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    Emes, Richard Thompson, Fiona Moore, Joyce Zang, Xingxing and Devaney, Eileen 2002. Cloning and characterisation of mmc-1, a microfilarial-specific gene, from Brugia pahangi. International Journal for Parasitology, Vol. 32, Issue. 4, p. 415.


    Michalski, Michelle L and Weil, Gary J 1999. Gender-specific gene expression in Brugia malayi. Molecular and Biochemical Parasitology, Vol. 104, Issue. 2, p. 247.


    Underwood, Anthony P. and Bianco, Albert E. 1999. Identification of a molecular marker for the Y chromosome of Brugia malayi. Molecular and Biochemical Parasitology, Vol. 99, Issue. 1, p. 1.


    Nembo, B. Duie, P. Garcia, M. Breton, P. Gayral, P. Porcheron, P. and Goudey-Perriere, F. 1993. Levels of ecdysteroid-like material in adults of Nippostrongylus brasiliensis during the intestinal phase. Journal of Helminthology, Vol. 67, Issue. 04, p. 305.


    Goudey-Perriere, Françoise Simo, Blandine Fokam Maccario, Jean Perriere, Claude and Gayral, Philippe 1992. Effects of ecdysteroids on reproductive physiology of Nippostrongylus brasiliensis (nematoda) in vivo. Comparative Biochemistry and Physiology Part C: Comparative Pharmacology, Vol. 103, Issue. 1, p. 105.


    BARKER, G. C. CHITWOOD, D. J. and REES, H. H. 1990. Ecdysteroids in helminths and annelids. Invertebrate Reproduction & Development, Vol. 18, Issue. 1-2, p. 1.


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Egg production in Brugia pahangi(Nematoda: Filarioidea)

  • C. J. Delves (a1), H. H. Rees (a2) and R. E. Howells (a1)
  • DOI: http://dx.doi.org/10.1017/S0031182000059746
  • Published online: 01 April 2009
Abstract
Summary

Oogenesis in Brugia pahangi has been studied by means of the aceto-orcein chromosomal squash technique and light-microscope autoradiography. The use of colchicine has demonstrated a 2–3 mm terminal germinative zone within the ovary, in which continuous and rapid mitotic division of germ cells occurs. In 80% of the gonads, oocytes within a 1–2 mm length of the ovary proximal to the germinative zone were at the prophase of meiosis I. Primary oocytes with markedly less condensed chromatin, apparently interphase cells, were observed in the corresponding region of the ovary in the remaining 20% of material examined. A cyclical or phased development of primary oocytes is suggested. Autoradiographic studies, concerned with the incorporation of [5-3H]uridine into germ cells of B. pahangi in vitro, further suggest that the onset of meiotic prophase is associated with the initiation of high RNA synthetic activity. Following meiotic prophase, oocytes complete meiosis I before entering a period of growth during which the chromatin material is decondensed. Recondensation of chromosomes prior to meiosis II is only observed after fertilization within the seminal receptacle. On completion of meiosis II, with the extrusion of a polar body, the haploid chromosome complement of the female unites with that of the male, re-establishing the diploid number of the zygote (2n = 10).

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Reprint requests to Professor R. E. Howells.
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Y. Sakaguchi , I. Tada , L. R. Ash & Y. Aoki (1983). Karyotypes of Brugia pahangi and B. malayi (Nematoda: Filarioidea). Journal of Parasitology 69, 1090–3.

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Parasitology
  • ISSN: 0031-1820
  • EISSN: 1469-8161
  • URL: /core/journals/parasitology
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