Identification of abundantly expressed novel and conserved genes from the infective larval stage of Toxocara canis by an expressed sequence tag strategy

被引:81
作者
Tetteh, KKA
Loukas, A
Tripp, C
Maizels, RM
机构
[1] Univ Edinburgh, ICAPB, Edinburgh EH9 3JT, Midlothian, Scotland
[2] Heska Corp, Ft Collins, CO 80525 USA
关键词
D O I
10.1128/IAI.67.9.4771-4779.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Larvae of Toxocara canis, a nematode parasite of dogs, infect humans, causing visceral and ocular larva migrans, In noncanid hosts, larvae neither grow nor differentiate but endure in a state of arrested development. Reasoning that parasite protein production is orientated to immune evasion, we undertook a random sequencing project from a larval cDNA library to characterize the most highly expressed transcripts. In all, 266 clones were sequenced, most from both 3' and 5' ends, and similarity searches against GenBank protein and dbEST nucleotide databases were conducted. Cluster analyses showed that 128 distinct gene products had been found, all but 3 of which represented newly identified genes. Ninety-five genes were represented by a single clone, but seven transcripts were present at high frequencies, each composing >2% of all clones sequenced. These high-abundance transcripts include a mucin and a C-type lectin, which are both major excretory-secretory antigens released by parasites. Four highly expressed novel gene transcripts, termed ant (abundant novel transcript) genes, were found. Together, these four genes comprised 18% of all cDNA clones isolated, but no similar sequences occur in the Caenorhabditis elegans genome. While the coding regions of the four genes are dissimilar, their 3' untranslated tracts have significant homology in nucleotide sequence, The discovery of these abundant, parasite-specific genes of newly identified lectins and mucins, as well as a range of conserved and novel proteins, provides defined candidates for future analysis of the molecular basis of immune evasion by T, canis.
引用
收藏
页码:4771 / 4779
页数:9
相关论文
共 75 条
[21]  
de Savigny D.H., 1975, Journal Parasit, V61, P781, DOI 10.2307/3279492
[22]   MOLECULAR-CLONING AND SEROLOGICAL CHARACTERIZATION OF A BRUGIA-MALAYI PEPSIN INHIBITOR HOMOLOG [J].
DISSANAYAKE, S ;
XU, M ;
NKENFOU, C ;
PIESSENS, WF .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1993, 62 (01) :143-146
[23]   CDNA EXPRESSED SEQUENCE TAGS OF TRYPANOSOMA-BRUCEI-RHODESIENSE PROVIDE NEW INSIGHTS INTO THE BIOLOGY OF THE PARASITE [J].
ELSAYED, NMA ;
ALARCON, CM ;
BECK, JC ;
SHEFFIELD, VC ;
DONELSON, JE .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 73 (1-2) :75-90
[24]  
FALCONE FH, UNPUB
[25]   Generation, identification, and evaluation of expressed sequence tags from different developmental stages of the Asian blood fluke Schistosoma japonicum [J].
Fan, JJ ;
Minchella, DJ ;
Day, SR ;
McManus, DP ;
Tiu, WU ;
Brindley, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 252 (02) :348-356
[26]  
*FIL GEN PROJ, IN PRESS PARASITOL T
[27]   Molecular cloning and in vitro expression of C-elegans and parasitic nematode ionotropic receptors [J].
Fleming, JT ;
Baylis, HA ;
Sattelle, DB ;
Lewis, JA .
PARASITOLOGY, 1996, 113 :S175-S190
[28]   AN ABUNDANT, TRANS-SPLICED MESSENGER-RNA FROM TOXOCARA-CANIS INFECTIVE LARVAE ENCODES A 26-KDA PROTEIN WITH HOMOLOGY TO PHOSPHATIDYLETHANOLAMINE-BINDING PROTEINS [J].
GEMS, D ;
FERGUSON, CJ ;
ROBERTSON, BD ;
NIEVES, R ;
PAGE, AP ;
BLAXTER, ML ;
MAIZELS, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (31) :18517-18522
[29]   An abundantly expressed mucin-like protein from Toxocara canis infective larvae: The precursor of the larval surface coat glycoproteins [J].
Gems, D ;
Maizels, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1665-1670
[30]   HUMAN TOXOCARIASIS [J].
GILLESPIE, SH .
JOURNAL OF APPLIED BACTERIOLOGY, 1987, 63 (06) :473-479