versão impressa ISSN 1870-3453
Rev. Mex. Biodiv. v.79 supl.ago México ago. 2008
A new species of Lentiella (Cestoda: Anoplocephalidae) from Proechimys simonsi (Rodentia: Echimyidae) in Bolivia
Una especie nueva de Lentiella (Cestoda: Anoplocephalidae) de Proechimys (Rodentia: Echimyidae) en Bolivia
Terry R. Haverkost and Scott Lyell Gardner*
Harold W. Manter Laboratory of Parasitology W529 Nebraska Hall, The University of Nebraska State Museum, University of Nebraska, Lincoln, Nebraska 685880514, USA.
Recibido: 15 agosto 2007
Aceptado: 26 febrero 2008
During a biodiversity survey of mammals and their parasites in the Beni, Bolivia in the summer of 2000, several spiny rats, Proechimys simonsi Thomas, 1900, were collected and examined for parasites. Herein we describe Lentiella lamothei n. sp. from one of these hosts. This species is can be distinguished from L. machadoi Rêgo, 1964 by having a greater total length but smaller maximum width, a greater number of segments, a smaller cirrus sac, a smaller scolex diameter, and in the eggs, a larger pyriform apparatus. In addition, we formally validate the genus Lentiella Rêgo, 1964, that had been placed in synonomy with Monoecocestus Beddard, 1914.
Key words: Echimyidae, Departamento del Beni, Bolivia, Anoplocephalidae, Lentiella lamothei.
Como parte del monitoreo de la biodiversidad de Bolivia, varias ratas espinosas (Proechimys simonsi Thomas, 1900) fueron examinadas en busca de parásitos durante el verano boreal del año 2000. En el presente trabajo se describe el céstodo Lentiella lamothei n. sp. recolectado en estos hospederos. Esta especie puede distinguirse de L. machadoi Rêgo, 1964 por tener una mayor longitud total pero menor ancho máximo, mayor número de proglótidos, bolsa del cirro más pequeña, escólex de menor diámetro, y un mayor aparato piriforme en los huevos. Además, se revalida formalmente al género Lentiella Rêgo, 1964, anteriormente sinonimizado con Monoecocestus Beddard, 1914.
Palabras clave: Echimyidae, Departamento del Beni, Bolivia, Anoplocephalidae, Lentiella lamothei.
This contribution is one of the many publications that have resulted from data collected as a result of our collaborative, longterm expeditionary research on the biodiversity of mammals and their parasites from the Republic of Bolivia (Gardner and Campbell, 1992; Anderson, 1997; Dick et al., 2007; Notarincola et al., 2007). In the year 2000, research teams from the Museum of Southwestern Biology and the Harold W. Manter Laboratory of Parasitology traveled through eastcentral lowland Bolivia and collected small and mediumsized mammals and their parasites from the departments of Beni and Santa Cruz. The work was primarily focused on a survey of potential hosts for Machupo virus, the causative agent of Bolivian hemorrhagic fever. During this survey, many species of mammals were obtained, examined, and deposited in museums. From our work, several specimens of spiny rats (Proechimys simonsi Thomas, 1900) were collected and examined for parasites and 2 individuals were found to be infected with an undescribed species of anoplocephalid cestode.
Species of the genus Proechimys Allen, 1899 occur throughout lowland tropical evergreen forests of South America from eastcentral Honduras (P. semispinosus (Tomes, 1860)) south through northern Paraguay (P. longicaudatus (Rengger, 1830)). Proechimys simonsi is known to occur in suitable habitats in Ecuador, Peru, Bolivia, and western Brazil (Eisenberg and Redford, 1992; Wilson and Reeder, 2005). During work carried out in the north eastern part of South America, the anoplocephalid cestode, Lentiella machadoi Rêgo ,1964 was described from 8 whole specimens taken from the small intestine of an individual of Proechimys guyannensis (Geoffroy, 1803) collected in Abaeté, Estado do Pará, Brazil (Rêgo, 1964). In this paper Rêgo (1964) established the genus Lentiella based on morphological characters of the species L. machadoi. For clarity we reproduce the original diagnosis of the genus here:
Lentiella Rêgo (1964)
Diagnose. Anoplocefalídeos de reduzidas dimensões e siples genitália. Escolex e ventosas grandes. Pescoço inexistente ou reduzido. Proglotes mais largos que longos, com segmentação linear. Póros genitais regular ou irregularmente alternos. Testículos pouco numerosos, dispostos nap arte posterior do segmento, em fila contínua, posteriormente ao ovário e vitelino. Bôlsa do cirro, grande, provida de cirro espinoso. Vagina ventral á bôlsa do cirro. Ovário bastante lobado, ligeiramente antiporal, Vitelino compacto, de posição mediana nos segmentos, mas poral em relação ao ovário. Receptáculo seminal pequeno. Útero tubular, que se ramitica, mas não ocupa a parte posterior dos segmentos. Ovos con aparéelo piriforme pouco desenvolvido. Sistema excretor? Adultos em roedores.
