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Series GSE132928 Query DataSets for GSE132928
Status Public on Jun 19, 2019
Title Pleiotropic Regulation of Virulence Genes in Streptococcus mutans by the Conserved Small Protein SprV
Organism Streptococcus mutans UA159
Experiment type Expression profiling by high throughput sequencing
Summary Streptococcus mutans, an oral pathogen associated with dental caries, colonizes tooth surfaces as polymicrobial biofilms known as dental plaque. S. mutans expresses several virulence factors that allow the organism to tolerate environmental fluctuations and compete with other microorganisms. We recently identified a small hypothetical protein (90 amino acids) essential for the normal growth of the bacterium. Inactivation of the gene, SMU.2137, encoding this protein caused a significant growth defect and loss of various virulence-associated functions. An S. mutans strain lacking this gene was more sensitive to acid, temperature, osmotic, oxidative, and DNA damage-inducing stresses. In addition, we observed an altered protein profile and defects in biofilm formation, bacteriocin production, and natural competence development, possibly due to the fitness defect associated with SMU.2137 deletion. Transcriptome sequencing revealed that nearly 20% of the S. mutans genes were differentially expressed upon SMU.2137 deletion, thereby suggesting a pleiotropic effect. Therefore, we have renamed this hitherto uncharacterized gene as sprV (streptococcal pleiotropic regulator of virulence). The transcript levels of several relevant genes in the sprV mutant corroborated the phenotypes observed upon sprV deletion. Owing to its highly conserved nature, inactivation of the sprV ortholog in Streptococcus gordonii also resulted in poor growth and defective UV tolerance and competence development as in the case of S. mutans Our experiments suggest that SprV is functionally distinct from its homologs identified by structure and sequence homology. Nonetheless, our current work is aimed at understanding the importance of SprV in the S. mutans biology.
 
Overall design Transcriptional profiling was performed using RNA extracted from cultures of S. mutans parent strain UA159 and the ∆sprV derivative grown in Todd-Hewitt medium supplemented with yeast extract.
 
Contributor(s) Manoharan S, Biswas I
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Submission date Jun 18, 2019
Last update date Jun 19, 2019
Contact name Indranil Biswas
E-mail(s) [email protected]
Phone 9135887019
Organization name University of Kansas Medical Center
Department Microbiology
Street address 3901 Rainbow Blvd
City Kansas City
State/province KS
ZIP/Postal code 66160
Country USA
 
Platforms (1)
GPL23431 Illumina HiSeq 2500 (Streptococcus mutans UA159)
Samples (2)
GSM3896452 Wild Type RNA Seq
GSM3896453 SprV Mutant RNA Seq
Relations
BioProject PRJNA549477
SRA SRP201775

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Supplementary file Size Download File type/resource
GSE132928_Manoharon_and_Biswas_UA159_vs_SMU_2137_diff.xlsx 279.5 Kb (ftp)(http) XLSX
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