directly into 90% ethanol for subsequent evaluation by staining, scanning electron and confocal laser scanning microscopy. The remaining three specimens were fixed in 95% ethanol for molecular studies.
Whole mounts of specimens (n = 7) were stained with Mayer’s paracarmine to highlight features of the internal anatomy. Specimens were measured using an eyepiece graticule and all measurements are given in micrometres as the range followed by the mean in parentheses, unless otherwise stated. The terminology of structures follows that of Williams; lengths refer to measurements taken along the longitudinal axis of the worm.
Additional ethanol fixed specimens (n = 5) were prepared for scanning electron microscopy by rehydrating down through a graded ethanol series to water and then by transferring them into 0.2 M sodium cacodylate buffer pH 8 for 24 h, post-fixed in 1% osmium tetroxide for 2 hours at room temperature and then dehydrated through a graded ethanol series. Specimens were then transferred to 50:50 100% ethanol: hexamethyldisilazane followed by 2 changes of 100% hexamethyldisilazane (45 min each), air dried overnight, mounted on 12.5 mm aluminium stubs (Agar Scientific Ltd., Stansted, UK) and then sputter‒coated with gold using an Edwards Sputter Coater S150B. Specimens were viewed under a Jeol JSM 6460 LV SEM, at an accelerating voltage of 10 kV.
A further three alcohol fixed specimens were processed for confocal laser scanning microscopy, by rinsing them in distilled water for 24 h and then transferring them to either 1) 40 mM chromotrope 2R (C2R) (Alfa Aesar, Heysham, UK) + 3 mM phosphotungstic acid (Sigma-Aldrich®, Poole, UK) + 0.5% acetic acid (Sigma-Aldrich®) for 4 h at room temperature to stain the attachment clamps and copulatory spines; or 2) 5 μl (0.2U μl-1 methanol) Alexa Fluor® 594 phalloidin (Invitrogen Molecular Probes, Eugene, Oregon, USA) in 100 μl distilled water in the dark, at room temperature for 5 h to stain the muscular components of the worm. After staining, the specimens were rinsed and mounted in distilled water and then examined on a Leica TCS SP2 AOBS laser scanning confocal microscope.
Illustrations were prepared from images captured using a Zeiss AxioCam MRc digital camera mounted on top of an Olympus BX51 compound microscope using a ×0.75 interfacing lens and ×10 to ×100 oil immersion objectives and MRGrab 126.96.36.199 (Carl Zeiss Vision GmbH, 2001) software.
Three individual monogeneans, previously fixed in 95% ethanol, were digested overnight at 56°C in DNA buffer containing 100 μg ml-1 proteinase K. Total DNA was extracted using a GeneMATRIX kit (EURx Poland) following the tissue protocol and used for PCR reactions. The small subunit ribosomal DNA (SSU rDNA) was amplified using the primers 18e, 390f, 870f/r and 18gM[6–9]. The D1-D2 domains of the large subunit ribosomal DNA (LSU rDNA) were amplified using the primers C1 and D2. PCR bands of the correct size were visualised and recovered from the PCR products using a GeneMATRIX PCR products extraction kit (EURx Poland). PCR reactions were performed in triplicate (three separate worms) according to the original descriptions and sequencing reactions were performed using BigDyeTM Terminator Cycle Sequencing chemistry utilising the same oligonucleotide primers used for the original PCRs. DNA sequencing was performed in both directions for all PCR products and contiguous sequences obtained manually using CLUSTAL_X and BioEdit. CLUSTAL_X was used for the initial sequence alignments and regions of ambiguous sequence alignments were manually edited using the BioEdit sequence alignment editor. Alignment files of related microcotylids, consisting of 947 characters of LSU rDNA sequence data, were used in the phylogenetic analyses. Phylogenetic analyses were performed using the maximum likelihood methodology in PhyML with the general time-reversible (GTR) substitution model selected and 1000 bootstrap repeats, and Bayesian inference (BI) analyses using MrBayes v. 3.0. Models of nucleotide substitution were evaluated for the data using MrModeltest v. 2.2. The most parameter-rich evolutionary model based on the Akaike Information Criterion (AIC) was the GTR + I + G (GTR + proportion Invariant + Gamma) model of evolution. Posterior probability distributions were generated using the Markov Chain Monte Carlo (MCMC) method with four chains being run simultaneously for 1,000,000 generations. Burn in was set at 2500 and trees were sampled every 100 generations making a total of 7500 trees used to compile the majority rule consensus trees.
