Hamacreadium cribbi n. sp. (Digenea: Opecoelidae) from Lethrinusminiatus (Forster) (Perciformes: Lethrinidae) from New Caledonian waters
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- Bray, R.A. & Justine, JL. Syst Parasitol (2016) 93: 761. doi:10.1007/s11230-016-9662-8
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A new species of Hamacreadium Linton, 1910, H. cribbi n. sp. is described from Lethrinus miniatus (Forster) from the waters off New Caledonia. It is compared with the other species of Hamacreadium reported from lethrinids and is characterised by the size of its eggs which tend to be larger [72–93 (84) vs 54–81 (56) µm long] than those of other species. Other characteristics, such as body size and shape and internal ratios, differentiate H. cribbi from other species; these differences are discussed in detail.
Hamacreadium Linton, 1910 is one of a group of plagioporine genera which are poorly defined morphologically and is ‘characterized by a combination of rather generalized plagioporine characters. Pre-eminent among those are the excretory vesicle extending into the forebody, deeply lobed ovary, distinctly submedian genital pore, and the vitelline follicles entering the forebody and extending beyond the testes to the posterior extremity’ (Cribb, 2005). The opecoelids are a group in need of a thorough molecular examination, and as a start we have sequenced a variety of worms, and have found that the Hamacreadium-like species found in Lethrinus miniatus (Forster) clusters with, but is distinct from worms identified as H. mutabile Linton, 1910 (see Justine et al., 2012b; Andres et al., 2014; Bray et al., 2016). To facilitate the discussion of this species in our phylogenetic studies we here describe and name this form.
Materials and methods
Fish were collected along the external slope of the reef, off Nouméa, New Caledonia. Digeneans were collected live, immediately fixed in nearly boiling saline (Cribb & Bray, 2010; Justine et al., 2012a) and then transferred to 80% ethanol. Whole-mounts were stained with Mayer’s paracarmine, dehydrated in an ethanol series, cleared in beechwood creosote and mounted in Canada balsam. Measurements were made through a drawing tube on an Olympus BH-2 microscope, using a Digicad Plus digitising tablet and Carl Zeiss KS100 software adapted by Imaging Associates, and are quoted in micrometres. The following abbreviations are used: BMNH, British Museum (Natural History) Collection at the Natural History Museum, London, UK; MNHN JNC, Muséum National d’Histoire Naturelle, Paris, France.
Family Opecoelidae Ozaki, 1925
Subfamily Plagioporinae Manter, 1947
Hamacreadium cribbin. sp.2
Type-host: Lethrinus miniatus (Forster) (Lethrinidae), Trumpet Emperor.
Type-locality: Récif Kué, External slope, New Caledonia (22°34′892S, 166°29′673E; 21.vi.2007).
Other localities: Off Ever Prosperity, external slope, depth 60 m, New Caledonia (22°27′S, 166°21′E; 22.viii.2006, 11.ix.2006, 07.xi.2006).
Type-material: Holotype: MNHN JNC2204a. Paratypes: MNHN JNC1924, 1952, 2114, 2162, 2184, 2186, 2202, 2203, 2204b, 2205, 2207, 2208, 2300, 2402, 2706, 2822B, 2824A; BMNH 2016.4.1.1-16.
Site in host: Digestive tract.
Prevalence: 83% (24 of 29).
Etymology: This species is named for our colleague Tom Cribb of the University of Queensland, the pre-eminent digenean taxonomist of the Indo-Pacific Region.
Description (Figs. 1–2)
Measurements (in μm) and ratios of type-series of Hamacreadium cribbi n. sp. ex Lethrinus miniatus (n = 25)
Body length (BL)
Pre-oral lobe length
Oral sucker length
Oral sucker width
Intestinal bifurcation to ventral sucker
Vitellarium to ventral sucker
Ventral sucker length
Ventral sucker width
Ventral sucker to ovary
Ovary to anterior testis
Anterior testis length
Anterior testis width
Distance between testes
Posterior testis length
Posterior testis width
Body width as % of BL
Forebody as % of BL
Sucker length ratio
Sucker width ratio
Oral sucker: pharynx ratio
Ventral sucker to ovary as % of BL
Post-testicular region as % of BL
Oesophagus as % of BL
Intestinal bifurcation to ventral sucker as % of BL
Vitellarium to ventral sucker as % of BL
Ovary to anterior testis as % of BL
Distance between testes as % of BL
Testes 2, oval to rounded, smoothly irregular, contiguous or slightly separated, in mid-hindbody, oblique. Cirrus-sac large, claviform, sigmoid, much wider proximally, reaches dorsally to ventral sucker, occasionally very slightly into hindbody, may be restricted to forebody in flattened specimens. Seminal vesicle long, coiled in posterior part of cirrus-sac. Pars prostatica and ejaculatory duct not clearly differentiated, long, coiled, complex coiling distally. Genital atrium distinct. Genital pore sinistral, ventral to left caeca or close, about halfway between bifurcation and ventral sucker.
