Raillietiella morenoi sp. n. (Pentastomida) from Gallotia atlantica (Peters and Doria, 1882) (Lacertidae) in the Canary Islands

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Parasitol Res (2006) 98: 425 429 DOI 10.1007/s00436-005-0068-9 ORIGINAL PAPER N. Abreu-Acosta. P. Foronda Rodriguez. B. Valladares. J. C. Casanova Raillietiella morenoi sp. n. (Pentastomida) from Gallotia atlantica (Peters and Doria, 1882) (Lacertidae) in the Canary Islands Received: 30 September 2005 / Accepted: 18 October 2005 / Published online: 28 December 2005 # Springer-Verlag 2005 Abstract Raillietiella morenoi sp. n., a new cephalobaenid pentastomid found in the lungs of Gallotia atlantica collected in the Canary Islands, is described. The new species belongs to the sharp-tipped posterior-hook type. The annulus number, morphology, and dimensions of copulatory spicules and the dimensions of anterior and posterior hooks separate Raillietiella sp. n. from the other raillietiedid sharp-tipped posterior-hook species of small lizard parasites in Africa. The host character of endemic protected species of G. atlantica in Alegranza Island posed great difficulty in obtaining more parasite materials. However, more studies are required to state the variability of this species and its possible distribution in other species in the Canary Islands, as well as in other Gallotia spp. Introduction Pentastomids of the genus Raillietiella Sambon, 1910, which has a sharp-tipped posterior hook and infects predominantly insectivorous small lizards, are a reduced species group with representatives in Australia, Africa, and America (Ali et al. 1985). These species are classified as N. Abreu-Acosta. P. Foronda Rodriguez (*). B. Valladares Department of Parasitology, Ecology, and Genetics, Faculty of Pharmacy, University of La Laguna, Avda. Astrofísico Fco. Sánchez s/n, 38203 Tenerife, Canary Islands, Spain e-mail: pforonda@ull.es Tel.: +34-922-318486 Fax: +34-922-318514 J. C. Casanova Laboratory of Parasitology, Faculty of Pharmacy, University of Barcelona, Avda. Diagonal s/n, 08028 Barcelona, Spain group I and are separated from blunt-posterior-hook species in small lizards, which are classified as group II (Ali et al. 1985). During a survey on the endoparasitic fauna of the endemic Atlantic lizard Gallotia atlantica (Peters and Doria, 1882) in Alegranza Island, cephalobaenid pentastomids were isolated from the lungs of two individual hosts. In this paper, both a description and a graphic representation of these parasitic individuals are presented. Materials and methods The Canary Islands are situated in the northeast Atlantic Ocean between 27 37 and 29 24 N and 13 23 and 18 8 W. Alegranza is one of the islands situated close to the continent at approximately 110 km off the northwest coast of Africa (Cabo Jubi). The island is uninhabited and belongs to a protected preserve. G. atlantica (Lacertidae) and Tarentola angustimentalis (Geckonidae), which are endemic species in the Canary Islands, are the only two reptiles that live on Alegranza. In the case of G. atlantica,it inhabits the islands of Lanzarote and Fuerteventura and the eastern islets, and there is a small introduced population on the east of Gran Canaria. In July 2000, the Canarian Government allowed the capture of ten individuals of each reptile species in Alegranza for parasitological study. Hosts were captured with live pitfall traps in Los Hornitos (G. atlantica) and El Cortijo (T. angustimentalis). The hosts were dissected after cervical dislocation, and live endoparasites were recovered from viscerae. Lung pentastomids were isolated from two individuals of G. atlantica (a male, an immature female, and a mature female), relaxed in saline solution (9% NaCl), and preserved in 70% ethanol prior to examination. Parasites were examined under a microscope. Annulus counting and both hook and spicule measurements were carried out following the methods described in Ali et al. (1981, 1982a c, 1984a,b). The maturity of the female was estimated from the percentage of fully developed eggs in the uterus, as stated by Ali and Riley (1983).