Taxa used in the phylogenetic analysis with respective GenBank accession numbers in parentheses: Atrispinum acarne Maillard et Noisy, 1979 (AF311702); Bivagina pagrosomi (Murray, 1931) Dillon et Hargis, 1965 (AJ243678); Cynoscionicola “branquialis” (AF382050); Diplostamenides sciaenae (Goto, 1894) Lebedev, Parukhin et Roitman, 1970 (FJ432589); Microcotyle arripis Sandars, 1945 (GU263830); Microcotyle erythrinii van Beneden et Hesse, 1863 (AM157221); Microcotyle sebastis Goto, 1894 (AF382051); Pagellicotyle mormyri (Lorenz, 1878) Mamaev, 1984 (AF311713); Polylabris sillaginae (Woolcock, 1936) Dillon, Hargis et Harrises, 1983 (GU289509); Sparicotyle chrysophryii (van Beneden et Hesse, 1863) Mamaev, 1984 (AF311719).
Type material examined
The following museum type specimens were examined: 1 paratype (CNHE 203) and 8 voucher specimens (CNHE 2822, 2824, 2827) of Pseudobivagina aniversaria (Bravo-Hollis, 1979) Mamaev, 1986 (syn. Neobivagina aniversaria Bravo-Hollis, 1979) from the Cortez sea chub Khyposus elegans (Peters) from the Colección Nacional de Helmintos, Instituto de Biologia, Universidad Nacional Autónoma de México, Mexico City, Mexico; 3 voucher specimens of Bivagina pagrosomi (NHM 19188.8.131.52-7) from the gills of the silver seabream Pagrus (syn. Chrysophrys) auratus (Forster); 4 voucher specimens of Microcotyle [labelled as Bivagina] centrodonti Brown, 1929 (NHM 19184.108.40.206-52) from the gills of the black seabream Spondyliosoma cantharus (L.); and 1 voucher specimen of Bivagina sp. (NHM 19220.127.116.11) from the gills of the red stumpnose bream Chrysoblephus gibbiceps (Valenciennes) from the national parasite collection maintained by the Parasites and Vectors Section, The Natural History Museum, London, UK. In addition, photographs of Bivagina tai (Yamaguti, 1938) from the gills of red sea bream Pagrus major (Temminck et Schlegel) were kindly provided for assessment by Professor Kazuo Ogawa from the Meguro Parasitological Museum, Tokyo, Japan. Although valuable type material of B. heterospina were not available for loan, photographs of paratype (acc. no. 12296) from the gills of A. spinifer caught in Mokura Bay, Kuria Muria Islands in the Arabian Sea on the 26th August 1969 were generously provided by Dr Pavel Gerasev from the Zoological Institute of The Russian Academy of Sciences (ZIRAS), St Petersburg, Russia.
Class Monogenea Carus, 1863
Family Microcotylidae Taschenberg, 1879
Subfamily Microcotylinae Monticelli, 1892
Omanicotyle n. gen.
Body lanceolate. Haptor symmetrical, with numerous clamps arranged in two equal rows. Clamps of microcotylid type of approximate equal size. No terminal anchors present. Paired muscular, unarmed, septate buccal organs. Oesophagus simple without diverticula. Intestinal crura not symmetrical, largely co-extensive with vitellaria extending into the haptoral peduncle. Testes numerous, post-ovarian. Genital atrium muscular, unarmed. Two large, paired, muscular, dorsal, vaginae, each armed with a crown of robust equal sized spines. Germarium U-shaped. Germinal part of germarium approximately ovoid. Large, fusiform, operculated eggs with two polar filaments, an extensive apical filament and a short posterior filament. Conspicuous Y-shaped vitelline duct. Vitellaria extending into the haptor.
Type species: Omanicotyle heterospina (Mamaev et Parukhin, 1974) n. comb.
Etymology: The generic name refers to the type locality, Oman.
Omanicotyle heterospina (Mamaev et Parukhin, 1974) n. comb.
Syn. Bivagina heterospina Mamaev et Parukhin, 1974.
