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Transcriptomic Analysis of the Adaptation of Listeria monocytogenes to Growth on Vacuum-Packed Cold Smoked Salmon.
Tang, Silin; Orsi, Renato H; den Bakker, Henk C; Wiedmann, Martin; Boor, Kathryn J; Bergholz, Teresa M.
Afiliação
  • Tang S; Department of Food Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York, USA.
  • Orsi RH; Department of Food Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York, USA.
  • den Bakker HC; Department of Food Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York, USA.
  • Wiedmann M; Department of Food Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York, USA.
  • Boor KJ; Department of Food Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, New York, USA.
  • Bergholz TM; Department of Veterinary and Microbiological Sciences, North Dakota State University, Fargo, North Dakota, USA teresa.bergholz@ndsu.edu.
Appl Environ Microbiol ; 81(19): 6812-24, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26209664
The foodborne pathogen Listeria monocytogenes is able to survive and grow in ready-to-eat foods, in which it is likely to experience a number of environmental stresses due to refrigerated storage and the physicochemical properties of the food. Little is known about the specific molecular mechanisms underlying survival and growth of L. monocytogenes under different complex conditions on/in specific food matrices. Transcriptome sequencing (RNA-seq) was used to understand the transcriptional landscape of L. monocytogenes strain H7858 grown on cold smoked salmon (CSS; water phase salt, 4.65%; pH 6.1) relative to that in modified brain heart infusion broth (MBHIB; water phase salt, 4.65%; pH 6.1) at 7°C. Significant differential transcription of 149 genes was observed (false-discovery rate [FDR], <0.05; fold change, ≥2.5), and 88 and 61 genes were up- and downregulated, respectively, in H7858 grown on CSS relative to the genes in H7858 grown in MBHIB. In spite of these differences in transcriptomes under these two conditions, growth parameters for L. monocytogenes were not significantly different between CSS and MBHIB, indicating that the transcriptomic differences reflect how L. monocytogenes is able to facilitate growth under these different conditions. Differential expression analysis and Gene Ontology enrichment analysis indicated that genes encoding proteins involved in cobalamin biosynthesis as well as ethanolamine and 1,2-propanediol utilization have significantly higher transcript levels in H7858 grown on CSS than in that grown in MBHIB. Our data identify specific transcriptional profiles of L. monocytogenes growing on vacuum-packaged CSS, which may provide targets for the development of novel and improved strategies to control L. monocytogenes growth on this ready-to-eat food.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Pesqueiros / Listeria monocytogenes Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Pesqueiros / Listeria monocytogenes Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article