A comparative study of five periodic human strains of Brugia malayi, originating from India, China, Korea, Malaysia and Indonesia, is given. This morphological analysis is based on males; the "standard" characters (oesophagus, papillae, spicules...) appear identical. On the contrary, the cuticular ornamentation of the posterior region--which is composed of the area rugosa and of a system of bosses and constitutes a secondary non-skid copulatory apparatus--differs following the geographical origin of the strain. A key is given, based on this character. 1(2) At 800-1,200 micron from the tip of tail, numerous cuticular bosses present on the right side of the body (fig. 2 and 8 B). 2(1) At 800-1,200 micron from the tip of tail, cuticular bosses absent or scarce on the right side of the body (fig. 8 D). 3(4) At 1,800-1,200 micron from the tip of tail (fig. 4), scarce and slightly projecting cuticular bosses on the dorsal side of the body contrasting with well projecting lateral cuticular bosses (fig. 9 E and F). Anterior extremity of the area rugosa made by a few stripes of tiny bosses linked transversally (fig. 9 A). 4(3) At 1,800-2,200 micron, numerous cuticular bosses on the dorsal side of the body (figs. 5, 6 and 7). Anterior extremity of the area rugosa made by the stripes of longitudinal rods (fig. 9C). 5(6) Oblong transversally stretched cuticular bosses on the dorsal and left sides of the body, anteriorly to the area rugosa (fig. 5); big oblong bosses on the left side (fig. 9 B). Transversal wrinkles and stripes of rods absent on the dorsal side of the body. 6(5) Round cuticular bosses on the dorsal and left sides of the body anteriorly to the area rugosa (figs. 6 and 7): no big oblong bosses on the left side. Transversal wrinkles or stripes of rods present on the dorsal side of the body (fig. 9 D). Nomenclaturally, such differences could be used in defining different taxa, but it could be useful to perform "blind determination" (material without labelling), to study conveniently the morphology of microfilariae (often an excellent indication for speciation in that group of Nematodes) and, evenly, to proceed to parallel studies on isoenzymes. However, whatever could be the taxonomical conclusion, the differences observed in Brugia malayi originating from different regions appear to the sufficient to consider the existence of four distinct diseases.
Many trichostrongyloid species parasitizing rodents in Malaysia were described in 1967 in a thesis that was never published. Some of these species have since been redescribed sometimes with, sometimes without reference to the thesis. The remaining species are redescribed using information given in the thesis and certain additional morphological data (in particular, the synlophe) taken from study of the paratypes. The species are reclassified according to criteria established in the most recent classification. The following genera are proposed: Brevistriatinae: - Macrostrongylus n. gen. characterized by a caudal bursa of Calypsostrongylus type and absence of synlophe. Nippostrongylinae: - Malaistrongylus n. gen. characterized by a synlophe of Heligmonoides type but with a larger number of ridges and by the fusion of rays 4 and 5 in the caudal bursa. - Rattus strongylus n. gen. characterized by small, subequal dorsal left ridges and a total number of ridges less than 20. - Sabanema n. gen. characterized by small subequal dorsal left ridges and a total number of ridges greater than 30. The species under consideration are the following: Hepatojarakus malayae Yeh, 1955; Pithecostrongylus bicapitatus n. sp. (= P. bicapitatus Ow Yang, 1967, in litt); Macrostrongylus ratti n. gen., n. sp. (= Macrostrongylus ratti Ow Yang, 1967, in litt.); Calypsostrongylus malayensis Durette-Desset, 1976 (= Brevistriata malayensis Ow Yang, 1967, in litt); Fissicauda callosciuri (Supperer et Kutzer, 1964); Fissicauda brevispicula n. sp. (= Brevistriata brevispicula Ow Yang, 1967, in litt.); Nippostrongylus brasiliensis (Travassos, 1914); Orientostrongylus tenorai Durette-Desset, 1970 (= Longistriata selangora Ow Yang, 1967, in litt.); O. krishnansamyi Durette-Desset et Lim-Boo-Liat, 1974 (= Longistriata malaccae Ow Yang, 1967, in litt.); Heligmonoides bulbosus n. sp. (= Heligmonina (Heligmonoides) bulbosa Ow Yang, 1967, in litt.); Heligmonoides lanceolatus n. sp. (= Heligmonina (Heligmonoides) lanceolata Ow Yang 1967, in litt.); Malaistrongylus odontospicularis n. gen., n. sp. (= Malaistrongylus odontospicularis Ow Yang, 1967, in litt.); Paraheligmonelloides triangulus n. sp. (= Longistriata triangulum Ow Yang, 1967, in litt.); P. annandalei n. sp. (= Longistriata annandalei Ow Yang, 1967, in litt.); P. rajah n. sp. (= Heligmonina (Heligmonoides) rajah Ow Yang, 1967, in litt.); Rattustrongylus odontoconus n. gen., n. sp. (= Longistriata odontocona Ow Yang, 1967, in litt.); R. rotundoconus n. sp. (= Longistriata rotundocona Ow Yang, 1967, in litt.); Sabanema sabana n. gen., n. sp. (= Longistriata sabana Ow Yang, 1967, in litt.); S. kepongi n. sp. (= Longistriata kepongi Ow Yang,
Edesonfilaria cynocephali n. sp., a parasite of Cynocephalus variegatus taylori (Thomas) in Malaysia, is described. Makifilaria Krishnasamy et coll., 1981 is placed in synonymy with Edesonfilaria and the new combination E. inderi (Krishnasamy et coll., 1981) n. comb. is proposed. Edesonfilaria and the closely related genus Macacanema constitute a small evolutionary line of Filariae with a hyperspecialized oesophagus (the glandular portion lacks lumen); the line is restricted to the Indo-Malaysian region and occurs in arboreal Dermopterans, Chiropterans and Primates.
