scholarly journals First record of Bulimulus tenuissimus (Mollusca) as potential experimental intermediate host of Angiostrongylus cantonensis (Nematoda)

2019 ◽  
Vol 79 (4) ◽  
pp. 686-696 ◽  
Author(s):  
F. G. Martins ◽  
J. S. Garcia ◽  
E. J. L. Torres ◽  
M. A. J. Santos ◽  
C. L. Massard ◽  
...  
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Amorphous Material ◽  
Angiostrongylus Cantonensis ◽  
Muscular Tissue ◽  
Wild Rodents ◽  
Intermediate Hosts ◽  
Post Exposure ◽  
The Third

Abstract Snails are essential to complete the life cycle of the metastrongylid nematode Angiostrongylus cantonensis, the causative agent of infections in domestic and wild animals, mainly rodents, and also of neural angiostrongyliasis or eosinophilic meningitis in humans. There are many reports of mollusks that can act as intermediate hosts of this parasite, especially freshwater snails and the African giant Achatina fulica. The terrestrial gastropod Bulimulus tenuissimus is widely distributed in Brazil and other species of the same genus occur in Brazil and other countries, overlapping regions in which there are reports of the occurrence of A. cantonensis and angiostrongyliasis. In spite of this, there are no records in the literature of this species performing the role of intermediate host to A. cantonensis. The present study analyzed the experimental infection with first-stage larvae of A. cantonensis, under laboratory conditions, of B. tenuissimus, by using histology and electron microscopy techniques. Three weeks after exposure to L1 larvae, it was possible to recover L3 larvae in small numbers from the infected snails. Developing larvae were observed in the cephalopedal mass (foot), ovotestis, and mantle tissues, being located inside a granulomatous structure composed of hemocyte infiltration, but there was no calcium or collagen deposition in these structures in significant amounts. In the third week post exposure, it was possible observe a sheath around the developing larvae. The infected snails presented reduction in the fibrous muscular tissue in the foot region, loss of the acinar organization in the digestive gland, with increase of amorphous material inside the acini and loss of epithelial pattern of nuclear organization in the acinar cells. However, the ovotestis seemed unaffected by the infection, since there was a large number of developing oocytes and spermatozoa in different stages of formation. The digestion of infected snails allows us the third-stage recovery rate of 17.25%, at 14 days post exposure to the L1. These L3 recovered from B. tenuissimus were used to infect rats experimentally, and 43 days post infection first-stage (L1) larvae of A. cantonensis were recovered from fresh feces. The results presented constituted the first report of the role of B. tenuissimus as an experimental intermediate host to A. cantonensis and shed some light on a possible problem, since the overlapping distribution of B. tenuissimus and A. cantonensis in Brazil and other countries where different species of Bulimulus occur enables the establishment and maintenance of the life cycle of this parasite in nature, with wild rodents as reservoirs, acting as a source of infection to humans, causing neural angiostrongyliasis.

Life cycle studies on two Digenea, Paradistomum geckonum (Dicrocoeliidae) and Mesocoelium sociale (Mesocoeliidae), in geckonid lizards from Indonesia

1987 ◽  
Vol 65 (10) ◽  
pp. 2491-2497 ◽  
Author(s):  
Murray J. Kennedy ◽  
L. M. Killick ◽  
M. Beverley-Burton
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Intermediate Hosts ◽  
Larval Stages ◽  
Hemidactylus Frenatus ◽  
Pulmonate Gastropod ◽  
First Intermediate Host

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.

scholarly journals Experimental life cycle of Lagochilascaris minor Leiper, 1909

1992 ◽  
Vol 34 (4) ◽  
pp. 277-287 ◽  
Author(s):  
Dulcinéa Maria Barbosa Campos ◽  
Lindomar G. Freire Filha ◽  
Miguel Alípio Vieira ◽  
Julieta Machado Paçô ◽  
Moacir A. Maia
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Subcutaneous Tissue ◽  
Cervical Region ◽  
Parasite Development ◽  
Mature Stage ◽  
Post Inoculation ◽  
Skeletal Musculature ◽  
Third Stage

