Initiation of a Sarcocystis neurona expressed sequence tag (EST) sequencing project:: a preliminary report

被引:19
作者
Howe, DK [1 ]
机构
[1] Univ Kentucky, Gluck Equine Res Ctr, Lexington, KY 40546 USA
关键词
Apicomplexa; equine protozoal myeloencephalitis; gene expression; sequence homology;
D O I
10.1016/S0304-4017(00)00418-0
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
To accelerate genetic and molecular characterization of Sarcocystis neurona, the primary causative agent of equine protozoal myeloencephalitis (EPM), a sequencing project has been initiated that will generate approximately 7000-8000 expressed sequence tags (ESTs) from this apicomplexan parasite. Poly(A)(+) RNA was isolated from culture-derived S. neurona merozoites, and a cDNA library was constructed in a unidirectional lambda phage cloning vector. Sixty phage clones were randomly picked from the library, and the cDNA inserts were amplified from these clones using the T3 and T7 primers that flank the multi-cloning site of the lambda vector. This analysis demonstrated that 100% (60/60) of the clones selected from this library contained recombinant cDNA inserts ranging in size from 0.4 to 4.0 kilobases (kb) with an average size of 1.23 kb. Single-pass sequencing from the 5' end of the 60 amplified cDNAs produced high-quality nucleotide sequence from 53 of the clones. Comparison of these ESTs to the current gene databases revealed significant matches for 10 of the ESTs, six of which are similar to sequences from other Apicomplexa (i.e,, Toxoplasma gondii). Importantly, none of the ESTs were of obvious mammalian origin, thus indicating that the cDNAs in this library were derived primarily from parasite mRNA and not from mRNA of the bovine turbinate host cells. Collectively, these data indicate that the described cDNA library will provide an excellent substrate for generating a portion of the ESTs that are planned from S. neurona. This sequencing project will greatly hasten gene discovery for this protozoan pathogen thereby enhancing efforts towards the development of improved diagnostics, treatments, and preventatives for EPM. In addition, the S. neurona ESTs will represent a significant contribution to the extensive database of sequences from the Apicomplexa. Comparative analyses of these apicomplexan sequences will likely offer a multitude of important information about the biology and evolutionary history of this phylogenetic grouping of parasites. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:233 / 239
页数:7
相关论文
共 17 条
[1]   Gene discovery by EST sequencing in Toxoplasma gondii reveals sequences restricted to the apicomplexa [J].
Ajioka, JW ;
Boothroyd, JC ;
Brunk, BP ;
Hehl, A ;
Hillier, L ;
Manger, ID ;
Marra, M ;
Overton, GC ;
Roos, DS ;
Wan, KL ;
Waterston, R ;
Sibley, LD .
GENOME RESEARCH, 1998, 8 (01) :18-28
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   ANALYSIS OF EXPRESSED SEQUENCE TAGS FROM PLASMODIUM-FALCIPARUM [J].
CHAKRABARTI, D ;
REDDY, GR ;
DAME, JB ;
ALMIRA, EC ;
LAIPIS, PJ ;
FERL, RJ ;
YANG, TP ;
ROWE, TC ;
SCHUSTER, SM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1994, 66 (01) :97-104
[4]   The protozoan parasite Toxoplasma gondii expresses two functional plant-like glycolytic enzymes -: Implications for evolutionary origin of apicomplexans [J].
Dzierszinski, F ;
Popescu, O ;
Toursel, C ;
Slomianny, C ;
Yahiaoui, B ;
Tomavo, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (35) :24888-24895
[5]   Experimental induction of equine protozoal myeloencephalitis in horses using Sarcocystis sp. sporocysts from the opossum (Didelphis virginiana) [J].
Fenger, CK ;
Granstrom, DE ;
Gajadhar, AA ;
Williams, NM ;
McCrillis, SA ;
Stamper, S ;
Langemeier, JL ;
Dubey, JP .
VETERINARY PARASITOLOGY, 1997, 68 (03) :199-213
[6]   EQUINE PROTOZOAL MYELITIS IN PANAMANIAN HORSES AND ISOLATION OF SARCOCYSTIS-NEURONA [J].
GRANSTROM, DE ;
ALVAREZ, O ;
DUBEY, JP ;
COMER, PF ;
WILLIAMS, NM .
JOURNAL OF PARASITOLOGY, 1992, 78 (05) :909-912
[7]   Development of molecular genetics for Neospora caninum: A complementary system to Toxoplasma gondii [J].
Howe, DK ;
Sibley, LD .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 13 (02) :123-133
[8]   Shikimate pathway in apicomplexan parasites [J].
Keeling, PJ ;
Palmer, JD ;
Donald, RGK ;
Roos, DS ;
Waller, RF ;
McFadden, GI .
NATURE, 1999, 397 (6716) :219-220
[9]   A plastid of probable green algal origin in apicomplexan parasites [J].
Kohler, S ;
Delwiche, CF ;
Denny, PW ;
Tilney, LG ;
Webster, P ;
Wilson, RJM ;
Palmer, JD ;
Roos, DS .
SCIENCE, 1997, 275 (5305) :1485-1489
[10]   Expressed sequence tag analysis of the bradyzoite stage of Toxoplasma gondii:: Identification of developmentally regulated genes [J].
Manger, ID ;
Hehl, A ;
Parmley, S ;
Sibley, LD ;
Marra, M ;
Hillier, L ;
Waterston, R ;
Boothroyd, JC .
INFECTION AND IMMUNITY, 1998, 66 (04) :1632-1637