Cestodes (tapeworms)

2020 ◽  
pp. 1520-1528
Author(s):  
Richard Knight

Adult tapeworms maintain anchorage to the host small-gut mucosa by means the scolex, a holdfast structure. The rest of the body forms the strobila and consists of a chain of flattened proglottids, which proliferate just behind the scolex. The life cycle then includes larval stages in one or more intermediate hosts. Many species of tapeworm, all zoonoses, infect humans as adult worms or larval stages. Serious disease can result when larval stages occur accidentally in humans, whereas infections by the adult stages often cause little harm. Two groups of cestode infect humans: the Cyclophyllidea and the Pseudophyllidea. The former have a terrestrial life cycle and cystic larvae; the latter have an aquatic cycle and worm-like larvae.

2016 ◽  
Vol 37 (1) ◽  
pp. 30 ◽  
Author(s):  
Andrew R Butcher

Brachylaimids are parasitic trematode fluke worms that have a terrestrial life cycle involving land snails and slugs as the first and/or second intermediate hosts for the cercarial and metacercarial larval stages. A wide range of mammals, birds, reptiles and amphibians are the definitive hosts for the adult worm. Brachylaima spp. have been reported from most continents including Europe, Africa, Asia, North and South America and Australia. There are over 70 described species in the genus with seven species indigenous to Australia. Although Brachylaima spp. are a cosmopolitan terrestrial trematode they have not been recorded to infect humans other than the three Brachylaima cribbi infections reported in two children and an adult from South Australia.


2020 ◽  
Vol 49 (6) ◽  
pp. 71-78
Author(s):  
О. M. Bonina ◽  
Е. А. Serbina

The results of studying the body structure of trematode cercariae of the families Opisthorchiidae and Notocotylidae and the features of their development in Western Siberia are presented. The data of long-term (1994–2019) studies on the spread of these pathogens of dangerous parasitic diseases in humans and animals are analyzed and summarized. The studies were conducted according to generally accepted methods in parasitology and hydrobiology. The species affi  liation of trematodes was determined in laboratory conditions on mature cercariae that independently left the shells of the host mollusks Bithynia tentaculata and B. troscheli. It was noted that the trematodes of the Opisthorchiidae and Notocotylidae families at the cercaria stage have the following similar features: a simple tail, pigmented eyes, and one oral sucking cup. Diagnosis of trematode cercariae of Opisthorchiidae and Notocotylidae families is possible by the following signs: the tail of the opisthorchis cercaria has a swimming membrane and is 2 times longer than the body, the tail of the notocotylid has no swimming membrane and is approximately equal in length to the body. Opisthor-chis cercariae have two pigment eyes, notocotilids – three. In the life cycle of opisthorchis, there are two intermediate hosts (bitinia and fi  sh), in the notocotylid cycle, one (bitinia). Opisthorchis cercariae have penetration glands, but notocotylids do not; the maximum daily emission of opisthorchis cercariae is ten times higher than that of notocotylids (6672 and 422 cercariae, respectively). The ability to diagnose opisthorchis and notocotilid at the cercaria stage allows the identifi cation of local foci of epidemiologically and epizootically dangerous diseases.


1987 ◽  
Vol 65 (10) ◽  
pp. 2491-2497 ◽  
Author(s):  
Murray J. Kennedy ◽  
L. M. Killick ◽  
M. Beverley-Burton

Life cycle studies of Paradistomum geckonum (Dicrocoeliidae) were attempted experimentally. The pulmonate gastropod Lamellaxis gracilis served as the first intermediate host; geckonid lizards (Cosymbotus platyurus, Gehyra mutilata, and Hemidactylus frenatus) served as definitive hosts. The life cycle of Mesocoelium sociale (Mesocoeliidae) was studied in naturally infected first intermediate hosts (L. gracilis, Huttonella bicolor) and experimentally in geckonid definitive hosts (C. platyurus, G. mutilata, and H. frenatus). Some naturally infected L. gracilis were infected concurrently with larval stages of both digeneans. Second intermediate hosts, presumed to be arthropods, were experimentally unnecessary. Metacercariae of P. geckonum were not found. Cercariae of M. sociale formed encysted metacercariae in the same individual snails.


