On behalf of the authors, we are pleased to announce a new publication that is available online in Genome Biology and Evolution detailing Brucella genetic variability in wildlife marine mammals populations relates to host preference and ocean distribution. Suárez-Esquivel M, KS Baker, N. Ruiz- Villalobos, G. Hernández Mora, E. Barquero-Calvo, R. González-Barrientos, A. Castillo-Zeledón, C. Jiménez-Rojas, C. Chacón Díaz, A. Cloeckaert, E. Barquero-Calvo, N. R Thomson, E. Moreno, C Guzmán-Verri. Brucella genetic variability in wildlife marine mammals populations relates to host preference and ocean distribution. Genome Biol Evol 2017 evx137. doi: 10.1093/gbe/evx137 or https://academic.oup.com/gbe/article/doi/10.1093/gbe/ evx137/3980255/Brucella-Genetic-Variability-in-Wildlife-Marine? guestAccessKey=ad938736-9a3c-4362-adc7-ecfb325445f8 ABSTRACT: Intracellular bacterial pathogens probably arose when their ancestor adapted from a free-living environment to an intracellular one, leading to clonal bacteria with smaller genomes and less sources of genetic plasticity. Still, this plasticity is needed to respond to the challenges posed by the host. Members of the Brucella genus are facultative-extracellular intracellular bacteria responsible for causing brucellosis in a variety of mammals. The various species keep different host preference, virulence, and zoonotic potential despite having 97-99% similarity at genome level. Here, we describe elements of genetic variation in *B. ceti* isolated from wildlife dolphins inhabiting the Pacific Ocean and the Mediterranean Sea. Comparison with isolates obtained from marine mammals from the Atlantic Ocean and the broader Brucella genus showed distinctive traits according to oceanic distribution and preferred host. Marine mammal isolates display genetic variability, represented by an important number of IS711 elements as well as specific IS711 and SNPs genomic distribution clustering patterns. Extensive pseudogenization was found among isolates from marine mammals as compared to terrestrial ones, causing degradation in pathways related to energy, transport of metabolites and regulation/transcription. *B. ceti* isolates infecting particularly dolphin hosts, showed further degradation of metabolite transport pathways as well as pathways related to cell wall/membrane/envelope biogenesis and motility. Thus, gene loss through pseudogenization is a source of genetic variation in *Brucella*, which in turn, relates to adaptation to different hosts. This is relevant to understand the natural history of bacterial diseases, their zoonotic potential and the impact of human interventions such as domestication. A pdf of this manuscript can be downloaded from the Genome Biology and Evolution website: DOI: 10.1093/gbe/evx137 or requests for reprints can be sent to gabbytica@gmail.com Cheers, Gabriela Gabriela Hernández Mora Bacteriology Area National Service of Animal Health (SENASA) Costa Rica