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  Babesia bovis Genome Sequencing Project

B. bovis is a tick-transmitted protozoan parasite of cattle that infects and results in the destruction of erythrocytes, causing severe anemia. Smith and Kilbourne’s classic work in the late 1800’s to elucidate the cause and mechanism of transmission of the Texas Fever agent was the first definitive demonstration of a vector-borne protozoan disease.

 

   
Babesia bovis Genome Sequencing Project
 

B. bovis and B. bigemina are important causative agents of bovine babesiosis in tropical and subtropical regions of the world, while Babesia divergens is more common in temperate climates. Babesiosis was a significant problem in the southern US till the 1940’s when it was controlled by eradication of the tick vectors by intensive acaricide dipping of cattle. However, the tick vectors are present in a buffer zone along the Rio Grande, in Mexico, and in US terriroties, and pose the threat of continual reemergence into the US as evidenced by occasional outbreaks of babesiosis in the border region. Emerging acaracide resistance of vector ticks in Mexico is a significant concern, since re-introduction of babesiosis into the US likely will occur via infected ticks. It is estimated that the first year cost of controlling vector ticks alone should they be introduced into the US is over $1.3 billion.  There is currently no babesial vaccine licensed for use in the US, and development of a vaccine is a high priority.

These apicomplexan parasites are related to Plasmodium spp (the causative agents of malaria) and Theilera parva (which causes theileriosis). Aside from being an agriculturally important pathogen, B. bovis resides within an important evolutionary branch within the phylogenic tree. Organisms from this branch of the tree have added substantially to our understanding of biology by the discovery of telomeres, catalytic RNA, the calvin cycle, GPI anchoring, and trans-splicing among others.

The Texas T2Bo strain was selected for genomic sequencing because the history of this isolate is well documented: it is known to be virulent, and it is tick transmissible. A combined clone by clone and whole genome shotgun approach was used to obtain the complete genome sequence for this organism. Phase 1 was end sequencing of a Bacterial Artificial Chromosome (BAC) library. Phase 2 was whole genome shotgun sequencing to 8X coverage. Phase 3 was gap closure.  The resulting sequence contains 9 contigs as indicated in the Table below.

Contig Chromosome
940 1
942 1
941 1
920 2
924 3
930 4
849 4
614 mitochondria
766 plastid

BLAST Babesia bovis contigs: BLAST on local server

Download Sequences  (Have Coordinates from BLAST search available)

This project is a collaboration between Washington State University, the Agricultural Research Service - Animal Disease Research Unit (ARS-ADRU) and The Institute for Genomic Research (www.tigr.org). Funding is provided by USDA/ARS CRIS 5348-32000-020-00D and SCA # 58-5348-2-683.

 
         
 
Revised June 26, 2006     |     Printer Friendly Version

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