ArticleInfection and immunity2000
Production of toxic shock syndrome toxin 1 by Staphylococcus aureus requires both oxygen and carbon dioxide.
Article in Infection and immunity, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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Who cites it
22 citing papers in PubMed.
- Vanillic acid-based pro-coagulant hemostatic shape memory polymer foams with antimicrobial properties against drug-resistant bacteria.Acta biomaterialia · 2024Article
- The host phylogeny determines viral infectivity and replication across Staphylococcus host species.PLoS pathogens · 2023Article
- The Association Between Onset of Staphylococcal Non-menstrual Toxic Shock Syndrome With Inducibility of Toxic Shock Syndrome Toxin-1 Production.Frontiers in microbiology · 2022Article
- The SrrAB two-component system regulatesProceedings of the National Academy of Sciences of the United States of America · 2020Article
- A study on the microbial quality of sealed products for feminine hygiene.Journal of preventive medicine and hygiene · 2018Article
- The effect of vaginal microbial communities on colonization by Staphylococcus aureus with the gene for toxic shock syndrome toxin 1 (TSST-1): a case-control study.Pathogens and disease · 2018Article
- Accessory gene regulator (Agr) functionality in Staphylococcus aureus derived from lower respiratory tract infections.PloS one · 2017Article
- Effects of Silver Sulphadiazine on Production of Extracellular Proteins by Strains of Staphylococcus Aureus Isolated from Burns Wound.Iranian journal of pharmaceutical research : IJPR · 2016Article
- Role of the siderophore transporter SirABC in the Staphylococcus aureus resistance to oxidative stress.Current microbiology · 2014Article
- Reduced aeration affects the expression of the NorB efflux pump of Staphylococcus aureus by posttranslational modification of MgrA.Journal of bacteriology · 2012Article
- At the crossroads of bacterial metabolism and virulence factor synthesis in Staphylococci.Microbiology and molecular biology reviews : MMBR · 2009Review
- CcpA mediates the catabolite repression of tst in Staphylococcus aureus.Infection and immunity · 2008Article
- The bicarbonate transporter is essential for Bacillus anthracis lethality.PLoS pathogens · 2008Article
- Effects of carbon dioxide on neurotoxin gene expression in nonproteolytic Clostridium botulinum Type E.Applied and environmental microbiology · 2008Article
- Anaerobic gene expression in Staphylococcus aureus.Journal of bacteriology · 2007Article
- Diversity of toxic shock syndrome toxin 1-positive Staphylococcus aureus isolates.Applied and environmental microbiology · 2004Article
- Characterization of virulence factor regulation by SrrAB, a two-component system in Staphylococcus aureus.Journal of bacteriology · 2004Article
- Molecular epidemiology of methicillin-resistant Staphylococcus aureus strains causing neonatal toxic shock syndrome-like exanthematous disease in neonatal and perinatal wards.Journal of clinical microbiology · 2003Article
- Bicarbonate ion stimulates the expression of locus of enterocyte effacement-encoded genes in enterohemorrhagic Escherichia coli O157:H7.Infection and immunity · 2002Article
- Repression of the Staphylococcus aureus accessory gene regulator in serum and in vivo.Journal of bacteriology · 2002Article
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2 authors.
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Abstract
The effect of O(2) and CO(2) on expression of toxic shock syndrome toxin 1 (TSST-1) by Staphylococcus aureus was investigated under controlled growth conditions with continuous-culture techniques. To stimulate TSST-1 production, air and anaerobic gas were premixed before delivery to the culture vessel. At a growth rate-or mass doubling time (t(d))-of 3 h, production of specific TSST-1 (expressed as micrograms per milligram of cell dry weight) was 5. 9-fold greater at an O(2) concentration of 4% than under anaerobic conditions. Increasing the O(2) concentration to 11% did not result in a significant increase (P> 0.05) in the rate of toxin production over that during growth in 4% O(2) but did result in a significant increase (4.9-fold; P<0.001) in the rate of toxin production over that during anaerobic growth. At a t(d) of 9 h, addition of 3.5% O(2) resulted in a 7.6-fold increase in specific TSST-1 production. When room air was sparged through a culture growing at a t(d) of 9 h, TSST-1 production increased significantly (by 3.4-fold) over that during anaerobic growth. When a growth environment of 4% O(2)-remainder N(2) was studied, no increase in TSST-1 production was observed; this was also the case with 8% O(2) at gas-flow rates of 0.1, 0.2, and 0.4 liters/min. In all experiments, production of biomass (expressed as milligrams of cell dry weight per milliliter) increased, indicating that O(2) was metabolized by S. aureus. Addition of CO(2) to the gas mix (4% O(2), 10% CO(2), 86% N(2)) resulted in a 5.1- to 6.8-fold increase in TSST-1 production over that during anaerobic growth and a 3.6-fold increase over that during growth in an environment of 4% O(2)-remainder N(2). The agr mutant strain tested produced 6.1-fold more specific TSST-1 in a growth environment of 4% O(2)-10% CO(2)-86% N(2) than during anaerobic growth. These data suggest that in this system, O(2) alone does not trigger production of TSST-1; rather, both CO(2) and O(2) are required.
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