As noted above, the details of the excretory system were not recorded; however, the general characteristics of the type species appear to be well enough defined that Rêgo (1964) was able to describe the species in a new genus (Lentiella n. gen.).
Beveridge (1994) examined the type specimens in the Helminthological Collection of the Instituto do Oswaldo Cruz (IOC 29.770a) and stated:
The testes lie in the posterior part of the medulla and the vagina, which is only clearly visible in 2 proglottids, opens to the genital atrium anterior to the cirrussac, in contradistinction to Rêgo's (1964) description. The uterus is prominently lobed and appears to be slightly reticulated; however, in the only specimen available, from the collection… …(IOC 29.779)[sic], the proglottids in which the critical stages of uterine development occur are damaged. More material is required for a detailed study of uterine development, and pending this, the genus is made a synonym of Monoecocestus.
We note here that in his description, Rêgo (1964) did not mention where the vagina enters the genital atrium; however, mediad from the genital atrium, the vagina passes ventrally to the cirrus sac. Therefore, based on our observations of both the description by Rêgo and of specimens that we collected in Bolivia, we verify that the genus Lentiella is valid and herein we describe a new species of anoplocephalid cestode collected from P. simonsi in the Beni Dept., Bolivia. The description is based on 5 fully developed specimens with gravid segments and sections of additional specimens.
Materials and methods
Captured mammals were processed immediately following standard protocols (Gardner, 1996). The complete gastrointestinal tract, liver, lungs, pleural, and peritoneal cavities were examined separately for helminths using a dissecting microscope. Cestodes found were placed immediately in a large volume of distilled water to relax the strobila for later morphological examination. Specimens were killed and preserved in either 10% formalin or 70% ETOH and were transported in the same solution to the laboratory for staining and subsequent study by light microscopy. Specimens used in the present study were stained in Semichon's acetic carmine or Erlich's acid hematoxylin, dehydrated in an alcohol series, cleared in terpineol and xylene, and mounted in Dammar gum. After staining, superficial tegument and tissues, including either dorsal or ventral longitudinal and transverse muscles, were removed from some specimens to allow observation of internal organs. Eggs were viewed by clearing a gravid proglottid with lactophenol and viewing free eggs with the aid of a microscope. Serial cross sections were prepared from one specimen to allow observation of the relative placement of organs.
All measurements were taken with the aid of an ocular micrometer. Figures were made with the aid of a drawing tube. Scolex length was measured from the anterior extremity to the posterior margin of the suckers. Neck length was measured from the posterior margin of the suckers to the first visible sign of segmentation. Genital pore alternation is presented as the number of times the genital pore switched sides per 100 proglottids. Thus, a higher number corresponds to more regular alternation. The widths of dorsal and ventral osmoregulatory canals were recorded at the midpoint of the proglottid on the antiporal side. Measurements of the cirrus sac were not taken if the cirrus was everted. Dimensions of the pyriform apparatus were measured from digital photographs. Testis distribution was measured as the distance between the 2 distal extreme testes (Haukisalmi et al., 2004). The index of asymmetry was calculated as the ratio of the distance between the midpoint of the vitellarium and the poral extremity/the total width of the proglottid (Sato et al., 1993). All measurements are provided in micrometers unless otherwise specified. Measurements provided include the mean measurement, followed by the range in parentheses, and the number of measurements if different than that given initially.
Measurements based on 5 whole gravid individuals from a single host. Measurements are summarized in Table I. Scolex 752 (673840) wide, 368 (341395) long. Suckers face laterally or anterolaterally. Width of suckers 293 (248348 n=20), sucker aperture 179 (132232 n=20). Neck 615 (360735) long, 502 (480540) wide at narrowest point. Specimens have 41 (3743) proglottids per gravid strobila. Strobila 19.4 (16.121.6) mm in total length. Width at widest point 1.37 (0.781.62) mm in mature proglottids. Immature proglottids 150 (120180) long, 894 (7801110) wide. Mature proglottids 449 (330660) long, 1323 (11101590) wide. Gravid proglottids 876 (780960) long, 1308 (12001500) wide. Genital pores alternate regularly, with an average of 90 (8296) switches per 100 proglottids.