426 Results Description of Raillietiella morenoi sp. n. The typical morphology of Raillietiella Sambon, 1910 from small lizards (Pence and Canaris 1973; Riley and Heideman 1998) is presented as follows: Male (holotype) Claviform-type morphology wider in the region of copulatory spicules, with gradual tapering posterior to bifid tail Holotype male: 5.7 mm long (Fig. 1d) Copulatory spicules curved (Fig. 1a) Base flaved and rounded hollow back involved in the sleeve of chitin Ornamented base overall length 124.2 μm, with opposite hollow back 631.5 μm long Oral cadre with 93.2 μm external diameter Female (allotype) Claviform-type morphology widest in the region of the first annuli, with gradual tapering posterior to bifid tail Allotype mature female: 25 mm long, with 36 annuli (Fig. 2h) Anterior hook: 258 (AB) 278 (BC) μm (Fig. 2e) Posterior hook: 309 (AB) 401.7 (BC) μm (Fig. 1c) and 236 (AB) 309 (BC) μm Oral cadre with 144.9 μm external diameter (Fig. 1b) Eggs: 84.2 53 μm (Fig. 2g) Taxonomic summary Type specimens: holotype male (TFMC/PE1), allotype female (TFMC/PE2), and paratype female (TFMC/ PE3) preserved in 70% ethanol in the parasite collection of the Natural History Museum of Tenerife Type host: G. atlantica (Peters and Doria, 1882) Common name: Atlantic lizard Fig. 1 Raillietiella morenoi sp. n. a The paired copulatory spicules of the holotype male. b Details of the oral cadre and the pharynx of the female holotype. c Details of a hook. d Head of the cleared male holotype showing the oral cadre, with two pairs of hooks relative to the copulatory spicules

427 Fig. 2 R. morenoi sp. n. e Anterior part of the cleared female allotype. f Eggs in the uterus. g Eggs. h Total female allotype Type locality: 27 37 and 29 25 N, 13 20 and 18 10 W, Los Hornitos, Alegranza, Canary Islands Site of infection: lung Prevalence of host: 2/10 Etymology: specific name referring to Juan Carlos Moreno ( Área de Medio Ambiente ), General Director of the Canary Government, who allowed the collection of the host material Remark The genus Raillietiella has been included several times in the families Cephalobaenidae Heymons, 1922 and Raillietiellidae Sambon, 1922 in the order Cephalobaenida and, more recently, in Raillietiellida (de Oliveira Almeida and Lindsey Christoffersen 1999), which is not in accordance with recent works (Riley et al. 2003; Spratt 2003). The taxonomy and systematics of the pentastomid genus Raillietiella were reviewed by Ali et al. (1985) in the description of Raillietiella cartagenensis and in the redescription of Raillietiella amphiboluri (Mahon, 1954), Raillietiella kochi (Heymons, 1926), Raillietiella shipleyi (Heimons, 1926), and Raillietiella indica (Gedoelst, 1921). Ali et al. (1985) reorganized the known and valid species of Raillietiella into five groups (small lizards, varanid lizards, amphisbaenians, snakes, and amphibians), which are mainly based on host characteristics (host type, ecology,

428 Table 1 Metrical data of raillietiellids possessing sharp-tipped hooks and infecting insectivorous lizards Species Female Male R. amphiboluri (Mahon, 1954) R. chamaeleonis (Greillat and Brygoo, 1959) R. aegypti (Ali, Riley, and Self, 1982) Length (mm) [mean (range)] Annulus number [mean (range)] Posterior hook Length (mm) Annulus number Posterior hook AB BC [mean (range)] [mean (range)] AB BC 32 (20 44) 32.5 (30 34) 208 (200 220) 370 27 29 15 18 17 22 277 6.5 23 26 26 (25 27) 247 (237 267) (61 69) (190 200) 384 (366 410) (315 325) <11 22 (21 24) 135 (118 153) (3.9 4.7) R. cartaginensis (Ali, Riley, and Self, 1985) R. morenoi sp. n. 25 36 309 401.7 5.7 30 192 267.8 Sources: Ali et al. (1985) and Greillat and Brygoo (1959) 212 (148 238) and zoogeography) (Riley and Heideman 1998). Two of these groups (groups I and II; after Ali et al. 1985) include species infecting small insectivorous lizards and are easily differentiated by