Why is bacillus cereus not a thermophile




















However, to date, we lack knowledge on the intracellular B. In particular, a fundamental challenge is to understand how antioxidant-oxidant interactions modulate B. Bacillus cereus adaptation to acid and low oxygen environments follows pathways that look quite similar to those that have been examined and described in great detail for other bacteria. However, there are also several clear differences that warrant the further examination of the adaptation mechanisms of B.

What is clearly lagging in B. Indeed, it is now evident that sRNAs play an essential role in gene regulation under various stress conditions Babu et al. Thus, it is crucial that we uncover this important regulatory layer in B. Another issue that requires attention is the importance of cell individuality in responding to stressors. Cells in a bacterial population, even in a very uniform environment, may differ considerably with respect to the genetic program that is operative under these conditions.

Such flexibility occurs in B. It would be interesting and important to find out whether culture heterogeneity also plays a role in the responses of B. Overall, it is expected that investigations of the stress physiology of B. Omics approaches available today will lead to important discoveries that can be applied in food safety. CD wrote the paper.

MJ and PS contribute to the writing of the part one of the manuscript. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Adak, S. Direct evidence for nitric oxide production by a nitric-oxide synthase-like protein from Bacillus subtilis. Agledal, L. The phosphate makes a difference: cellular functions of NADP. Redox Rep.

Alonso-Hernando, A. Effects of exposure to poultry chemical decontaminants on the membrane fluidity of Listeria monocytogenes and Salmonella enterica strains.

Food Microbiol. Alvarez-Ordonez, A. Acid adaptation sensitizes Salmonella enterica serovar Typhimurium to osmotic and oxidative stresses. Acid tolerance in Salmonella typhimurium induced by culturing in the presence of organic acids at different growth temperatures. Arginine and lysine decarboxylases and the acid tolerance response of Salmonella Typhimurium. Andreeva, Z. Purification and cytotoxic properties of Bacillus cereus hemolysin II. Protein Expr. Antikainen, J. Armengaud, J.

Exoproteomics: exploring the world around biological systems. Expert Rev. Proteomics 9, — Babu, M. Nanobiotechnology Baida, G. Complete nucleotide sequence and molecular characterization of hemolysin II gene from Bacillus cereus. FEMS Microbiol. Banfalvi, G. Acta , — Acta Microbiol. Google Scholar.

Beecher, D. Enterotoxic activity of hemolysin BL from Bacillus cereus. Bergman, N. Transcriptional profiling of Bacillus anthracis during infection of host macrophages.

Berk, P. Acid resistance variability among isolates of Salmonella enterica serovar Typhimurium DT Bohm, M. Comparative bioinformatics and experimental analysis of the intergenic regulatory regions of Bacillus cereus hbl and nhe enterotoxin operons and the impact of CodY on virulence heterogeneity. Boonchai, N. Study on cytotoxicity and nucleotide sequences of enterotoxin FM of Bacillus cereus isolated from various food sources.

Booth, M. Discussion on simultaneous intraesophageal impedance and pH measurement of acid and nonacid gastroesophageal reflux: effect of omeprazole.

Gastroenterology Browne, N. Acid stress in the food pathogen Bacillus cereus. Budin-Verneuil, A. Bueno, E. Bacterial adaptation of respiration from oxic to microoxic and anoxic conditions: redox control.

Redox Signal. Canet, S. Involvement of phospholipids in resistance and adaptation of Escherichia coli to acid conditions and to long-term survival. Cao, Y. Crystal structure of a phosphorylation-coupled saccharide transporter. Nature , 50— Carlsson, J. Acta Vet. Ceuppens, S. Enterotoxin production by Bacillus cereus under gastrointestinal conditions and their immunological detection by commercially available kits.

Foodborne Pathog. Gastrointestinal passage of Bacillus cereus. Chen, Y. Analysis of Streptococcus salivarius urease expression using continuous chemostat culture. Streptococcus salivarius urease: genetic and biochemical characterization and expression in a dental plaque streptococcus.

