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Digestion in the tick,Argas persicus, Oken.

Published online by Cambridge University Press:  06 April 2009

R. J. Tatchell
Affiliation:
The Molteno Institute, University of Cambridge*

Extract

1.Studies on the histological changes during digestion in Argas persicus reveal that the ingestion of blood is accompanied by the destruction of the existing gut epithelial cells.

2.The blood remains unlysed for 2–3 days while a new epithelium develops which contains cells that secrete a saliva-fast PAS-positive colloid that causes haemolysis.

3.Other epithelial cells remove the freed erythrocytic nuclei by phagocytosis.

4.Most of the gut cells then absorb protein from the lumen and intracellular digestion takes place leaving pure haematin granules as the waste product of the digestion of haemoglobin.

5.After the initial rapid phase of digestion only relatively few cells show signs of absorptive and digestive activity.

6.Absorption of protein is accompanied by increased alkaline phosphatase activity in the microvilli of the cell border; this activity is lost once absorption finishes and digestion begins.

7.Strong aminopeptidase activity can be demonstrated at the border of some of the protein vacuoles.

8.In vitro tests show that the gut proteinase is active only in the acid range with peaks at pH 2·6 and 3·8 and has a Km of 0·32 % with bovine serum albumin as substrate.

9.In vivo data show that digestion, after haemolysis has occurred, takes place in two phases; the first is rapid and lasts approximately 1–2 weeks and is followed by the second phase which is slow and remains constant until the next blood feed.

10.The proportion of the blood meal which remains after the rapid phase of digestion is determined by the sex and developmental stage of the tick and within each category it is constant and serves, in the absence of significant fat and glycogen reserves, as a food reserve.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1964

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References

REFERENCES

Balashov, Y. S. (1961). The structure of digestive organs and the blood digestion in argasidae. Mag. Parasit., Moscow, 20, 185225.Google Scholar
Christophers, S. R. (1906). The anatomy and histology of ticks. Sci. Mem. med. sanit. Dep. India (N.S.), 23, 155.Google Scholar
Frame, E.G., Russel, J. A. & Wilhemi, A. E. (1943). The colorimetric estimation of amino nitrogen in blood. J. biol. Chem. 149, 255–70.CrossRefGoogle Scholar
Fraser, A., Ring, R. A. & Stewart, R. K. (1961). Intestinal proteinases in an insect, Calliphora vomitoria L. Nature, Lond, 192, 9991000.CrossRefGoogle Scholar
Gózony, L., Hindle, E. & Ross, P. H. (1914). Serological tests. J. Hyg., Camb. 14, 354–9.CrossRefGoogle ScholarPubMed
Greenberg, B. & Paretsky, D. (1955). Proteolytic digestion in the house-fly, Musca domestica. Ann. ent. Soc. Amer. 48, 4650.CrossRefGoogle Scholar
Heatley, N. G. (1936). The digestive enzymes of the Onychophora (Peripatopsis spp.). J. exp. Biol. 13, 329–43.CrossRefGoogle Scholar
Hughes, T. E. (1954). Some histological changes which occur in the gut epithelium of Ixodes ricinus females during gorging and up to oviposition. Ann. trop. Med. Parasit. 48, 397404.CrossRefGoogle ScholarPubMed
Keilin, D. & Wang, Y. L. (1947). Stability of haemoglobin and of certain endoerythrocytic enzymes in vitro. Biochem. J. 41, 491500.CrossRefGoogle ScholarPubMed
Kitaoka, S. (1961). Physiological and ecological studies on some ticks. VI. Rate of digestion of blood meal and nitrogen, iron and sterol economy during the ovipositing process in the tick. Nat. Inst. Animal Hlth. Quart. 1, 105–12.Google Scholar
Lambremont, E. N., Fisk, F. W. & Ashrafi, S. (1959). Pepsin-like enzyme in larvae of stable flies. Science, 129, 1484–5.CrossRefGoogle ScholarPubMed
Lees, A. D. (1946). Chloride excretion and the function of coxal glands in ticks. Parasitology, 37, 172–84.CrossRefGoogle Scholar
Llewellyn, J. (1954). Observations on the food and the gut pigment of the Polyopisthocotylea (Trematoda: Monogenea). Parasitology, 44, 428–37.CrossRefGoogle ScholarPubMed
Pearse, A. G. E. (1960). Histochemistry. Theoretical and Applied. London: J. and A. Churchill Ltd.Google Scholar
Pickford, G. E. (1942). Studies on the digestive enzymes of spiders. Trans. Conn. Acad. Arts Sci. 35, 3372.Google Scholar
Robinson, L. E. & Davidson, J. (1914). The anatomy of Argas persicus (Oken). II. Parasitology, 6, 217–56.CrossRefGoogle Scholar
Roesler, R. (1934). Histologische, physiologische und serologische Untersuchungen über die Verdauung bei der Zeckengattung Ixodes Latr. Z. Morph. ökol. Tiere, 28, 297317.CrossRefGoogle Scholar
Russel, J. A. (1944). Note on the colorimetric determination of amino-nitrogen. J. biol. Chem. 156, 467.CrossRefGoogle Scholar
Till, W. M. (1961). A contribution to the anatomy and histology of the brown ear tick Rhipicephalus appendiculatus Neumann. Mem. ent. Soc. S. Afr. 6, 1124.Google Scholar
Tomarelli, R. M., Charney, J. & Harding, M. L. (1949). The use of azo-albumin as a substrate in the colorimetric determination of peptic and tryptic activity. J. Lab. clin. Med. 34, 428–33.Google Scholar
Weitz, B. & Buxton, P. A. (1953). Rate of digestion of blood meals of various haematophagous arthropods as determined by the precipitin test. Bull. ent. Res. 44, 445–50.CrossRefGoogle Scholar
Wigglesworth, V. B. (1959). A simple method for cutting sections in the 0·5 to range and for sections of chitin. Quart. J. micr. Sci. 100, 315–20.Google Scholar