The life cycle of Lagochilascaris minor was studied using material collected from human lesion and applying the experimental model: rodents (mice, hamsters), and carnivorae (cats, dogs). In mice given infective eggs, orally, hatch of the third stage larvae was noted in the gut wall, with migration to liver, lungs, skeletal musculature and subcutaneous tissue becoming, soon after, encysted. In cats infected with skinned carcasses of mice (60 to 235 days of infection) it was observed: hatch of third stage larvae from the nodules (cysts) in the stomach, migration through the oesophagus, pharynx, trachea, related tissues (rhino-oropharynx), and cervical lymphonodes developing to the mature stage in any of these sites on days 9-20 post inoculation (P.I.). There was no parasite development up to the mature stage in cats inoculated orally with infective eggs, which indicates that the life cycle of this parasite includes an obligatory intermediate host. In one of the cats (fed carcass of infected mice) necropsied on day 43 P.I., it was observed the occurence of the self-infective cycle of L. minor in the lung tissues and in the cervical region which was characterized by the finding of eggs in different stages of development, third stage larvae and mature worms. It's believed that some component of the carnivorae gastrointestinal tracts may preclude the development of third stage larvae from L. minor eggs what explains the interruption of the life cycle in animals fed infective eggs. It's also pointed out the role of the intermediate host in the first stages of the life cycle of this helminth.

Observations on the suitability and importance of the domestic intermediate hosts of Echinococcus granulosus in Uttah Pradesh, India

1989 ◽  
Vol 63 (1) ◽  
pp. 39-45 ◽  
Author(s):  
M. Irshadullah ◽  
W. A. Nizami ◽  
C. N. L. Macpherson
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Echinococcus Granulosus ◽  
Frequency Distribution ◽  
Host Species ◽  
Control Measures ◽  
The Other ◽  
Hydatid Cysts ◽  
Intermediate Hosts ◽  
Cyst Size

ABSTRACTThe present study investigated the suitability and importance of buffaloes, camels, sheep, goats and pigs in maintaining the life-cycle of Echinococcus granulosus in Aligarh, India. A total of 565 (36%) of 1556 buffaloes, 20 (2%) of 1208 goats, 5 (1%) of 559 pigs, 6 (6%) of 109 sheep and two of three camels were found to harbour hydatid cysts. The frequency distribution of the hydatid cysts in each intermediate host species was over-dispersed and in buffaloes cyst fertility increased with increasing cyst size. Of 2171, 95 and four buffalo, goat, and camel cysts examined 327 (15%), two (2%) and three cysts respectively were fertile. No pig or sheep cysts were found to contain protoscoleces. The unfenced buffalo abattoir and the large number of dogs allowed access to the abattoir coupled to the number of buffaloes slaughtered in comparison to the other potential hosts, indicates that the buffalo is the most significant host for maintaining the life-cycle of the parasite in this area of India. Applicable control measures for the region are suggested.

The Life-Cycle and Morphology of Stemmatostoma-Pearsoni, Gen Et Sp-Nov, With Notes on the Morphology of Telogaster-Opisthorchis Macfarlane (Digenea, Cryptogonimidae)

1986 ◽  
Vol 34 (2) ◽  
pp. 279 ◽  
Author(s):  
TH Cribb
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Freshwater Fish ◽  
Oral Sucker ◽  
Intermediate Hosts ◽  
Redial Generation ◽  
Adult Morphology ◽  
Mother Sporocyst ◽  
First Intermediate Host ◽  
Prosobranch Snail

Stemmatostoma pearsoni, gen. et sp. nov., is described from the intestine of Leiopotherapon unicolor (Gunther) and Macquaria novemaculeata (Steindachner) in Queensland. Stemmatostoma is placed within the Neochasminae and is distinguished by its long oesophagus, compact ovary, short caeca, pre-ovarian vitellaria, simple gonotyl and funnel-shaped oral sucker. The diagnosis of the Neochasminae is emended excluding Parspina Pearse. Telogaster opisthorchis Macfarlane is recorded from the intestine of Anguilla reinhardtii Steindachner from Victoria. The spinose oral suckers of S. pearsoni and T. opisthorchis are capable of being retracted into tegumental pockets. It is postulated that this arrangement may be widespread amongst spinose cryptogonimids. The first intermediate host of S. pearsoni is Posticobia brazieri (Smith), a prosobranch snail. The second intermediate hosts are freshwater fish: Hypseleotris galii (Ogilby), H. compressus (Krefft), Mogurnda mogurnda (Richardson), M. adspersa (Castelnau), Philypnodon grandiceps (Krefft), Gobiomorphus australis (Krefft), and Pseudomugil signifer Kner. Within the snail there is a mother sporocyst generation, a redial generation and a cercarial generation. Development of the mother sporocyst is similar to that described for other opisthorchioids. Cryptogonimid cercariae are characterized by 16 flame-cells, pre-vesicular penetration glands, dorso-ventral caudal finfolds and absence of body pigmentation. On the basis of cercarial and adult morphology it is proposed that Pseudexorchis Yamaguti be excluded from the Cryptogonimidae.

