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Transcriptome profiling of Lactococcus garvieae strains in response to growth temperature

ABSTRACT: Analysis of the changes in the transcriptome of two different Lactococcus garvieae strains (21881 & 8831) at different temperatures of growth (18/37 ºC)

ORGANISM(S): Lactococcus garvieae

PROVIDER: GSE40318 | GEO | 2013/11/04

SECONDARY ACCESSION(S): PRJNA173482

REPOSITORIES: GEO

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Transcriptome profiling of Lactococcus garvieae strains in response to growth temperature

Project description:Analysis of the changes in the transcriptome of two different Lactococcus garvieae strains (21881 & 8831) at different temperatures of growth (18/37 M-BM-:C) Reference design experiment comparing samples of 21881 and 8831 strains of Lactoccocus garvieae, with three biological replicates for each condition grown at 18 and 37 degrees Celsius. The results were referenced to a equimolar mixture of both strains grown at 29 degrees Celsius

2013-11-04 | E-GEOD-40318 | biostudies-arrayexpress

Transcriptome profiling of Lactococcus garvieae 21881 in response to different stress conditions

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Transcriptome analysis of Lactococcus garvieae strain 8831 grown at 13ºC and 18ºC

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Analysis of the genome content of Lactococcus garvieae by genomic interspecies microarray hybridization

Project description:Background: Lactococcus garvieae is a bacterial pathogen that affects different animal species and human. Despite the widespread distribution and emerging clinical significance of L. garvieae in both veterinary and human medicine, there is almost a complete lack of knowledge about the genetic content of this microorganism. In the present study the genomic content of L. garvieae CECT 4531 was analyzed by bioinformatic tools and microarray-based comparative genomic hybridizations (CGH) experiments, using Lactococcus lactis subsp. lactis IL1403 and Streptococcus pneumoniae TIGR4 as reference microorganisms. Results: The combination and integration of in silico analyses and in vitro (CGH) experiments performed between the reference microorganisms allowed establishing an inter-species hybridization framework with a detection threshold based on the sequence similarity ≥70%. With this threshold value, 267 genes were identified as having an analogue in L. garvieae, most of which (n = 258) have been documented for the first time in this pathogen. Most of these genes are related to ribosomal, sugar metabolism or energy conversion systems. Some identified genes could be involved in the pathogenesis of L. garvieae infections. Conclusions: In this study a comparative analysis based on microarray interspecies hybridization and the use of bioinformatic tools were used for the first time to study the genetic content of L. garvieae CECT 4531. Towards this approach, we identified 267 potentially present genes in L. garvieae CECT 4531, some of which could be involved in the pathogenesis of L. garvieae infections, such as als or mycA. These results provide the first insight into the genome content of L. garvieae.

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