Ovary usually lobate (3–5 lobes; see Fig. 2), oblique to and overlapping anterior testis. Seminal receptacle oval, dorsal to ovary. Mehlis’ gland pre-ovarian. Laurer’s canal opens dorsally to Mehlis’ gland. Uterus pre-ovarian, mainly intercaecal. Eggs tanned, operculate. Metraterm thick-walled, reaches level of ventral sucker. Vitellarium follicular, fields reach from bifurcal level of ventral sucker, to close to posterior extremity, lateral to caeca and encroaching slightly over dorsal and ventral surface of caeca, almost confluent in bifurcal and post-testicular regions, usually continuous at level of ventral sucker, occasionally interrupted on one or both sides.
Excretory pore terminal. Vesicle I-shaped, reaches to about level of genital pore.
Vitellarium anterior extent: At level of intestinal bifurcation: 52 specimens (58%); distinctly post-bifurcal, but not to ventral sucker: 38 specimens (42%).
Vitellarium interruptions at ventral sucker level: Continuous, no interruption: 73 specimens (81%); interruptions both sides: 7 specimens (8%); interruptions one side: 9 specimens (10%).
Cirrus-sac reach (continuum): To about mid ventral sucker level: 49 specimens (54%); to posterior part of ventral sucker, occasionally very slightly into hindbody: 41 specimens (46%).
Ovary lobation. Not always clear, sub-lobes complicate the picture: Three lobes: 69 specimens (77%); four lobes: 15 specimens (17%); Five lobes: 6 specimens (7%).
Several species of Hamacreadium have been reported from Lethrinus spp., including two reports from L. miniatus. Unfortunately, neither is accompanied by descriptions. Durio & Manter (1968) reported the type-species of Hamacreadium, H. mutabile, from L. miniatus from New Caledonia, but molecular evidence and other evidence (see below) suggests that this species occurs only in lutjanid fishes. Shen (1985) reported H. lethrini Yamaguti, 1934 from L. miniatus from off the Xisha Islands (or Paracel Islands) in the South China Sea. These species will be discussed below, along with the other Hamacreadium spp. from Lethrinus spp.
1.Hamacreadium balistesiNagaty & Abdel Aal, 1962 was originally reported from the Spangled Emperor Lethrinus nebulosus (Forsskål) and the White-banded Triggerfish Rhinecanthus aculeatus (Linnaeus) (Balistidae) from the Red Sea (Nagaty & Abdel Aal, 1962b) and was considered as synonym of H. mutabile by Bray & Cribb (1989). As is discussed below, H. mutabile is probably a specific parasite of lutjanids. The cirrus-sac in H. balistesi is said to be ‘preacetabular’. Nagaty & Abdel Aal (1962b) mention that the vitelline fields ‘may be interrupted at acetabular level’ and differentiate it from H. interruptus by, inter alia, ‘vitelline follicles constantly arranged or may be interrupted at acetabular level instead of their constant interrupted arrangement’, but see the Fischthal & Kuntz (1965) description of H. interruptus Nagaty, 1941 (discussed below). Ramadan (1983) considered H. balistesi a synonym of H. interruptus. The ventral sucker to ovary distance is relatively distinctly greater than in H. cribbi n. sp. (Fig. 5) and the eggs are smaller (Fig. 3). The excretory system is neither described nor illustrated.
2.Hamacreadium diacopaeNagaty & Abdel Aal, 1962 was originally reported from the Dory Snapper Lutjanus fulviflamma (Forsskål) (Lutjanidae) from the Red Sea (Nagaty & Abdel Aal, 1962a) and later from the ‘bec de cane’ Lethrinus sp. (most probably L. nebulosus) from New Caledonia (Durio & Manter, 1968). The only description was based on a single specimen. It is small, broad (width 42% of body length, BL), with a long forebody (49% BL), the ventral sucker tends to be relatively larger [sucker-width ratio 1:1.83–2.00 (1:2.22)], it has a short post-testicular region (12% BL), the ovary overlaps the ventral sucker and the vitellarium reaches to the oesophagus. The excretory system is neither described nor illustrated.
3.Hamacreadiumegyptiael Abdou, Heckmann, Beltagy & Ashour, 2001 was described from Lethrinus nebulosus and the Sky Emperor Lethrinus mahsena (Forsskål) in the Red Sea (el Abdou et al., 2001). Although reported from two hosts, measurements of only one specimen are given and these measurements vary between the description and the table. The illustrations and the tiny gonads clearly show that the worm is immature and we consider it unrecognisable.
