The Presence of Plasmids in Lactococcus lactis IL594 Determines Changes in the Host Phenotype and Expression of Chromosomal Genes.
Katarzyna KosiorekAnna Koryszewska-BagińskaMarek SkonecznyLidia Stasiak-RóżańskaTamara Aleksandrzak-PiekarczykPublished in: International journal of molecular sciences (2023)
The L. lactis IL594 strain contains seven plasmids (pIL1 to pIL7) and is the parental strain of the plasmid-free L. lactis IL1403, one of the most studied lactic acid bacteria (LAB) strain. The genetic sequences of pIL1 to pIL7 plasmids have been recently described, however the knowledge of global changes in host phenotype and transcriptome remains poor. In the present study, global phenotypic analyses were combined with transcriptomic studies to evaluate a potential influence of plasmidic genes on overall gene expression in industrially important L. lactis strains. High-throughput screening of phenotypes differences revealed pronounced phenotypic differences in favor of IL594 during the metabolism of some C-sources, including lactose and β-glucosides. A plasmids-bearing strain presented increased resistance to unfavorable growth conditions, including the presence of heavy metal ions and antimicrobial compounds. Global comparative transcriptomic study of L. lactis strains revealed variation in the expression of over 370 of chromosomal genes caused by plasmids presence. The general trend presented upregulated energy metabolism and biosynthetic genes, differentially expressed regulators, prophages and cell resistance proteins. Our findings suggest that plasmids maintenance leads to significant perturbation in global gene regulation that provides change in central metabolic pathways and adaptive properties of the IL594 cells.
Keyphrases
- escherichia coli
- genome wide
- single cell
- klebsiella pneumoniae
- gene expression
- rna seq
- poor prognosis
- heavy metals
- dna methylation
- lactic acid
- bioinformatics analysis
- copy number
- induced apoptosis
- drinking water
- multidrug resistant
- signaling pathway
- binding protein
- crispr cas
- cell proliferation
- cell death
- quantum dots
- mesenchymal stem cells