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The Development of Heligmosomum muris Yokogawa, a Nematode from the Intestine of the Wild Rat1

Published online by Cambridge University Press:  06 April 2009

Sadamu Yokogawa
Affiliation:
Professor of Pathology, Medical School of Formosa.

Extract

1. Heligtnosomum muris proved to be very favourable material for the study of nematode development, since it will develop perfectly normally in culture rats, infection is easily carried out and since sexual maturity is reached in 7–10 days after infection.

2. The post-embryonal development of H. muris is divided into five stages, two free and three parasitic, with three moults. There is only one moult during free life, the second and third stages being separated by change of habitat brought about by entrance into the host. Sexual maturity is attained soon after the completion of the third moult. The mature worm has two cuticular layers, the outer of which is separated by a space from the inner. This outer cuticula is probably the beginning of a fourth moult which is never completed.

3. Under favourable conditions the eggs hatch in about 20 to 24 hours after being passed with the faeces.

4. The first two stages of post-embryonal development, which are passed in free life, are separated by a relatively long moult during which the larva changes from the rhabditiform type to the filariform type. During this period there is a rapid division of the cells lining the intestine, which frees masses of these cells into the lumen and leaves the intestine of the filariform larva lined with flattened cells.

5. The infective stage is not enclosed in a sheath and tends to work its way out of the culture onto the glass or along the edges of the filter paper. At this stage it is impossible to distinguish the sexes.

6. Infection of the rat can be accomplished both by way of the mouth or through the skin although the latter method is by far the most effective. The larvae reach the lungs about 14 to 20 hours after penetration through the skin. They remain in the lungs until about 35 to 65 hours after infection. The majority of them reach the intestine 50 to 65 hours after infection, although in a few they were found as early as 45 hours.

7. In the lungs the larvae increase rapidly in size and moult just before they migrate to the intestine. Early in the development in the lungs the sexes can be distinguished by: (1) the migration toward the posterior end of the genital primordium of the female, (2) structural differences in the caudal region, and (3) differences in shape of the genital primordium.

8. After reaching the intestine the larvae grow rapidly and enter into the third moult from 96 to 108 hours after infection. In the fourth larval stage between the second and third moults growth and differentiation are most marked. It is during this stage that the differentiation of the organs of the reproductive system occurs.

9. Shortly after the completion of the third moult sexual maturity is reached and later the cuticula separates into two layers.

10. During the course of development the changes in size and shape and in the character of the cuticula were traced step by step and the differentiation of the digestive and excretory systems were followed as completely as the material would permit. However it was in following the details of the development of the reproductive organs that the investigation was most fully carried out.

11. In the male reproductive system the testes, vas deferens, seminal vesicle, cement gland and ejaculatory duct arise by differentiations of the genital primordium and are therefore called internal sex-organs, while the bursa and the spicules which are not developed from the genital primordium are known as the external sex-organs.

12. Toward the end of the third larval stage (first parasitic stage) the genital primordium of the male becomes separated into two parts by an extremely delicate strand of tissue. The anterior half of this genital primordium grows forward up to the oesophageal region and forms the testes, the narrow strand connecting the two parts develops into the vas deferens, and the posterior part grows backward to the posterior end, becomes tubular and forms the seminal vesicle, cement gland and ejaculatory duct.

13. The bursa is formed from the walls of the posterior end of the male which become very much inflated, and the spicules develop from secretions of a group of spindle-shaped cells which are early differentiated in the posterior region.

14. In the development of the female reproductive system the ovary, oviduct, seminal receptacle, uterus and the anterior part of the ovijector arise from the differentiation of the genital primordium and are therefore called internal sex-organs, while the vulva, vagina and posterior part of the ovijector arise from invagination and differentiation of subcuticular cells of the posterior end and are therefore called external reproductive organs.

15. After the genital primordium has migrated backward to a position on the ventral side just in front of the anus, it elongates very greatly and grows forward. The anterior part remains as a solid mass of cells and differentiates into the ovary. The rest of the primordium becomes tubular and differentiates into the oviduct, seminal receptacle, uterus and ovijector.

16. A group of cells just in front of the rectum and just over the posterior part of the genital primordium increases in number, invaginates, becomes differentiated into a tube which joins with the posterior part of the genital primordium. This tube differentiates into the vulva and vagina. Where it joins the posterior end of the internal reproductive organs there is an overlapping so that the posterior end of the ovijector has a double origin.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1922

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References

Leuckart, R. (1887). Neue Beiträge zur Kenntniss des Baues und der Lebensgeschichte der Nematoden. Abhandl. d. math.-phys. Cl. d. k. sächs. Gesellsch. d. Wissensch. Leipzig, XIII. 565704, 3 pls.Google Scholar
Looss, A. (1897). Notizen zur Helminthologie Egyptens. 2. Centralbl. f. Bakt. u.Parasitenk. (etc.), Jena, XXI. 913–26, 10 figs.Google Scholar
Looss, A. (1905). The Anatomy and Life History of Agchylostoma duodenale (Dub.). A Monograph. Part I. Records of the Egyptian Government School of Medicine, III. 1158, 10 pls.Google Scholar
Looss, A. (1911). The Anatomy and Life History of Agchylostoma duodenale (Dub.). A Monograph.Part II. Records of the Egyptian Government School of Medicine, IV. 167611.Google Scholar
Neuhaus, C. (1903). Die post-embryonale Entwickelung der Rhabditis nigrovenosa. Jenaische Ztschr. f. Naturw. Jena, XXXVII. 653–90, 2 pls. and 1 fig. in text.Google Scholar
Theiler, H. and Robertson, W. (1915). Investigations into the Life History of the Wireworm in Ostriches. 3rd and 4th Reports of the Director of Veterinary Research, Department of Agriculture, Union of South Africa, pp. 293336, 9 pls.Google Scholar
Veglia, F. (1915). The Anatomy and Life History of the Haemonchus contortus (Rud.). 3Ard and 4th Reports of the Director of Veterinary Research, Department of Agriculture, Union of South Africa, pp. 349–47, 22 pls.Google Scholar
Yokogawa, S. (1920). A New Nematode from the Rat. Journ. Parasit. VII. 2933, 2 pls.CrossRefGoogle Scholar