4.Hamacreadium epinepheliYamaguti, 1934, now known as Cainocreadium epinepheli, is a widely reported parasite of Indo-Pacific serranids, including those from New Caledonian waters (Bray & Justine, 2007; Justine et al., 2010a) and has been reported in the Chinese Emperor Lethrinus haematopterus Temminck & Schlegel, off Japan by Yamaguti (1934). Nagaty (1941) considered H. epinepheli a synonym of H. mutabile, which he reported from serranids, lethrinids and lutjanids, but later (Nagaty, 1956), recognised the species as distinct. Shen (1985) recorded Cainocreadium epinepheli in L. haematopterus, from off the Xisha Islands. The median genital pore distinguishes Cainocreadium from Hamacreadium.
5.Hamacreadium interruptusNagaty, 1941 was originally reported from the Pink Ear Emperor Lethrinus lentjan (Lacépède) (as Lethrinus mahsenoides Valenciennes) from the Red Sea (Nagaty, 1941). Fischthal & Kuntz (1965) recorded H. interruptus from the Smalltooth Emperor Lethrinus microdon Valenciennes and the Asian Swamp Eel Monopterus albus (Zuiew) (Synbranchidae) off Jesselton, North Borneo. They considered Plagioporus longivesicula Yamaguti, 1952 and Hamacreadium lethrini Nagaty & Abdel Aal, 1962 as synonyms. Hafeezullah & Dutta (1980) described H. interruptus from an unidentified marine fish off Chiria Tapu, Andaman Islands. The lack of an identified host reduces the value of the description and it is not used in comparison here. Tadros et al. (1978) reported this species from the type-host also in the Red Sea. Nagaty (1941) described and illustrated a large lateral gap in the vitelline fields at the level of the ventral sucker. Fischthal & Kuntz (1965) stated that the vitelline fields are ‘interrupted at acetabular level on both sides in 12, on left side only in 4, on right side only in 1, and uninterrupted on both sides in 3’. The eggs are smaller than those in H. cribbi n. sp. (Fig. 3). The excretory system is neither described nor illustrated.
6.Hamacreadium khaliliRamadan, 1983 was originally reported from L. mahsena and L. nebulosus from the Red Sea (Ramadan, 1983). El-Labadi et al. (2006) reported the species from the Lavender Jobfish Pristipomoides sieboldii (Bleeker) (Lutjanidae) and the Yellow-edged Lyretail Variola louti (Forsskål) (Serranidae), from the Gulf of Aqaba in the Red Sea, without descriptive matter. The species is differentiated from H. interruptus in a key by ‘Testes globular and lobulated, cirrus pouch triangular’. The vitelline follicles are ‘aggregated in two sets, a posterior and an anterior, with a gap between them’. The eggs are smaller than those in H. cribbi n. sp. (Fig. 3). The anterior extent of the excretory vesicle was not traced.
7.Hamacreadium koshariNagaty & Abdel Aal, 1962, originally reported in Serranus sp. (Serranidae) and Lethrinus mahsena from the Red Sea (Nagaty & Abdel Aal, 1962b), has vitelline fields restricted to the hindbody and Bray & Cribb (1989) considered it likely that it belongs on the genus Apopodocotyle Pritchard, 1966, now considered a synonym of Cainocreadium Nicoll, 1947 (see Cribb, 2005).
8.Hamacreadium krusadaiensisGupta, 1956 was originally reported from a ‘marine cat-fish’ from the Gulf of Mannar (Gupta, 1956). Hafeezullah (1971) redescribed the species from Lethrinus nebulosus (syn. L. frenatus Valenciennes) from the Gulf of Mannar off Tuticorin. Gibson (1976) transferred the species to Neolebouria Gibson, 1976 and it has been included in the two most recent keys to that genus (Bray & Justine, 2009; Dronen et al., 2014).
9.Hamacreadium nagatyiLamothe Argumedo, 1962 (syns H. lethrini Nagaty & Abdel Aal, 1962 nec Yamaguti, 1934; H. lenthrium Manter, 1963) is based on a single large specimen from Lethrinus lentjan (as Lethrinus mahsenoides) from the Red Sea (Nagaty & Abdel Aal, 1962a). As the name is pre-occupied, it has been replaced twice, by Lamothe-Argumedo (1962) and Manter (1963). At 7,220 µm long, this species is larger than any other reported lethrinid Hamacreadium. Cirrus-sac is entirely within the forebody. The ventral sucker to ovary distance is relatively distinctly greater than in H. cribbi n. sp. (Fig. 5) and the eggs tend to be smaller (Fig. 3). The excretory system is neither described nor illustrated.
