Global regulation by (p)ppGpp and CodY in Streptococcus mutans
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Lemos, Jose A.
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Univ Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USAUniv Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Lemos, Jose A.
[1
,2
]
Nascimento, Marcelle A.
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Univ Florida, Coll Dent, Dept Oral Biol, Gainesville, FL 32610 USAUniv Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Nascimento, Marcelle A.
[3
]
Lin, Vanessa K.
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Univ Florida, Coll Dent, Dept Oral Biol, Gainesville, FL 32610 USAUniv Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Lin, Vanessa K.
[3
]
Abranches, Jacqueline
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Univ Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USAUniv Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Abranches, Jacqueline
[1
,2
]
Burne, Robert A.
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Univ Florida, Coll Dent, Dept Oral Biol, Gainesville, FL 32610 USAUniv Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
Burne, Robert A.
[3
]
机构:
[1] Univ Rochester, Med Ctr, Ctr Oral Biol, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
The RelA, RelP, and RelQ enzymes are responsible for the production of the alarmone (p)ppGpp in Streptococcus mutans. A strain lacking all three synthetases (Delta relAPQ) does not grow in minimal medium lacking the branched-chain amino acids (BCAA) leucine or valine but grows well if isoleucine is also omitted. Here, we investigated whether there was a correlation between growth in the absence of leucine and valine with (p)ppGpp pools and the activation of CodY. By using a combination of single, double, and triple mutants lacking the (p)ppGpp synthetase enzymes, we demonstrated that the ability to grow in the absence of leucine or valine required basal levels of (p) ppGpp production by RelP and RelQ. The introduction of a codY mutation into the Delta relAPQ strain fully restored growth in medium lacking leucine or valine, revealing that the growth-defective phenotype of Delta relAPQ was directly linked to CodY. Lowering GTP levels through the addition of decoyinine did not alleviate CodY repression or affect the expression of genes involved in BCAA biosynthesis, suggesting that S. mutans CodY is not activated by GTP. The results of phenotypic studies revealed that the codY mutant had a reduced capacity to form biofilms and that its growth was more sensitive to low pH, showing a role for CodY in two key virulence properties of S. mutans. Microarray results revealed the extent of the CodY regulon. Notably, the identification of putative CodY-binding boxes upstream of genes that were downregulated in the codY mutant indicates that CodY may also function as a transcriptional activator in S. mutans.