V. Radev

REDESCRIPTION OF ECHINOSTOMA TRIVOLVIS (CORT, 1914) (TREMATODA: ECHINOSTOMATIDAE) WITH A DISCUSSION ON ITS IDENTITY

The life-cycle of Echinostoma trivolvis (Cort, 1914) has been completed experimentally and the validity and identity of this species are discussed. Synonyms for cercariae and adults of E. trivolvis are as follows: Cercaria trivolvis Cort, 1914, C. trisolenata Faust, 1917, C. acanthostoma Faust, 1918, C. complexa Faust, 1919; Distoma echinatum Zeder, 1803, of Leidy (1888, 1904) and Hassall (1896); E. echinatum (Zeder, 1803) of Hassall (1896), Stiles & Hassall (1895), Barker & Laughlin (1911), Barker (1916) and Swales (1933); E. revolutum (Frölich, 1802) Dietz, 1909 of Johnson (1920), Fallis (1934), Beaver (1937) and Fried & co-workers (1968–1989); E. armigerum Barker & Irvine, 1915; E. coalitum Barker & Beaver, 1915; E. callawayensis Barker & Noll, 1915; E. paraulum Dietz, 1909 of Miller (1937); E. multispinosum Vigueras, 1944; and Echinoparyphium contiguum Barker & Bastron, 1915. The first intermediate host is the planorbid snail Helisoma trivolvis. Second intermediate hosts are various pulmonate and prosobranch snails, mussels, planarians, fishes, frogs, tadpoles and freshwater turtles. Final hosts are various birds and mammals. E. trivolvis occurs only in North America.

LIFE HISTORY AND IDENTIFICATION OF PHILOPHTHALMUS LUCIPETUS FROM ISRAEL

A Philophthalmus species whose larval stages have been isolated from Melanopsis praemorsa snails collected in Israel and formerly identified as probably belonging to Philophthalmus palpebrarum has now been reevaluated as belonging to Philophthalmus lucipetus. The present determination is based on a detailed study of all the stages of the parasites life cycle--eggs, intramolluscan stages, cercariae, and adults. They were compared to the original species P. lucipetus, recently reexamined and redescribed from source material in Vienna, Austria. The identity of the eyefluke from Israel and P. lucipetus was further confirmed by successful cross-infections employing miracidia of the Israeli isolate in European (Bulgarian) Fagotia acicularis acicularis snails on the one hand and miracidia of P. lucipetus from Bulgaria in Israeli Melanopsis praemorsa on the other hand, but none infected Melanoïdes tuberculata snails from Israel.

LIFE CYCLE AND IDENTIFICATION OF AN EYEFLUKE FROM ISRAEL TRANSMITTED BY MELANOIDES TUBERCULATA (MÜLLER, 1774)

A philophthalmid species from Israel using the freshwater snail Melanoides tuberculata as intermediate host was studied. The biological and morphological characteristics of all developmental stages of the life cycle of this philophthalmid were described, and compared to those of Philophthalmus lucipetus Rudolphi, 1819 from Israel, Philophthalmus gralli Mathis and Leger, 1910 from Jordan, Philophthalmus palpebrarum Looss, 1899, Philophthalmus nocturnus Looss, 1907, Cercaria distomatosa Looss 1896 from Egypt, and Philophthalmus lucknowensis Baugh, 1962 from India. The possible identity with 1 of these species is discussed. On the basis of comparative analysis of the data for all parasite stages in the life cycle, geographical distribution, snail hosts, and snail host specificity, we propose to designate the Israeli Melanoides tuberculata-transmitted eye fluke to Philophthalmus distomatosa n. comb. (Looss, 1896), (Digenea: Philophthalmidae).