1989 ◽  
Vol 67 (6) ◽  
pp. 1421-1424 ◽  
Author(s):  
Cheryl A. Macdonald ◽  
Daniel R. Brooks

Pseudotelorchis compactus from the oviducts of Emydoidea blandingi is redescribed and its phylogenetic affinities examined. The Ochetosomatidae is considered the sister group of the Telorchiidae based on the shared presence of a well-developed glandular and muscular metraterm, and on the use of tadpoles as second intermediate hosts in the life cycle. The monophyly of the Ochetosomatidae is supported by the presence of relatively short caeca and testes located near the posterior ends of the caeca. The monophyly of the Telorchiidae is supported by the presence of postuterine testes located near the posterior end of the body. Orchidasma is excluded from the Telorchiidae because it possesses a spinose cirrus, spinose metraterm and distal portion of the uterus, and testes separated widely in the hind body by the uterus. Pseudotelorchis is considered monophyletic by virtue of having ovaries with irregular rather than smooth margins, testes that vary from side by side to tandem rather than being consistently tandem, and by inhabiting the oviducts rather than the intestine of the definitive hosts. Pseudotelorchis is the sister group of Loefgrenia plus Telorchis, the latter group diagnosed by having ovaries that are at least half an ovarian diameter posterior to the posterior margin of the ventral sucker rather than proximal to it. Loefgrenia is diagnosed by the absence of an esophagus, while Telorchis is diagnosed by strictly tandem testes with smooth margins and well-ordered ascending and descending uterine loops.