Clair, G. Restricting fermentative potential by proteome remodeling: an adaptative strategy evidenced in Bacillus cereus. Proteomics 11, M CrossRef Full Text. OhrRA functions as a redox-responsive system controlling toxinogenesis in Bacillus cereus. Proteomics 94, — Expanding the known repertoire of virulence factors produced by Bacillus cereus through early secretome profiling in three redox conditions.

Contreras-Zentella, M. A novel double heme substitution produces a functional bo3 variant of the quinol oxidase aa3 of Bacillus cereus. Purification and paratial characterization. Cotter, P. Surviving the acid test: responses of gram-positive bacteria to low pH. Presence of GadD1 glutamate decarboxylase in selected Listeria monocytogenes strains is associated with an ability to grow at low pH.

Dawes, C. Salivary concentrations of urea released from a chewing gum containing urea and how these affect the urea content of gel-stabilized plaques and their pH after exposure to sucrose.

Caries Res. De Angelis, M. Arginine catabolism by sourdough lactic acid bacteria: purification and characterization of the arginine deiminase pathway enzymes from Lactobacillus sanfranciscensis CB1. De Biase, D. Glutamate decarboxylase-dependent acid resistance in orally acquired bacteria: function, distribution and biomedical implications of the gadBC operon. De Sarrau, B. Influence of anaerobiosis and low temperature on Bacillus cereus growth, metabolism, and membrane properties.

Deutscher, J. How phosphotransferase system-related protein phosphorylation regulates carbohydrate metabolism in bacteria. Didier, A. Monoclonal antibodies neutralize Bacillus cereus Nhe enterotoxin by inhibiting ordered binding of its three exoprotein components. Dubbs, J. Peroxiredoxins in bacterial antioxidant defense.

Subcell Biochem. Duport, C. Ebner, P. Excretion of cytoplasmic proteins in Staphylococcus is most likely not due to cell lysis. Excreted Cytoplasmic proteins contribute to pathogenicity in Staphylococcus aureus.

Eisenreich, W. C isotopologue perturbation studies of Listeria monocytogenes carbon metabolism and its modulation by the virulence regulator PrfA.

Esbelin, J. ResDE-dependent regulation of enterotoxin gene expression in Bacillus cereus : evidence for multiple modes of binding for ResD and interaction with Fnr.

ApoFnr binds as a monomer to promoters regulating the expression of enterotoxin genes of Bacillus cereus. BMC Microbiol. Fagerlund, A. Bacillus cereus Nhe is a pore-forming toxin with structural and functional properties similar to the ClyA HlyE, SheA family of haemolysins, able to induce osmotic lysis in epithelia.

Microbiology , — Fang, Z. Cross-functionalities of Bacillus deacetylases involved in bacillithiol biosynthesis and bacillithiol-S-conjugate detoxification pathways. Fortier, L. Fozo, E. Low pH-induced membrane fatty acid alterations in oral bacteria. Shifts in the membrane fatty acid profile of Streptococcus mutans enhance survival in acidic environments.

Frees, D. Identification of proteins induced at low pH in Lactococcus lactis. Garcia, L. The succinate:menaquinone reductase of Bacillus cereus : characterization of the membrane-bound and purified enzyme. Geng, H. Characterization of ResDE-dependent fnr transcription in Bacillus subtilis. Gohar, M. The PlcR virulence regulon of Bacillus cereus.

Gonzalez-Flecha, B. Metabolic sources of hydrogen peroxide in aerobically growing Escherichia coli. Gotz, F. Excretion of cytosolic proteins ECP in bacteria. Griswold, A. Characterization of the arginine deiminase operon of Streptococcus rattus FA Gueriri, I. The Pta-AckA pathway controlling acetyl phosphate levels and the phosphorylation state of the DegU orphan response regulator both play a role in regulating Listeria monocytogenes motility and chemotaxis.