Type host: King soldier bream, Argyrops spinifer (Forsskål) (Sparidae); wild (current study;).
Other hosts: Soldierbream, Argyrops filamentosus (Valenciennes).
Site on the host: Gills.
Type locality: Kuria Muria Islands, Arabian Sea (17° 28′ 06.14″ N; 55° 35′ 55.18″ E).
Other localities: Sea of Oman landed at the port of Muttrah (23° 37′ 08.65″ N; 58° 35′ 33.76 E) (current study).
Type material: Holotype (acc. no. 226/IO-1628) deposited in the Helminthology Laboratory of General Biology and Soil Science of the USSR FESC. Paratypes (acc. no. 12296) are stored in the Laboratory of Parasitology of the Zoological Institute of the USSR.
Voucher material: Seven Mayer’s paracarmine stained whole mounts prepared for the current study. Three voucher specimens (acc. no. NHMUK 2013.5.13.1-3) are deposited in the parasite collection of the Parasites and Vectors Section, The Natural History Museum (NHM), London. A further two specimens (USNPC acc. no. 106952.00) are deposited in the United States National Parasite Collection (USNPC), Beltsville, MD, USA; and two additional voucher specimens (acc. no. AHC 35684) are deposited in the Australian Helminthological Collection (AHC) of The South Australian Museum (SAMA), North Terrace, Adelaide.
Molecular sequence data: A complete SSU rDNA sequence of 1968 bp and a partial LSU rDNA sequence of 949 bp have been deposited in GenBank under the accession numbers JN602094 (SSU) and JN602095 (LSU), respectively.
General: To comply with the regulations set out in article 8.5 of the amended 2012 version of the International Code of Zoological Nomenclature (ICZN), details of this species have been submitted to ZooBank with the Life Science Identifier (LSID) zoobank.org:pub: CDEC0135-BA59-4754-B213-5C748A02C818. In addition, a species profile including taxonomic traits, host details and additional metadata are provided on http://www.monodb.org.
The original specimens of Omanicotyle [Bivagina] heterospina (Mamaev et Parukhin, 1974) n. comb. were collected from Kuria Muria Islands in the Arabian Sea, off the coast of Oman in July-August 1967 and in August-September 1969. This represents a separate water body, as recognised by the International Hydrographic Organisation, to the material collected from the Sea of Oman for the current study. There are, however, some small differences in the number of vaginal spines between the two collections. The material collected from the Arabian Sea have 20–25 spines (25 spines on paratype ZIRAS acc. no. 12296) each measuring 48–54 in length, whilst the specimens collected for the current study have 16–18 spines, measuring 24–28 in length.
Each Omanicotyle specimen (18 individuals from 30 fish) was positioned on the outer hemibranch of the gill arch to which they were attached, orientated along the length of a single primary filament, the anterior end of the worm pointing towards the distal tip, with their clamps attached to the second lamellae; the posterior part of the haptor curling round the filament. The function of the numerous C2R positive droplets along the lateral margins of the anterior haptor is unknown and can only be speculated upon. Given their high number and aggregation, it is unlikely that these represent the precursors for the synthesis of new clamps, i.e. they are not in close association with developing clamps. It could be suggested that these function as papillae increasing the surface area of this part of the haptor and make a contribution to the attachment of the worm. Unfortunately, this area was not visible on the specimens prepared for SEM; further specimens are therefore required to determine whether these structures are visible externally. According to Mamaev, parasites belonging to the subfamily Microcotylinae Monticelli, 1892 have either a single medio-lateral or rarely a dorso-laterally positioned vagina or occasionally two dorso-laterally situated vaginae. Given the large size of the vaginae, which occupy almost the entire width of the worm, it cannot be said that they are strictly dorso-lateral or medial.