scholarly journals Rat lungworm Angiostrongylus cantonensis (Chen, 1935) (Nematoda: Strongylida: Metastrongylida)

EDIS ◽  
2013 ◽  
Vol 2013 (9) ◽  
Author(s):  
John Capinera ◽  
Heather S. Walden
Keyword(s):  
Life Cycle ◽  
Angiostrongylus Cantonensis ◽  
Intermediate Hosts ◽  
Fact Sheet ◽  
The World ◽  
Rat Lungworm

Like many pest and disease problems, rat lungworm has been slowly spreading around the world. First described by Chen from rats in China, the medical significance of this parasite was overlooked until 1944 when it was found infecting humans in Taiwan. Even then, because the report was published in Japanese, its importance remained largely unknown. In 1955, Mackerras and Sandars found this nematode among rats in Brisbane, Australia, and described its life cycle, including the importance of its molluscan intermediate hosts. This 4-page fact sheet was written by John Capinera and Heather S. Walden and published by the UF Department of Entomology and Nematology, September 2013. http://edis.ifas.ufl.edu/in1007

Role of T cell subpopulations in mice infected with Angiostrongylus cantonensis

1996 ◽  
Vol 70 (3) ◽  
pp. 211-214 ◽  
Author(s):  
J.D. Lee ◽  
J.J. Wang ◽  
J.H. Chang ◽  
L.Y. Chung ◽  
E.R. Chen ◽  
...  
Keyword(s):  
T Cells ◽  
T Cell ◽  
Immune Responses ◽  
Angiostrongylus Cantonensis ◽  
T Helper ◽  
The Third ◽  
Cell Subpopulations ◽  
T Cell Subpopulations

AbstractWhen C57BL/6 mice were infected with Angiostrongylus cantonensis, the percentage of T helper (CD4+) cells and T supressor (CD8+) cells in peripheral blood increased weekly until the third and seventh week respectively, and then gradually decreased. C57BL/6 mice were depleted of CD4+ and CD8+ T cells by in vivo injection of anti-CD4 and anti-CD8 monoclonal antibodies, respectively, and then infected with A. cantonensis. There were significantly more and less worms recovered in the mice depleted of CD4+ and CD8+ T cells respectively than in undepleted mice. Discrete subpopulations of T cells from mice exposed to A. cantonensis for 3 weeks or 7 weeks were adoptively transferred to syngeneic recipients which were then given a challenge infection. Protection was mediated by a CD4+ T cell population present in mice after 3 weeks of infection but was not demonstrable with cells taken 7 weeks after infection. When CD4+ T cells obtained from 3-week infected mice were mixed with 5% CD8+ T cells obtained from mice infected for 7 weeks, no significant transfer of resistance was observed. Thus, immune responses to A. cantonensis in mice were regulated by discrete subpopulations of T lymphocytes.

The development of Neoechinorhynchus buttnerae (Eoacanthocephala: Neoechinorhynchidae) in its intermediate host Cypridopsis vidua in Brazil

2018 ◽  
Vol 63 (2) ◽  
pp. 354-359 ◽  
Author(s):  
Felipe de Sousa Lourenço ◽  
Germán Augusto Murrieta Morey ◽  
José Celso de Oliveira Malta
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Intermediate Hosts ◽  
Experimental Procedure ◽  
Stage Of Development ◽  
Lack Of Information ◽  
Brazilian Amazon Region ◽  
The Family ◽  
Cypridopsis Vidua