Gusarov, I. S-nitrosylation signaling in Escherichia coli. Bacterial nitric-oxide synthases operate without a dedicated redox partner. Hanna, M. Hardy, S. CytK toxin of Bacillus cereus forms pores in planar lipid bilayers and is cytotoxic to intestinal epithelia. Helmann, J.

Bacillithiol, a new player in bacterial redox homeostasis. Henderson, B. Bacterial virulence in the moonlight: multitasking bacterial moonlighting proteins are virulence determinants in infectious disease. Higuti, I. Studies on the ATPase of Bacillus cereus. Cell Biochem. Hoe, C. Bacterial sRNAs: regulation in stress.

Imlay, J. The molecular mechanisms and physiological consequences of oxidative stress: lessons from a model bacterium. Ivanova, N. Genome sequence of Bacillus cereus and comparative analysis with Bacillus anthracis. Nature , 87— Jayaraman, G. Transcriptional analysis of the Streptococcus mutans hrcA, grpE and dnaK genes and regulation of expression in response to heat shock and environmental acidification.

Jessberger, N. From genome to toxicity: a combinatory approach highlights the complexity of enterotoxin production in Bacillus cereus. Jiang, D. Jobin, M. Acid tolerance response is low-pH and late-stationary growth phase inducible in Bacillus cereus TZ Kalkowski, I. Metabolism of nitric oxide in denitrifying Pseudomonas aeruginosa and nitrate-respiring Bacillus cereus.

Kanjee, U. Mechanisms of acid resistance in Escherichia coli. Kayser, M. Dichloromethane metabolism and C1 utilization genes in Methylobacterium strains. Kieboom, J. Arginine-dependent acid resistance in Salmonella enterica serovar Typhimurium. Korner, H. Phylogeny of the bacterial superfamily of Crp-Fnr transcription regulators: exploiting the metabolic spectrum by controlling alternative gene programs.

Kreft, J. Cloning and expression in Escherichia coli and Bacillus subtilis of the hemolysin cereolysin determinant from Bacillus cereus. Kullen, M. Kwon, Y. Induction of acid resistance of Salmonella typhimurium by exposure to short-chain fatty acids.

Survival of a Salmonella typhimurium poultry isolate in the presence of propionic acid under aerobic and anaerobic conditions. Anaerobe 4, — Lage, C. Laouami, S. Lactate dehydrogenase A promotes communication between carbohydrate catabolism and virulence in Bacillus cereus.

Le Lay, J. Reducing activity, glucose metabolism and acid tolerance response of Bacillus cereus grown at various pH and oxydo-reduction potential levels. Li, Y. Cell density modulates acid adaptation in Streptococcus mutans : implications for survival in biofilms. Lidder, S. Vascular effects of dietary nitrate as found in green leafy vegetables and beetroot via the nitrate-nitrite-nitric oxide pathway.

Lindback, T. Characterization of the Bacillus cereus Nhe enterotoxin. CodY, a pleiotropic regulator, influences multicellular behaviour and efficient production of virulence factors in Bacillus cereus. Liu, Y. Mycothiol protects Corynebacterium glutamicum against acid stress via maintaining intracellular pH homeostasis, scavenging ROS, and S-mycothiolating MetE. Loi, V. Redox regulation by reversible protein S-thiolation in bacteria.

Lumppio, H. Rubrerythrin and rubredoxin oxidoreductase in Desulfovibrio vulgaris : a novel oxidative stress protection system. Lund, T. A new cytotoxin from Bacillus cereus that may cause necrotic enteritis.

Luo, S. Methionine in proteins defends against oxidative stress. Mackay, E. The concentration of urea in the blood of normal individuals. Madegowda, M. Proteins 71, — Madeira, J. Time dynamics of the Bacillus cereus exoproteome are shaped by cellular oxidation. Data Brief. Deciphering the interactions between the Bacillus cereus linear plasmid, pBClin15, and its host by high-throughput comparative proteomics.

