cDNA was generated by using Superscript III RT (Invitrogen) according to the manufacturer’s protocol. 1 μl of the resulting cDNA was used for each PCR. As a negative control, reactions were also run on RNA templates without RT treatment, selleck and as a positive control, each reaction was also made with purified genomic DNA as template. The cycling parameters were 30 cycles of 94°C for 30 s, 55°C for 30 s, and 72°C for 1.5 min. The resulting amplicons were analyzed in 0.8% agarose gels. Primers were designed with Primer3 software [34]. Genomic data and analysis The complete MGCD0103 mw genome sequence and annotation of the B. abortus 2308 strain was
obtained fron GenBank (Accession numbers AM040264 and AM040265 for chromosomes LY2109761 datasheet I and II respectively). Blast comparisons against the microbial genome database were performed via web at the NCBI Blast server [35]. Statistical analysis A statistical analysis was performed using Prism3, version 3.0(GraphPad Software, San Diego, CA). Statistical significance wascalculated using either a nonparametric Mann-Whitney test or an unpaired t test. A P value of < 0.05 was considered statistically significant.
Acknowledgements This work was supported by grants BIO2007-63656 from the Spanish Ministerio de Educación y Ciencia, and API 07/01 from Fundación Marqués de Valdecilla to FJS. We thank Matxalen Llosa and Olga Draper for critical reading and copyediting of the manuscript, Regis Hallez and Xavier de Bolle for providing plasmid pRH016, and Dominique Schneider for providing plasmid pDS132. References 1. Sangari FJ, Seoane A, Rodriguez MC, Aguero J,
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