Expression of the filarial nematode phosphorylcholine-containing glycoprotein, ES62, is stage specific

被引:29
作者
Stepek, G
Auchie, M
Tate, R
Watson, K
Russell, DG
Devaney, E
Harnett, W [1 ]
机构
[1] Univ Strathclyde, Dept Immunol, Glasgow G4 0NR, Lanark, Scotland
[2] Univ Strathclyde, Dept Biosci & Biotechnol, Glasgow G4 0NR, Lanark, Scotland
[3] Univ Glasgow, Dept Immunol, Glasgow G11 6NT, Lanark, Scotland
[4] Cornell Univ, Coll Vet Med, Dept Microbiol & Immunol, Ithaca, NY 14853 USA
[5] Univ Glasgow, Dept Vet Parasitol, Glasgow G61 1GH, Lanark, Scotland
关键词
ES62; Acanthocheilonema viteae; Brugia pahangi; expression;
D O I
10.1017/S0031182002001920
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
ES62, an immunomodulatory phosphorylcholine-containing glycoprotein secreted by the rodent filarial nematode Acanthocheilonema viteae, has previously been shown to be produced by L4 larvae and adult worms only. However, homologous sequences to ES62 have recently been found in L1 and L3 cDNA libraries of certain human filarial nematodes. Therefore, the various stages of A. viteae were re-examined and it was again found that only the post-L3 stages secreted ES62. Synthesis but not secretion by earlier stages was ruled out by examination of the protein content of whole worm extracts and by immunoelectron microscopy. However, examination by PCR of the mRNA for ES62 revealed that it was found in the L1 and L3 larvae. This may explain why homologous sequences to ES62 have been found in Brugia malayi and Onchocerca volvulus larval cDNA libraries. It also suggests that filarial nematodes, in general, may secrete ES62. To obtain evidence for this, we investigated production by Brugia pahangi, a close relation of B. malayi. We found that ES62 was indeed secreted but, as with A. viteae, only by the post-L3 stages, although again the mRNA for ES62 could be detected in the earlier stages. Overall our results suggest that production of ES62 is not species specific, that it is indeed stage specific, and that this may be due to post-transcriptional control of expression.
引用
收藏
页码:155 / 164
页数:10
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