Selenium exists in the soil as trace element and is very important component of human diet, while its high concentration is toxic Rayman Rayman MP.

The importance of selenium to human health. Three forms of selenium selenate, selenite and elemental selenium are more prominent in nature. Selenate and selenite are toxic while elemental selenium being the insoluble in water is less mobile and usually remains in the soils posing a smaller risk to the environment Fesharaki et al. Biosynthesis of selenium nanoparticles using Klebsiella pneumoniae and their recovery by a simple sterilization process.

Braz J Microbiol. Biological methods for the remediation of toxic forms of chromium and selenium are environment friendly Hunter Hunter W. An Azospira oryzae syn Dechlorosoma suillum strain that reduces selenate and selenite to elemental red selenium. Curr Microbiol. Bio-Reduction of selenite to elemental red selenium by Tetrathiobacter kashmirensis.

Genetic correlation between chromium resistance and reduction in Bacillus brevis isolated from tannery effluent. J Appl Microbiol. Bioremediation is inexpensive and established technology, which is commonly used in the environment without posing any damaging effects to the ecosystem Khan et al. Role of plant growth promoting rhizobacteria in the remediation of metal contaminated soils. Environ Chem Lett.

The purpose of this study was to isolate novel microbes, especially from some extreme environment and to utilize them for the bioremediation of chromium and selenium polluted soils and wastewater. Bacterial strains used in this study were isolated from the northern hilly ft geothermal springs of Hunza Gilgit, Pakistan.

Water and soil samples were collected and transported to the laboratory in controlled conditions. Water and soil samples were diluted and spread on nutrient agar plates and incubated at different temperatures. After 24 h, different colonies of strains were picked and purified. The strains were basically characterized morphologically and biochemically following Gerhardt et al.

Methods for general and molecular bacteriology. American Society for Microbiology, Washington, D. C; Metal resistance profile of the isolated strains was also determined against copper, cadmium, mercury, manganese, zinc, arsenic, chromium and selenium. Reduction of hexavalent chromium by Pseudomonas fluorescens LB in batch and continuous cultures. Appl Microbiol Biotechnol. About mL of chromium reduction media was prepared and inoculated with 1. On regular time period, flasks along with samples were withdrawn and Cr VI reduction was estimated by using 1,5-diphenylcarbazide following Clesceri et al.

Standard methods for the examination of water and waste water. All the selenite reduction experiments were carried out under aerobic conditions. Selenite reduction was monitored at same temperatures, pH, incubation times and initial Na 2 SeO 3 concentrations as in the above experiment.

Two hundred and fifty milliliter of selenite reduction medium was prepared and inoculated with 1. Medium was also amended with sodium acetate 2. At 48 and 96 h incubation, cultures were withdrawn taking 1.

An automated fluorimetric method for determination of nanogram quantities of selenium. Analytica Chimica Acta. For the exact identification of these strains TA2 and TA4 , ribotyping was carried out. More than 50 bacterial strains were isolated from the soil and water of geothermal springs of Chillas.

On the basis of various morphological, biochemical, physiological and 16S rRNA gene sequencing study, both the strains were identified as Bacillus cereus Table 1. The accession number of strains B. Cereulide intoxication is frequently associated with the consumption of starchy, cooked food such as rice or pasta dishes. Only a minority of B. These enterotoxins are sensitive to heat, acid and proteolysis and typically cause abdominal pain and diarrhea toxicoinfection.

The incubation time of the diarrheal disease is 6 to 24 hours. In contrast to the spores, most ingested cells as well as potentially present enterotoxins are inactivated during gastro-intestinal passage. It is assumed that only vegetative cells that rapidly reach the mucus layer of the small intestine can contribute to enterotoxin production.

Opinion 1 Date Title Size Follow us: Recommend page Print page Bookmark page. Department 4 Biological Safety. BfR-Committees Biological Hazards. Cookie Notice This site only uses cookies to offer you a better browsing experience. Bacillus cereus bacteria in foodstuffs may cause gastrointestinal diseases.



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