AbstractThe family Neoechinorhynchidae includes seven species ofNeoechinorhynchusfrom freshwater fishes of Brazil. Although severalNeoechinorhynchusspecies are cited infecting different fish species in Brazil, there is a lack of information concerning to their life cycle and the identification of the intermediate hosts. Thus, the aim of the present study was to describe the development ofNeoechinorhynchus buttneraein its intermediate host collected in a fish farm located in Rio Preto da Eva, Amazonas, Brazil. To verify the presence ofN. buttneraein the fish pond, twentyColossoma macropomumwere captured and analyzed, being corroborated the presence of this parasite species. Samples of plankton were also collected, finding the ostracodCypridopsis viduaas the intermediate host. For the description of the larvae development, a laboratory experimental procedure was conducted by feeding the collected ostracods with the eggs of the adult specimens taken from the sampled fish. To observe the stages of development an artificial hatch was performed. Every stage of development was photographed, measured, drawn and described. The time of development of the immature stages ofN. buttneraewas 29 days, reporting the stages: acanthor, acanthella (with eight developmental changes) and cystacanth. As high infections byN. buttneraecauses morphological damages to the intestine and may compromise the quality ofC. macropomumand in consequence the production of fish farmers in the Brazilian Amazon region, the knowledge of its intermediate host and the understanding of its life cycle represents a useful information to prevent and combat infections by this parasite.

Studies on resistance in calves to experimental infection with the nodular worm, Oesophagostomum radiatum (Rudolphi 1803). II. The role of the respective stages of the parasitic life cycle in the stimulation of resistance

1963 ◽  
Vol 14 (5) ◽  
pp. 704 ◽  
Author(s):  
FHS Roberts ◽  
RF Riek ◽  
RK Keith
Keyword(s):  
Life Cycle ◽  
Fourth Stage ◽  
Development Stages ◽  
The Third ◽  
Surgical Implants ◽  
Series Of Experiments ◽  
Parasitic Life Cycle ◽  
Fourth Stage Larva ◽  
Stimulation Of

Investigations are reported which attempted to define the role of the respective stages of the parasitic life cycle ofOesophagostomum radiatum in the stimulation of resistance in calves to reinfection with this parasite. In one series of experiments with calves reared worm-free, infection was restricted to known stages by treatment with an anthelmintic, and in another series by surgical implants of worms. Subsequent reinfection showed that the early development stages of the parasite up to the early fourth stage larva in the gut lumen, and the exsheathing fluid released at the third and fourth ecdyses, were not essential for the stimulation of resistance. The results also suggest that ability to stimulate resistance increases as the worms mature.

On the Experimental Transmission of Syngamus trachea from Starlings to Chickens

1935 ◽  
Vol 13 (1) ◽  
pp. 1-2 ◽  
Author(s):  
Phyllis A. Clapham
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Eisenia Foetida ◽  
Intermediate Hosts ◽  
Experimental Transmission ◽  
Syngamus Trachea

In a previous paper (1934) it was shown that the life-cycle of S. trachea proceeds best when an intermediate host is involved. By means of Eisenia foetida, an annulate worm, it was possible to induce heavy and certain infestations of gapeworm in chickens with material obtained from the partridge, pheasant, rook and chicken. Other earthworms were shown to be possible intermediate hosts but this was found to be the best and most successful.

A study on the life-cycle and epidemiology of Pseudanoplocephala crawfordi Baylis, 1927

1990 ◽  
Vol 64 (1) ◽  
pp. 54-61 ◽  
Author(s):  
Jiang Taijing ◽  
Jin Zhehao ◽  
Wu Hui ◽  
Cui Chunquan
Keyword(s):  
Life Cycle ◽  
Intermediate Host ◽  
Tribolium Castaneum ◽  
Rattus Norvegicus ◽  
Control Measures ◽  
Intermediate Hosts ◽  
New Host ◽  
Epidemiological Factors ◽  
New Host Records

ABSTRACTA study of the life-cycle and epidemiology of Pseudanoplocephala crawfordi Baylis, 1927 is reported. Intermediate hosts are Tenebrio obscurus, T. molitor, Carpophilus dimidiatus and Tribolium castaneum. The first three species are new host records. Development in the intermediate host takes 1–1.5 months. The completion of the life-cycle takes 2–2.5 months. Surveys of intermediate hosts, pigs, humans and rats were carried out. In Rattus norvegicus, the prevalence was as high as 22%. Epidemiological factors and suggestions for control measures are discussed.

Sign in / Sign up

Export Citation Format

Share Document