The following measurements are based on 15 mature proglottids with 3 proglottids measured per strobila. Testes ovoid, 27 (1837) per proglottid, 47 (3266 n=75) in diameter. Testis distribution 522 (410650). Testes dorsal and ventral to transverse excretory canal. Cirrus sac 210 (123310) long, 120 (76158) wide. Internal and external seminal vesicle absent. Seminal receptacle 116 (73163) long, 69 (41107) wide. Vitelline gland 95 (70111) long, 96 (70114) wide. Index of asymmetry 0.61 (0.560.65). Ovary 224 (180284) long, 277 (234332) wide. Midline of ovary 801 (658983) from poral extremity, midline of vitelline gland 694 (573867) from poral extremity. Vagina dilated distally, when dilated, usually overlapping cirrus sac. Vaginal dilation reaching maximum length of 237 long and 114 wide, appearing in immature segments, not seen or absent in mature proglottids. Vagina 422 (316664) long, entering genital atrium anterior to cirrus sac. Uterus dorsal to seminal receptacle and ovary, ventral to testes, if contacted. Uterus crosses ventral excretory canals rarely, in gravid segments only. Uterus may cross osmoregulatory canals ventrally or dorsally. Gravid uterus with anterior, posterior, and lateral diverticula. Genital organs crossing excretory canals dorsally. Dorsal and ventral excretory canals present. Ventral canals 25 (1639) in width, dorsal canals 13 (421) wide, transverse canals 18 (843) wide. Eggs round, 46 (4351 n=25) in diameter containing an oncosphere 12 (1014 n=25) wide surrounded by pearshaped pyriform apparatus. Pyriform apparatus simple, with 2 short horns and no filaments, 31 (2534 n=12) along its axis.
Typehost: Proechimys simonsi Thomas 1900, Symbiotype (see Frey, et al., 1992) deposited in the University of New Mexico, Museum of Southwestern Biology Mammal Division (MSB), MSB98787.
Site of infection: small intestine.
Typelocality: Puesto Militar Casarabe, Dept. Beni, Bolivia, 5.5 km South of Casarabe by road, 14o 53' 44" S 64o 25' 59" W, 188 m elevation.
Typespecimen: holotype, mounted on a microscope slide, collected 26 May, 2000, HWML70023, 9 paratypes from same host symbiotype, mounted on slides, HWML70024, preserved in formalin, HWML63382. All specimens deposited in the Harold W. Manter Laboratory of Parasitology, Division of Parasitology, The University of Nebraska State Museum, University of Nebraska, Lincoln, Nebraska.
Prevalence and intensity: 2/6 (33%), average 40 specimens from duodenum.
Etymology: this species is named after Dr. Rafael LamotheArgumedo, teacher, taxonomist, and one of the leaders in helminthology at UNAM in Mexico.
Lentiella Rêgo, 1964, emended.
Diagnosis. Anoplocephalids of small size. Scolex and suckers large. Proglottids wider than long in immature, mature, and gravid segments, posterior penultimate and ultimate segments devoid of eggs, always longer than wide. Genital pores regularly alternating. Small but numerous testes, located in posterior part of segment, in continuous line, posterior to ovary and vitelline gland. Testes overlap transverse, but not ventral or dorsal osmoregulatory canals. Cirrus sac large, cirrus spined. Vagina enters gential atrium anterior to cirrus sac. Lateral genital ducts (vagina and cirrus sac) cross osmoregulatory canals dorsally. Ovary lobed, slightly antiporal. Vitelline gland compact, posterior and poral to the ovary. Small seminal receptacle present. Vaginal dilation present in immature segments. Internal and external seminal vesicles absent. Tubular uterus arching anteriorly from center, not occupying posterior part of the segments. Uterine development abrupt, filling with eggs before uterine wall fully developed. Uterus crosses ventral excretory canals rarely, in gravid segments only. Uterus may cross osmoregulatory canals ventrally or dorsally. Gravid uterus with anterior, posterior, and lateral diverticula. Anapolytic with eggs generally absent from terminal senescent segments. Eggs with simple pyriform apparatus. Adults in rodents, South America.