2021 ◽  
Author(s):  
◽  
Rosemary Jennifer Hurst

<p>The life cycle of Anisakis simplex in New Zealand waters is described from observations on the morphology, distribution and behaviour of free-living and parasitic stages. Comparison with the life cyles of two other anisakids, Phocanema decipiens Myers 1959 and Thynnascaris adunca Rudolphi 1802 shows differences in distribution, degrees of host specificity, the status of invertebrate hosts, the factors influencing infestation levels of teleost hosts, and the location and pathological effects of infestation. Larval stages occurring in intermediate and paratenic hosts were identified by comparison of larval and adult morphometrics. A. simplex larvae were also positively identified by in vitro cultivation through to adults. Some morphometric variations compared to overseas descriptions are apparent. The ventriculus of A. simplex larvae is shorter relative to body length and the intestinal caecum of P. decipiens is longer relative to ventriculus length. Egg and free-living larval stages were obtained from in vitro cultivation of (A. simplex) and collection of eggs from mature adults from definitive hosts (T. adunca). Eggs of P. decipiens were not obtained. Eggs of A. simplex and T. adunca hatch in 8-11 days at 15 [degrees] C. A. simplex eggs hatch in 6 days at a temperature of 22 [degrees] C and did not hatch in 16 days at 10 [degrees] C. Eggs and free-living stage III larvae of A. simplex and T. adunca are similar in morphology with little differentiation of internal structures. Examination of the stomach contents of pelagic fish infested with anisakids indicated that possible intermediate hosts of A. simplex are the euphausiid Nyctiphanes australis and the decapod Munida gregaria. Possible hosts of T. adunca and M. gregaria are a wide variety of smaller zooplanktonic groups, e.g. decapod larvae and copepods. Larvae of A. simplex were found in one of 8850 N. australis; larvae of T. adunca were found in 69 of 3999 chaetognaths (Sagitta spp.) a medusa and a decapod larva. These larvae are morphologically similar to Stage III larvae from teleosts. No anisakids were found in 3956 Euphausia spp., 1147 M. gregaria and 740 prawns. Twenty five T. adunca larvae and adults were found in 818 freshly eaten M. gregaria in teleost stomachs, indicating that this invertebrate may act as a paratenic and a definitive host. Experimental infection of N. australis and M. gregaria with stage II larvae of A. simplex and T. adunca was unsuccessful. The location of anisakid infestation in three pelagic teleost species, Thyrsites atun, Trachurus novaezelandiae and Trachurus declivis is described. A. simplex larvae are found mainly in the body cavity of all species, at the posterior end of the stomach, with less than one percent occurring in the musculature. Distribution of A. simplex larvae does not change with increasing size of the host or increasing total worm burden. Thyrsites atun have a higher proportion of larvae in the stomach wall (8-13%) compared to Trachurus spp. (< 4%). T. adunca larvae are found infrequently in the body cavity of all three species, on the pyloric caeca and in the stomach wall. Adults and larvae of T. adunca are found more commonly in the alimentary canal, indicating that these teleosts are more important as definitive hosts in the life cycle of this anisakid. P. decipiens larvae are found only in Thyrsites atun and occur mainly in the muscles (98.5%). No quantitative pathogenic effects of anisakid infestation on these teleosts hosts were detected. The main factors influencing the infestation of the three teleost species are age of the host, locality and season. Sex of the host and depth (over the continental shelf, 0-250 m) are not important. A. simplex infestation increased with age in all host species examined, and was higher in Trachurus declivis from the southern-most locality, suggesting the existence of at least two distinct populations of this species. Significant differences in infestation of Thyrsites atun with P. decipiens suggests that this anisakid may be more common in southern localities also. The infestation of Thyrsites atun by larval and adult T. adunca in the alimentary canal is most influenced by season and closely related to diet. Nematode samples were obtained from the marine mammals Arctocephalus forsteri, Kogia breviceps and Phocarctos hookeri. Adult A. simplex were recorded from A. forsteri (a new host record) and Kogia breviceps; preadults from Phocarctos hookeri. Adult P. decipiens were recorded from Phocarctos hookeri; preadults from Arctocephalus forsteri and K. breviceps. Other anisakids found were Anisakis physeteris (Baylis 1923), Contracaecum osculatum Rudolphi 1802 and Pseudoterranova kogiae (Johnston and Mawson 1939) Mosgovoi 1951. These records are all new for the New Zealand region except P. decipiens from P. hookeri and C. osculatum from Arctocephalus forsteri. A. simplex and C. osculatum were found associated with gastric ulcers in Arctocephalus forsteri.</p>


