A study of acetylcholinesterase throughout the life cycle of Nippostrongylus brasiliensis

Parasitology ◽  
1971 ◽  
Vol 62 (3) ◽  
pp. 367-373 ◽  
Author(s):  
Barbara E. Sanderson ◽  
Bridget M. Ogilvie

Acetylcholinesterase activity, measured per unit wet weight, is relatively low in the eggs and infective larvae of N. brasiliensis. It increases rapidly during the parasitic phase, especially in the late 3rd- and early 4th-larval stages. Activity in normal adults is extremely high (× 15 egg activity) and this is doubled again in immune-damaged adults. Possible functions of N. brasiliensis acetylcholinesterase are discussed.It is a pleasure to acknowledge the technical assistance of Miss Anne Cronin and Miss Beryl Crooks.

1955 ◽  
Vol 29 (1-2) ◽  
pp. 27-32 ◽  
Author(s):  
H. M. Gharib

It is well known that the first two larval stages in the life cycle of nematodes belonging to the superfamily Strongloidea, have a freeliving existence. During this time, the larva which hatches from the egg feeds actively, undergoes two moults and grows considerably before reaching the infective stage, when it is ready to invade a definitive host. Under natural conditions this external development takes place in the faeces, which have been deposited by the infected host on ground likely to be contaminated with various bacteria.


Parasitology ◽  
1964 ◽  
Vol 54 (1) ◽  
pp. 1-41 ◽  
Author(s):  
B. L. James

1. Parvatrema homoeotecnum sp.nov. from the oystercatcher, Haematopus ostralegus occidentalis Neumann at Aberystwyth is described and compared with other species of the genus.2. The life cycle of this species is unique. The larval stages occur in the gastropod, Littorina saxatilis (Olivi) subsp. tenebrosa (Montagu) and include germinal sacs which have a structure and development similar to an adult digenean. There are no free-living stages and only one intermediate host.3. The significance of this unique life cycle is discussed.4. The family Gymnophallidae Morozov, 1955, is reviewed. Emended definitions are given for the family, subfamilies and genera. Keys, diagnostic features and brief notes of the species are included.I am very grateful to Dr Gwendolen Rees, who suggested the investigation which led to the discovery of this species, for her advice and indispensable assistance throughout the work and the preparation of this paper. I am also grateful to the late Professor T. A. Stephenson for his interest and for the provision of working facilities; to Mr W. A. Ballantine, Mr A. H. Clarke, Jr., Mr C. Curtis, Miss G. P. F. Evans, Dr V. Fretter, Professor L. A. Harvey, Mr D. H. Jones and Dr J. Lewis who sent me specimens of Littorina saxatilis; to Professor R. M. Cable and Emerit. Professor G. R. La Rue for helpful suggestions; to Mr J. R. Hirst and Mr D. Hemingway Jones for photographic and technical assistance and to the Department of Scientific and Industrial Research for a grant which made the work possible.


Parasitology ◽  
1972 ◽  
Vol 64 (2) ◽  
pp. 229-233 ◽  
Author(s):  
R. M. Connan

Rats were infected with 1000 larvae at the time of mating and they were given a second infection while suckling a new-born litter some 3½ weeks later. Although they did have significantly more worms than immune controls such rats were nevertheless highly resistant to challenge with infective larvae. However, when challenged with adult worms, immunized lactating rats were unable to eliminate the second infection.That the failure of self-cure in this case was not because adult worms are less antigenic in lactating rats was shown in the third experiment. Lactating rats were immunized by infection either with adult worms only or with larvae allowed to complete their life-cycle. When subsequently challenged with infective larvae during the same lactation, both groups were equally resistant. It is therefore concluded that in lactating rats the gut phase of N. brasiliensis infection is in some way protected from the self-cure mechanism. This may be due either to absence of an essential factor operating late in the process, or to the presence of a potentiating factor which allows the worms to survive.The author would like to thank Professor W. I. B. Beveridge in whose Department this work was carried out, and the Agricultural Research Council for their financial assistance. It is also a pleasure to acknowledge the technical assistance of Mr J. A. Wilson and Mr P. W. Holmes.