Omanicotyle n. gen. can be differentiated from the other 24 genera in the subfamily Microcotylinae on the basis of vaginal number (single or paired) and its relative armature, and also by armature of the genital atrium. The species belonging to the following genera all possess a single, unarmed vagina: Atriostella Unnithan, 1971; Caballeraxine Lebedev, 1972; Diplostamenides Unnithan, 1971; Gamacallum Unnithan, 1971; Jaliscia Mamaev et Egorova, 1977; Magniexcipula Bravo-Hollis, 1981; Paramicrocotyloides Rohde, 1978; Paranaella Kohn, Baptista-Farias et Cohen, 2000; Pauciconfibula Dillon et Hargis, 1965 (syn. Bradyhaptorus Unnithan, 1971); Polymicrocotyle Lamothe-Argumedo, 1967; Pseudoaspinatrium Mamaev, 1986; Sciaenacotyle Mamaev, 1989 (single opening with paired vaginal ducts); and, Solostamenides Unnithan, 1971. Whilst those belonging to Monomacracanthus Mamaev, 1976 and Sebasticotyle Mamaev et Egorova, 1977 possess a single, armed vagina. Species belonging to the genus Microcotyle van Beneden et Hesse, 1863, also have a single, typically mid-dorsally positioned, vagina that is unarmed although the genus also includes species with an armed vagina (e.g. Microcotyle pamae Tripathi, 1954; see). The remaining genera in the subfamily possess paired vaginae. Species belonging to the following genera have unarmed vaginae: Bivagina Yamaguti, 1963 (certain species within the genus); Diplasiocotyle Sandars, 1944; Lutianicola Lebedev, 1970; Neobivagina Dillon et Hargis, 1965 [based on Neobivagina canthari (van Beneden et Hesse, 1863) Dillon et Hargis, 1965 which was nominated by Mamaev as the type species, following the reallocation of the other species in the genus to other genera]; Pseudobivagina Mamaev, 1986; and Pseudoneobivagina Mamaev, 1986. The remaining genera, which also include Omanicotyle n. gen., all have armed vaginae, i.e. Bivagina Yamaguti, 1963 (certain species within the genus); Kahawaia Lebedev, 1969; and Neobivaginopsis Villalba, 1987. Omanicotyle n. gen. can be readily discriminated from the other genera. The vaginae in Bivagina are typically small but heavily muscularised structures armed with a crescent of short spines; the vaginal ducts connecting the two vaginae are typically clearly visible. Kahawaia possesses two cuticularised, pyriform pads armed with spines, interpreted as vaginae. The vaginae of Neobivaginopsis are large, muscular, contractile structures the openings of which have lightly sclerotised borders. The vaginae of Omanicotyle n. gen. by comparison, are large, muscular structures with a full corona of spines, which near abut against each other and occupy almost the entire width of the worm and as such obscure the vaginal ducts (which could not be seen in the specimens examined for the current study).
Omanicotyle n. gen. can also be discriminated from almost all the other genera on the relative armature of the genital atrium and/or that of the cirrus/penis when present. The following genera have both an armed genital atrium and an armed cirrus: Caballeraxine; Diplostamenides; Lutianicola; Neobivagina; Neobivaginopsis; Pseudobivagina; Pseudoneobivagina; Sciaenacotyle; and Sebasticotyle. Atriostella possesses an armed genital atrium but an unarmed cirrus, whilst species belonging to the genera Diplasiocotyle, Kahawaia, Jaliscia, Microcotyle, Paranaella, Polymicrocotyle and Solostamanides possess an armed genital atrium but no differentiated cirrus. The genera Gamacallum, Magniexcipula and Monomacracanthus have an unarmed genital atrium but an armed penis/cirrus, whilst species belonging to Paramicrocotyloides, Pauciconfibula and Pseudoaspinatrium have both an unarmed genital atrium and an unarmed cirrus. Only the genera Bivagina and Omanicotyle n. gen. have an unarmed genital atrium and no differentiated cirrus. The latter two genera, however, can be readily separated on the size and armature of their vaginae, as discussed above.