2021 ◽  
Author(s):  
◽  
Rosemary Jennifer Hurst

<p>The life cycle of Anisakis simplex in New Zealand waters is described from observations on the morphology, distribution and behaviour of free-living and parasitic stages. Comparison with the life cyles of two other anisakids, Phocanema decipiens Myers 1959 and Thynnascaris adunca Rudolphi 1802 shows differences in distribution, degrees of host specificity, the status of invertebrate hosts, the factors influencing infestation levels of teleost hosts, and the location and pathological effects of infestation. Larval stages occurring in intermediate and paratenic hosts were identified by comparison of larval and adult morphometrics. A. simplex larvae were also positively identified by in vitro cultivation through to adults. Some morphometric variations compared to overseas descriptions are apparent. The ventriculus of A. simplex larvae is shorter relative to body length and the intestinal caecum of P. decipiens is longer relative to ventriculus length. Egg and free-living larval stages were obtained from in vitro cultivation of (A. simplex) and collection of eggs from mature adults from definitive hosts (T. adunca). Eggs of P. decipiens were not obtained. Eggs of A. simplex and T. adunca hatch in 8-11 days at 15 [degrees] C. A. simplex eggs hatch in 6 days at a temperature of 22 [degrees] C and did not hatch in 16 days at 10 [degrees] C. Eggs and free-living stage III larvae of A. simplex and T. adunca are similar in morphology with little differentiation of internal structures. Examination of the stomach contents of pelagic fish infested with anisakids indicated that possible intermediate hosts of A. simplex are the euphausiid Nyctiphanes australis and the decapod Munida gregaria. Possible hosts of T. adunca and M. gregaria are a wide variety of smaller zooplanktonic groups, e.g. decapod larvae and copepods. Larvae of A. simplex were found in one of 8850 N. australis; larvae of T. adunca were found in 69 of 3999 chaetognaths (Sagitta spp.) a medusa and a decapod larva. These larvae are morphologically similar to Stage III larvae from teleosts. No anisakids were found in 3956 Euphausia spp., 1147 M. gregaria and 740 prawns. Twenty five T. adunca larvae and adults were found in 818 freshly eaten M. gregaria in teleost stomachs, indicating that this invertebrate may act as a paratenic and a definitive host. Experimental infection of N. australis and M. gregaria with stage II larvae of A. simplex and T. adunca was unsuccessful. The location of anisakid infestation in three pelagic teleost species, Thyrsites atun, Trachurus novaezelandiae and Trachurus declivis is described. A. simplex larvae are found mainly in the body cavity of all species, at the posterior end of the stomach, with less than one percent occurring in the musculature. Distribution of A. simplex larvae does not change with increasing size of the host or increasing total worm burden. Thyrsites atun have a higher proportion of larvae in the stomach wall (8-13%) compared to Trachurus spp. (< 4%). T. adunca larvae are found infrequently in the body cavity of all three species, on the pyloric caeca and in the stomach wall. Adults and larvae of T. adunca are found more commonly in the alimentary canal, indicating that these teleosts are more important as definitive hosts in the life cycle of this anisakid. P. decipiens larvae are found only in Thyrsites atun and occur mainly in the muscles (98.5%). No quantitative pathogenic effects of anisakid infestation on these teleosts hosts were detected. The main factors influencing the infestation of the three teleost species are age of the host, locality and season. Sex of the host and depth (over the continental shelf, 0-250 m) are not important. A. simplex infestation increased with age in all host species examined, and was higher in Trachurus declivis from the southern-most locality, suggesting the existence of at least two distinct populations of this species. Significant differences in infestation of Thyrsites atun with P. decipiens suggests that this anisakid may be more common in southern localities also. The infestation of Thyrsites atun by larval and adult T. adunca in the alimentary canal is most influenced by season and closely related to diet. Nematode samples were obtained from the marine mammals Arctocephalus forsteri, Kogia breviceps and Phocarctos hookeri. Adult A. simplex were recorded from A. forsteri (a new host record) and Kogia breviceps; preadults from Phocarctos hookeri. Adult P. decipiens were recorded from Phocarctos hookeri; preadults from Arctocephalus forsteri and K. breviceps. Other anisakids found were Anisakis physeteris (Baylis 1923), Contracaecum osculatum Rudolphi 1802 and Pseudoterranova kogiae (Johnston and Mawson 1939) Mosgovoi 1951. These records are all new for the New Zealand region except P. decipiens from P. hookeri and C. osculatum from Arctocephalus forsteri. A. simplex and C. osculatum were found associated with gastric ulcers in Arctocephalus forsteri.</p>


2006 ◽  
Vol 80 (4) ◽  
pp. 327-332 ◽  
Author(s):  
K. Umadevi ◽  
R. Madhavi

AbstractThe life cycle of the heterophyid fluke, Haplorchis pumilio is elucidated for the first time from the Indian region. Various stages in the life cycle were established based on observations made on natural infections found in snails and fish in a freshwater stream at Visakhapatnam, India and experimental infections carried out in the laboratory. The thiarid snail, Thiara tuberculata served as the first intermediate host and a wide range of freshwater fish as second intermediate hosts. Natural infections with adult flukes were found in the piscivorous birds Ardeola grayii and Bubulcus ibis. Adults were raised experimentally in day-old chicks. Distinguishing features of the cercaria of H. pumilio are: a large body size (200–224×92–96 μm), body–tail ratio of 1:2.1 and densely distributed pigment granules in the parenchyma imparting a brownish tinge to the body. Natural infections with metacercariae were found in the freshwater fish Channa punctatus, C. orientalis, Puntius sophore, Gambusia affinis and fingerlings of Cyprinus carpio and Liza macrolepis. Additionally, experimental infections were established in Therapon jarbua, Esomus danricus and Oreochromis mossambica. Metacercariae were embedded in the caudal muscles of fish and heavy infections induced mortality. Metacercariae were infective at about 15 days of age.