Parasitology ◽  
1968 ◽  
Vol 58 (2) ◽  
pp. 415-430 ◽  
Author(s):  
G. W. Seifert ◽  
P. H. Springell ◽  
R. J. Tatchell

The erythrocytes and plasma of a British and Brahman crossbred steer were labelled with51Cr and125I respectively. The radioactivity levels were subsequently maintained as constant as feasible by injecting the steers with calculated amounts of the appropriate labelled material on 3 consecutive days. The steers had previously been heavily infested withBoophilus microplusto ensure that all stages in the parasite's life-cycle would be present during the 4-day period, when the steers were being treated with isotopes.Various stages ofB. micropluslarvae, nymphs and adults were collected and the uptake of red cells and plasma at each stage assessed by radioassay. In certain calculations, corrections were made for the uptake of blood fractions before the animals were made radioactive.A relationship between the weight of the tick and its dietary intake was established. At all the stages of larval and nymphal feeding the plasma content of the diet was greater than that of the host blood. However, erythrocytes were detectable even in the earliest larval stages examined. Dropped fully engorged adult females contained more red cells per individual, and generally also more plasma, than engorged ticks removed from the host.Fully engorged adult females took up as much as twice their own weight of blood components, but in none of the earlier stages did the tick concentrate its blood meal.No obvious differences could be demonstrated statistically between the behaviour of the parasites on the two hosts. However, indications are that recently attached larvae took up more erythrocytes from the British animal.We wish to thank Messrs A. K. Duffield, A. J. Short, B. Wilson, and Miss S. J. Shepherd, for skilful technical assistance.


Parasitology ◽  
1965 ◽  
Vol 55 (1) ◽  
pp. 173-181 ◽  
Author(s):  
D. L. Lee

The cuticle of adults ofNippostrongylus brasiliensishas been described using histological, histochemical and ultrastructural techniques.The cuticle has the following layers: an outer triple-layered membrane; a single cortical layer; a fluid-filled layer which is traversed by numerous collagen fibrils; struts which support the fourteen longitudinal ridges of the cuticle and which are suspended by collagen fibrils in the fluid-filled layer; two fibre layers, each layer apparently containing three layers of fibres; and a basement lamella.The fluid-filled layer contains haemoglobin and esterase.The muscles of the body wall are attached to either the basement lamella or to the fibre layers of the cuticle.The mitochondria of the hypodermis are of normal appearance.The longitudinal ridges of the cuticle appear to abrade the microvilli of the intestinal cells of the host.Possible functions of the cuticle are discussed.I wish to thank Dr P. Tate, in whose department this work was done, for helpful suggestions and criticism at all stages of this work, and Mr A. Page for technical assistance. I also wish to thank Professor Boyd for permission to use the electron microscope in the Department of Anatomy.


Parasitology ◽  
1961 ◽  
Vol 51 (1-2) ◽  
pp. 133-172 ◽  
Author(s):  
J. C. Pearson

1.Neodiplostomum intermediumPearson is recorded from four new hosts; as an adult from the water rat,Hydromys chrysogasterGeoffroy, and as a metacercaria (diplostomulum), from tadpole and adult of an undescribed tree frog,Hylasp., tadpole of (Hyla latopalmata(Günther)Mixophyes fasciolatusGünther and frog of an unidentified leptodactylid.2. The life cycle ofNeodiplostomum intermediumwas followed experimentally; the hosts were:Pettancylus assimilis(Petterd), a fresh-water limpet, as first intermediate host; tadpole ofHyla pearsoniCopland as second intermediate host;Hyla caerulea(Shaw) a tree frog, andHemisphaerodon gerrardiPeters, the pinktongued skink, as paratenic hosts; andRattus assimilis(Gould) and laboratory rats as definitive hosts.3. Descriptions are given of the morphology of the miracidium, mother sporocyst, daughter sporocyst, cercaria, and diplostomulum, with special reference to the structure of the miracidium and of the cercarial tail.4. Observations are given on the embryology of the miracidium, hatching of the egg, transformation of the miracidium into the mother sporocyst with special reference to the germinal cells, the route and manner of escape of cercariae from the snail host, the development of the diplostomulum with special reference to the reserve excretory system, and the movements of diplostomula during metamorphosis of the tadpole host.5. The haploid chromosome number is ten, as determined from squashes of testes. One paratype and a series of experimental adults have been compared with and found different fromNeodiplostomum(Fibricola)sarcophilusn.comb. The orthography and formal proposing of the names of the species ofFibricolatransferred toNeodiplostomumby Pearson (1959b) are corrected.The writer wishes to thank Dr M. J. Mackerras, Queensland Institute for Medical Research, for generously supplying water rats; Professor J. F. A. Sprent, University of Queensland Veterinary School, for his criticism of the manuscript; Mr K. Webber and his sons for their assistance in catching rats and for permission to collect snails, frogs and tadpoles from their streams; and Mr R. J. Ballantyne for technical assistance. This study was supported by a grant from the Rural Credits Fund of the Commonwealth Bank of Australia.