Compared to the only other species in the genus, L. lamothei n. sp. differs from L. machadoi by having a greater total length but smaller maximum width, a greater number of segments, a smaller cirrus sac, a smaller scolex diameter, and in the eggs, a larger pyriform apparatus. Other measurements may prove useful in distinguishing the 2 taxa. However, due to the condition of the material from Rêgo (1964), we recommend that new material be collected and measured so a comparison can be made with properly relaxed specimens of L. machadoi. Currently, including this report, species of Lentiella are known only from hystricognath rodents of the genus Proechimys in the Neotropics (Brazil and Bolivia).
Species assigned to the genus Lentiella appear superficially similar to species of Monoecocestus in that the vagina enters the genital atrium anterior to the cirrus sac. However, Lentiella has a tubular uterus while the developing uterus of all known species of Monoecocestus is reticular in nature. In addition, the vitelline gland in Lentiella is posterior to the ovary and on the poral side compared with the vitelline gland in known species of Monoecocestus which are central and posterior to the ovary.
The 2 species of Lentiella can be readily distinguished from species of Viscachataenia Denegri et al., 2003 with the former having only a single set of genital organs per segment and a tubular uterus.
Comparing L. lamothei to known forms of the Anoplocephalidae that also have a uterus that is tubular in nature, it is evident that only species of Nearctic Anoplocephaloides have this type of uterine development and structure. However, L. lamothei can be recognized as distinct from species of Anoplocephaloides in having a uterus that remains diffuse until the uterine wall becomes immediately recognizable and the uterus is full of eggs. In species of Anoplocephaloides, the tubular uterus develops more slowly, forming a definitive uterine wall and lumen before becoming gravid. Finally, the testes of Lentiella are always posterior to the ovary and vitelline gland compared to species of Anoplocephaloides that have testes that are largely antiporal.
Species of Proechimys are known to eat seeds, fruits, and fungi (Eisenberg and Redford, 1992), and with the discovery of this cestode, it is clear that they also eat some kind of arthropod. Assuming the close relationship of Lentiella spp. to Monoecocestus spp., this arthropod is likely an Oribatid mite, since the life cycle of at least one species of Monoecocestus has been experimentally verified (Freeman, 1952). We assume the close relationship of Lentiella and Monoecocestus from the relative position of the vagina to the cirrus sac at the genital atrium, and the posterior position of the testes in the proglottids.
Development of the uterus has been one of the most important taxonomic characters of species included in this family of cestodes, especially in the Anoplocephalinae, where the uterus does not degenerate in gravid proglottids (Rausch, 1976; Spasskii, 1951). It has been established that the development of the early uterus (e.g. reticulate, tubular) is homoplasic (Wickström et al., 2005), but general structure and development of the uterus is still used to discriminate between and among species within a genus. The development of the uterus in L. lamothei n. sp. appears to be most similar to Anoplocephaloides in that it is not reticulate early in development, but differs from Anoplocephaloides species in the nature of the development. The uterus in L. lamothei n. sp. appears in the segment less than 5 proglottids before it becomes prominent in the strobila; appearing as an aggregation of cells that spans the proglottid, not unlike most other anoplocephalids. However, in Anoplocephaloides the uterus develops a recognizable uterine wall and lumen prior to becoming full of developing eggs (Fig. 8). In L. lamothei n. sp., development from a simple aggregation of cells to fully gravid uterus takes place in the span of one proglottid, and in the newly formed uterus undeveloped eggs occupy a majority of the uterine area (Fig. 9). The uterine wall in this fully gravid proglottid is has not completely developed, and still looks like an aggregation of densely packed cells. In the following proglottids the uterus grows rapidly, but the number of eggs does not follow its fast development, leaving the uterus partially filled in subsequent proglottids. Soon the uterus develops the anterior and posterior diverticula common in Monoecocestus and other anoplocephalid species until it becomes saclike, filling with eggs. Many specimens examined followed developmental pathways noted by Rêgo (1964) in that the eggs would sometimes be completely expelled from the last 2 or 3 proglottids. Those senescent segments appear in sharp contrast to those proglottids before them, as they became 2 to 3 times longer than wide.