the initial ideas of Self (1969) in species with sharp-tipped posterior hooks (group I) and blunt-tip posterior hooks (group II). Species differentiation in these two groups is mainly based on a combination of characteristics, including body size, annulus number, posterior-hook dimensions, and size and shape of the male copulatory spicule (Riley and Heideman 1998). The sharp-tipped posterior-hook Raillietiella includes four well-characterized species (Ali et al. 1985): R. amphiboluri Mahon, 1954 in Australian bearded lizard Amphibolurusbarbatus; Raillietiella chamaeleonis Gretillat and Brygoo 1959 in Chamaeleo oustaleti and Chamaeleo verrucosus from Madagascar; Raillietiella aegypti Ali, Riley, and Self, 1982 in different small lizards from Egypt; and R. cartagenensis Ali, Riley, and Self, 1985 in Hemidactylus sp. and Gonatodes sp. from Colombia. The reported presence of Raillietiella affinis Bovien, 1927 in Lepidactyluslugutris from the British Salomon Island awaits confirmation (Ali et al. 1982a) and also that in Lioheterodonmodestus from Madagascar due to the inclusion of R. chamaeleonis as a host (Gretillat and Brygoo 1961). Raillietiella sp. n. could be distinguished from Raillietilla sharp-hooked species of small lizards at the level of males and mature females (Table 1). Different combinations of characteristics, such as measurements of body length, annulus number, anterior-hook and posterior-hook size, and dimensions of the copulatory spicule, differentiate Raillietiella sp. n. from other similar species in group I of Ali et al. (1985). Posterior hooks of both sexes in the new species are substantially larger than those described in the latter species. There is only an overlap in the length of the hook (dimension BC) with mature females of R. aegypti only. The taxonomic and systematic morphological characteristics stated by Ali et al. (1985) and others referring to male hooks (Riley and Heideman 1998) are reliable in distinguishing group I Raillietiella spp. and in separating Raillietiella sp. n. from the rest. More specimens are required in order to state the variability of this species, but the endemic character of the hosts and the status of the protected species make it difficult to obtain more specimens for parasitological studies. Lacertids of the genus Gallotia are endemic species of the Canary Islands. Lizard fauna of the genus Gallotia comprises seven species all endemic in the Canary Islands and represented by at least ten subspecies with restricted distribution in a particular island (Delgado 2001). G. atlantica is an omnivorous lizard that feeds mainly on arthropods. The Gallotia species living in the Canary Islands have been surveyed for endoparasites, but no species of pentastomid have been reported (Cordero del Campillo et al. 1994). This is the first report of a pentastomid in a reptile species from the Canary Islands. Known endoparasites from Canarian lacertids and geckonids are restricted to platyhelminths and nematodes (Cordero del Campillo et al. 1994). In view of the parasitic helminth fauna found in Gallotia spp. and Tarentola spp. in Canarian islands other than Alegranza, it is clear that host isolation offers a good scenario for parasitic speciation, particularly in oxyurid nematodes. Moreover, the helminth fauna of Gallotia spp. reveals similar characteristics (Fain and Bannert 2000). This phenomenon is also known to be present in the endoparasitic fauna of reptiles in Madagascar and concretely in pentastomids (Gretillat and Brigoo 1959; Gretillat et al. 1962). Acknowledgements We wish to thank the Exmo. Cabildo Insular de Lanzarote for permission to capture samples of G. atlantica in Alegranza Island, as well as the Exmo. Cabildo Insular de Tenerife and 2001 SGR00088 project by the Comissionant por la Recerca y Universitats de la Generalitat de Catalunya (Catalonia Government) for their support.