Collar spine models in the genus Echinostoma (Trematoda: Echinostomatidae)

This paper discusses collar spine arrangements in the genus Echinostoma. All arrangements are of uneven numbers of collar spines on the oral collar. The total number of collar spines in these arrangements ranges from a low 31 to a high 51. There are 11 models of collar spine arrangements in the Echinostoma consisting of spine numbers 31, 33, 35, 37, 39, 41, 43, 45, 47, 49, and 51. Representative species with these collar spine arrangements are given in the article. The number of collar spines in a species is identical in both the larval and adult forms. Reports of even numbered spine counts in the genus Echinostoma are erroneous and probably reflect counts on worms with lost, retracted, or supernumerary spines.

Life-cycle, delimitation and redescription of Catatropis verrucosa (Frölich, 1789) Odhner, 1905 (Trematoda: Notocotylidae)

The life-cycle of Catatropis verrucosa (Frölich, 1789) Odhner, 1905 has been completed experimentally starting from infected snails collected along the River Danube in Europe. Each stage of the life-cycle is redescribed. Taxonomic problems are discussed and the main features of the species are listed. Synonyms for C. verrucosa are Fasciola verrucosa Frölich, 1789, F. anseris Gmelin, 1790, Monostoma verrucosa (Frölich, 1789) Zeder, 1800, and Catatropis charadrii Skrjabin, 1915. Other names, such as Notocotylus triserialis Diesing, 1839, Notocotyle triseriale (Diesing, 1839) Diesing, 1850, Monostoma verrugueux Dujardin, 1845, “Monostoma sp. du canard” of Blanchard (1847), Notocotyle verrucosum (Frölich, 1789) Monticelli, 1892, N. verruqueux Railliet, 1895, and Distoma verrucosum (Frölich, 1789) Wolffhugel, 1900, were found to represent adults and/or larvae of C. verrucosa. Conversely, but less often, adults and larvae of other species were found described and illustrated as C. verrucosa. One of these, C. verrucosa of Joyeux (1922), was renamed Pseudocatatropis joyeuxi Kanev & Vassilev, 1986. Occasionally, authors actually working with C. verrucosa ascribed their results to different species. Based on experimental life-cycle studies, the following facts were demonstrated. (1) The first intermediate hosts are the prosobranch freshwater snails Bithynia tentaculata (Linnaeus, 1758) and B. leachi (Leach, 1818). (2) The same snails are also first intermediate hosts for Notocotylus imbricatus (Looss, 1893) Szidat, 1935, N. parviovatus Yamaguti, 1934, and N. ponticus Tschiaberaschvili, 1966. In all these species, the species characteristics are expressed by the adult morphology only, and the larvae cannot be identified by morphological criteria. It is proposed that tri-oculate monostome cercariae found in naturally infected B. tentaculata and B. leachi be referred to as “Cercaria imbricata group”. These cercariae include Cercaria imbricata Looss, 1893, C. helvetica I Dubois, 1928, C. triophthalmia Faust, 1930, C. fennica I Wikgren, 1956; C. ephemera of Lutta (1934); C. monostomi of Mathias (1925), Lutta (1934) and Zdun (1961), Cercaria Notocotylus attenuatus of Francalanci & Manfredini (1969), and Monostome cercaria I Emmel, 1943. (3) There is no second intermediate snail host in the life-cycle of C. verrucosa. (4) The final hosts are birds. (5) The adult worms possess, on the ventral body surface, a median ridge and two lateral rows of 12 (range 11–14) papillae per row.

Argentophilic Structures of the Miracidium of Echinostoma trivolvis (Cort, 1914) (Trematoda: Echinostomatidae)

Argentophilic structures of the miracidium of Echinostoma trivolvis were described from 80 specimens reared from material originally collected in eastern Pennsylvania, U.S.A. Miracidia were impregnated with 0.5% aqueous silver nitrate solution. The miracidium has 18 epidermal plates arranged in 4 rows of 6 + 6 + 4 + 2 = 18. Up to 20 papillalike structures on the terebratorium were arranged along 3 axes and in 5 groups. A single papilla was located at the base of each of the 6 epidermal plates of the first row. The eyespots were located posterior to the first row of plates and 2 excretory pores were located anterior to the last row of plates.