10.Hamacreadium lethriniYamaguti, 1934, was originally reported from Lethrinus haematopterus, from the Pacific coast of Wakayama Prefecture, Japan (Yamaguti, 1934). Fischthal & Kuntz (1964) redescribed, but did not illustrate, the species from the Longfin Emperor Lethrinus erythropterus Valenciennes (as Lethrinus hypselopterus Bleeker) and the Humpback Red Snapper Lutjanus gibbus (Forsskål) (Lutjanidae) from Puerto Princesa, Palawan Island. Philippines. The species has been reported two further times, but with no descriptive matter. Dyer et al. (1988) reported as host the Thumbprint Emperor Lethrinus harak (Forsskål) from Okinawa, Japan and Shen (1985) reported Lethrinus miniatus and the Grey Large-eye Bream Gymnocranius griseus (Temminck & Schlegel) (Lethrinidae) as hosts off Xisha Islands (or Paracel Islands) in the South China Sea. The original description is very similar to H. cribbi n. sp., but the testes are described and illustrated as irregularly indented, not the usual condition in H. cribbi. Fischthal & Kuntz (1964) described the post-testicular distance as 0–585 µm, indicating that at least one of their specimens was damaged. The eggs are generally smaller than in H. cribbi (Fig. 3). The excretory system reaches to about the same level as in H. cribbi.
11.Hamacreadium mehsenaNagaty, 1941, reported from Lethrinus ‘mehsena’ (presumably Lethrinus mahsena) from the Red Sea (Nagaty, 1941) differs from Hamacreadium in that the vitellarium does not reach into the forebody. Pritchard (1966) placed the species in her new genus Apopodocotyle Pritchard, 1966, but Cribb (2005) replaced in its original genus. It appears closest to the genus Podocotyle Dujardin, 1845, but while the testes are described as oblique, they appear almost symmetrical in the illustration. This form cannot be confused with H. cribbi. The excretory system is neither described nor illustrated.
13.Hamacreadium nebulosaeNagaty & Abdel Aal, 1962 is known only from three specimens found in L. nebulosus in the Red Sea (Nagaty & Abdel Aal, 1962b). According to the measurements given the sucker-width ratio is about 1:1, whereas in the illustration this ratio is about 1:1.8. The excretory vesicle is said to reach to the mid-level of the ventral sucker. The eggs are distinctly smaller than those of H. cribbi (Fig. 3).
14.Plagioporus(Plagioporus)longivesiculaYamaguti, 1952 is known from two gravid and three immature specimens from Lethrinus sp., off Makassar, southern Sulawesi (Yamaguti, 1952). Fischthal & Kuntz (1965) considered Plagioporus longivesicula a synonym of Hamacreadium interruptus and Bray & Cribb (1989) went further and listed it as a synonym of H. mutabile. The excretory vesicle reaches into the pre-bifurcal region. The eggs are distinctly smaller than those in H. cribbi (Fig. 3).
The description of this species was considered desirable as it is included in a wider study of opecoelid phylogeny and systematics based on LSU and SSU rDNA sequences. A small section of the resultant tree is included here as Figure 6 and details of the techniques are as in Bray et al. (2016). Hamacreadiummutabile is a widely reported parasite mainly of lutjanid fishes, and our worms from a lutjanid from New Caledonia, labelled as Hamacreadium ‘mutabile’, were identified as this species by Justine et al. (2012b). Morphologically this New Caledonian form appears practically identical to the Gulf of Mexico form, but the molecular evidence indicates that it is one of a group as closely related, but distinct, worms (Fig. 6). The Gulf of Mexico H. mutabile material (based only on a LSU rDNA sequence) is from the type-host in the eastern Gulf of Mexico, close to the type-locality of Dry Tortugas, Florida (Linton, 1910; Andres et al., 2014). Hamacreadiumcribbi clusters weakly with H. mutabile, it is probably more realistic to consider the Hamacreadium species to be related by a polytomy.
Our thanks are due to the many students who were involved in the collection of lethrinid parasites and are listed in Justine et al. (2010b).
The generation of sequences was funded by a Life Sciences Molecular Taxonomic Support grant from the Natural History Museum, London.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
All applicable institutional, national and international guidelines for the care and use of animals were followed. Annual permits for collecting fish and parasites were issued by Province Sud, New Caledonia, to IRD, from 2003 to 2010.
|Funder Name||Grant Number||Funding Note|
|Life Sciences Molecular Taxonomic Support grant from the Natural History Museum, London|
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