There are 24 genera in the subfamily Microcotylinae, which, according to Mamaev includes microcotylids that possess a symmetric or sub-symmetric, well-delineated haptor, adults that lack haptoral anchors, intestinal limbs with lateral branches/appendages without anastomoses, an armed or unarmed genital atrium, and, usually a single, medio-lateral, vagina, rarely latero-dorsal, but occasionally two, dorso-laterally or ventro-laterally positioned, vaginae. The subfamily Microcotylinae was revised by Unnithan to include six new genera (Atriostella, Diplostamenides, Manterella Unnithan, 1971, Nudimasculus Unnithan, 1971, Polynemicola Unnithan, 1971 and Solastamenides Unnithan, 1971), alongside the four existing genera Metamicrocotyla Yamaguti, 1953, Microcotyle van Beneden et Hesse, 1863, Microcotyloides Fujii, 1944 and Prosomicrocotyla Yamaguti, 1958. This was subsequently revised by Mamaev who moved Polynemicola and Microcotyloides to the subfamily Polynemicolinae Mamaev, 1986; Metamicrocotyla to the subfamily Metamicrocotylinae Yamaguti, 1963; Prosomicrocotyla to the subfamily Prosomicrocotylinae Yamaguti, 1963. Despite their removal from the Microcotylinae, however, no additional comment on the placement of Manterella and Nudimasculus was made. Mamaev then moved a further 14 genera (Bivagina, Caballeraxine, Diplasiocotyle, Gamacallum, Jaliscia, Kahawaia, Lutianicola, Magniexcipula, Monomacracanthus, Neobivagina, Neobivaginopsis, Paramicrocotyloides, Pauciconfibula, Polymicrocotyle, Pseudoaspinatrium, Pseudobivagina, Pseudoneobivagina and Sebasticotyle) into the Microcotylinae. The genera Paranaella and Sciaenacotyle were subsequently added.
Although the number of monogeneans encountered in the current study was low, it is not known what impact these polyopisthocotyleans may pose to stock when A. spinifer is reared under intensive aquaculture conditions. Given the recorded pathogenicity of other microcotylids on captive held fish stocks (e.g. Bivagina tai[24, 26]; Microcotyle sebastis; Sciaenacotyle panceri (Sonsino, 1891); Sparicotyle chrysophrii (van Beneden et Hesse, 1863) Mamaev, 1984; and Zeuxapta seriolae (Meserve, 1938)[29–31]), a full assessment of the potential impact Omanicotyle heterospina n. gen. et n. comb. may have is advised before production is initiated.
The polyopisthocotylean Omanicotyle heterospina n. gen. et n. comb. collected from the gills of the sparid A. spinifer is the first monogenean to be described from the Sea of Oman and is assigned to a new genus within the subfamily Microcotylinae (Microcotylidae), based on consistent morphological and molecular differences discriminating it from other genera in the subfamily. Morphologically, Omanicotyle n. gen., which possesses two large, fully-armed vaginae, can be discriminated from the genus Bivagina (e.g. B. pagrosomi) on differences in the armament of the vaginae and a characteristic circular, dorsal region of folded tegument. Sequencing of the LSU rDNA (949 bp) revealed only a 95.2% percentage similarity with B. pagrosomi (identities = 876/920 (95%); gaps = 10/920 (1%)), lending support to the proposal that these specimens are placed as a new taxon within the Microcotylinae. A full assessment of the disease potential of Omanicotyle heterospina n. gen. et n. comb. and how it may impact on the production of A. spinifer in Omani waters is advised before production begins.
We thank Professor Ian D. Whittington from the South Australian Museum, Adelaide, Australia for his invaluable comments relating to microcotylid morphology; to Dr Gerardo Pérez Ponce de León and Mr Luis García-Prieto from the Instituto de Biología, Universidad Nacional Autónoma de México, Mexico City for the loan of type specimens of Neobivagina from the Coleccion Nacional de Helmintos, Instituto de Biologia, UNAM, Mexico; Mrs Eileen Harris and Tracey Heath from the Parasites and Vectors Section, The Natural History Museum, London for the loan of type specimens of Bivagina and for their assistance in accessing some of the Russian literature relating to microcotylids; Professor Kazuo Ogawa from the Meguro Parasitological Museum, Tokyo, Japan for providing images of B. tai; and, Dr Pavel Gerasev from the Zoological Institute of Russian Academy of Sciences, St Petersburg, Russia for providing images of a paratype of B. heterospina. The authors also gratefully acknowledge the support provided by Mrs Nashwa Al-Mazrooei, Director of Fishery Quality Control Center, Ministry of Agriculture and Fisheries Wealth, Oman throughout this project and for her contribution to Omani fish and fisheries research. This study was supported through projects IG/AGR/FISH/13/02, Sultan Qaboos University, Oman, whilst the DNA component of the study was supported by a University of Malaya HIR grant No: UMC/625/1/HIR/027.
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