Identification problems with species in the Echinoparyphium recurvatum complex from physid snails in the USA

This study was done to help us answer numerous requests that we get about the identity of 45-collar-spined echinostomes in the genus Echinoparyphium. We examined 45-collar-spined cercariae from physid snails collected in Europe and the USA. Morphological observations of these cercariae showed considerable similarities in most of the characteristics we examined in these cercariae. Similar findings were made of adults obtained from natural and experimentally infected avian hosts in Europe and the USA. We suggest that these echinostomes be considered as species in the Echinoparyphium recurvatum complex, until further morphological and molecular studies be done on this group.

Argentophilic structures of miracidia and cercariae of Philophthalmus lucipetus (Philophthalmidae : Trematoda) from Israel

Argentophilic structures of Philophthalmus lucipetus miracidia and cercariae from Israel are described. Eighty-four of 87 miracidia examined displayed an epidermal plate arrangement of 6:8:4:2 = 20, similar to other Philophthalmus species. Twenty papilla-like structures are arranged on the terebratorium in 3 groups, along 1 axis. Sixteen body papillae are located at the bases of epidermal plates of row 1. Eyespots are mediodorsal, between rows 1 and 2. Excretory pores are lateral, between rows 2 and 3. Features common to Israeli and Bulgarian isolates, differentiating them from other species, include the presence of 16 body papillae as opposed to 10 in other species, and a maximum of 20 papillae on the terebratorium as opposed to 19 in the others. About 3% of the miracidia displayed different plate arrangements. Among the argentophilic structures of P. lucipetus cercariae, the Israeli and Bulgarian P. lucipetus show a common pattern of 2–4 excretory pores in the tail, but arrangement of cephalic CI3 and CI5 papillae in the 2 isolates is insufficiently unequivocal for species determination. The data presented show that miracidial characteristics, rather than those of cercariae, aid in determining the species of philophthalmids. They also support former evidence attesting to the identity of the Bulgarian and Israeli species.

ARGENTOPHILIC STRUCTURES OF THE MIRACIDIA AND CERCARIAE OF PHILOPHTHALMUS DISTOMATOSA N. COMB. FROM ISRAEL

The morphology and patterns of distribution of the argentophilic structures of miracidia and cercariae of Philophthalmus distomatosa n. comb. are described. The epidermal plate arrangement of the vast majority (94.2%) of miracidia studied conformed to the formula 6:8:4:2 = 20. The rest (5.8%) displayed the following patterns of arrangement of epidermal plates: 6:7:4:2 = 19; 6:6:4:2 = 18; and 6:4:4:2 = 16. Twenty papillalike structures were observed on the terebratorium. They were arranged along 1 axis, in 3 groups. Most commonly, 16 papillae were present on the body, located between epidermal plates of the first and second rows. The eye spots were located dorsally, near interepidermal space S1. The numbers, arrangements, and locations of the excretory pores varied. Patterns of distribution of the tegumentary papillae of P. distomatosa n. comb. cercariae are given, including those of the cephalic regions, periacetabular region, and tail. Argentophilic structures of the mentioned larval stages and of other parameters clearly distinguishing between the presently described species and those of P. lucipetus from Israel are summarized. On the basis of comparison of the presently described larval stages and those of other Melanoides tuberculata-associated larval stages of Philophthalmus in Israel and Jordan, the possibility exists that a third species occurs in Israel.

History of echinostomes (Trematoda).

Echinostomatidae (Trematoda) is the largest family within the class Trematoda. Members of this family have been studied for many years in relation to their utility as basic research models in biodiversity and systematics and also as experimental models in parasitology since they offer many advantages. Echinostomes have contributed significantly to numerous developments in many areas studied by parasitologists and experimental biologists. In this review, we examine the history of the echinostomebased studies from the beginnings to the present. For this purpose, we have divided the history of echinostomes into four periods (i.e. 18th and 19th centuries, first half of the 20th century, second half of the 20th century and the late 20th and 21th century) according to the types of studies performed in each of them. Moreover, we also briefly review the history of echinostome infections in humans.