429 References Ali JH, Riley J (1983) Experimental life-cycle studies of Raillietiella frenatus Ali, Riley, Self, 1981: pentastomid parasites of Geckos utilizing insects as intermediate host. Parasitology 86:147 160 Ali JH, Riley J, Self JT (1981) A revision of the taxonomy of the blunt-hooked Raillietiella, pentastomid parasites of African, South-East-Asian and Indonesian lizards, with a description of a new species. Syst Parasitol 3:193 207 Ali JH, Riley J, Self JT (1982a) A description of a new species of Raillietiella (Pentastomida: Cephalobaenida) from Egyptian lizards with a reassessment of the taxonomic status of Raillietiella geckonis (Diesing, 1850) Sambon, 1910 and Raillietiella affinis Bovien, 1927. Syst Parasitol 4:169 180 Ali JH, Riley J, Self JT (1982b) A revision of the taxonomy of Raillietiellaboulengeri (Vaney and Sambon, 1910) Sambon, 1910, R. orientalis (Hett, 1915) Sambon, 1922 and R. agcoi Tubangui and Masiluñgan, 1956 (Pentastomida: Cephalobaneida). Syst Parasitol 4:285 301 Ali JH, Riley J, Self JT (1982c) Amphibians as definitive hosts for pentastomids: Raillietiella bufonis n. sp. from Bufo lemur in Puerto Rico and a reassessment of Raillietiella indica Gedoelst, 1921. Syst Parasitol 4:279 284 Ali JH, Riley J, Self JT (1984a) A revision of the taxonomy of pentastomid parasites (genus Raillietiella, Sambon, 1910) from American snakes and amphisbaenians. Syst Parasitol 6:87 97 Ali JH, Riley J, Self JT (1984b) Further observations of blunthooked raillietiellids (Pentastomida: Cephalobaneida) from lizards, with descriptions of three new species. Syst Parasitol 6:147 160 Ali JH, Riley J, Self JT (1985) A review of the taxonomy and systematics of the pentastomid genus Raillietiella Sambon, 1910 with a description of a new species. Syst Parasitol 7:111 123 Cordero del Campillo M, Castañón L, Reguera A (1994) Índice- Catálogo de Zooparásitos Ibéricos, 2nd edn. Secretariado de Publicaciones, Universidad de León, León Delgado G (2001) División Chordata. In: Izquierdo I, Martín JL, Zurita N, Arechavaleta M (eds) Lista de especies silvestres de Canarias (Hongos, Plantas y Animales terrestres) 2001. Consejería de Política territorial y Medio Ambiente Gobierno de Canarias, pp 285 290 de Oliveira Almeida W, Lindsey Christoffersen M (1999) A cladistic approach to relationships in Pentastomida. J Parasitol 85 (4):695 704 Fain A, Bannert B (2000) Two new species of Ophionyssus Megnin (Acari: Macronyssidae) parasitic on lizards of the genus Gallotia boulenger (Reptilia: Lacertidae) from the Canary Island. Int J Acarol 26(1):41 50 Gretillat S, Brygoo ER (1959) Raillietiella chamaeleonis n. sp. Première espèce de Cephalobaenidae (Pentastomida) signalèe a Madagascar. Ann Parasitol Hum Comp 34(1 2):12 20 Gretillat S, Brygoo ER (1961) Les dilatateurs de copulation chez Raillietiella (Heimonsia) hemidactyli et valeur taxonomique possible de ces organes chez les Pentastomida. Arch Inst Parasitol Madagascar 29:71 74 Gretillat S, Brygoo ER, Domergue CA (1962) Pentastomes de reptiles malgaches. Ann Parasitol Hum Comp 37:295 313 Pence DB, Canaris AG (1973) Observations on the pentastome Raillietiella gehyrae Bovien, 1927 (Cephalobaenida: Cephalobaenidae) from Mabuya homalocephala in Kenia. Z Parasitenkd 41:1 10 Riley J, Heideman NJL (1998) A new blunt-hooked pentastomid belonging to the genus Raillietiella Sambon, 1910, from two species of agamid lizards in Namibia. Syst Parasitol 41:41 46 Riley J, Oaks JL, Gilbert M (2003) Raillietiella trachea n.sp., a pentastomid from the trachea of an oriental white-backed vulture Gyps bengalensis taken in Pakistan, with speculation about its life-cycle. Syst Parasitol 56:155 161 Self JT (1969) Biological relations of the Pentastomida. A bibliography on the Pentastomida. Exp Parasitol 24:63 119 Spratt DM (2003) Rileyella petauri gen. nov., sp. nov. (Pentastomida: Cephalobaenida) from the lungs and nasal of Petaurus breviceps (Marsupialia: Petauridae) in Australia. Parasite 10:235 241