A description is given of cercarial chaetotaxy of two Centrocestinae (Heterophyidae, Opisthorchioidea) from Malaysia: Centrocestus formosanus and Centrocestus sp.--Comparison with cercarial chaetotaxy of taxonomically related groups indicates that 1. The chaetotaxy of the Centrocestinae agrees with that of other Opisthorchioidea, 2. There is an important difference between chaetotaxy of Centrocestinae and other Heterophyidae which suggest that the family is heterogeneous.
Onchocerca dewittei n. sp. was collected from a wild Boar at the metatarse level (tendons and subcutaneous connective tissue); it can be differentiated from other species by the female cuticle showing straight ridges which overlap in the lateral fields, and by its relatively thick microfilaria (length 228-247 mu and width 6-7 mu). This suidean Onchocerca displays some primitive characters such as straight ridges and persistency of ten pairs of caudal papillae in the male; but as a whole this species is undoubtedly more highly evolved than O. raillieti Bain, Müller and coll., 1976, a parasite of Equidae.
Hepatocystis bainae n. sp., parasite on the Microchiropteran bat, Hipposideros galeritus is described and differentiated from Hepatocystis rodhaini; it is characterized by the type of the microgametocytes ("diffuse"), the small size of the hepatic schizonts and the repartition of the colloide.
An immature merocyst of Hepatocystis malayensis and gametocytes of H. brayi were studied with the electron microscope. The merocyst consisted of a highly complex cytoplasmic reticulum ramifying through an amorphous matrix: the entire complex was enclosed by a simple unit membrane. The host cell was apparently destroyed completely during growth of the cyst. Immature gametocytes were highly amoeboid and showed extensive vacuolisation or attenuation of the cytoplasm. The nucleus contained one or two prominent nucleoli. Mature gametocytes had compact cytoplasm and contained pyriform osmiophilic bodies which were believed to function in the release of the parasites from the host cells. Macrogametocytes were distinguished from microgametocytes by cytoplasmic differences in numbers of ribosomes, and cristate mitochondria and in the extent of development of the smooth endoplasmic reticulum. The compact nuclei of the macrogametocytes had inconspicuous DNA but prominent nucleoli whereas those of the microgametocytes were irregular and showed a central aggregate of DNA. In microgametogenesis karyokinesis of the parent nucleus was delayed until axoneme formation was complete. Then the nuclear buds were extruded into emerging microgametes. At fertilisation the plasmalemmas of the two gametes fused and the single axoneme and nucleus of the microgamete moved into the cytoplasm of the macrogamete.
Description of four new species of Heligmosome Nematodes parasites of the gut of Trichys lipura: --Heligmonella limbooliati n. sp. has a synlophe of Heligmonella-type and a bursa related to Cordicauda. --Cordicauda trichysi n. sp. is characterized by the relatively small dorsal lobe of the bursa, numerous cuticular ridges and the origin of the 8th rib at the distal third of the dorsal rib. --C. malayensis is closely related to C. trichysi (the female of the two species are morphologically identical but the two species can be separated by the larger dorsal lobe of the bursa and the longer spicula of C. malayensis). --C. magnabursa n. sp. is separated from the other species of the genus by the peculiar morphology of the bursa and the female's tail, dorsally bent. The fauna of Trichys is compared to that of Atherurss africanus, which is parasitized by 8 coparasites species: One Heligmonella and seven Paraheligmonina. From a phyletic as well as an ecological point of view (relative abundance and species location in the gut) the two fauna seem to have evolved in a parallel way, one in Africa, one in Asia, from a single Heligmonella type Nematode, after the host's partition.
Tarsubulura perarmata (Ratzel, 1868) is described from a primate Tarsius bancanus and from Tupaidae: Tupaia glis and T. minor in Malaysia (Kuala Lumpur). Its biological cycle is done by the experimental infestation of crickets belonging to the genera Valanga and Oxya. The infective larvae are obtained after three weeks of development of 28 degrees C in the intermediate host. They differ from third stage larvae obtained from Subulurinae by the development of cuticular pharyngeal lobes. The early apparition of this ontogenetic character confirms the isolation of the genus Tarsubulura as compared to the general evolution of the Subuluridae.
