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Gene expression profile of early in vitro biofilms of Streptococcus pneumoniae

Authors
Yadav, Mukesh KumarKwon, Seong KeunCho, Chang GunPark, Seok-WonChae, Sung-WonSong, 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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