2013 ◽  
Vol 47 (6) ◽  
pp. 37-42 ◽  
Author(s):  
O. S. Kudlai ◽  
L. N. Yanovich

Abstract Rhopalocercous cercariae were found in the gonads of duck mussels, Anodonta anatina (Linnaeus, 1758) collected from the Sluch River (Zhytomyr oblast, Ukraine). The morphological features observed led to conclusion that this species belonged to the genus Phyllodistomum Braun, 1899. Obtained results suggested that the second intermediate hosts in the life cycle of this trematode were absent. Free-swimming cercariae were observed encysting in water. This species is similar to Phyllodistomum pseudofolium Nybelin, 1926 by overall body proportions and ratio of suckers: lengths of oral to ventral sucker 1 : 1.1; widths of the same organs 1 : 1.2. To confirm the taxonomic position of the species found and establish a possible relationship between it and P. pseudofolium an experimental infection of fish Carassius carassius (Linnaeus, 1758) as potential definitive host was performed. The infection was not successful. Descriptions and figures of all detected larval stages of Phyllodistomum sp. are provided.


2018 ◽  
Vol 93 (05) ◽  
pp. 580-588 ◽  
Author(s):  
A.L. May-Tec ◽  
A. Martínez-Aquino ◽  
M.L. Aguirre-Macedo ◽  
V.M. Vidal-Martínez

AbstractWe describe the larval developmental stages and life cycle of the dracunculid nematodeMexiconema cichlasomaein both the intermediate,Argulus yucatanus(Crustacea: Branchiura), and definitive hosts,Cichlasoma urophthalmus(Perciformes: Cichlidae), from the Celestun tropical coastal lagoon, Yucatan, Mexico. The morphological analyses showed significant differences between the total length of L1 found inM. cichlasomaegravid female and L2–L3 inA. yucatanus.This result indicates that theM. cichlasomaelarval development occurs in the intermediate host. We obtained sequences from the small subunit (SSU) ribosomal marker from larval stages ofM. cichlasomaeinA. yucatanusand adult nematodes inC. urophthalmus. Our morphological and molecular results support conspecificity betweenM. cichlasomaelarvae inA. yucatanusand the adult stages inC. urophthalmus. We briefly discuss the phylogenetic position ofM. cichlasomaeamong the Daniconematidae, and provide evidence of the monophyly of the daniconematids associated with branchiurid intermediate hosts. Based on the phylogenetic results, we support the transfer of theMexiconemagenus to the family Skrjabillanidae and do not support the lowering of family Daniconematidae to subfamily.


2018 ◽  
pp. 375-402
Author(s):  
J. Antonio Baeza ◽  
Emiliano H. Ocampo ◽  
Tomás A. Luppi

In the subphylum Crustacea, species from most major clades have independently evolved symbiotic relationships with a wide variety of invertebrate and vertebrate hosts. Herein, we review the life cycle disparity in symbiotic crustaceans. Relatively simple life cycles with direct or abbreviated development can be found among symbiotic decapods, mysids, and amphipods. Compared to their closest free-living relatives, no major life cycle modifications were detected in these clades as well as in most symbiotic cirripeds. In contrast, symbiotic isopods, copepods, and tantulocarids exhibit complex life cycles with major differences compared to their closest free-living relatives. Key modifications in these clades include the presence of larval stages well endowed for dispersal and host infestation, and the use of up to 2 different host species with dissimilar ecologies throughout their ontogeny. Phylogenetic inertia and restrictions imposed by the body plan of some clades appear to be most relevant in determining life cycle modifications (or the lack thereof) from the “typical” ground pattern. Furthermore, the life cycle ground pattern is likely either constraining or favoring the adoption of a symbiotic lifestyle in some crustacean clades (e.g., in the Thecostraca).


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