Location: Animal Diseases Research
Title: Molecular Characterization of Babesia bovis Strains Using PCR Restriction Fragment Length Polymorphism Analysis of the msa2-a/b Genes Authors
|Wilcowsky, Silvina -|
|Farber, M -|
|Gil, G -|
|Echaide, I -|
|Mosqueda, J -|
|Alcaraz, E -|
|Florin-Christensen, M -|
Submitted to: Annals of the New York Academy of Sciences
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: December 1, 2007
Publication Date: December 15, 2008
Repository URL: http://www3.interscience.wiley.com/cgi-bin/fulltext/121569920/PDFSTART
Citation: Wilcowsky, S., Farber, M., Gil, G., Echaide, I., Mosqueda, J., Alcaraz, E., Suarez, C.E., Florin-Christensen, M. 2008. Molecular Characterization of Babesia bovis strains using PCR restriction length polymorphism analysis of the msa2s/b genes. Annals of the New York Academy of Sciences. 1149:141-144. Interpretive Summary: Babesia bovis is a tick borne apicomplexan pathogen that remains an important constrain for the development of cattle industries worldwide. The disease can be produced by distinct B. bovis stains with different levels of virulence and other characteristics. This manuscript describes a simple method for the differentiation of such strains occurring in the Americas.
Technical Abstract: The merozoite surface antigen-2 (msa-2) family of Babesia bovis is a group of variable genes that share conserved 5' and 3' ends and encode for membrane-anchored glycoproteins that have been postulated as vaccine candidates. In this work, we analyzed the sequences of three of these genes (msa-2a1, a2, and 2b) from two geographically distant strains and detected a certain degree of genotypic diversity that could be exploited to work out new molecular tools for the discrimination of B. bovis field samples. Here we describe a PCR restriction assay that was developed based on this observation and tested on several B. bovis strains and isolates. The results show a strain-specific band pattern in geographically distant isolates, indicating the presence of differentially located BspMI restriction sites. This approach provides a simple method for the differentiation of American B. bovis strains.