Parasitology ◽  
2009 ◽  
Vol 137 (1) ◽  
pp. 159-171 ◽  
Author(s):  
H. J. McSORLEY ◽  
J. R. GRAINGER ◽  
Y. HARCUS ◽  
J. MURRAY ◽  
A. J. NISBET ◽  
...  

SUMMARYThe transforming growth factor-β (TGF-β) gene family regulates critical processes in animal development, and plays a crucial role in regulating the mammalian immune response. We aimed to identify TGF-β homologues from 2 laboratory model nematodes (Heligmosomoides polygyrus and Nippostrongylus brasiliensis) and 2 major parasites of ruminant livestock (Haemonchus contortus and Teladorsagia circumcincta). Parasite cDNA was used as a template for gene-specific PCR and RACE. Homologues of the TGH-2 subfamily were isolated, and found to differ in length (301, 152, 349 and 305 amino acids respectively), with variably truncated N-terminal pre-proteins. All contained conserved C-terminal active domains (>85% identical over 115 amino acids) containing 9 cysteine residues, as in C. elegans DAF-7, Brugia malayi TGH-2 and mammalian TGF-β. Surprisingly, only the H. contortus homologue retained a conventional signal sequence, absent from shorter proteins of other species. RT-PCR assays of transcription showed that in H. contortus and N. brasiliensis expression was maximal in the infective larval stage, and very low in adult worms. In contrast, in H. polygyrus and T. circumcincta, tgh-2 transcription is higher in adults than infective larvae. The molecular evolution of this gene family in parasitic nematodes has diversified the pre-protein and life-cycle expression patterns of TGF-β homologues while conserving the structure of the active domain.


2011 ◽  
Vol 8 (4) ◽  
pp. 870-876 ◽  
Author(s):  
Baghdad Science Journal

The study aimes to investigate the effects of leaves & fruits ethanolic extract of Duranta repens L. on biological performance for all stages of life cycle of the mosquito Culex pipiens piepiens L., For this purpose the mosquitoes were reared in the laboratory till the fourth generation .Different concentrations of leaves (800,1000,1200,1400ppm) and fruits (800,1000,1200ppm) were tested on (eggs,larval stages,pupal stages and the adult stages). The results revealed that the extracts gave highest mortality rate for the eggs at(100%) compared with control,fruits extract shown highest mortality rate of the four larval instars (100%)at 1200ppm compared with leave extract at(80,50,33.33,20%).Also the extract caused a high mortality rate for pupal stage compared with fruits extract at(76.66,53.33%)respectively.Also ethanolic extract caused a 83.33,76.66% for male &femail. Developmental deformation was observed.. In conclusion, the findings of the present study indicate that the leaves &fruits extracts of Duranta repens L., , can be widely and effectively used in the control of mosquito.


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.


Author(s):  
Jan A. Pechenik

I have a Hardin cartoon on my office door. It shows a series of animals thinking about the meaning of life. In sequence, we see a lobe-finned fish, a salamander, a lizard, and a monkey, all thinking, “Eat, survive, reproduce; eat, survive, reproduce.” Then comes man: “What's it all about?” he wonders. Organisms live to reproduce. The ultimate selective pressure on any organism is to survive long enough and well enough to pass genetic material to a next generation that will also be successful in reproducing. In this sense, then, every morphological, physiological, biochemical, or behavioral adaptation contributes to reproductive success, making the field of life cycle evolution a very broad one indeed. Key components include mode of sexuality, age and size at first reproduction (Roff, this volume), number of reproductive episodes in a lifetime, offspring size (Messina and Fox, this volume), fecundity, the extent to which parents protect their offspring and how that protection is achieved, source of nutrition during development, survival to maturity, the consequences of shifts in any of these components, and the underlying mechanisms responsible for such shifts. Many of these issues are dealt with in other chapters. Here I focus exclusively on animals, and on a particularly widespread sort of life cycle that includes at least two ecologically distinct free-living stages. Such “complex life cycles” (Istock 1967) are especially common among amphibians and fishes (Hall and Wake 1999), and within most invertebrate groups, including insects (Gilbert and Frieden 1981), crustaceans, bivalves, gastropods, polychaete worms, echinoderms, bryozoans, and corals and other cnidarians (Thorson 1950). In such life cycles, the juvenile or adult stage is reached by metamorphosing from a preceding, free-living larval stage. In many species, metamorphosis involves a veritable revolution in morphology, ecology, behavior, and physiology, sometimes taking place in as little as a few minutes or a few hours. In addition to the issues already mentioned, key components of such complex life cycles include the timing of metamorphosis (i.e., when it occurs), the size at which larvae metamorphose, and the consequences of metamorphosing at particular times or at particular sizes. The potential advantages of including larval stages in the life history have been much discussed.


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