Eimeria nebulosa n. sp. and Klossia pachyleparon n. sp. are described from the monitor lizard Varanus nebulosus in Malaysia. The flask shaped oocysts of E. nebulosa average 20.7 by 12.6 mum. The oocyst wall is composed of a single layer. There is a single polar granule but no residuum. Ellipsoidal sporocysts average 11.1 by 5.6 mum. A sporocyst residuum is present. Endogenous stages develop in the epithelial cells of the small intestine. The splerical oocysts of K. pachyleparon average 33.6 mum in diameter. The wall is about 2.5 mum thick and is composed of 3 layers. The spherical sporocysts average 10.8 mum in diameter. Sporocysts contain 4 sporozoites and residuum. Developmental stages were not observed.
Description of the male Pterygodermatites nycticebi (Mönnig, 1920) unknown until the present study, and a study of the cephalic and cuticular structures of the female. This rictularid has a morphological evolution comparable to that of other males of the Rictulariidae parasitic in viverrid carnivores and in primates.
Redescription of the female of Setaria thomasi Sandosham, 1954, parasite of Sus scrofa jubatus; description of the female of Papillosetaria malayi n.sp. from Tragulus javanicus. The study of the buccal region of Papillosteria leads the authors to consider this genus as an ancestral form of Setaria.
Description of Trichospirura willmottae n. sp. parasite of the salivary ducts of Tupaia glis and T. sp. (single virgin female) parasite of the intestine of Myotis mystacinus in Malaysia. The two species are very closely related to the type species, a parasite of the pancreatic ducts of brasilian Primates, and can be differentiated mainly by the mensurations of the posterior extremities of the bodies. While the genus Rhabdochoma, parasite of the intestine of fresh-water fishes, underwent a very similar, but more or less pronounced, morphological evolution, it became adapted to many different hosts: Sea-fishes, Saurians, Mammals and to many locations. This evolutionary line includes six genera; Trichospirura, the only parasite in Mammals, is one of the more evolved. Some remarks are made on the host-distribution of Trichospirura, on the relationships between Rabdochonidae and Cystidicolidae and on the osmo-excretory apparatus of Trichospirura. The hypertrophy of this apparatus, which could be the consequence of the passage during the course of evolution from aquatic to terrestrial life, is comparable to that of the Pneumospirurinae.
Morphological study of two Spirura parasites of the oesophageal and the gastric wall of Tupaia and Nycticebus in Malaysia. -- Spirura malayensis n. sp. is found both in Tupaia in the District of Selangor (West Malaysia) and in Nycticebus coucang in Borneo. Its very primitive characteristics relate it to S. diplocyphos Chabaud, Brygoo and Petter, 1965, parasite of lemurs from Madagascar. Its larval development was obtained experimentally in Blatella germanica. -- Spirura aurangabadensis (Ali and Lovekar, 1966) described from a microchiroptera in India is found in west Malaysia in a Nycticebus coucang, and in a Tupaia glis. -- The distribution of the different species and the comparative study of the larval and adult cephalic structures show that the genus Spirura arose and became diversified in the old world in very primitive hosts according to two main evolutive lines.
1. a) List of Nematodes collected by Professor Aellen in european Microchiroptera. Additionnal morphological data to the study of Molinostrongylus alatus, M. panousei, M. skrjabini. Description of M. aelleni n. sp. b) Description of M. richardae n. sp., M. benexae n. sp. et M. bauchoti n. sp., parasites of malagasian Molossidae. c) Description of M. colleyi n. sp. and M. owyangi n. sp., parasites of Malaysian Vespertilioninae, and of Allintoschius dunni n. sp., discovered in Myotis mystacinus from Malaysia and Pipistrellus nanus from Africa. 2. Taking into account the characteristics of the synlophe, the 17 species of the genus Molinostrongylus may be divided into five groups, each one being reasonably well characteristic of the genus of their Chiropteran host. 3. The composition of the Trichostrongyloidea fauna of Chiroptera and its relationship with Trichostrongyloidea from other Mammals (Tupaiidae, Pholidotes, Primates, Sciuridés) are analysed. Six groups are separated and divided into two well defined lines: 1) genus Strongylacantha, and 2) 12 genera stemming more or less directly from the Molineinae, 4. The three conical outgrowths at the tip of the female tail which differenciate presently the Anoplostrogylinae from the Molineinae appear to be an unreliable characteristic. The two subfamilies form a complex group which will be better understood if the evolution of the synlophe and that of the caudal bursa of the males are taken into account.
Description of a new species of Oxyurid: Syphacia (Syphatineria) callosciuri n. sp. parasite of a Sciurid rodent Callosciuris caniceps in Malaysia. In rodents belonging to the genus Callosciurus in Malaysia two species: S callosciuri n. sp. and S. owyangi Quentin, 1975, show morphological characteristics which are intermediate between the primitive Syphacia and two different lines of species parasite of recent rodents. These observations appear to indicate that the adaptation of Syphacia of Sciurids to the modern rodents has occured in South-East Asia.