Gene expression profile of early in vitro biofilms of Streptococcus pneumoniae
- Authors
- Yadav, Mukesh Kumar; Kwon, Seong Keun; Cho, Chang Gun; Park, Seok-Won; Chae, Sung-Won; Song, Jae-Jun
- Issue Date
- 9월-2012
- Publisher
- WILEY-BLACKWELL
- Keywords
- biofilm; gene expression; microarray; Streptococcus pneumoniae
- Citation
- MICROBIOLOGY AND IMMUNOLOGY, v.56, no.9, pp.621 - 629
- Indexed
- SCIE
SCOPUS
- Journal Title
- MICROBIOLOGY AND IMMUNOLOGY
- Volume
- 56
- Number
- 9
- Start Page
- 621
- End Page
- 629
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/107540
- DOI
- 10.1111/j.1348-0421.2012.00483.x
- ISSN
- 0385-5600
- Abstract
- In this study, the gene expression profile of early in vitro Streptococcus pneumoniae biofilm with respect to planktonic cells in cDNA microarray analysis is reported. Microarray analysis with respect to planktonic cells was performed on total RNA extracted from biofilms grown in 24-well microtiter plates. To validate the microarray results, real-time RT-PCR was performed on 13 differentially expressed genes and one constitutively expressed gene. The cDNA-microarray analyses identified 89 genes that were significantly differentially expressed in biofilm and planktonic cells. Genes involved in isoprenoid biosynthesis, cell wall biosynthesis, translation and purine and pyrimidine nucleotide metabolic pathways were exclusively expressed in the biofilms, whereas transcription regulator genes were exclusively expressed in planktonic cells. The real-time RT-PCR results of 13 differentially regulated genes were completely in agreement with the microarray data. The exclusive up regulation in biofilms of genes involved in the mevalonate pathway, cell wall biosynthesis, translation and purine and pyrimidine nucleotide metabolic pathways suggests that expression of these genes may be required for initial biofilm formation, and growth and survival of bacteria in biofilms. The up regulation of related genes suggests that cells in biofilms may be under stress conditions and possibly actively involved in the protein synthesis required to adapt to a new environment.
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