We thank the Colección Boliviana de Fauna of the Museo de Historia Natural in La Paz for long term logistic support during our years of field work in Bolivia. We also thank the 2 anonymous reviewers whose comments helped shape and focus the discussion. This work was supported by US. National Science Foundation Grants: BSR8612329, BSR9024816, DEB9496263, and DEB9631295 to S.L.G.
Anderson, S. 1997. Mammals of Bolivia, taxonomy and distribution. Bulletin of the American Museum of Natural History 231:1652. [ Links ]
Beveridge, I. 1994. Family Anoplocephalidae Cholodkovsky, 1902. In Keys to the cestode parasites of vertebrates, L. F. Khalil, A. Jones and R. A. Bray (eds.). CAB International, Cambridge. p. 315366. [ Links ]
Denegri, G., M. C. Dopchiz, M. C. Elissondo and I. Beveridge. 2003. Viscachataenia n. g., with the redescription of V. quadrata (von Linstow, 1904) n. comb. (Cestoda: Anoplocephalidae) in Lagidium viscacia (Rodentia: Chinchillidae) from Argentina. Systematic Parasitology 54:8188. [ Links ]
Dick, C. W., D. Gettinger and S. L. Gardner. 2007. Bolivian ectoparasites: a survey of bats (Mammalia: Chiroptera). Comparative Parasitology 74:372377. [ Links ]
Eisenberg, J. F. and K. H. Redford. 1992. Mammals of the Neotropics: the central Neotropics, volume 3. University of Chicago, Illinois. 609 p. [ Links ]
Freeman, R. S. 1952. The biology and life history of Monoecocestus Beddard, 1914 (Cestoda: Anoplocephalidae) from the porcupine. Journal of Parasitology 38:111129. [ Links ]
Frey, J. K., T. L. Yates, D. W. Duszynski, W. L. Gannon and S. L. Gardner. 1992. Designation and curatorial management of type host specimens (symbiotypes) for new parasite species. Journal of Parasitology 78:930932. [ Links ]
Gardner, S. L. 1996. Field parasitology techniques for use with mammals. In Measuring and monitoring biological diversity: standard methods for mammals, D. E. Wilson, F. R. Cole, J. D. Nichols, R. Rudran and M. S. Foster (eds.). Smithsonian Institution, Washington, D.C. p. 291298. [ Links ]
Gardner, S. L. and M. L. Campbell. 1992. Parasites as probes for biodiversity. The Journal of Parasitology 78:596600. [ Links ]
Haukisalmi, V., L. M. Wickström, H. Henttonen, J. Hantula and A. Gubányi. 2004. Molecular and morphological evidence for multiple species within Paranoplocephala omphalodes (Cestoda, Anoplocephalidae) in Microtus voles (Arvicolinae). Zoologica Scripta 33:277290. [ Links ]
Notarnicola, J., F. A. JiménezRuiz and S. L. Gardner. 2007. A new species of Dipetalonema (Filarioidea: Onchocercidae) from Ateles chamek from the Beni of Bolivia. Journal of Parasitology 93:661667. [ Links ]
Rausch, R. L. 1976. The genera Paranophlocephala Luhe, 1910 and Anoplocephaloides Baer, 1923 (Cestoda: Anoplocephalidae) with particular reference to species in rodents. Annales de Parasitologie Humaine et Comparée 51:513562. [ Links ]
Rêgo, A. A. 1964. Lentiella machadoi g. n., sp. n. e Raillietina (R.) trinitatae (Cameron and Reesal, 1951), parasitos de roedor (Cestoda, Cyclophyllidea). Revista Brasileira de Biologia 24:211220. [ Links ]
Sato, H., H. Kamiya, F. Tenora and M. Kamiya. 1993. Anoplocephaloides dentatoides sp. n. from the graybacked vole, Clethrionomys rufocanus bedfordiae, in Hokkaido, Japan. Journal of the Helminthological Society of Washington 60:105110. [ Links ]
Spasskii, A. A. 1951. Essentials of cestodology, anoplocephalate tapeworms of domestic and wild animals. Academy of Sciences of the USSR, Moscow. 783 p. [ Links ]
Wickström, L. M., V. Haukisalmi, S. Varis, J. Hantula and H. Henttonen. 2005. Molecular phylogeny and systematics of anoplocephaline cestodes in rodents and lagomorphs. Systematic Parasitology 62:8399. [ Links ]
Wilson, D. E. and D. M. Reeder. 2005. Mammal Species of the World. Johns Hopkins University, Baltimore. 2142 p. [ Links ]